13572 Closed Entry-Level Biotechnology & Life Science Job Postings
This list includes jobs asking for Associates, Bachelors or Masters degrees and is available in three formats: chronological, alphabetical and geographical. We also keep records of all the old jobs we have posted that are no longer open: Entry-level History
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| Job Information | Description | Date Added | |
| 1 | Eyepoint Pharmaceuticals Watertown, MA Process Engineer I Bachelor of Science, Engineering Exp: 1-2 years |
EyePoint is seeking a motivated Process Engineer I with excellent interpersonal skills to join our team. This person will be responsible for process sustaining and improvement of all components, device and packaging related projects. This position requires the application of continuous improvement, equipment oversight, trending, layout plans, testing, data analysis and report writing to resolve and improve manufacturing efficiencies. Candidate must be able to effectively collaborate with internal R&D, Quality, Regulatory and Operations departments and with external vendors and suppliers to deliver against project timelines and maintain process sustaining activities. The ideal candidate possesses the ability to develop credibility and trust as a technical resource to contribute to the company’s growth, productivity, and innovation. | 11/27/2024 |
| 2 | Freudenberg Carpinteria, CA Manufacturing Quality Engineer I Bachelor of Science Degree in Engineering or related field Exp: 0-3 years |
Participate in Measurement System Analysis activities including Gage RnR, Test Method Validations, Test Procedures, etc. as part of the Design Transfer process. Aid standardization initiatives for Quality Engineering at the site level and partners with other Freudenberg Medical facilities. Support and develop validation protocols and reports (IQ/OQ/PQ) and provide objective evidence that equipment, processes, test methods and product meet requirements and are compliant with applicable regulations. Uses statistical tools (Minitab, etc) to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE). Assist Quality Engineering on MRB review of nonconforming products; recommends disposition and corrective actions. Performs complaint analysis investigations and trend reporting. Audit the Line’s production paperwork for accuracy; help drive the Line toward 100% first pass yield on DHR | 11/27/2024 |
| 3 | FUJIFILM Diosynth Biotechnologies Thousand Oaks, CA Quality Control Associate Operations Bachelor’s degree Exp: 0-3 years |
The QC Associate Operations position is responsible for executing sample management activities, which include control, receipt, and distribution of product, intermediates, raw materials samples, sample retention, reference samples, and stability samples at Fujifilm Diosynth Biotechnologies California (FDBC). The QC Associate Operations position will interact regularly with internal QC, Quality Assurance, Manufacturing, Warehouse and Facilities groups. In addition to external Quality representatives supporting client requests and/or notifications. This position is expected to carry out all their activities in compliance with FDBC Quality processes, the requirements of the Quality Management System, and in compliance with regulation requirements governing laboratory controls and manufacturing. Individuals in this role are customer service-oriented, demonstrate fundamental awareness of verbal and written communication, problem solving, critical thinking, and time management. And role model company core values of trust, delighting our customers, Gemba, and Genki. | 11/27/2024 |
| 4 | Cook Medical Bloomington, IN Senior Material Scientist Master of Science degree in Materials Science or Polymer Science Exp: 1 year |
Support pre/post-market engineering by solving material problems to develop and improve medical devices and manufacturing processes and advance the strategic goals of the company. | 11/11/2024 |
| 5 | Abbott Sylmar, CA Technical Services Engineer I Bachelors Degree - (Preferred Electrical Engineering, Biomedical Engineering ) Exp: 0-2+ years |
Functioning under general supervision, provides independent clinical and technical support in response to inquiries from physicians, health care professionals, patients and field staff using professional knowledge and judgment. This level of the Technical Service Engineer (TSE) provides the clinical and technical interface between the medical community and various departments through consultation. Requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more biomedical engineering or other medical-related academic course of study. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness. Stays abreast of and consults on technical advancements. Promotes the process of continuous quality improvement and risk management, and coordinates solutions for technical and project issues. | 11/04/2024 |
| 6 | Catalent San Diego, CA Process Engineer I Master’s degree of Engineering Exp: 0+ years |
Catalent Pharma in San Diego, CA is hiring a Pharmaceutical Process Engineer I. The Pharmaceutical Process Engineer I reports to the Process Engineer Supervisor. An individual at the level of Process Engineer I will be expected to understand and execute basic setup, operation, troubleshooting, breakdown, and cleaning of designated small scale and pilot scale pharmaceutical manufacturing equipment under limited supervision. Equipment maintenance activities may include the purchasing and installation of spare parts and supplies. This individual will complete projects and demonstration batches, evaluating the formulation, equipment set points, and process procedures with supervision. Analysis of various product characteristics will be completed with minimal supervision. The Process Engineer I will participate in the technology transfer process to the manufacturing group and may participate in the batch record review process to identify risks. Other duties include supporting the manufacturing group in the GMP (Good Manufacturing Practices) suites as subject matter expert for designated projects. Other duties include the revision of SOPs (Standard Operating Procedures), as well as researching and onboarding new equipment under the direction of a senior engineer. | 11/04/2024 |
| 7 | Catalent San Diego, CA Quality Control Chemist I Bachelor’s degree in Chemistry or Biochemistry highly preferred Exp: No exp |
Catalent Pharma in San Diego, CA is hiring a Quality Control (QC) Chemist I. The QC Chemist I will be responsible for performing various analytical techniques and common standard lab practices in order to assess the quality of pharmaceutical products under cGMPs (as applicable) and limited supervision. This position gives opportunities to broaden analytical understanding and learn the common operations in a fast-paced, early Phase-focused, dynamic Quality Control group. | 11/04/2024 |
| 8 | Catalent San Diego, CA Process Engineer I Master’s degree of Engineering Exp: No exp |
Catalent Pharma in San Diego, CA is hiring a Pharmaceutical Process Engineer I. The Pharmaceutical Process Engineer I reports to the Process Engineer Supervisor. An individual at the level of Process Engineer I will be expected to understand and execute basic setup, operation, troubleshooting, breakdown, and cleaning of designated small scale and pilot scale pharmaceutical manufacturing equipment under limited supervision. Equipment maintenance activities may include the purchasing and installation of spare parts and supplies. This individual will complete projects and demonstration batches, evaluating the formulation, equipment set points, and process procedures with supervision. Analysis of various product characteristics will be completed with minimal supervision. The Process Engineer I will participate in the technology transfer process to the manufacturing group and may participate in the batch record review process to identify risks. Other duties include supporting the manufacturing group in the GMP (Good Manufacturing Practices) suites as subject matter expert for designated projects. Other duties include the revision of SOPs (Standard Operating Procedures), as well as researching and onboarding new equipment under the direction of a senior engineer. | 11/04/2024 |
| 9 | Catalent Madison, WI Associate Engineer – Engineering Bachelor's degree in Engineering or related scientific field Exp: 1-2 years |
The Associate Equipment Engineering candidate will work on the Equipment team within the Engineering department. The candidate will interact with Operations, Supply Chain, Process Development, Validation, Procurement, Manufacturing Science and Technology (MS&T) and Quality. | 11/04/2024 |
| 10 | Catalent Madison, WI Process Engineer - Manufacturing Science & Technology Master’s degree in a STEM discipline Exp: 0+ years |
The Manufacturing Sciences and Technology (MS&T) department’s primary function is to serve as an agile technical services team to support process & technology transfer (e.g., mAbs, fusion proteins, enzymes, mRNA, new modalities, etc.), process readiness and execution support related to documentation, equipment, consumables and materials, and technical writing. The MS&T organization supports the Madison facility as well as the Catalent Biologic’s network through client- facing support, on-the-floor or on-call technical coverage, as well as continuous improvement and site strategy projects. The Technology Transfer groups (Upstream and Downstream) are the technical liaisons between Process Development (internal or external) and at-scale GMP manufacturing relating to process transfer. This function includes drafting and supporting required batch documentation (i.e., gap assessments, reports, batch records, product impact), as well as process modeling and facility fit including initial bill-of-material development. | 11/04/2024 |
| 11 | MilliporeSigma San Jose, CA Process Development Scientist Master’s degree in Chemical Engineering, Pharmaceutical Sciences, Life Sciences, Chemistry, or Biochemistry Exp: 1+ years |
MilliporeSigma is looking for a Process Development Scientist to join the technical branch of the commercial organization in the greater San Francisco Bay area. The Process Development Scientist is part of a worldwide team of engineers and scientists reporting into the technical support group for MilliporeSigma’s Process Solutions business. | 11/04/2024 |
| 12 | MilliporeSigma Miamisburg, OH Associate Quality Scientist Bachelor’s Degree in Chemistry, Biology, or other Life Science Discipline Exp: 1+ years |
Evaluate stable isotope products, raw materials and in process materials according to established procedures. | 11/04/2024 |
| 13 | MilliporeSigma Bedford, MA Scientist - Viral Vector Applications Bachelor’s degree in Chemical Engineering, Cell Biology, or other Science discipline Exp: 1+ years |
The Viral Vector Applications Scientist at MilliporeSigma in Bedford, MA will play a pivotal role in supporting development of cutting-edge tools and technologies for the rapidly evolving cell and gene therapy market. The successful candidate will join a dynamic Applications team within Process Solutions R&D, specializing in upstream viral vector processing. This group is responsible for generating application data to address customer needs, enhance knowledge in the field, and demonstrate the performance of products and processes for Adeno-Associated Virus (AAV) manufacturing. The scientist in this strategic lab-based position will independently manage experiments, execute studies, analyze data, and effectively communicate results. Collaboration is essential, as the role requires close interaction with a diverse range of technical and non-technical stakeholders encompassing both internal teams and external partners. | 11/04/2024 |
| 14 | Cepheid Sunnyvale, CA Scientist II Master’s degree Exp: 0-2 years |
The Scientist II is a bench-level job focusing on real-time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001-compliant organization. The candidate will plan and execute laboratory research and demonstrate appropriate technical proficiency, scientific creativity, and collaboration with cross-functional departments. | 11/04/2024 |
| 15 | Cepheid Sunnyvale, CA Scientist II Master’s degree in Molecular biology/Microbiology/Bioinformatics or related field Exp: 1+ years |
The Scientist II position is primarily a bench level R&D job focusing on real time PCR and RT-PCR assay and product development in an FDA-QSR and ISO9001 compliant organization. This position is part of Assay R&D and will be located in Sunnyvale, CA (Onsite). At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 16 | Cepheid Lodi, CA Manufacturing Engineer Master's degree Exp: 0+ years |
The Manufacturing Engineer II is responsible for sustaining and improving Medical Injection molding tools and processes to achieve plant manufacturing objectives for safety, quality, on-time performance, and customer satisfaction. This position will give me the opportunity to gain knowledge of using the Danaher Business Systems (DBS) tools in a manufacturing environment. This position is part of the Manufacturing Engineering Department and will be located in Lodi, CA. At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 17 | Cepheid Sunnyvale, CA Senior Scientist I Master’s degree in Molecular biology/Microbiology/Bioinformatics or related field Exp: 1+ years |
The Senior Scientist I position is a bench-level job focusing on real-time PCR and RT-PCR assay verification across GeneXpert platform instruments. The candidate will plan and execute analytical studies and demonstrate appropriate technical proficiency, scientific creativity, and collaboration with cross-functional departments. May lead small studies with manageable risks and resource requirements as well as lead others to resolve project related issues. This position is part of Assay R&D and will be located in Sunnyvale, CA (Onsite). At Cepheid, our vision is to be the leading provider of seamlessly connected diagnostic solutions. | 11/04/2024 |
| 18 | Cepheid Lodi, CA Process Engineer - Day Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role would 5am-1pm, Thursday-Monday, with Tuesday and Wednesday off. | 11/04/2024 |
| 19 | Cepheid Lodi, CA Process Engineer- Split Shift Bachelor’s degree Exp: 0-1+ years |
The Process Engineer supports manufacturing operations with scientific expertise to ensure successful transfer of new products from development to manufacturing ensuring robust manufacturing processes at commercialization; failure investigation of commercialized products; support processes to ensure performance within expected parameters. Includes laboratory roles. Schedule for this role will be 1pm-9pm, Monday- Friday with Saturday and Sunday. | 11/04/2024 |
| 20 | BioLegend San Diego, CA Research Associate I - Antibody Applications Bachelor’s Degree in Biology, Immunology, Biochemistry, Neuroscience or other related fields Exp: 1 year |
Biolegend’s Research Associate position conducts antibody characterization and supports product development in Immunology, Oncology, Stem Cells and Neuroscience, encompassing various antibody applications including SDS-Page and Western blot, Immunoprecipitation, ELISA, flow cytometry, immunocytochemistry, immunohistochemistry, etc. This position will be responsible for effectively collecting, communicating and summarizing experimental data. | 10/28/2024 |
| 21 | BioLegend San Diego, CA Biochemist I - ELISA BS/BA in Biology, Chemistry, or other life science related field Exp: 1+ years |
BioLegend is seeking a highly motivated Manufacturing Associate to join the Biomarker Immunoassay team in San Diego. The Manufacturing Associate will be working closely with others in the team to ensure timely manufacturing of high-quality immunoassay products under ISO13485 standards. This role will be responsible for all aspects of product manufacturing including planning/scheduling, making and testing immunoassay components and kits, troubleshooting issues associated with product quality, and documenting and reviewing production batch records to ensure accuracy and completeness. Additional responsibilities include working with the Product Development team to ensure proper transfer of new products from Product Development to Manufacturing, filling daily immunoassay kit orders from inventoried components, and making and testing custom products in a timely manner. | 10/28/2024 |
| 22 | Bio-Rad Hercules, CA Quality Engineer I Bachelor’s degree or equivalent in a related scientific discipline Exp: 0-2+ years |
The candidate will attend cross function Daily Management meetings and represent QA following up on blocking issues and implementing countermeasures. The candidate will manage the Material Review Board and ensure thorough documentation of non-conformities and risk based determination of CAPA. The candidate will review data for trends, manage corrections and corrective action and support GSC and business partners as requested. | 10/28/2024 |
| 23 | Bio-Rad Hercules, CA QC Specialist I - Temporary Bachelor's degree or equivalent in a life science (Chemistry, Biology) or related field Exp: 0-2 years |
A typical day will involve completion of testing on assigned batches and completing paperwork/data entry into SAP to document results for review/product release. This role requires communication and coordination between team members, the supervisor and the planners to ensure that we are keeping on top of priorities to avoid backorder. Besides routine testing, a day will include attending the daily Tier 1 meetings to report on safety, quality, delivery and inventory updates. | 10/28/2024 |
| 24 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline Exp: 1-6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 10/28/2024 |
| 25 | AustinPx Georgetown, TX Process Engineer I Bachelor’s Degree in Engineering, Chemical Engineering Exp: 0-2 years |
Work within a cGMP quality system, including participating in manufacturing activities under limited supervision. Complete process development and scale up activities in collaboration with formulation development and manufacturing to enable clinical trial material manufacturing. Prepare master batch records (MBRs). Utilize statistical design of experiment and process control schemes to optimize outcomes. Solve technical issues relating to the manufacture of dose form/product using process analysis tools. Design Experiments to investigate the relationships between material attributes, process parameter/equipment selection, and product quality. Generate process development/optimization protocols and reports. Assist with all necessary activities to procure and install equipment, including developing requirements, setting up, qualification protocol writing & execution, SOP development. Scale up of manufacturing processes from pilot to commercial scale. Participate in process technical transfer of manufacturing processing to 3rd party Contract Development and Manufacturing Organizations (CDMOs) to enable commercial manufacturing. Travel to CDMOs to oversee process transfer and manufacturing. Develop a strong understanding of specific equipment utilized internally and at CDMOs. | 10/22/2024 |
| 26 | Avantor Sciences Bridgewater, NJ Associate Scientist - Upstream (mRNA) BS (biochemistry, molecular biology, cell biology, chemical engineering, bioengineering or related). Exp: 1+ year |
The successful Associate Scientist - Upstream (mRNA) candidate will bring an eagerness to learn, strive for highly productivity, be well-organized and self-motivated. This high potential role will be responsible for the hands-on execution of cell culture laboratory experiments for the process development and basic analytical studies. The hired candidate will make detailed observations, analyze data, interpret results, and exercise appropriate technical judgment in the execution of studies. | 10/22/2024 |
| 27 | Baxter Saint Paul, MN Sterility Associate I BS Degree in Science, Engineering or Math or other relevant field Exp: 1+ year |
As the site Sterility Associate, you will serve as the primary resource for the team and support development, validation and maintenance of sterilization processes and cleanroom certification. This position plays a substantial role in the qualification and/or validation of sterilization, cleanroom, equipment, raw materials, and manufacturing processes. In this role you will directly impact the health and safety of our end-users, our patients. | 10/22/2024 |
| 28 | Baxter Hayward, CA Analyst I, Quality Control Lab Bachelor’s degree in Chemistry or Biological Sciences with Analytical Chemistry Exp: 0-2 years |
Conduct specific chemical and physical analysis on medical devices through all stages of the manufacturing process from incoming raw materials to finished goods. Responsible for overall sample and materials management activities supporting the QC laboratory. | 10/22/2024 |
| 29 | Baxter Round Lake, IL Quality Lab Associate I Bachelors degree in Chemistry or Science related degree Exp: 6+ months |
The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. **This is a first shift position that will be required to work on Saturday to Tuesday to support training of analysts and to support projects and/or production, as required.** A candidate must not be allergic to Penicillin and Cephalosporin or their related products and /or materials. | 10/22/2024 |
| 30 | Baxter Cleveland, MS Process Engineer - Injection Molding Bachelor's Degree in Engineering Required (Mechanical, Industrial, Electrical, Chemical, or Polymer Science degrees are preferred) Exp: 0-2 years |
This position is a key role in the Injection Molding Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Injection Molding Operations. You will also be involved in Multi-functional project management within this role. | 10/22/2024 |
| 31 | Baxter Cleveland, MS Process Engineer - Bottled Solutions Bachelor's degree in engineering required. (Mechanical, Industrial, Electrical, or Computer degrees are preferred) Exp: 0-2 years |
This position is a key role in the Bottled Solutions Operations. Primary focus will be on implementing continuous improvement, new business, and capacity expansion projects. Additional focus will also be on manufacturing equipment reliability and process support work within the Bottled Solutions Operations. Multi-functional project management will be involved in this role as well. | 10/22/2024 |
| 32 | Baxter Mountain Home, AR Quality Lab Associate Bachelor of Science in Chemistry Exp: 0-2 years |
Responsible for the outgoing quality, safety, and efficacy of product produced at Mountain Home (relative to Chemistry Laboratory analyses) involving complex routine and non-routine testing and validation in the Chem Lab. | 10/22/2024 |
| 33 | Inotiv Raleigh, NC Associate Scientist Bachelors Degree biology or related field Exp: 0-1+ years |
Conduct GLP and non-GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays). Maintain and dose cultured cells, including primary cells and stem cells. Perform laboratory maintenance tasks (e.g. material storage and disposal, equipment monitoring/maintenance, etc.). Assist in the maintenance of supply inventories. Maintain study books. Handle data (e.g. organize data, prepare data tables). Train others in basic lab skills. Perform peer reviews of laboratory records and study documentation. Participate in the Quality Assurance audit process. | 10/22/2024 |
| 34 | Inotiv Raleigh, NC Associate Scientist Bachelors Degree biology or related field Exp: 0-1+ years |
Conduct GLP and non-GLP genetic toxicology assays (i.e. Ames, Comet, and micronucleus assays). Maintain and dose cultured cells, including primary cells and stem cells. Perform laboratory maintenance tasks (e.g. material storage and disposal, equipment monitoring/maintenance, etc.). Assist in the maintenance of supply inventories. Maintain study books. Handle data (e.g. organize data, prepare data tables). Train others in basic lab skills. Perform peer reviews of laboratory records and study documentation. Participate in the Quality Assurance audit process. | 10/22/2024 |
| 35 | Beckman Coulter Diagnostics Chaska, MN Manufacturing Controls Engineer II Master's degree in engineering Exp: 0+ years |
The Manufacturing Engineer II for Beckman Coulter Diagnostics is responsible for supporting our reagent operations equipment, assessing equipment for optimization, qualifying replacements, monitoring our processes and driving to exceed our customer’s demands to ensure our patients have the tests they need. This position is part of the Reagent Operations located in Chaska and is on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Manufacturing Engineering team and report to the Process Engineering Manager responsible for the design, implementation and support of manufacturing processes, and equipment. If you thrive in a fast-paced role and want to work to build a world-class manufacturing organization. | 10/22/2024 |
| 36 | Beckman Coulter Diagnostics Miami, FL System Integration Engineer Master’s degree in a related Engineering discipline (Electrical Engineering, Mechanical, Biomedical, Systems Engineering) Exp: 0+ years |
The Systems Integration Engineer for Beckman Coulter Diagnostics will be a critical team member working cross-functionally on programs developing new products, and in supporting legacy instrumentation in cost reduction, product design changes due to regulatory and environmental standard revisions, and customer driven product enhancements. This position is located in Miami, FL with the Hematology/Urinalysis Business Unit, and is on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will work within the Systems Engineering team and report to the Senior Manager of Systems and Hardware, New Product Development responsible for leading design tasks that create novel hardware, fluidics and electronics, and for integrating these systems, along with reagents and algorithms, into world-class clinical diagnostics analyzers. If you thrive in an amazing, innovation-oriented, challenging role and want to work to build an amazing systems engineering and test organization. | 10/22/2024 |
| 37 | Beckman Coulter Diagnostics Carlsbad, CA Technician Production Operations Bachelor’s degree Exp: 0-1+ years |
The Reagent Formulations Technician for Beckman Coulter Diagnostics is part of a formulation team responsible for the manufacturing of reagents used in the medical diagnostics field. This role is critical to the healthcare industry and to allow doctors and lab technicians to diagnose patients quickly and accurately all over the world. This fully onsite position reports to the Supervisor for Aqueous Formulations and is part of the Production Operations Department located in Carlsbad, CA. If you thrive in a fast paced, detail-oriented role and want to work to build a world-class, quality focused manufacturing organization—read on. | 10/22/2024 |
| 38 | Beckman Coulter Diagnostics Chaska, MN Quality Assurance Scientist I Bachelor´s degree in Science or Engineering related discipline Exp: 0-2 years |
The Quality Assurance Scientist I for Beckman Coulter Diagnostics is responsible for investigating customer complaints for the Immunoassay product line. This position is part of the Complaint Handling Unit located in Chaska, Minnesota and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Post Market Surveillance organization and report to the Post Market Quality Assurance Manager responsible for ensuring complaints are correctly classified, records are populated per the current procedures and policies, and are investigated in a timely manner. If you thrive in a multifunctional role and want to work to build a world-class post market surveillance organization. | 10/22/2024 |
| 39 | BD Mebane, NC Associate Quality Scientist Bachelor’s degree in Biology, Microbiology or other related Life Science Exp: 1-2 years |
Reporting to the Quality Scientist/Lab Supervisor, the BD Mebane Associate Quality Scientist is responsible for applying basic scientific principles to routine laboratory work, executing product testing, applying/interpreting scientific data of moderate complexity, ensuring good laboratory practices, and processing data generated from Quality Control testing. | 10/22/2024 |
| 40 | BD Warwick, RI Product Development Engineer 1 Bachelor's degree in engineering or other applicable science field Exp: 1 year |
Direct project responsibility for design, development of new and improved products. Performance against schedule affects commitments made in the division business plan. Recommends product specifications, drawings, documents and changes as they pertain to any new products or product modifications. | 10/22/2024 |
| 41 | Biofidelity Morrisville, NC Molecular Technologist II (2nd shift) Master’s degree in medical laboratory science or biological or chemical sciences Exp: 1+ years |
Biofidelity is seeking a Molecular Technologist II to perform high complexity diagnostic testing using Biofidelity’s ASPYRE technology, histology, and nucleic acid extraction workflows. With minimal oversight from the Supervisor, the Molecular Technologist II will be responsible for the efficient and quality execution of sample accessioning, processing, data generation, and reporting in the clinical laboratory. The ideal candidate has strong molecular biology technical skills, is collaborative, trustworthy with ability to work in a fast-paced clinical environment. This role reports to the Molecular Tech III, Team Lead. | 10/22/2024 |
| 42 | AstraZeneca Frederick, MD Quality Control Analyst (Sun-Wed) Bachelor’s degree in scientific/ biotech/ pharmaceutical or relevant field of study Exp: 0-3 years |
Join our Operations team as a Quality Control Analyst, where will be responsible for performing laboratory testing. This is an exciting opportunity to accelerate our Lean journey and take advantage of the huge opportunities to drive efficiencies in our processes and produce better-quality outputs. As a Quality Control Analyst, you will perform selected quality control testing activities, including raw materials, in process, finished product, and stability testing according to standard operating procedures. You will be responsible for conducting troubleshooting equipment problems, entering data evaluated for compliance to specifications, and reporting abnormalities. You will also be involved in writing new standard operating procedures or revising existing documentation. Your role will require you to apply critical thought to solving problems and work on problems requiring an in-depth knowledge of scientific methods and techniques. | 10/15/2024 |
| 43 | AstraZeneca Santa Monica, CA Associate, Quality Control Analytical Master's degree in Biological Sciences or related field Exp: 1 year |
We are looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis, and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 10/15/2024 |
| 44 | AstraZeneca Mount Vernon, IN Validation Engineer Bachelor’s degree in Engineering, Chemistry, Biology, or Pharmaceutical Sciences Exp: 0-3 years |
As a Validation Engineer, you will perform installation and operational and performance qualification (IQ/OQ/PQ) of critical manufacturing equipment, facilities, and utility systems. Your responsibilities will include developing and reviewing qualification protocols and reports, coordinating system and equipment documentation collection, and executing protocols. You will also solve qualification and cleaning validation execution issues using critical analysis skills and develop sound, reasoned solutions and recommendations. | 10/15/2024 |
| 45 | AstraZeneca Waltham, MA Scientists, ADC/RC Target Biology Masters degree experience in Biology, Oncology, Biochemistry, Pharmacology, Molecular Biology, Cell Biology, or a related field. Exp: 1+ years |
We are currently seeking a highly motivated Scientist (non-PhD) with strong scientific excellence and technical expertise in oncology research to join our ADC Biology and Development team at Waltham, MA USA, within the Oncology Targeted Discovery (OTD) group. | 10/15/2024 |
| 46 | Aldevron Fargo, ND Quality Control Environmental Analyst I Bachelor’s degree in microbiology or related scientific field Exp: 0-1 years |
This position is part of the Quality Control department located in Fargo, ND and will be an on-site position. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Control Environmental Monitoring Team and report to the QC Environmental Monitoring Supervisor, and be responsible for sampling, detecting, quantifying, and identifying possible contaminants that may interfere with the quality of the product during the different stages of the manufacturing process. | 10/08/2024 |
| 47 | Aldevron Madison, WI Associate Scientist II, R&D BS or MS degree in biology, molecular biology, biochemistry, chemistry, or related discipline Exp: BS: 1+ years; MS: 0+ years |
This position is part of the Research and Development Department located in Madison, WI and will be onsite. At Aldevron, we combine best-in-class products and service with the ideal operating environment to lay the groundwork for vital new discoveries worldwide. You will be a part of the Analytical Method Development team and report to the Senior Scientist responsible for analytical method development and new method research. | 10/08/2024 |
| 48 | Alloy Therapeutics Waltham, MA Research Associate – Oligonucleotide Discovery B.S. or M.S. degree in Biology or related science Exp: 1-3 years |
As a Research Associate, you will work within the RNA Medicine team in Waltham, MA. You will also collaborate with internal/external partners on nucleic acid drug discovery projects to ensure timely execution of the experiments, and delivery of high-quality data. This role will have an autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! This role will report to our RNA Senior Scientist with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! | 10/08/2024 |
| 49 | Amgen Thousand Oaks, CA Sr. Associate (Process Development) Master’s degree in Chemical Engineering, Biomedical Engineering, Biochemistry, Biotechnology, Pharmaceutics or related subject area Exp: 1+ years |
Amgen is currently seeking a Process Development Senior Associate for our Pivotal Drug Product Technologies Group in Thousand Oaks, CA. This group is responsible for late stage drug product formulation and fill/finish process development for large molecule modalities (e.g. monoclonal antibodies, bispecific T-cell engagers (BiTEs) and fusion proteins). The Sr. Associate will work closely with a team of engineers and scientists responsible for the technical aspects of Amgen’s drug product commercialization and lifecycle management. | 10/08/2024 |
| 50 | Abeona Therapeutics Cleveland, OH Quality Assurance Specialist, Supplier Quality Bachelor’s degree in related field Exp: 1 year |
The Specialist I, Supplier Quality will perform routine activities associated with manufacturing of cell and gene therapy products at the Abeona Therapeutics Inc. site in Cleveland, OH. This position supports the release of materials in support of cGMP Operations. The Specialist I, Quality Assurance will report to the Supervisor, Quality Assurance or above. | 09/30/2024 |
| 51 | Abeona Therapeutics Cleveland, OH Quality Control Transport/Microbiology Associate BS in biology, microbiology, molecular biology or other relevant discipline Exp: 1-4 years |
The Quality Control Transport/Microbiology Associate assists in all aspects of Transport of Drug Products to treatment centers for the associated drug product. In addition, Transport associate will assist in Microbiology activities in support of GMP testing for Quality Control. Interacts with employees internal and external to Quality Control. | 09/30/2024 |
| 52 | Abeona Therapeutics Cleveland, OH Sr. Associate, Manufacturing - Logistics QMS BS in life sciences, engineering, or other relevant discipline Exp: 1-4 years |
The Manufacturing Logistics QMS Senior Associate is responsible for working independently and with others to perform Quality Management System activities pertaining to the Manufacturing Department. This individual serves as an embedded quality assurance representative within the Manufacturing Department. | 09/30/2024 |
| 53 | AstraZeneca Gaithersburg, MD Associate Specialist Clinical Biologics Bachelor's degree Exp: 0-4 years |
As an Associate Specialist/Specialist in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and skillsets to perform large scale clinical development activities. You will join a collaborative and driven team in an elite biopharmaceutical company. | 09/30/2024 |
| 54 | AstraZeneca New Haven, CT Associate Scientist II, Injectable Drug Product Development Master’s degree in Chemistry, Biochemistry, Chemical Engineering, Pharmaceutical Sciences, or relevant Engineering/Life Sciences field Exp: 1+ years |
The Associate Scientist III will join Injectable Drug Product Development group to support the formulation and drug product process development of Alexion’s biotherapeutic candidates. This individual will lead and support execution of stability studies, develop fit for purpose analytical methods, perform analytical testing, and draft reports for the executed studies. This individual will work independently in a dynamic team environment and routinely collaborate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply. A general understanding of protein chemistry and machine learning based image analysis is preferred. | 09/30/2024 |
| 55 | AstraZeneca Santa Monica, CA Associate, Quality Control Analytical Master's degree in Biological Sciences or related field Exp: 1 year |
Neogene is looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis, and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 09/30/2024 |
| 56 | AstraZeneca Gaithersburg, MD Scientist, OTD Target Validation Master’s Degree in relevant discipline Exp: 1+ years |
We are seeking highly a motivated independent lab Scientist with wet-bench laboratory experience to join our Tumor Targeted Delivery team in Early Oncology in Gaithersburg, MD USA. As a Scientist, you will support target validation efforts for tumor-targeted therapies, such as antibody-drug-conjugates (ADCs) and targeted radio-conjugates. You will work collaboratively with cross-functional teams to advance pipeline programs and deepen our understanding of all aspects of target biology. | 09/30/2024 |
| 57 | AstraZeneca Santa Monica, CA Senior Associate, Quality Control Microbiology MS/MA Exp: 1+ years |
We are seeking an individual with cell therapy quality control background to join our Quality team. You will contribute to the advancement of our product pipeline by performing environmental monitoring, lot release testing and other assigned tasks. You will also be expected to independently organize, analyze results, and present conclusions. You will ensure that the QC Microbiology Laboratory is operating as expected. | 09/30/2024 |
| 58 | AstraZeneca Gaithersburg, MD Scientist in vivo - Immunology MS Exp: 1 year |
The successful candidate will be a key member of an in vivo team within the Early Respiratory & Immunology in vivo Department, performing in vivo and ex vivo studies to support a diverse range of immunology-related projects. This role specifically involves working as a lab-based scientist in the area of in vivo pharmacology. As a strongly self-motivated and independent individual you will be adept at working across functional areas, enabling you to maximize value from the available resources. The role will sometimes involve implementing protocols over timelines that extend outside of normal working patterns. The successful candidate will assist with the design, execution and analysis of experiments to generate data in support of pipeline projects. You will be expected to utilize your expertise to run various in vivo disease models, as well as provide input for the establishment of new in vivo models. | 09/30/2024 |
| 59 | AstraZeneca Frederick, MD Electrical Engineer BA/BS in Engineering/Life Sciences Exp: 0-5 years |
As an Electrical Engineer, you will be responsible for a wide range of tasks including troubleshooting motor controls, performing BMS changes, supporting automation for electrical and utility systems, and implementing operational improvements to reduce energy consumption. You will also be involved in project management, problem-solving, and communication with internal teams and external vendors. Your work will contribute to the completion of milestones associated with specific activities and you will be expected to lead moderate cross-functional teams to complete work. | 09/30/2024 |
| 60 | H.B. Fuller St. Paul, MN Scientist Master’s degree in chemistry or chemical engineering Exp: 1+ years |
The Scientist has primary responsibility for conducting research tasks coordinated by more experienced scientists and managers. In general, a Scientist conducts laboratory bench work tasks, physical testing and supports QA and Operations in trouble shooting manufacturing issues. This position is responsible for product development, cost saving initiatives, and production support. This person will be dealing primarily with moisture curing one-part and solvent free two-part technologies for adhesives, sealants, and coatings for the North America Construction Adhesives business. This includes building envelope, flooring, DIY, and other construction applications. | 09/30/2024 |
| 61 | B. Braun Medical Irvine, CA QC Chemistry Associate II (Chromatography) Bachelor's degree in a Science related field Exp: 1-2 years |
Perform routine laboratory analysis of In-Process, finished product, raw material, stability samples and environmental monitoring according to established specifications and procedures using wet chemistry techniques or various laboratory apparatus and instruments (e.g. HPLC, UV/Visible Spectrophotometer, FTIR, TOC, pH meter etc.) in compliance with B. Braun, cGMP, GLPs, SOPs, USP and FDA guidelines. | 09/30/2024 |
| 62 | Vyriad Rochester, MN Quality Control Analyst Bachelor’s degree in a science related field. Exp: 1 year |
Responsible for performing and validating analytical methods essential for quality control and release of drug product. Performs environmental monitoring of critical manufacturing areas, thus ensuring that manufacturing processes and products meet quality specifications, under moderate direction of managers and senior team members. The analyst shall maintain quality assurance processes, be responsible for testing products, recording, and analyzing data during product development and manufacturing. The analyst will follow through on set processes and ensure adherence to best production practices and product quality standards, as well as monitors the efficiency and cost-effectiveness of product output. Receives general instructions on routine work and detailed instructions on new projects or assignments. | 09/24/2024 |
| 63 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate I - In Vivo Pharmacology Bachelors in Biology related field preferred Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly motivated Research Associate I to support our in vivo pharmacology team for various projects. | 09/24/2024 |
| 64 | HD Biosciences, Inc. (Wuxi) San Diego, CA Research Associate I Bachelors in Life Sciences or related field preferred Exp: 0-1 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its Discovery Biomarkers team. We’re seeking a highly motivated Research Associate I to support our in vitro/ex vivo immunology team for various projects. | 09/24/2024 |
| 65 | WuXi AppTec Marietta, GA Associate Laboratory Technician Bachelor’s Degree Exp: 1 year |
Perform Sterility Testing in compliance with applicable Regulations, International Standards following SOPs in cleanroom type environment, perform QA/QC tasks, prep carts. | 09/24/2024 |
| 66 | WuXi AppTec Philadelphia, PA Quality Control Environmental Monitoring Associate I Bachelor’s degree with a major in Biology, Microbiology, or related Life Science Exp: 0-3 years |
The Quality Control Environmental Monitoring Associate I is responsible for performing sampling and testing in support of manufacturing and validation activities, under the direction of a Supervisor or higher. Works in a team environment with various laboratory staff. | 09/24/2024 |
| 67 | WuXi AppTec Philadelphia, PA Manufacturing Associate I - 2nd Shift Bachelor’s (science preferred) degree Exp: 0-2 years |
The Manufacturing Associate I is responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/24/2024 |
| 68 | Xilis Durham, NC Research Associate - Research & Innovation B.S. or M.S. degree in cancer biology, immunology, molecular biology or equivalent Exp: 1+ years |
The candidate will execute critical experiments in the laboratory to nurture and support Xilis' research and development team. Working very closely with thought leaders in immunology, cancer biology, and assay development, the candidate will process samples, gather data, keep meticulous notes, and participate in a detailed analysis, drawing conclusions, and formulation of next steps / experimental designs. The successful candidate will have a strong work ethic and bring exceptional skills to the laboratory with an ability to independently run complex experiments. He or she will have prior experience in primary cell culture, flow cytometry assays, molecular biology techniques, and a demonstrated ability to operate and maintain lab instrumentation and lab automation. Cross-functional team support and communication are central for this position. The candidate will report to the R&D program lead. By joining the team at an early stage, the candidate will have an outsized impact on fundamentally advancing precision cancer care therapy. | 09/24/2024 |
| 69 | YMC Devens, MA Automation Engineer – Software Bachelor’s Degree in Chemical Engineering or Electrical Engineering preferred Exp: 0-2 years |
Automation Engineer will develop, implement, and test automation/control solutions for our products. This position is customer-driven and focused and is responsible for working with current and potential clients/customers. | 09/24/2024 |
| 70 | BD Sparks, MD Quality Engineer II (Instrument Plant) MS in Mechanical or Electrical or Industrial Engineering, Biological Sciences, Chemistry, and/or Computer Science or other related field. Exp: 1 year |
The Quality Engineer II is responsible for the application and interpretation of the plant/department procedures to ensure consistency/compliance with Quality Systems. The Quality Engineer II uses the Company Quality Systems to ensure overall compliance and has the knowledge necessary to apply the appropriate statistical and analytical tools. Works with variable enterprise systems/Corporate directives to support new and/or current product lines and processes. Typical assignments may include, supporting one or more instrument platforms on sustaining items such as complaints, non-conformances and day to day issues, supporting audits, actively participating on teams, ensures documentation compliance, processing of CAPAs, change controls, and deviation waivers. Frequent interaction with other functional areas such as Research and Development, Operations, etc. is routine. The Quality Engineer II may take the lead in root cause investigations for issues of moderate complexity. | 09/24/2024 |
| 71 | BD Covington, GA Lab Technician Bachelor’s degree in Biological Science (microbiology preferred) or related scientific discipline Exp: 1+ years |
BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Become a maker of possible with us. | 09/24/2024 |
| 72 | BD Sparks, MD Quality Engineer II, Chemistry MS in Biological Sciences, Chemistry, Engineering, Computer Science and/or Regulatory Affairs or other related field is required. Exp: No Exp |
The Quality Engineer is responsible for the application and interpretation of the plant/department procedures to ensure consistency/compliance with Quality Systems. The Quality Engineer uses the Company Quality Systems to ensure overall compliance and has the knowledge necessary to apply the appropriate statistical and analytical tools. Works with various enterprise systems/Corporate directives to support new and/or current product lines and processes. Typical assignments may include performing tasks, of moderate complexity, within planned schedules and timelines, test review for ROH release, water testing and OOS support, support for Validations of equipment and test methods, audits, actively participating on teams, ensuring documentation compliance, processing of CAPAs, change controls, and deviation waivers. Frequent interaction with other functional areas such as Research and Development, Operations, Facilities, etc. | 09/24/2024 |
| 73 | Blue Life Solutions Irvine, CA Entry-Level Microbiology Associate Bachelor’s degree in microbiology, Biology, or a closely related field. Exp: Entry Level |
Blue Life Solutions, LLC is seeking a dedicated and detail-oriented Entry-Level Microbiology Associate to join our dynamic research team. The successful candidate will assist in conducting microbiological experiments, analyzing data, and maintaining laboratory equipment and records. This role offers an excellent opportunity for recent graduates to gain hands-on experience in a collaborative and innovative environment. This position is full time, fixed term (Duration: 2 years, with reevaluation for potential extension). | 09/24/2024 |
| 74 | TScan Therapeutics Waltham, MA Senior/Principal Research Associate, New Technology & Product Development M.S. in biology, immunology, pharmacology, or related field. Exp: 0-2+ years |
TScan Therapeutics is a clinical-stage biotech seeking to revolutionize life-changing therapeutics for patients by identifying novel T cells and epitopes. We are looking for an experienced researcher to join our team as Senior/Principal Research Associate, supporting the New Technology and Product Development Team. The incoming candidate will have the opportunity to work at the intersection of biology and engineering to develop the next generation of TCR-T cell products. The ideal candidate should have relevant experience in T cell immunology, primary and tumor cell culture, cell-based assays, and flow cytometry, and enjoy exciting, collaborative and vibrant startup culture. A team player with a sense of urgency will thrive in this role. | 09/18/2024 |
| 75 | Beckman Coulter Life Sciences Remote - Chicago, IL Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 76 | Beckman Coulter Life Sciences Remote - Southern, IL Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 77 | Beckman Coulter Life Sciences Remote - Milwaukee, WI Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 78 | Beckman Coulter Life Sciences Remote - St. Louis, MO Associate Field Service Engineer Bachelor's degree (B.S./B.A.) in mechanical, electrical, biological science, engineering Exp: No Exp |
The Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and repair of Beckman Coulter products at customer sites. This entry-level position works under close supervision and mentoring by a manager, regional specialist, and senior engineers within the territory. Tasks are performed independently as proficiencies are developed. This position is remote based in either Chicago, IL, Southern, IL, Milwaukee, WI, OR St. Louis, MO | 09/18/2024 |
| 79 | Vaxcyte San Carlos, CA Associate Scientist II, Analytical Development MS in Chemistry, Analytical Chemistry preferred, Organic / Biochemistry Exp: 1-4 years |
Looking for an energetic and talented individual to join our Analytical Development team. Primary responsibility for the incumbent will be to support the developmental activities currently on going in the laboratory as assigned. | 09/18/2024 |
| 80 | Velocity Clinical Research Union, SC Clinical Research Coordinator I Bachelor’s degree in Science or Engineering Discipline preferred. Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 09/18/2024 |
| 81 | Velocity Clinical Research Albuquerque, TX Clinical Research Coordinator I Bachelor’s degree in Science or Engineering Discipline preferred. Exp: 1 year |
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. | 09/18/2024 |
| 82 | VGXI Conroe, TX Process Development Technician Bachelor’s degree Exp: 1-3 years |
Conduct research scale production of plasmid DNA on an ongoing basis. Perform and document routine maintenance on PD equipment. Assist the execution and analysis of data for the purpose of fermentation and purification process development. Assist the analysis of samples from cGMP seed banking, fermentation and purification processes. Assist experiments to evaluate new technologies as designed and supervised by senior team members. Maintain a clean and organized laboratory environment. | 09/18/2024 |
| 83 | Stryker Remote, Customized Implant Design Engineer Bachelor of Science in Engineering, Mechanical Engineering, or Biomedical Engineering Exp: 0+ years |
Stryker is seeking to hire a Design Engineer to support Stryker Craniomaxillofacial (CMF) Division. This role has a direct impact on healthcare by designing customized patient implants. This is a remote role supporting the West Coast, and it requires working standard business hours in either the Pacific or Mountain Time Zone. | 09/11/2024 |
| 84 | Sunbird Bio Cambridge, MA Research Associate BS or MS in biology, chemistry, biochemistry, or biomedical/chemical engineering or similar discipline Exp: 1-3+ years |
The Product Development team at Sunbird Bio's U.S. headquarters in Cambridge, Massachusetts, is searching for an innovative, motivated, and inquisitive Research Associate to help advance our neurodegenerative disease programs along the development pipeline. The ideal candidate will leverage their technical immunoassay experience to discover new biomarkers to further understand neurodegenerative disease signatures in blood samples. | 09/11/2024 |
| 85 | Sunflower Therapeutics Medford, MA Bioprocess Engineer Bachelor’s degree in chemical engineering or equivalent Exp: 1-3 years |
Sunflower Therapeutics is recruiting a motivated and highly organized individual to support its mission to deliver protein manufacturing solutions that anyone can use to create innovative new medicines, food products, and other bio-based products. Sunflower is advancing “right-sized” and ecient approaches to democratize protein manufacturing using strain engineering, integrated process development, and automated small-footprint facilities Reporting to the Director of Engineering Operations, the Bioprocess Engineer will be responsible for supporting engineering operations at Sunflower Therapeutics to enable the advancement of Sunflower’s protein manufacturing equipment prototypes. This individual will assist in the design, development, testing, and implementation of biomanufacturing systems for recombinant proteins. A successful candidate will be able to utilize bioprocess data to interpret product and process requirements and ensure the hardware design meets specified and operational standards. This individual will diagnose technical problems across system functions and suggest and carry out creative and timely solutions. As Sunflower grows, the Bioprocess Engineer will contribute to the continuous improvement of Sunflower’s automated multi-product protein manufacturing systems. | 09/11/2024 |
| 86 | Takeda Boston, MA Associate Product Manager / Product Manager, Shared Platforms & Services BS/BEng in a technically relevant field of study (e.g. Engineering, Information Technology, Computer Science, Computer Engineering) Exp: 1-3 years |
Are you looking for a patient-focused, innovation-driven company that will inspire and empower you to shine? Join us as a Product Manager on the Shared Platforms & Services Team in Takeda’s Global Data, Digital, and Technology (GDD&T) team based in Cambridge, Massachusetts. The Shared Platforms & Services Team is a global team that allows Takeda to design, develop, and deploy externally facing digital solutions to patients and healthcare professionals (HCPs). Our team of software engineers and IT professionals share a passion for building trail-blazing digital solutions, while ensuring quality and compliance are followed to the highest standards. Our team works closely with local business teams, commercial, drug product teams, and research & development as key compliance enablers for both internal and external partners developing digital health solutions. The Product Manager will own the vision and product strategy for an internally facing compliance platform and the administration of Takeda’s digital asset compliance process framework. | 09/11/2024 |
| 87 | Takeda Boston, MA Cell Therapy Data Engineer Master’s degree in Information Technology, Information Systems, Data Analytics, Engineering, Computer Science, or related field Exp: 1 year |
Takeda Development Center Americas, Inc. is seeking a Cell Therapy Data Engineer in Cambridge, MA with the following requirements: Master’s degree in Information Technology, Information Systems, Data Analytics, Engineering, Computer Science, or related field plus 1 year of related experience. Prior experience must include: Utilize computing languages including R, C/C++, Python, and Java; Apply knowledge in distributed computing, databases (e.g., SQL), relational databases (e.g., PostgreSQL), and Amazon Web Services; Demonstrate experience in database programming and development of dashboards; Demonstrate experience in data integration, programming, and the objective evaluation & utilization of analytical tools & libraries. | 09/11/2024 |
| 88 | Takeda Social Circle, GA Sr QA Technician Bachelor's degree in scientific discipline Exp: No exp |
As the Sr QA Technician, you will be responsible for inspection of production materials, components, and chemicals to the Manufacturing facility. You will identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Takeda Quality practices. You will demonstrate effectiveness in task completion, decision-making and handling multiple projects. The hours of this position are 12PM-8:30PM, Monday-Friday; weekend and holiday work. Overtime may be required. | 09/11/2024 |
| 89 | Takeda Boston, MA Senior Research Associate I, IVS Imaging Technician MS in a scientific discipline (or equivalent) Exp: 1+ years |
Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a Senior Research Associate I, IVS Imaging Technician in our Cambridge, MA location. As a Senior Research Associate I, IVS Imaging Technician, you will perform complex animal manipulations for imaging procedures, supporting multiple therapeutic areas of the Company including Oncology, Drug Metabolism and Pharmacokinetics, CNS, GI and Imaging. You will also perform advanced dosing and biomethodology, sample collection, and animal procedures with efficiency, accuracy and attention to detail. As part of the Comparative Medicine team, you will report to Associate Director, Comparative Medicine and work with other groups within Preclinical and Translational Sciences. | 09/11/2024 |
| 90 | Takeda Boston, MA Research Senior Associate, IBD/GI MS in a scientific discipline (or equivalent) Exp: 1+ years |
At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Research Senior Associate, IBD/GI, Inflammation Research where you will e part of a team focused on validation of novel targets and the evaluation of drug candidates for the treatment of chronic fibroinflammatory diseases. | 09/11/2024 |
| 91 | TG Therapeutics Remote, NY Research and Development Associate BS/BA or MS/MA/PhD degree in a scientific discipline Exp: 1 year |
We are seeking a dynamic and proactive Research and Development Associate to join our Regulatory Affairs team. This role will be instrumental in supporting the various aspects of product development including nonclinical and clinical research. The ideal candidate will have a strong life sciences background, with a passion to build a career in the pharmaceutical industry. We are looking for a highly motivated individual, who can be a team player and an independent thinker. This role will report to the Associate Director, Regulatory and Development Strategy. We are looking to fill this role in the Summer of 2024. | 09/11/2024 |
| 92 | Thermofisher Greenville, NC QC Scientist II (Lab Services) Master's of Science in Chemistry, Biochemistry, Biology, or related physical science. Exp: 1-2 years |
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or growing productivity in their laboratories, we are here to support them. You will make an impact to our society by ensuring drug products manufacture onsite are safe and have excellent quality by performing various tests in a GMP laboratory. | 09/11/2024 |
| 93 | Thermofisher Remote/Knoxville, TN Engineer II, Field Service - SEM/TEM/FIB University degree in electronics, physics, engineering, computer science or similar field preferred Exp: 1-5 years |
The Field Service Engineer II for the Materials and Structural Analysis Division (MSD) of Thermo Fisher Scientific is responsible for performing the on-site installation, servicing and repair of complex equipment and systems. Engineers investigate and improve operational quality of system equipment; Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Small/Large Dual Beam (SDB/LDB); instruct customers in the operation and maintenance of the system; serve as company liaison with customer on administrative and technical matters for assigned projects; and conduct on-site installations of the full range of Thermo Fisher Scientific electron microscopy systems and their associated options. | 09/11/2024 |
| 94 | Thermofisher Greenville, NC Formulation Technician II Bachelor’s Exp: No exp |
The Formulation Technician II will be responsible to produce sterile injectables and work on problems of moderate scope where analysis of situations or data requires a review of a variety of factors. This colleague follows written and verbal instructions when performing the following duties. | 09/11/2024 |
| 95 | Thermofisher Remote/Boston, MA Engineer I, Field Service Bachelor’s degree in engineering, biology, chemistry, or related field. Exp: 1-3 years |
The Field Service Engineer (FSE) performs customer installs, repairs and preventative maintenance on a variety of laboratory instruments in assigned territory. The FSE engages with customers and provides the highest quality of service in a professional and timely manner. | 09/11/2024 |
| 96 | Thermofisher Logan, UT Engineer II, Mechanical Master's degree in Engineering (mechanical or chemical) Exp: 1 year |
Thermo Fisher Scientific is seeking a motivated Sustaining Engineer to join our R&D engineering team in Logan, UT. As part our Bioproduction Group, you will have the opportunity to support the developers and manufacturers of biological-based therapeutics and vaccines. Drive process and product innovation by adapting both existing and novel single-use technologies. Support new and existing product development pipeline through collaboration with the R&D teams to generate new product ideas, evaluate existing product and evaluate new technologies for feasibility and application into bioprocess workflows. Drive activities, including hands-on and delegated testing, writing test plans and results, presentations, interpretation of data and collaborate multi functionally to meet the business needs. | 09/11/2024 |
| 97 | Revvity San Diego, CA Research Associate I - Antibody Applications (IHC, ICC, Flow Cytometry, WB) Bachelor’s or Master's Degree in Biology, Immunology, Biochemistry, Neuroscience or other related fields Exp: 1 year |
Biolegend’s Research Associate position conducts antibody characterization and supports product development in Immunology, Oncology, Stem Cells and Neuroscience, encompassing various antibody applications including SDS-Page and Western blot, Immunoprecipitation, ELISA, flow cytometry, immunocytochemistry, immunohistochemistry, etc. This position will be responsible for effectively collecting, communicating and summarizing experimental data. | 09/05/2024 |
| 98 | Revvity San Diego, CA Research Associate I - Tissue Culture Bachelor of Science in biology or a related field Exp: 1+ years |
This position is responsible for developing cutting-edge recombinant protein/antibody products in the Molecular & Cellular Biology (MCBio) group. The research associate will be involved in developing new lines of recombinant protein/antibody products by supporting projects and team members. The duties include preparing buffer solutions and cell culture media, maintaining cells cultures, and purifying recombinant proteins/antibodies according to standard operating procedures. Other job responsibilities include transferring the products to other groups for testing, preparing product/project-related documentation, and maintaining the inventory and record for recombinant protein/antibody products. This role will also support R&D projects to increase efficiencies or develop new technologies for the group. | 09/05/2024 |
| 99 | Revvity Lafayette, CO Scientist I Bachelor's degree in chemistry or a life sciences discipline Exp: 1-3 years |
Revvity has a rewarding and exciting opportunity for an enthusiastic Scientist 1 for our Custom Synthetic Manufacturing laboratory. The Scientist 1 position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO, Key responsibilities for this position include a wide array of duties related to the manufacturing of RNA and DNA oligonucleotides. This includes custom synthesis, cleaving, quality and quantity determination of product for customers. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 09/05/2024 |
| 100 | Hologic San Diego, CA Research Associate 2 B.A. /B.S. Molecular Biology, Chemistry, Biochemistry or related field Exp: 1-3 years |
Hologic is seeking a Research Associate 2 responsible for designing and performing experiments to support assay development including: feasibility, design transfer, assay integration and assay verification. Candidate accountable for effectively communicating results, collaborating with team members, and troubleshooting. | 09/05/2024 |
| 101 | Hologic Newark, DE Senior EMC/RF Compliance Engineer Master’s Degree Exp: 1-3 years |
The Senior Compliance Engineer will be responsible for defining and executing product compliance strategies, policies, and processes to ensure that the company’s products meet regulatory standards and compliance certifications are obtained and maintained for global markets (e.g., ISO, FCC, UL, IEEE). The Senior Compliance Engineer will work closely with regulatory agencies and is the technical subject matter expert for regulatory compliance. Apply today! | 09/05/2024 |
| 102 | Hologic San Diego, CA Mechanical Design Engineer 1 BS in Mechanical Engineering Exp: 0-3 years |
In this role, you will be part of a multidisciplinary engineering team developing and sustaining medical diagnostic instruments including mechanical design and manufacturing. You will be expected to bring hands-on experience and knowledge in mechanical design and manufacturing while utilizing sound engineering judgement and first principals. You will be expected to design, prototype, and test various electromechanical concepts to provide rapid feedback and direction to the broader development team to drive fast and decisive decisions. Interfacing with outside vendors on rapid prototyping, machining, molding, and advanced manufacturing processes is required. This is a fast-paced position that demands the ability to quickly adapt to evolving changes within the instrument, assay, and user needs. You will be working across functional groups such as Systems Engineering, Assay Development, Manufacturing, and Process Transfer. Clear communication, the ability to collaborate with others, and being a self-starter are a must. | 09/05/2024 |
| 103 | HD Biosciences San Diego, CA Research Associate I Bachelors in Life Sciences or related field preferred Exp: 0-1 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its Discovery Biomarkers team. We’re seeking a highly motivated Research Associate I to support our in vitro/ex vivo immunology team for various projects. | 09/05/2024 |
| 104 | WuXi Advanced Therapies Philadelphia, PA Manufacturing Associate I - 1st Shift Bachelor’s (science preferred) degree Exp: 0-2 years |
The Manufacturing Associate I is responsible for manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 09/05/2024 |
| 105 | HD Biosciences San Diego, CA Research Associate II (Temp/Contingent) Master degree in Molecular and Cell Biology or Bachelor degree Exp: 1-2 years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 09/05/2024 |
| 106 | Stability Biologics San Antonio, TX QA Specialist BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.) Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 09/05/2024 |
| 107 | RayzeBio Indianapolis, IN Radiopharmaceuticals Production Operator II Bachelor’s Degree in a STEM field Exp: 1-4 years |
The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is right the first time and that the production area is kept in order at our manufacturing site in Indianapolis IN. You will be responsible for the production of RayzeBio drug products, strictly complying with good manufacturing practice and aseptic requirements. Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. As RayzeBio expands the production site and its portfolio of new products, the Production Operator will support validation work for future company initiatives, and support management with internal projects and new hire training. The Radiopharmaceuticals Production Operator will report directly to the Production Manager. Operator level will be evaluated with experience and qualifications. | 08/30/2024 |
| 108 | RayzeBio San Diego, CA Associate Scientist I/II, Chemistry BS or MS in Chemistry or related field with strong understanding of organic and analytical chemistry Exp: BS 2-5 years’ or MS 0-4 years’ |
The Associate Scientist will work as part of a team of scientists to synthesize and design analogs to optimize potency, pharmacokinetics, and in vivo efficacy of potential drug candidates. | 08/30/2024 |
| 109 | Reckitt St. Peters, MO Project Engineer B.S. Engineering Discipline (Electrical, Chemical, Mechanical) Exp: 1-3 years |
Seeking an engineering leader eager to make an impact! As the Engineering Manager within one of our agile-factory teams, you'll be the spark that drives project efficiency and innovation. Be at the forefront of managing an exceptional team, turning strategic plans into reality and leading the charge in our manufacturing success. Standard engineering is not what we do – we're about pioneering. If you're passionate about leading change and enhancing how we operate, you could be the perfect fit for us. | 08/30/2024 |
| 110 | Regeneron East Greenbush, NY Associate Process Characterization & Technology Scientist B.S in Biology, Chemistry, Biochemistry or related life sciences field. Exp: 0-2 years |
Regeneron is currently looking for a Process Characterization & Technology Scientist to join the process characterization and controls cell culture team within the Process Sciences department. This is a lab based position with a 1st shift, Wednesday- Saturday, 6am-4:30pm schedule. The Process Characterization and Technology Scientist is responsible for characterizing the cell culture manufacturing operations through laboratory-scale experiments, drawing conclusions via statistical analysis, and authoring technical summary reports. | 08/30/2024 |
| 111 | Regeneron Tarrytown, NY Laboratory Assistant II, Analytical Chemistry BS Exp: 0-2+ years |
The Laboratory Assistant II will support the staff members in the Analytical Chemistry group through general administrative duties as well as laboratory and equipment upkeep. | 08/30/2024 |
| 112 | Regeneron Tarrytown, NY Associate Scientist - DNA Core BS/MS Exp: 0-3 years |
We are seeking a collaborative and motivated Associate Scientist to join the DNA Core. Our group provides Regeneron laboratories with services vital for conducting scientific research, including plasmid preparation and purification. | 08/30/2024 |
| 113 | Regeneron East Greenbush, NY Associate Process Characterization & Technology Scientist B.S in Biology, Chemistry, Biochemistry or related life sciences field. Exp: 0-2 years |
Regeneron is currently looking for a Process Characterization & Technology Scientist to join the process characterization and controls cell culture team within the Process Sciences department. This is a lab based position with a 1st shift, Wednesday- Saturday, 6am-4:30pm schedule. The Process Characterization and Technology Scientist is responsible for characterizing the cell culture manufacturing operations through laboratory-scale experiments, drawing conclusions via statistical analysis, and authoring technical summary reports. | 08/30/2024 |
| 114 | Regeneron Rensselaer, NY QC Analyst - Sample Management BS/BA in Life Sciences, or related field Exp: 12-18+ months |
Regeneron is currently looking to fill a QC Analyst position in our QC Sample Management department with a 3rd shift schedule, Saturday-Wednesday, 10pm-8:30am. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Quality Control’s role is to ensure product quality and patient safety. Our QC Sample Management department acts as the gatekeepers of QC, accessioning and triaging samples as they are submitted for testing; the QC Analyst position performs a variety of sample receipt functions as well as routine sample inventory and disposal. | 08/30/2024 |
| 115 | Regeneron Tarrytown, NY Associate Scientist BS degree or MS degree in a scientific field Exp: 0-3+ years |
Regeneron's Clinical Bioanalysis group, located in Tarrytown NY, is seeking an Associate Scientist. Train on bioanalytical methods (manual, hybrid, and automated) and completes methods to perform bioanalysis for clinical studies under supervision. Analyze multiple plates within the same day and may perform multiple assays within the same day. Interpret data to assess plate acceptance criteria and adjust sample dilutions accordingly. Complete vital operations in LIMS (requesting samples, building analysis plates, tracking sample movement, tracking pending analysis and performing data entry). Uses the ELN for data documentation purposes. Prepares and qualifies reagents, and re-orders laboratory supplies and reagents, as needed. Ensures compliance, as appropriate, for all laboratory work and documentation in accordance with working practices, company SOPs, bioanalytical method procedures (BMPs), and regulations. | 08/30/2024 |
| 116 | Regeneron Rensselaer, NY Associate Biotech Production Specialists BS/BA in Life Sciences or related field Exp: Entry Level, New Grad |
Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our Associate Biotech Production Specialists are on the front line, producing our life changing products and have a passion for assisting those in need by using biotechnology. They perform all tasks necessary for the manufacturing operations of both clinical and commercial manufacturing programs. | 08/30/2024 |
| 117 | Renaissance Lakewood, NJ Compounder II, 3rd shift Bachelor’s Degree Exp: 0 years |
Primary Responsibility for execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. | 08/30/2024 |
| 118 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors Exp: 0+ years |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as a Production Technician - Vaccine within our Packaging Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people. | 08/30/2024 |
| 119 | Sanofi Chattanooga, TN Quality Control Chemist Lab I (2nd shift) Bachelor’s degree in chemistry or related field Exp: 0-3 years |
The Quality Control Lab Chemist will perform routine testing to support production and release of product in compliance with established specifications. Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented, and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures.Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 08/30/2024 |
| 120 | Sanofi Swiftwater, PA Production Technician - Vaccine Bachelors Exp: 0+ years |
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as a Production Technician - Vaccine within our Packaging Team, will have the potential to transform the practice of medicine, turning the impossible into possible for millions of people. | 08/30/2024 |
| 121 | Sanofi Chattanooga, TN Quality Control Lab Chemist I Bachelor’s degree in chemistry or related field Exp: 1-3 years |
The Quality Control Lab Chemist will perform routine testing to support production and release of product in compliance with established specifications. Perform testing of ingredients as required to support production requirements. Assure that testing is properly documented, and that the ingredient is dispositioned in accordance with the results of the test and the appropriate standard operating procedures.Perform routine laboratory testing for bulk and finished product to support production or shipping requirements. Assure that testing is properly documented and that the bulk or finished product is dispositioned in accordance with the results of the test and the appropriate standard operating procedures. Perform stability testing in support of the room temperature stability program. Assure that stability testing is completed in a timely manner and within the designated time frame. Complete stability testing documentation as appropriate. Knowledge of and ability to use lab instruments including but not limited to: UV-VIS, HPLC, GC, ICP, AA, and FTIR. | 08/30/2024 |
| 122 | Sanofi Waltham, MA Senior Associate Scientist MSc or BSc Exp: MSc: +1 year; BSc: +1-3 years |
The primary responsibilities of the Senior Associate Scientist, Virology will be to support covid vaccine projects by generating and characterizing SARS-CoV-2 pseudovirus materials and maintaining the production lab. Individual will support optimization of pseudovirus capabilities and assay development as needed for the project and departments. The successful candidate will be required to generate, analyse and document data and to communicate their results internally. The candidate will be required to liaise effectively with the team. | 08/30/2024 |
| 123 | Q² Solutions Durham, NC Immunoassay Associate Scientist Bachelor’s degree in chemistry or a related field Exp: 1 year |
We are seeking an Immunoassay Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 08/21/2024 |
| 124 | Q² Solutions Durham, NC Associate Immunoassay Scientist Bachelor’s degree in chemistry or a related field Exp: 1 year |
We are seeking an Immunoassay Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Immunoassay Associate Scientist, you will execute laboratory experiments with precision, contribute innovatively to scientific procedure design, and uphold the highest standards of Good Laboratory Practices (GLP) for our clients. You’ll not only set up and conduct experiments but also manage laboratory equipment, ensuring protocols are meticulously followed under the guidance of a dedicated lab services manager, researcher, or scientist. | 08/21/2024 |
| 125 | Q² Solutions Austin, TX Associate Scientist, Assay Development Bachelor's degree in relevant scientific discipline. Exp: 1 year |
We are seeking an Associate Scientist, Assay Developmentto join Q² Solutions, IQVIA’s laboratory business in Austin, TX. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As an Associate Scientist, you will be responsible for maintaining acceptable and accurate levels of raw and batched inventory in support of reagent manufacturing and production testing. | 08/21/2024 |
| 126 | Q² Solutions Ithaca, NY Associate Scientist, Sample Preparation Bachelor’s Degree Exp: 1 year |
We are seeking an AssociateScientist, Sample Prepto join Q2 Solutions, IQVIA’s laboratory business atIthaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Scientist, Sample Prep, you will be responsible for sample preparation duties, including troubleshooting routine experiments, preparing solutions and reagents, and driving process improvements. You will also play a key role in training junior level staff. | 08/21/2024 |
| 127 | Q² Solutions Durham, NC Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology. Exp: 6 months |
We are seeking an Associate Scientist to join Q² Solutions, IQVIA’s laboratory business in Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist will be instrumental in conducting and documenting analytical procedures, ensuring compliance with SOPs and regulatory guidelines, and contributing to the advancement of our laboratory operations. | 08/21/2024 |
| 128 | Q² Solutions Durham, NC QC Specialist Bachelor’s Degree in medical technology or equivalent. Exp: 1 year |
We are seeking a Quality Control Specialist to join Q2 Solutions, IQVIA’s laboratory business at Durham, NC. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. As a Quality Control Specialist, you will be responsible for supporting lab quality control processes and improvements, ensuring accuracy and compliance with regulations and SOPs. | 08/21/2024 |
| 129 | Q² Solutions Ithaca, NY Scientist, Lab Operations Bachelor’s Degree in applied/laboratory sciences with direct laboratory coursework. Exp: 0-2 years |
We are seeking aScientist Laboratory Operationsto join Q2 Solutions, IQVIA’s laboratory business atIthaca, NY. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. Responsible for the accurate execution of laboratory experiments and contributing to the design of scientific procedures. This position aids in the development of scientific discovery and supports Good Laboratory Practices (GLP) for the customer. | 08/21/2024 |
| 130 | Nova Biomedical Waltham, MA Quality Engineer I BS degree in engineering, the sciences, or another technical discipline. Exp: 1-2 years |
Nova Biomedical is hiring a Quality Engineer I on-site (hybrid) in our Waltham, MA facility. This role will support Quality Assurance activities within the corporate Quality Management System (QMS). Responsibilities include providing expertise and general oversight for the management and improvement of design and development, validations, quality planning, internal auditing, investigations, process controls, change management, quality records, corrective and preventive activities, data management, employee training, and other duties as assigned. | 08/06/2024 |
| 131 | Novartis San Diego, CA Research Scientist - In Vitro Pharmacology B.S. in molecular biology, cell biology, biochemistry, bioengineering, or related scientific discipline Exp: 0+ years |
We are seeking a highly skilled and motivated Research Scientist I to join our dynamic in vitro pharmacology team In San Diego dedicated to advancing gene therapy and siRNA for neurological and neuromuscular diseases. As a key member of our research team, you will play a critical role in supporting various aspects of research including tissue sample processing, biodistribution, biomarker assay development, antibody screening campaigns, as well as oversee lab operation activities. Join us in our mission to transform the treatment landscape for neurological and neuromuscular diseases through cutting-edge gene therapy approaches. Apply now to make a meaningful impact on the lives of patients worldwide! | 08/06/2024 |
| 132 | Novasenta Pittsburgh, PA Research Associate, Assay Development Master’s Degree or bachelor’s degree from an accredited institution Exp: 1+ years |
Conducts routine and non-routine lab procedures and assays for molecular, cellular, and metabolic characterization of relevant samples from mouse models of cancer and human clinical cancer tissue. This includes the conduct of relevant exploratory experiments and control experiments, applying basic scientific principles. As needed, supports the development and validation of new technologies for molecular, cellular and metabolic characterization of samples. Supports the development of biological, immunological assays to investigate mechanisms of immune-mediated effects of novel identified targets. Contributes to the profiling and validation of novel, druggable, immunotherapy targets. Documents and maintains a detailed and precise record of work performed. Performs lab management, which includes ordering supplies and maintaining inventory, ensuring safety, service and maintain laboratory instruments of the lab,etc. Atively participates in the scientific dialogue of the group and proactively collaborates with colleagues. Performs all other duties as assigned | 08/06/2024 |
| 133 | Novavax Gaithersburg, MD Research Associate II Bachelor’s or Master’s degree in Immunology/Virology or relevant field Exp: 1+ years |
We are seeking a highly motivated individual to serve as a Research Associate who takes on the responsibility in support of study projects on cellular assays for Adjuvant and Vaccine candidates. This position will require the incumbent to develop and qualify assays for analyzing samples from preclinical and clinical studies, mainly by using Flowcytometric staining, but can extend to other cellular assays such as Elispot and cytotoxicity assay. This position will mostly involve hands-on laboratory work. | 08/06/2024 |
| 134 | Novavax Gaithersburg, MD Research Associate II - Vaccine Immunology B.S. or M.S. in Immunology, Biology, Molecular Biology, Virology, Genetics or related field. Exp: 1+ years |
Novavax, Inc (Nasdaq:NVAX) is a biotechnology committed to helping address serious infectious diseases globally through the discovery, development and delivery of innovative vaccines to patients around the world. We have more than a decade of experience contending with some of the world’s most devastating diseases, and we are here to make a difference. Hard-won lessons and significant advances illustrate that our proven technology based on solid science tested by decades of research, has tremendous potential to make a substantial contribution to public health worldwide. | 08/06/2024 |
| 135 | Novavax Gaithersburg, MD Analytical Development Associate I/II (Contract) Bachelor’s degree OR Master’s degree Exp: BS: 1-2 years or Master's: Some industry internshnip or co-op exp |
Novavax is seeking an Associate II, Analytical Development to provide technical and documentation support in a laboratory setting. This role is responsible for contributing to the method development, qualification, and technology transfer for analytical methods. The qualified individual will bring experience in relevant analytical technologies, such as ELISA, SRID, Luminex, or BLI. The position will perform in-process testing, as needed, to support the Process Development, Formulation Development, and Manufacturing teams, in addition to method development and qualification. | 08/06/2024 |
| 136 | Novitium East Windsor, NJ Specialist Preventive Maintenance Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6+ months |
Responsible for developing and carrying out a scheduled preventive maintenance program for plant utilities and manufacturing equipment; Troubleshoot existing equipment for issues, change or modify to improve efficiency; Work closely with EHS to maintain facility compliance with applicable OSHA and DEP regulations; Prepare and assist Plant Shut-Down plans and coordinate with all departments to execute the plans; Develop, maintain, and oversee Spare Parts Inventory system and its procurement in collaboration with Purchasing Manager; Manage the organization and maintenance of spare parts warehouses and workshops; Set in service for an existing system to manage Work Orders; Discuss heating/cooling system malfunctions with users to isolate problems or to verify that problems have been corrected; Record and report all faults, deficiencies and other unusual occurrences as well as time and materials expended on work orders. | 08/06/2024 |
| 137 | Novitium East Windsor, NJ Regulatory Specialist Bachelors in Pharmaceutical sciences / biology / microbiology / chemistry / chemical / Regulatory Affairs Exp: 1+ years |
Review, manage and write regulatory submissions electronically which include New ANDA filings, Complete Response letters, Information requests, Amendments to the ANDA’s (Labeling, Chemistry & Bioequivalence) of different dosage forms (Tablet, Capsule, Liquid & Solutions); responsible for filing the Post Approval Supplements like CBE-0, CBE-30 (Changes being effective in 30 days) and Prior Approval Supplements (PAS); submitting dossiers electronically after the approval of initial product submissions (ANDA); review of the leachable and extractable reports generated for the oral Liquid & Solution drug products. | 08/06/2024 |
| 138 | Novitium East Windsor, NJ Sr. Software Engineer Master’s in computers / electronics / electrical / related Exp: 6+ months |
Design and implement Netapp storage systems, including installation, configuration, software upgrades, and storage provisioning; deploy NetApp tools (OCUM,WFA,DFM,snapcreator) to support production operation; configure ifgroups, IPSapce, Vlan’s and Braodcast domains; administer Fiber Channel SAN fabrics, including installation, configuration, zoning, software upgrades, and maintenance of switches; responsible to code and maintain system scripts to support operations of the storage systems; perform architectural planning, designing, coding, and prepare test plans; deploying & configuring new virtual systems and ecosystems. | 08/06/2024 |
| 139 | Novitium East Windsor, NJ Instrumentation Engineer Bachelor’s in Instrumentation / industrial / electronics / electrical / mechanical / related Exp: 6+ months |
Responsible for Instrument and Equipment’s of entire Plant; Installation, troubleshooting & calibration of instruments such as TOC Analyzer, HMI, PLC, Flow Meters, Temperature controller, transmitter, pressure transmitter, gas analyzer; Maintaining minimal instrument downtime through troubleshooting & maintenance activities; Maintaining data backup, instrument documentation, and Spares Inventory & Annual Maintenance contracts; Pro-active Support for Quality Control, Production & Compliance group’s activities; Follow-ups and closures of instrument Change controls, deviations instrument related incidents, & CAP A (corrective and preventive action); Procurement of qualified equipment’s as per GLP & Pharmacopeia requirements, and responsible for IQ, OQ, DQ and PQ for instruments and manage all paperwork. | 08/06/2024 |
| 140 | Novitium East Windsor, NJ Quality Control Analyst Bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related Exp: 1+ years |
Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development and application, quantitative and qualitative analysis, and improvement of analytical methodologies; conduct testing and analysis of pharmaceutical raw materials like drug substance, excipients and packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry; Conduct testing and analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions. The dosage forms include food supplements like vitamin capsules, mineral tablets, and multivitamin syrups. | 08/06/2024 |
| 141 | OraSure Technologies Bethlehem, PA Formulations Specialist Bachelor of Science in chemistry, biochemistry, or equivalent sciences Exp: 1-3 years |
The formulations specialist manufactures chemical formulations necessary for production of finished goods, documents production information, and performs routine maintenance on equipment/machinery. | 08/06/2024 |
| 142 | Novonesis Wausau, WI Process Engineer Bachelor of Science degree in Engineering Exp: 1-3 years |
This position works under general direction and is primarily responsible for developing and improving manufacturing processes by studying product and manufacturing methods. The Process Engineer is responsible for commissioning manufacturing equipment and ensuring equipment operates and performs as intended. | 08/06/2024 |
| 143 | Novonesis Franklinton, NC Process Engineer I BS or MS in Engineering Exp: 0+ years |
You will have the opportunity to work closely with production to ensure things operate smoothly and efficiently. You will be able to drive process improvements, work with capital projects, and support upscaling new processes from development. | 08/06/2024 |
| 144 | Noxilizer Hanover, MD R&D Lab Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1+ years |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 08/06/2024 |
| 145 | Globus Medical West Carrollton, OH Associate Engineer, Manufacturing Bachelor's Degree in Electrical Engineering Exp: 0-2 years |
As part of the manufacturing team, the Associate Manufacturing Engineer needs to have strong technical skills, be hands-on, and be creative with minimum supervision. The job requires a team player with the ability to function well in a challenging, fast-paced environment. This person must be enthusiastic, positive, even-tempered, and have strong skills in areas of communication, dependability, interpersonal relationships, flexibility, and maturity. | 08/06/2024 |
| 146 | Ocular Therapeutix Bedford, MA Microbiology Analyst I B.S. degree in Microbiology, Biology or related scientific field. Exp: 1 year |
The Microbiology Analyst I is responsible for performing QC activities in microbiology lab such as Environmental Monitoring of the cleanrooms and support in performing testing of product and raw materials according to established specifications and procedures. This position also manages EM excursions and data entries. | 08/06/2024 |
| 147 | Ofni Systems Raleigh, NC Computer Systems Validation Engineer BS or equivalent degree in math, science or engineering Exp: 1 year |
We are hiring a Validation Engineer to be on the cutting edge of automated validation techniques. You will be responsible for implementing our validation solutions while working with industry-leading companies. Ideal candidates are experts on the requirements of 21 CFR 11, have excellent critical thinking and interpersonal skills, and are motivated to meet client needs for compliance. If you are an A-level engineer who enjoys the challenge of solving real-world compliance problems then we would like to talk with you. | 08/06/2024 |
| 148 | OncoPep Cambridge, MA Research Associate (In Vitro) BS Exp: 1 year |
We are looking to expand our Research team by recruiting a skilled Research Associate in cellular/molecular biology to join our growing team. The candidate will primarily work with molecular and cell biology techniques including culture of primary cells and cell lines, flow cytometry, ELISA, and western blot. He/She will play an important role in the discovery and development of novel biotherapeutics for immuno-oncology. He/she will be responsible for generating the tools necessary for evaluation and screening of lead candidate therapeutics. He/she will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and generate standard operating procedures. | 08/06/2024 |
| 149 | Orbital Therapeutics Cambridge, MA Research Associate, Molecular Immunology B.S. or M.S. in Immunology, Biology, or related field. Exp: 1-4 years |
Orbital Therapeutics is currently seeking a highly motivated, self-driven, and creative individual with extensive experience in molecular immunology, looking to join an outstanding research team dedicated to designing and executing studies using a new generation of RNA medicines. This individual will enjoy working in a pioneering, fast-paced, and collaborative start-up environment with the opportunity to coordinate studies focused on immunomodulation, while also exploring ways to unleash the power of Orbital’s core technologies. This individual will join a culture of intellectual rigor, scientific curiosity, and collegiality, cross functionally contributing to research across the organization. The candidate will be an important team member whose contributions will be critical to our success in developing new therapeutics to improve the lives of patients. | 08/06/2024 |
| 150 | Organogenesis Norwood, MA QC Analyst I-Cell Culture Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Cell Culture performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. The QC Analyst I performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 08/06/2024 |
| 151 | Organogenesis Norwood, MA QC Analyst I - Chemistry Bachelor’s degree in biology or related field Exp: 1-3 years |
The QC Analyst I, Chemistry performs quality activities in support of product production and release for ASA Product. This position interacts with other internal departments, including Production, Quality Assurance, Validation, Calibration, Materials, and Logistics. The position also interacts with external entities including contractors and suppliers. Performs a variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending, and reporting results. | 08/06/2024 |
| 152 | OriGen Biomedical Austin, TX Quality Engineer I Bachelor’s degree in Engineering Exp: 1-2 years |
The Quality Engineer I is responsible for technical duties within the Quality organization including validation and qualification, calibration, and customer contact. These duties will support manufacturing operations, customer service, process improvement, and regulatory requirements. | 08/06/2024 |
| 153 | Packgene Biotech Houston, TX Quality Control Specialist I - HPLC Bachelor's degree in bioscience, chemistry or related field Exp: 1-2 years |
The Quality Control Specialist I or II- HPLC will undertake laboratory work under the guidance of senior scientists. The Quality Control Specialist I or II is responsable to operate and maintain HPLC instruments; execute HPLC assays. The Quality Control Specialist I will have chance to learn Gene Therapy concepts and cGMP practice, etc | 08/06/2024 |
| 154 | Padagis New Hope, MN QC Chemist II Bachelor's degree Exp: 1+ years |
We are hiring for a QC Chemist II, 2nd Shift, in New Hope, MN who performs inspection on a range of work to detect defects and maintain quality standards. The hours for this role are Monday through Friday 2pm-10pm with some flexibility. | 08/06/2024 |
| 155 | Endo Rochester, MI Quality Associate Specialist, Product Release (Midnight shift) BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 08/06/2024 |
| 156 | Endo Rochester, MI Quality Associate Specialist, Product Release (Days) BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. All incumbents are responsible for following applicable Division & Company policies and procedures. | 08/06/2024 |
| 157 | Endo Horsham, PA Quality Associate Specialist, MQA BA/BS degree in a related discipline Exp: 0-1 years |
The Quality Associate Specialist, under close supervision, performs routine collection of environmental and utility monitoring samples. This role also reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. May participate in “on the floor” activities during product manufacturing. | 08/06/2024 |
| 158 | Paradromics College Station, TX Preclinical Research Assistant Bachelor’s or Master’s degree in Science or Engineering Exp: 1+ years |
The Paradromics Neuroscience team is seeking strongly motivated Research Assistants to contribute to the preclinical testing of our Connexus® Direct Data Interface in large animal models. This role is a temporary position with a fixed period of a year with the possibility of renewal at the end of the contract. This role involves interfacing with veterinarians, neuroscientists, electrical engineers, software engineers, and data engineers. Excellent communication and interpersonal skills are crucial for excelling at this role. This role requires an individual with a “can-do,” self-starter attitude. This position is based on-site in College Station, Texas. We are building next-generation brain implants to treat serious conditions in mental and physical health. If you want to use your skills in a positive, impactful way, if you like to be intellectually challenged, and if you want to be surrounded by hard-working and passionate co-workers, this work will be highly fulfilling. | 08/06/2024 |
| 159 | Paragon 28 Englewood, CO Associate Quality Engineer - Rotational Bachelor’s in engineering or technical discipline Exp: 0-2 years |
The Rotational Associate Quality Engineer has varied responsibilities to assist both the Quality-Production and Quality-Design teams in ensuring Paragon 28’s compliance to regulations and standards. The role will split time and/or rotate through day-to-day tasks and exposure to the supplier quality engineering, design quality engineering and production quality engineering roles at Paragon28 for a 12-month period, with the intention of aligning a candidate’s skills and passion with business needs for permanent placement within the quality department | 08/06/2024 |
| 160 | PCI Pharma Philadelphia, PA Process Engineer-AM Weekends Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout. **This is a weekends position. Friday, Saturday, & Sunday 7am to 7pm.** | 08/06/2024 |
| 161 | PCI Pharma Philadelphia, PA Process Engineer I-2nd Shift Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout. *This is a 2nd shift position. The hours are 3pm to 11pm, Monday to Friday. | 08/06/2024 |
| 162 | PCI Pharma San Diego , CA QA Specialist - Sterile Fill & Finish Bachelor’s degree Exp: 1-2 years |
This full-time position will report to the Quality Manager - Sterile Fill Finish focusing on supporting the Quality department with review and release of executed batch records, product inspection, product or raw material release, document control, production monitoring, environmental monitoring, tracking quality metrics and assisting with validations, preventative actions, audits and continuous improvement. This position is responsible for performing quality activities within the Sterile Fill and Finish group in accordance with all applicable procedures, regulations, and safety directives. This individual’s primary job function will be review and release finished lots of drug product vials and syringes manufactured by PCI. Other job functions may be required at the discretion of management and include but are not limited to drafting procedures, sampling raw materials or finished products, assisting in general operations of the zero human intervention isolators all in accordance with GMPs and established SOPs | 08/06/2024 |
| 163 | Pel-Freez Biologicals Rogers, AR Quality Control Technician Bachelor's degree in science Exp: 1 year |
Under supervision, the QA Technician I will perform quality control testing and assist with the implementation of the Pel-Freez quality management system in accordance with ISO 9001. The role will be required to understand and promote the Quality System as part of the Company's overall goal toward continual improvement through strict adherence to all company policies, procedures, principals, and values. | 08/06/2024 |
| 164 | Penumbra Alameda, CA Manufacturing Engineer II BS degree in Mechanical, Biomedical, Chemical, or Materials Engineering, or a related discipline required Exp: 1+ years |
As a member of the Manufacturing Engineering group at Penumbra, you will be called upon to solve complex problems and implement innovative solutions. You will provide manufacturing technology and robust solutions aimed at commercializing new products and continuously improving production processes. Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement adaptations and modifications to the production line and to quality systems. | 08/06/2024 |
| 165 | Penumbra Alameda, CA Manufacturing Engineer II BS degree in Mechanical, Biomedical, Chemical, or Materials Engineering, or a related discipline required Exp: 1+ years |
As a member of the Manufacturing Engineering group at Penumbra, you will be called upon to solve complex problems and implement innovative solutions. You will provide manufacturing technology and robust solutions aimed at commercializing new products and continuously improving production processes. Working cross-functionally with engineering groups across the company, as well as with Production, Quality Control and Quality Assurance, you will resolve problems encountered on the production floor and throughout the business, and will apply your engineering knowledge and creativity to implement adaptations and modifications to the production line and to quality systems. | 08/06/2024 |
| 166 | Penumbra Alameda, CA Quality Engineer I Bachelor’s or Master's degree in an engineering or scientific discipline required Exp: 1+ years |
As a Quality Engineer I, you will be charged with the quality behind Penumbra's game-changing medical devices used to address some of the world's toughest disease states! Unlike quality engineering roles in other companies, at Penumbra, we provide our quality engineers with highly technical problems to solve. Your efforts will directly impact the safety of patients around the world who use our products. You will apply your passion for creative problem solving throughout all stages of the process, from concept to commercialization and into continuous improvements. | 08/06/2024 |
| 167 | Performance Validation Grand Rapids, MI Level I/II Validation Engineer/Specialist BS degrees in Biomedical Engineering, Chemical Engineering or Mechanical Engineering Exp: 1+ year |
Performance Validation is seeking a full-time Level I or Level 2 Validation Engineer/Specialist to join our team in Grand Rapids, Michigan. Level I/II Validation Engineer/Specialist reports directly to the Division Director or Manager and will be assigned to one or more project teams headed by a Project Leader. | 08/06/2024 |
| 168 | Pfizer Pearl River, NY Associate Scientist– Viral Vaccines & Immunology Bachelor's Degree in a relevant field of science Exp: 0-2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will have the important role to generate high-quality immunoassay data in a regulated Good Laboratory Practices (GLP) setting to support Pfizer’s vaccine programs according to Standard Operating Procedures. You will support the preclinical evaluation and early clinical development of mRNA and protein based viral vaccines. You will perform various assays to monitor the immune responses elicited by respiratory virus, herpesvirus, and influenza virus vaccine candidates. In addition, you will maintain cell lines and prepare preclinical and early clinical samples for testing. Your strong foundation in general scientific practice, its principles and concepts will help in meeting critical deadlines. Your strong work ethic and collaborative spirit will be an integral part of our dynamic team. You will be relied on as a technical contributor to assess the assigned tasks and make decisions that involve direct application of your knowledge. | 08/06/2024 |
| 169 | Pfizer Pearl River, NY Associate Scientist - Sample Logistics and Solutions Bachelor of Science Degree or Bachelor of Arts Degree in a relevant scientific discipline Exp: 0-5 years |
The primary purpose of this job role is to function as a member of the Sample Logistics and Solutions (SLS) team within Pfizer Vaccine Research and Development (VRD). The incumbent will be responsible for receiving samples from global clinical/study trials according to approved protocols and processes. The individual will participate in all aspects of tracking and documenting the chain of custody of samples. The incumbent’s role will include sample receipt, documentation, storage, tracking, aliquoting, distribution to the testing labs, and sample disposal. The colleague will work in a team setting and will share roles and responsibilities as assigned by the team leader/manager. | 08/06/2024 |
| 170 | NAMSA Northwood, OH Microbiology Technologist Bachelor Degree Exp: No Experience |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions, Accurately collects and records raw data in logbooks and on worksheets, May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures, May be required to perform required specific testing as applicable, May be required to operate specified laboratory equipment, May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable), Other duties as assigned. | 07/17/2024 |
| 171 | NAMSA Minneapolis, MN Associate Pathology Technician Bachelor degree or equivalent in Biological Sciences or related discipline Exp: 0-2 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Supports or independently performs necropsy procedures, including complete necropsies and perfusion procedures. Assists and performs routine gross examination as required by GLP standards, and performs accurate and timely record keeping. Assists in coordinating and performing the shipping of all pathology related specimens to the appropriate designated facility. Performs thorough recordkeeping of shipping and receipt logs. Performs tissue trimming according to established guidelines. Performs photography and high-resolution x-ray imaging and film developing. Maintains proficiency in all appropriate designated departmental SOPs with knowledge of lab processes. Assists in the review of protocols that include pathology services, and assists with modifying pathology-related SOP’s. Maintains a clean, GLP-compliant lab and ensures all logbooks are reviewed and correct. Maintains laboratory equipment according to applicable SOPs. Performs calibration or validation activities to specialized equipment. Other duties as assigned. | 07/17/2024 |
| 172 | NAMSA Minneapolis, MN Associate Pathology Technician Bachelor degree or equivalent in Biological Sciences or related discipline Exp: 0-2 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Supports or independently performs necropsy procedures, including complete necropsies and perfusion procedures. Assists and performs routine gross examination as required by GLP standards, and performs accurate and timely record keeping. Assists in coordinating and performing the shipping of all pathology related specimens to the appropriate designated facility. Performs thorough recordkeeping of shipping and receipt logs. Performs tissue trimming according to established guidelines. Performs photography and high-resolution x-ray imaging and film developing. Maintains proficiency in all appropriate designated departmental SOPs with knowledge of lab processes. Assists in the review of protocols that include pathology services, and assists with modifying pathology-related SOP’s. Maintains a clean, GLP-compliant lab and ensures all logbooks are reviewed and correct. Maintains laboratory equipment according to applicable SOPs. Performs calibration or validation activities to specialized equipment. Other duties as assigned. | 07/17/2024 |
| 173 | NAMSA Irvine, CA Senior Lab Technician - Sterility Assurance Bachelor degree Exp: 1 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description:May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. Performs routine calculations and may participate in analyzing and interpreting results. Maintain all test equipment and supplies for various testing. Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents. Assist in the preparation of items for testing. Monitor raw materials and final finished media for conformance with applicable material specifications and SOPs. May be responsible for extractions, which may include: test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. | 07/17/2024 |
| 174 | NAMSA Irvine, CA Associate Microbiologist Bachelor degree Exp: 1 years |
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. Job Description: Independently perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs, and according to applicable work instructions. Prepare or participate in the preparation of test specifications in conjunction with the requirements of the applicable standards and/or client instructions. May have direct client contact as needed. Responsible for review of incoming test articles and paperwork for appropriateness and accuracy and for taking all concerns to management as required. Accurately collects and records raw data in logbooks and on worksheets. Responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in SOPs. | 07/17/2024 |
| 175 | Nanomix San Leandro, CA Associate Scientist, Assay Development Bachelor’s degree (or equivalent) in in Biology, Bioengineering, Chemistry, Chemical Engineering, or related field Exp: 0-2 years |
Nanomix has developed tests for the diagnosis of sepsis, acute kidney injury, and COVID-19, and is looking for an Assay Development Associate Scientist to help accelerate these programs and the development of other IVD assay products in the pipeline. This is an opportunity to work with a world class team to deliver an advanced, mobile medical diagnostic platform of urgent need to the healthcare industry. The successful candidate will apply scientific & technical skills in all phases of developing diagnostic assay products. Assist in developing Nanomix eLab biosensor cartridge assays to detect various biomarkers &/or viral/bacterial antigens. | 07/17/2024 |
| 176 | Element Bend, OR Chemist I/Chemist II Bachelor’s Degree in Chemistry or related field is required. Exp: Some experience (for Chemist I) or 2 years experience (for Chem II) in a laboratory setting |
Element has an opening for a Chemist I or Chemist II position at our extractables and leachables (E&L) testing Center of Excellence in Bend, OR. This position will work in a cGMP-regulated environment under the direction of a Team Lead or other senior staff member in laboratory and office settings. The position will work with a team completing E&L project work using internal methods, protocols and SOPs according to customer specific requirements. This position requires working in a collaborative manner with other team members to accomplish organizational goals, providing ideas to improve efficiency and actively contributing to positive co-worker/customer relationships through efficient interaction on current projects. The Chemist I or Chemist II will also contribute to team continuous improvement initiatives. | 07/17/2024 |
| 177 | Element Wixom, MI Project Manager - Engineer Bachelor of Science degree in a science or testing related field including but not limited to: Metallurgical Engineering, Materials Science, and Polym Exp: 0-5 years |
Element has an opportunity for an Engineer to join our rapidly expanding Project Management team in our Wixom, MI Lab. The Project Manager will be coached to be able to provide quotations, manage testing programs, write technical reports, and support the other team members. Our Engineers perform a variety of routine and non-routine testing assignments and insures timely and accurate test results under minimal direct supervision. The project manager position must be proficient in a number of core business and technical skills as well as compliance to established safety rules, code of conduct, and company policies and procedures. | 07/17/2024 |
| 178 | Element Fremont, CA Electromagnetic Compatibility Compliance Engineer Bachelor’s Degree in Engineering Exp: 0-2+ years |
Element, has an opportunity for Electromagnetic Compatibility Compliance Engineer in the Regulatory Division of our Fremont, CA. This position applies engineering concepts for testing and evaluation of electronic and wireless RF devices for US federal and international regulatory compliance. Determining compliance requires the understanding and application of test standards, diagnosing problems, analyzing results, and troubleshooting unexpected performance in a fast-paced environment and industry. All training provided. | 07/17/2024 |
| 179 | Element Huntington Beach, CA Associate Engineer Bachelor of Science degree in a science or testing related field Exp: 0-1 years |
Join us as an Associate Test Engineer and see how your variety of routine and non-routine testing make a difference and how critical it is to helping us deliver on our purpose and achieve our goals. Element is a world renown Aerospace Testing Company with clients such as Boeing, SpaceX and Blue Origin. At Element our shared purpose of ‘Making tomorrow safer than today’ is what brings us together. We are energized by our ambition to make the world a better place and create a safer future for people. This is what sets us (and you, if you join us…) apart from the crowd. | 07/17/2024 |
| 180 | NantWorks Culver City, CA Battery Engineer B.S/M.S. in Mechanical Engineering, Chemical Engineering, Materials Science, or related technical field Exp: BS - 2 years; MS - 0+ years |
The Battery Engineer will be responsible for development, selection and validation active materials across the anode and cathode portfolio, assisting in development and implementation of R&D tools, and general engineering tasks. This includes developing and characterizing active/passive materials, developing slurry and coating recipes, building cells, and cell testing, leading engineering design and construction. This individual will be a key contributor in advancing NantG Power's competitive advantage to drive energy density, power density, safety, and materials sustainability improvements at scale. The ideal candidate will have a strong record of scientific achievement in the areas of Li-ion batteries, nanomaterials, and/or electrochemistry. | 07/17/2024 |
| 181 | LGC Biosearch Technologies Alexandria, MN Quality Control Technician I - Laboratory Bachelor’s degree in a relevant scientific discipline Exp: 0-2 years |
The Quality Control (QC) Technician I focuses on the performance of analytical testing activities within the consumable product lines. They are responsible for testing intermediate and finished products, analysing the results of Quality Control testing and comparing results to established specification and/or customer requirements. In addition, they may perform testing and/or review of incoming goods. | 07/17/2024 |
| 182 | LGC Biosearch Technologies Cumberland Foreside, ME Manufacturing Chemist I Bachelors degree in life science field or other related science or medical Exp: No Experience |
The Manufacturing Chemist I fulfills the essential role of preparing reagents, buffers, stocks, and other solutions using established procedures within the operations laboratory. They will use general laboratory equipment and techniques to perform these tasks under both direct and indirect supervision. They are expected to perform routine analysis and interpretation of test results against established acceptance criteria with limited judgment. | 07/17/2024 |
| 183 | LGC Biosearch Technologies Middleton, WI Lab Services Technician Bachelor's degree in a scientific field of study (e.g. biology, chemistry, physics) Exp: 0+ years |
The Lab Services Technician provides foundational support to the processing and preparation of client samples for the Lab Services team at a specific operational site. In agreement with other Lab Services team members, this position is responsible for driving their operational duties by supervisor direction as well as standard operating procedures (SOPs) and work instructions. | 07/17/2024 |
| 184 | LGC Biosearch Technologies North Charleston, SC Production Chemist I Bachelor of Science degree is required, chemistry degree preferred Exp: 0-2 years |
The Production Chemist I is responsible for the manufacturing of reference standard solutions by following routine procedures and operations of laboratory equipment. This is a highly collaborative position and requires a high level of teamwork and productivity. We are looking for individuals that can thrive in a fast-paced laboratory setting and demonstrate ability to prioritize and organize work with guidance from team leads and supervisor. Our site manufactures both catalog and custom solutions for customers requiring focused bench work, detailed record keeping and flexibility in daily tasks. | 07/17/2024 |
| 185 | LGC Biosearch Technologies Petaluma, CA Oligonucleotide Production Technician - Liquid Handling Bachelors Degree or Master's Degree preferred in Life Sciences. Exp: 0-2 years |
The Oligonucleotide Production Technician I will perform tasks associated with the production of modified oligonucleotides in a high throughput time sensitive manufacturing environment in compliance with company procedures and external regulatory requirements. | 07/17/2024 |
| 186 | Sotera Health Salt Lake City, UT Lab Analyst - Analytical Chemistry Bachelors Degree, relevant Life Science Exp: No Exp |
Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. | 07/17/2024 |
| 187 | Nemagen Discoveries Newark, NJ Research Scientist B.S. in a Biological Science orin a related field Exp: 0+ years |
NemaGen Discoveries’ mission is to advance therapies to treat mast cell-related and chronic inflammatory diseases. Under the direction of NemaGen’s Principal Scientist, you’ll work in an exciting and fast-paced start-up environment where you’ll assist with the development of NemaGen’s research programs. NemaGen is looking for candidates with a strong scientific background that have an interest in entrepreneurship and helping grow NemaGen in the coming years. If you want to be a part of cutting-edge research and improve the lives of patients, we encourage you to apply! Design and perform cell culture assays related to the development of innate immune cells with novel chemical compounds. Phenotypically and functionally characterize the activation state of various immune cell populations. Perform in-vitro efficacy studies. Operate standard laboratory equipment including, but not limited to, centrifuges and flow cytometers. | 07/17/2024 |
| 188 | AstraZeneca Santa Monica, CA Associate, Quality Control Analyical BS in biological sciences or a related field is required. Exp: 0+ years |
Neogene is looking for an energetic and experienced person with cell therapy quality control background to join our Quality Control (QC) team. You will contribute to the advancement of our product pipeline by performing QC analytical method qualification, complete sample analysis and other assigned tasks. You will also independently organize and present results and conclusions. You will ensure that the QC Analytical laboratory is operating as expected. | 07/17/2024 |
| 189 | NeoGenomics Laboratories Durham, NC Molecular Laboratory Technologist, Temporary Bachelor’s Degree in one of the chemical, physical, or biological sciences Exp: 1+ years |
The Laboratory Technologist works under minimal supervision and consistently and independently performs the complex level of clinical tests by following department procedures. You will drive initiative for prompt, accurate performance of test results with appropriate documentation of result. | 07/17/2024 |
| 190 | Neolight Scottsdale, AZ Biomedical Engineer Bachelor's or Master's Degree in Electrical Engineering Exp: No Experience |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 07/17/2024 |
| 191 | Neuralink Austin, TX Associate Chemist Bachelor OR M.S. of Science in Chemistry, Biochemistry, or a related field Exp: 1-2 years |
The Associate Chemist role will work with teams across the Neuralink organization to analyze the chemical and biological characteristics of manufacturing processes and finished devices. This will include various levels of product testing during R&D and release to obtain data that may be required for product approvals. Additionally, this data may be used to confirm patient safety of our products by applicable global regulations, regulatory guidelines, or voluntary consensus standards. Daily responsibilities may involve drafting internal procedures and test protocols, sample preparation, laboratory testing, method development, inventory management, and other miscellaneous laboratory tasks. The primary goal will be to assist in medical device chemical and biological characterization to support patient safety and regulatory approval. | 07/17/2024 |
| 192 | Revvity San Diego, CA Biochemist I - Proteogenomics Bachelor’s degree in Physical Sciences, Life Sciences, or other related fields Exp: 1+ years |
BioLegend (a division of Revvity, Inc.) has an opening for a self-motivated individual with production experience in a fast moving and dynamic environment to join our Proteogenomics team! The biotechnician will be an integral member of a team, that manufactures and provides high-plex oligonucleotide conjugated antibodies panels to enable studies for novel applications in precision medicine, oncology, immunology, neuroscience, and stem cell research. This position will report to a team lead and will ensure the highest quality of our finalized antibody products. This is a great opportunity to work in a fast-paced and dynamic environment for you to enhance your knowledge in the biotechnology industry! In this position you will perform column chromatography manually and via automation, troubleshooting of problematic errors, continue to improve methodologies for efficiency, follow Standard Operating Procedures (SOP)s, and cross train on a variety of other supporting tasks. | 07/18/2024 |
| 193 | Revvity San Diego, CA Research Associate I - Immunoassay (LEGENDplex BS in a Biology, Chemistry or other related field Exp: 1+ years |
This position is responsible for supporting immunoassay products development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneously detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experiences in growing business in a fast-pace biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 07/18/2024 |
| 194 | Revvity San Diego, CA Research Associate II - Immunoassay (LEGENDplex) BS in a Biology, Chemistry, or other related field Exp: 1+ years |
This position is responsible for supporting immunoassay product development and manufacturing in the Biomarker Immunoassay group. The Research Associate will be involved in all aspects of the product development processes including designing, initiating, testing, troubleshooting, testing materials manufacturing, technical instruction transferring, and product launching. More specifically, he or she will be working with an experienced scientist on testing new hybridoma clones, qualifying the raw materials used for immunoassay products manufacturing and new immunoassay product development and launching. These immunoassay products may allow simultaneous detection of up to 13 important biomarkers for inflammatory diseases, stem cells, cancer, cardiovascular disease, or neuron degenerative diseases, and will be very useful tools for the biomedical research community. This position is a great opportunity for gaining working experience in growing business in a fast-paced biotech industrial environment. He or she will be able to manage the assigned function and tasks with great communication skills in a timely manner with independence after appropriate training. | 07/18/2024 |
| 195 | Revvity San Diego, CA Biochemist I - GMP Beads Conjugation BS degree in chemistry/biochemistry, material science or life science. Exp: 0-1 years |
This biochemist role will be an integral member of our GMP team that develops and manufactures BioLegend’s regulated magnetic beads and antibody reagents produced in our US FDA registered cGMP manufacturing facility. This position will report to a GMP MOJO Scientist. The desired candidate must be a team-player who is organized and is able to work in a fast-paced environment to meet deadlines. Great attention to detail is also a skill that will allow the candidate to be successful. | 07/18/2024 |
| 196 | Revvity San Diego, CA Research Associate I - Molecular Cloning Bachelors of Science in Biological Sciences Exp: 1+ years |
This position is responsible for developing recombinant protein/antibody research products in the Molecular Cellular Biology group. The research associate will be involved in the early stage of product development for recombinant protein/antibody products. The duties include preparing cell culture media, DNA purification, PCR and molecular cloning, bacterial and mammalian cell cultures, and purifying recombinant proteins/antibodies with several affinity tags, and weekly presentations of results to internal and external groups. This position offers a significant opportunity for learning molecular biology techniques and career growth in the biotechnology industry. | 07/18/2024 |
| 197 | Revvity San Diego, CA Quality Control Associate I Bachelor’s degree in a scientific discipline Exp: 1+ years |
At BioLegend we are dedicated to commercializing high quality reagents to support the research community for legendary discoveries. The Associate for BioLegend’s Quality Control group will test products such as antibodies and proteins in the following application(s): flow cytometry, immunohistochemistry, western blotting, ELISA, multiplex immunoassays and/or functional bioassays. The candidate will perform all aspects of the assays following SOPs and ISO requirements. Additional responsibilities include culturing mammalian cell lines, isolating primary cells, and maintaining laboratory equipment and supplies. We are looking for a highly motivated person who loves science and wants to be part of a dynamic and fast paced team. | 07/18/2024 |
| 198 | Revvity Boston, MA Associate Chemist B.S. degree in Chemistry, Biochemistry, Chemical Engineering Exp: 0-2 years |
We are seeking an Associate Chemist to join our team of scientists in the Research Reagents group manufacturing synthetic chemical products used throughout the world in scientific research applications. The Associate Chemist will also have an opportunity to work on the Microfluidics product line. This position will function as a member of the production staff and will participate in the transfer, implementation and on-going production of products in the laboratory. This is an on-site role based at our Boston South End manufacturing site. | 07/18/2024 |
| 199 | Neurona Therapeutics South SF, CA Research Associate, Process Sciences Bachelor’s or master’s degree in chemistry, biology or biochemistry. Exp: 0-5 years |
Our ideal candidate is a self-motivated individual who has a passion for method development and qualification that can thrive in a fast-paced dynamic environment. The successful candidate will work as a member of the Process Sciences department and will be responsible for projects requiring design and qualification of process equipment. In addition, the candidate will interface with Manufacturing, Process Science, Facilities, Validation, QA, and Contract Engineering/vendor firms to produce detailed designs for procurement, construction, installation, start-up, and validation of process systems including systems for shipping product to clinical sites. This is a fantastic opportunity to join a small team, work on transformative science, and take part in building an exciting, science-driven company. | 07/18/2024 |
| 200 | Q2 Solutions Marietta, GA Associate Scientist, Flow Cytometry Bachelor’s Degree in a scientific field including chemistry, biology or medical laboratory technology. Exp: 6+ months |
In this vital role, you'll support daily laboratory functions, including inventory management, pre-analytical sample handling, and more, ensuring efficient and effective operations. What you’ll be doing: Performing and documenting analytical procedures, adhering to SOPs and regulatory guidelines, and upholding our laboratory's high-quality standards. Analyzing routine data, identifying deviations or unusual results, and reporting these findings promptly to senior lab personnel to safeguard our scientific work's integrity. Engaging in quality investigations, preparing necessary materials for analyses, and demonstrating your commitment to scientific accuracy and rigor. Mentoring entry-level staff, facilitating their onboarding, and participating in continuous education initiatives to strengthen our team's expertise foundation. Taking part in cross-functional projects, communicating effectively across various teams, and advocating for safety, quality, and adherence to organizational standards and initiatives. | 07/18/2024 |
| 201 | Q2 Solutions Indianapolis, IN Associate Scientist, Biotransformation Bachelor’s degree in a relevant scientific discipline Exp: 6+ months |
We are seeking an Associate Scientist, Biotransformation to join Q2 Solutions, IQVIA’s laboratory business in Indianapolis, Indiana. We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. What You’ll Be Doing: Perform routine analysis and laboratory testing procedures to obtain data from pre-clinical and/or clinical specimens. Document analytical procedures in accordance with methods and regulatory guidelines. Assess whether analytical procedures are proceeding according to expectations and ensure results are within acceptable tolerances. Identify abnormal progress, potential quality failures, or unusual results and escalate to senior lab personnel. Prepare data analysis results for upload to LIMS system under the guidance of senior-level staff. Assist in writing laboratory procedures and techniques. | 07/18/2024 |
| 202 | Q2 Solutions Durham, NC Associate Scientist Bachelor’s Degree in a chemical, physical, biological, or clinical laboratory science, medical laboratory technology, or cytotechnology. Exp: 6+ months |
We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development. The Associate Scientist will be instrumental in conducting and documenting analytical procedures, ensuring compliance with SOPs and regulatory guidelines, and contributing to the advancement of our laboratory operations. | 07/18/2024 |
| 203 | Q2 Solutions Marietta, GA Laboratory Assistant, Inventory Control Bachelor’s Degree or equivalent combination of education Exp: 6+ months |
As a Laboratory Assistant, Inventory Control you will be providing lab support, necessary to assist the local inventory process. You will also be managing reagent inventory for the Flow and PBMC departments. | 07/18/2024 |
| 204 | NJ Bio Princeton, NJ QC Scientist (I&II) BS, MS, or PhD degree in chemistry, biology, biochemistry, or related discipline Exp: 1+ years |
The primary role is to provide analytical support for GMP manufacturing and process development. The QC scientist will develop, qualify, and execute analytical test methods for raw materials, highly potent APIs, antibody-drug conjugates (ADCs), and other pharmaceutical products in a GMP setting. | 07/18/2024 |
| 205 | Avecia Cincinnati, OH Associate Chemist BS degree in Chemistry or related areas Exp: 0+ years |
As an Associate Chemist, you will execute chemistry and related activities for manufacturing, packaging and shipping of OliGrow oligonucleotides according to company processes. | 07/18/2024 |
| 206 | Noah Medical Sunnyvale, CA Clinical Engineer Bachelor’s degree in Engineering or Science; Master’s degree preferred Exp: 0-5 years |
The Clinical Engineering Team at Noah Medical is dedicated to ensuring the products Noah is developing meet all of the clinical and user needs. We collaborate closely with our end users (physicians) to understand their needs and the clinical value Noah’s products will bring them. The Clinical Engineering team also works closely with cross-functional development teams to represent clinical value propositions for patients and providers throughout the design and development of new products. Join us to contribute to Noah Medical's growth and to shape the future of medical robotics. | 07/18/2024 |
| 207 | Noble Life Sciences Sykesville, MD Research Technician Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1+ years |
Job Description: Compliance: Perform assigned tasks and responsibilities under the direction of the Scientist(s) and/or the Study Director(s) and in accordance with relevant study protocols, regulations, and Standard Operating Procedures (SOPs); Training: Ensure personal training is documented according to Noble SOPs prior to the performance of associated procedures; Procedure Preparation: Label tubes and other supplies needed for collecting and processing specimens. Prepare reagents needed for collection or processing of specimens. Performance of Procedures: Process various blood and tissue samples. Maintain quality, safety, and/or infection control standards. Perform procedures using various instrumentation according to Noble SOPs; Documentation: Maintain lab notebooks and document experimental procedures and associated data. Assist in writing deviations and preparing responses to quality assurance audits related to duties performed. Laboratory Maintenance: Take ownership of assigned laboratories. | 07/18/2024 |
| 208 | NorthStar Beloit, WI Radiopharmaceutical Manufacturing Associate Associate’s or Bachelor’s degree in a STEM discipline Exp: 0-1 years |
The Radiopharmaceutical Manufacturing Associate performs duties to support the development and manufacturing of radiopharmaceuticals for NorthStar operations. This includes equipment preparation, product dissolution, and dispensing of medical radioisotopes while complying with procedures, instructions, and prescribed routines. All duties and responsibilities will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 07/18/2024 |
| 209 | NorthStar Beloit, WI Quality Control Analyst/Senior Quality Control Analyst Bachelor’s Degree in Chemistry, Biology, or other related scientific discipline Exp: 1+ years |
The primary role of this position is to conduct and validate various biological and analytical quality control assays associated with the processing of radiopharmaceutical isotopes and drugs to ensure compliance with established standards. This role requires extensive training on radiation safety including ALARA (“as low as reasonably achievable”) principles. Duties will be completed in compliance with applicable regulatory agency standards. This position supports production in a 24-hour manufacturing facility which means your schedule provides days off during the week when weekend work is required. Early morning, late evening, weekend, and some holiday work will be required with occasional overtime. | 07/18/2024 |
| 210 | Machine Solutions Flag Staff, AZ Medical Device Testing Technician Bachelor’s level degree, preference for engineering or technical experience or Exp: 0+ years |
Machine Solutions testing equipment is used to evaluate and quantify the performance of our customers’ interventional devices such as stents, catheters, and guide wires. Testing/applications technicians are responsible for lab-based tasks, which include sample processing, contract testing, measuring, recording, analyzing results and generating reports on MSI equipment with in-house or customer product. The technician will learn how to operate Machine Solutions equipment and use this knowledge to host customer training and perform quality inspections to ensure equipment meets operational specifications. An ideal candidate will be someone who enjoys working with their hands and enjoys the challenge of finding unique solutions to meet our customer’s needs. | 07/01/2024 |
| 211 | Macrogenics Rockville, MD Manufacturing Associate II - Cell Culture Bachelor’s degree in a related discipline and a minimum of three years of related biopharmaceutical manufacturing experience in FDA regulated, control Exp: 1+ years |
The Manufacturing Associate II participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Protein Purification area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 07/01/2024 |
| 212 | Macrogenics Rockville, MD Manufacturing Associate I - Cell Culture Bachelor’s degree in a related discipline Exp: No Experience |
The Manufacturing Associate I participates in the manufacturing of biopharmaceutical drug product to support MacroGenics’ multiple clinical programs in the Cell Culture area. This position will work in the manufacturing suite under GMP (Good Manufacturing Practices) to ensure that materials manufactured meet required specifications and regulatory requirements. | 07/01/2024 |
| 213 | MagBio Genomics Gaithersburg, MD Production and Fulfilment Associate Bachelor's Degree in Biology or equivalent science-related field; or equivalent combination of education and experience. Exp: 0-2+ years |
This position is responsible for the timely and efficient scheduling production, packaging and shipping of standard and custom products, and for providing support to other areas of manufacturing to ensure timely product delivery. Responsibilities with reagent production, shipping, and order fulfilment. | 07/01/2024 |
| 214 | Magnolia Medical Technologies Seattle, WA Engineering Intern, Product Development (Hybrid) Pursuing an engineering degree, or related BA/BS degree, or pursuing a related MA/MS. Exp: Entry Level |
The Engineering Intern performs, under direct supervision, and contributes to the Engineering and Product Development Department of Magnolia Medical Technologies, Inc. The Intern is exposed to the medical device industry and Magnolia Medical's company culture through partnering with the organization’s teams, department supervisors and leaders who provide informal mentoring and coaching towards success. The Engineering Intern develops working knowledge of product development, works in a changing environment, and will further develop skills utilized industry wide in regulatory environments. | 07/01/2024 |
| 215 | Mallinckrodt Pharmaceuticals St. Louis , MO Chemical Process Technician Minimum of a Bachelor's degree in Chemistry, Biology or other science degree. Exp: 1-3+ years |
Develop and produce pharmaceutical products via multiple methodologies, follow standard operating procedures, maintain compliance with Good Manufacturing Practices. | 07/01/2024 |
| 216 | Mallinckrodt Pharmaceuticals Hobart, NY Quality Technician I - First Shift Bachelor Degree in science related field (Chemistry, Biology) is preferred Exp: I: Class/previous work exp in science related field II: Working knowledge of chemistry required III: Min 1-3 years of exp in cGMP facility |
Perform basic wet chemistry, preparation of reagents/solutions, and sample reconciliation following approved methods. | 07/01/2024 |
| 217 | Mallinckrodt Pharmaceuticals Hobart, NY Validation Technician III Bachelor Degree in engineering discipline, life sciences or technical field related to pharmaceutical manufacturing is preferred Exp: 0-1 years |
Assists with multiple cross-functional projects from development through release for commercial implementation. Supports departmental priorities and senior level engineers with guidance from the department manager. May support the execution of validation studies as needed, including assisting in pre-run training, product sampling, and review of documentation for completeness and alignment with good documentation practices. Assists in the analysis and review of data generated by validation studies performed within the department. | 07/01/2024 |
| 218 | Mallinckrodt Pharmaceuticals Hobart, NY Validation Engineer I Bachelor Degree in engineering discipline, life sciences or technical field related to pharmaceutical manufacturing is preferred Exp: 1-2 years |
Assists with multiple cross-functional projects from development through release to production. Projects include new facilities startup, manufacturing equipment and packaging line FATs and qualifications. Independently executes activities in support of the Validation Department priorities with minimal guidance from the department manager. Provides technical assistance during investigations of equipment/process/product issues. Supports validation deviations related to equipment/process/product. Execute validations as needed, including assisting in product sampling, auditing and technical review functions as defined in study protocols. Analyzes data, utilizing appropriate statistical methods, generated by validation studies performed by the Validation group to determine process capabilities. | 07/01/2024 |
| 219 | Mallinckrodt Pharmaceuticals Madison, WI Quality Analyst Bachelor’s Degree Exp: 1+ years |
The Quality Analyst ensures that all materials, activities, processes, and specified conditions involved in daily device manufacturing, processing, and packaging meet current GMP standards and comply with relevant procedures and standards to maintain product quality integrity. Additionally, the Quality Analyst manages nonconforming material reports, plans material review board meetings, and oversees the status of quarantined and scrapped materials. | 07/01/2024 |
| 220 | Mammoth Biosciences Mammoth Brisbane, CA Research Associate II/Senior Research Associate – LNP Formulation Bachelor's degree in chemistry, pharmaceutical sciences, bioengineering, chemical engineering, or related discipline with 1+ years of experience or Ma Exp: 0-1 years |
In this role, the successful candidate will be contributing to the formulation efforts of Mammoth’s proprietary CRISPR nuclease systems, supporting the formulation and physiochemical characterization of the candidates for a variety of therapeutic indications. In addition, this candidate will be contributing to the analytical method development to support the formulation discovery and production of test articles to support Mammoth’s ex-vivo and in vivo studies. | 07/01/2024 |
| 221 | Mariana Oncology Watertown, MA GMP Manufacturing Technician Bachelor’s Degree, Associate Degree, or 5 years of experience working in a GMP manufacturing environment in the pharmaceutical or biotechnology indust Exp: 0-5 years |
Mariana Oncology is focused on an extremely exciting field of oncology of precision radiopharmaceuticals to treat unmet need in solid tumors. We are at the vanguard in developing best in class alpha and beta emitting radio ligands targeting cancer tumors while mitigating destruction to healthy tissue and cells. We have built a fully integrated, leading radiopharmaceutical platform, that is bringing together novel target biology insights, innovative multimodal ligand discovery, and enabling translational infrastructure. We are seeking an experienced GMP Manufacturing Technician to join Mariana’s Manufacturing organization, advancing personalized medicine and radiopharmaceuticals. | 07/01/2024 |
| 222 | Mariana Oncology Watertown, MA Quality Control Analyst I/II Master’s degree in biochemistry, chemistry or related discipline with 0-2 years exp, or Bachelor's degree with 2-4 years exp Exp: 0-2 years |
We are seeking an experienced Quality Control Analyst I/II to join Mariana’s Clinical Manufacturing organization, advancing personalized medicine and radiopharmaceuticals. You will be responsible for supporting the release and stability testing of our clinical therapies produced in our GMP manufacturing suite in Watertown. This person will play a role in creating and maintaining the highest standard of excellence for our therapies to treat cancer patients. | 07/01/2024 |
| 223 | Marvel Biome Woburn, MA Research Associate BS or MS in Molecular Biology, Microbiology, or Cell Biology required Exp: 0-2 years |
We are seeking a full-time Research Associate to join a highly collaborative team using the latest molecular biology, protein biochemistry, and -omics analysis techniques to develop microbiome-based therapies. In addition, there will be opportunities to assist in the execution of pre-clinical studies to evaluate treatment efficacy. The ideal candidate is obsessed with the question of how to best design and execute experiments to identify treatment-improving therapies. This is a unique opportunity to work at a nimble, forward-thinking microbiome start-up and help build the foundation for microbiome as therapeutics. | 07/01/2024 |
| 224 | MatTek Ashland, MA Production Associate I Bachelor’s degree in biology or equivalent with no previous work experience Exp: 0+ years |
Participates in duties associated with manufacturing of MatTek tissue models according to SOPs where applicable. May also perform duties assigned under Laboratory Assistant, as needed. | 07/01/2024 |
| 225 | Maze Therapeutics San Francisco, CA Research Associate, In Vivo Pharmacology Bachelors degree in biology, pharmacology, or other relevant field is required Exp: 1+ years |
Are you driven by a passion for scientific discovery and a desire to make a tangible impact on human health? We're seeking a passionate, creative, and dedicated Research Associate to join our in vivo pharmacology team. In this role, you will be pivotal in conducting pharmacokinetic studies that drive our research projects forward, while also contributing to preclinical pharmacodynamic and disease models. Under the guidance of the Director of Pharmacology, your work will directly support the discovery of new drug candidates and advance our understanding of disease mechanisms. Additionally, as a rapidly growing biotech company, we offer an exciting and collaborative work environment where every team member plays a vital role in our success. | 07/01/2024 |
| 226 | Mdxhealth Irvine, CA Product Development Associate Bachelor's degree with 1-2 years of experience working in research & development or Master's degree with 0 to 3 years’ experience. Exp: 0-3 years |
The Product Development Associate is involved in assisting with the planning, conducting, and analyzing experiments leading to validation of diagnostic tests in the field of oncology. The PD Associate works in a team and needs to communicate relevant information to professional colleagues and to participate constructively in discussions that will impact the performance of the final product. | 07/01/2024 |
| 227 | Mdxhealth Irvine, CA Inventory Control Associate High School Diploma or Bachelor's Degree Exp: 1-2+ years |
The function of an Inventory Control Associate is to keep track of the goods and supplies of the Operations teams, both incoming receipt and outgoing release to the laboratories. The Inventory Control Associate is to keep records of inventory counts, generate and place purchase orders, coordinate with vendors, maintain inventory of items in stock, and perform data entry of this information. The Inventory Control Associate is to monitor and handle purchases to ensure arrival in a timely fashion in the quantity and quality that upholds mdxhealth standards while maintaining supplier and interdepartmental relationships. | 07/01/2024 |
| 228 | MedAbome Fremont, CA Research Associate (Molecular Biology) M.S. or B.S. degree in life science with academic or industrial experience in biological research Exp: 0+ years |
Perform molecular biology experiments to support drug discovery and development; Participate in antibody engineering, cell line generation, in vitro and in vivo assays. | 07/01/2024 |
| 229 | MedAbome Fremont, CA Research Associate (Cell Biology) M.S. or B.S. degree in life science with academic or industrial experience in biological research Exp: 0+ years |
Maintain cell lines and perform cell-based assays to support antibody drug discovery; Participate in antibody generation and characterization, such as fusion, ELISA, FACS and other cell-based assays; Participate in small animal studies. | 07/02/2024 |
| 230 | Medmix Flowery Branch, GA Technical Project Engineer Bachelor’s degree in mechanical or industrial engineering Exp: 1+ years |
We are looking for a Technical Project Engineer to join us at medmix. This exciting opportunity will allow you use your skills to identify areas of improvement and propose recommendations to management. You will lead and drive the implementation of your recommendations and assess its impact to the business. If you are eager to learn, strive for personal development, are highly motivated and organized, and a great communicator, you can help us drive medmix to the next level. As a Technical Project Engineer you will help us to take effective project management to the next level. Responsibilities: Realization of injection molding life cycle projects in the segments industry, dental and surgery, Lead interdisciplinary project teams, Create and update of project plans and necessary documents, Reach the goals set for cost, time and quality, Delegate and control tasks and execution of work packages within the projects, Execution of mile stone meetings | 07/02/2024 |
| 231 | Medpace Cincinnati, OH Laboratory Technologist - Sample Processing Bachelor's degree in a Biological Science field or Chemical Science field Exp: 1+ years |
Our biorepository activities are growing rapidly, and we are looking to add to our sample processing team! The Laboratory Technologist will aid in the development and growth of the biorepository sample processing department. The ideal candidate will have strong critical thinking and problem solving abilities. This position will be a full-time, position in Cincinnati, OH. | 07/02/2024 |
| 232 | Medpace Irving, TX Clinical Research Associate (CRA) Must have a minimum of a Bachelor’s degree in a health or science related field Exp: 0+ years |
The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you! | 07/02/2024 |
| 233 | Medpace Cincinnati, OH Chemistry Laboratory Technician A minimum of a Bachelor's degree, with previous experience in a research laboratory Exp: 1+ years |
Responsibilities: Prepare samples according to project protocol and/or related SOPs; Maintain compliant laboratory documentation; Perform data analysis and data checking; Interpret results obtained for accuracy and acceptability; Clean and sterilize laboratory equipment; and Other duties deemed necessary. | 07/02/2024 |
| 234 | Medpace Cincinnati, OH Laboratory Quality Assurance (QA) Auditor Bachelor’s degree in the science or a related field Exp: 1-3 years |
The QA Auditor role will be responsible for both internal and external audits, as well as coordinating, conducting, and tracking company-wide Regulatory Training, CAPA Investigations and Metric Analysis. This role will also ensure Compliance to Standard Operating Procedures (SOPs), current Regulations, and Standards. In addition, the Auditor will assist in the creation and maintenance of Controlled Documents. This role is highly visible to Medpace Internal and External Clients; therefore, this role requires excellent Communication Skills, a Proactive Enthusiasm, and Critical Thinking. | 07/02/2024 |
| 235 | Medpace Cincinnati, OH Laboratory Technologist Bachelor's degree in a Biological Science field or Chemical Science field Exp: 0+ years |
The Laboratory Technologist at Medpace Reference Laboratories plays a pivotal role in research based drug development within the pharmaceutical industry. Due to our recent growth, we are in need of qualified and focused driven individuals, like yourself! You would have the unique opportunity to work on the laboratory side of the fast paced medical world by conducting routine and esoteric testing on blood, tissue, and body fluids. If you have an analytical mind set, and enjoy working in a team-oriented laboratory setting, this could be the opportunity for you! | 07/02/2024 |
| 236 | MedPharm Durham, NC Associate Scientist-Performance Testing Bachelors degree, education may be used in lieu of experience Exp: 0-2 years |
The Associate Scientist is an essential member of the laboratory team. They work with the Performance Testing team to conduct in vitro permeation and release testing for topical and transdermal formulations. They also conduct analysis of research projects and results and help develop nonstandard tests. Associate Scientists have the opportunity to collaborate with fellow scientists in study planning, formulation development, analytical, and tissue culture. We are looking for an eager individual who wants to develop personally and professionally. You should have a strong attention to detail, be a go-getter, and be continuously striving for self-improvement. You are passionate about good science and want to help out in any way possible. We are looking to invest in someone who wants to grow not only in this role but also in their scientific career. | 07/02/2024 |
| 237 | Medtronic Fridley, MN Hardware Engineer I Bachelors degree in Electrical Engineering, Computer Engineering or related field required Exp: No Experience |
This position will provide Electrical Design and System Test support for the Translational Research System team on Neuromodulation & Pelvic Health Implantable products such as cutting-edge neurostimulator systems for Deep Brain Stimulation, Spinal Cord Stimulation, and Sacral Nerve Modulation. The individual will support all phases of development including definition, design, troubleshooting, characterization, and verification of medical device research systems. The individual will be an integral part of the R&T organization delivering the highest quality, life changing technology to our patients. This role requires a strong background in hardware development and testing, system integration and testing, and a passion for improving healthcare through technology. | 07/02/2024 |
| 238 | Medtronic Danvers, MA Process Engineer I Bachelors Degree in a related engineering discipline (i.e., mechanical, biomedical, industrial, materials science) Exp: No Experience |
As a Process Engineer I, you will be involved with process development, setting up manufacturing operations, and interfacing cross-functionally with other key engineering expertise to develop a product. In this role, you will part of a team but will be able to work independently to determine and develop approaches to solutions. You will communicate with internal and external customers and suppliers. Your work will involve collaboration and dynamic interactions with R&D and Design Assurance regarding products in the development pipeline and with operation team members for new or iterative product implementation. | 07/02/2024 |
| 239 | Medtronic North Haven, CT Manufacturing Engineer I Bachelors degree, preferred in Engineer Exp: No Experience |
The Manufacturing Engineer will be working with highly motivated team members and dynamic work environment. This is a great opportunity to interact and work with broad cross-functional groups including different manufacturing sites engineering, quality, share-services, marketing team and extensive business platforms, and suppliers to continuously improve the manufacturability. | 07/02/2024 |
| 240 | Meissner Camarillo, CA Quality Assurance Coordinator Bachelor’s Degree from a 4-year accredited college or university Exp: 1-3 years |
As part of the Quality Assurance team, you will work closely with Quality Control, Customers, Engineering, Manufacturing, Sales and Marketing teams to ensure that solutions in development and in production meet the needs of our customer base and are compatible with the regulatory environment of our industry. As part of the Quality Assurance team, you will work closely with Quality Control, Customers, Engineering, Manufacturing, Sales and Marketing teams to develop and improve our Quality Management System (QMS). Work collaboratively with the team to develop, implement, maintain and ensure the performance of the company’s QMS. Utilizing leading-edge technology, you will support customer inquiries by monitoring Meissner’s Quality inbox, coordinating responses and assigning inquiries to the appropriate parties. Support and ensure compliance with established company policies and procedures, objectives, quality assurance program. Support implementation of QA procedures and documents. Review SOPs to ensure alignment with quality guidelines and documents. | 07/02/2024 |
| 241 | Meissner Camarillo, CA R&D Scientist I Bachelor’s degree required in STEM-related field Exp: 1-5 years |
Are you a passionate scientist ready to push the boundaries of research and development? Join our dynamic R&D team as an R&D Scientist I, where you’ll spearhead groundbreaking experiments, analyze cutting-edge data, and contribute to revolutionary product advancements. If you thrive in a collaborative environment and are driven by discovery, we want you on our team! Our customers use our products and technologies to develop new therapeutics and many familiar products that support our modern lifestyle. At the core of these products, are in-house technologies that are developed and maintained by highly talented and self-driven engineers and scientists. Participate in technology development projects, Assist in technology transfer of R&D Activities to manufacturing, Support our technologies to continuously improve our products and processes. | 07/02/2024 |
| 242 | Teva Pharmaceuticals Salt Lake City, UT Quality Control Analyst I Bachelor’s degree, preferably in the sciences or any combination of equivalent education Exp: 0+ years |
Teva has an opportunity for a passionate Chemist to join our team. As a key part of our dedicated, friendly, and collaborative Product Quality Team, you’ll play an essential role in laboratory testing of pharmaceutical product in support of commercial product release. This role is great role to learn the pharmaceutical manufacturing process. Many of our entry level lab analysts advance into other roles in Science, Quality and Production. | 07/02/2024 |
| 243 | Mercury Bio Santa Fe, NM Research Associate BS or MSc in related fields and previous research experience Exp: 1+ years |
Mercury Bio has immediate openings for Research Associates with expertise in molecular genetics, biochemistry, bioinformatics, immunology and microbial or human cell culture. Ideal candidates should have a BS or MSc in related fields and previous research experience. This position requires creative and critical thinking, as well as the ability to work independently. Mercury Bio is located in Santa Fe, NM and focuses on the development of RNA therapeutics to control gene expression in humans in a safe and dose-dependent manner. | 07/02/2024 |
| 244 | Meridian Bioscience Memphis, TN Quality Assurance Associate Bachelor’s degree from accredited institution in life science, chemistry, pharmaceutical science, statistics, or health/human services related field. Exp: 0-5 years |
The Quality Assurance (QA) Associate will support QA processes, programs, and conduct QA activities. This position will uphold standards, methods, and procedures for all stages of production. This position will identify continuous process improvement areas, in compliance with Good Manufacturing Practices (GMP) and Good Documentation Practices (GLP) processes and documentation for quality control activities. This requires excellent technical skills and abilities, analytical and mathematical skills, organizational and time-management skills, verbal, and written communication skills, plus ability to apply attention to detail. | 07/02/2024 |
| 245 | Meridian Bioscience Memphis, TN Quality Control Analyst Bachelor's degree in a scientific discipline or equivalent Exp: 1 years |
The Quality Control Analyst position performs testing and inspection of raw materials, in-process and finished products, and audits the corresponding documentation in compliance with internal SOPs and applicable regulatory requirements, participates in test method validation development and execution, and assists in the training and development of new Quality Control Analysts. The Quality Control Analyst is also responsible for performing duties required in the application and continued improvement of the company’s Quality System. | 07/02/2024 |
| 246 | Meridian Bioscience North Billerica, MA Research Associate Bachelor of Science degree required, experience with analytical chemistry strongly preferred Exp: 0+ years |
Primary role is to run experiments, acquire and record data.Tasks/Duties/Responsibilities: Support projects by conducting experiments, acquiring, and accurately documenting data. Contribute to completion of milestones associated with specific projects. Expected to grow and develop in this role and be able to draw conclusion from studies and design experiments. | 07/02/2024 |
| 247 | Meridian Bioscience Memphis, TN Lab Production Associate (Antigens and Cell Culture) Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecular Exp: 0+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 07/02/2024 |
| 248 | Merit Medical South Jordan, UT Mfg Engineer I Bachelor’s or Master's Degree in Engineering Exp: 0+ years |
Performs routine technical work such as the design, manufacture and operation of structures, machines and systems under general supervision and guidelines. Performs routine technical work requiring the application of standard techniques, procedures, and criteria in carrying out engineering tasks. Uses limited amounts of discretionary judgment in making decisions regarding technical alternatives. Performs work of some higher technical level for training purposes, and work is screened to ensure correct application of scientific principles. Works on special projects, writes ECN's, and may create prototypes under general direction. Performs other related duties and tasks as required. | 07/02/2024 |
| 249 | Merit Medical South Jordan, UT R&D Engineer II - (Endovascular) Part-time Bachelor’s Degree in Engineering or technical field related to the department of assignment Exp: 0+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. This position is 20 hours a week in the RND Endovasular division of Merit Medical. | 07/02/2024 |
| 250 | Merit Medical South Jordan, UT Engineer II (Annual) Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision Exp: 0+ years |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. | 07/02/2024 |
| 251 | Merit Medical South Jordan, UT Technician III Bachelor's Degree with 1 year of exp, Associate's Degree with 3 years of 3 years tech exp, or High school Diploma with 5 years of tech exp Exp: 1+ years |
Performs non-routine technical assignments of substantial variety and complexity. Performs assignments and may assist in planning assignments of a non-routine nature for which operational precedents are not fully applicable. Prepares test specimens, adjusts and operates equipment, and records test data, pointing out deviations resulting from equipment malfunction or observational errors. Extracts engineering or other data from various reports, processes the data, and presents the data. Receives technical advice from engineers or supervisor for complex problems. Working overtime may be required for this position. Performs other duties and tasks as required. | 07/02/2024 |
| 252 | Meso Scale Diagnostics Gaithersburg, MD Scientist I, Bioanalytical Lab Bachelor's degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 1+ years |
The Bioanalytical Scientist I provides supervision of daily laboratory operations, offers guidance, leadership and direction to lab personnel to ensure on-time completion of customer projects. This includes leading initiatives for the transfer of newly developed assays that have been developed for customers to the company's Bioanalytical Lab, supporting new instrumentation intended for use in sample testing services and managing studies performed in accordance with relevant regulations. This position will directly supervise the work of others in their group and/or across interdisciplinary teams. The Bioanalytical Scientist I will lead and/or direct the work of others, to include establishing the scope of work assignments, experiments and work schedules/deadlines. They are expected to independently manage multiple projects yielding high quality results, and provide oversight and guidance to other team members as needed. | 07/02/2024 |
| 253 | Meso Scale Diagnostics Rockville, MD Quality Control Analyst I Bachelor’s degree in relevant field preferred. Associate’s degree in relevant field required. Exp: 0+ years |
Under general supervision, the Quality Analyst I performs routine quality control inspection, testing and data analysis for various incoming, in-process, and final products within MSD’s protein-based immunoassay catalog. This position will execute various laboratory cleaning activities to help support overall operations of Quality/Product Control. | 07/02/2024 |
| 254 | Meso Scale Diagnostics Gaithersburg, MD Bioanalytical Associate I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, or other related area is req Exp: 0-2 years |
A Bioanalytical Associate I is responsible for handling biological samples, reagents, and materials in support of sample testing and assay service projects. This is a laboratory based position whose primary function will be sample management and handling, under direct supervision and direction. The incumbent may also perform protein-based immunoassays on a routine basis with relatively high throughput (2-8 plates per day). The incumbent is expected to adhere to all standard operating procedures and policies established for execution of Bioanalytical studies and sample testing projects under applicable regulatory compliance requirements. | 07/02/2024 |
| 255 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Mechanical Bachelor’s degree in Mechanical Engineering Exp: 0+ years |
The Mechanical Engineer I is responsible for mechanical design, testing, and documentation of new instrumentation and support of exisiting instrumentation for the biodefense, clinical and life-science markets. Design work will include the design of precision mechanisms and complex assemblies that include machined, molded and sheet-metal components. | 07/02/2024 |
| 256 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Automation Bachelor’s degree in Computer Science or Electrical, Mechanical, or Systems Engineering is required Exp: 0-1+ years |
The Automation Engineer I will design and build high performance, automated process equipment used for manufacturing and/or laboratory automation systems. These systems include, but are not limited to automated reagent dispensers, assembly, machine vision, and liquid handling systems for micro-plate test kit and micro-fluidic assay cartridges used in the biodefense, clinical, and life-science markets. | 07/02/2024 |
| 257 | Meso Scale Diagnostics Rockville, MD Production Control Technician I Bachelor’s degree in life sciences, protein sciences, cellular/molecular biology, chemistry, biochemistry, biotechnology, engineering or a related fie Exp: 0-1+ years |
The Production Control Technician I is responsible for assisting in the control of production, documentation and inventory maintenance for multiple groups within Consumable Operations. | 07/02/2024 |
| 258 | Meso Scale Diagnostics Gaithersburg, MD Engineer I, Systems Bachelor’s degree in Systems, Mechanical, or Electrical Engineering or a closely related field Exp: 0-1+ years |
The Systems Engineer I is responsible for assisting in the development and management of requirements and specifications, system integration and testing of electromechanical, fluidic, thermal control, and imaging systems, and formal verification and validation testing. | 07/02/2024 |
| 259 | MethodSense Morrisville, NC Quality and Safety Engineer Bachelor’s degree in biomedical engineering or alternative engineering degree. Exp: 1-7 years |
We are looking for talented Quality and Safety Engineers to join our experienced team. If you can commit yourself to supporting a passionate regulatory affairs and quality assurance business dedicated to their clients, you can have a career with us. We need someone with honesty, integrity and excellent communication and interpersonal skills. The position requires the ability to work with client company executives, test labs and FDA regulators. It also requires agility and love for knowledge. If you want to join a high energy purposed team, please apply. | 07/02/2024 |
| 260 | Metrohm Charlotte, NC Field Service Technician - Lab Equipment A degree or certification in Chemistry (or related STEM field) is preferred. Exp: 0+ years |
Field Service Technicians provide on-site preventative maintenance and basic service for Metrohm laboratory instruments. You will attend training classes at our headquarters in Tampa, FL. Field Service Technicians get to travel to a diverse group of labs, meet different people and see various instrument applications at work. You will have the resources to support the client face to face, via phone, email and Microsoft Teams. This is a remote position that requires some overnight travel in the NC/SC region. | 07/02/2024 |
| 261 | MicroAire Surgical Instruments Charlottesville, VA Design Verification Engineer (Test Development) Bachelor’s in Mechanical or Biomedical Engineering required. Exp: 0+ years, internship exp applies |
Develops Plans for the Appropriate Verification and Validation (testing) of new products, line extensions, and product redesigns. | 07/02/2024 |
| 262 | MicroVention Aliso Viejo, CA Engineer I, R&D Bachelor’s degree in Engineering or Scientific field. Exp: 6 months |
Support development of medical device products with work including writing or verifying specifications; designing new products and fixtures; testing processes and equipment; and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. Job duties: Develop new product concepts and products. Provide engineering design and process development.Generate intellectual property; write invention disclosures. Supervise assemblers, technicians, and specialists. Partially self-directed and capable of meeting project goals with supervision. Some travel required. Perform additional responsibilities as assigned. | 07/02/2024 |
| 263 | Mikart Inc Atlanta, GA Quality Control Analyst Bachelor of Science in Chemistry with 0 yrs exp or Bachelor of Science degree in a related science plus 1 year of applicable exp Exp: 0-1 years |
The Quality Control Analyst for Mikart, LLC is responsible for conducting analyses on various components, in process materials and finished dosage forms. Document all analyses performed through the use of notebooks and official forms. Immediately report any anomalies to the Team Leader. Enter data into spreadsheet templates and verify accuracy by performing minimal manual calculations. Assure the accuracy of all data used for batch calculations. Conduct all operations in strict accordance with applicable regulations, guidance documents, SOPs and Mikart policies and procedures, including computer data acquisition and integrity policies. Assure that all laboratory areas and workspaces are maintained in a neat and orderly fashion. Perform necessary cleaning, maintenance, and calibration of instrumentation, as required. Maintain or request appropriate supplies and materials necessary to complete all assignments. Assist in maintaining accurate documentation of all supplies and chemicals received and used. Maintain appropriate records of waste storage and disposal in accordance with Mikart procedures and appropriate regulations. Assure that laboratory reagents, solutions, standards, samples, and controlled substances are used and stored properly and in accordance with all applicable regulations and guidelines. Secure all assigned samples while testing is in progress. Assure all materials used in analyses are within their established expiry period. | 07/02/2024 |
| 264 | Mikart Inc Atlanta, GA Quality Control Analyst (Microbiologist) Bachelor of Science in Biology with 0 yrs exp or B.S. degree in a related science plus one-year applicable experience, or other appropriate combinatio Exp: 0-1 years |
The Quality Control Analyst (Microbiologist) for Mikart, LLC is responsible performing analyses on incoming samples requiring microbiological testing. Receive incoming samples, including water, environmental, raw material and dosage form samples, and insure that information is accurately and promptly entered into logs. Perform microbiological or other testing required on incoming samples safely and in accordance with all GMP, USP and Mikart specifications and procedures. Document all analyses performed through the use of notebooks and official forms. Immediately report any anomalies to the supervisor. Report any discrepant, suspect or out-of-specification results to the Microbiology Supervisor immediately. Accurately follow investigation plan directives issued by supervisory personnel. Assure proper handling of materials under test, including controlled substances, and ensure proper storage of all samples. Assure that all waste is processed according to procedures before disposal. Complete usage and maintenance logs accurately and promptly for instruments and equipment present in the micro lab. Receive and assure that all laboratory reagents, solutions, standards, samples, and controlled substances are used, stored properly and in accordance with all regulations and guidelines. Secure all assigned samples while testing is in progress. Assure all materials used are within their established expiry period. Verify that all laboratory equipment is within the active calibration period. | 07/02/2024 |
| 265 | Miltenyi Biotec Boston, MA Clinical Trial Associate Bachelor's Degree Exp: 0-2 years |
The Clinical Trial Associate (CTA) will support the clinical trial team, ensuring that all essential documentation is collected, maintained and filed during the study. Collaborate with Clinical Trial Manager(s) to assist in the operational and logistical aspects of clinical trial management tasks (e.g. start-up, maintenance, and close-out activities) according to ICH-GCP and standard operating procedures. Liaise with CROs and other clinical vendors to ensure deliverables are met and communication is efficient. Partner with Investigators and clinical site staff to ensure optimal Sponsor-Site relationships. Assist in the management of study to ensure adherence to timelines and achievement of study goals while ensuring high quality. | 07/02/2024 |
| 266 | Mission Bio South SF, CA Sr Bioinformatics Scientist, Remote Master's or PhD degree in Computational Biology, Bioinformatics Exp: Relevant grad/postdoc experience are also welcome |
We are seeking a talented and motivated Computational Biologist/Bioinformatics Specialist to join our team. This role will be pivotal in supporting our pharma accounts, driving product development and clinical traction by utilizing advanced data analysis techniques, algorithm development, and effective communication with customers. The ideal candidate will have a strong background in data analysis, with a focus on single-cell analysis, and possess the skills necessary to refine algorithms for production environments and ensure compliance with regulatory standards. | 07/02/2024 |
| 267 | Moderna Norwood, MA Engineer I, Process Engineering Bachelor’s degree in chemical engineering, mechanical engineering, or related field. Exp: 0-2 years |
In this role, you will support the operability and reliability of GMP manufacturing process equipment at Moderna's manufacturing facility in Norwood, MA. This individual will assist Facilities and equipment End Users with routine troubleshooting and optimization of process equipment. Applicants should enjoy working in a fast-paced, dynamic, and innovative environment. | 07/02/2024 |
| 268 | MP Biomedicals Solon, OH Production Chemist Bachelor of Science in Chemistry, Biochemistry, or Biology or equivalent work/school experience. Exp: 0-3 years |
The production chemist will be trained on two different product lines. This position will rotate training through two manufacturing areas that include Immunology and Molecular Biology Liquids. Learn and be responsible for a wide variety of product formulation tasks. Follow and optimize production processes while following safety protocols. Produce quality research products in a timely fashion to meet customer demand. Responsibilities will include: Operation of lab equipment including spectrophotometer, plate reader, centrifuges, pipettors, etc., Purification of antibodies from whole antisera using affinity chromatography methods. Conjugation of antibody to enzymes/fluorochromes. Maintenance of detailed records of products in production. Perform Quality Control testing for Immunology products (UV-VIS, Immunoelectrophoresis, and ELISA). | 07/02/2024 |
| 269 | Myriad Genetics Salt Lake City, UT Research Associate (Onsite) BA/BS or MS in Molecular Biology, Cell Biology, Genetics, Biochemistry, Biophysics, Chemistry, or a related discipline Exp: 1+ years |
We are looking for a Research Associate to join our interdisciplinary R&D team that includes scientists in Salt Lake City and South San Francisco (this posting is for a role in Utah). The ideal candidate will have hands-on experience with a range of current molecular biology techniques, with particular focus on NGS. We are seeking a collegial teammate who is curious and rigorous, an individual who shares our enthusiasm for improving people’s lives by building the products that power precision medicine. | 07/02/2024 |
| 270 | AlloyTx Waltham, MA Research Associate, Antibody Discovery B.S. in Immunology, Molecular Biology, or related discipline. Exp: 0-2 years |
As a Research Associate, Antibody Discovery, you will work with our ADS team to build new antibody technologies for the discovery of antibody-based therapeutics. You will be using the very latest single-cell techniques with the goal of identifying drug candidates in close collaboration with our partners. This role requires strong molecular biology skills, and the ability to plan and execute lab activities efficiently. This role will report to Head of In-Vivo Antibody Discovery with autonomy owning various stakeholders, projects, and tasks in a dynamic start-up environment while keeping up the pace of Alloy. This is you! | 5/17/2024 |
| 271 | AlStem Bio Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM, INC is a growing research biotechnology company located in Richmond, CA. ALSTEM is a nimble provider of tools specializing in virus packaging, genome editing, cell engineering and stem cells for life science research. ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 5/17/2024 |
| 272 | Alta Sciences Columbia, MO Associate Scientist, DCA M.S. Exp: +1year |
In the performance of their respective tasks and duties, the Associate Scientist, Dose Concentration Analysis are expected to be engaged in the conduct of or responsible for the supervision of a nonclinical laboratory study shall have the education,training and experience, or combination thereof, to enable that individual to perform their assigned functions. They will also need to comply with Good Laboratory Practices (GLP), and all regulatory requirements applicable to the position. They will need to develop, revise, review and implement Standard Operating Procedures {SOPs) as applicable to the position. The Associate Scientist will need to understand and incorporate the information contained in the Employee Handbook into day to-day job performance and strive to demonstrate the Company's values in all work-related activities. They'll need to provide technical and scientific leadership in the area of analytical chemistry. This role requires them to plan and execute projects, identify and acquire the necessary facilities equipment and procedures for research projects by performing the below duties. | 5/17/2024 |
| 273 | Alta Sciences Everett, WA Research Associate - Flow Cytometry Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate I, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting our Flow Cytometry team. | 5/17/2024 |
| 274 | Alta Sciences Everett, WA Research Associate II - Biomarker Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate II, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting our Biomarker assay team. | 5/17/2024 |
| 275 | Alta Sciences Scranton, PA Research Associate - Laboratory Animals BS/BA in a scientific discipline preferred. Exp: 0-2 years |
Do you love working with animals? Do you want to contribute to advancing human health science research? Do you like to work in small teams? Altasciences is seeking Research Associates at all levels of experience that have a passion for scientific research. In this position your focus will be working directly with animals in the collection of data and in support of the development of human medicine. You will perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different animal models: mice, rats, non-human primates, swine and canine and you will have the opportunity to become a proficient, highly skilled expert in this field. Multiple shifts available. | 5/17/2024 |
| 276 | Alta Sciences Everett, WA Research Associate PCR - Laboratory Sciences Associate degree in scientific discipline. Exp: 6 months |
As a Research Associate III, you will be at the forefront of groundbreaking research, contributing to the success of our laboratory through diverse responsibilities that go beyond the ordinary. Engage in hands-on activities such as equipment maintenance, supply stocking, and general cleaning while supporting and executing data collection activities involving qPCR, ddPCR, and DNA isolation, . | 5/17/2024 |
| 277 | Alta Sciences Columbia, MO Research Associate II, Laboratory Sciences Associates/Bachelor’s degree in Immunology/ Biology/ Chemistry or equivalent scientific discipline. Exp: 1-3 years |
The Research Associate II, Laboratory Sciences role works independently in the day-to-day laboratory operation, collection, and review of data for the Laboratory Sciences department. Support and perform data collection activities including ligand binding assays, and/or flow cytometry, and/or cell-based assays, and/or mass-spectrometry, and/or as assigned. Participates in the creation of study worksheets, SOPs and other documents as assigned. Provides support for general laboratory equipment and maintenance as assigned. | 5/17/2024 |
| 278 | Alta Sciences Everett, WA Research Associate I - Small Animal Unit BS/BA in a scientific discipline preferred. Exp: 0-2 years |
Do you love working with animals? Do you want to contribute to advancing human health science research? Do you like to work in small teams? Altasciences is seeking Research Associates at all levels of experience that have a passion for scientific research. In this position your focus will be working directly with animals in the collection of data and in support of the development of human medicine. You will perform technical procedures to support advancements in pharmaceutical development. In this position you will learn and perfect complex procedures including learning the skills to operate laboratory equipment, specimens collection techniques and data acquisition. At Altasciences Preclinical Services, we work with many different animal models: mice, rats, non-human primates, swine and canine and you will have the opportunity to become a proficient, highly skilled expert in this field. Multiple shifts available. | 5/17/2024 |
| 279 | Aluna Alameda, CA Scientist I - Research and Development BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field. Exp: 1-3 years |
Alveo Technologies is looking for a Research and Development Scientist 1 to support R&D efforts of projects in disease detection. A successful candidate will assist in planning and executing protocols, and conducting experiments at the bench to meet objectives. The candidate should be able to review, understand and follow the instructions, protocols and SOPs provided by R&D. | 5/17/2024 |
| 280 | Alvogen Norwich, NY Quality Systems Specialist I Level I: Associate or Bachelor of Science in Chemistry, Life Science, Engineering or combination of training, education, and experience that is equiva Exp: 1 - 3 years |
The Quality Systems Specialist provides system administration and support of daily quality activities to ensure compliance with global regulatory requirements and guidelines (FDA, ICH, EU, WHO, etc.). | 5/17/2024 |
| 281 | Alvogen Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline. Exp: 0-3 years |
The Quality Control Chemist I / Microbiologist I: Performs routine testing to assess the conformance of raw materials, finished products, and/or stability samples to predetermined product specifications. Performs routine testing in conformance with approved procedures, accurately and concisely documents data, and reports results. Demonstrates a basic knowledge of SOP’s and GMP regulations as related to the pharmaceutical quality control laboratory. | 5/17/2024 |
| 282 | Amber Bio San Francisco, CA Research Associate Bachelor’s or Master’s degree in Biology, Biochemistry, Chemical Engineering, Biological Engineering, or a related field. Exp: 1 year |
Responsibilities: ● Work in a highly collaborative team focused on advancing our gene editing platforms. ● Support technology development strategy and design/build/test improved systems. ● Support engineering and characterization of editing systems with high-throughput experimentation. ● Maintain detailed, well-organized, and timely documentation of experiments and data. ● Effectively analyze and present data, and communicate research plans and timelines to the core team. ● Live Amber Bio’s core values of being biologically inspired, being honest and rigorous about our research, and fostering a supportive environment. | 5/17/2024 |
| 283 | Amplify Bio West Jefferson, OH Asst./Associate Scientist, Analytical Sciences Bachelor’s degree in molecular biology, Biochemistry, Immunology, Molecular Genetics, or related field. Exp: 1 year |
AmplifyBio is currently seeking to hire an Assistant/Associate Scientist to join our growing Analytical Sciences team! The Assistant/Associate Scientist is responsible for performing analytical testing using a variety of cellular and/or molecular biology analysis platforms. Level of position and title will be based on experience and will report to a supervisor or senior scientist of Analytical Sciences. | 5/17/2024 |
| 284 | ANI Pharmaceuticals Baudette, MN Quality Assurance Specialist Bachelors degree is required. Chemistry, medical technology, microbiology preferred. Exp: 1-2 years |
This position is responsible for providing support to the Manufacturing and Packaging Operations to ensure relevant procedures are followed and meet GMP requirements. This includes, but is not limited to the following: 2nd Shift Monday -Friday 3:15 pm to 11:15 pm | 5/17/2024 |
| 285 | ANI Pharmaceuticals Baudette, MN Quality Control Chemist Bachelors degree in chemistry, biochemistry, microbiology or closely related field/major. Exp: QC Chemist – 1-3 years experience |
The QC Chemist position is responsible for independently performing testing in a pharmaceutical Quality Control laboratory. All work will be conducted in accordance with standard operating procedures and test methods. This includes performing testing on raw material, in-process and finished product samples. Execute compendia method validations, method transfers and validation support of new product development. Set up and confirm suitable operation of equipment and instrumentation. Collect data and generate/report results in accordance with governing test methods and SOPs. | 5/17/2024 |
| 286 | Aphena Pharma Easton, MD Manufacturing Engineer BSME or equivalent experience. Exp: 1+ years |
Aphena Pharma Solutions is looking for a Manufacturing Engineer to join our team in Easton, MD! Aphena Pharma Solutions is a dynamic pharma solutions provider focused on contract packaging, repackaging and manufacturing for the pharmaceutical, OTC, dietary supplement, animal health and medical device marketplaces. | 5/17/2024 |
| 287 | Appia Bio Culver City, CA Research Associate I/II MS in Biology or related major. Exp: 0-4 years |
We are seeking a creative and driven Research Associate I/II ready to take on the challenge and opportunity presented by the frontiers of creating novel engineered cell therapies. The individual will be part of the Molecular Biology team and support the efforts to generate and deliver critical gene expression plasmids and lentivirus preparations. The individual will primarily be working directly with an Appia Bio Scientist and will be required to work both independently and as a team in a fast-paced environment to support ongoing discovery projects. The Research Associate I/II will join a culture of intellectual rigor and collegiality that has been built at Appia. | 5/17/2024 |
| 288 | Applied Medical Rancho Santa Margarita, CA Plastics Process Engineer II Bachelor’s degree in Polymer, Materials, Plastics, or Manufacturing Engineering (or equivalent). Exp: 1-2 years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. As a Plastics Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 5/17/2024 |
| 289 | Aptitude Medical Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry Level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 5/17/2024 |
| 290 | AAVIS Pharmaceuticals Hoschton, GA Quality Control Chemists (Hoschton, GA) Master’s Degree in Chemistry, Analytical Chemistry, or Pharmaceutical Science. Exp: 1+ years |
Develop and optimize quality control methods for drug product and drug substances; Perform testing of raw materials, intermediates and finished product using HPLC/Empower, GC, Dissolution apparatus/Autosampler, UV/Vis, and FTIR; Perform routine testing of residual solvents for raw materials and finished products; Develop and perform method validation and method transfer for ANDA and QC methods for Assay, Dissolution, Impurities, and residual solvents per USP and ICH guidelines; Calibrate and troubleshoot HPLC system, Dissolution, PH meter and KF apparatus; Perform wet chemistry tests, including LOD, pH, titration, residue on ignition and Heavy metals in compliance with cGMP and cGLP. | 5/10/2024 |
| 291 | Abbott Minnetonka, MN Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Minnetonka, MN location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Quality Engineer I is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within new product development, manufacturing, or system/services support. | 5/10/2024 |
| 292 | Abbott Sylmar, CA Mechanical Development Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Mechanical Development Quality Engineer I assures new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs | 5/10/2024 |
| 293 | Abbott Sylmar, CA Development Quality Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Development Quality Engineer I assures products, processes, and quality records conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross-functional team members that facilitates organizational success by protecting patient safety and meeting business needs. | 5/10/2024 |
| 294 | Abbott Temecula, CA Associate Engineer - Product Performance Bachelor's degree. Exp: 0-2 years |
In this role you will identify, analyze, investigate, monitor and document patterns and trends in post marketing surveillance data as part of the CAPA system. Analyze and investigate product complaints from the field as part of post market surveillance requirements. Communicate and educate management, R&D, marketing, sales organization and other departments, as well as external customers about product performance. Ensure that information and insight gained from the investigations and corrective actions is fed back to the R&D and marketing organizations as part of the risk management and design input systems. Develop Post Market Surveillance Plans and provide engineering support for complaint investigation readiness of new products. | 5/10/2024 |
| 295 | Abbott Sylmar, CA Risk Management Engineer I Bachelors Degree Or an equivalent combination of education and work experience. Exp: 0-2 years |
This position works out of our Sylmar, CA location in the Cardiac Rhythm Management division. As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats. Risk Management Engineer I works closely with development/manufacturing/quality engineering to establish and ensure compliance and quality for product related risk management documentation. Ensure risk management assessments and evaluations for products conform to established standards and agency regulations. | 5/10/2024 |
| 296 | Abbott Pleasanton, CA Systems Engineer I Bachelor’s Degree in Engineering (Mechanical, Computer, Electrical, or Software), Computer Science, or related discipline. Exp: 6 months’ |
We are recruiting a Systems Engineer to join our Abbott Heart Failure team in Pleasanton, CA, where we are focused on helping people with heart failure manage their health to ultimately change and save lives. The engineer will be primarily working on the CardioMEMS HF portfolio, which remotely monitors changes in pulmonary artery (PA) pressure, which is used to prevent worsening heart failure, lower heart failure mortality rates, and improve quality of life for our heart failure patients. Systems engineering defines, designs, tests, and integrates components, disciplines, and products within the CardioMEMS HF System, including implantable sensors, external reader systems used by clinicians and patients, mobile application software, and cloud-based web applications. The System Engineer will help execute tasks during design change projects and development of next generation products, including requirements definition and management, design documentation, and system testing, verification, and validation. | 5/10/2024 |
| 297 | Abbott Minnetonka, MN R&D Engineer I Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, biological sciences, medical/clinical science or equivale Exp: 1+ years’ |
As R&D Engineer I, at our Plymouth, MN or St. Paul, MN location, you will be part of our Electrophysiology (EP) product development team focused on delivering the future in diagnostic, imaging, and ablation therapy catheters. In Abbott’s Electrophysiology (EP) division, we’re advancing the treatment of heart and vascular disease through breakthrough medical technologies, allowing people to restore their health and get on with their lives. | 5/10/2024 |
| 298 | Abbvie North Chicago, IL Veterinary Technician AS/BS degree. CVT required. Exp: 0-4+ years |
The Veterinary Technician carries out daily activities in the vivarium and provides clinical nursing care and research support for lab animals. Works independently on weekends and holidays. Contributes to specific projects in support of Comparative Medicine initiatives. Provides exemplary animal care. Adheres to all department and AbbVie regulatory expectations, as well as USDA and FDA regulations. Provides veterinary care in support of the AbbVie drug discovery and development process. | 5/10/2024 |
| 299 | Abbvie North Chicago, IL Associate Scientist I/II – DMPK-BA: Drug Metabolism, Pharmacokinetics, and Bioanalysis Master’s Degree or equivalent education. Exp: 0+ years |
Quantitative, Translational & ADME Sciences Department at AbbVie has an open position for an Associate Scientist II position in North Chicago, IL. The successful candidate will be responsible for non-regulated quantitative LC-MS/MS bioanalysis of small molecules from in vivo and in vitro samples, including data analysis and interpretation. | 5/10/2024 |
| 300 | Abbvie North Chicago, IL Associate Scientist II/ Scientist I - Process Chemistry MS degree in chemistry. Exp: 0+ years |
Process Research and Development is responsible for inventing and executing the chemical processes and preparing active pharmaceutical ingredient (API) to enable clinical trials, toxicology studies and drug product development for Abbvie’s pre-clinical and clinical candidates. We create valuable intellectual property through composition of matter, chemical processes, and technology resulting in a cost-effective commercial manufacturing process. We develop the supply chain for APIs, prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We seek a highly motivated scientist with strong synthetic skills to work under the mentorship of a supervisor and to work in a multi-functional team environment. Opportunities may also exist to contribute to high-throughput experimentation, automation, and data science. | 5/10/2024 |
| 301 | Abbvie South San Francisco, CA Associate Scientist II orScientist I, CMC Drug Substance Cell Line Development Group Associate Scientist II - Master’s Degree or equivalent education. Exp: 0+ years |
The Development Sciences Biologics CMC Drug Substance Cell Line Development Group in South San Francisco, CA is seeking a Scientist to join a talented and collaborative team developing CHO cell lines for GMP applications. In this laboratory position, the candidate will perform hands-on molecular characterization studies in a well-supported and dynamic environment to help advance novel therapies to human clinical studies. The work will encompass molecular, cellular, and bioprocess development studies relating to the generation and characterization of optimized CHO cell lines for production of our pipeline candidates. | 5/10/2024 |
| 302 | Abbvie Worcester, MA Associate Scientist or Scientist I, Recombinant Production BS or MS in biology or related field. Exp: BS: 0-5+ years; MS: 0-2+ years |
Discovery Biotherapeutics at AbbVie is seeking a highly-motivated research scientist to join a dynamic team supporting biologics drug discovery. This position will impact projects through purification and characterization of biopharmaceutical products such as monoclonal antibodies in high throughput. The ideal candidate has direct experience with mammalian tissue culture, protein purification, proficiency in standard chromatography techniques, protein characterization (e.g., MS, SEC), and binding assays (e.g., ELISA and flow cytometry). The applicant should be able to analyze, document, and report data. She/he should possess excellent communication skills and be comfortable presenting in group settings. | 5/10/2024 |
| 303 | Abeona Therapeutics Cleveland, OH Associate, Quality Control BS in biochemistry, biology, microbiology, molecular biology or other relevant discipline. Exp: 1 to 4 years |
The Quality Control Associate performs routine laboratory activities in support of GMP testing for Quality Control. Testing includes raw material, packaging components, in-process and finished product. Interacts with employees internal and external to Quality Control. | 5/10/2024 |
| 304 | Absci Vancouver, WA Laboratory Technician Bachelor’s degree in Molecular Biology, Biochemistry, Microbiology, or a related discipline. Exp: 1+ years |
The Laboratory Technician will join the NGS Development team and support innovative research that advances Absci’s proprietary Drug Creation PlatformTM. The NGS team is integral to the success of most projects at Absci, and this role will involve delivering NGS results for library screens and strain construction. Primary responsibilities include providing core support to sequencing and analysis activities. The individual will work closely with other members of the NGS team in day-to-day sample preparation and operation and maintenance of Illumina and PacBio instruments. The individual should be able to master new laboratory skills rapidly and will take on additional technical responsibilities outside of the NGS team. This position will require the ability to work a weekend shift as needed. We seek candidates who are passionate about building a collaborative, multidisciplinary company culture and committed to making a transformative impact on our industry. To be successful in this role, the candidate should be a team player, have an innovative mindset, possess applicable technical experience, and be excited about working in a dynamic startup environment. An ideal candidate will demonstrate initiative and follow-through, a passion for scientific advancement, and a strong commitment to excellence. | 5/10/2024 |
| 305 | Absci Vancouver, WA Research Associate II - Disease Biology Senior Research Associate: MSc in biology, cell biology, immunology or a relevant field. Exp: 1+ years |
As part of the Disease Biology Team, you will work on engineering cell lines for various programs and contribute to the development and optimization of cell-based assays, including, but not limited to, ligand-binding potency, cellular uptake, cytotoxicity, ADCC, CDC, ADCP, and proliferation assays. This role requires experience with mammalian cell culture techniques and understanding mechanism of action (MOA) assays. This position requires strategic thinking and a high level of collaboration across multidisciplinary teams within Absci. It also requires excellent communication, technical, and organizational skills and demonstrated success in delivering under tight timelines. Individuals who enjoy working with a sense of urgency and thrive in a dynamic team and high-performance culture will be successful and thrive in this role. | 5/10/2024 |
| 306 | Accelerated Diagnostics Tucson, AZ Research Associate (Pilot Lab) BS in a scientific discipline. Exp: 1 year |
Accelerate Diagnostics is seeking a motivated Research Associate who would like to gain hands-on experience in an R&D pilot lab supporting antimicrobial susceptibility test (AST) assay development. The successful candidate will be passionate, well-organized, detail-oriented, and work independently as well as in a team environment. The candidate will spend approximately 70% of their time on basic laboratory techniques and the remaining 30% on assisting technical staff with routine lab and office work including equipment maintenance and cleaning, data entry and data management. The work schedule is Monday-Friday, 8:00 am - 5:00 pm. | 5/10/2024 |
| 307 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology. Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. | 5/10/2024 |
| 308 | Astrazeneca Waltham, MA Research Associate Bioscience Immunology, Early Respiratory And Immunology BS or MS degree in biology, immunology or a relevant discipline. Exp: 1 year |
As a part of our growing Immunology Bioscience team within the Early R&I department, we are seeking a highly motivated scientist with diverse laboratory skills to join our collaborative team. This candidate would ideally have experience in immunology or related disciplines such as biology, biomedical engineering, virology, genetics or microbiology. This is a lab-based position, and the role will be based in Waltham, Massachusetts within AstraZeneca’s state-of-the-art laboratories where you will follow the science to help drive innovation and advance medicine to help improve patient lives. This position offers a unique opportunity to work in a dynamic and innovative environment developing your career at the interface of research and drug discovery. | 5/10/2024 |
| 309 | Astrazeneca Gaithersburg, MD Associate Scientist - Viral Clearance Bachelor’s degree. Exp: 1 – 2 years |
This role will focus on viral clearance, part of the protein purification development function in the PAS department. The major responsibilities include: Design and execute studies to demonstrate virus removal or inactivation capabilities for protein purification unit operations, initially with guidance and gradually become independent. In collaboration with existing team members, plan studies, manage logistics, documentation, data verification and interpretation, report writing, and participate in regulatory submissions. Make periodic presentations in group meetings, project team meetings, and in one-on-one situations. Support purification process development, technology transfer to manufacturing sites, and production incident resolution as appropriate. Participate in new technology evaluations | 5/10/2024 |
| 310 | Astrazeneca Lexington, MA Engineer - Downstream, Viral Vector Product Development BS or MS degree in Biological Engineering, Chemical Engineering, Biochemistry, or related discipline. Exp: 0-3 years |
The candidate contributes to the Viral Vector Product Development group through the design and execution of experiments based around downstream AAV (Adeno-Associated Virus) manufacturing processes. They will assist the purification team to generate, interpret, and present experimental data to inform and recommend process operating conditions with the goal of developing a robust and scalable manufacturing process. They will additionally draft documentation and provide expertise to assists in scale-up and tech transfer to clinical/commercial manufacturing facilities as well as submission of regulatory filings. | 5/10/2024 |
| 311 | Astrazeneca Lexington, MA Engineer - Upstream, Viral Vector Product Development BS or MS degree in Biological Engineering, Chemical Engineering, Biochemistry, or related discipline. Exp: 0-3 years |
The candidate contributes to the Viral Vector Product Development group through the design and execution of experiments based around upstream AAV (Adeno-Associated Virus) manufacturing processes. They will assist the upstream team to generate, interpret and present experimental data to inform and recommend process operating conditions with the goal of developing a robust and scalable manufacturing process. They will additionally draft documentation and provide expertise to assist in scale-up and tech transfer to clinical/commercial manufacturing facilities as well as submission of regulatory filings. | 5/10/2024 |
| 312 | Astrazeneca New Haven, CT Engineer II, Injectable Drug Product Development MS degree in Biochemistry, Chemistry, Chemical Engineering or related field from an accredited university. Exp: 1+ years |
The Engineer II will design and implement experiments to develop injectable drug product formulations and process characterization studies, including analyzing samples and authoring technical reports. Work on an impactful dynamic team and routinely collaborate to innovate with other members of Injectable Drug Product Development as well as other groups in Product Development and Clinical Supply! | 5/10/2024 |
| 313 | Astrazeneca Frederick, MD Production Technician I -Day Shift BS/BA Degree in STEM field. Exp: 1+ years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 5/10/2024 |
| 314 | Astrazeneca Gaithersburg, MD Associate Specialist (Clinical Biologics) Bachelor's degree. Exp: 0+ years |
As an Associate Specialist in the Clinical production team within Biopharmaceutical Development, you’ll build broad knowledge of bioprocessing in a cGMP environment to launch your career in the biopharmaceutical industry. In this role you will take an adaptable, science driven approach to everything you do. You will become an integral part of process development, accelerating product candidates into the clinic and gaining knowledge and experience in cell culture, purification and critical support activities. Under the supervision of highly trained personnel, you will gain the process knowledge and abilities to perform large scale clinical development activities. You will join a collaborative and driven team in an extraordinary biopharmaceutical company. | 5/10/2024 |
| 315 | Active Motif Carlsbad, CA Research Associate I-III RA I: Bachelor's degree in Biological sciences (in Molelcular Biology, Genetics, Life Sciences or related fields). Exp: 0-1 year |
Supports Epi-Services customer projects received by Operations & Services Team Performs next generation sequencing (NGS) lab bench work assigned in a time dependent, quality dependent manner Executes assigned lab bench experiments in a time dependent manner and quality dependent manner Train and follow SOP for each Assay Service Record, document and store data & results as per the SOP/receipt and logging of samples in LIMS tracker Ensure, contribute and support team goals achievements Performs regular clean-up of the lab bench space / equipment utilized Performs and follows safety requirements as outlined Keeps detailed record of lab experiments, logs of instruments utilized Sets up and follows quality control requirements Contributes and supports Group Leader with customer projects data analysis Will perform up to 4 different Assay Services with varying sample batch sizes Other duties as required and/or assigned | 5/10/2024 |
| 316 | Adapt Immune Philadelphia, PA Manufacturing Cell Therapy Specialist Bachelor degree in a cell biology, bioengineering or medical technology related field, or equivalent experience is required. Exp: 1+ years’ |
This role will provide support for the manufacturing of gene modified autologous T-cell product at our manufacturing site in the Philadelphia Navy Yard. The Specialist will perform cell processing activities, media formulation, product sampling, and other manufacturing needs as necessary, commensurate with the level of training and experience of employee. Work is primarily in Grade B and Grade C aseptic manufacturing environment, but may also include support of process development runs in the Manufacturing Science and Technology laboratory. | 5/10/2024 |
| 317 | Adaptive Biotech Seattle, WA Accessioning Specialist II Bachelor’s degree in Biology, Molecular Biology, Immunology or Chemistry. Exp: 1+ years |
The Biological Sample Management Accessioning Specialist II will be an entry level lab operations team member who is able to accession for the clinical or research accessioning teams or assist in sample management. This role is expected to spend approximately 90% of their time inside the lab and 10% of their time working on various tasks assigned by the department. A successful Accessioning Specialist II will complete the responsibilities described below while working to support clinical and research sample management within Molecular Laboratory Operations. Shift: Tuesday - Saturday 9:30am-6:00pm PT | 5/10/2024 |
| 318 | Adaptive Biotech Seattle, WA Material Handler II BS/BA degree preferred. Exp: 1 year |
As a Material Handler II at Adaptive, you’ll be responsible for assisting the clinical laboratory operations and research labs maintain the right levels of inventory. We are seeking team-oriented and energetic individuals who have previous experience in highly regulated environments. Material Handlers reconcile receipts, move, store, and distribute various non-hazardous and hazardous materials, laboratory components, and business supplies. Working with closely related departments, you’ll conduct an array of activities to replenish raw materials and supplies where they are needed. | 5/10/2024 |
| 319 | Adaptive Biotech Seattle, WA Research Associate I Bachelor’s degree in biology, molecular biology, immunology, or similar discipline. Exp: 0-3 years |
Adaptive is seeking a Research Associate I with an aptitude for learning to join our dynamic and collaborative R&D Operations team. You will join the high throughput molecular lab team to aid in the development of new and existing assays for cellular and computational biology research across Adaptive. In this job, you will master a variety of molecular biology techniques and participate in immune system profiling by next generation sequencing jointly with other researchers and computational biologists. As such, high attention to detail and willingness to learn is crucial for success in the role. | 5/10/2024 |
| 320 | Adare Pharma Solutions Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/10/2024 |
| 321 | Adhezion Mansfield, TX Process Engineer BS Degree in Chemical or Mechanical Engineering. Exp: 1+ years |
The Process Engineer will report to the Plant Manager. This position will lead the plants Process Improvement and EHS programs and be responsible for driving manufacturing productivity by improving process efficiencies, reducing wastes, improving quality, and increasing capacities as well as ensuring profitable growth through successful new product commercialization. Key processes in this adhesives and sealants manufacturing facility include solids conveying, mixing, compounding, chemical reactions, and packaging. Engineer will be coming in on the ground floor of a newly installed wood flooring urethane production line, with the ability to work with a diverse group of experienced operators in a positive culture environment. | 5/10/2024 |
| 322 | Adimab Lebanon, NH Research Associate - Mammalian Cell Culture B.S. Exp: 1-3+ years |
We are seeking a Research Associate with experience in mammalian cell culture and protein expression to join our team. This role will support Adimab's novel antibody discovery, maturation, and production platform and closely interface with the Antibody Discovery, Protein Analytics, Molecular Core, and Computational Biology teams. | 5/10/2024 |
| 323 | Adma Biologics Boca Raton, FL QA Specialist I - Product Release Bachelor's Degree required. Exp: One to two years |
The QA Specialist I - Product Release will have the primary responsibility consisting of the review of controlled documents for accuracy and completeness prior to Quality Assurance (QA) release of product. | 5/10/2024 |
| 324 | Adma Biologics Boca Raton, FL Technician III, Manufacturing Fractionation - Night Bachelor's degree. Exp: 1+ years |
The Technician III, Manufacturing Fractionation - Night Shift position is under direct supervision of the Group Leader. This experienced position is responsible for the manufacture of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. | 5/10/2024 |
| 325 | Adma Biologics Boca Raton, FL Technician II - Manufacturing Fractionation - Night Bachelor's degree. Exp: 1+ years |
The Manufacturing Technician II, Fractionation - Night Shift position is under direct supervision of the Group Leader. This experienced position is responsible for the manufacture of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. | 5/10/2024 |
| 326 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years ; MS: 1 year |
Admera Health is looking for an Associate Scientist I/II to join our growing team! • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing • Carry out genomic assays under Biosafety Level II Policies and in regulatory compliance. • Perform Operational Qualification and Performance Qualification on Next Generation Sequencers. • Strictly follow standard operating procedures set forth for processing biological specimens while complying with laboratory safety protocols. • Strict recordkeeping of all laboratory procedures. • Continue acquiring next generation sequencing knowledge to support molecular biology techniques. • Collaborate within the group and cross departmental to achieve goals. | 5/10/2024 |
| 327 | ACDBio Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex Assays. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 5/10/2024 |
| 328 | ACDBio Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 5/10/2024 |
| 329 | ACDBio Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
he Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 5/10/2024 |
| 330 | EyeCRO Oklahoma City, OK Research Associate I Bachelor's degree in a biology related field. Exp: 1 year |
We are looking for a Research Associate to join our team. The ideal candidate will be responsible for participating in a wide variety of animal-based activities and performing routine wet chemistry. This position plays a critical role in our mission to support groundbreaking scientific research and development. We highly value individuals who thrive in a dynamic team setting. Our team's success is built on a foundation of mutual support, shared goals, and a commitment to excellence. | 5/2/2024 |
| 331 | Frontida BioPharm Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/2/2024 |
| 332 | Frontida BioPharm Vandalia, OH 3rd Shift QC Chemist Bachelors Degree in Chemistry or related field. Exp: 1+ years |
The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 5/2/2024 |
| 333 | Fujifilm Diosynth College Station, TX Manufacturing Technician II Associates degree. Exp: one (1) year |
Summary: The Manufacturing Technician III will work directly with a range of technologies. Dependent Upstream Unit: Single-Use Cell Culture Vessels/Bioreactors up to 2000L Bacterial Fermentation Culture Vessels up to 2000L Alpha Wasserman Continuous Flow Centrifuge Disposable Magnetic Mixing Bags and Totes Cell Expansion and Propagation Banking/Cryopreservation of Cell Lines and Viruses Hyperstack, Cellstack, and other Adherent Cell Technologies Plate counting, microscopic examination Monitor cultures, take samples, turn-around of bioreactor and fermenters, sterilization, and inoculation Downstream Unit: Medium to Large-scale filtration systems including Tangential Flow Filtration (TFF), Hollow Fiber Tangential Flow Filtration (HFTFF), Nanofiltration and depth filtration Medium to Large-scale Chromatographic systems (ÄKTA). Pre-Packed Columns from 1L to 100L Single use mixing systems (Pall & GE) Single Use connectivity types such as GE DAC and Colder AseptiQuik Bulk filling Aseptic process simulation and drug product filling Plate counting, microscopic examination Alpha Wasserman Continuous Flow Centrifuge | 5/2/2024 |
| 334 | Fujifilm Diosynth College Station, TX Quality Control Visual Inspection Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 1+ year |
Summary: The Visual Inspection Analyst I will be responsible for assisting the drug product visual inspection program at FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. External US Essential Functions: Perform visual inspection for Final Product Fills and Aseptic Process Simulations (APS) for AQL level inspections Participate in threshold study (POD) executions and training exercises for visual inspection Participate in particulate identifications and investigations, as required. Sub-visible particulate testing (USP <787>, <788> (Method 1 and Method 2), <789>), as appropriate Secondary functions could include: environmental monitoring (Total Air, Viable Air and Viable Surface) in a cleanroom/controlled environment, plate count enumeration and characterization, routine QC laboratory cleaning, management of inventory items for the laboratory Ensure the lab is maintained (organized, clean, & properly supplied). Perform other duties as assigned. Required Skills & Abilities: Must be able to pass a visual acuity test given upon hire, with corrective lenses if necessary. Ability to follow safety procedures outlined in the Chemical Hygiene Plan. Good attention to detail and ability to utilize problem solving/trouble shooting skills. Good computer skills. Demonstrated written and oral communication skills. Ability to multi-task and prioritize work assignments with little supervision. Strong organization and analytical skills | 5/2/2024 |
| 335 | Fujifilm Diosynth Holly Springs, NC Manufacturing Associate 3 - Drug Product BA/BS, preferably Life Sciences or Engineering. Exp: 1+ year |
This role as Manufacturing Dssociate 3 in Drug Product, will mainly include the operation of the filling line including all the related tasks. This role will support projects, which will influence the manufacturing processes for Drug Product Manufacturing. This includes, training new colleagues, maintaining compliance of cGMP documents and assisting in the qualification of equipment as well as all other aspects of the startup of the DPFG facility. This manufacturing facility will be 24/7 operational and the role may require to be flexible with working hours and shift rotation. While in project phase, the schedule will be Monday-Friday during normal business hours. Upon transitioning to operations, this position will transition to a day or night shift that will be defined prior to the transition. During the project phase Contribute to the preparation for operational readiness related to bulk drug product manufacturing Possible assignments include, supporting projects related to procedure review and/or creation, development or transfer of manufacturing business processes and testing and commissioning support Travel up to 0-25% (international or domestic) may be required during the project phase In operations Lead, execute and document manufacturing processing steps and/or manufacturing support activities as well as process monitoring and control Perform in-process testing (pH, conductivity, visual inspection) Execute validation protocols according to cGMP Standard Operating Procedures (SOPs) Maintain training to perform all required manufacturing activities Assist and/or lead cycle counts and manage materials for the assigned manufacturing functional area Perform Operations for all aspects of filling line Assist the lead with tasks in manufacturing activities Assist with the coordination of daily shift activities This role requires shift work (weekend and potential for nights) Perform other duties as assigned | 5/2/2024 |
| 336 | Waters Milford, MA Design Quality Engineer Minimum of a Bachelor’s degree in Engineering or Science related function. Exp: 1+ year |
This position will be responsible for concurrent quality engineering science activities associated with the consumables and lab automation product development business unit, on-market design change, risk management, quality systems and Waters requirements for columns, kits and chemistry products. Primary responsibility will be to provide chemistry/scientific and product support in the following areas: design controls, risk management, change control, post market review, quality planning, continuous improvement, establishment of appropriate requirements management and traceability. This is a Hybrid position based in Milford, MA | 5/2/2024 |
| 337 | InBios International Seattle, WA Research Associate I A bachelor’s degree in a biologicals science. Exp: 1-2 years |
You have a biologicals, life sciences degree, academic or commercial lab experience with good simple buffer knowledge and experience and a firm scientific foundation, and you are eager to put your skills and knowledge to use in the commercial biotech assay research and development field. You also thrive in a fast-paced work environment where priorities and projects may change quickly. You are attentive and teachable and have a strong desire to learn new skills and you want hone those skills you have already begun to master under the supervision and instruction of the team’s lead scientist. You are a good teammate who is responsible and motivated and comfortable working closely in a team environment, where you openly share ideas and collaborate. You may or may not already have lateral flow immunoassay experience. (Prior experience with LFI is not required for the Research Associate I position.) | 5/2/2024 |
| 338 | InBios International Seattle, WA Manufacturing Associate I - ELISA Bachelor’s degree with emphasis on life science OR Associate of Applied Science degree preferred but not required. Exp: 1-year |
We are searching for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale ELISA diagnostic test components in a BSL-2 laboratory. If you are seeking an entry-level, full-time, on-site position where you can gain experience and grow at the forefront of medical diagnostic biotechnology, this is a great opportunity for you. | 5/2/2024 |
| 339 | InBios International Seattle, WA Manufacturing Associate I- Rapid Spray (2nd Shift 3:30PM - 12:00AM) Bachelors degree in life sciences or a similar field. Exp: 1 year |
We have an immediate opening for entry-level candidates to join our Biotech manufacturing team to support efforts in producing EUA-approved Covid-19 antigen tests and other InBios products. This position is ideal for someone who wants to start out working in a biotech laboratory/manufacturing environment, learn industry standard good manufacturing practices (GMP), is ready to learn new skills and procedures and is comfortable working with machines and with your hands. We would like to see your resume if you have general industrial or academic laboratory experience and a willingness to learn more lab skills. This position provides opportunity for working with a team and independently on a variety of tasks including preparing buffers, running semi-automated machines, and producing large-scale lateral flow diagnostic test components. If you are seeking an entry-level position with opportunities for experience and growth at the forefront of medical diagnostic biotechnology this is a great opportunity for you. This position operates on two schedules. This opportunity is for our 2nd shift, which is from 3:30 PM - 12:00 midnight Monday - Friday. | 5/2/2024 |
| 340 | Pace Analytical Maplewood, MN Laboratory Technician Minimum requirement: Associate degree in science or equivalent laboratory experience. Exp: 1 year |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for maintaining the lab spaces and supplies to support research and development laboratories. This includes maintaining equipment, supplies, and lab cleanliness that support the development of a variety of healthcare products. This role may include basic solution and sample preparation. | 5/2/2024 |
| 341 | Pace Analytical Maplewood, MN R&D Lab Tech B.S. in a chemistry, biology or related area of study. Exp: 1+ years |
Join us as an R&D Lab Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. A candidate for this position will have excellent lab skills across a variety of techniques to support a research lab focusing on development of medical adhesives and other devices | 5/2/2024 |
| 342 | Pace Analytical Maplewood, MN Bioanalyst B.S. in molecular biology, biochemistry, biology, chemistry or related science. Exp: 0+ years |
Join us as a Bioanalyts, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for performing bioassays and application development to support biopharmaceutical filtration devices. These analyses include ELISAs, PCR, DNA and more that support cell culture production. In addition the candidate will be supporting the development of new applications of current filtration products. Join us as a Bioanalyts, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. | 5/2/2024 |
| 343 | Pace Analytical Maplewood, MN Physical Properties Technician - Entry Level Bachelors degree in a science field. Exp: 0+ years |
Join us as a Physical Properties Technician, where you’ll put your love of science to work in the Scientific Insourcing Solutions division. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The Scientist will prepare and test samples in the lab for adhesive products, and assist with lab maintenance | 5/2/2024 |
| 344 | Pace Analytical Maplewood, MN Product Engineering Techician B.S. in Chemistry, Biochemistry, Materials Science or related science. Exp: 1+ years |
Join us as an Engineering Product Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This position will actively support the testing of healthcare products crucial to patient’s safety efforts within the healthcare industry. This role includes performing lab-scale polymerization reactions, coating adhesive solutions into films, and physical properties testing. Work is performed as part of a team in a fast-paced environment | 5/2/2024 |
| 345 | Pace Analytical Maplewood, MN Laboratory Technician Minimum requirement: Associate degree in science or equivalent laboratory experience. Exp: 1 year |
Join us as a Laboratory Technician, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. This candidate will be responsible for maintaining the lab spaces and supplies to support research and development laboratories. This includes maintaining equipment, supplies, and lab cleanliness that support the development of a variety of healthcare products. This role may include basic solution and sample preparation. | 5/2/2024 |
| 346 | Pace Analytical Brooklyn Park, MN Microbiologist Bachelor's degree in Microbiology, Biology or a related discipline required. Exp: 1 year - 4 years |
Join us as a Microbiologist, where you’ll put your love of science to work in the Scientific Insourcing Services department. You’ll receive all the training you need to successfully take on your new role and grow an exciting laboratory sciences career at Pace®. The main function of the QC Microbiologist is to perform supportive activities for general lab readiness, conducting critical biological tests, and following SOPs to perform methods using analytical skills and understanding of biological and chemistry techniques and principles. Note: This position is expected to last 9 months up to 1 year. Note: Training will occur for 2-3 weeks standard 8-hour days M-F. Regular schedule will be Saturday - Tuesday, 10 hour days | 5/2/2024 |
| 347 | Vigene Biosciences Rockville, MD QC Associate I - Environmental Monitoring - 4 - 10 hour shifts, Thursday - Sunday from 8am - 6pm 1 B.S in Biology or related field. Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Associate I – Environmental Monitoring will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 5/2/2024 |
| 348 | Vigene Biosciences Malvern, PA Technician II Mammalian Cell Banking Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 1 to 2 years |
Under direct supervision, responsible for performing basic daily laboratory and clean room tasks as they relate to the operations performed within the Manufacturing department, including mammalian cell banking and vaccine preparation activities, data analysis and writing client batch records and SOPs. | 5/2/2024 |
| 349 | Vigene Biosciences Malvern, PA Sample Processing Materials Technician Bachelor's degree (B.A./8.S.) or equivalent in scientific discipline preferred. Exp: 1 to 3 years |
Responsible for performing a wide variety of tasks involved in sample processing and inventory management of critical components, critical laboratory supplies, specialty reagents, client-supplied raw materials, and internal and external cell banks. Performs a variety of activities related to log in, sample processing, storage, shipping of stored materials and client support | 5/2/2024 |
| 350 | Vigene Biosciences Memphis, TN Biomanufacturing Technician I - Shift C Tuesday-Friday: 11:30am-10:00pm EG AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
NOTE: This position is: Shift C: Tuesday thru Friday 11:30am - 10:00pm (Saturday, Sunday, Mondays off) The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 5/2/2024 |
| 351 | Vigene Biosciences Wayne, PA Technician I Environmental Monitoring Bachelor's degree (B.S.) or equivalent in biology or related discipline. Exp: 0 to 1 year |
Responsible for performing daily laboratory tasks as they relate to the Environmental Monitoring and Contamination Control Department. | 5/2/2024 |
| 352 | Vigene Biosciences Memphis, TN QC Specialist 1 Microbiology Bachelor's degree in biology or relevant scientific discipline preferred. Exp: 1 years |
The QC Specialist I for the QC Microbiology Department will be responsible for reviewing laboratory data, writing laboratory and environmental monitoring excursion reports, and executing simple tasks within projects/CAPAs/Change controls. The position requires the utmost attention to detail, good organizational skills, computer proficiency, and a basic understanding of microbiology and laboratory instrumentation. In addition, effective communication skills and the ability to function in a fast-paced, highly technical environment with minimal supervision are essential for success. | 5/2/2024 |
| 353 | Pharmaceutical Calibrations and Instrumentation Indianapolis, IN Applications Engineer - FP/Sentinel - Indianapolis, IN Degree in engineering, mechanical preferred. Exp: 1+ years |
As an Applications Engineer you will assist our sales force with technical expertise for the design of fluid power systems and customer system integrations. This includes preparing hydraulic schematics, test procedures and recommend components. You will provide integral project management for these systems. | 5/2/2024 |
| 354 | Boston Scientific Arden Hills, MN Analytical Chemist I - Extractables and Leachables Bachelor’s degree or higher in chemistry-focused field with aptitude for analytical chemistry. Exp: 1+ years |
The Analytical Chemist I will support chemical characterization (extractables & leachables) testing of medical devices. This role will involve significant hands-on laboratory work, including solution preparation and testing. The medical device products supported include products across the Boston Scientific portfolio. | 5/2/2024 |
| 355 | Boston Scientific Arden Hills, MN R&D Technician II - 1st Shift Associates in Arts degree/diploma. Exp: 1 Year |
Executes and supports testing of implantable medical device batteries often involving specialized equipment in a laboratory environment during the design, development, and production life cycles of medical devices batteries. Your work will directly impact the quality and reliability of BSC products and improve the lives of our patients. You will be directly involved in characterizing and evaluating the performance of implantable medical device batteries. Take pride that the work you do helps save lives and improve the quality of life for millions of people around the world. | 5/2/2024 |
| 356 | Boston Scientific Arden Hills, MN Manufacturing Tech II - 3rd Shift Associate in Arts degree/diploma. Exp: 1+ years |
Responsible for performing functions associated with all manufacturing operations, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, subassemblies, and final assemblies. Determines and may assist in developing methods and procedures to control or modify the manufacturing process. Works with engineers in conducting experiments. | 5/2/2024 |
| 357 | Boston Scientific Arden Hills, MN Manufacturing Tech II - 2nd Shift AA degree. Exp: 1 year |
Responsible for performing functions associated with all manufacturing operation, including manufacturing equipment support, calibration tasks, equipment optimization, OEE utilization. In battery manufacturing we have a diverse roster of equipment. You will support automation systems, electrical test equipment, laser systems, fixturing, vacuum systems, and much more. This is a great opportunity to further your technical career within a winning, people-oriented company. | 5/2/2024 |
| 358 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Monday through Friday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. We have an exciting opportunity for a Research Technician I (Monday through Friday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 5/2/2024 |
| 359 | Charles River Laboratories Ashland, OH Research Analyst I - Immunology Bachelor's degree (B.A. / B.S) or equivalent in laboratory science or related discipline required. Exp: Zero to two years |
We are seeking a Research Analyst 1- Immunology for our Safety Assessment site located in Ashland, OH. Essential Duties and Responsibilities: • Perform assays such as ELISA, multiplex, immunophenotyping, comet, and micronucleus. • Perform density gradient cell separations. • May act a lead/primary technician on basic studies. • Utilize micropipettes for all assays. • Perform study preparation activities including ordering supplies, preparing/verifying paperwork, and tube labeling. • Receive and log in reagents, solutions, and samples. • Prepare simple to complex lab solutions. • Assist in method development studies, method validation studies, and equipment validations as needed. • Operate, perform quality control and maintenance procedures on equipment such as microplate readers, plate washers, cell counters, multiplex instruments, flow cytometers, freezers, liquid scintillation counter, gamma counter, and eyewash stations. • Maintain clean work areas by cleaning dishes/glassware, wiping down countertops, and sweeping/mopping floor as needed. • Collect and record data in compliance with Good Laboratory Practices (GLPs), Standard Operating Procedures (SOPs), protocols, and study plans. • Input, print, and edit basic to complex data. • Prepare materials for shipment and archival. • Review documentation for quality control. • Perform all other related duties as assigned. | 5/2/2024 |
| 360 | Leica Biosystems Vista, CA Software Engineer (Hybrid) Bachelor’s in (completed or in progress) in computer science, software engineering, or similar. Exp: 0-2+ years |
The Software Engineer for Leica Biosystems will located in Vista, CA, is hybrid, and will report to a Senior Manager, Software Development. This Software Engineer is responsible for helping perform maintenance and make modifications on existing and new software products. | 5/2/2024 |
| 361 | Genesis Therapeutics San Diego, CA Research Associate, Biochemistry B.S./M.S. in Biochemistry, Biology, or a related field. Exp: 1 year |
Genesis Therapeutics is pioneering artificial intelligence guided rational drug design to address severe unmet medical needs for patients. Our lab in San Diego is looking for a motivated and enthusiastic candidate to support in vitro biochemical assay screening efforts. You will be producing biochemical activity & binding data using various technologies that will help drive rapid progress in our drug programs across a variety of different targets. | 5/2/2024 |
| 362 | Genoptix Ft Myers, FL; Tampa, FL; Nashville,, FL Clinical Laboratory Technologist Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a Clinical Laboratory Technologist Dry Lab you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 363 | Genoptix Houston, TX; Ft Myers, FL; Tampa, F, TX Clinical Laboratory Technologist II Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a Clinical Laboratory Technologist I Dry Lab you will work under general supervision and you will be responsible for accurately performing highly complex laboratory testing procedures. You will determine acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. You will also analyze specimens, review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 364 | Genoptix Aliso Viejo, CA Clinical Laboratory Technologist- Molecular Bachelor’s Degree from an accredited college or university in one of the chemical, physical, or biological sciences. Exp: one year |
As a technologist, you will work under general supervision. You will be responsible for performing highly complex laboratory testing procedures. You will figure out acceptability of specimens for testing, prepare clinical specimens and identify specimen related problems. In this position, you will need to analyze specimens and review and release test results. You will have the means to prepare stock solutions, reagents and cocktails used in the laboratory. You will then test these based on standard criteria and document all observations. | 5/2/2024 |
| 365 | MEDTOX Raritan, NJ Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! Pay Based on Experience -- Starting @ 28.50/hour Sign-On Bonus of $5,000 ( External Candidates Only ) The work schedule for this position will be Sunday - Thursday 10:00 pm - 6:30 am | 5/2/2024 |
| 366 | MEDTOX Holyoke, MA Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Holyoke, MA. In this position, you will work in a fast-paced, customer-focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! The work schedule for this position will be Tuesday - Saturday 10:00 pm - 6:30 am | 5/2/2024 |
| 367 | MEDTOX Binghamton, NY Clinical Laboratory Technician Associate degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team Guthrie Lourdes Hospital in Binghamton, NY. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Pay Range: $20.40 - $40.14 + 10% shift differential on weekdays or 15% shift differential on weekends Work Schedule: 3x8 hour shifts: Weekdays, 3:00pm- 11:30pm and rotating weekends | 5/2/2024 |
| 368 | MEDTOX Westborough, MA Clinical Laboratory Technologist - Molecular Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
Pay Based on Experience -- Starting @ 26.00/hour Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, The Integrated Genetics Division of LabCorp is seeking a Molecular Technologist to join their Molecular Diagnostics team in Westborough, MA! In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, Real-time PCR, Sanger Sequencing, MLPA, Methylation PCR and Fragment Analysis to test for specific genetic diseases such as Cystic Fibrosis, Spinal Muscular Atrophy and Fragile X Syndrome to name just a few. Work Schedule: Sunday - Thursday, 7:00am - 3:30pm. | 5/2/2024 |
| 369 | MEDTOX Lowell, MA Clinical Laboratory Technologist Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology. Exp: 1 year |
$10,000 sign on bonus (external candidates only) Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team at Lowell General Hospital Saints Campus in Lowell, MA. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Work Schedule: Monday- Friday, 7:00am - 3:30pm & every 3rd weekend | 5/2/2024 |
| 370 | Steris Mentor, OH Associate Scientist I Bachelor degree in Biology, Microbiology, Molecular Biology is preferred. Exp: 1-5 years |
Position Summary The Associate Scientist I will work in the Product Development team performing microbiology methodologies with several strains of BSL1 and BSL2 test organisms, including bacteria, fungi, and viruses. The position will require implementing established methodologies to evaluate the microbiocidal activity of disinfectants and sterilization processes. The position will also perform testing to develop and evaluate sterility assurance products (i.e. biological indicators). The position will require accurately maintaining, recording, and reporting test data. Additionally, applicant must possess the ability to perform and accurately document tasks according to established microbiocidal test standards, work instructions, and written protocols in a timely manner, while working both independently and within a team on multiple studies at different stages of the process. This position is located onsite in Mentor, OH. | 4/22/2024 |
| 371 | Steris Richmond, CA Quality Engineer Bachelor Degree in Engineering or Computer Science Exp: 1+ years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR, and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems | 4/22/2024 |
| 372 | Steris Spartanburg, SC Quality Analyst Bachelor's Degree Exp: 1-5 years |
The Quality Analyst is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. This role leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances. Responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting. | 4/22/2024 |
| 373 | Stryker Portage, MI Design Engineer – Electrical, RISE B.S or M.S. in Electrical Computer Engineering, Electrical Engineering or related engineering discipline; we will only consider candidates with Decemb Exp: 0+ years |
Stryker, a global leader in medical technology takes great pride in their people, and that’s why we’re looking to expand our talent. As a result, we are looking for the best and brightest graduates to strengthen our team and drive our business going forward. The Rotational Intensive Specialized Experience (RISE) Program, which lasts 2 years and includes 4 six-month rotations, is designed specifically for highly talented engineers who are looking for exposure to and experience in different disciplines of engineering. Participants will be immersed into new product development (design engineering), quality, product testing, simulation, and so much more. Each individual’s rotations are tailored to fit their passion and skill sets along with current business needs. RISE engineers will not only gain a broad knowledge of our Research & Development functions but will also have the opportunity to attend additional leadership and personal development trainings, seminars, and product labs. The RISE Engineering program also offers exposure to senior leadership with end of rotation presentations, townhalls, and small group forums. Upon successful completion of the program, participants are eligible to apply to any open roles within Stryker. | 4/23/2024 |
| 374 | Stryker Portage, MI Mechanical Engineer, R&D – Sustainment Bachelor’s Degree in Mechanical Engineering or related Exp: 0+ years |
Stryker is seeking to hire a Mechanical Engineer, R&D to support Medical’s Acute Care Product Engineering team. This role is onsite, in Portage, MI with the expectation to come into the office 4-5 days a week. Stryker Bed Frames Stryker Stretchers and Transport Chairs | 4/23/2024 |
| 375 | WuXi Apptec San Diego, CA Research Associate III Master degree in Molecular and Cell Biology Exp: 0+ years |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate III to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 376 | WuXi Apptec San Diego, CA Research Associate Must have Master’s degree in Biochemistry, Cellular and Molecular Biology, Biomedical Engineering, or Biotechnology. Exp: 1+ years |
Research Associate (San Diego, CA) – Skills and knowledge in Biological Macromolecules, Protein/ligand Binding, Cell-cell Interactions, Gene Delivery, Stem Cells Engineering, Polymer Synthesis/processing. Perform assay in cell-based format and biochemical assays using Biological Macromolecules, Protein/ligand Binding, Cell-cell Interactions, Gene Delivery, and Mammalian cell culture; Perform compound management work; Perform incucyte analysis to determine cell doubling time and seeding density for cytotoxicity study using Stem Cells Engineering, Polymer Synthesis/processing; Perform assays in cell-based format suitable for SAR screening in 96 and 386-well formats; Support cell banking and maintain cell line inventory; Execute validated assays for compound screening. | 4/24/2024 |
| 377 | WuXi Apptec San Diego, CA Research Associate II - In Vivo Pharmacology Master degree in Molecular and Cell Biology or Bachelor degree. Exp: MS: 0 years; BS: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate II to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 378 | WuXi Apptec San Diego, CA Research Associate II (Temp/Contingent) Master degree in Molecular and Cell Biology or Bachelor degree. Exp: MS: 0 years; BS: 1 -2 year |
HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly skilled and motivated Research Associate III to support our in vivo pharmacology team for various projects. | 4/24/2024 |
| 379 | WuXi Apptec Philadelphia, PA Laboratory Technician I Associates’/Bachelor’s (science preferred) degree. Exp: 0-2 years |
The Laboratory Technician I performs cell culture and cell-biology based assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Under direct supervision, completes batch records and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs additional Research & Development activities as required. | 4/24/2024 |
| 380 | WuXi Apptec Cranbury, NJ Associate Scientist I (Contingent/Temp) Bachelor’s degree in animal science, biology, or a related discipline. Exp: 0-3 years |
Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. Operates lab equipment including oxidizers, centrifuges, LS counters, and cage/tunnel washers. **Please note that this is a contingent/temp position and not eligible for benefits.** Schedule: Monday to Friday 6:30 AM - 3:00 PM (occasional weekend rotations | 4/24/2024 |
| 381 | WuXi Apptec Philadelphia, PA Bioprocessing Associate I AS/BS Exp: 0+ years |
The Bioprocessing Associate I is responsible for providing support in performance of activities within production facilities to support manufacture of Master and Working Cell Banks Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). The Bioprocessing Associate I is responsible for providing support in performance of activities within production facilities to support manufacture of Master and Working Cell Banks Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs). | 4/24/2024 |
| 382 | Cel-Sci Baltimore & Elkridge, MD Validation Technician B.S. in science or engineering or a related discipline or 2-year degree. Exp: AS: 1 to 2+ years |
The Validation Technician is responsible for supporting validation activities of GMP equipment and systems. Assists in specifying and selecting equipment. Maintains all records related to qualification and validation. Prepares validation reports, suggests, and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Technician reports to the Validation Engineer. | 4/24/2024 |
| 383 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline. Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 4/24/2024 |
| 384 | Cogent Professionals Indianapolis, IN Pharma Lab Technician AS degree in chemistry, biology or related science and/or equivalent college coursework in the sciences. Exp: 0+ years |
We currently have a role available for a Pharmaceutical Lab Technician. Job duties include, but are not limited to, the following: General lab organization: order lab gases; put away clean glassware; refill lab solvents; maintain cleanliness and organization of labs, hallways, back-up hoods, waste disposal stations, and storage areas. Chemical preparation: Basic reagent and solvent preparation and transporting to different labs as needed. Instrument care: submit maintenance requests and coordinate with service providers; defrost lyophilizers; check balances for correct operation and appropriate cleanliness; fill liquid nitrogen for NMRs; clear NMR sample carousel; refill LC-MS solvents and QC vials; prepare LC-MS wash solvents; check LC-MS standards; routine preventative maintenance of vacuum pumps. Purification instrument duties: fill solvents and collection racks for flash systems; ensure consumables are properly stocked; dispose of waste solvents and tubes; refill wash bottles; clean and properly store reusable columns. Stockroom support: deliver chemicals from and return items to chemical inventory system; appropriately segregate chemicals; inventory reconciliation; assess safety labeling of compounds to maintain appropriate labels | 4/26/2024 |
| 385 | Concuir Consulting Los Angeles, CA Project Engineer II/III BS Engineering degree required, Chemical, Mechanical or Biomedical preferred. Exp: 1-4+ years’ |
As a full-time employee of Concuir, Inc, you will provide consulting services to pharmaceutical, biotech and/or medical device manufacturing clients. In this role, you will quickly learn common client practices, recommend and implement improvements to reach project goals, and have the opportunity to scale-up and bring new products into manufacturing. You will be able to utilize your experience as well as benefit from Concuir’s portfolio of project management and cGxP best practices to drive your overall success. Projects range from design through qualification of production equipment, utilities modification, implementation of new facilities and process scale ups. | 4/26/2024 |
| 386 | Cosette Pharmaceuticals Lincolnton, NC Chemist I - 1st shift and 2nd shift BS or BA in Chemistry or related science. Exp: 0+ years |
Basic Purpose: Provide technical support to plant operations Essential Functions and Responsibilities: Basic wet chemical and instrumental testing of raw materials, in-process, finished product, and stability samples Basic maintenance of instrumentation and equipment in support of laboratory testing Inventory control and maintenance of laboratory chemicals and supplies Adherence to policies of EHS Other duties as assigned by management | 4/26/2024 |
| 387 | Cytokinetics South San Francisco, CA Research Associate I B.S. in scientific discipline. Exp: 0-2 years |
We are currently in search of a highly motivated Research Associate who possesses a strong passion for the field of Medicinal Chemistry, to become an integral part of our dynamic team. The ideal candidate will bring forth their expertise and enthusiasm to actively contribute to and enhance our ongoing efforts and initiatives in the realm of pharmaceutical research and development. | 4/26/2024 |
| 388 | Cytokinetics South San Francisco, CA Contract - Research Associate (DMPK) Bachelor's or Master's degree in Pharmaceutical Sciences, Chemistry, Biochemistry, or a related field. Exp: 1+ years |
We are seeking a highly motivated Junior Research Associate with a focus on Drug Metabolism and Pharmacokinetics (DMPK) to join our team. The ideal candidate will contribute to our efforts in screening, plasma protein binding, and microsomal assays. This role offers an exciting opportunity to work in a collaborative and fast-paced environment, supporting the development of cutting-edge therapies for cardiovascular and skeletal muscle disorders. | 4/26/2024 |
| 389 | Dewpoint Therapeutics Boston, MA Research Associate II - Compound Management M.Sc. or higher in Science, Chemistry, Engineering, or a related field. Exp: 1 year |
We are looking for a creative, energetic individual to join our Lead Discovery and Lead Evaluation team, working directly on compound management and lab informatics. If you’re looking to jump start your career as a Researcher while gaining experience and knowledge in a collaborative and empowering environment, this is the ideal role for you. As the ideal candidate, you will bring experience in managing inventories of both small molecules and biological materials and have a desire to build a career in an industry-leading & cutting edge HTS team. In this position you’ll be part of an energizing and supportive startup culture engaged in continuous learning, and part of an exceptional international team. This role is based at our site in Boston's Seaport district. Dewpoint offers competitive salary, great benefits, and amazing perks. | 4/26/2024 |
| 390 | Dicerna Pharmaceuticals West Lebanon, NH Quality Control Coordinator Associate’s degree or equivalent. Exp: one (1) or more years |
This position is responsible for coordinating/supporting/assisting the Quality Control team including offsite and onsite calibrations, quality system interaction, management of sample collection and drop-off, communication of production schedule and ad-hoc testing requests, troubleshooting, performing a variety of highly diverse and complex administrative tasks and activities requiring sound planning, organization, judgement, adaptability, and accountability. This position is located in West Lebanon, New Hampshire and will require onsite work and collaboration. It is a full time (40 hour per week) position and the standard schedule is Monday-Friday (8am-5-pm). We offer a competitive salary, commensurate with experience. | 4/26/2024 |
| 391 | Dicerna Pharmaceuticals West Lebanon, NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 4/26/2024 |
| 392 | Elicio Therapeutics Boston, MA Scientist I/II, Translational Medicine MS. Exp: 0-3 years |
Reporting to the Senior Scientist I of Translational Medicine, this individual will serve as an integral team member with exposure to multiple facets of business operations. The Scientist I will be responsible for conducting immunogenicity assays that measure vaccine efficacy, such as ELISpot/Fluorospot, ICS, and other flow cytometry-based assays. As part of the organization's Translational Medicine team, this individual will interact collaboratively with the Clinical Operations and Analytical Chemistry departments to successfully progress current and future clinical programs. Additional attributes of the position include responsibility for performing in vivo mouse experiments to characterize the immune response to vaccine candidates. Elicio (ELTX) is a growing organization based out of the Seaport area of Boston, Massachusetts with additional staff functioning in a virtual-based environment from the Greater Boston area and throughout the United States. | 4/26/2024 |
| 393 | BostonGene Waltham, MA Biospecimen Inventory Technician Minimum BS in a Biological or Life Science. Exp: one year |
The candidate will report to the Lab Manager and under their supervision support BostonGenes laboratory teams with sample management and tracking systems/protocols. The candidate will create and oversee a new sample inventory tracking system using the existing Lab Information Management System (LIMS) and Benchling software. Once created they will assist in the transition to an end-to-end barcoding-based system for sample tracking and continuously update and improve the process as new tests are added. This candidate will also be responsible for handling and processing blood specimens for specific projects. This will involve basic blood processing techniques such as blood fractionation, plasma clarification, and cell isolation for downstream biobanking. | 4/16/2024 |
| 394 | BPS Bioscience San Diego, CA Research Associate I, Molecular & Cellular Biology Bachelor's. Exp: Entry-level |
The position requires the ability to perform and somewhat independently interpret molecular cloning and protein expression experiments. The successful candidate will be tasked with duties in molecular biology, cell culture and transfection techniques. These include standard cloning, PCR techniques, and plasmid preparation and analysis. Expression systems of focus will be mammalian cells (293). This position will include assisting other researchers with their experiments and with lab maintenance. | 4/16/2024 |
| 395 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 4/16/2024 |
| 396 | Cabaletta Bio Philadelphia, PA Research Associate/Sr. Research Associate, Molecular Biology B.S degree in Life Sciences or closely related discipline. Exp: 0-2 years |
Reporting to the Associate Scientist, Molecular Biology group, we are seeking an experienced and motivated Research Associate or Senior Research Associate. Under scientific and technical supervision, the candidate will design and execute cell-based assay advancing multiple discovery programs. The position offers growth into additional areas such as cell biology and molecular biology, immunology, and cell therapy. The position involves both technical and operational responsibilities. | 4/16/2024 |
| 397 | Caraway Therapeutics Rahway, NJ Specialist, Process Engineering Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Sterile GMP Clinical Manufacturing facility. As the facility is nearing the completion of its construction, the selected candidate will contribute to equipment and facility commissioning/qualification, regulatory certification, as well as other workstreams’ critical activities to enable facility startup and operational readiness. To support these business-critical activities, night and weekend work may be required. Once the facility is operational, this role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 4/16/2024 |
| 398 | Caraway Therapeutics Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related field. Master’s degree in Chemical Engineering, Chemistry, Ph Exp: BS: 1 year |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 4/16/2024 |
| 399 | Bayer Luling , LA Chem Production Engineer Bachelor’s of Science degree in Chemical Engineering, including May 2024 B.S. Chemical Engineering graduates. Exp: 0-3 years |
The Chemical Production Engineer provides support to plan, coordinate, and execute technical activities needed to support manufacturing operations. Also, ensures the safe, efficient, productive, and environmentally sound manufacture of active ingredients or intermediates. | 4/17/2024 |
| 400 | Bayer Berkeley, CA Associate Electrical Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 4/17/2024 |
| 401 | Bayer Huxley, IA Agronomic Research Specialist II (Field) - Huxley, IA Bachelor’s degree completed by start date. Bachelor’s or Master’s degree in agronomy, life sciences, engineering. Exp: 1+ years |
As a field-facing Agronomic Research Specialist II, you will be responsible for contributing to an R&D Field Trial program for corn and soybeans. Your primary responsibilities will be to coordinate with growers on leased land space and assist with acquiring and supervising local staffing during in-season activities. You will conduct in-season research activities such as phenotyping, study management, and data analytics review as part of overseeing and executing research trials that feeds the R&D pipeline. Additionally, you will have the opportunity to partner with other Agronomic Research Specialists on site, as well as other cross-site functions on initiatives to improve data quality, standard operating procedures, or quality/compliance actions. This is an onsite role (site and surrounding production fields), primarily day shift (with extended hours during peak season) at our Huxley, IA research facility.As a field-facing Agronomic Research Specialist II, you will be responsible for contributing to an R&D Field Trial program for corn and soybeans. Your primary responsibilities will be to coordinate with growers on leased land space and assist with acquiring and supervising local staffing during in-season activities. You will conduct in-season research activities such as phenotyping, study management, and data analytics review as part of overseeing and executing research trials that feeds the R&D pipeline. Additionally, you will have the opportunity to partner with other Agronomic Research Specialists on site, as well as other cross-site functions on initiatives to improve data quality, standard operating procedures, or quality/compliance actions. This is an onsite role (site and surrounding production fields), primarily day shift (with extended hours during peak season) at our Huxley, IA research facility. | 4/17/2024 |
| 402 | AstraZeneca Frederick, MD Production Technician I - Night Shift BS/BA degree preferred. Degree in STEM field. Exp: 1+ years |
In this role, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also train with a qualified Technician on activities related to operating process equipment with the requirement of qualification. Additionally, you will follow and execute cGMP documentation, utilize Manufacturing Execution systems (MES), contribute to problem-solving activities for non-routine activities on the production floor, and participate in continuous improvement activities for Manufacturing. Adherence to AstraZeneca values and behaviors is expected. | 4/17/2024 |
| 403 | AstraZeneca Frederick, MD Production Technician I/II - Nights BS/BA degree preferred. Degree in STEM field. Exp: 0-1 years |
Your responsibilities will include operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. You will be expected to demonstrate advanced equipment/process knowledge to diagnose issues and participate in first-line troubleshooting and root cause analysis. You will also be responsible for maintaining qualifications in Production Technician duties, executing work orders within the system, and leading continuous improvement initiatives. | 4/17/2024 |
| 404 | AstraZeneca Frederick, MD Production Technician II-Night Shift BS/BA degree preferred. Degree in STEM field. Exp: 0-1 years |
As a Production Technician, you will be responsible for the operation of processing equipment according to established SOPs, MPRs, & SPRs in accordance with cGMPs. Your duties will include solution preparation, cell culture, purification & formulation, and supporting activities. You will also be a qualified trainer on-the-floor, follow and execute cGMP documentation, maintain qualifications in Production Technician duties, and utilize Manufacturing Execution Systems (MES). Furthermore, you will contribute to problem-solving activities and troubleshooting for non-routine activities on the production floor. You will lead indirect processing activities in support of MFG operations and continuous improvement initiatives. Adherence to AstraZeneca values and behaviors is a must. | 4/17/2024 |
| 405 | Bachem Vista, CA Process Engineer Bachelor’s degree in mechanical, electrical, chemical, manufacturing engineering or science related field. Exp: 1-3 years |
The process engineer is responsible for supporting and maintaining critical and supporting equipment and instruments to ensure the manufacturing process is continuously in operation with minimal downtime. Concurrently, through process mapping, the process engineer is responsible to develop process improvement projects to create efficiency in the process. The process engineer will also be responsible for identifying and researching background for equipment purchases and making recommendation to management. | 4/18/2024 |
| 406 | Covance Burlington, NC Molecular Diagnostic Specialist for DNA Identification Bachelor's Degree in Biology, Chemistry or Life Science. Exp: 1 year |
The DNA Identification Building in Burlington, NC is seeking a Molecular Diagnostic Specialist. The Molecular Diagnostic Specialist helps to support the operations team, the quality team and the laboratory in various ways while also maintaining the laboratory equipment and their records. As a Molecular Diagnostic Specialist, this role will help support the development and optimization of new and existing molecular diagnostic tests. Conducts routine to complex experimental procedures within overall scope of a research project and/or diagnostic test development project. Maintains all appropriate records regarding data collection and interpretation of results. Daily activities include scripting for automation, validation of equipment and consumables, general instrument repairs, and monitoring PMs. The MDS team is vital in constant lab streamlining and preventing down time in lab processing. LabCorp's Consumer Genetics operation is one of the world's largest genotyping facilities, having genotyped millions of samples for SNP (Single Nucleotide Polymorphism) analysis since 2013. SNPs are single base changes in DNA that give rise to genetic variation. These variations can be used for ancestry typing, health and disease risk factors, carrier conditions, and curiosity testing! The working schedule for this position will be: Monday - Friday 2 pm - 10:30 pm, 10% shift differential offered for 2nd shift. | 4/18/2024 |
| 407 | Covance Burlington, NC Technologist for Moleclar Micro Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 1 year |
Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our lab team as a Technologist in Burlington, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives." This position is also responsible for supporting the COV2 team to include duties such as assay building and releasing results. The schedule for this position will be: 2nd shift, Tuesday-Sat, 2:00pm-10:30pm. Eligible for 10% shift differential due to 2nd shift hours. | 4/18/2024 |
| 408 | Covance Raritan, NJ Clinical Laboratory Technologist - Molecular Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced clinical laboratory professional looking for leadership opportunity? Are you detail oriented, process focused, and enjoy leading others? Are you looking for an industry leading company that offers growth and stability? LabCorp is seeking a Clinical Laboratory Technologist to join our Core Laboratory team in Raritan, NJ. In this position, you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". Work Schedule: Tuesday - Saturday: 3:00 pm - 11:30 pm | 4/18/2024 |
| 409 | Covance Raritan, NJ Clinical Laboratory Technologist - Chemistry Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 0+ years |
Are you an experienced Clinical Lab Professional? Are you looking to looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team in Raritan NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. Work Schedule: Work Schedule: Tuesday - Saturday (12:00am - 8:30am) and alternating Saturdays (11:30pm- 8:00am) New Grads Welcome – Full Training Provided | 4/18/2024 |
| 410 | Covance Raritan, NJ Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! Pay Based on Experience -- Starting @ 28.50/hour Sign-On Bonus of $5,000 ( External Candidates Only ) The work schedule for this position will be Sunday - Thursday 10:00 pm - 6:30 amAre you an experienced Medical Lab Professional? | 4/18/2024 |
| 411 | Covance Raritan, NJ Clinical Laboratory Technologist - Forensics Toxicology Bachelor’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet localregulatory (CLIA & State) requirem Exp: 0+ years |
Are you an experienced Clinical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Clinical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Raritan, NJ. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: “Improving Health, Improving Lives”. New Grads Welcome - Full Training Required Work Schedule: Tuesday – Saturday - 7:00 am - 3:30 pm | 4/18/2024 |
| 412 | Covance Holyoke, MA Clinical Laboratory Technologist - Microbiology Bachelor's degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) require Exp: 1 year |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Technologist in Holyoke, MA. In this position, you will work in a fast-paced, customer-focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". New Graduates Welcome! The work schedule for this position will be Tuesday - Saturday 10:00 pm - 6:30 am | 4/18/2024 |
| 413 | Dexcom San Diego, CA Mechanical Engineer II Master’s degree in a technical discipline. Exp: 0-2 years’ |
The R&D Mechanical Engineering Characterization Team is responsible for the feasibility and development of next-generation products at Dexcom. We’re seeking a cross-functionally disciplined engineer with subject matter expertise across mechanics, materials, and human tissue/device interaction to support characterization and test of novel patch materials and designs. Positioned within the Mechanical Engineering team, this is a high visibility, high impact role in achieving Dexcom’s product performance and reliability goals through delivering functional excellence in the research, development, and characterization of technologies/designs & their integration to a product ecosystem. | 4/18/2024 |
| 414 | Emergent BioSolutions Baltimore, MD Analyst II, Quality Assurance - 3rd-Shift BS or BA degree in Science or Engineering. Exp: 0-2 years |
The Analyst II on the Floor is responsible for assuring the quality of products manufactured at the Emergent BioSolutions Baltimore Facility. The Analyst II will perform Quality on the Floor functions. Our QA Department provides expertise in problem-solving and process improvements. The QA Specialist will interact with manufacturing personnel and Quality Engineers to provide guidance necessary to maintain and improve CGMP compliance at the company. | 4/18/2024 |
| 415 | Emergent BioSolutions Baltimore, MD Analyst II, QA on the Floor BS or BA degree in Science or Engineering. Exp: 0-2 years |
This role is responsible for monitoring Warehouse areas, Printed Material inventory management,Packaging Operations support, and Warehouse Quality on the Floor continuous improvement. | 4/18/2024 |
| 416 | Emergent BioSolutions Baltimore, MD Analyst II, QC Microbiology, 3rd Shift (Wed-Sat) MS in Microbiology/Biology or related field. Exp: 0-2 years |
The Analyst II, QC Microbiology position supports the Quality Control group at Emergent BioSolutions Camden Campus to maintain process optimization and manufacturing activities. The Microbiologist is responsible for performing activities in support of the Microbiology, Environmental Monitoring, and Utility testing programs, which includes microbiological product testing, monitoring of the manufacturing production space, and supporting quality initiatives. The individual routinely conducts monitoring, testing, and SOP generation and revision. This is a 3rd-shift/4 day work week position -working hours 10pm-8:30am-Wednesday through Saturday. Hours may vary to meet business and training needs. | 4/18/2024 |
| 417 | Emergent BioSolutions Winnepeg, MB, CA Analyst I, QC Laboratory Services - Limited Term University degree or technical diploma in microbiology, biology or related field of study. Exp: 0-2 years |
The Analyst I, QC Laboratory Services performs GMP compliant microbiological testing as required to support Raw Material testing, In-process, Finished Product release & Stability or nonclinical/ clinical studies. The Analyst I may also perform testing required to support assay and process validations. He/She will perform testing to support release of lab specific material (media, standards). | 4/18/2024 |
| 418 | Emergent BioSolutions Rockville, MD Sr Bioprocess Associate BS/BA in Biology, Chemistry, or related discipline. Exp: 1-3 years’ |
The primary role of this position is to provide technical support for all fill finish operations with strict adherence to cGMP compliance. The candidate will also provide guidance for all on-floor activities including aseptic fill operations, visual inspection, labeling, and packaging of bulk product with minimal supervision. This position requires proficiency in aseptic technique, and deliberate movements inside various isolators. The candidate for this position will be working in close association with Technical Operations, Quality Assurance, Quality Control, and Material Management to overcome challenges in meeting the production schedule. | 4/18/2024 |
| 419 | Leidos Biomedical Research San Antonio, TX Research Associate Master’s degree or equivalent. Degree should be in a related field. Knowledge of animal anatomy and physiology. Exp: 1+ years |
Are you ready for an opportunity to make a difference in the lives of those who serve our country? Leidos Health Solutions is currently looking for a Research Associate with molecular biology experience to support the Directed Energy (DE) department at the Naval Medical Research Unit, San Antonio (NAMRU-SA) in San Antonio, TX. NAMRU-SA conducts gap driven combat casualty care, craniofacial, and directed energy research to improve survival, operational readiness, and safety of Department of Defense personnel engaged in routine and expeditionary operation. | 4/19/2024 |
| 420 | Leidos Biomedical Research Dayton , OH Electrical Engineer Bachelor’s degree in an engineering discipline (electrical, computer, or similar). Master’s degree or higher in electrical or computer engineering. Exp: BS: 0-3 years |
Leidos is searching for an Electrical Engineer to support AFRL’s Dynamic Infrared Missile Evaluation (DIME) Laboratory located on Wright Patterson Air Force Base, OH. The successful candidate will utilize a strong engineering background designing, testing, modeling, simulating, and analyzing the next generation of infrared countermeasure techniques. This position will support multiple simultaneous research efforts within the laboratory requiring skills including hands-on experimentation, digital modeling using graphical programming, modeling and simulation of aircraft/missile engagements, and computer application development involving interfacing with hardware systems and real-time processing. Addressing our customers’ challenging mission requirements necessitates research and development of new capabilities as well as making improvements to existing systems. The successful candidate will be required to quickly develop an understanding of legacy efforts and engineer improvements to meet new requirements. Additionally, the engineer will be called upon to develop new and innovative solutions to challenging problems, helping our customers provide solutions for the warfighter. The successful candidate will work as part of an integrated team but should also be proficient at conducting independent research. | 4/19/2024 |
| 421 | Leidos Biomedical Research Huntsville, AL Entry-Level Firmware Engineer Bachelor of Science in Electrical Engineering or equivalent degree from an ABET-accredited institution with a 3.0 or higher GPA. Exp: 1+ years |
Primary Responsibilities In this role, project assignments could be focused in one or multiple of the following areas: Design, simulation, and testing of firmware using hardware description languages (HDL) to drive custom hardware. Testing and integration of RF electronics such as high speed DACs used for waveform generation and ADCs used for signal processing. Utilizing cutting edge AMD/Xilinx FPGA and SoC families and design tools such as the RFSoC. Testing and debugging hardware using lab equipment such as spectrum analyzers and oscilloscopes. Working on multidisciplinary teams to debug problems when integrating firmware and PCB designs with Radar and Seeker hardware. | 4/19/2024 |
| 422 | Leidos Biomedical Research Huntsville, AL Penetration Tester- Entry Level Master’s degree in Cyber Security, Computer Science, Computer Engineering, Electrical Engineering. Exp: 1+ years |
Leidos Defense Systems is seeking a full-time, talented, and motivated Penetration Tester to perform penetration tests on customer systems in the defense, space, cyber, and commercial fields. The ideal candidate will possess technical skills in networking, operating systems, and programming, as well as the ability to think creatively about potential threats. They will also possess the ability to analyze both open and closed-source intelligence to determine potential cyber threat Tactics, Techniques, and Procedures (TTPS), attack vectors, and risks to systems of various size and complexity. | 4/19/2024 |
| 423 | Leidos Biomedical Research Patuxent River, MD Junior Network and Computer Systems Administrator (ROD) Bachelor’s Degree in Computer Science, Mathematics, or Engineering from an accredited college or university. Exp: 1+ years |
The Leidos Defense Group is seeking an entry level Network and Computer Systems Administrator to provide networking support as part of the Range Operations Division (ROD) Range Support Branch of the Atlantic Test Range (ATR) in Patuxent River, Maryland. Members of this dynamic team design and develop complex hardware and software network architectures to support real-time Research, Development, Test, & Engineering (RDT&E) test and fleet training events conducted by ATR in support of customers’ requirements. | 4/19/2024 |
| 424 | Eli Lilly Indianapolis, IN Biologist - In Vivo Neuroscience BS/MS in Biology, Animal Sciences, Pharmacology, or a related field. Exp: 1+ years |
Lilly Neuroscience is seeking an experienced scientist (Bachelors or Masters) to join the Neurodegeneration team to facilitate its mission of discovering novel medicines for the treatment of Alzheimer’s disease, Parkinson’s disease, ALS, and other related neurodegenerative conditions. The individual will join a laboratory focused on in vivo research to support our expanding neurodegeneration portfolio, and they will leverage their technical expertise to lead high quality studies and sample collection to support identification/development of novel targets for Neurodegenerative conditions. A key focus of the scientist will be the utilization of multiple in vivo techniques including complex surgical models to support therapeutic investigations in pre-clinical animal models. Importantly, the individual will collaborate with colleagues across the Neurodegeneration group to facilitate both exploratory and portfolio workstreams. The scientist must possess a strong work ethic and an ability to quickly master numerous new techniques. Lilly has a proud record of drug development for neurodegenerative diseases that has been driven by a highly collaborative and diverse team of accomplished scientists. | 4/19/2024 |
| 425 | Eli Lilly Indianapolis, IN Associate Biologist BS or MS in biology/animal science/veterinary technology or a closely related field. Exp: 1 year |
The Lilly Diabetes, Obesity and Complications Therapeutic Area (DOCTA) is focused on discovery and development of new therapeutics for the treatment of medical complications arising from type 2 diabetes and obesity. The cardiorenal team is looking for a biologist to conduct experiments using animal models of renal and metabolic diseases. The ideal candidate should be goal-oriented and dedicated, capable of conducting thorough research studies with minimal oversight. This biologist will design and perform experiments independently and within team-based environments, as well as interact with internal and external collaborators. Are you ready to actively engage in cardiorenal drug hunting teams and serve as a scientific and technical advisor to project teams? Apply now to join the Lilly Team! | 4/19/2024 |
| 426 | Eli Lilly Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 4/19/2024 |
| 427 | Eli Lilly Cambridge, MA Scientist - In Vivo Surgical Associate Bachelors or Masters degree in neuroscience or related fields preferred. Exp: 1+ years |
The Next Generation Therapeutics group is a newly formed team with a focus on using novel therapeutic modalities to deliver medicines for chronic pain and neurodegenerative disorders. The group, based at our Cambridge Innovation Center in Kendall square, will work with internal and external partners to identify, and deliver new novel therapies into patients at speed. The team is seeking experienced and inspiring scientists to join our fast-paced, interdisciplinary team as we leverage innovative RNA/oligonucleotide/gene and genomic based therapeutics to enhance our portfolio. | 4/19/2024 |
| 428 | Eli Lilly Lebanon, IN Manufacturing Scientist - Lebanon API Manufacturing Master's Degree in STEM Discipline (Chemistry preferred). Exp: 1 year |
The Manufacturing Scientist is part of the TSMS (Technical Services/Manufacturing Science) team that provides the technical support required to achieve reliable and compliant manufacturing of API molecules. This role will be part of the Manufacturing Process Team for its respective area, providing daily oversight to ensure safe and reliable supply of medicines. The Manufacturing Scientist executes technical projects (experimental, modeling and/or production data analysis) to improve and optimize process control, yield, purity, and/or productivity. In addition, the manufacturing scientist should be capable and of setting up and executing a variety of experiments at laboratory scale and conducting research on manufactured product for process improvements and troubleshooting in the technical services and manufacturing sciences laboratory. | 4/19/2024 |
| 429 | Eli Lilly Lebanon, IN Associate- Laboratory Support - Quality Control - Advanced Therapies Bachelors (4-year) degree in a science field related to chemistry, microbiology, biology, or other science discipline. Exp: 1+ years |
The Laboratory Support Associate is a support role in the Quality Control Laboratory helping to ensure proper and efficient functioning of laboratory operations. The Laboratory Support Associate is responsible for operational excellence and continuous improvement in the laboratory. They will manage laboratory samples, materials, reagents, equipment usage, ordering, organization, and may include management of laboratory system access. | 4/19/2024 |
| 430 | Eli Lilly Lebanon, IN Process Engineer - API Manufacturing Bachelor's Degree in Chemical, Biochemical, Bioprocess, Process, or Mechanical Engineering. Exp: 1+ years |
We are seeking Process Engineers to support the API Manufacturing Business in Lebanon. Process Engineering is core to delivering our product pipeline across batch and continuous API production and development. | 4/19/2024 |
| 431 | Meridian Medical Technologies Cambridge, MA Associate Scientist, Protein Production & Engineering, BioMedicine Design Bachelor’s degree is required with a Life Science major. Exp: 0 to 3 years |
Pfizer’s BioMedicine Design (BMD) is seeking a highly motivated Cell and Molecular Biologist to join Biotherapeutics Expression and Purification group (BEP) located in Pfizer Worldwide Biotherapeutics Research campus of Cambridge MA. Qualified candidate will play an essential role in support of large-scale non-GMP transient protein lead production across Pfizer’s diverse biotherapeutics discovery portfolio to enable Pfizer’s research units and their pre-clinical therapeutics in-vitro and in-vivo needs. This individual will work in the area of therapeutic protein production and engineering in mammalian cells. The individual will perform mammalian cell culture, molecular biology, large-scale mammalian cell expression, and protein production analysis for supporting protein therapeutics discovery efforts. The individual will perform this function with supervision, toward considerable independence, and will display initiative in learning new techniques. The candidate will contribute to the group wide deliverables and be required to work on several projects simultaneously presenting results and updates at group meetings. | 4/19/2024 |
| 432 | Meridian Medical Technologies Andover, MA Associate Scientist, Cell Line Development B.S in cellular/molecular biology or related life science field. Exp: 0-3 years |
A technical, lab-based position is available within Pfizer’s Molecular and Cellular Technologies organization. The position will be primarily involved in mammalian cell line development (CLD) portfolio advancement, novel technology development and process optimization. Working with a group of scientists, the successful candidate will be responsible to perform platform cell line development activities to fulfill the need of moving Pfizer’s biotherapeutics pipeline projects towards either clinical or commercial developmental phase. This role will involve all aspects of cell line development from vector design/construction, cell culture maintenance, clone screening, and cell line characterization. The successful candidate will possess excellent aseptic technique and have experience with mammalian cell culture and recombinant protein expression. | 4/19/2024 |
| 433 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
This position is responsible for the developing and or formulation of standards, controls, calibrators, and intermediates in the production and development of Bio-Techne's Luminex, Q-kit, DuoSet, and Simple Plex product lines. Day to day responsibilities involve hands on work in a production laboratory running assays for ELISA and Luminex Assays. You will draft and revise standard operating procedures, manage a production schedule, and analyze assay data to further the ongoing development of new and existing products within Bio-Techne’s evolving portfolio. | 3/27/2024 |
| 434 | Advanced Cell Diagnostics Minneapolis, MN Advanced Quality Technician An associate degree. Exp: 0+ years |
The responsibilities of an Advanced Quality Technician are to perform tasks in the process of inspecting and testing science products. Duties may require interpreting results, inventory, and participation in complaint investigations. This position will participate in the continuous improvement of our products and customer-centered culture. | 3/27/2024 |
| 435 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate MS degree in the biological sciences. Exp: 0-2 years |
As an Advanced Research Associate you will work in the Immunocytochemistry Department on the validation of antibodies for immunocytochemistry applications. You will be knowledgeable of animal anatomy and histology and familiar with histological examination of tissues, frozen and paraffin-embedded tissue sections, immunohistochemistry protocols, microscopy systems; collect digital images, digital image post-processing and enter data into a database. | 3/27/2024 |
| 436 | Advanced Cell Diagnostics Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 3/27/2024 |
| 437 | Advanced Cell Diagnostics Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
The Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 3/27/2024 |
| 438 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/27/2024 |
| 439 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Are you passionate about science, an adaptable self-starter with an insatiable curiosity and have a drive to innovate and further develop your skills with a multitude of analytical tools to study and characterize biomolecules? As a Research Associate in the Analytical Services team, you will be responsible for performing routine Quality Control (QC) testing, and participating in troubleshooting efforts for released products and new products that are still in development through the application of biophysical analysis of proteins and antibodies focusing on our capillary electrophoresis systems, but may also include chromatography, immunoassays, light scattering and other analytical tools, with the aid of fully defined SOPs. You will also actively take part in group projects, participate in process improvement efforts to improve lab protocols with the goal of facilitating innovation, efficiency and productivity, and perform additional duties as assigned. | 3/27/2024 |
| 440 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Associate I - Mid-Shift Bachelors in a science or engineering discipline preferred. Exp: zero to two (2) years |
We are currently seeking a Drug Product Manufacturing Associate I who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. | 3/27/2024 |
| 441 | Akcea Therapeutics Carlsbad, CA Research Associate II/ Senior Research Associate, Core Antisense Research Master’s degree preferred in biochemistry, molecular biology or cell biology, or a B.S. Exp: MS: 0+ years; BS: >1-2 years |
We are seeking a highly qualified and motivated individual to perform basic research to increase our understand on how ASOs target RNA to modulate the expression of genes. The position offers the opportunity to do groundbreaking science and make discoveries that will create the next generation of ASO medicines. The selected candidate will become an integral part of an interdisciplinary and energetic team of scientists in the Ionis Core Research group. | 3/27/2024 |
| 442 | Akouos Indianapolis, IN Analytical Chemist - Bioproduct Research & Development MS in Analytical Chemistry, Biochemistry, Chemistry, or a related field. Exp: 0+ years |
The Bioproduct Research and Development (BR&D) organization delivers new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and gene therapy systems. BR&D is a multidisciplinary group with deep technical expertise that works collaboratively with our discovery and manufacturing colleagues. Located in Indianapolis, IN, scientists have full access to Lilly’s deep pharmaceutical development expertise and engineering capabilities. In this role, you will be part of a diverse team of analytical chemists, pharmaceutical scientists, and engineers delivering product and process understanding across a broad range of platforms. Ideal candidates will possess experience across multiple analytical techniques, demonstrate an aptitude in technical problem solving, and be motivated to work both independently and collaboratively in a dynamic environment. | 3/27/2024 |
| 443 | Akouos San Francisco, CA Research Associate - DMPK BS or MS in chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based Research Associate to join our Drug Metabolism and Pharmacokinetics (DMPK) team. This individual will be a key contributor to performing standard ADME/DMPK assays, such as microsomal stability, plasma protein binding, and metabolite identification. The individual will also be responsible for operating LC-MS instruments (QQQ and HRMS) with minimal direction. Do you have experience in mass spectrometry while doing enzyme related work? This role may be perfect for you! | 3/27/2024 |
| 444 | Akouos Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 3/27/2024 |
| 445 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Downstream Process Development MS degree in Biochemistry, Chemistry, Chemical Engineering or related discipline from an accredited university. Exp: 0+ years |
The Associate Scientist II is responsible for performing assigned experimental tasks to support the development and optimization of manufacturing processes for Alexion’s biotherapeutic candidates. The Associate Scientist II will work routinely in collaboration with other members of Biologics Process Development, Technology Transfer and Analytical Sciences, including all other groups in Product Development and Clinical Supply. | 3/27/2024 |
| 446 | Alexion Pharmaceuticals New Haven, CT Associate Scientist II, Pilot Plant Operations MS. Exp: 1+ years |
The Associate Scientist II will perform assigned tasks to support the operational scale up of Pilot-scale manufacturing processes for Alexion’s bio-therapeutic candidates. Work routinely in collaboration with other members of Process Development and other groups in Product Development and Clinical Supply organization. | 3/27/2024 |
| 447 | Ampac Analytical Rancho Cordova, CA Automation Engineer II Master's Degree in Engineering or Computer Science. Exp: 0-2 years |
Mid-level Automation Engineer will be responsible for PLC Programming, Citect HMI Development, and cGMP documentation development and execution. Additional responsibilities will include developing, testing, and maintaining custom software applications to solve unique problems in a manufacturing environment. Execute small internal control system projects, manage larger vendor supported control system projects. Coordinate and advise process engineering on control system requirements. Engineer must be able to perform industrial field work which may involve some lifting, use of ladders, and stairs. Works under general supervision. | 3/28/2024 |
| 448 | Ardelyx Fremont, CA QA Specialist III (CSV) Bachelor’s degree in a technical discipline, science /engineering discipline preferred but not required equivalent experience may be considered. Exp: 1-7 years |
We are seeking a highly skilled and detail-oriented QA Computer System Specialist to join our team. The ideal candidate will be responsible for overseeing the quality assurance for all GxP computer systems within our organization. The person in this role will work with the functional teams to ensure that all GxP regulated systems are purchased, audited, installed and maintained according to industry best practices (e.g. GAMP5) and regulatory requirements (e.g. 21CFR Part 11 and relevant FDA Guidance). The position will also support plan and organize QA activities for computer system validation projects. Specific duties of this role include, but are not limited to, overseeing and approving validation- related documents, conducting risk assessments, determining which elements of projects should be validated, assessing and/or coordinating impact of proposed changes to computerized systems, and support activities to prepare for inspections (both external and internal) related to computer system validation. The candidate will also be responsible for maintaining GxP computer systems in a validated state in addition to support designing work processes for users and administrators of these systems. In addition, this position will involve interacting with regulatory agencies and corporate partners during inspections and audits and may require travel to audit computerized system vendors off-site. The incumbent will also develop and implement strategies to ensure compliance with CSV requirements and consistent application of relevant policies and processes. | 3/29/2024 |
| 449 | Arrowhead Pharmaceuticals Verona, WI Associate Manufacturing Scientist I (2nd shift) BS or MS in chemistry, biochemistry, engineering, or related scientific field. Exp: Entry level to 3 years |
The Associate Manufacturing Scientist I (second shift) supports the production of drug substances and drug products. Their responsibility will focus on the preparation of solutions and reagents by following standard protocols. This technically focused second shift position supports lab work, helps solve problems, and effectively communicates with colleagues. | 3/29/2024 |
| 450 | Arrowhead Pharmaceuticals Verona, WI Associate Scientist, CMC Process Development BS or MS in chemistry or biochemistry with an excellent understanding of organic and analytical chemistry. Exp: 1+ years |
Chemist in the Development Chemistry Group focusing on oligonucleotide synthesis development. This is an ideal position for an individual with an organic or biological chemistry background who has an interest in projects related to novel technology in synthesis and purification of oligonucleotides and bioconjugates. | 3/29/2024 |
| 451 | Atec Spine Carlsbad, CA Quality Engineer Minimum Bachelor’s degree (BS) from a four-Year College or university in Mechanical, Industrial and Systems, Biomedical, or Manufacturing Engineering. Exp: 1-5 years |
Develop and improve, with an emphasis on implementation, inspection methods, gages, process control techniques, standard operating procedures, inspection plans, test protocols and test reports to ensure safety, reliability and efficacy of new products and processes. | 3/29/2024 |
| 452 | Atec Spine Carlsbad, CA Validation Engineer Bachelor’s degree from four-year College or university in Engineering, or equivalent experience. Exp: 0-3 years |
Validation Engineering for New Product Development & Sustaining Engineering with a focus on software systems. Under minimal supervision, the Validation Engineer will work closely with QE, R&D, Marketing, Product Development teams, Supply Chain, and Regulatory to bring products to market while ensuring compliance to applicable standards and regulations. | 3/29/2024 |
| 453 | Aurora Biolabs San Diego, CA Research Associate I Bachelors or Masters in science related field. Exp: 0-1 year |
Aurora Biolabs, LLC is seeking a motivated research associate I in cell and molecular biology, biochemistry or related field in San Diego, CA. The individual will be a critical part of our products development team, development a new line of recombinant protein products for drug discovery and commercial use. This position requires extensive hands-on experience with a broad range of techniques including protein expression and purification, molecular cloning, PCR, mammalian cell, insect cells and bacterial culture, ELISA, as well as in vitro cell-based/immuno-based assays. You will work in an atmosphere that is stimulating, innovative, and customer focused. | 3/29/2024 |
| 454 | Beam Therapeutics Durham, NC Manufacturing Associate (Multiple Openings) BS, MS a plus, in Life Sciences or Engineering. Exp: 0-5 years |
Beam is expanding our geographical footprint to RTP, NC with the recent announcement of a 100,000 square foot manufacturing facility in addition to our laboratory-based facilities located in Cambridge, MA. We are looking for highly energetic Manufacturing Associates to support start-up and scaling of cGMP manufacturing at our new RTP site. The successful candidates will provide manufacturing, operational & technical experience around commissioning, training, qualification, and start-up. The ideal candidates will have experience in cell or gene therapy, along with demonstrated ability in a GMP environment. They will also possess the ability to successfully interface with multidisciplinary teams and build strong cross-functional relationships in a team environment. | 3/29/2024 |
| 455 | Beam Therapeutics Durham, NC QC Analyst Bachelor’s degree required, preferably in a chemistry, life science, or related discipline. Exp: 1-3 years |
Beam is seeking a highly motivated and energetic Analyst to join our growing QC analytical team. The Quality Control Analyst will be responsible for performing various analytical methods to evaluate the quality of critical in-process samples to support cGMP manufacturing operations across multiple site programs. This role will also be responsible for daily laboratory operations including reagent receipt and inventory management and equipment maintenance. This position will support deviation initiation and investigations as well as implementation of continuous improvements. The Analyst will support critical analytical method implementation workstreams in support of program start-up and scale up. This role will work closely with team members in Quality Assurance, Manufacturing, MS&T and Analytical Development. The position will report to the Senior QC Manager. The Analyst I is expected to be an on-site resource at Beam’s manufacturing facility in RTP, North Carolina to support project start-up and routine clinical and commercial operations. | 3/29/2024 |
| 456 | Berkshire Sterile Manufacturing Lee, MA Formulation Associate I Associates Degree in a science-related discipline. Exp: Zero to two (0-2) years’ |
Perform all formulation operations in the area of assignment and support start-up/changeovers/tech transfer activities. This position works under the immediate direction of the Formulation Supervisor and all work is conducted following a high standard of GMP compliance and written SOP and batch records. | 3/29/2024 |
| 457 | Berkshire Sterile Manufacturing Lee, MA Manufacturing Associate- 2nd Shift Associates Degree. Exp: zero (0) to two (2) or more years |
Perform all production operations in the areas assigned within the facility. Perform production support operations in areas assigned and support start-up, changeovers and tech transfer activities. | 3/29/2024 |
| 458 | Berkshire Sterile Manufacturing Lee, MA Process Engineer Process Engineer: Bachelor’s degree in Chemical Engineering, Chemistry, Biology, or Pharmaceutical Science. Exp: One (1) to three (3) years |
The Process Engineer will lead tech transfer projects from client or small scale to manufacturing/large scale in a manner that meets safety, quality, and operational performance expectations. The key function of this role will be to deliver effective, safe and efficient manufacturing processes for parenteral drug products. | 3/29/2024 |
| 459 | Berkshire Sterile Manufacturing Lee, MA Facilities Engineer Bachelors or Master’s engineering degree. Exp: Up to two (2) years |
The Facilities Engineer will supply engineering expertise to support and continually improve mechanical systems at BSM within the requirements of relevant regulations, cGxPs and the BSM Quality Management System. The Facilities Engineer will perform all work under the supervision and direction of the Senior Engineering Manager. | 3/29/2024 |
| 460 | BioLife Solutions Bothell, WA Aseptic Technician I Bachelor’s degree; or Associate degree / Biotech cert. Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology.The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 461 | BioLife Solutions Indianapolis, IN Aseptic Technician I Minimum: Two years of college-level biological coursework, i.e. in Chemistry, Biology, Physics, etc.Minimum: Two years of college-level biological cou Exp: Entry-level |
Daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is entry level and an effective way to get started in a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 462 | BioLife Solutions Bothell, WA Aseptic Technician II Bachelor’s degree. Exp: 1 year |
The Aseptic Technician is a core team member of the manufacturing team. The Aseptic Technician is responsible for daily production including environmental monitoring, formulating, and filling of aseptic GMP manufactured products according to batch records and SOPs. This position is for an experienced manufacturing professional with knowledge of GMP, aseptic technique, and problem-solving skills. This position provides an opportunity to solve challenges in a fast-growing industry. BioLife is a fast-growing company that is the leading cell preservation specialist within the fields of biotechnology and pharmaceuticals. This position allows for exposure to many department’s ways of working and opportunities for cross functional projects. Allows for insight into the world of biotechnology. | 3/29/2024 |
| 463 | BioLife Solutions Bothell, WA Quality Specialist I Bachelor’s degree. Exp: 0-2 years |
The Quality Assurance Specialist is a core team member of the Quality department. The Quality Assurance Specialist ensures the Quality Management System (QMS) programs flow in a timely and accurate fashion, and that the programs are in compliance with all business requirements. Quality Assurance is a trusted partner to other departments and builds strong relationships both internally and externally. This position must demonstrate abilities to work cross-functionally throughout the company with superior communication skills. A motivated self- starter and attention to detail finisher is key to the core role of Quality Assurance, ensuring that all procedures are processed in a timely fashion and right the first time. | 3/29/2024 |
| 464 | Biomerics Salt Lake City, UT Design Transfer Engineer I A bachelor’s degree in engineering or a related field (mechanical, biomedical, chemical) is required. (Required). Exp: 1+ years |
The Design Transfer Engineer I will be responsible for designing and manufacturing transfer of class II medical and surgical devices in a dynamic, customer-focused organization. The Design Transfer Engineer I will be expected to work with customers to understand product and process specifications, develop and transfer manufacturing processes, and build and test devices to those specifications. All activities will be expected to be documented according to design control requirements in a design history file (DHF). The Design Transfer Engineer I will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. The Design Transfer Engineer I will work within the constraints of budget, schedule, and scope while managing risk and ensuring adherence to established processes & regulations. The Design Transfer Engineer I may be an individual contributor and participate as part of a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. | 3/29/2024 |
| 465 | Biomerics Brooklyn Park, MN Industrial Engineer A bachelor’s degree in industrial engineering or an engineering degree is required. Exp: 1+ years |
This position will play an integral role at BAC by driving and implementing continuous improvement throughout the business. The IE works cross-functionally across the plant to eliminate waste and improve product, material, and information flow. | 3/29/2024 |
| 466 | Biotium Fremont, CA CHEMISTRY TECHNICIAN I (CHEMISTRY) B.S. or M.S. degree in Chemistry. Exp: 1+ years |
Under the direct supervision from a senior chemist, perform chemical purifications using chromatography including preparative HPLC or gravity chromatography; carry out chemical synthesis using standard protocols; carry out chemical analyses using modern instruments including analytical HPLC, LC-MS, TLC, UV/Vis and fluorescence spectrophotometry. | 3/29/2024 |
| 467 | Biotium Fremont, CA RESEARCH ASSOCIATE I, BIOSCIENCE B.S. in Biology, Molecular Biology, Biochemistry or a related field. Exp: 1+ years |
Under direct supervision from the VP of Research and Development, perform synthesis, purification, and characterization of antibody/biomolecule conjugates of fluorescent dyes, fluorescent proteins, tandem dyes, enzyme reporters, and polymeric scaffolds. Research and development leading to commercialization of bioconjugates for research applications. The successful candidate will possess a strong background in chemistry and bioconjugation chemistry and have experience performing bioconjugation reactions, protein purification, and requisite analytical techniques. | 3/29/2024 |
| 468 | Visby Medical San Jose, CA Product Transfer Engineer I Bachelor’s degree in engineering or related field. Exp: 1-2 years |
The Product Transfer Engineer plays a vital role in transitioning products from design and development to full-scale production. The individual will also be responsible for root cause investigations under the guidance of senior team members to ensure smooth operations. | 3/29/2024 |
| 469 | Boston Analytical Salem, NH Analytical Chemist I, Raw Materials Qualification include a Bachelor’s degree in Chemistry or a related discipline is required. Exp: 0-2 years |
The Chemist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties include performing analysis of Raw Materials using AA, UV-Vis, and Wet Chemical Analysis according to USP/EP methods. | 3/29/2024 |
| 470 | Boston Analytical Salem, NH Microbiologist QC I - Framingham Qualifications include a BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. Location: Framingham, MA | 3/29/2024 |
| 471 | Boston Institute of Biotechnology Southborough, MA Research Associate – Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 3/29/2024 |
| 472 | Boston Institute of Biotechnology Southborough, MA Assoc. Scientist – Downstream Process Development MS degree in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≥1 year |
The Associate Scientist is responsible for development and execution of downstream related projects with moderate direct supervision. The individual reports to a more senior scientist level or above on relevant projects. The individual will provide expertise in the development and optimization of downstream processes. | 3/29/2024 |
| 473 | KCAS Bioanalytical Olathe, KS Associate Scientist - Pharma LC-MS/MS Bachelor’s degree in Chemistry, Biochemistry, or related field. Exp: 1-3 years |
When you work as an Associate Scientist on the Pharma LC-MS/MS team, you get to further our mission by being a contributing scientist on studies, with the ability to carry out all aspects from study setup and development, through reporting with some assistance. You will need to utilize a strong base in scientific principles/theory to assess data integrity and troubleshooting, while independently completing experiments. | 3/18/2024 |
| 474 | KCAS Bioanalytical Olathe, KS Analyst II - Pharma LC-MS/MS BS/BA degree in Chemistry, Biochemistry, or other life science field. Exp: one year |
When you work as an Analyst II in the Pharmaceutical Liquid Chromatography Mass Spectrometry (LC-MS/MS) lab at KCAS, you get to further our mission by working under senior Pharma LC-MS/MS scientists to contribute to the success of our clients. | 3/18/2024 |
| 475 | Latitude Pharmaceuticals San Diego, CA QC Associate Minimum BS degree in Chemistry or chemistry-related field. Exp: 1+ years |
LATITUDE Pharmaceuticals Inc., a San Diego-based contract drug developer and manufacturer, is seeking a Quality Control Associate to be a key member of the QC group. A successful candidate should have some experience in drug product manufacturing and analytical testing techniques under GMP. This is a full-time position and will report to the Director of Quality. The position will be located in San Diego, California. | 3/18/2024 |
| 476 | Lodo Therapeutics Cambridge, MA Operations Engineer 1, DNA Synthesis (Weekend Shift) at Ginkgo Bioworks Inc. Bachelor's degree in biology, biochemistry or biomedical engineering. Exp: 1+ years |
We're seeking a DNA Synthesis Operations Engineer to join our team to execute, improve, and scale our state-of-the-art manufacturing process flows. You’ll apply molecular biology protocols to perform efficient and high-quality lab-work in a fast-paced setting. You will use your excellent communication skills and flexibility to work effectively within a diverse team. You’ll display your breadth by leveraging the technology, software, automation, and instrumentation acumen required by our detailed processes flows. Please note that this position is to be filled at our Cambridge, MA location and will cover a four day, 10 hour per day work schedule (Thursday to Sunday - 10AM to 8PM). | 3/18/2024 |
| 477 | Regulus Therapeutics San Diego, CA Temp/Hire: Research Associate – Senior Research Associate, Drug Discovery Biology MS in Biology or related discipline. Exp: 1+ years |
We are excited to invite a dedicated and driven individual to join our Research Biology team. This role is designed for a qualified candidate who seeks the opportunity to evolve as a drug discovery scientist, with a specific focus on microRNA biology, oligonucleotide therapeutics, and CNS-related diseases. The successful candidate will serve as a hands-on cell and molecular biologist, contributing valuable research experience and skills to the organization. The role encompasses a spectrum of drug discovery efforts, spanning early-stage target identification to advanced IND-related activities. The ideal applicant should possess direct experience in various molecular techniques, a robust understanding of cell biology, and excellent organizational and presentation skills. This position presents an exciting prospect to contribute to the exploration of innovative oligonucleotide therapeutics addressing areas of high unmet medical need. | 3/20/2024 |
| 478 | AGC Biologics Seattle, WA Downstream Manufacturing Associate I/III Bachelor’s degree or Biotech certificate, quality systems regulations (cGMP) knowledge. Exp: 1+ years |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. The Manufacturing Support Technician will be responsible for fulfillment of immediate requests from the Manufacturing Operations departments including, but not limited to, assembly preparation, washing parts, autoclaving of parts, kitting parts for delivery and facility sanitizations. The deadline for applications is the 31st of March. | 3/20/2024 |
| 479 | AGC Biologics Boulder, CO Quality Assurance Associate I-III (In Plant Operations) Bachelor’s degree in Biology, Chemistry or other relevant science/engineering discipline. Exp: Associate II – 0 - 2 years |
The Quality Assurance Associate I- III (In Plant Operations) is responsible for providing (24/7/365) Quality support to the activities listed below at the Boulder, CO site. SCHEDULE: 2-2-3 Blue Days | 3/20/2024 |
| 480 | AGC Biologics Seattle, WA Quality Control Associate I BS/BA degree. Exp: 1-3 years |
The Quality Control Associate I will perform QC analysis and document activities according to SOPs following good manufacturing processes (GMP). This individual will also demonstrate the ability to learn QC methods, procedures and systems. | 3/20/2024 |
| 481 | AGC Biologics Seattle, WA Upstream Manufacturing Associate I/III Bachelor’s degree or Biotech certificate, quality systems regulations (cGMP) knowledge. Exp: 1 year |
The role of the Manufacturing Associate is to act as a controller, providing essential duties to support the respective production suite, Supervisor and Manager. On a daily basis, the Manufacturing Associate is expected to have a full understanding of the schedule and required tasks; promoting adequate assessment and response of any production demands. The Manufacturing Support Associate will be responsible for fulfillment of immediate requests from the Manufacturing Operations departments including, but not limited to, assembly preparation, washing parts, autoclaving of parts, kitting parts for delivery and facility sanitizations. | 3/20/2024 |
| 482 | AGC Biologics Seattle, WA; Boulder & Longmont, CO, US Upstream Process Development Associate I A.A./B.S. in a life science or engineering. Exp: 1-3 years |
This is a Development Associate I position in the Upstream Process Development group. Primary responsibility will be to support mammalian cell culture processes used for the manufacture of therapeutic recombinant proteins. The successful candidate will be responsible for supporting shake flask and bioreactor experiments, sampling, inoculating, feeding & harvesting bioreactors. Under general supervision, this person carries out routine to moderately complex experiments or procedures. The deadline for applications is the 31st of March. | 3/20/2024 |
| 483 | Aptitude Medical System Santa Barbara, CA Research Associate Bachelor’s degree or Master’s degree in a relevant discipline. Exp: Entry-level |
We are seeking to hire multiple capable and driven entry-level Research Associates to join our tight-knit research and development team. In this position, you will be working closely with a cross-functional team of mission-driven scientists and engineers to drive the invention and development of novel diagnostic products. | 3/21/2024 |
| 484 | Aura Biosciences Brighton, MA Sr. Associate Scientist, Upstream Degree in biochemical engineering, biological sciences, biochemistry or related discipline. M.S. Exp: 1+ years |
Reporting to the Upstream Process Development Lead, the (Sr) Associate Scientist will be responsible for the development of upstream production processes and the production of material for routine in-house development use. This includes all assays associated with cell culture production. The incumbent will also participate in the transfer of the upstream process to support biopharmaceutical product development at Contract Manufacturing Organizations (CMOs). The scientist will interact with the in-house team and the CRO/CMO to ensure timely progress in technology development, documentation, and manufacturing readiness. | 3/21/2024 |
| 485 | Bio-Concept Laboratories Westborough, MA Entry Level Scientist 1 - 2nd Shift Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: Entry-level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Sunday - Thursday 4:00 pm - 12:30 am What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 486 | Bio-Concept Laboratories Sheridan, WY Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory workJoin us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 3/21/2024 |
| 487 | Bio-Concept Laboratories Westborough, MA Entry Level - Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Sunday - Thursday 8 am - 4:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 488 | Bio-Concept Laboratories Mt. Juliet, TN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory wor | 3/21/2024 |
| 489 | Bio-Concept Laboratories Mansfield, MA Scientist 1 -Metals- Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Find your place at Pace® Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Monday - Friday 3 pm - 11:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 490 | Bio-Concept Laboratories Mansfield, MA Scientist 1 - Metals - Early Mornings Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. Schedule: Monday - Friday 5 am - 1:30 pm What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 491 | Bio-Concept Laboratories Greensburg, PA Environmental Scientist - Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field, or an equivalent combination of education, training and experience. Exp: Entry-level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. What you’ll do Facilitate and support the analysis, administration and oversight of air, water and soil samples using standard chemistry/ biochemistry policies, programs, and practices Clean, maintain and calibrate equipment Maintain detailed and organized documentation on all laboratory work | 3/21/2024 |
| 492 | Biofactura Frederick, MD Quality Control Analyst Bachelor’s degree required. Exp: 1+ years |
The QC Analyst will support the establishment and growth of BioFactura’s QC department. Responsibilities include, but are not limited to, performing QC testing of DS/DP release and stability samples in support of BioFactura programs; ensuring compliance with established regulatory practices and standards; working with Analytical Development (AD) on the transfer of qualified assays to QC; assisting with assay validation activities; and authoring and review of SOPs, protocols, and reports. | 3/22/2024 |
| 493 | BioRestorative Therapies Melville, NY cGMP Bio -Manufacturing Engineer MSc degree in cell biology or similar discipline. Exp: 1 to 6 years |
BioRestorative Therapies, Melville, NY is recruiting for a cGMP bio-manufacturing engineer. This role provides outstanding opportunities for talented self-motivated individuals, ideally with experience in (stem) cell biology, immunology, and/or molecular biology, who can contribute to our ongoing efforts to generate clinical grade cell-based therapeutics. We are most interested in connecting with qualified individuals who aspire to support the development of therapeutics and/or life science products and tools to support research endeavors. | 3/22/2024 |
| 494 | ChemPacific Baltimore, MD Chemist Master’s degree in Chemistry or Organic Chemistry. Exp: one year |
Perform multi-step organic synthesis in solution and/or solid support: Optimize conditions to achieve desired yield; perform and interpret data analysis such as LC/MS and NMR; perform purification steps such as extraction, recrystallization, silica gel column chromatography and LC/MS purification; perform cGMP synthesis of pharmaceutical ingredients; and perform process development and scale-up for kilogram quantities; and clearly record and communicate results and challenges to coworkers/supervisor. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. Please send your resume to xtan@chempacific.com | 3/22/2024 |
| 495 | CRISPR Therapeutics Boston, MA Research Associate II, in vivo Oligonucleotide Chemistry MS degree in Chemistry, Chemical Engineering, Biochemistry, Bioengineering, Pharmaceutical Sciences or related field. Exp: 1+ years |
CRISPR Therapeutics is seeking a highly motivated Research Associate to join our In Vivo Technical Operations department in Boston, Massachusetts. The incumbent will be responsible for the oligonucleotide synthesis, purification, desalting, and analysis to support the process development of guide RNA production in various scales. This position will also support therapeutic programs in multiple disease areas in R&D department. Prior experience in oligonucleotide synthesis, purification, and characterization is desired | 3/22/2024 |
| 496 | GenEdit South San Francisco, CA Lab Technician, Chemistry (Part Time) Associate degree (or) bachelor’s degree in any science field or equivalent experience. If the candidate is willing to be promoted to RA I, the positio Exp: RA I: 0-2 years |
GenEdit is seeking a highly self-motivated Lab Technician to provide support to the Chemistry team. The Lab Technician will be responsible for assisting the Medicinal Chemistry Team in cataloging and organizing the inventory of synthesized polymers, alongside routine lab maintenance and aliquot distribution. They will have a key role in chronicling the various modes of organic, polymer, and analytical chemistry performed at GenEdit. A successful candidate will be collaborative, resourceful, and enthusiastic to work in a team environment. This candidate will report to the Principal Scientist in the Chemistry Department and communicate with all interdisciplinary groups like formulation, in vitro and in vivo teams. This position may convert into a full time Research Associate (RA I) in a year subject to candidate’s performance and the requirement by the Chemistry department. Upon promotion to RA, the candidate will be working in organic synthesis of bio-synthetic polymer, macromolecule and/or complex organic molecule characterization utilizing various separation and detection techniques in support of research, regulatory and business efforts. They will be responsible for synthesis of novel polymer molecules, assist with developing, implementing, and validating analytical methods to characterize novel polymers for gene delivery nanoparticles. This position will also participate in the development and routine performance of polymer characterization assays for identity and purity, preparation of certificates of analysis (COA), and preparation of standard operating procedure (SOP). Additional duties and responsibilities may be required as needed. | 3/22/2024 |
| 497 | Immucor Norcross, GA MQA Technician II Associate’ Degree (AA) or equivalent from a two-year college or technical school; Bachelor’ degree is highly preferred. Exp: six months to one year |
We are seeking an experienced Manufacturing Quality Assurance (MQA) Technician II to join our team. Our company is a growing medical technology firm that offers challenging positions, opportunities for professional growth, and competitive benefit packages to all employees. Our company is founded on and guided by our corporate mission and values: respect, integrity, teamwork, and achievement. If you have the necessary skills and experience to excel in this position, we want to hear from you! | 3/22/2024 |
| 498 | Indivior Raleigh, NC Controls Engineer Bachelor of Science in Engineering or related field. Exp: 1+ years |
The Controls Engineer is a technical resource to the engineering, maintenance, validation and operations departments, to meet all regulatory and Company specific policy requirements and objectives, and to improve plant efficiency, capacity, capability and modernization. This person is responsible for the research, development, design, layout, building, testing, troubleshooting, repairs and improvement of all manufacturing control systems, including the Building Management System (BMS), HVAC, and Utility Control Systems. The position is also responsible for implementing improvements to increase equipment efficiency and prevent obsolescence, as well as ensuring the validated state of all applicable equipment, systems and facilities. This position will maintain compliance with all company standard operating procedures (SOPs) and applicable cGMP, OSHA, EPA, and local government regulations. | 3/22/2024 |
| 499 | Indivior Raleigh, NC Environmental Monitoring Technician II Bachelor of Science degree in a life science or equivalent. Exp: 1-3 yrs |
This position reports to the EM Supervisor for the functional area to which they are assigned and has no direct reports. This individual holding the position of EM Technician II shall be responsible for performing routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms, critical utilities and controlled environments. | 3/22/2024 |
| 500 | Lampire Biological Labs Everett, PA Laboratory Technician BS in relevant field. Exp: 1-2 years |
Job Description: To facilitate daily operations at the Coopersburg Laboratory by supporting the whole blood, plasma/serum, anticoagulant, brokered and abattoir departments as necessary. | 3/22/2024 |
| 501 | NeuMoDx Molecular Ann Arbor, MI MANUFACTURING SPECIALIST, REAGENT College Degree (BS/BA) in science or chemistry field. Exp: 1 year |
Manufacturing Specialists are required to have a strong knowledge of manufacturing methods and techniques, process development experience, work flow understanding, ability to understand formulations and follow recipes and testing protocols for any in-process Quality checks • In this position, Manufacturing Specialists, will maintain manufacturing equipment, create work instructions, train others, often be asked to contribute to or lead projects, be cross functionally trained to work in several areas as needed. • This role requires a self-starter, ability to work independently, understanding of departmental goals-working as a team to achieve those goals within set timelines. | 3/22/2024 |
| 502 | Physical Sciences Andover, MA Chemical Engineer BS or MS degree in Chemical Engineering, Chemistry or Materials Science. Exp: 0 to 2 years’ |
Physical Sciences Inc., located just north of Boston in Andover, has a career opportunity for a Chemical Engineer with a strong background in reaction kinetics, heat and mass transfer, and separations. We are seeking an applicant who can assist with developing and scaling-up materials production from laboratory/batch processes to pilot-scale/continuous processes. The applicant we seek would benefit from material development, purification and characterization experience. We are looking for a strong worker, who can safely and effectively execute on their ideas as a member of a team and sometimes as an individual contributor. This Chemical Engineer will be asked to work on innovative programs, in areas such as atmospheric water harvesting, continuous process development, and waste conversion to high performance materials. Experience with wet chemistry laboratory procedures and related analytical techniques is essential. Hands on experience with hardware assembly for chemical processes is preferred. Working knowledge of analytical laboratory techniques (e.g. GC-MS, FTIR, NMR, DSC, TGA, tensile testing) and chemical engineering software packages (e.g. Comsol) is highly desirable. | 3/22/2024 |
| 503 | Physical Sciences Andover, MA Optical Engineer Bachelor’s degree in optical or mechanical engineering, physics or equivalent. Exp: 1+ years |
Physical Sciences Inc., a 100% Employee-Owned company located just north of Boston in Andover, seeks an Optical Engineer with professional experience to support development of emerging optical technologies. The candidate will support optical systems design, construction, and testing needs for illuminators, projectors, integrated spectrometers and/or metasurfaces. A strong basic understanding of optical system layout and construction is sought. | 3/22/2024 |
| 504 | Physical Sciences Andover, MA Experimental Physicist Bachelor or Masters degree in Physics, Applied Physics, Optics, or Related Discipline. Exp: 0-5 years |
Physical Sciences Inc., located just north of Boston in Andover, MA, seeks an experimental physicist with experience in laser-based tools related to applications such as atom sensing, integrated photonics, or optical materials development. The candidate will join teams at PSI and contribute to invention, demonstration, and deployment of technology platforms targeting these application areas. The ideal candidate will have a bachelor’s or master’s degree in physics or related disciplines and should be interested in applied research and development with strong experimental, hardware, and leadership skills. | 3/22/2024 |
| 505 | The Ritedose Corporation Columbia, SC Microbiologist Technician Technical degree in life science or related field. Exp: 1+ years |
The Microbiologist Technician is responsible for all duties related to performing environmental monitoring, personnel monitoring. Other responsibilities include data entry, data review, ensuring calibration of equipment, maintaining and ordering inventory of laboratory supplies, and maintaining the Microbiology laboratory by ensuring its cleanliness and order. | 3/22/2024 |
| 506 | Sedia Biosciences Beaverton, OR Production Technician I High School diploma, Training Certificate, or Associates degree (technical field preferred). Exp: Entry level |
Production Technicians at Sedia will be responsible for the production of Sedia’s products. This includes the formulation of reagents, application of reagents to various materials, dispensing of testing reagents into vials, tubes, or bottles, capping and labeling of components and assembly of components into finished test kits. Technicians will be working with standard laboratory equipment as well as automated and semi-automated production equipment. | 3/22/2024 |
| 507 | Sedia Biosciences Beaverton, OR QC Technician I High School diploma, Training Certificate, or Associates degree (technical field preferred). Exp: Entry-level |
This position works under direct supervision to perform Quality Control functions including the inspection and testing or raw materials, components, and finished products in a medical diagnostic manufacturing environment. Works in compliance with the Quality Management System and under applicable quality standards such as ISO-13485 and CFR 21 part 820 cGMPs. | 3/22/2024 |
| 508 | Acceleron Pharma Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 509 | Acceleron Pharma Rahway, NJ Specialist, Process Engineering Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Sterile GMP Clinical Manufacturing facility. As the facility is nearing the completion of its construction, the selected candidate will contribute to equipment and facility commissioning/qualification, regulatory certification, as well as other workstreams’ critical activities to enable facility startup and operational readiness. To support these business-critical activities, night and weekend work may be required. Once the facility is operational, this role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of sterile clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Sterile Process Engineering Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 510 | Acceleron Pharma Rahway, NJ Specialist, Analytical Research and Development Advanced and relevant industry experience for applicants with a Bachelor of Science degree, or beginner, relevant industry experience for applicants w Exp: 1+ years |
The Small Molecule Analytical Research and Development group has an opening for a Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Specialist, you will be part of a team of Specialists working on cross-functional scientific teams to enable development of novel small molecule, peptide, and oligonucleotide drug development through laboratory-based analytical characterization of our raw materials including excipients and package components. | 3/22/2024 |
| 511 | Acceleron Pharma Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 3/22/2024 |
| 512 | Acceleron Pharma Rahway, NJ Specialist, Quality Assurance (Hybrid) Bachelor degree (B.S.) in an appropriate Science or Engineering discipline (engineering, chemistry, biology, biochemistry, microbiology). Exp: 1+ years |
The Rahway based Specialist, Global Development Quality Operations - API, is responsible for review and approval of documentation to support Good Manufacturing Practice (GMP) clinical supply API manufacture, testing, release and maintenance in support of our company's clinical supply programs. This person will also review and approve documentation accompanying the disposition of API materials (including new modalities) to ensure conformance to appropriate regulatory and company requirements for clinical supply manufacture and/or regulatory inspections. Performs audits of batch documentation, data, information, procedures, equipment and systems, and/or facilities to ensure the compliance with Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMPs) and other applicable worldwide regulations and our Company procedures. The Specialist will become knowledgeable in regulatory requirements, cGMPs and our company's procedures to assure API (including new modalities) manufacturing and testing is in compliance and will gain competency in their responsibilities. | 3/22/2024 |
| 513 | Tris Pharma Monmouth Junction, NJ Associate QC Analytical Chemist Bachelors in Chemistry or related scientific field. Exp: 0-3 years |
We have an immediate opening in our Monmouth Junction, NJ QC Lab for an (Associate) QC Analytical Chemist. This is an entry level scientific position and we will train qualified candidates who meet listed requirements. Recent college graduates are welcome to apply. The (Associate) Quality Control (QC) Analytical Chemist performs analytical testing of raw materials, packaging components, in-process (IP), finished product (FP), and/or stability samples (ST). She/he is also responsible for following Analytical Methods, current Good Manufacturing Practices (cGMPs), Protocols, Standard Operating Procedures (SOPs) and company policies. | 3/11/2024 |
| 514 | Turn Biotechnologies Mountain View, CA Research Associate - Synthetic Chemistry, CMC BS/MS in organic/synthetic chemistry or related discipline. Exp: 1-3 years |
Turn Biotechnologies is seeking an excellent Research Associate with strong knowledge and hands on experience in synthetic/organic chemistry to work in our CMC team. The ideal candidate should have experience in synthesizing, purifying and characterizing small molecules, in particular lipids. Additionally, experience in polymer chemistry is a plus. | 3/11/2024 |
| 515 | Vor Biopharma Cambridge, MA GMP Operations Associate BS in Biology or related field. Exp: 1 - 3 years |
Vor Bio is seeking a GMP Operations Associate who is an enthusiastic and driven individual to support cGMP manufacturing for clinical phase cell therapy manufacturing facility. The candidate will be responsible for providing assistance in the support area for the manufacturing of Vor’s gene-edited cell therapies and maintaining compliance of cGMPs in manufacturing areas. | 3/15/2024 |
| 516 | Wright Medical Portage, MI Electrical Design Engineer Bachelor's degree in EE or related discipline required. Exp: 0+ years |
This role is on the Electrical Engineering team at Stryker Medical division's Acute Care business unit. We primarily work with patient handling and patient care equipment within the hospital space such as stretchers, hospital beds, and support surfaces. This role falls under the team addressing the high-acuity market, with a focus on products that often come into direct contact with patient. It includes gaining a deep understanding of customer needs through research and partnership with upstream marketing and through direct interactions with customers. Working with a diverse team, you will design, develop, modify, evaluate, and verify electrical components and sub-systems for medical devices. The role includes the full development process from research to product launch. | 3/15/2024 |
| 517 | Wright Medical Mahwah, NJ Operations Engineer Bachelor’s degree in engineering- Required. Exp: 1 year |
Stryker Orthopedics is seeking to hire an Operations Engineer to support the manufacturing of joint replacement products in Mahwah, New Jersey. As an Operations Engineer with the operations team you will provide manufacturing engineering support and direct projects for assigned cells. | 3/15/2024 |
| 518 | ZeptoMetrix Raleigh, NC Production Scientist I Bachelor’s degree in Chemistry, Engineering or related field from an accredited higher learning institution. Exp: Up to 2 years |
The Production Scientist I will involve all manufacturing tasks related to the production of the company’s organic products. Responsibilities include manufacturing, handling, and packaging various classes of organic compounds as per standard operating procedures. The incumbent must be a dynamic individual who can multi-task and perform various activities associated with manufacturing operations while adhering to all safety policies and high quality Standard Operating Procedures. This position requires hands on chemistry lab work and will report to the Organic Manufacturing Lead. | 3/15/2024 |
| 519 | ZeptoMetrix North Charleston, SC Scientist I, Quality Bachelor's degree in Chemistry or related field. Exp: 1 year |
The Quality Control (QC) Scientist is primarily responsible for the quality control of starting materials, in-process materials and the finished goods. The incumbent must be a dynamic individual who can work in a diversified group and able to handle multi-tasks within QC operations. The candidate must possess a good working knowledge of Analytical Chemistry. This position requires hands on chemistry lab work and troubleshoot instruments and solve complex spectroscopic problems. | 3/15/2024 |
| 520 | Zimmer Biomet Warsaw, IN Development Engineer I Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mec Exp: 1 - 3 years |
*Please note, this role is a hybrid position, partially onsite in Warsaw, IN and partially remote. You have a key support role with responsibility for new product design, development, and commercialization; and/or to maintain in the market innovative medical device products in order to further Zimmer Biomet’s mission and grow Zimmer Biomet’s market leadership position | 3/15/2024 |
| 521 | Zimmer Biomet Warsaw, IN Technician College/University courses in Microbiology, Biology, Chemistry, Engineering Mechanics, Medical Technology or other related field preferred. Exp: 0 – 3 years |
Responsible for supporting the daily operations of the laboratory at all Zimmer Biomet Warsaw facilities and for operating and maintaining laboratory equipment for the necessary assigned tasks per area work instructions. May also be responsible for ensuring that equipment calibration and maintenance (preventive and/or corrective) is performed. | 3/15/2024 |
| 522 | Zimmer Biomet Warsaw, IN Development Engineer I Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mec Exp: 1-3 years |
*This is a hybrid position, partial remote/partially onsite, in Warsaw, IN. Responsible for the design, development, and processing of patient specific implants and instruments based upon individual patient anatomy or conditions. Work is expected to encompass both the development of new products and maintenance of existing products. Position will lead small scope project as a project leader or portions of larger scope project as a core team member as well as individual patient cases within the Patient Matched Implants (PMI) department. | 3/15/2024 |
| 523 | Z-Medica Morrisville, NC Associate R&D Engineer, Sustaining Possession of bachelor’s degree in engineering. Exp: One year |
This is an entry level engineering position that will support the sustaining engineering group for the Emergency Medicine product families. However, assignments may include work for other products within the Teleflex portfolio. Experience and background requirements should focus on disposable products. Incumbent organizes and manages multiple projects and ensures projects are completed in a timely manner; Assignments may focus on sustaining engineering assignments providing creative solutions to existing products when problems arise, or modifications are requested. Performs other duties as required or assigned. | 3/15/2024 |
| 524 | Z-Medica Morrisville, NC Associate R&D Engineer, Sustaining Possession of bachelor’s Degree in Engineering. Exp: One year |
This is an entry level engineering position that will support the sustaining engineering group for the anesthesia products lines. However, assignments may include work for other products within the Teleflex portfolio. Experience and background requirements should focus on disposable products. Incumbent organizes and manages multiple projects and insures projects are completed in a timely manner; Assignments may focus on sustaining engineering assignments providing creative solutions to existing products when problems arise, or modifications are requested. Performs other duties as required or assigned | 3/15/2024 |
| 525 | Z-Medica Jaffrey, NH Associate Manufacturing Engineer Bachelor's Degree in Polymer/Plastics Engineering or equivalent field required. Exp: 0-2 years |
Results-driven professional is dedicated to constant learning and training. We are looking for an Polymer or Chemical Engineer to join our team. You will be responsible for assisting, planning, designing, and completing projects in extrusion manufacturing utilizing six sigma/lean/DMAIC or like methodologies. The ideal candidate would have experience working with manufacturing equipment and processes to optimize production and increase capacity. Must have equipment acumen, with the ability to be creative and troubleshoot when necessary. Technical aptitude, people-centric, and ability to assist the PTFE and melt extrusion departments. | 3/15/2024 |
| 526 | Z-Medica Maple Grove, MN Environmental Technician Bachelor’s Degree in Biology, Chemistry, Microbiology or other related science or engineering field. Exp: 0 - 2 years |
Responsible for the environmental/microbial control in the Teleflex manufacturing facilities. Complete planning, coordination and execution of deliverables related to environmental control, microbial control, sterilization qualifications and cleaning/disinfection control of manufacturing areas. | 3/15/2024 |
| 527 | Z-Medica Maple Grove, MN Microbiologist I Bachelor’s Degree required in a related scientific discipline. Exp: No previous professional experience required. |
This role is responsible for complete execution of deliverables related to microbiology testing, contamination control, cleaning/disinfection validation of manufacturing areas, product release testing, and controlled environment monitoring/certification. This will require review of samples to ensure testing is performed according to provided work instruction. Fulfill microbiology role supporting new product development, production, controlled environments, and sterilization. | 3/15/2024 |
| 528 | Z-Medica Morrisville, NC Service Engineer Minimum AA/AS/BS or demonstrated equivalent. Exp: 1 year |
This individual is responsible for the troubleshooting, service and repair of VPS products following established procedures and work instructions at the Morrisville, NC Service Center. They will support critical business activities related to servicing VPS capital equipment products focused on the customer experience, continuous improvement and workflow efficiencies This role will collaborate with VPS service globally, working with other Teleflex sites, third parties and distributors to maintain a consistent approach to service | 3/15/2024 |
| 529 | Zymo Research Irvine, CA Bioinformatics Associate I Holds a master’s or bachelor's degree in Biology, Bioinformatics, Computer Science, Mathematics, Statistics, or a related discipline. Experience may s Exp: 1+ years |
Zymo Research is seeking a highly motivated individual to join our Bioinformatics team! The qualified individual will play a key role in developing analysis pipelines for Next-Generation Sequencing data and performing cutting-edge data science to support Zymo Research’s global product strategy. As part of the Bioinformatics team, you will leverage your skills and familiarity with NGS-based sequencing methods in the research and development of new data analysis pipelines for our services, applications, and exciting research projects! | 3/15/2024 |
| 530 | ZebraSci Mannford, OK; Tempe, AZ; Vernon Hil, OK R&D Engineer II B.S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other related engineering field. Mechanical Engineering degree Exp: 1-3 years |
Hybrid, Multiple Locations. This position is a limited term assignment which will include benefits such as (medical, health, dental, 401K). Eligibility for these benefits will be based on the eligibility requirements as determined by the BD Total Rewards policy and is anticipated to last approximately through 12/20/24. This position works multi-functionally and leads R&D activities needed in the development and transfer to manufacturing of products, processes, test methods and equipment for medical device manufacturing. Hybrid, Multiple Locations. This position is a limited term assignment which will include benefits such as (medical, health, dental, 401K). Eligibility for these benefits will be based on the eligibility requirements as determined by the BD Total Rewards policy and is anticipated to last approximately through 12/20/24. This position works multi-functionally and leads R&D activities needed in the development and transfer to manufacturing of products, processes, test methods and equipment for medical device manufacturing. | 3/15/2024 |
| 531 | ZebraSci Lexington, MA Analytical Chemist Bachelor of Science degree required; Master of Science degree preferred. Exp: 1-year |
This position will be involved in many aspects of producing and developing biomaterials, including the analysis, production, isolation, purification and testing of biomaterials within well-defined guidelines. The associate will need to use appropriate analytical tools to characterize and qualify the biomaterials, such as gas chromatography (GC), gel permeation chromatography (GPC) and mechanical testing. S/he will interact with contract testing laboratories to conduct appropriate testing on the materials and may also provide supervision and guidance to junior level technicians. | 3/15/2024 |
| 532 | ZebraSci Branchburg, NJ Combination Product Test Engineer Bachelors of Engineering, Biomedical, Chemistry, Biology, or equivalent is preferred. Exp: 1+ years |
Responsibilities Conducts timely sample intake, including receipt, proper identification, storage and return shipments as needed Conducts testing as assigned utilizing appropriate test methods, protocols specifications and equipment (includes product and/or equipment testing), including adhering to test schedules (e.g. stability pulls, aging pulls). Conducts data analysis as per protocol or specifications utilizing variety of data analysis tools (e.g. excel, JMP, MiniTab) Communicate challenges, scheduling or testing conflicts and other issues to management in timely manner Maintains inventory of lab supplies, including but not limited to; general supplies (e.g. PPE, wipes, cleaners…) and chemicals use for routine testing and/or cleaning Conducts routine sample disposition (e.g. return to client, disposal), including coordination of hazardous waste disposal Responsible to maintain the lab and storage areas in a clean an organized manner. Includes routine lab cleaning Adheres to ZebraSci Quality Systems, including but not limited to; timely identification, and notification of potential Quality Events (e.g. OOS, Deviations, CAPA…) and the subsequent forward processing and investigation of such events | 3/15/2024 |
| 533 | ZebraSci Louisville, CO Staff Reliability Engineer BS in engineering or a related technical field (i.e., physics, materials science, mathematics). BS in engineering or a related technical field (i.e., Exp: 1-year |
The Staff Reliability Engineer is responsible for providing project support to ensure reliability targets are achieved according to project plans. The reliability engineer should have a demonstrated broad technical base in all aspects of reliability engineering. The ideal candidate would have experience in electrical, mechanical and software engineering fundamentals, including PoF (Physics of Failure) understanding. The candidate will work closely with R&D members and be a sole contributor to conduct system and component level reliability activities for sustaining product and new product development within the franchise and division. The reliability engineer will have the technical skills necessary to effectively challenge the design concepts as they pertain to overall reliability. An exciting part of the role includes opportunities to work on reliability initiatives for key R&D business critical projects. At the heart of reliability engineering is testing and we are looking for expertise that will help us become a Center of Excellence. The reliability engineer will lead troubleshooting and failure analysis investigation activities to determine design weaknesses and root-cause. Ideally the candidate will grow and be able to direct efforts of individuals around reliability process and deliverables | 3/15/2024 |
| 534 | ZebraSci Temecula, CA Combination Product Test Engineer (Onsite) Bachelor’s degree in science or math related fields, such as biology, chemistry or engineering is preferred. Exp: 1 year |
The primary role of the Engineering Technician is the timely and accurate execution of testing as scoped within individual projects and per client requirements. This includes but is not limited to; sample receipt, prep, storage, and shipping, as well as protocol and report generation, data review and summary. This role utilizes standard and custom laboratory equipment. | 3/15/2024 |
| 535 | ZebraSci Mebane, NC Associate Quality Scientist Bachelor’s degree in Biology, Microbiology or other related Life Science. Exp: 1-2 years |
Reporting to the Quality Scientist/Lab Supervisor, the BD Mebane Associate Quality Scientist is responsible for applying basic scientific principles to routine laboratory work, executing product testing, applying/interpreting scientific data of moderate complexity, ensuring good laboratory practices, and processing data generated from Quality Control testing. | 3/15/2024 |
| 536 | ZebraSci Columbus, NB Quality Engineer I Bachelor's Degree Required Field(s) of Study: Science-related field, Quality Assurance, Engineering, Mathematics/Statistics Exp: 0-5 years |
Support Quality and Production groups by using process and regulatory knowledge combined with a data driven approach to problem solving. Become a subject matter expert in application of statistical tools, measurement systems analysis, and root cause analysis. Take ownership of projects and drive to completion, whether working independently or in a team. Will interact professionally with BDM, PS customers in project management and problem solving activities. Regular, punctual attendance is an essential job function. Ability to speak, read and write English. Ensures compliance with BD quality systems, policies, procedures and practices and all local, state, federal and BD safety regulations, policies and procedures. The applicant pool includes an identified internal candidate. All applications are welcomed | 3/15/2024 |
| 537 | Accurus Biosciences Richmond, CA Research Associate Bachelor’s or Master’s degree in Biology. Exp: 0-3 years |
The successful candidate will perform a range of duty critical to our research service business. The primary responsibility of this position is general molecular biology which includes DNA cloning, site directed gene mutagenesis, plasmid DNA preparation and DNA restriction analysis. Additional responsibilities for this position may include mammalian cell culture, protein transient production, stable cell line generation and general lab maintenance. If interested, please send your resume to hr@accurusbio.com. | 3/15/2024 |
| 538 | Affinivax Rockville, MD Biopharmaceutical Associate I Bachelor of Science / Bachelor of Art / Associates Degree in biological sciences, chemical sciences, engineering or equivalent technical discipline. Exp: 1+ years |
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Basic understanding and knowledge of the following areas and ability to perform the activity with some supervisory guidance: Follow appropriate standard operating procedures (SOPs), protocols and batch records/logbooks to safely perform process operations and document compliantly with good documentation and data integrity practices. Perform the set-up, operation, cleaning and break-down of process equipment. Perform sampling procedures on various analytical instruments to analyze cell culture, solution and/or product concentration characteristics. Operate Filter integrity devices to confirm the integrity of filters pre and post use. Perform process operations, equipment and instrument monitoring and trending to enable proactive identification of issues to escalate and correct with applicable departments. Follow all related safety policies and procedures and Put safety first by playing an active role in identifying and correcting unsafe behaviors and conditions. | 3/15/2024 |
| 539 | Affinivax King of Prussia, PA Biopharm Manufacturing Associate II BS/BA degree OR an Associate’s degree from Montgomery county community college in Biotechnology or related technical field. Exp: 1+ years |
Posted Date: Mar 15 2024 Thank you for your interest in our Bio Pharm Manufacturing Associate II (Evergreen) position. Applicants for this role will not be receiving immediate feedback regarding their applications. If you are looking for an immediate opportunity, please take a look at the GSK careers page for opportunities that would align with your skill-set. I have included the link here for your convenience: Careers | GSK US . As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep. Will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. Will participate in safety and compliance initiatives, as well as investigations. Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance. | 3/15/2024 |
| 540 | Affinivax King of Prussia, PA Associate Manufacturing Specialist Bachelors of Science, or Bachelors of Arts. Exp: 1+ years |
The Associate Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. The associate manufacturing specialist, with support from team leads and supervisors, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role will support will follow the lifecycle of new products, more specifically: Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. | 3/15/2024 |
| 541 | Affinivax King of Prussia, PA Associate Microbiologist BS in science field. Exp: 1+ years |
GSK is currently looking for an Associate Microbiologist to join our team in Upper Merion, PA. In this role, the Microbiologist performs quality testing for In process and bulk biopharmaceutical ingredients, finished biopharmaceutical products. Reviews and revise SOP’s when needed. | 3/15/2024 |
| 542 | Affinivax King of Prussia, PA Manufacturing Specialist Bachelors of Science, or Bachelors of Arts. Exp: 1+ years |
The Associate Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. The associate manufacturing specialist, with support from team leads and supervisors, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role will support will follow the lifecycle of new products, more specifically: Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. | 3/15/2024 |
| 543 | Affinivax Hamilton, MT QC System Support Specialist Bachelor's Degree in a scientific discipline. Exp: 1+ years |
The QC Systems Support Specialist will manage non-testing laboratory support systems and processes for QC, including: Maintaining SAP Modules, Master Data/Monograph Creation, Compendial Review, Equipment Qualification/Lifecycle, and Method Validation/Transfer. Serve as a Lead Investigator for select QC Unplanned Events, as well as change coordinator for selected QC Change Controls. Author QC Technical Documents, such as validation and trend reports and provide data for annual PQR. Works collaboratively with global teams (ASAT) and the GSK network to maintain compliance and alignment, and to deliver both local and global projects as per established timelines. | 3/15/2024 |
| 544 | Carmot Therapeutics Berkeley, CA Research Associate I/Research Associate II, Pharmacology BSc, MSc in pharmacology, biology or related field. Exp: 1-5 years |
In this position, you will assist with the design and execution of in vivo pharmacology experiments in rodents. In particular, you will be utilizing mouse models of obesity and diabetes to support compound characterization and mechanism of action studies. These efforts will support lead discovery and translational biology for clinical compounds. The position may also involve in ex vivo and in vitro pharmacology experiments. The environment at Carmot is fast paced, requiring you to be excellent at multitasking and working within a team to achieve common goals. | 3/15/2024 |
| 545 | Cirtec Medical Sturtevant, WI Engineer I Manufacturing A bachelor’s degree in engineering. Exp: 0 years |
This position is primarily responsible for developing and implementing robust cost-effective manufacturing processes and methods in accordance with product specifications and Class III medical device quality standards. This position recommends and implements improvements to sustained production processes, methods and controls; as well as coordinates the launch of new products into pilot production. | 3/15/2024 |
| 546 | Integrity Bio/ LyoTip Albuquerque, NM Mechanical Engineer Bachelor's degree (B.S.) in Mechanical Engineering. Exp: Entry level |
The Engineering Department provides the capacity to manufacture pharmaceuticals in an efficient, timely, and safe manner, thereby contributing to the profitability of the business unit by maintaining or modifying production equipment and related systems. The Mechanical Equipment Engineer will work in supporting manufacturing operations both on the manufacturing floor and off, spending time within the manufacturing operations is required and will be a priority at times. | 3/15/2024 |
| 547 | Integrity Bio/ LyoTip Springfield, MO Process Engineer I or Process Engineer II The following required knowledge and proficiency skills are required for this position to be acquired through a minimum of a Chemical Engineering degr Exp: PE I: 0-3 years; PE II: 1-3 years. |
The primary purpose of the Process Engineer position is to design, implement and continuously improve chemical manufacturing processes using appropriate chemical engineering and scientific principles. Process design involves preparation of process flow diagrams, piping and instrument diagrams, mass and energy balances, equipment specifications, process safety information and operating procedures necessary to implement the process. Implementation involves development of construction task lists, participating in risk assessments, performing training, supporting start up and leading troubleshooting efforts. Continuous improvement includes identification of opportunities to improve quality, safety and economic performance of processes through proactive engineering evaluation as well as incident investigation and corrective/preventative action identification and implementation. Secondary purposes include configuration, modification and optimization of site control systems and to provide technical assistance to other site departments (QA, QC, Accounting, Maintenance, EH&S, etc.) in support of Curia's general business objectives and requirements. | 3/15/2024 |
| 548 | Integrity Bio/ LyoTip Albany, NY Research Scientist I; Analytical Development Bachelor’s or Master’s Degree in Chemistry or a related field. Chemical Hygiene training. Exp: 1+ years |
The Research Scientist I-Analytical Development is an integral part of the Curia team, contributing to our success by supporting the manufacturing department and external customers. The routine functions of the laboratory are testing of raw materials, in-process, end product, and stability samples. The principal responsibility of the Research Scientist I is the analysis by multiple procedures of compounds. The Research Scientist I is expected to demonstrate proficiency in both the theoretical and practical aspects of analytical chemistry. | 3/15/2024 |
| 549 | Integrity Bio/ LyoTip Albany, NY Research Scientist I; Analytical Development Bachelors or Masters Degree with major in Natural Science or Pharmacy or equivalent. Chemical Hygiene training. Exp: 1+ years |
The principal responsibility of the Research Scientist I is the analysis by multiple procedures of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist's performance rating will be based on productivity. | 3/15/2024 |
| 550 | Integrity Bio/ LyoTip Rensselaer, NY Production Technician in Rensselaer, NY - 12 Hour Nights Associates or Bachelor's degree. Exp: 1+ years |
The Production Technician is an integral part of the team, contributing to our success by weighing out chemicals and preparing various types of solutions for use in process. | 3/15/2024 |
| 551 | Integrity Bio/ LyoTip Burlington, MA Quality Assurance Specialist I, Sun-Wed 7a-5p Bachelor’s degree (or foreign equivalent) in Biology, microbiology, biotechnology or related life science field. Exp: 0-3 years’ |
The Quality Assurance Specialist I is responsible for maintaining Quality databases and providing on-the-floor QA presence and oversight to the manufacturing operation. The QA Specialist’s role will include identifying compliance risks in the operation prior to and during execution, avoiding deviation whenever possible as well as managing immediate corrective action such that a) adherence to cGMP’s and internal procedures/policies is maintained, b) appropriate immediate corrective action is implemented and effectively documented in order to provide traceability and substantiation of any claims to be made in the investigation. This position primarily works in the cGMP production areas to manage adherence to the quality system and to initiate and assist in the initiation and resolution of deviations. | 3/15/2024 |
| 552 | Integrity Bio/ LyoTip Albuquerque, NM Aseptic Core Monitor I BS, preferably in Microbiology or a related field. Exp: 1+ years |
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Aseptic Core Monitor (Albuquerque, NM) will oversee all activities in the aseptic environment to ensure continual compliance with cGMP and provide mentoring on aseptic techniques for all aseptic personnel. This position requires expertise in all aspects of aseptic manufacturing of the sterile product, the ability to work hands-on, strong leadership skills, and the ability to collaborate in a cross-functional environment. The individual will work closely with all departments in the manufacturing environment and reports metrics to site management regularly. Join our talented workforce, where a commitment to excellence and a customer-focused attitude is everything. We pursue excellence because our work has the power to improve patient’s lives with the pharmaceuticals we develop and manufacture. | 3/15/2024 |
| 553 | Roche Seattle, WA Research Associate Bachelor’s, Master’s or PhD degree in Biological/Life Sciences, Chemistry, Organic Chemistry, Chemical Engineering, Biochemistry or related field. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its unique chemistry that advances DNA sequencing by nanopore, Sequencing by eXpansion (SBX™). You will develop, process and purify the molecular building blocks for our novel technology. These building blocks translate DNA sequences into a simple to measure surrogate, the Xpandomer, which significantly improves the accuracy and throughput of nanopore sequencing. The Molecular Engineering group is passionate about the novel molecules they have developed and the impact SBX technology can have on advancing sequencing and patient outcomes. We are looking for people who are excited to collaborate with us to make SBX successful. Please include a cover letter outlining why you want to work with us, your specific interest in our technology and how you would contribute. | 3/5/2024 |
| 554 | Roche Branchburg, NJ Senior Lab Technician Associates degree required; Bachelor's Degree preferred. Exp: < 1 year |
Branchburg is the molecular diagnostics manufacturing engine within Global Operations and a Polymerase Chain Reaction (PCR) center of excellence. As the largest DIA manufacturing site in North America, our teams deliver a broad portfolio of PCR-based in-vitro diagnostic tests. Our operations include reagent and active diagnostic ingredient (ADI) production, filling and packaging. Our 63-acre site with ~1400 people is currently under expansion, fueled by our culture of agility, innovation and transformation. Each day we focus on delivering the value of Roche Diagnostics to patients around the world. | 3/5/2024 |
| 555 | Roche Carlsbad, CA Mechanical Engineer I BS degree. Exp: 0-2 years |
We are looking for a highly motivated and team-oriented individual who is passionate about technology and product development for IVD assays. As a Mechanical Engineer I, you will work under supervision from senior contributors for concept-to-market and sustaining engineering efforts of IVD instrumentation. Apply hands-on involvement in on-market support for existing and new products, troubleshooting and root cause analysis, creation and maintenance of input and output specifications, concept and feasibility activities, prototyping, testing, and transfer to manufacturing. | 3/5/2024 |
| 556 | Roche Santa Clara, CA Product Engineer B.S. in Biology, Chemistry, Biochemistry, Molecular Biology, Mechanical Engineering or a related field. Exp: 1-3 years |
As a Product Engineer at Roche Sequencing Solutions, you will be instrumental in the development of the consumable prototype manufacturing process. In this dynamic role, you will lead the charge in innovation, contributing to the advancement of highly automated DNA sequencing pipelines and diagnostic applications. Your expertise will play a critical role in shaping the future landscape of genetic diagnostics. Roche is seeking a motivated and collaborative individual with strong analytical skills to join our team. As a Product Engineer, you will drive the development of high-quality devices, serving as a key player in the development and technology transfer of our prototype manufacturing process. This position entails close collaboration with internal and external hardware and software developers within the RSS team, as well as active engagement with the CD development team. | 3/5/2024 |
| 557 | Roche Carlsbad, CA Process Engineer I - Night Shift Bachelor’s degree in Engineering or a related technical discipline. Exp: 1+ years |
The work schedule for this position is a night shift from Sunday through Friday from 10 PM to 6:30 AM. As a Process Engineer you are responsible for driving stable, reliable production processes. You are instrumental in troubleshooting, testing , and supporting for existing products and new product lines. Under minimal supervision, you will apply engineering principles to resolve complex manufacturing equipment issues that arise and implement initiatives to reduce equipment downtime and improve throughput yields. | 3/5/2024 |
| 558 | Roche Carlsbad, CA Quality Control Specialist I - Mon-Fri 4:30 PM to 1 AM B.S. degree required, in basic sciences, life sciences, or engineering. Exp: 1 - 3 years |
This position conducts incoming, in-process and final release QC testing in a controlled manufacturing environment. This position may also execute validation studies, execute test protocols, analyze data, generate analytical reports, investigate Non-Conformances, evaluate processes & procedures, utilize statistical techniques, review specifications, and inspect & test equipment. May conduct training on quality related tools, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 3/5/2024 |
| 559 | Roche Tucson, AZ IQC Technician II Bachelor's Degree preferred. Exp: < 1 year |
The Incoming Quality Control (IQC) Technician – Instruments Manufacturing, will be an integral part of a team that performs inspection of raw materials, components and sub-assemblies using established operation procedures, work instructions, engineering parts drawings. The individual will be responsible for the review, generation and sign-off of inspection reports and related quality documentation. The individual will be responsible for interfacing with highly complex systems and controls in an ISO 13485 and GMP manufacturing environment. The individual will maintain areas in high state of inspection preparedness by maintaining equipment, records and IQC environment in order to comply with regulatory requirements utilizing current regulations and Operating Procedures (OP). Additionally, maintains incoming inspection documents, assists in the investigation of incoming parts and instruments manufacturing non-conforming parts, manufacturing exception events and works independently with general guidance from senior team members. | 3/5/2024 |
| 560 | RPRD Diagnostics Wauwatosa, WI Clinical Lab Technician I Bachelor's degree in genetics, biology, molecular biology, chemistry, biochemistry or related discipline. Exp: 1 year |
RPRD Diagnostics, LLC is seeking a Clinical Lab Technician I to join our team. At RPRD, we believe that comprehensive genetic testing offers an unprecedented opportunity to improve the outcomes for millions of patients who are prescribed drugs, so we are developing next-generation pharmacogenetics testing services to improve clinical decision making. We aim to enable hospitals, clinicians, and their patients to better understand and manage their treatment choices on the basis of each individual's unique genetic profile. Additionally, our team is committed to continuous innovation in order to advance knowledge and deliver cutting edge services and care to our clients and their patients. The Clinical Lab Technician I performs high complexity molecular techniques such as genotyping, next generation sequencing, data analysis and interpretation. They are further responsible for recognizing the clinical significance of each test performed, maintaining the confidential and sensitive nature of patient information and results, and reporting results within established time frames. This position also assists with the validation of new applications in the clinical laboratory and works collaboratively as part of a team to help ensure the smooth operation of the lab. | 3/5/2024 |
| 561 | SAMDI Tech Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Sunday through Thursday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 3/5/2024 |
| 562 | SAMDI Tech Worcester, MA Research Technician I - 2nd Shift Hours Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Monday through Friday 2nd shift hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 3/5/2024 |
| 563 | SAMDI Tech Mattawan, MI Technician 1 - Histology, 2nd Shift Bachelor’s degree (BA/BS) or equivalent in a biological science, preferred. Exp: 0+ months |
We are seeking an experienced Technician 1 - Histology for our 2nd Shift Pathology Services Team in Mattawan MI. A Technician 1 – Histology is in training to perform and become proficient in on-boarding skills, procedures, and cooperating in a team environment. The technician is learning basic skills required to conduct a study, which may include handling tissues and organs, trimming tissues, embedding, measuring organ weights; microtomy, slide preparation, staining; inventory and quality control, and shipping of tissues. The technician is working under close supervision to gain proficiency. | 3/5/2024 |
| 564 | SAMDI Tech Cambridge, MA Research Associate /Imaging Bachelor’s degree (B.A./B.S.) or equivalent in Animal Science or related field. Exp: One to two years |
We are seeking an Research Associate/ Imaging for our Insourcing Solutions Department based in Cambridge, MA. As the Research Associate/Imaging, you will perform multi-modality imaging studies, preclinical imaging data acquisition, image data processing and analysis, may also work with other scientists for in vivo and ex vivo imaging experiments. | 3/5/2024 |
| 565 | SAMDI Tech Horsham, PA Formulations Technician I Bachelor’ degree (B.S.) preferred. Exp: 0 to 1 years |
Full Time – 40 Hours/Week $1000 SIGN ON BONUS (external applicants eligible only) Perform routine preparation of vehicles and test article dosage solutions for use in toxicology studies with close supervision. | 3/5/2024 |
| 566 | SAMDI Tech Wayne, PA Technician I Molecular Biology Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 0-1 years |
Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services. | 3/5/2024 |
| 567 | SAMDI Tech Malvern, PA Technician I Microbiology Bachelor's degree (B.A./B.S.) or equivalent in Biology or related discipline. Exp: 0-1 years |
Under direct supervision, responsible for performing daily laboratory tasks as they relate to Molecular Biology Testing Services. | 3/5/2024 |
| 568 | Sanofi Pasteur Framingham, MA Purification Development Research Associate Bachelor's degree in Chemical Engineering, Biochemical Engineering, Biochemistry or related discipline Exp: 1+ years |
We are looking for candidates for the position of Research Associate. This individual will join a dynamic and motivated team to develop downstream purification processes in support of early and late stage drug development programs. In addition, the Research Associate will support the tech transfer of the developed process into the clinical manufacturing team or Industrial Affairs organization, while ensuring the highest standards of safety, environmental, and regulatory compliance are maintained in the workplace. | 3/5/2024 |
| 569 | Sanofi Pasteur Swiftwater, PA Production Technician - Vaccine Associates or Bachelor’s Exp: AS: 1 + yrs; BS: 0 + yrs |
This is a third shift position. Must be able to work weekends and holidays as needed. Flexibility for changing schedule required. | 3/5/2024 |
| 570 | ScienCell Research Laboratories Carlsbad, CA Associate Molecular Biologist Bachelor’s or Master’s degree in life science. Exp: one-year |
We are searching for an energetic and self-motivated candidate with a positive attitude and strong work ethic to fill our associate molecular biologist position in our R&D department. Responsibilities include, but are not limited to, working on cell-derived DNA, RNA, and proteins purification, gene expression analysis, performing PCR/RT-PCT/qPCR, SDS PAGE and UV spectrum for quantitation. Candidates should be familiar with electrophoresis, spectrophotometer, centrifugation and other basic laboratory techniques. General lab logistical skills such as record keeping, ordering supplies and ensuring general laboratory safety and cleanliness are also required. | 3/5/2024 |
| 571 | SeaGen Groton, CT Associate Scientist, Sustainable Chemistry Data Bachelor’s Degree in Chemistry, Environmental Science or related field. Exp: 0 to 2 years |
As an Associate Scientist, you will be at the center of our operations and you’ll find that everything we do, every day, is in line with an unwavering commitment to quality. You will become a member of Pfizer Chemical Research and Development (CRD) Sustainability Team, and will work under the guidance of the Sustainable Chemistry Lead. Your work alongside the entire department will help implement an overall strategy for the collection, analysis, management, and communication of sustainability related data and metrics. You will help execute the CRD Vision by measuring key sustainable metrics evolution over time as we commit to the development of greener processes to manufacture Pfizer APIs from clinical to commercial. Your role will support the company towards its goal of becoming Net Zero by 2040. You are able to work independently or within a small team under guidance from strategy leaders.Essential skills include excellent oral and written communication, proficient office computer software knowledge including data management (Microsoft Office, Spotfire) and teamwork-oriented mindset. Ideally, you have a solid knowledge of organic chemistry and you are passionate about data collection as well as sustainability. | 3/5/2024 |
| 572 | SeaGen Bothell, WA Manufacturing QA Associate III Bachelors Degree Exp: 0+years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. It is your hard work and commitment that will make Pfizer ready to achieve new milestones and help patients across the globe. | 3/5/2024 |
| 573 | SeaGen Rocky Mount, NC Associate Validation Engineer Bachelors degree Exp: 0+years |
You will be a member of Pfizer’s dedicated and highly effective Validation team. You will be responsible for the creation, review and approval of validation master plan, SOPs, protocols and reports. Your methodological approach will help us ensure compliance of our quality systems with company standards and government regulatory requirements. Your problem-solving ability will help us troubleshoot validation problems for equipment and performance processes and conduct statistical analysis of testing results and process anomalies. Your documentation skills will guide the writing, review and approval of validation process documents and technical reports related to equipment, facilities, utilities, computer systems, products and processes. As an Associate Validation Engineer you will be responsible for validating/qualifying the systems, equipment, utilities used to manufacture and/or clean drug products within a large manufacturing facility located in North Carolina, USA. You will help to demonstrate systems are running according to necessary specifications and operate within regulations to ensure data integrity and the production of quality products. | 3/5/2024 |
| 574 | SeaGen Kalamazoo, MI QC Laboratory Analyst II Bachelor’s degree in Chemistry, Biochemistry or related science. Exp: 0-1 years |
This position is for a testing analyst in the Kalamazoo QO API Non-LC Laboratory working on first shift. Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the API NonLC Laboratory include GC, Particle Size, X-Ray Crystallography, Karl Fisher, UV, and general analytical procedures. | 3/5/2024 |
| 575 | Seracare Life Sciences Cumberland Foreside, ME Quality Control Technologist I Associates in Medical Laboratory Science or a Bachelor’s degree in Medical Technology (preferred) or related science degree (i.e. biology, chemistry, Exp: 1-3 years |
Follows standardized procedures and prepares samples for testing. Analyzes test results for accuracy, acceptability, and critical limits. Relies on limited independent judgment to plan and accomplish goals. Performs a variety of tasks. A limited degree of creativity and latitude is required. | 3/5/2024 |
| 576 | Shionogi San Diego, CA Laboratory Assistant, Qpex BioPharma, wholly-owned subsidiary of Shionogi Inc. in San Diego, CA. Associates degree or a relevant certificate in a laboratory science field. Exp: 1+ years |
As a Lab Assistant you will play a vital role in supporting scientific and research activities within Qpex’s research laboratory. | 3/6/2024 |
| 577 | Sigmapharm Laboratories Bensalem, PA Quality Assurance Associate At minimum, an associate’s degree in any life science. Exp: 1 to 3 years |
· Responsible for assisting the Head of Quality Assurance (QA) to ensure all pharmaceutical processes and documentation that may impact the safety, identity, strength, quality and purity of any drug product or drug substance manufactured at Sigmapharm Laboratories, LLC (Sigmapharm) complies with all applicable Standard Operating Procedures (SOPs) and regulatory requirements and is prepared or performed in a way that maintains quality and reduces potential risks. · Responsible for the review and approval of all product and process-related Official Documents. · Responsible for the review and approval of qualification related Documents such as protocols and reports. · Responsible for aiding in the control and organization of CGMP documentation, recorded information or data generated and maintained in document control. · Responsible for auditing batch records and overall operational procedures. | 3/6/2024 |
| 578 | Smithers West Trenton, NJ Scientist (PCR and Molecular Biology) MS in Biological or Physical Sciences. Exp: 1-2 years |
Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance. PDS works with customers to develop new methods, validate existing methods, and perform the assays necessary to analyze samples from patients on more than 100 clinical trials. PDS is seeking a Scientist with experience in Molecular Biology to join our team. The successful candidate is able to apply prior experience and knowledge to successfully perform in a laboratory environment under regulated conditions. | 3/6/2024 |
| 579 | Smithers Darien, IL Associate Chemist I - Smithers Cannabis Testing Services, Darien, IL BS degree in Chemistry or related field. Exp: 6 months |
Smithers Cannabis Testing Services is seeking an Associate Chemist I at our Darien, IL location. Job Summary The Associate Chemist I performs critical sample processing and extraction duties to prepare cannabis samples for analysis and enters sample information in the laboratory information management system (LIMS) to facilitate subsequent analysis. The position is responsible for maintenance of laboratory stock reagents. Operates and may maintain, under supervision, test equipment and apparatus. | 3/6/2024 |
| 580 | Smithers Wareham, MA Assistant Biologist - Ecotoxicology - Smithers Wareham, MA Bachelors or better in Biology or related field. Exp: 0+ years |
Smithers Environmental Risk Sciences division is seeking an Assistant Biologist in the Ecotoxicology Department at our Wareham, MA location. Often, duties include recording instrument and apparatus readings, making observations of various biological effects in exposures and compiling study data books. Incumbent will be introduced to mathematical and statistical procedures used to reduce and analyze study data. Responsible for maintaining cleanliness of the labs, storage and culture areas including maintenance and calibration of equipment used in any of these settings. May require routine involvement in seawater and/or sediment collection. Assignments are completed with minimal supervision. Assists with organization, direction and training of technicians. Assists in coordinating internal requirements for testing (i.e. chemistry support, Quality Assurance, reporting). Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations and company policies. | 3/6/2024 |
| 581 | Smithers Wareham, MA Associate Chemist I - Environmental Fate and Metabolism B.S. degree in chemistry or related field. Exp: 6 months |
Position is expected to perform a variety of routine tasks and often complex and difficult procedures independently and under supervision, in support of the conduct of normal laboratory operations. Individual is expected to detect and report problems in standardized procedures due to instrumental, sample, or test system failures. Performs a variety of routine, laboratory-based procedures. Responsible for understanding and routinely performing applicable Standard Operating Procedures, study specific protocol procedures and other laboratory assignments. This often includes recording instrument and apparatus readings on standard forms, preparation of test systems and recording and compiling laboratory data in real time in a complete and thorough manner for individual assignments. Responsible for maintaining cleanliness of the labs, storage and chamber areas as well as executing regular maintenance/calibration of equipment used on a regular basis. Employee is responsible for understanding and adhering to all safety and Good Laboratory Practice regulations as well as company policies. Duties are performed with minimal supervision. | 3/6/2024 |
| 582 | Smith and Nephew Pittsburgh or Andover, PA Software Engineer (Pittsburgh, PA or Andover, MA) Bachelor’s degree required (Software Engineering or Computer Science preferred). Exp: 0 - 2 years |
Software Engineer (Pittsburgh, PA or Andover, MA) Life Unlimited. At Smith+Nephew, we design and manufacture technology that takes the limits off living. The Software Engineer will be involved in research/design/testing of medical devices | 3/6/2024 |
| 583 | Spherotech Lake Forest, IL Manufacturing Associate Bachelor's degree in Chemistry or related field. Exp: 0+ years |
Spherotech, Inc. seeks a college graduate for a Manufacturing Associate opening. Duties include polymer synthesis, bottling, packaging, documentation, etc. | 3/6/2024 |
| 584 | Spherotech Lake Forest, IL Quality Control Associate Bachelor's degree in Chemistry or related field. Exp: 1 year |
Spherotech, Inc. seeks a college graduate for a Quality Control Associate opening. Duties include final product inspection, documentation, Quality Control testing etc. | 3/6/2024 |
| 585 | Stability Biologics San Antonio, TX QA Specialist - San Antonio, TX BS degree in a scientific discipline (Chemistry, Biology, Physics, Bio-Medical Engineering/Chemical Engineering, etc.). Exp: 1 year |
The Quality Assurance Specialist (QAS) will be a member of the Stability Biologics Quality Dept. to perform quality record reviews, batch release, record retention, data entry, auditing, investigations and document control activities. The QAS will be responsible for quality assurance metrics, CAPA/NCMR and maintaining all quality records/batch records in a secure and controlled manner. The QA Specialist will also be responsible for ensuring all policies and procedures are in compliance with appropriate FDA, AATB, states, and Stability Biologics standard operating procedure. | 3/7/2024 |
| 586 | StageBio Frederick, MD Laboratory Technician I/II/III · College degree preferred. Exp: 0+ years |
StageBio is seeking a full-time Laboratory Technician II to join our Frederick, Maryland facility. Primary Responsibilities Include: Individuals will be trained to perform tissue grossing, processing, embedding, microtomy, staining (H&E & special staining), quality control and general histology duties Maintain a safe working environment by following all safety and chemical regulations as outlined in StageBio’s SOPs Prompt and accurate recording of data Daily cleaning of work area and equipment Other duties assigned by management | 3/7/2024 |
| 587 | Stellartech Research Milpitas, CA Quality Engineer II Typically requires a BS degree or equivalent. Exp: 1-3 years |
Stellartech is looking for a Quality Engineer to join our Team. | 3/7/2024 |
| 588 | Tempus Durham, NC Molecular Technologist - Lead Trainer (Monday-Friday, 2:30pm-11:00pm) MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of said data. Here at Tempus, we believe the greatest promise for the detection and treatment of cancer lies in the deep understanding of molecular activity for disease initiation, progression, and efficacious treatment based on the discovery of unique biomarkers. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We're looking to build a laboratory team who are passionate and focused on developing state of the art techniques to processing and creating and interpreting vast amounts of genomic and molecular data. | 3/8/2024 |
| 589 | Tempus Durham, NC Molecular Technologist - Lead Trainer (Monday-Friday, 8:00am-4:30pm) MS in medical technology, clinical laboratory science, chemical, physical or biological science. Exp: 1 year |
Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time. With the advent of genomic sequencing, we can finally decode and process our genetic makeup. We now have more data than ever before but providers don't have the infrastructure or expertise to make sense of said data. Here at Tempus, we believe the greatest promise for the detection and treatment of cancer lies in the deep understanding of molecular activity for disease initiation, progression, and efficacious treatment based on the discovery of unique biomarkers. We're on a mission to connect an entire ecosystem to redefine how genomic data is used in clinical settings. We're looking to build a laboratory team who are passionate and focused on developing state of the art techniques to processing and creating and interpreting vast amounts of genomic and molecular data. | 3/8/2024 |
| 590 | NeoLight Scottsdale, AZ Biomedical Engineer Bachelor's Degree in Electrical Engineering (Required) from an accredited university or college. A Master's degree is preferred. Exp: entry-level or 1-2 years |
We seek a full-time entry-level Biomedical Engineer focusing on Electrical Engineering. In this role, you will provide strong, independent technical support to teams that contribute to resolving significant electrical and embedded system issues for the next generation and on-market products. A successful candidate will be a productive individual contributor who works independently with general supervision on larger, moderately complex projects/assignments. In addition, the candidate sets objectives for their job area to meet the objectives of projects and assignments. | 3/8/2024 |
| 591 | TransMedics Andover, MA Mechanical Engineer I - Product Development BS in Mechanical Engineering, Plastics Engineering, Biomedical Engineering, or equivalent is required. Exp: 0-2 years |
Reporting to the Director of Mechanical Engineering, the Mechanical Engineer 1 will work with the cross- functional Product Development team to develop new products. The ideal candidate should be self- motivated and have a strong desire to learn and take on new responsibilities. The candidate will support larger programs under the mentorship of Sr. Staff and lead smaller projects with guidanace. The candidate will contribute to the full design process from concept to production. This position will have several opportunities to develop engineering skills including: CAD, technical analysis, technical writing, problem solving, engineering best practicices, and hand-on use of lab and machine shop equipment. | 3/8/2024 |
| 592 | TransMedics Andover, MA Cardiothoracic Research Specialist Bachelor's degree in Biology, Biochemistry, Biomedical Sciences or related field. Exp: 1–2-year |
If you’re looking for a career with a company where you can make a difference, earn a competitive salary, and have ample professional growth opportunities, this is it. TransMedics is a publicly traded, medical technology company revolutionizing what’s possible in organ transplant through innovation, collaboration, and commitment. We’re growing and transforming the transplantation industry through our Organ Care System (OCS™) technology platform & National OCS Program, preserving organs used in heart, lung, and liver patienttransplants for safe transport nationwide. We are seeking a highly motivated and detail-oriented Cardiothoracic Research Specialist to joinour Cardiothoracic Research team. This position offers an excellent opportunity for an early career researcher to gain hands-on experience in cardiothoracic research while contributing tomeaningful projects within our dynamic research and lab environment. | 3/8/2024 |
| 593 | Pharmaron San Diego, CA In Vivo Research Associate I, Ophthalmology Associates degree (preferred) in veterinary technology or BS. Exp: AS: 1-2 years; BS: 1 year |
Pharmaron (San Diego) is seeking to hire an outstanding candidate to join our Ocular department at the Research Associate I level. The Research Associate will play an important role by supporting in vivo studies to test devices being developed for various ocular disorders. | 2/27/2024 |
| 594 | Pharmaceutics International Hunt Valley, MD Microbiologist (EM) B.S / M.S. in a life sciences discipline. Exp: 0-2 years |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensuring their delivery in an accurate and timely manner following proper safety precautions. | 2/27/2024 |
| 595 | Phitonex Fremont, CA Scientist I, Formulations BS/BA in scientific field in Chemistry, Biochemistry, ore related technical discipline. Exp: 1+ years |
You will be responsible for manufacturing products for the Bulk Formulations Toxicology team and complete associated cGMP documentation. You will work with chemicals and biologicals to manufacture reagents, calibrators, and controls for IVD immunoassay use and participate in process improvements projects. | 2/27/2024 |
| 596 | Phitonex Florence, SC Scientist I - Process R&D BS/BA degree in chemistry or life science. Exp: 0-3 years |
You will join a team of synthetic organic chemists in the manufacturing of pharmaceutical ingredients at the Florence, SC site. Many of our products are already in the market serving patients and we work on a variety of projects for existing and new clients. In this position, you will perform hands-on experimentation and learn knowledge and skills for the process development of pharmaceutical products. We have a fast-paced working environment while keeping a good work-and-life balance. | 2/27/2024 |
| 597 | Phitonex Cincinnati, OH R&D/Mfg Scientist I (onsite) Associates or Bachelor’s Degree in physical science; Chemistry or Biology preferred. Exp: 1-2 years |
As a Quality Laboratory Team Member, you will coordinate with your supervisor and collaborate with colleagues in diverse groups to assure that critical timelines are met. You will have the opportunity to collaborate with your peers within the laboratory and those in other departments such as formulations, operations, project management and quality assurance on a regular basis. You will perform analytical methods for elaborate testing for validated and experimental methods and other tests as needed to support lab operations. You will participate in the validation of analytical test methods when additional resources are required. | 2/27/2024 |
| 598 | Phitonex Middletown, VA Formulation Scientist I B.S. in Science or Medical Technology is preferred. Exp: 0+ years |
Work in a Value Stream environment and organize, carry out, monitor, multi-stage production processes to prepare and formulate serum, clinical diagnostic assays and reagents for use in research and commercial scientific products for the IVD industry with compliance to specifications and GMP/FDA requirements. The formulations range in scale from 1 mL to 50,000 L and are manufactured using protocols/batch records in an environmentally monitored lab space. Data is recorded in batch records following good documentation practices as required for regulated industries. | 2/27/2024 |
| 599 | Plex Pharma San Diego, CA Research Associate, Biology & Protein Chemistry BS or MS in molecular and biology, protein chemistry or related field. Exp: 1-3 years |
Plex Pharmaceuticals (www.plexpharma.com), a biotechnology company with a focus on developing novel drugs targeting misfolded and aggregated proteins, has an immediate opening for a Research Associate. The successful candidate will contribute to drug discovery efforts by performing cloning, expression and purification of protein drug targets, as well as assisting in assay development and characterization of compounds. | 2/27/2024 |
| 600 | Poochon Proteomics Solutions Frederick, MD Lab Assistant Associate degree or above in medical technology, or related life science is preferred. Exp: 1+ year |
We are seeking a Lab Technician to join our DNA Sequencing and Mass Spectrometry team. | 3/1/2024 |
| 601 | PPD Middleton, WI Entry Level Biochemist Bachelor's degree or equivalent. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 602 | PPD Highland Heights, KY Assistant Scientist - 2nd Shift Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 603 | PPD Highland Heights, KY Assistant Scientist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 3/1/2024 |
| 604 | Prevail Therapeutics Boston, MA Associate Scientist, Early Preclinical Development - Inner Ear Biology Bachelor's Degree. Exp: 0+ years |
The Early Preclinical Development (EPD) Team is seeking an Associate Scientist with experience in inner ear histology to support discovery and IND-enabling animal studies. The ideal candidate will have experience in histologic techniques specific to the inner ear, such as microdissection of the mouse and non-human primate (NHP) inner ear tissues into discrete anatomical regions, and further processing of these tissues using various histologic techniques, in addition to imaging, analysis, and preparation of data for presentation. Cross-functional work may be required to advance Company goals. The successful candidate will be self-motivated and creative, with a desire to succeed at the highest level in a highly collaborative and fast-paced environment. | 3/1/2024 |
| 605 | Prevail Therapeutics San Francisco, CA Research Associate - DMPK DICE BS or MS in chemistry. Exp: 0-6 years |
We seek an exceptional full-time lab-based Research Associate to join our Drug Metabolism and Pharmacokinetics (DMPK) team. This individual will be a key contributor to performing standard ADME/DMPK assays, such as microsomal stability, plasma protein binding, and metabolite identification. The individual will also be responsible for operating LC-MS instruments (QQQ and HRMS) with minimal direction. Do you have experience in mass spectrometry while doing enzyme related work? This role may be perfect for you! | 3/1/2024 |
| 606 | Preventice Solutions Arden Hills, MN Quality Engineer I - Electrical Bachelor's degree or higher in Electrical Engineering. Exp: Entry-Level |
The Electrophysiology (EP) Design Quality Assurance team is looking for an engineer to evaluate manufacturing and design changes. EP has a broad portfolio of capital equipment used in the field to support ablation and diagnostic procedures. The EP Design Quality assurance team is growing, and the timely evaluation of design changes is key to maintaining a robust EP Capital Equipment portfolio to reduce potential safety and quality issues. This role provides visibility across the Research and Design organization. The selected candidate will collaborate with Manufacturing, Product Complaints, Regulatory, and Field Servicing engineering. This is a significant role for an entry-level engineer with opportunities to grow into Computer Programming, Cybersecurity, Risk, or Electrical Design. The selected candidate will be mentored by a Senior Electrical Engineer. | 3/1/2024 |
| 607 | Preventice Solutions Maple Grove, MN Quality Engineer I University degree or the equivalent combination of education and experience required. Exp: 0-2 years |
Develops, establishes and maintains quality engineering methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Serves as a Quality representative to improve awareness, visibility, communication on quality initiatives to support departmental, functional, site, divisional and corporate quality goals and priorities. Provides focused quality engineering support within new product development, operational, or system/services support. | 3/1/2024 |
| 608 | Procept BioRobotics San Jose, CA Electrical Engineer Bachelor's degree (B.S.) in Electrical Engineering or equivalent. Advanced degrees are a plus. Exp: 1-5 years |
The Electrical Engineer works within the Electrical Engineering group within the R&D Capital Equipment department. The position will be responsible for supporting electrical systems for PROCEPT’s electro-mechanical products, including electronics feasibility, requirements definition, design, design verification, test system development, manufacturing procedure development, and production transfer activities at various stages of the product development cycle. Development will be conducted in accordance with PROCEPT’s quality system. | 3/1/2024 |
| 609 | ProteinSimple Minneapolis, MN Advanced Research Associate MS degree in the biological sciences. Exp: 0-2 years |
As an Advanced Research Associate you will work in the Immunocytochemistry Department on the validation of antibodies for immunocytochemistry applications. You will be knowledgeable of animal anatomy and histology and familiar with histological examination of tissues, frozen and paraffin-embedded tissue sections, immunohistochemistry protocols, microscopy systems; collect digital images, digital image post-processing and enter data into a database. | 3/1/2024 |
| 610 | ProteinSimple Newark, CA Senior Research Associate, PAS MS in molecular biology, biochemistry, cell biology or related field. Exp: 0-2 years |
The Senior Research Associate (SRA) will serve as a key member of the ACD Professional Assay Services (PAS) department, performing RNAscope assay services for industrial, pharmaceutical, and academic sponsors to detect RNA targets of interest. An additional critical work component will be the application of immunohistochemistry (IHC) to look for specific protein targets. The position will have an opportunity to work closely with scientists and investigators from a broad customer base. It is expected that the Sr. Research Associate will independently collect and interpret data based on project expectations, which has implications for many downstream applications, such as biomarker validation and cell and gene therapy. The SRA will also be expected to independently utilize available resources for any required troubleshooting and communicate clearly with sponsors through both electronic mail and teleconference channels. The SRA must also coordinate with internal research and development (R&D) team to learn new techniques quickly and be able to adapt to shifting priorities in a fast- paced and growing start-up environment. | 3/1/2024 |
| 611 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/1/2024 |
| 612 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of methylcellulose, methylcellulose-containing media, and stem cell and gene therapy (SCGT) media. Perform QC testing and analysis of some methylcellulose-containing media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Perform additional duties as assigned. Skills used include cell culture, high attention to detail, strong communication and organizational skills. | 3/1/2024 |
| 613 | ProteinSimple Minneapolis, MN Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Are you passionate about science, an adaptable self-starter with an insatiable curiosity and have a drive to innovate and further develop your skills with a multitude of analytical tools to study and characterize biomolecules? As a Research Associate in the Analytical Services team, you will be responsible for performing routine Quality Control (QC) testing, and participating in troubleshooting efforts for released products and new products that are still in development through the application of biophysical analysis of proteins and antibodies focusing on our capillary electrophoresis systems, but may also include chromatography, immunoassays, light scattering and other analytical tools, with the aid of fully defined SOPs. You will also actively take part in group projects, participate in process improvement efforts to improve lab protocols with the goal of facilitating innovation, efficiency and productivity, and perform additional duties as assigned. | 3/1/2024 |
| 614 | ProteinSimple Minneapolis, MN Quality Assurance Specialist B.S degree in Biology related disciplines. Exp: 0 to 5 years |
The responsibilities of this position are to engage and support various improvement projects for Document Control (Label design and document writing, routing, approval etc) and Quality Assurance activities, including but not limited to Supplier Management, Non-Conformance, CAPA and Change Management etc. | 3/1/2024 |
| 615 | ProteinSimple Minneapolis, MN Quality Technician, Hematology QC Lab MLT/MLS degree, bachelor’s degree in biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 3/1/2024 |
| 616 | QPS Newark, DE Associate Scientist II - Bioanalytical Dept Bachelor’s degree. Exp: 1-2 years |
As an Associate Scientist II in our Bioanalytical department, you will be a fully supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. | 3/1/2024 |
| 617 | QPS Newark, DE Associate Scientist I - TLM Bachelor’s Degree Biology, Molecular Biology, Biochemistry, Immunology, Pharmacology, Medical Technology, or a related field. Exp: 0+ years |
Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies Assist supervisor in performing analysis of drug or other targets in complex biologic matrices Set-up, use and maintain complex instrumentation Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Perform routine mathematical & chemical calculations | 3/1/2024 |
| 618 | Quanterix Billerica, MA Manufacturing Associate I BS in Chemistry, Biology or related Life Sciences. Exp: 0+ years |
We are looking for an experienced and highly motivated Manufacturing Associate I located in Billerica, MA to join our Planar Manufacturing team. individual will work with a team of individuals to prepare solutions, conjugate beads, reconstitute antigens and perform filling activities to support a diverse assay menu. Hours for this position are 8am-4:30pm. | 3/1/2024 |
| 619 | Quidel Rochester, NY Scientist I, Quality Labs BS degree in scientific or related field. Exp: 0 to 2 years |
As we continue to grow as QuidelOrtho, we are seeking a Scientist I in the Reference Laboratory. The Scientist I assures the Calibration Traceability by executing complex analytical testing of patient samples and other fluids to support the release process, stability testing, accuracy testing, and new method development. This testing uses a variety of instrumentation including, but not limited to, pH meter, manual spectrophotometers, Olympus AU400, Beckman AU480, flame photometers, atomic absorption, RIA, and HPLC. The Scientist I will maintain instrumentation, calibrates, runs quality control and analyzes requested samples. Position requires summary reports, analysis of technical data, evaluation of quality control, and instrument troubleshooting. Completion of Non-Conformance Records and/or Quality Investigations in a timely manner is required for this position. Work is scheduled, supervised, and follows established methods and procedures. Business decisions and product accuracy is dependent upon the technical ability of this individual and reproducibility of the analytical methods. This position is located on-site in Rochester, New York. | 3/1/2024 |
| 620 | Quidel Rochester, NY Quality Analyst I (Fluid Release / Microbiology) Bachelor’s degree in Microbiology, Biology, Medical Technology, Biochemistry. Exp: 1+ years |
As we continue to grow, we are seeking Quality Analyst I to execute complex analytical testing of VITROS Calibrators, Control and other product fluids to support the formulation, release process, stability testing and accuracy of the VITROS products. This testing uses a variety of instrumentation including, but not limited to, VITROS 5,1 Chemistry System, pH meter, Chloride meter, conductivity meter and manual spectrophotometers. Will maintain VITROS instrumentation, calibrates, run quality control and analyze requested samples. In addition to support as a floater the Microbiology Laboratory testing. Works under the guidance of senior laboratory staff and management to resolve routine to complex analytical quality issues, assist in laboratory investigations and assures the product performance meets specification and claims. This position is located in Rochester, NY. | 3/1/2024 |
| 621 | Quidel Athens, OH QC Technician II Bachelor’s degree in Chemistry, Biology, Life Science or similar discipline. Exp: 1-3 years |
The Quality Control Technician II is primarily responsible for performing Quality Control testing products at various stages of Production, as well as occasional basic technical tasks such as document control, maintenance of work areas and may perform inventory control. The QC Technician II will be expected to maintain proficiency in all areas such that re-assignment will be seamless when there are changes to workload and/or company focus. This role is located in Athens, Ohio. | 3/1/2024 |
| 622 | Reckitt Benckiser Pharmaceutical Montvale, NJ R&D Microbiology Lab Scientist/Assistant, Equity, Claims, Compliance Bachelors Degree in a Biological Science (with microbiology focus preferred). Exp: 6 months to 2 years. |
• Conduct disinfection and sanitization efficacy tests (e.g. AOAC, ASTM, CEN,) to evaluate the antimicrobial efficacy of experimental formulations, finished products and ingredients. • Conduct required stability tests (preservative challenge tests, microbial limits) for personal care product development and launch support. • Help create new microbiological methods to foster a pipeline of innovative claims. • Manage multiple projects and provide microbiological support within the required project timelines (including testing and reporting of results) to various project teams. • Act as a subject matter expert in Microbiology. • Work with external partners in a professional and productive manner. • Perform appropriate laboratory practices and procedures, and consistently maintain laboratory records and notebooks in compliance with Good Laboratory Practice standards. • Review/author existing laboratory Standard Operating Procedures and apply them to lab and testing responsibilities. • A solid understanding of microbiology and techniques used for isolating, growing and identifying bacteria. Propagation and maintenance of appropriate microbial stocks. | 3/1/2024 |
| 623 | Reckitt Benckiser Pharmaceutical Montvale, NJ R&D Assistant, Chemistry and Measurement Sciences- Analytical BS/BA in Chemistry or related field. Exp: 0-2 years |
Reckitt Research and Development CMS (Montvale, NJ) is seeking a self-motivated analytical chemist to join our team in the role of Assistant in the Analytical lab. The successful candidate would work independently with supervision in the lab, supporting analytical measurement for Health & Hygiene global new product development, including the Lysol, Dettol, and Harpic brands. | 3/1/2024 |
| 624 | Reaction Biology Malvern, PA Research Associate I Bachelor of science degree. Exp: 1+ years |
To provide ground level lab work following standard protocols according to department needs. The employee will support other team members in the execution of routine lab procedures, as well as to help sustain the functionality of the lab through regular cleaning, stocking inventory, and maintenance. | 3/1/2024 |
| 625 | Reata Pharmaceuticals Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred) OR BioWork Certificate or Associate’s Degree. Exp: 1+ years |
Our Manufacturing Associates perform processing steps and manufacturing support activities in our Drug Substance facility in Research Triangle Park (RTP). These teams are the backbone of our operations – each playing a critical role in delivering our therapies to the patients who need them. Our teams are organized by the steps in the biomanufacturing process that they operate in; with two main areas/disciplines – Upstream (Cell Culture) and Downstream (Purification). MAs perform these critical steps within Current Good Manufacturing Practice (cGMP) biosafety cabinets and cleanroom suites. | 3/1/2024 |
| 626 | Reata Pharmaceuticals Research Triangle Park, NC Associate II, QA - Swing Shift Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Quality Assurance Associate II is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identifying gaps in existing Quality systems and proposing solutions to site management. The QA Associate will perform all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures and also adhere to all regulatory licenses and regulations, interfacing with key Quality and manufacturing customers, and coordination of investigations impacting the RTP site. The QA Associate may participate in internal compliance audits; assess and approve discrepancies from site, corporate, and regulatory guidance. The QA Associate will also ensure compliance with training policies. Please note that this is a Swing Shift position and will work a traditional 2-2-3 Manufacturing Rotation from 12pm to 12am, on a 12hr/shift schedule. There is a 10% pay differential for this position. | 3/1/2024 |
| 627 | Reata Pharmaceuticals Research Triangle Park, NC Associate II, Quality Assurance Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Associate II, Quality Assurance is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identify gaps in existing Quality systems and propose solutions to site management. | 3/1/2024 |
| 628 | R&D Systems Minneapolis, MN Advanced Manufacturing Technician Bachelor degree. Exp: 1-3 year |
The responsibilities of a Manufacturing Technician are to support the laboratory staff with the process of building and manufacturing science products. This position will perform a variety of tasks within a laboratory setting that may include labeling, recording data, operating equipment, formulation and plate coating. | 3/1/2024 |
| 629 | R&D Systems Wallingford, CT Research Associate, Reagent Manufacturing Bachelors’ Degree in Biology, Chemistry, Biochemistry or related biological science. Exp: 1+ years |
The candidate will be responsible for providing accurate, efficient and quality production tasks in a cutting-edge molecular biology laboratory. The individual must exhibit a high degree of attention to detail and follow multi-step complicated technical protocols and processes accurately and rapidly. A basic molecular biology or biochemistry laboratory skill set is required as is experience in the use and maintenance of multiple types of biological instrumentation and systems. This position requires the ability to function with minimal oversight and convert customer demands into finished product. The individual will execute production protocols and ensure continual operation of equipment to meet production targets assigned by management, effectively and immediately communicate any complications that arise during manufacturing, and then be able to work across teams to establish and maintain a solution and provide detailed documentation of manufacturing activities, on a daily basis. | 3/1/2024 |
| 630 | R&D Systems Minneapolis, MN Senior Manufacturing Technician Bachelor’s Degree in Science or Engineering. Exp: 1+ years |
The responsibilities of this position are to organize and stage different types of vials and bottles for filling. The position requires that the candidate has the ability to fill antibodies and protein solutions into vials. The candidate may be required to perform calculations based on volume and purity. The candidate must have the ability to cap and label vials of antibodies and proteins quickly and accurately. The candidate will be required to complete computer inventory entries and track supplies accurately. The candidate must have the ability to work in a laminar flow hood and fill (pipetting) products for extended periods of time. The candidate must have the ability to inspect vials with product and identify defects. The candidate will be required to operate cap torqueing and labeling automation. The candidate's ability to trouble shoot automation is an added skill set that would be desirable. The candidate will be required to learn nationalization process. The candidates' ability to complete paperwork accurately is critical. The candidate's ability to work in a fast-paced regulatory environment as a team is critical. The candidate must have the ability to gown and work in a clean room. The candidate performs pipette calibration accurately. The candidate may work on new production introduction, implementation, and filling. The candidate will help with yearend inventory counting and perform additional duties as assigned. The candidate will be required to exhibit EPIC behaviors aligned with the corporate vision. | 3/1/2024 |
| 631 | R&D Systems Minneapolis, MN Advanced Research Associate Master’s degree. Exp: 1+ years |
In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques such as cell culture, flow cytometry, qPCR, and other analytical methods. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 3/1/2024 |
| 632 | Roche Seattle, WA Lab Assistant BS in Chemistry, Biochemistry, Biology or related field. Exp: 1+ years |
Roche Diagnostics acquired Stratos Genomics (SBX Nanopore Sequencing) in 2020 for its novel Sequencing by eXpansion (SBX™) technology. SBX™ uses unique applications from chemistry, biochemistry, and protein engineering to sequence DNA by nanopore in rapid time with high accuracy and low cost. We are looking for people who are excited to collaborate with us to make SBX successful. You will join the SBX Central Services team of Lab Assistants and play a crucial role in the day-to-day operations of the lab. | 3/1/2024 |
| 633 | Nexus Pharmaceuticals Lincolnshire, IL Quality Control Chemist I BS or MS in chemistry or related field with a minimum of 20 hours of chemistry coursework. Exp: one year |
The Quality Control Chemist I is responsible for the execution of wet chemistry and analytical chemistry techniques during testing of Raw Materials and finished products. This testing includes: Instrumental analysis such as HPLC, GC, UV and FTIR as well as wet chemistry such as titrations, LOD and chemical identification tests. The Quality Control Chemist I performs method development or method transfer testing. The Quality Control Chemist I works in the laboratory in a safe and effective manner. | 2/20/2024 |
| 634 | Nostrum Laboratories Bryan, OH Chemist I Bachelors Degree. Exp: 0 - 4 years |
Responsible for development and validation of analytical methods in support of product development and IND/NDA/ANDA filings. Perform routine wet chemical and instrumental analysis on raw materials, in-process, finished and stability products. Accurately compiles and reports data. Gather, compile and compose documents needed for regulatory submissions. | 2/20/2024 |
| 635 | Nostrum Laboratories Bryan, OH QC LAB TECHNICIAN I Associates Degree. Exp: 1-2 years |
The QC Technician I is responsible for conducting non-complex analytical tests for raw materials, components, in-process materials, finished products, other samples as assigned, in accordance with cGMP regulations, regulatory filings, and approved procedures. | 2/20/2024 |
| 636 | Novartis Cambridge, MA Research Scientist II, Cell Pharmacology – CVM MS degree in biochemistry, molecular or cell biology, biophysics, biomedical engineering or a related field. Exp: 0+ years |
We are seeking a highly motivated Research Scientist II to join our Cell Pharmacology team. You will advance our understanding of disease biology, contribute to target identification efforts, and work towards the discovery and optimization of new drugs for The Cardiovascular and Metabolic Disease Area (CVM) of Biomedical Research. The work involves collaboration with research scientists across multiple disciplines as well as translational medicine colleagues who support bringing our drugs to patients. | 2/22/2024 |
| 637 | Novartis San Diego, CA Research Scientist II, CGT Biodistribution and Technology Scientific background with an BS in Biological Sciences or a closely related discipline. Masters preferred. Exp: 1+ years |
We are seeking a highly motivated scientist to contribute to gene therapy development as part of the global community of investigators in the Cell & Gene Therapy (CGT) group within BRC. The successful candidate will work at the cutting edge of gene therapy biodistribution, platform and technology research to model and test priorities in translational research. The successful candidate will be a collaborative scientist experienced in molecular biology experiments, liquid handling automation and/or NGS sequencing. | 2/22/2024 |
| 638 | Novartis Emeryville, CA Research Scientist, Comparative Medicine Bachelor’s degree (B.A./B.S.) in animal or life sciences field preferred. Exp: 1+ years |
Comparative Medicine (CM) provides high quality husbandry and in vivo research work and support to enable drug discovery research and development. We are looking for a Research Scientist in CM to provide husbandry and vivarium Operations support, and to help run in vivo research studies and projects to support the diverse and exciting project portfolio at GH. The candidate should be action-oriented, Experienced with rodent husbandry and vivarium operations, skilled in in vivo procedures used to perform in vivo experiments with high technical and ethical standards and provide best in class animal care. The role will require an ability to work independently as well as in close collaboration with other CM colleagues, research scientists, the IACUC and animal welfare team. | 2/22/2024 |
| 639 | Novartis Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 2/22/2024 |
| 640 | Novartis Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 2/22/2024 |
| 641 | Novo Nordisk Durham, NC Manufacturing Operator I - Future 2nd Shift Associate’s degree preferred. Exp: one (1) year |
Efficiently, effectively & safely clean, setup & operate manufacturing equipment to achieve production goals, while adhering to applicable cGMPs & SOPs. | 2/22/2024 |
| 642 | Novo Nordisk West Lebanon, NH Manufacturing Science and Analytical Technology Associate I Bachelor’s degree or equivalent in Biochemistry, Chemistry, Engineering or a closely related field. Exp: one year |
This position has the responsibility of working with senior level Scientists to execute laboratory scale process development or validation studies in support of process or assay development, or process troubleshooting or scale-up. The scientific knowledge in this position will range from familiarity with details of manufacturing process, process chemistries, development studies and relevant assay methods and instruments. This position will be one of the interfaces between MSAT and Manufacturing or Quality. | 2/22/2024 |
| 643 | Novo Nordisk Clayton, NC Associate Process Engineer - FP - TECH SUPPORT - Assembly - Nights - Team C Bachelor’s degree in Chemical Engineer, Mechanical Engineering, or related discipline. Exp: One (1) year |
Responsible for assisting with design and implementation of manufacturing processes, instrumentation and equipment start-ups from the laboratory through manufacturing scale. | 2/22/2024 |
| 644 | Novo Nordisk West Lebanon, NH Manufacturing Technician- Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 2/22/2024 |
| 645 | Novo Nordisk Durham, NC Maintenance Technician I - 2nd Shift AA/AS/AAS degree from an accredited university in a relevant field required. Exp: one (1) year |
Improve systems & equipment reliability on assigned process, reduce system/equipment downtime on assigned process & support operation of assigned process. | 2/22/2024 |
| 646 | Noxilizer Hanover, MD Research and Development Laboratory Scientist Bachelor’s degree in Biology, Biotechnology, Biomedical Engineer, Material Science or related field preferred. Exp: 1 year |
The R&D Lab Scientist is responsible for performing, documenting and reporting microbiological sterilization studies for Noxilizer’s customers. Noxilizer’s customers range from Fortune 500 pharmaceutical, biotech and medical device companies to start-ups that are in the US, Europe and Asia. These studies are the first critical step in the customer’s evaluation of nitrogen dioxide sterilization and their product, as well as an important revenue-generating area for the company. The R&D Laboratory Scientist will join a high-performing team of experts to solve sterilization challenges while they grow their skills for future career opportunities. | 2/22/2024 |
| 647 | NxStage Ogden, UT Biocompatibility Engineer I Bachelor's Degree in related Engineering or scientific discipline required. Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 2/23/2024 |
| 648 | NxStage Southaven, MS Medical Lab Scientist - Microbiology Bachelor's Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 - 3 years' |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 649 | NxStage Rockleigh, NJ Medical Lab Scientist - Diagnostic Immunology Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 650 | NxStage Southaven, MS Medical Lab Scientist - Hematology Bachelor’s Degree in Medical Laboratory Sciences or Biological Sciences required. Exp: 0 – 3 years’ |
Performs a wide variety of moderately and highly complex tasks and analysis of human fluids and tissues, using manual procedures as well as operating various laboratory equipment and automated analyzer systems. Responsible for acceptable quality control accurate testing, and release of accurate patient results in collaboration with the Lead, Supervisor or Manager. | 2/23/2024 |
| 651 | NxStage Mesa, AZ Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 652 | NxStage Richmond, VA Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 653 | NxStage Saint Peters, MO Biomedical Equipment Technician Associate Degree in electronics / biomedical technology, or equivalent a plus. Exp: 0 – 1 year |
Entry level position focuses on the development of Knowledge, Skills, and Abilities (KSA) in a supervised environment with the intent of developing performance and effective, efficient independent functioning under close supervision upon completion of various training processes over time. Under close supervision and consistent with completed training and qualifications, schedules and performs routine repair and maintenance activities of medical equipment, water systems and the physical plant in assigned facilities that ensures patient safety and staff operating equipment in accordance with company policies and procedures, manufacturer’s documentation, industry standards and local, state and federal regulatory requirements. Responsible for efficient use of resources related to repair and maintenance costs. | 2/23/2024 |
| 654 | Ocean Ridge Biosciences Exton, PA Lab Assistant Associate or bachelor’s degree preferred. Exp: 1+ years |
The Lab Assistant will work under the supervision of laboratory staff or researchers to assist in the smooth functioning of laboratory operations. This role involves a combination of technical and administrative tasks to support ongoing laboratory activities and required documentation. Additionally, the Lab Assistant will provide crucial support for clinical trial kitting activities and sample receipt. | 2/23/2024 |
| 655 | Ocean Ridge Biosciences Chicago, IL Assistant/Associate Toxicologist BS degree in animal/veterinary science, biology, or related disciplines. Exp: Assoc: 0-3 years |
The Associate/Assistant Toxicologist plays a key, hands on role in the conduct of preclinical studies and supports the Study Director to ensure that Sponsor studies are conducted properly and according to FDA guidelines. | 2/23/2024 |
| 656 | Ocean Ridge Biosciences Hayward, CA Research Associate M.S. degree in related scientific discipline. Exp: 0-3 years |
1) Perform Watson design according to Study Protocols 2) Conduct basic method development and validation studies. 3) Ability to troubleshoot and solve basic technical and instrumental issues. 4) Conducts and documents work in a regulated environment. 5) Reviews the data package and notebooks for junior chemists 6)Writing up analytical methods, protocols, and reports under supervision 7) Perform project communication with client, study director, and project management team under supervision | 2/23/2024 |
| 657 | Ocean Ridge Biosciences Exton, PA Associate Scientist/Scientist Scientist: M.S.; Associate Scientist: B.S./B.A. Exp: Scientist: 1-5 years; Associate Scientist: 1-5 years |
This is a technical scientific position within the Biologics Service Team. The Biologics Service Team is responsible for conducting bioanalytical methods related to large molecule biotherapeutic drug development across all therapeutic areas, spanning nonclinical studies to post-market clinical development. | 2/23/2024 |
| 658 | Ocean Ridge Biosciences Exton, PA Lab Technician High School diploma, associate degree, or bachelor’s degree. Exp: 0-2+ years |
Frontage Laboratories, Inc. is hiring a Laboratory Technician I/II in the CMC Analytical Services division. The Laboratory Technician is responsible for supporting scientists in laboratory testing activities. The Laboratory Technician’s duties include following procedures, recording data, working with laboratory equipment, ordering supplies, and maintaining an inspection ready work environment. | 2/23/2024 |
| 659 | Ocean Ridge Biosciences Exton, PA Lab Technician Bachelor’s degree in molecular biology, Biology, Biochemistry, Chemical Engineering, Mechanical Engineering, or equivalent. Exp: 1-5 years |
We are looking for a qualified Lab Technician to join our team. The role will perform and support laboratory procedures and controls within Biologics, Gene, and Cell Therapy (BGC) Department to maintain efficiency and compliance for the laboratory. The ideal candidate needs to have an entrepreneurial spirit that enables her/him to wear multiple hats as we scale-up the laboratory business. The candidate will have experience in working in a laboratory environment, preferably within biologics/or GCT lab. The candidate will be well-trained to maintain safety conditions in the lab and expected to be passionate in working in a matrix organization environment. The goal is to optimize lab compliance and maintaining the smooth running of the lab. | 2/23/2024 |
| 660 | Ocean Ridge Biosciences Exton, PA Associate Scientist Bachelor’s or master’s degree in molecular biology, cell biology, biochemistry, or a related field. Exp: 1+ years |
The Cell-based Assay Core Lab, based at our Exton headquarters, stands as a premier provider of diverse cell-based assays. These include potency assays, neutralizing antibodies assays, EliSpot, virus plaque assay, TCID50 Assays etc. We are seeking a candidate with a fundamental understanding of Cell Biology, Biochemistry, and Molecular Biology. The ideal candidate should be highly organized, self-motivated, enthusiastic about learning, and capable of managing multiple projects concurrently | 2/23/2024 |
| 661 | Ocular Therapeutix Bedford, MA Manufacturing Operator Associate degree or biotechnology certificate strongly preferred. Exp: 1-3 years |
The Manufacturing Operator is responsible for performing all manufacturing processes related to the Ocular Therapeutix’s products. The Operator is an integral part of our team and will be responsible for manufacturing activities by following appropriate SOP(s) and supervisor direction, in accordance with current good manufacturing practices and company policy and procedures. | 2/23/2024 |
| 662 | Ocular Therapeutix Bedford, MA Device Engineer I Bachelor’s degree (in Mechanical Engineering, Biomedical Engineering or related discipline. Exp: 0 - 2 yrs |
We are seeking a motivated engineer to join the Product Development team. The individual is responsible for contributing to the design and manufacture of injectors and applicators used for the delivery of hydrogel drug product to treat various ophthalmic conditions. Responsibilities include product design (CAD modeling), design verification, design validation and other elements of Design Control. The role also includes process development activities, line layout, fixture design, equipment procurement, and supporting GMP manufacturing of clinical trial material. This individual will participate in defining voice of the customer requirements and product and material specifications. They will also perform risk analysis activities and design verification testing. This role will require a mix of cross-functional collaboration as well as execution of key laboratory experiments to achieve program objectives. The position is set in a dynamic and fast-paced environment. Critical areas of immediate focus include planning and execution of laboratory experiments, CAD design and maintenance of engineering drawings, Design for Manufacturability, process development and incorporation of fixture design and semi-automated processes to support development of manufacturing processes for late-stage clinical production that are capable, scalable, and sufficiently robust for transfer to commercial manufacturing. We are seeking a motivated engineer to join the Product Development team. The individual is responsible for contributing to the design and manufacture of injectors and applicators used for the delivery of hydrogel drug product to treat various ophthalmic conditions. Responsibilities include product design (CAD modeling), design verification, design validation and other elements of Design Control. The role also includes pr | 2/23/2024 |
| 663 | OriGen Biomedical Austin, TX Manufacturing Engineer I Bachelor’s degree in Engineering. Exp: 0-2 years’ |
The Manufacturing Engineer I will evaluate and develop processes to ensure quality, cost, and efficiency requirements are met. S/he will troubleshoot problems with production and take corrective actions and will research and make recommendations on the purchase of equipment and/or upgrades to existing equipment and support manufacturing as needed. | 2/23/2024 |
| 664 | Parexel West Point , PA Scientist II - Microbiologist Bachelor’s degree required; concentration in a scientific or applied discipline strongly preferred. Exp: 1-2 years |
We are looking to fill a Scientist 2 position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. | 2/23/2024 |
| 665 | Parexel Rahway, NJ Scientist 3 - Drug Product Microbiologist Bachelor’s degree required; concentration in a scientific or applied discipline strongly preferred. Exp: 1-2 years |
We are looking to fill a microbiologist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in Rahway, NJ. | 2/23/2024 |
| 666 | Parexel Rahway, NJ Crystallization Engineer III MS degree or equivalent in Engineering, Chemistry, Chemical Engineering, or a related field is required. Exp: 1-2 years’ |
We are looking to fill an Engineer 3 position working as a full-time employee of Parexel on long-term assignment onsite at one of our clients in Rahway, NJ. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship. Overview / Responsibilities The Chemical Engineering Research and Development department of one of our clients in Rahway, NJ has a position available that will have primary accountability for lab process development specifically around API crystallization, isolation, drying, and particle physical attribute control. Activities will include working with gram quantities at the bench scale to a few kilograms at the Unit Operations and Preplab scales utilizing wet and dry processing equipment within these labs (e.g., crystallization vessels, filtration and drying equipment, and wet and dry milling tools, etc.). The department offers fast-paced, hands-on research that requires a high degree of technical skills and contributions. Secondary activities may include experiments and the use of instruments associated with process safety evaluation when needed, and the general support of Specialty Labs operations within the Chemical Engineering R&D Department. | 2/23/2024 |
| 667 | Par Pharmaceutical Rochester, MI Microbiologist I Bachelor of Science degree in microbiology, biology or related field with microbiology coursework required. Exp: 1+ years |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 2/23/2024 |
| 668 | Par Pharmaceutical Horsham, PA Associate Scientist, Bioprocess Technical Operations Bachelor’s degree in a biological, chemical, or related discipline is required. Exp: 1+ years |
The Associate Scientist will perform lab duties under the direct supervision of senior Biotech Ops (BTO) staff. Key areas of focus/support include preparation of buffers as well as execution of one or two specific methods or processes. | 2/23/2024 |
| 669 | Par Pharmaceutical Rochester, MI Quality Associate Specialist, Product Release (Afternoon Shift) BA/BS degree in a related discipline. Exp: 0-1 year |
The Quality Associate Specialist, Product Release, under close supervision, reviews all pertinent records, including Batch Production Records and laboratory Certificates of Analysis to confirm accuracy and, with guidance, makes the determination of acceptability for product release. In addition, confirms that all related Quality events such as CAPAs, Change Controls, etc. are closed prior to releasing the product. Partners with other departments to ensure that errors are addressed and corrected. Identifies errors that have potential product impact, escalates to supervision, and takes action to place lots on Quality Hold as needed. Ensures release meets internal requirements and is performed in a timely and accurate manner. | 2/23/2024 |
| 670 | Partner Therapeutics Lynnwood, WA Quality Control Lab Support Technician I (Contract/Onsite) B.S. or equivalent degree in science (Biology, Chemistry, Biochemistry, etc.) or related field (Chemical Engineering, etc.) strongly preferred. Exp: 1 year |
The Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine which includes testing raw materials, process intermediates, Bulk Drug Substance (“BDS”), and Drug Product (“DP”). The Lab Support Technician I role is an individual contributor who maintains and prepares the onsite laboratories to perform required testing. This position is an ONSITE role requiring a presence 5 days per week at our Lynnwood, WA plant which is a cGMP production scale manufacturing facility for our product, Leukine® (sargramostim), a therapeutic glycoprotein. | 2/23/2024 |
| 671 | Partner Therapeutics Lynnwood, WA Quality Control Lab Support Technician I (Onsite) B.S. or equivalent degree in science (Biology, Chemistry, Biochemistry, etc.) or related field (Chemical Engineering, etc.) strongly preferred. Exp: 1 year |
The Quality Control Department is responsible for all testing related to the manufacturing and release of Leukine which includes testing raw materials, process intermediates, Bulk Drug Substance (“BDS”), and Drug Product (“DP”). The Lab Support Technician I role is an individual contributor who maintains and prepares the onsite laboratories to perform required testing. This position is an ONSITE role requiring a presence 5 days per week at our Lynnwood, WA plant which is a cGMP production scale manufacturing facility for our product, Leukine® (sargramostim), a therapeutic glycoprotein. | 2/23/2024 |
| 672 | PeproTech St. Louis, MO Lab Technician II-Formulations Associate’s degree in science field or or Bachelor’s degree in science or engineering field. Exp: AS: 1+ years; BS: 0+ years |
The candidate will be responsible for the performance of operations in support of the BPS Cell Culture Development Team. You will carry out a variety of functions related to Upstream Process Development operations with primary focus on medium and buffer formulations. Additional functions may include but are not limited to activities such as supply stocking and organization, and equipment maintenance including basic troubleshooting, cleaning, and performance maintenance on supporting equipment. | 2/23/2024 |
| 673 | Merieux NutriSciences Minnetonka, MN Microbiology Lab Tech Associate's degree in STEM degree preferred. Exp: 1+ year |
We are looking for a Microbiology Lab Tech in 11585 K-Tel Dr, Minnetonka, MN 55343 USA. Your mission will be to: Purpose (Objective): The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 2/12/2024 |
| 674 | Merieux NutriSciences Stone Mountain, GA Microbiology Laboratory Technician Associates degree or equivalent work experience. Exp: 1+ year |
We are looking for a Microbiology Laboratory Technician in 2169 West Park Court, Stone Mountain, GA 30087 USA. Your mission will be to: Purpose (Objective):The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. | 2/12/2024 |
| 675 | Merieux NutriSciences Salt Lake City, UT Chemistry Technician Associates degree or Bachelors degree. Exp: AS: 1+ years; BS: 0+ years |
We are looking for a Chemistry Technician in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: Composting and grinding of samples for analysis as required. Perform chemical analyses such as protein, moisture, fat, ash, and other components. Prepare sample for analysis according to procedure. Retrieve samples from designated areas (e.g. log-in, sample storage). Perform chemical analyses of macronutrients, micronutrients or other parameters as designated. Extract desired component from sample with appropriate processes so that concentration can be determined. Prepare standards and reagents that are needed for the analysis procedure. Write/label all samples throughout the process so that Client and sample numbers can be tracked. Perform calculations, checking and interpretation of results where applicable. Track status of designated tests as assigned to ensure Client turn around time commitments are met and inform supervisor of non compliance. Assist other departmental personnel with analysis tasks so that testing can proceed according to specified time limits. | 2/12/2024 |
| 676 | Merieux NutriSciences Minnetonka, MN Media Technician Associate's degree in STEM degree preferred. Exp: 1+ years |
We are looking for a Media Technician in 11585 K-Tel Dr, Minnetonka, MN 55343 USA. Your mission will be to: Purpose (Objective): The incumbent prepares sample for processing and maintains documentation of process to facilitate analysis procedures. | 2/12/2024 |
| 677 | Merieux NutriSciences Springfield, MO Microbiologist I Associates degree required, Bachelors preferred or equivalent work experience. Exp: One (1)- 2 years |
We are looking for a Microbiologist I in 2835 N Oak Grove, Springfield, MO 65803 USA. Your mission will be to: Purpose (Objective): The incumbent is responsible for the testing of samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. Schedule is 11:30-8p, Tuesday-Saturday. | 2/12/2024 |
| 678 | Merieux NutriSciences Crete, IL Microbiologist III Masters degree. Exp: 1-2 years |
We are looking for a Microbiologist III in 3600 Eagle Nest Dr, North Building, Crete, IL 60417 USA. Your mission will be to: The incumbent is responsible for the testing of food samples using various microbiological analyses. The incumbent provides analytical support for the lab by ensuring that laboratory procedures are being performed within specified quality guidelines. This position serves as a technical resource and provides ongoing technical support related to method and process implementations. This position spends the majority of time or all of their time in diagnostics. | 2/12/2024 |
| 679 | Merieux NutriSciences Gainesville, FL Microbiology Lab Technician Associates degree. Exp: 0+ years |
We are looking for a Microbiology Lab Technician in 2183 SE Hawthorne Rd, Gainesville, FL 32641 USA. Purpose (Objective):The incumbent prepares samples for processing and maintains documentation of process to facilitate testing procedures. | 2/12/2024 |
| 680 | Meso Scale Discovery Gaithersburg, MD Research Associate Bachelor’s degree in life sciences, or related area is required. Master’s degree a plus. Exp: 1+ years |
This position is responsible for executing experiments and analyzing the resulting data in support of reagent and assay development projects with close supervision. This is a laboratory-based position responsible for advancing research and/or development objectives focused on leading-edge biomarker measurements and technology. | 2/12/2024 |
| 681 | Meso Scale Discovery Rockville, MD Product Transfer Associate I Bachelor degree in Biology, Chemistry, Biotechnology, Engineering or related field, or associate’s degree with equivalent experience. Exp: One year |
This position is responsible for manufacturing assay kit components during development phases, meeting production schedules and troubleshooting. The role is cross-disciplinary and requires coordination across multiple departments (Operations, Quality, Research & Development, etc). | 2/12/2024 |
| 682 | Microbiologics Saint Cloud, MN Quality Control Technician Four-year microbiology or related degree required. Exp: 1+ years |
We are currently looking to add a Quality Control Lab Technician to our St. Cloud, MN team. In this role, you will perform Quality Control Testing, Shelf-Life Testing, and Packaging Event Evaluations on Microbiologics products in accordance with the appropriate Company Device Master Record (DMR), policies and procedures with the objective to release only production products that meet all of Microbiologics acceptance criteria. | 2/12/2024 |
| 683 | Microbiologics Lexington, KY Microbial Production Technician Bachelor’s degree in Biology, Microbiology or closely related field. Exp: 0+ years |
We are currently looking to add a Microbial Production Technician to our team in Lexington, KY. In this role, you will be responsible for manufacturing of microorganism product line, fungal serology, proficiency materials, and custom and retail products, in addition to other duties listed below. | 2/12/2024 |
| 684 | Microbiologics Saint Cloud, MN Research & Development Technician Four (4) year degree in relevant field (e.g., biology, microbiology, virology, cell biology molecular biology). Exp: 1+ years |
We are currently looking to add a R&D Technician to our team in Research & Development. In this role you will be responsible for assisting with supervised experiments using microbiology and molecular biology techniques and/or cell culture and virology techniques as well as other applicable methodologies leading to new products or process improvements. | 2/12/2024 |
| 685 | Mirati Therapeutics Summit West, NJ Specialist, QA Engineering Bachelor of Science degree required. Exp: 1 year |
The Specialist is responsible for providing quality oversight for Site Validation activities and Quality Control Laboratory method and equipment validation in accordance with BMS policies, standards, procedures and Global cGMP. Functional responsibilities for the incumbent include ensuring accurate and timely maintenance and review of validation and qualification documents for all equipment, laboratory, and facility activities; support data integrity initiatives for the site. | 2/15/2024 |
| 686 | Mirati Therapeutics Devens, MA Specialist, Validation Engineer I, Cleaning Validation Knowledge of Engineering and Quality Assurance generally attained through studies resulting in a B.S., in engineering, a related discipline. Exp: 0-2 years |
Supports the design and maintenance of a robust cleaning validation lifecycle for process equipment and systems, that includes a bench-scale cleaning program, a cleaning monitoring program, and a cleaning verification changeover program for a fully automated, multi-product biologics manufacturing facility. Performs cleaning validation lifecycle activities, including work arising from change controls, capital projects, shutdown/changeover activities, cleaning validation bench-scale studies, and cleaning monitoring programs. Works collaboratively with peers within Validation, Manufacturing Systems, Information Technology, Manufacturing, Manufacturing Engineering and Quality Effectively manages workload to address priorities, meet schedules, maximize productivity, reduce costs, and increase efficiencies. Ensures alignment with site validation master plans and philosophies, BMS policies, and industry guidelines on validation and quality engineering. | 2/15/2024 |
| 687 | Miromatrix Medical Woburn, MA Research Associate I, Cell Production and Tissue Engineering Bachelor’s Degree in cellular biology, developmental biology, biomedical engineering, or a related field. Exp: 1+ years |
The Research Associate I is responsible for helping to derive and expand the necessary cell types to develop and build autologous tissue constructs as a solution to end-stage renal disease and other disorders. This position is part of a multidisciplinary team led by experienced stem cell and developmental biologists and engineers. This individual is experienced in human primary cell and stem cell derivation, expansion, and differentiation. Technical expertise in multiple cell biology techniques including quantitative polymerase chain reaction, fluorescence microscopy, flow cytometry and other immune-based assays are critical to this position. | 2/15/2024 |
| 688 | Miromatrix Medical Eden Prarie, MN Research Associate II/Senior Research Associate, Cell Development & Characterization Research Associate II: Master’s degree in biology, cellular and molecular biology, biomedical sciences, biomedical engineering, or biomanufacturing. Exp: 1+ years’ |
The Senior Research Associate/Associate II, Cell Development and Characterization, is responsible for performing cellular analysis of primary kidney and liver cells using flow cytometry, immunofluorescence, immunocytochemistry, and qPCR. This individual must be self-motivated with demonstrated ability to culture and characterize mammalian cells, creatively solve problems, should be excellent at troubleshooting, and able to work independently and in collaboration with a diverse team of multidisciplinary scientists and engineers diligently and carefully. This role, and team, will be tasked with characterization of kidney and liver cells for cellularization efforts in Bioengineered Organ Development, and with developing GMP level protocols and release tests in preparation of IND filing. | 2/15/2024 |
| 689 | Moderna Therapeutics Norwood, MA Research Associate, Technical Development Operations BS in Biochemistry, Molecular Biology, or a related field. Exp: 1-2 years |
Moderna is seeking a molecular biologist to join Technical Development newly established Sequencing Center. In this laboratory-based position, the individual will routinely process sequencing samples, operate, and troubleshoot instruments including ABI 3730xl, Echo, Illumina MiSeq, NovaSeq, plate readers and liquid handlers. Experience with lab automation is a plus. The candidate must thrive in a fast pace high throughput environment, have a collaborative spirit, and be curious and willing to learn new techniques to push process development forward. | 2/16/2024 |
| 690 | Moderna Therapeutics Norwood, MA Research Associate, Analytical Development A BS with a focus on microbial sciences. Exp: 1+ years |
We seek a motivated individual with experience in a microbiology laboratory setting to support microbial testing in Technical Development. Candidates should have experience with various microbial techniques such as aseptic sample handling, filtration and pipetting. In this laboratory-based role, the Research Associate will be responsible for supporting daily laboratory operations and following microbiology test protocols for analysis of in-process and final product bioburden and endotoxin release testing of development samples (DNA plasmid, protein, mRNA, and LNP sample types). In addition, the Candidate would contribute to method optimization, testing in support of rapid microbiological method qualifications and maintain the microbiology laboratory and equipment. | 2/16/2024 |
| 691 | Moderna Therapeutics Norwood, MA Research Associate, Drug Product Development Masters or Bachelor’s Degree in on one of the following fields: Chemical Engineering, Biochemical or Biomedical Engineering, Pharmaceutical Sciences, Exp: 0 – 2 years |
We are seeking a highly skilled and motivated Research Associate in Drug Product Development respiratory team, to work in a team developing Moderna’s sterile drug product processes and products that enable clinical and future commercial supply. The primary role for this position will be to support product concept development including process development and scale-up work, container development and conditions of use studies. The incumbent will support the development of compositions, aseptic fill/finish unit operations through the development and use of scale-down models, process characterization studies etc. Applicants should have relevant pharmaceutical sciences related experience with various aspects of drug product development. The applicant should have exceptional ability to plan, execute and report, to communicate and collaborate, and requires strong attention to detail while working in a fast-paced, interdisciplinary environment. | 2/16/2024 |
| 692 | Moderna Therapeutics Norwood, MA Engineer II, MST Biochemical engineer, Chemical engineer, Biochemistry or Biology background. MS. Exp: 1 to 3 years’ |
The Engineer II, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross-functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Wednesday through Saturday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 693 | Moderna Therapeutics Norwood, MA Engineer I, MS&T Biochemical engineer, Chemical engineer, Biochemistry or Biology background. BS. Exp: 1 to 2 years |
The Engineer I, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Sunday through Wednesday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 694 | Moderna Therapeutics Norwood, MA Engineer I, MS&T Biochemical engineer, Chemical engineer, Biochemistry or Biology background. BS. Exp: 1 to 2 years |
The Engineer I, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Individualized Neoantigen Therapies (INT). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 3rd shift role, working a Wednesday through Saturday schedule from 10:00pm until 8:00am. | 2/16/2024 |
| 695 | Moderna Therapeutics Norwood, MA Engineer II, MST - PCV Biochemical engineer, Chemical engineer, Biochemistry or Biology background. MS. Exp: 1 to 3 years’ |
The Specialist, MS&T will be part of Moderna’s Manufacturing Science and Technology team responsible for process implementation, technical support, and person-in-plant coverage to ensure the robust End-to-End production of our new mRNA Personalized Cancer Vaccine (PCV). The individual will work collaboratively with cross functional stakeholders such as Technical Development, Manufacturing, Regulatory, and Quality, to ensure all technical aspects of production are successfully executed. This will be a 1st shift role and the individual will be working a Wednesday through Saturday schedule from 6:00am until 4:00pm. | 2/16/2024 |
| 696 | Nanostring Bothell, WA Manufacturing Assembly Technician I 2-year degree in a Life Science related discipline (Chemistry, Molecular Biology, Biotechnology, etc.) Exp: 0+ years |
The Manufacturing Lab Technician is responsible for supporting the production of reagents used in various NanoString Analysis Systems, for example, nCounter® and GeoMx®. The role requires learning and performing both manual and automated production processes for the manufacturing of raw, intermediate, and final reagents needed for the multiplexed detection and the quantification of many different types of target molecules from biological samples. In this role, the Lab Tech will learn the skills to operate semi-automated and automated scientific equipment, perform Standard Operating Procedures (SOPs), navigate Document Control systems, Enterprise Resource Planning (ERP) systems, etc. | 2/16/2024 |
| 697 | Nanosyn Mississauga, Ontario Canada, CA Chemist I (Trace Metals) B.Sc. in chemistry or related field. Exp: 1 -2 years’ |
Under the supervision of the Supervisor, Trace Metals and Manager, Trace Metals and GMP Testing, this position is responsible for the following: Perform routine chemical and physical analysis on the full range of analytical samples in accordance with in-house methods, customer’s method or compendial method primarily using Inductively Coupled Plasma Mass Spectrometry (ICP-MS)/ Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES)/ Atomic Absorption Spectroscopy (AAS) Perform and maintain Trace Metals instruments- performance verifications, troubleshoot when required Assists with method development, method validation testing and analytical method transfer testing using ICP-OES/ ICP-MS/ and AAS Prepare analytical reports, method validation protocols and reports for validations and verifications performed Maintain documentation, including lab notebooks, equipment logbooks and instrument raw data in accordance with applicable SOPs Inform and discuss with Manager any atypical / OOS result and deviations Perform pipette calibrations, washing of glassware, disposal of samples in accordance with in-house SOPs Assist Supervisor and Manager with other laboratory duties as required | 2/16/2024 |
| 698 | Nanosyn Acton, MA Microbiologist I (Entry Level) Graduation in microbiology / equivalent. Exp: 1-2 year |
Element has an opportunity for a Microbiologist I whose primary responsibility is to support laboratory operations by conducting the relevant microbiological testing. | 2/16/2024 |
| 699 | Nanosyn Midland, MI Chemist Bachelors. Exp: 0-2 years’ |
Element has a current opening for a Chemist to join our growing team in Midland, MI. The Chemist executes analytical methods and perform testing using a variety of technologies, under the supervision of more senior staff members and supervisor. | 2/16/2024 |
| 700 | New England Biolabs Ipswich, MA Research Technician B.A or B.S. in Biology, Molecular Biology or related field. Exp: 1+ years |
The Sequencing Core at New England Biolabs Inc. (NEB) is seeking a Research Technician to support Next-Generation sequencing (NGS) and DNA analysis operations of the group. As a member of the Sequencing Core, this individual will interface with scientists across the Research, Product Development, and Production departments to deliver high-quality data. | 2/16/2024 |
| 701 | NorthEast BioLab Hamden, CT Associate Scientist, Central Laboratory Services B.S. in Physiological Science, Epidemiology, Microbiology, Immunology, Genetics, Biology, Molecular Biology, Cell Biology, Biotechnology, Biochemistry Exp: Entry Level |
NOTE: PLEASE SUBMIT BOTH RESUME AND COVER LETTER TO APPLY FOR THIS JOB. KINDLY DISCUSS YOUR MOTIVATION, RELEVANT EXPERIENCE, SALARY REQUIREMENTS, AND VISA STATUS IN YOUR SUBMISSION. Role Gain an overall understanding of drug development and maintenance of the full chain of sample custody for regulatory compliance Support implementation of Laboratory Information management System (Watson LIMS) for sample management and storage Sample management and reconciliation, kit preparation and verification, and document preparation related to biological sample collection, storage, and shipment for clinical trials Streamline inventory management, consumable ordering, and other documentation requests for Quality Assurance Unit Help maintain ultra-low temperature (ULT) freezers and refrigerators and associated electronic logs and records Learn bioanalytical techniques for the analysis of drug and biomarkers in biological matrices Follow appropriate safety and study requirements by reading, understanding, and following Standard Operating Procedures (SOP), Good Laboratory Practices (GLP) requirements, and Sponsor Study protocols Support business development and marketing activities, foster client relationships, and help onboard new sponsors | 2/16/2024 |
| 702 | Nelson Laboratories Taylorsville, UT Lab Analyst - Routine Chemistry (Day Shift, Mon-Fri) Bachelors Degree is relevant Life Science preferred. Exp: No Experience |
Laboratory Analysts conduct testing under supervised conditions in accordance with established procedures. Successful lab analysts are people who enjoy conducting tests following written instructions, who pay close attention to detail to make sure everything is done correctly, and who have high standards of personal integrity so that they deliver high-quality results. | 2/16/2024 |
| 703 | Nephron Pharmaceuticals West Columbia, SC Quality Assurance Associate High School diploma with Bachelor of Arts or Science degree preferred. Exp: 1 year |
Manages the sampling, inspection, and release of production components, raw materials, as well as related corresponding documentation for use in manufacturing operations. Serves as primary reviewer for DHR documents and product release. Quality assurance process improvements. Coordinate incoming inspection equipment usage and maintenance. Assists with additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 2/16/2024 |
| 704 | Nephron Pharmaceuticals West Columbia, SC Microbiology Environmental Monitoring Technician - (Days & Nights Available) Associates of Science minimum; Bachelor’s degree with a science background preferred. Exp: 1+ years |
The Microbiology Environmental Monitoring (EM) Technician I is an entry level position that performs monitoring of air quality, environmental, and personnel throughout the facility. EM Technician I collects samples of water for injection (WFI) and performs enumeration. EM Technician I assists EM Leads, Supervisors, and Management with additional responsibilities as delegated. EM Technician I must uphold cGMP and Nephron’s core beliefs. | 2/16/2024 |
| 705 | Nephron Pharmaceuticals West Columbia, SC Nitrile-QA Incoming Inspector Bachelor’s degree preferred. Exp: 1 year |
Receives, samples, inspects, and releases raw material chemicals within Nephron Nitrile’s electronic inventory system and process corresponding documentation necessary in manufacturing operations. Samples, inspects, and releases production components within Nephron Nitrile’s electronic inventory system. Ensures correct paperwork was obtained by warehouse personnel. Work with other departments to ensure receipts, sampling, and releases are within compliance and completed in a timely manner. Assists and performs additional work duties or responsibilities as evident or required. | 2/16/2024 |
| 706 | Nephron Pharmaceuticals West Columbia, SC Microbiology Gowning Certification Coordinator Bachelor’s degree with a science background preferred. Exp: 1+ years |
The Microbiology Gowning Certification Coordinator is an expert on gown certification. Microbiology Gowning Certification Coordinator will lead all gown certification training and plating, as well as follow up with any re-training or re-certification necessary. Microbiology Gowning Certification Coordinator will maintain the certification schedule. When EM Trainer is unavailable, Microbiology Gowning Certification Coordinator will train EM Technician I and EM Technician II. Microbiology Gowning Certification Coordinator must uphold cGMP and Nephron’s core beliefs. | 2/16/2024 |
| 707 | Neurocrine Biosciences San Diego, CA Associate Scientist, Analytical Chem Research Bachelor's degree in Chemistry, Biochemistry or similar discipline. Exp: 1+ years |
Assists medicinal chemistry efforts in purifying and analyzing small molecules by LC-MS and SFC. Supports a range of activities, including design, operation, and maintenance of all analytical instrumentation, including HPLCs, SFCs, mass spectrometers, liquid handlers, and solvent evaporators. | 2/16/2024 |
| 708 | Nexcelom Bioscience San Diego, CA Research Associate I - Diagnostics Bachelor’s degree in a Life Sciences-related field. Exp: 1 years |
BioLegend (a division of Revvity, Inc.) is seeking a highly motivated Product Development Research Associate to join our Diagnostic Product Development Team. This position will actively participate in the development of flow cytometry reagents for diagnostic use. The responsibilities include: perform experiments, analyze and report results, troubleshoot, manage and maintain documentation. After three months in this role, you should be able to work independently to perform flow cytometry experiments, analyze data and document report. | 2/16/2024 |
| 709 | Nexcelom Bioscience San Diego, CA Research Associate I - Antibody Development Bachelor of Science or equivalent degree with coursework in cell biology, immunology, and biochemistry. Exp: 1+ years |
This person would be responsible for developing monoclonal (or polyclonal) antibodies in BioLegend derived from immunized animals by performing antigen preparation, host immunization, bleed analysis, cell fusion, and small-scale antibody purification. Techniques involved in this job include antigen formulation, animal immunization and tissue harvesting, cell culture, cell fusion, and antibody analysis using ELISA, WB, and other techniques. | 2/16/2024 |
| 710 | Lifecore Biomedical Chaska, MN Associate Manufacturing Engineer - Automation BS in Engineering or Automation Engineering Technology Degree. Exp: entry level |
This full-time position offers incredible benefits, your choice of a 2nd shift - 4 day work week or a weekend shift - 3 day work week, and a company culture focused on development and growth which include promotion opportunities. In this entry level engineering role you'll have the opportunity to utilize and enhance your skills in a highly regulated industry by supporting automated manufacturing processes by designing and implementing improvements and troubleshooting and resolving issues. | 2/5/2024 |
| 711 | Lifecore Biomedical Chaska, MN QC Lab Coordinator I Bachelor’s Degree in life science or equivalent combination of education and experience. Exp: 1-3 years |
This full time position offers incredible benefits, your choice of a 4 ½ or 5 day work week, and a company culture focused on development and growth which include promotion opportunities. As the QC Lab Coordinator, you will support the Quality Control department in meeting their goals and accountabilities by trending department data and reporting key metrics. You will manage scheduling and coordinate with other departments to ensure timelines are maintained. You will also perform LIMS and ERP transactions, coordinate with external vendors, and assist with creating, updating, and reviewing supporting QC documentation. | 2/5/2024 |
| 712 | Lonza Durham, NC Cell Culture Technician AA degree Exp: 1-3 years |
Lonza Durham has an exciting opportunity for a Cell Culture Technician to perform tissue culture, tissue isolations and media production with a high degree of aseptic and technical skill. The Cell Culture Technician facilitates departmental function including training lower-level technicians, laboratory maintenance and cleaning, assisting with planning and ordering, writing protocols, performing and reporting on experiments, upholding departmental standards, and reviewing batch records. The Cell Culture Technician is responsible for the manufacture and assembly of products used in clinical research including operation of production equipment, maintaining records, and laboratory environment to comply with Good Manufacturing Practices (GMP), ISO 9000 regulations, and Standard Operating Procedures. The Cell Culture Technician may assist with in process testing to assure batches meet specifications. The training schedule, following orientation, will be Monday – Friday, 8am – 5pm for up to 12 weeks. After training, the work schedule will be Tuesday - Saturday, 8am – 5pm. Occasional evening and weekend work required | 2/5/2024 |
| 713 | Lonza Portsmouth, NH Manufacturing Project Associate 2 (Biologics Manufacturing) A.S. or B.S. degree preferred, with a focus in Biotechnology, Biology, Chemistry, or related STEM discipline. Exp: 1+ years |
The Manufacturing Project Associate Level II is an intermediate level position for an individual with technical manufacturing knowledge and preferably prior proven projects experience. As a level II, the individual is responsible for medium to large sized suite and process specific projects and projects that span across suites and/or the entire Manufacturing organization. The individual is responsible for owning and driving manufacturing improvement projects from concept to completion, with a particular focus on creating efficiencies that contribute to quality, cost, on-time delivery and right first time. The Project Associate supports by working cross-functionally and in collaboration with internal support departments, vendors, and Manufacturing suites to implement new systems, technology and/or procedures, update/create associated documentations and provide essential trainings. The individual will be expected to manage a number of projects at various stages of completion; managing priorities and ensuring on time and quality delivery of all assigned projects. In this level, individuals may become introduced to more customer and campaign focused responsibilities, including IPT/JPT and pre-campaign initiatives. | 2/5/2024 |
| 714 | Lonza Portsmouth, NH Manufacturing Project Specialist (Biologics Manufacturing) A.S. or B.S. degree highly preferred, with a focus in Biotechnology, Biology, Chemistry, or related STEM discipline. Exp: 1+ years |
The Manufacturing Project Specialist works closely with Manufacturing Management to support the achievement of department goals, interdepartmental readiness and batch release requirements, and maintain due dates to support the on time release of batches. The Project Specialist supports by working cross-functionally and in collaboration with internal support departments, customers and Manufacturing suites to develop or update procedures or steps, identify and escalate risks, communicate changes and plan for execution. The Project Specialist is responsible for owning and driving manufacturing improvement projects from concept to completion, with a particular focus on creating efficiencies that contribute to quality, cost, on-time delivery and right first time performance. This role falls under Lonza's Hybrid Work Policy, which requires 3 days a week onsite. | 2/5/2024 |
| 715 | Lonza Portsmouth, NH Biotechnologist Level 1 (A Shift Days) AS/BS preferred; Science related discipline. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Biotechnologist/Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks | 2/5/2024 |
| 716 | Lonza Portsmouth, NH Biotechnologist Level 2 (Upstream) - A Shift Days AS/BS preferred in relevant STEM field. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH The Biotechnologist Level 2 is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level II associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 2/5/2024 |
| 717 | Lonza Portsmouth, NH Biotechnologist Level 1 (B-Nights) - Biotech Manufacturing AS/BS preferred; Science related discipline. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7pm-7am, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for night shift and for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Biotechnologist/Manufacturing Associate I is responsible for the manufacture of therapeutic proteins (API) under current Good Manufacturing Practices (cGMP) conditions. Level I associates are expected to execute process recipes, follow written Standard Operating Procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to demonstrate a strong understanding of cGMP compliance while operating under supervision, and aseptic technique in handling of products and materials. Level II Operators may also be asked to troubleshoot equipment events, initiate deviations, review batch records and logbooks. | 2/5/2024 |
| 718 | Lonza Portsmouth, NH Biotechnologist Level 1 - Cell Therapy A.S., B.S., or vocational certificate in relevant STEM field is a plus. Exp: 1+ years |
Shift Schedule: The shift schedule is from 7am-7pm, on a rotational schedule every other week: Week 1: M/T/F/SAT/SUN Week 2: W/TH Shift differentials are included for weekends worked Initial 2 week training period on day shift Monday-Friday upon hire for new hires The Cell & Gene Therapy Biotechnologist/Manufacturing Associate will help to provide a safe, controlled work environment in all areas of expertise. Be aware of the site safety objectives and make sure they are communicated and understood. Biotechnologist/Manufacturing Associates will be proficient in an assigned area (i.e. Cell Growth, Drug Product Filling, etc.) and work in a team environment during manufacturing operations (i.e. harvest, fill/finish, visual inspection, etc.). | 2/5/2024 |
| 719 | Loop Genomics San Diego, CA Research Associate, Surface Chemistry Bachelor’s degree in chemistry, materials science, biochemistry, bioengineering, physics, or similar fields. Exp: 0-2 years |
We are seeking a Research Associate, who has a curious mind and a great desire to learn new techniques in new areas of study to join our interdisciplinary research team. You will be learning experiment design pertaining to surface coating characterization assays, explore optimal surface coating process and support custom surface production needs. The preferred candidate will have scientific research lab experience, demonstrated by any combination of prior curricular, extracurricular undergraduate research lab work, scientific paper, poster, or presentations. | 2/5/2024 |
| 720 | LSI Solutions Victor, NY Manufacturing Engineer - 8:00AM to 5:00PM Level I: BS Engineering or Engineering Technology; or Level II: MS. Exp: Level I: 0-2 years; Level II: 1 to 5 years |
The Manufacturing Engineer is responsible for developing and improving manufacturing processes. They design and refine production equipment and processes to improve capability, enhance productivity, reduce waste, reduce risk, and elevate overall product quality. Manufacturing Engineers introduce new technologies, perform root cause analysis, implement corrective actions, and leverage problem solving skills and equipment expertise to support ongoing production. | 2/5/2024 |
| 721 | Lumen Bioscience Seattle, WA Lab Technician, Physiology BA/BS degree in molecular biology, microbiology, biochemistry, chemistry, biotechnology, biochemical engineering, or related field of study Exp: 1-3 years |
Lumen is seeking a highly motivated, innovative Lab Technician to join our team. The Laboratory Technician will support scientists in the Physiology research and development group. The work will involve several projects aimed at culturing Lumen’s spirulina-based platform organism. The individual will be focused on operating bioreactors under various run conditions and analyzing samples. The candidate is also expected to independently perform and learn new laboratory techniques, use specialized laboratory instruments, perform delicate manual procedures, follow and apply standard laboratory protocols and provide reliable, independent, and versatile support to biotechnology research. The position requires strong organizational skills and meticulous laboratory record keeping. Effective communication skills are crucial in coordinating with Lumen’s research and production scientists, in providing status updates, and in raising quality or troubleshooting issues as they may arise. | 2/5/2024 |
| 722 | Lumen Bioscience Seattle, WA Lab Technician, Clinical B.S. in immunology, biochemistry, cell biology, microbiology, or related field of study. Exp: one year |
Lumen Bioscience Clinical Program Management is seeking a laboratory technician with clinical research laboratory experience. Working with scientists, the technician will support assay development efforts across multiple active clinical projects. The position also involves coordinating assay development internally with Lumen’s research, manufacturing, and quality teams. The technician will support equipment and supply requisition and inventory. In addition, the technician will maintain the clinical specimen archive. The position requires strong communication skills and an empathic understanding of where others are experiencing issues. Efficient problem-solving are crucial to keep pace with our growing company. Personal initiative and organizational skills will drive your career growth. | 2/5/2024 |
| 723 | Luminex Madison, WI Design Assurance Engineer Bachelor's Degree Bachelor degree required, in a life science/engineering discipline required. Exp: 1+ Years |
The Design Assurance Engineer acts as the quality representative on design core teams for electromechanical instruments, reagents and assays for the life science and in-vitro diagnostics market. Design Assurance Engineer is responsible for guiding the development teams through the Design Control process ensuring compliance with FDA, ISO, QSR, quality, safety and environmental regulations and internal procedures. The Design Assurance Engineer may also provide support for quality initiatives, post market design changes/improvements and quality surveillance activities. | 2/5/2024 |
| 724 | Luminex Northbrook, IL Manufacturing Associate I, Microarray Associate's Degree in Chemistry, Life Sciences, Biotechnology, or Medical Technology related fields required. Exp: 1+ Years |
Delivering manufacturing requirements against production schedule within a focused manufacturing operation and/or product segment. Work schedule may include alternate shifts. Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System. | 2/5/2024 |
| 725 | Luminex Cypress, CA Cell Culture Technician II Requires Bachelor’s Degree in Biology or related field or equivalent experience. Exp: 1+ Years |
Responsible for manufacturing and assembly of clinical and commercial products. Operates production equipment. Weighs, measures and checks raw materials to assure batches manufactured contain proper ingredients and quantities. Performs Cell Culture activities using aseptic technique. Maintains records and laboratory environment to comply with regulatory requirements, Good Manufacturing Practices and Standard Operating Procedures. Assist with in-process testing to assure batches meet specifications. Assignments are moderately complex in nature where judgment is required in resolving problems and making routine recommendations. Supports all applicable regulations including but not limited to FDA, ISO, and CMD/CAS requirements. | 2/5/2024 |
| 726 | Luminex Stillwater, MN Process Scientist I Bachelor's or Master's degree in Chemistry, Biology, Medical Technology or related science field. Exp: 1+ years |
This position is responsible for material processing, reagent formulation, technical manufacturing, in-process and final quality control of reagents, components and in-vitro diagnostic products. | 2/5/2024 |
| 727 | Luminex Stillwater, MN Engineering Technician BS in Engineering Exp: 1-2 years |
As an Equipment Technician, you will be an administrator and expert of the equipment used in the manufacture of in vitro diagnostic products. In addition, you will drive operational improvement activities that involve equipment procurement, validation, or the transfer of information from equipment. This is a fast-paced, deadline-driven department that provides centralized support to the organization. Be a Subject Matter Experts (SME) for equipment and equipment validations to implement changes to business systems and processes, interacting and working collaboratively with teams across Diasorin. | 2/5/2024 |
| 728 | Horizon Therapeutics Thousand Oaks, CA Engineer Master’s degree in Engineering Exp: 0 - 2 years |
Let’s do this! Let’s change the world! In this dynamic role you will serve as the system owner for process equipment in a state of the art bulk biopharmaceutical manufacturing facility. | 2/7/2024 |
| 729 | Horizon Therapeutics Holly Springs, NC Engineer - Plant Utilities Master’s Degree in Chemical or Mechanical Engineering Exp: 0 - 2 years |
Let’s do this! Let’s change the world! The Engineer System Owner will be joining the Facilities & Engineering (F&E) group to partner closely with the corporate engineering team to design, build, commission, and qualify new equipment and systems needed for drug substance production, as well as developing subject matter expertise to support operations upon start up. | 2/7/2024 |
| 730 | HRA Pharma Covington, OH Microbiologist I - Nights A four-year college degree in Microbiology or Biological Science. Exp: One years |
Perrigo Nutritionals, located in Covington, OH is looking to add a Night shift Microbiologist to their team. The hours for this position are, 6pm - 6am working a rotating 2/2/3 schedule Scope of the Role The successful candidate will be able to work in a safe and efficient manner in accordance with current GLP’s, SOP’s, analytical methods, and work instructions. Excellent communication skills, attention to detail, and the ability to work both independently and as part of a team are desired. A thorough understanding of aseptic technique is essential. Microbiological testing is performed on raw materials, in-process samples, finished products, water samples, and environmental swab samples. | 2/7/2024 |
| 731 | HRA Pharma Georgia, VT Chemistry Analyst I - 2nd Four-year college degree in chemistry or related science. Exp: 1-2 years |
The incumbent performs a variety of standard analyses on raw material, in-process, and finished product samples using chemical analysis techniques, according to compendia (i.e. USP, FCC, or AOAC) or Perrigo methodologies. Performs routine analyses of raw material and finished product samples as assigned, demonstrates proficiency in 5 – 10 separate Analytical Methods (AM’s). Analytical instrumentation used in this group is primarily NMR Fat Analyzer, Nitrogen Analyzer, NIR Spectroscopy, and HPLC (High Pressure Liquid Chromatography). | 2/7/2024 |
| 732 | ICU Medical Austin, TX Chemistry Analyst I - Night Shift - (24300022) Bachelor’s Degree is required: Chemistry, Chemical Engineering, or Chemical Science. Exp: 0-2 year |
The Chemistry Analyst I will work under direct supervision or be partnered with an experienced analyst to perform wet chemistry analyses, preparation of reagents, standardization of solutions, and instrumentation testing and documentation in a cGMP environment. May be cross-trained to work in other laboratory areas as dictated by the needs of the department. | 2/7/2024 |
| 733 | Integrated DNA Technologies Coralville, IA Technician II Associate’s (2 year) degree. Bachelor’s (4 year) degree preferred. Science related field preferred. Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Sunday – Thursday 3:00PM – Midnight | 2/7/2024 |
| 734 | Integrated DNA Technologies Coralville, IA Job Posting Title Technician II (Synthesis -Long Oligo) Associate or bachelor’s degree in a Science related field preferred. Exp: 12 months |
This position is part Shipping, Receiving and Distribution department of the located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Monday-Thursday 9:00pm-7:30am | 2/7/2024 |
| 735 | Integrated DNA Technologies Coralville, IA Technician II (Synthesis - MNP) Associate or bachelor’s degree in a Science related field preferred. Exp: 12 months |
This position is part Shipping, Receiving and Distribution department of the located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Wednesday -Friday 7PM-7AM. | 2/7/2024 |
| 736 | Integrated DNA Technologies Coralville, IA Technician II, Stock Product Associate’s (2 year) degree or comparable combination of education and experience required. Bachelor’s (4 year) degree preferred. Science related fi Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Sunday – Thursday 3:00PM – Midnight | 2/7/2024 |
| 737 | Integrated DNA Technologies Coralville, IA Technician II (Formulation - GMP) - Overnight Associate’s (2 year) degree or comparable combination of education and experience required. Bachelor’s (4 year) degree preferred. Science related fi Exp: 1+ years |
This position is part of the Production department located in Coralville, IA and will be on-site. At IDT, we are one global team. We celebrate our differences, engage in healthy debate, and are inclusive. Together, we accomplish great things. Shift: Weekday Overnight; Monday – Thursday 8:30pm-7:00am | 2/7/2024 |
| 738 | Illumina San Diego, CA Scientist 1: Assay Product Development BS/MS in Biochemistry, Molecular Biology, Chemistry, Biology, Bioengineering, or related disciplines. Exp: 1-2 years |
We are looking for a contract Scientist 1 to join the assay development team within Illumina Product Development. This person will be contributing to new technologies and workflows for Illumina customers as part of a collaborative team. This is a hands-on position where you will primarily be responsible for the design, execution, and analysis of experiments to support assay development and optimization. | 2/7/2024 |
| 739 | Lyophilization Services of New England Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 2/8/2024 |
| 740 | Lyophilization Services of New England Madison, WI QC Chemist I Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study. Exp: 0-3 years |
The QC Chemist I will have responsibility to support various activities in the Quality Control Laboratory. This includes testing the following sample types R&D, in-process, finished product, stability, as well as raw materials. Job duties may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management | 2/8/2024 |
| 741 | Lyophilization Services of New England Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 2/8/2024 |
| 742 | Maverick Therapeutics Social Circle, GA Manufacturing Technician II AA or higher. Exp: 1+ years |
As a Manufacturing Tech II, you will execute all processes in production while strictly following cGMP, environmental health and safety guidelines and any other related regulations which could apply. In addition to making routine revisions to documents, you may rewrite complex procedures or initiate new procedures as applicable. You will have enough applied technical knowledge to perform complex trouble shooting tasks and may even assist during the transfer of new technologies into manufacturing. You will have technical and administrative competence to organize and lead production activities, including demonstrating leadership in cGMP compliance, and environmental health and safety skills. You will report to Manufacturing Supervisor. | 2/9/2024 |
| 743 | Maverick Therapeutics Thousand Oaks, CA Manufacturing Associate - Day Bachelor's degree preferred. Exp: 0-2 years |
Under the general direction of the Manufacturing Lead and overall direction of the Supervisor, the Manufacturing Associate executes all processes in the production area while strictly adhering to CGMP, environmental health and safety guidelines and any other related regulations. | 2/9/2024 |
| 744 | Maverick Therapeutics Round Lake Beach, IL Manufacturing Technician II AA or higher. Exp: 1+ years |
As a Manufacturing Technician II, you will implement all processes in production while strictly following cGMP, environmental health and safety guidelines and any applicable related regulations. You will have technical and administrative competence to organize and lead production activities. You will participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include assisting with the movement of Flexbumin between the different stages of inspection to packaging within the value stream. You may act as line lead, and will ensure the line operates smoothly and keeps up with daily goals. You will also document your process activities on routers or in the electronic batch management system (EBM). You will report to the Supervisor, Manufacturing. | 2/9/2024 |
| 745 | Maverick Therapeutics Thousand Oaks, CA Manufacturing Associate - Night Shift Bachelor's degree preferred. Exp: 0-2 years |
Under the general direction of the Manufacturing Lead and overall direction of the Supervisor, the Manufacturing Associate executes all processes in the production area while strictly adhering to CGMP, environmental health and safety guidelines and any other related regulations. This position is a night shift role. | 2/9/2024 |
| 746 | Medtronic Cherry Hill, MA Microbiologist II Bachelors degree required. Exp: one year |
Responsibilities may include the following and other duties may be assigned. Interacts with Purchasing and Contract Sterilization/Test Facilities to ensure that the Sterilization requirements and product testing procedures are clear, complete and understood. Works with the internal personnel as well as with the Contract Sterilization and Test facilities to establish specifications and coordinates the new product sterilization validations as well as the quarterly validations. Work with different Subject Matter Expert to evaluate changes impacting the product families, controlled rooms and critical systems. Coordinates yearly and quarterly product re-verifications (Irradiation & Ethylene Oxide)Coordinate lethality testing for EO product, or process qualifications Product Release (EO & Gamma) Develop and Coordinate Steam Sterilization Studies Develop and Coordinate Reusable Device Validation (Cleaning Studies) Develop and Coordinate Profiling Protocols | 2/9/2024 |
| 747 | Medtronic Northridge, CA Biomedical Engineer II Masters of Science in Biomedical Engineering, Chemical Engineering, or related disciplines. Exp: 0+ years |
As a member of the Medtronic Diabetes – Continuous Glucose Monitoring Sensor R&D team this Product Development Engineer II will support the development of next generation CGM products. This position will play a key role in the early stage development of various new/improved chemistry layers/coatings of glucose sensors by designing and executing design optimization and characterization studies in preclinical & clinical studies. The role includes process development for feasibility clinical manufacturing. To this end, you will be responsible for driving the product build documentation, coordinating the fabrication & builds of prototype sensors for benchtop, preclinical and clinical evaluations, execute data trending & statistical process analysis. Upon successful proof-of-concept through feasibility studies, this role will subsequently support tech transfer to process & manufacturing teams. You will manage deliverables for multiple projects and maintain an effective system for tracking progress. You will be interfacing with Managers, Engineers &Technicians in R&D and New Product Introduction (NPI) Operations teams as well as Quality and Clinical groups to accomplish day to day activities. The candidate must have strong organizational skills, attention to details, an analytical mindset and ability to communicate effectively with multiple stakeholders. | 2/9/2024 |
| 748 | Medtronic Bedford, MA Quality Engineer II Advanced degree in related engineering discipline required (Biomedical, mechanical, manufacturing, etc.). Exp: 0 years |
In this exciting role as a Quality Engineer II in the Bedford/Billerica facilities, you will have responsibility for supporting the quality and daily manufacturing of high-quality and complex catheters to support the Cardiac Ablation Solutions Business. In this role you will be part of a team that grows the operations capacity over 8X to support our customer needs in this newly acquired product portfolio. You will lead improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies. | 2/9/2024 |
| 749 | Medtronic Billerica, MA Manufacturing Engineer II Advanced degree. Exp: 0 years |
Responsibilities may include the following and other duties may be assigned. Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. | 2/9/2024 |
| 750 | Genentech Hillsboro, OR MANUFACTURING ASSET ENGINEER I/II, HTO B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 0-2 years’ |
The Asset Engineer I/II is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 1/25/2024 |
| 751 | Genentech Hillsboro, OR MANUFACTURING TECHNICIAN (CONTRACTOR) Graduate of a two-year Associates Degree program in Electrical/Mechanical Technology (or equivalent) is a plus. Exp: 1 to 2 years (within the last 7 years) |
Under the direction of the Process Unit Lead, perform a wide variety of tasks and operations that are required to formulate, fill, inspect and package sterile pharmaceutical products in a state-of-the-art, automated production and packaging facility. Troubleshoot, maintain, assemble, install, and repair all electronic, mechanical, and instrumentation devices on production equipment as required. Assist on major equipment overhauls, repairs, and installations as necessary. All operations carried out in compliance with cGMPs, Standard Operating Procedures (SOPs), product recipes, and Genentech standards. Duration: 6-month contract with possible extensions up to 3 years Day Shift, 6:00 am – 6:30 pm, Sunday -Tuesday plus every other Wednesday Day Shift, 6:00 am – 6:30 pm, Thursday -Saturday plus every other Wednesday Day Shift, 5:30 am - 4:00 pm, Monday - Thursday Swing Shift, 12:00 pm -10:30 pm Monday - Thursday Night Shift, 6:00 pm -6:30 am, Sunday-Tuesday plus every other Saturday Night Shift, 6:00 pm – 6:30 am, Wednesday – Friday plus every other Saturday | 1/25/2024 |
| 752 | Genentech Hillsboro, OR MANUFACTURING ASSET ENGINEER I, HTO (TWO YEAR TERM) B.S or higher in Mechanical Engineering, Electrical, Chemical, Biochemical, or related discipline. Exp: 1-2 years’ |
The Asset Engineer is responsible for supporting the design, operation, control and optimization of manufacturing equipment at HTO. The position serves as the equipment owner and is engaged in development, qualification, data analysis, troubleshooting, and continuous improvement activities. The Asset Engineer plays a key role in day-to-day operations, as well as design and delivery of local and major capital projects, and interacts with a cross-functional team to deliver on business objectives. | 1/25/2024 |
| 753 | Genentech Vacaville, CA MANUFACTURING TECHNICIAN-BIOPROCESS (CONTRACTOR) Desirable but not required: AS/BS/BA in Biological Sciences, Physical Sciences. Exp: 1+ years |
As a Manufacturing Technician, you will be responsible for producing innovative bio-therapeutic medicine by interfacing with highly automated production systems and controls in a current Good Manufacturing Practices (cGMP) environment. You will maintain areas in a high state of inspection preparedness and will utilize business systems for inventory and process management. You will maintain records to comply with regulatory requirements utilizing cGMP and Standard Operating Procedures (SOPs) and will participate in the routine production of mammalian cell culture products within the Vacaville Manufacturing Facility, operating in at least one of the following production areas: Upstream Manufacturing (UM): Primary focus is the cleaning, sterilization and operation of fixed vessel systems for media preparation, fermentation, and harvest operations; perform seed train operations; perform dispensing of components; handle and aliquot hazardous materials. Downstream Manufacturing (DM): Responsibilities include the operation and cleaning of fixed tank systems, the operation and cleaning of filtration systems, large-scale buffer preparation, and the operation of column chromatography systems; perform dispensing of components; handle and aliquot hazardous materials | 1/25/2024 |
| 754 | Genentech Oceanside, CA BIOPROCESS MANUFACTURING TECHNICIAN (CONTRACT) Preferred - Degree in Life Sciences/Engineering, Associate’s or Biotech certificate from approved program. Exp: 1+ years |
At Genentech, we are dedicated to pursuing groundbreaking science to discover and develop medicines for people with serious and life-threatening diseases. As a Bioprocess Manufacturing Technician, you will be responsible for producing medicine in a highly automated and controlled environment. Each product has a specific recipe; you will follow this recipe, along with the standard operating procedures, to operate the production equipment across various areas, including raw material dispensing/aliquoting, cell culture and purification. You will maintain records and follow all the steps necessary to comply with regulatory requirements within a current Good Manufacturing Practices (cGMP) environment. This is a contract role with the possibility of conversion to a permanent employee position. | 1/25/2024 |
| 755 | Genentech Oceanside, CA ENGINEER I Bachelor's or Master's degree in Engineering or Life Sciences. Exp: 0-4 years |
Responsible for supporting operations in the Oceanside Pilot Plant and Process Engineering Purification/Analytical Lab. Deliverables include but are not limited to: HPLC-based analytics, rapid bioburden/endotoxin, lab scale and pilot scale chromatography, UFDF operations, buffer prep, column packing, equipment maintenance and preparation of technical reports. May commission new equipment, troubleshoot equipment and systems, develop new equipment requirements and operating parameters, and provide factory and site acceptance testing. Provide scientific and technical support to GMP Manufacturing Operations in a multi-product, large scale, automated biopharmaceutical facility. Support process validation through large and small-scale studies, protocol and report preparation, validation sampling, and sample shipments. | 1/25/2024 |
| 756 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Chemist I Bachelor’s degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology). Exp: 1-3 years |
The Quality Control Chemist is responsible for supporting quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include, but are not limited to, providing general laboratory support for raw material, in-process, stability, and finished product testing. | 1/25/2024 |
| 757 | Grand River Aseptic Manufacturing Grand Rapids, MI QC Lab Technician Bachelor’s degree in a related field (Biochemistry, Biotechnology, etc.). Exp: 0-2 years’ |
The QC Lab Technician supports quality systems as they relate to the manufacturing and testing of cGMP drug products. These duties will include but are not limited to providing general laboratory support for sampling of raw material, incoming stability and finished product sample processing, basic physical testing, and inventory administration. | 1/25/2024 |
| 758 | Grand River Aseptic Manufacturing Grand Rapids, MI Aseptic Manufacturing Associate (2nd and 3rd shifts) Bachelor’s degree, or equivalent experience. Exp: 0-1 year |
The Aseptic Manufacturing Associate (AMA) is responsible for performing various routine manufacturing tasks following established procedures and cGMP regulations under guidance of a production supervisor and/or senior management. | 1/25/2024 |
| 759 | GreenLight Biosciences Rochester, NY Bioprocess Technician 4-year degree in Chemistry, Biochemistry, Biotechnology, Chemical Engineering. Exp: 1+ years |
GreenLight Biosciences is seeking a highly motivated Bioprocess Technician with education/experience in biotechnology, microbiology and biochemistry process operations at development scale. The successful candidate will become a member of the Rochester, NY pilot plant team and support their overall mission of delivering high performance RNA production processes and products to the market. Exact level dependent on qualifications including relevant experience. | 1/25/2024 |
| 760 | Grifols Clayton, NC Utilities Project Engineer Bachelor's Degree in Engineering or related field. Exp: Engineer I: 0 years |
The Utilities Project Engineer will be responsible for the oversight of utilities projects for an industry leading biological therapeutic product manufacturer, Grifols as a member of the Facilities NA Project Engineering Team. The position will be stationed in Clayton, NC and will oversee Grifols projects on the east coast of the United States primarily, with the potential to oversee projects at other North American sites. Projects will include installation of clean and dirty utilities such as refrigeration systems, chillers, cooling towers, boilers, water purification systems, steam systems, waste systems, pumped distribution systems, and others, with some civil/structural oversight. Candidate should have a good understanding of the theory behind these types of systems as some system design and design reviews will be required. Candidate, through experience, should have knowledge of industry standards and best practices for utilities systems. Candidate must be willing to adjust working hours to meet the needs of the project(s), including some weekend work when required to match the schedule of project crafts. Some travel will be required - up to 25%. The position has the potential to progress into an engineering role / management role of increasing responsibility. | 1/25/2024 |
| 761 | Grifols Vista, CA Manufacturing Technician Associates Degree or Bachelor’s degree preferred. Exp: 1-2 years’ |
Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 1/25/2024 |
| 762 | Grifols Vista, CA Manufacturing Technician Associates Degree or Bachelor’s degree preferred. Exp: 1-2 years’ |
Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The Tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. | 1/25/2024 |
| 763 | Grifols Los Angeles, CA QC Chemist Bachelor’s degree in Chemistry, Biochemistry, Biology or closely related scientific discipline is required. Exp: 1+ years |
The QC Chemist is responsible for performing routine and non-routine chemical and biochemical assays on protein-based therapeutics and raw materials. | 1/25/2024 |
| 764 | Grifols Clayton, NC Quality Control Assistant/Associate Materials Eval. Coord. Associates degree with an emphasis in sciences or mathematics. Exp: one year |
Location: Clayton NC Shift: M-F 8am - 4:30pm The Quality Control Assistant/Associate Materials Evaluation Coordinator evaluates critical quality attributes (visual, dimensional, functional), coordinates required chemical and/or biological testing, and executes approved usage decisions on all quality managed material used at the facility. These evaluations are performed on a wide variety of materials including, but not limited to, chemicals, labeling components, primary drug container components, process hoses, sterilizing filters, and other critical raw materials. This is done by verifying compliance to specifications and testing requirements and ensuring required documentation is complete and accurate thus minimizing the possibility that the safety and efficacy of final products manufactured and tested using these quality managed materials is compromised or adulterated. The Coordinators perform the last detailed review of these materials prior to release for use thus sound judgment is essential. The QC Assistant/Associate Materials Evaluation Coordinator inspects product final container reserve samples according to approved standard operating procedures. The QC Assistant/Associate Materials Evaluation Coordinator may perform in the warehouse as a Quality representative for sampling, auditing, and making Quality decisions. In this area, the QC Assistant/Associate Materials Evaluation Coordinator audits raw material batches using designated ANSI sampling plans. Decisions made by QC Coordinators have major compliance and monetary implications for Grifols | 1/25/2024 |
| 765 | GRO Biosciences Cambridge, MA RA/Senior RA, Application Sciences BS degree. Exp: 1 year |
We’re seeking an RA or a Senior RA with synthetic chemistry, protein biochemistry, and/or glycobiology experience who’s interested in learning new things, “wearing many hats”, and having a large impact on the growth of an early-stage company. Major responsibilities include experimental design, experiment execution, data analysis, and collaborating across a matrixed research team. Ideal candidates are collegiate, transparent, data-driven, motivated by novel challenges, and will think critically yet creatively about the company’s strategies for therapeutic development. | 1/25/2024 |
| 766 | GlaxoSmithKline Marietta, PA Process Equipment Engineer BS Degree in engineering. Exp: 1 or more years |
Are you looking for an engineering role that allows you to leverage your technical knowledge in a state-of-the-art manufacturing environment? If so, this Process Equipment Engineer role could be an ideal opportunity to explore. The Process Equipment Engineer supports primary (bulk) vaccine adjuvant manufacturing in a 24/7 production facility as part of an Engineering and Maintenance Team. The team is responsible for maintaining equipment in a state of readiness through routine preventive maintenance and upgrades to extend its useful life. The Process Equipment Engineer will also lead continuous improvement projects to achieve Safety, Quality and Commercial objectives. As system experts, Engineers are relied upon to lead technical investigation impacting manufacturing processes | 1/25/2024 |
| 767 | GlaxoSmithKline King of Prussia, PA Automation Engineer BS/BA in engineering, life sciences, biology or equivalent technical discipline. Exp: 3+ months |
As an Automation Engineer, you will provide engineering and technical support for process controls and manufacturing execution systems in the Biopharmaceutical Operations facility. Evaluate and develop technology, plan and implement modifications, troubleshoot and support process controls and manufacturing execution systems | 1/25/2024 |
| 768 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 769 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Wed - Sat 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 770 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Sun - Wed 7am - 5:30pm) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 771 | Gyroscope Therapeutics Morris Plains, NJ Associate Scientist (Hours: Sun - Wed 2:30pm - 1:00am) BA or MS in chemistry, biochemistry, microbiology, or other related science. Exp: 0 - 5 years |
Under general direction, perform testing and other activities in functions supporting the Quality Control department (Micro/EM, QC Bio-assay, and raw materials, as appropriate). | 1/26/2024 |
| 772 | Gyroscope Therapeutics Morris Plains, NJ Cell Processing Specialist I (Tuesday-Saturday am shift) Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline. Exp: 0 - 1+ years |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. Cell Processing Specialist I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 1/26/2024 |
| 773 | Gyroscope Therapeutics Durham, NC BioProcess Engineer I - Upstream (2-2-3 rotation day shift) Bachelor of Science Degree in Biology, Chemistry, Biotechnology or applicable field. Exp: Entry level |
The BioProcess Engineer I is responsible for assisting with organizing, running, and sustaining the manufacturing operations process at the plant/site. | 1/26/2024 |
| 774 | Gyroscope Therapeutics Morris Plains, NJ Cell Processing Specialist I Sun-Thurs. PM shift) Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline. Exp: 1 - 1+ years |
The Cell Processing Specialist is responsible for cell washing operations and verifying cell processing intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. Cell Processing Specialist I will also be responsible for the formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. | 1/26/2024 |
| 775 | HelixBind Boxborough, MA Research Associate BS in a Physical or Life Sciences/Engineering discipline. Exp: 1+ years |
We are seeking a talented and motivated individual to join our R&D Team as a Research Associate. The position offers the exciting opportunity to grow along with the Company as it takes its initial product through to FDA clearance and market launch while it, in parallel, grows its pipeline of impactful syndromic diagnostic assays. This is a great time to join the team, with plenty of opportunities to grow and lead new projects. | 1/26/2024 |
| 776 | Helmer Scientific Noblesville, IN Electromechanical Engineer I BS degree in Engineering or Engineering Technology. Exp: 0-5 years |
This role supports Helmer Scientific, part of Trane Technologies Life Sciences Portfolio. Helmer Scientific designs, integrates, manufactures, markets, and distributes specialized medical and laboratory equipment to clinical and life science customers in over 125 countries, as well as provide after-market service and support. Provides electromechanical engineering support to Engineering department through the development, documentation and production support for Helmer product development. Develop specs for mechanical and electrical engineering requirements based on directions given by Manager. Have fundamental knowledge from educational background, while tasks are managed or directed by others | 1/26/2024 |
| 777 | Heska Mississauga, On Temporary-Laboratory Generalist 1 - (Overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. Shift: Monday - Friday 11pm - 7:30am Saturday on rotation | 1/26/2024 |
| 778 | Heska West Palm, FL Stat Lab - Lab Generalist I Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
HOURS: The hours for this position are Monday - Friday from about 12:30pm - 6:30pm. PURPOSE OF JOB: Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. | 1/26/2024 |
| 779 | Heska Chantilly, VA Lab Generalist I (overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. Shift: Monday - Friday 11:30pm - 8:00am Alternating Saturdays 10:00pm - 7:00am Includes night shift differential. ESSENTIAL DUTIES AND RESPONSIBILITIES: | 1/26/2024 |
| 780 | Heska Irving, TX Lab Generalist I (Overnight) Associates/Bachelor’s Degree in Science related field or Veterinary Technician. Exp: 1 year |
Receives and prepares samples for laboratory analysis and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. May perform a variety of client service activities for internal and external stakeholders. | 1/26/2024 |
| 781 | Heska Mississauga, O Microbiology Technician I(Day Shift)Temporary 4 year degree in Science-related field preferred. Exp: 6 months |
The Microbiology Laboratory Technician I performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. Shift: Monday - Friday 9:00am - 5:30pm. Weekends would be on rotation. | 1/26/2024 |
| 782 | Heska Oak Brook, IL Parasitology Technician 2, 3 or 4 year degree in Science-related field. Exp: 6 months |
The Parasitology Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. | 1/26/2024 |
| 783 | Heska Atlanta, GA Parasitology Technician - Day Shift 2, 3 or 4 year degree in Science-related field. Exp: 6 months |
The Parasitology Laboratory Technician performs laboratory analyses and tests. Prepares samples, sets up instruments, runs tests and reads, interprets and releases results. SHIFT: Monday-Saturday 8am-430pm | 1/26/2024 |
| 784 | Hikma Cherry Hill, NJ Chemical Process Operator I - 3rd Shift Associates Degree in Science or equivalent Exp: 1-year |
Using company procedures and guidelines, the Chemical Process Operator I is responsible for a limited spectrum of duties within the department. This may include weighing, mixing, equipment cleaning, tank cleaning, tank movement and PM activities, etc. This job has no supervisory responsibilities; however, the ability to assume higher level responsibilities and/or have demonstrated leadership abilities is preferred. | 1/26/2024 |
| 785 | Hillrom Marion, NC Quality Lab Associate I - Bioburden (3rd Shift: M-Thu) B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 1/26/2024 |
| 786 | Hillrom Plymouth, MN Engineer I - R&D Disposables (Hybrid) BS in Mechanical, Plastics, Biomedical Engineering or a related field, MS preferred. Exp: 0 - 1 year |
Document engineering concepts. Create, modify, and maintain design documentation per company procedures. Assist in the design and building of basic tooling, test fixtures and assembly equipment. Build prototypes and models and may operate machine tools. Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies. Write technical reports based on design verification analysis/testing for design changes and product design activities. Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis. Identify, investigate, and solve engineering problems. | 1/26/2024 |
| 787 | Hillrom Marion, NC Quality Associate l (2nd shift:3pm-11pm) Bachelor's degree strongly preferred. Degree in engineering or life science preferred. Exp: 1+ years |
Responsible for working with the manufacturing departments to address defects with the finished products. | 1/26/2024 |
| 788 | Hillrom Marion, NC Quality Lab Associate I- Bioburden (5th Shift- 6AM to 6PM) B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Conduct microbiological analysis on raw materials, solution, and components following approved Standard Operating Procedures in an accurate and timely manner. | 1/26/2024 |
| 789 | Hillrom Saint Paul, MN Manufacturing Engineer I B.S. degree in Engineering or Science (Biomedical Engineer, Chemical Engineer, Mechanical Engineer, Electromechanical). Exp: 1+ years |
As a member of St. Paul's Engineering team, the Manufacturing Engineer supports daily initiatives from manufacturing teams to equipment to integrate new products within production goals (i.e., quality, delivery, cost, productivity, and safety). In this role you will support engineering improvement projects, participate in R&D activities, support key development and continuous engineering projects, drive KPI implementation and follow up. | 1/26/2024 |
| 790 | Companion Medical Danvers, MA Microbiologist II Bachelors degree required. Exp: 1-2 years |
Responsibilities may include the following and other duties may be assigned. Interacts with Purchasing and Contract Sterilization/Test Facilities to ensure that the Sterilization requirements and product testing procedures are clear, complete and understood. Works with the internal personnel as well as with the Contract Sterilization and Test facilities to establish specifications and coordinates the new product sterilization validations as well as the quarterly validations. Work with different Subject Matter Expert to evaluate changes impacting the product families, controlled rooms and critical systems. Coordinates yearly and quarterly product re-verifications (Irradiation & Ethylene Oxide)Coordinate lethality testing for EO product, or process qualifications Product Release (EO & Gamma) Develop and Coordinate Steam Sterilization Studies Develop and Coordinate Reusable Device Validation (Cleaning Studies) Develop and Coordinate Profiling Protocols Develop Equipment Validations (steam, dry heat, incubators Documentation of all test procedures and validations Provide guidance to other non-exempt personnel within/outside the department | 1/18/2024 |
| 791 | Companion Medical Bedford, MA Quality Engineer I Bachelors degree required. Exp: 0 years |
In this exciting role as a Quality Engineer I in the Bedford/Billerica facilities, you will have responsibility for supporting the quality and daily manufacturing of high-quality and complex catheters to support the Cardiac Ablation Solutions Business. In this role you will be part of a team that grows the operations capacity over 8X to support our customer needs in this newly acquired product portfolio. You will lead improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies. | 1/18/2024 |
| 792 | Companion Medical Rice Creek, MN Quality Engineer I Bachelors degree required. Exp: 0 years |
In this exciting role, the Quality Engineer I will have responsibility for products built at Rice Creek Pharma Operations manufacturing site. Manufacturing Platform East employs the full breadth of our talent, technologies, products, services, and solutions to address the needs of customers and patients across the globe. The Manufacturing East Platform offers devices and therapies to treat abnormal heart rhythms, as well as cardiac diagnostic and monitoring solutions. Rice Creek Pharma Operations, or Fridley, offers devices within the defibrillation solutions, surgical infection control, and diabetes management portfolios. | 1/18/2024 |
| 793 | Companion Medical Rice Creek, MN Software Engineer I Bachelors degree required. Exp: 0 years |
We are currently seeking a passionate Software Engineer I to join our Advanced Manufacturing Engineer (AME) Team. The Software Engineer I will support the design, development, and validation of Non-Product Software to support the automation and software integration operations for the development and commercialization of new combination devices (device/drug) | 1/18/2024 |
| 794 | Companion Medical Plymouth, MN Manufacturing Engineer I Bachelors degree required. Exp: 0 years |
Engineers are indispensable to achieving our Mission. That’s why we empower you to bring the best of your experience to bear on our market-leading portfolio of innovations. Apply your existing skills and develop new ones, with the training, mentorship, and the guidance you need to continue to develop your expertise. Today, we’re partnering across the industry to confront systemic healthcare challenges – this requires bold leadership. If you want a challenging, energizing, rewarding career that changes lives, join us. We are currently hiring a Manufacturing Engineer I at our Plymouth, MN site. Make an impact on your community and the lives of others by leading sustaining efforts of cutting-edge medical devices. This Engineer would be responsible for first shift technical support of Cardiac Surgery product such as mechanical heart valves. Cardiac surgery represents end-state treatment in the care continuum for many cardiovascular diseases. There are approximately 1.8 million cardiac surgical procedures in the world on an annual basis. Cardiac surgery remains extremely important in treating complex disease and remains the gold standard on which many of the other therapies being developed in Cardiovascular are based upon. | 1/18/2024 |
| 795 | Cook Biotech Winston Salem, NC Research and Development Engineer 2 Bachelor's degree in Engineering/Technology is required. Exp: 1-2 years |
The primary purpose of the Research and Development Engineer at Cook Winston-Salem is to design, test and technically document the feasibility, construction and production process of new and/or changed medical products. | 1/18/2024 |
| 796 | Cook Biotech Winston Salem, NC Research and Development Engineer 1 Minimum four year degree in Engineering/Technology. Exp: 0+ years |
The primary purpose of this position is to design, test and technically document the feasibility, construction and production process of new and/or changed medical products. | 1/18/2024 |
| 797 | Cook Biotech Bloomington, IN Manufacturing Engineer 1 Bachelor’s degree in Engineering or related field. Exp: 0 - 3+ years |
Responsible for providing technical support for the day-to-day production activities in the manufacture of custom, plastic components used in the assemblies of various medical devices. This is a hands-on position with visibility on the manufacturing floor and requires a high level of interaction with the production, product development, and quality teams. The engineer is responsible for supporting product development activities, continuous improvement, complaint resolution, CAPA investigations and other quality initiatives. | 1/19/2024 |
| 798 | CordenPharma Boulder, CO QC Analyst - Nights Bachelor's Degree (BA) from 4-year college or university. Exp: 0 - 1 year |
Performs all technician tasks accurately and efficiently without supervision. Initiates expert technical advice to customers and completes all tasks in the Technician Training Manual. Maintains a high level of housekeeping and attention to detail. | 1/19/2024 |
| 799 | Contract Pharmacal Hauppauge, NY Microbiologist; Quality Control Bachelor’s degree in a science related field. Exp: 1 - 9 years |
The Microbiologist is responsible for and has experience in performing microbial analysis for the QC Microbiology laboratory which is responsible for the analysis and disposition of commercial materials (raw materials, finished product release, stability, validation, investigation), and environmental samples, as assigned, and documenting results in accordance with SOPs. | 1/19/2024 |
| 800 | Contract Pharmacal Hauppauge, NY Scientist I; Analytical R&D Bachelor’s or Master’s degree in chemistry or analytical chemistry. Exp: 1-2 years |
Design and conduct routine laboratory analysis using various analytical instruments and software such as HPLC, UPLC, ICP, and UV-Vis. | 1/19/2024 |
| 801 | Contract Pharmacal Hauppauge, NY Lab Tech Associate degree. Exp: 1+ years |
The Laboratory Technician has primary responsibility for conducting basic routine lab analysis and maintaining all laboratory equipment, chemicals, and logbooks per CPC SOPs. | 1/19/2024 |
| 802 | Crown Bioscience San Diego, CA Research Associate I - Biomarker & Diagnostic Tech Bachelor of Science degree or above in biotechnology, cell biology, immunology, oncology or other related disciplines. Exp: one year |
The purpose of the Research Associate I position is to provide support on biomarker discovery studies to meet company's goals, objectives and quality standards. | 1/19/2024 |
| 803 | Crown Bioscience San Diego, CA Research Associate I - Cell Culture Technician Bachelor's degree in Biology, Biochemistry or related area. Exp: 1-2 years |
The purpose of the Research Associate I is to provide support with in vitro client studies and help with in vivo studies aligned with Company's goals, objectives and quality standards. | 1/19/2024 |
| 804 | Cyprotex Framingham, MA Research Assistant BA/MS or equivalent experience in a relevant Biological or Chemical scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro ADME/Tox assays and maintaining mammalian cells. Training opportunities will be provided for high throughput screening, mammalian cell culture and LC-MS/MS. Some cell culture and LC-MS experience are preferred. | 1/19/2024 |
| 805 | Cyprotex Framingham, MA Research Associate BS/ MS in a relevant bio scientific discipline. Exp: 0-2 years |
The team is looking for a highly motivated Research Associate and/or Research Assistant that will be responsible for routine screening of compounds in various in vitro toxicology assays. | 1/19/2024 |
| 806 | Cytovance Biologics Oklahoma City, OK AD Associate II MS in a life science field. Exp: 1+ years |
The AD Associate I/II position develops, optimizes, and qualifies analytical methods for biopharmaceutical products. The associate also supports drug development departments, such as Purification Department and Cell Culture Department, by performing analytical testing. | 1/19/2024 |
| 807 | DiaCarta Richmond, CA Research Associate Sc. degree in molecular biology or a related field OR S. degree in molecular biology or a related field. Exp: Sc.: 0-1 years; S.: 0-2 years |
DiaCarta is seeking a highly motivated, independent, and interactive Research Associate to join the R&D function in the company. The new team member will participate in R&D activities with the goal of developing and launching new qPCR, NGS, and branched DNA tests for IVD cancer diagnostics applications. The successful candidate will have outstanding attention to detail, enjoy working in a fast-paced multidisciplinary team environment, and have exceptional hands-on laboratory skills. DiaCarta is a rapidly growing company, so the candidate must be highly motivated and committed to launching their career in an innovative area of molecular diagnostics. This is a full-time role in Richmond, and you will be reporting to the Senior Scientist. | 1/19/2024 |
| 808 | DiscGenics Salt Lake City, UT Lab Calibration Technician Bachelors in Biological, Biochemical, or Chemistry related field. Exp: 1-2 years’ |
The Lab Calibration Technician is responsible for inspection, calibration, verification and maintenance of all laboratory equipment to meet established conformance standards. The Lab Calibration Technician will be responsible for performing routine maintenance according to the maintenance schedule or coordinating with external vendors or in-house experts to complete all tasks on time. The role may also be required to perform or coordinate non-routine repairs or calibration to ensure equipment is performing to internal standards. This role interacts with all levels of the organization in a collaborative and positive way with colleagues to facilitate department and organizational initiatives for cultural cohesion aligned to the DiscGenics Values. | 1/19/2024 |
| 809 | Distributed Bio Seattle, WA Research Associate I B.S. in either animal science or similar discipline preferred. Exp: 6-12 months |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings. | 1/19/2024 |
| 810 | Distributed Bio S. San Francisco, CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
In this role you will observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. You will handle routine handling, restraint, identification (including ear notching, tagging) and sexing of common laboratory animals. Ability to distinguish various common laboratory animal strains in accordance with standardized genetic nomenclature and phenotype identification. You will also perform technical functions required by research protocols such as assist with dilution and dosing calculations; dosing administrations (PO, SQ, IP, IM, and IV); blood collections (Submandibular, Cardiac); basic necropsy and tissue collection; tumor measurement and body weights. Assist Vet Techs and Veterinarians with follow-up checks, treatments and procedure if needed. Perform health surveillance sample collection procedures. Actively interact with research staff to provide technical assistance. | 1/19/2024 |
| 811 | Distributed Bio Spencerville, OH In Vivo Technician II Associate (A.A./A.S.) or Bachelor’s degree (B.A./B.S.). Exp: 6 months |
We are seeking an In Vivo Technician II for our In Vivo Team at our Safety Assessment site located in Spencerville, OH. A Technician II is performing basic tasks and procedures within a team. The technician is assigned to work on study, performing and becoming more efficient in tasks required of the department training plan which may include collecting and recording data with minimal supervision in the performance of studies. Responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. Administer test substances by various basic methods. The technician is usually working closely with a trainer or buddy but becoming more independent | 1/19/2024 |
| 812 | Distributed Bio Memphis, TN Biomanufacturing Technician I - Shift C Tuesday-Friday: 11:30am-10:00pm AS or BS in a scientific field strongly preferred. Exp: Zero to 1 year |
NOTE: This position is: Shift C: Tuesday thru Friday 11:30am - 10:00pm (Saturday, Sunday, Mondays off) The BioManufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to work night, weekends, and holidays. Must be able to meet physical requirements established in this job description. | 1/19/2024 |
| 813 | Distributed Bio Newark, DE Molecular Technologist-1 Sequencing Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred. Exp: 0-3 years |
Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE. This position is Monday - Friday 10:00am to 6:30pm. The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance. | 1/19/2024 |
| 814 | Distributed Bio Memphis, TN Biomanufacturing Technician I - Shift A Sun - Wed 7:30am - 6:00pm 1 AS or BS in a scientific field required. Exp: Zero to 1 year |
The Biomanufacturing Technician I is responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products including compliance with regulatory agencies and associated guidelines. Must be able to meet physical requirements established in this job description. The hours are as follows: Shift A: Sun – Wed, 7:30am – 6:00pm (Thursday, Friday and Saturdays off) | 1/19/2024 |
| 815 | Distributed Bio Ashland, OH Technician II, Formulations Bachelor’s degree (B.A./B.S.) in a relevant field. Exp: no experience |
A Technician II will prepare basic to complex dosing material and samples for vehicles, solutions, suspensions, diets, and dispensations independently with some oversight. Hours for the position are 9:00am-5:30pm Mon -Fri with potential overtime and/or weekend work. | 1/19/2024 |
| 816 | Element Biosciences San Diego, CA Research Associate, Surface Chemistry Bachelor’s degree in chemistry, materials science, biochemistry, bioengineering, physics, or similar fields. Exp: 0-2 years |
We are seeking a Research Associate, who has a curious mind and a great desire to learn new techniques in new areas of study to join our interdisciplinary research team. You will be learning experiment design pertaining to surface coating characterization assays, explore optimal surface coating process and support custom surface production needs. The preferred candidate will have scientific research lab experience, demonstrated by any combination of prior curricular, extracurricular undergraduate research lab work, scientific paper, poster, or presentations. | 1/19/2024 |
| 817 | EMD Serono Kankakee, IL Process Engineer Bachelor’s degree in Biology, Chemistry, or other Scientific discipline. Exp: 1+ years |
MilliporeSigma in Kankakee, IL is hiring a Process Engineer. In this role, you will identify KPIs to enhance processing and efficiencies. You will also assess new technologies to enhance production capabilities as well as reduce variation within the processes. | 1/19/2024 |
| 818 | EMD Serono Sheboygan Falls, WI Associate Quality Control Chemist (Laboratory) Bachelor's Degree in chemistry, biochemistry,?chemical engineering or other life science discipline. Exp: 1+ year |
The Associate Quality Control Chemist will perform routine assignments using existing procedures and evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 1/19/2024 |
| 819 | EMD Serono St. Louis, MO Associate Quality Scientist Bachelor’s Degree in Chemistry, Biochemistry, Biology, or other life science discipline. Exp: 1+ year |
Within the Life Sciences division of Millipore Sigma (CTDMO), the Associate Scientist (QC) position will perform quality control activities in support of GMP products at our Cherokee site. The position is within the Analytical Testing team. The job responsibilities include analytical testing and other activities in support of GMP manufacturing. The position will report to the QC Supervisor. | 1/19/2024 |
| 820 | EMD Serono St. Louis, MO Associate Quality Scientist Bachelor's Degree in Cemistry, Biochemistry, Biology, or other life science discipline. Exp: 1+ years |
As an Associate Quality Scientist, you will be responsible for reviewing the documentation and data generated for analysis of GMP products at our Cherokee site. This review may include data supporting raw materials, in-process, and/or final products. You will be responsible for verifying that documentation and raw data meet good documentation requirements, are technically acceptable, all calculations are appropriate, and specifications are met. Additional expectations may include the review of new or updated procedures for both technical soundness and allowance for appropriate documentation. Review of audit trials, data integrity and GDP. Shift: Monday-Friday 2:00PM to 10:30PM. | 1/19/2024 |
| 821 | EMD Serono St. Louis, MO Analytical Scientist Master’s Degree in Chemistry, Biochemistry, Engineering, or other scientific discipline. Exp: 1+ years' |
MilliporeSigma is looking for an Analytical Scientist to add to the team at our Cherokee site. In this role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma. This role will serve as an individual contributor in the Process and Analytical Development organization. You will be involved in working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will require problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations. This role will be reporting to Rodney Zollars. | 1/19/2024 |
| 822 | EMD Serono St. Louis, MO Analytical Scientist Master’s Degree in Chemistry, Biochemistry, Engineering, or other scientific discipline . Exp: 1+ years' |
MilliporeSigma is looking for an Analytical Scientist to add to the team at our Cherokee site. In this role, you’ll be working in the Contract Testing, Development, and Manufacturing Organization (CTDMO) within the Life Sciences group of MilliporeSigma. This role will serve as an individual contributor in the Process and Analytical Development organization. You will be involved in working in a lab setting on analytical method development and optimization for external customers in the field of Antibody Drug Conjugates (ADC). The role will require problem solving, working within project timelines, and contributing to documentation for method qualification and transfer into GMP manufacturing and quality control organizations. This role will be reporting to Robert Guilmett. | 1/19/2024 |
| 823 | EMD Serono Sheboygan Falls, WI Associate Production Scientist - 12 Hour Night Shift Bachelor’s Degree in Chemistry, Chemical Engineering, or other life science discipline. Exp: 1+ years |
The Associate Production Scientist at MilliporeSigma will manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 1/19/2024 |
| 824 | Endo Pharmaceuticals Rochester, MI Microbiologist II Master of Science degree in microbiology, biology or related field. Exp: 1+ year’ |
Performs Quality laboratory microbiological analyses of materials including water testing, finished product testing, raw material testing, and method validation. Supports laboratory investigations of moderate scope and complexity while abiding by GMPs and GLPs. Has working knowledge of, and stays current with, regulatory guidance and compendia relevant to laboratories and pharmaceutical manufacturing. | 1/19/2024 |
| 825 | Foxx Life Sciences Londonderry, NH Product Manager Lab, must be local Bachelor’s Degree in an appropriate Engineering discipline such as Mechanical, Biomedical or Chemical Engineering. Exp: 1 – 3 years |
POSITION SUMMARY: The product manager will interact with sales, marketing, Engineering and Leadership teams to provide strategic oversight to develop, launch, and grow new product offerings and solutions. Product manager works in a fast-paced environment. They are organized, can dynamically prioritize short-term and long-term business needs and are driven to work at the intersection of science and business. | 1/19/2024 |
| 826 | Frenova Renal Research Ogden, UT Biocompatibility Engineer I Bachelor's Degree in related Engineering or scientific discipline required Exp: 0 - 2 years' |
The entry level Engineer will participate in designing, executing, and championing research and development activities of Fresenius' products. As a member of a tech team, the Engineer I environment is mentored - with oversight from higher level Engineers to complete pre-defined work. The Engineer I may be involved in quality planning, internal audits, data collection and analysis, specification development and review and design review and qualification. The Engineer I will work with cross-functional teams to develop, commercialize, and maintain high quality. | 1/19/2024 |
| 827 | Fresenius Kabi Melrose Park and Chicago, IL Scientist I Possess a B.S. in Chemistry, Biology or related physical science. Exp: 1-4 years |
The Scientist I is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 1/19/2024 |
| 828 | Fresenius Kabi Melrose Park and Chicago, IL Scientist I Possess a B.S. in Chemistry, Biology or related physical science. Exp: 1-4 years |
The Scientist I is responsible for an intermediate level of expertise in analytical chemistry, chromatographic methods of analysis and instrumentation, including troubleshooting. Independently executes protocols, verifications, method transfers in support of senior level personnel. Directs and provides guidance to associate scientists. | 1/19/2024 |
| 829 | Fresenius Kabi Melrose Park and Chicago, IL Associate Scientist (Nights) BS/BA degree in Science or related field. -or- AS/AA degree. Exp: BS: 0+ years; AS: 1-3 years |
The Associate Scientist is responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Reports testing results and documents in compliance with cGMP and GLP standards. Provides support to Scientist, Lead Scientist, and Supervisor. Prepares media, reagents, sanitizing solutions and equipment for use in testing. | 1/19/2024 |
| 830 | Bio-techne Minneapolis, MN Quality Assurance Specialist B.S degree in Biology related disciplines. Exp: 0 to 5 years |
The responsibilities of this position are to engage and support various improvement projects for Document Control (Label design and document writing, routing, approval etc) and Quality Assurance activities, including but not limited to Supplier Management, Non-Conformance, CAPA and Change Management etc. | 1/8/2024 |
| 831 | Bio-techne Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 1/8/2024 |
| 832 | Bio-techne Minneapolis, MN Quality Technician, Hematology QC Lab MLT/MLS degree, bachelor’s degree in biology, or related field of study. Exp: 0-1 year |
This position will require setup, maintenance, basic troubleshooting, and operation of Hematology analyzers. This position will test hematology products for homogeneity during the bottling process by following established methods. The expectation for this position is to set up and test product on all laboratory instruments and troubleshoot as necessary within 12 months of hire. This position will adhere to safety regulations. Understand the basic ISO protocols and other applicable standards. Perform additional duties as assigned. | 1/8/2024 |
| 833 | Bio-techne Minneapolis, MN Advanced Research Associate, QC Bioassay Master’s degree om the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires experience with ELISAs, PCR, Western Blotting, and cell culture, including maintenance of cell lines and isolation of primary cells for use in the bioassays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 1/8/2024 |
| 834 | Bio-techne Minneapolis, MN Advanced Research Associate Bachelor’s degree in Biology, Biotechnology, Biochemistry or equivalent. Exp: 0 to 2 years |
In this position you will build custom made-to-order kits for our rapidly growing Luminex product line, including qualification of assay components, formulation of intermediates, and preparation for packaging. | 1/8/2024 |
| 835 | Bio-techne San Jose, CA Process Engineering Technician - Instruments Associate degree or equivalent in a relevant technical field (e.g., electrical engineering, mechanical engineering, or similar). Exp: Entry |
We are seeking a skilled and detail-oriented Process Engineering Technician to join our team. In this role, you will be responsible for supporting the development, testing, and maintenance of complex electro-mechanical instruments used in our manufacturing processes. Your expertise will be crucial in ensuring the efficient operation and optimization of these instruments, contributing to the overall success of our organization. | 1/8/2024 |
| 836 | Bio-techne Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 1/8/2024 |
| 837 | Camber Spine King of Prussia, PA Associate Project Engineer Bachelor’s degree in Mechanical Engineering (preferred), Biomedical Engineering, or other relevant technical discipline. Exp: 0-3 years |
The Associate Project Engineer will be involved with legacy and new product projects, including project planning, execution, while adhering closely to project timeline and budget. | 1/10/2024 |
| 838 | Cambrex Marlborough, MA Clean Room Analyst - Microbiological Environmental Monitoring Entry Level: Associate’s degree in Microbiology or related field; Expert Level: Bachelor’s degree or higher in Microbiology or related field. Exp: 12 months |
Our Clean Room Services team is looking for both entry level and veteran Environmental Monitoring Analysts that are passionate about leveraging their talents to provide an outstanding customer experience. If you’re interested in receiving excellent training and working as part of a team of experts with opportunities for growth, you’ll be a great fit in our strong company culture. As a Cleanroom Services Analyst you will perform environmental monitoring and cleanroom qualifications within controlled environments. You will travel to regional client sites to provide your expertise with equipment, procedures, policies and regulations to ensure that their cleanrooms meet the requirements for safe manufacturing of medical devices, pharmaceuticals and other patient products. | 1/10/2024 |
| 839 | Advanced Sterilization Products Malvern, PA Associate Scientist, Bioassay Methods Development Master’s degree in Biology, Pharmacology. Immunology, Biochemistry or a related scientific discipline is preferred. Exp: 1 year |
The Associate Scientist, Bioassay Methods Development, will be responsible for the development of cell-based bioassays and binding assays to be used as Quality Control (QC) potency assays and in support of structure-function and biological characterization studies, to better understand mechanism of action for new molecular entities in clinical development and for commercial products. The individual will be accountable for method development, qualification, validation and transfer activities as well as the evaluation of new technologies. | 1/10/2024 |
| 840 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Solid Tumor (2nd & 3rd Shift) Bachelor’s degree in a science related field. Exp: Less than 1 year |
The Molecular Technologist is responsible for performing various molecular techniques that include, but are not limited to, formalin-fixed paraffin-embedded tissue macro-dissection, RNA/DNA extractions, PCR, DNA methylation analysis, equipment maintenance, laboratory inventory, sample tracking, ordering supplies and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 841 | Caris Life Sciences Phoenix, AZ Technician - Digital Pathology Operations Associate degree with preferred major in Biological and/or Physical Sciences: or, an equivalent combination of education and experience. Exp: 1+ years |
The technician is responsible for the overall slide-scanning functions of the clinical laboratory including the routine operation and basic troubleshooting of the Whole Slide Scanners, retrieval of glass slides to be digitized, QC by visual inspection of the generated Whole Slide Images, and the testing of new software solutions to support the department. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 842 | Caris Life Sciences Phoenix, AZ Molecular Technologist - Liquid Profiling Bachelor’s degree in a science field is required. Master’s degree in a science field is preferred. Exp: 1+ years |
The Molecular Technologist – Liquid Profiling is responsible for performing various molecular techniques that include, but are not limited to, blood processing and buffy coat extraction, RNA/DNA extractions, PCR, DNA methylation analysis, Next-Generation Sequencing, equipment maintenance, laboratory inventory, sample tracking and receiving packages. This position works under the direction of the supervisor and follows standard laboratory procedures and policies. | 1/11/2024 |
| 843 | Catalog Boston, MA Associate Computational Biologist, R&D – Future Technologies B.S. or M.S. in computational biology, molecular biology, biomedical engineering, or a related discipline. Exp: 1+ years |
CATALOG, a Boston-based pioneering startup, is making significant strides in the field of data storage and computation by harnessing the power of DNA. DNA, known for its millennia-long stability, unrivaled information density, and cost-effective replicability, offers revolutionary potential for latency-tolerant high-density data storage and massively parallel computation. We're seeking a motivated Associate Computational Biologist with an interest in synthetic biology to join our interdisciplinary team and contribute to the development of CATALOG's DNA-based data storage and computation platform. | 1/11/2024 |
| 844 | Catalog Boston, MA Research Associate or Senior Research Associate, DNA Computing BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: 1+ years |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 1/12/2024 |
| 845 | Catalog Boston, MA Research Associate/Senior Research Associate Tech Ops BS or MS in biology, molecular biology, biochemistry, or a related discipline. Exp: 1+ years |
We are actively seeking a Research Associate or Senior Research Associate with a solid grounding in molecular biology or chemistry. In this role, you'll be instrumental in helping to build CATALOG's innovative DNA-based data storage and computation platform. You'll collaborate with our dynamic team of computer scientists and biologists, developing novel storage and computing architectures and translating them into scalable chemical operations. Your work will contribute to the optimization of a molecular instruction set that underpins the world’s first DNA storage and computing platform. | 1/12/2024 |
| 846 | Cellares South San Francisco, CA Cell Therapy Manufacturing Specialist Bachelor’s Degree or diploma in a scientific or related field is required. Exp: 1+ years |
We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform. The primary focus of this position will be to support manufacturing operations, as well as day-to-day lab operations. This is a hands-on position that will train in Process Development, Analytical Development, and/or MSAT prior to joining the Manufacturing Group. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. | 1/12/2024 |
| 847 | Cenetron Diagnostics Milwaukee, WI Tissue Recovery Specialist - Full-time Associate's Degree degree from an accredited college or university in a related healthcare field required. Exp: 1-3 years |
Under the direction of the Supervisor, the Tissue Recovery Specialist (TRS) is responsible for the surgical recovery and acquisition of tissue from donors from referring agencies. | 1/12/2024 |
| 848 | Cenetron Diagnostics Milwaukee, WI Organ Recovery Specialist - Surgical Tech Associate's Degree or Bachelor’s Degree from an accredited college or university in a related healthcare field required. Exp: 1-3 years |
Under the direction of the Supervisor, Recovery Services the Organ Recovery Specialist is responsible for coordinating, assisting, and performing many of the key aspects related to the surgical recovery process of organ donation. | 1/12/2024 |
| 849 | Cenetron Diagnostics Indianapolis, IN Associate Technologist Laboratory Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 1/12/2024 |
| 850 | Cenetron Diagnostics Milwaukee, WI Associate Technologist Laboratory - Molecular Oncology and Genetics Laboratory Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1+ years |
Under direct supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts at a basic level with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment . | 1/12/2024 |
| 851 | Cenetron Diagnostics Wauwatosa, WI Research Technologist II - Deininger Lab Bachelor's Degree from an accredited college or university in biology, chemistry or equivalent scientific discipline required. Exp: 1-3 years |
Develops, improves, and implements laboratory techniques and performs complex experiments and/or tests to contribute to the timely and accurate completion of the research project(s). | 1/12/2024 |
| 852 | Cenetron Diagnostics Milwaukee, WI Technologist Laboratory HLA - $3,500 sign on bonus!!!! Bachelor's Degree from an accredited college or university in biology, chemistry, molecular biology, immunology, clinical laboratory science, medical Exp: 1-3 years |
Under supervision by department leadership, performs CLIA regulated and clinical contract research testing. Interacts with customers, providing a high level of customer service to resolve customer concerns about sample acceptability and results. Supports preparation of laboratory reagents and routine maintenance of laboratory equipment. Supports the training of junior and peer staff members. Performs higher level interpretation of testing results and test panels. | 1/12/2024 |
| 853 | Cenetron Diagnostics Wauwatosa, WI Research Technologist - Dr. Dipa Lab Bachelor's Degree from an accredited college or university in biology, chemistry, scientific discipline or equivalent combination of education and exp Exp: 1-3 years |
Under the direction of the Principal Investigator, performs laboratory assays and complex experiments to elucidate novel research questions. | 1/12/2024 |
| 854 | Champions Oncology Rockville, MD Formulations Technician I BS degree in chemistry, pharmacology, or related field.preferred. Exp: 1 year |
The Formulations Technician will support in vivo oncology research studies in mice. Duties and responsibilities include: Receive, distribute, and disposition test compounds, vehicles, and reagents. Formulate test compounds, vehicles, and reagents. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Willing to work the following schedule: Friday, Saturday, Sunday, Monday and Tuesday - weekly 11:00am to 7:30pm | 1/12/2024 |
| 855 | Champions Oncology Rockville, MD Research Associate I, Cell Culture In-Vivo BS degree. Exp: 0- 2 years |
The research associate will perform cross-functional laboratory assays with a focus on in vitro/In vivo studies. Assist in the development and execution of novel assays including collecting and processing data. | 1/12/2024 |
| 856 | Champions Oncology Rockville, MD Research Technician, Support Team BS degree in animal science, biology, pharmacology, or related field preferred. Exp: 3 to 6 months |
A Research Technician on the Support Team provides general technical support for in vivo oncology studies in mice. | 1/12/2024 |
| 857 | Champions Oncology Rockville, MD Laboratory Animal Care Technician BS degree in biology, pharmacology, or related field. Exp: 0 - 1+ years |
Support in vivo oncology studies in mice as a member of the Vivarium Operations Team. Duties and responsibilities: Provide animal care including handling, receipt and husbandry procedures Provide animal care including feeding and watering with food and water consumption monitoring Conduct animal observation for general health and overall well-being Clean equipment, rooms and facility according to a schedule devised by senior personnel; including floor sweeping and washing, cage washing and sterilization, and waste removal Document and initial required information in relevant room and log books Material and supply distribution and waste handling Record data using laboratory information management systems | 1/12/2024 |
| 858 | Champions Oncology Rockville, MD Animal Research Technician I, Study Services BS degree in animal science, biology, pharmacology, or related field. Exp: 1 year |
Support in vivo oncology research studies in mice as a member of the Study Services Team. Duties and responsibilities: Perform in-life technical procedures on mice, including handling, restraint, body weight measurement, tumor volume measurement with calipers or imaging device, compound administration, blood collection, and euthanasia. Record study data within the laboratory information management system. Read, understand, and adhere to study protocols. Perform general study preparation and organizational activities, including sample tube labeling, supply organization and stocking, and laboratory organization. Work weekends and holidays on rotating basis. | 1/12/2024 |
| 859 | Cisbio Boston, MA Lab Equipment Support Specialist Associates Degree in a Science/Engineering Field or Bachelor’s degree in a Science/Engineering Field. Exp: AS: 1-2 years; BS: 0+ years |
Enhance the existing LAMP infrastructure to track equipment preventative maintenance (PM). Service work will be performed by LAMP/OEMs and customer Facilities engineers. Support System Admin functions Provide the following compliance support activities: Enter all PM and corrective maintenance (CM) service requests and reports in customer logbook (ELN). Confirm each maintenance event receives a signed service report (electronic preferred). Review documents for accuracy. Confirm MS performance checks are done at least monthly, compile results and distribute to staff. Compile service information as needed to support internal QA and agency audits. Manage pipet calibration with record keeping in customer ELN. Generate out of calibration impact memos if there is a pipette calibration failure for customer review and approval. Maintain balance inventory and coordinate with the CUSTOMER MIC centre to support service/calibration report archival by the CUSTOMER assigned personnel. Escalate to customer corporate management if there are issues getting the appropriate support. Confirm Fume hoods/enclosures are PMed on schedule by the customer assigned personnel. Escalate issues to customer’s corporate management. PH meter maintenance – check calibration, electrode storage, and buffer expirations monthly. | 1/12/2024 |
| 860 | Cisbio Collegeville, PA Chemical Management Specialist Bachelor's degree. Exp: 1+ years |
Performs efficiency studies (assays) and pre-clinical exploratory safety studies. Performs testing of clinical, research and quality control proficiency; evaluates instruments. Evaluates and analyzes clinical research data. Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives. Manages storage of research samples. | 1/12/2024 |
| 861 | Cisbio Bothell, WA Lab Support Coordinator Associates degree. Exp: 1+ years' |
Serve as point of contact for customer lab staff, facilitating and coordinating laboratory needs and activities. This role will work closely with other teams to seamlessly deliver lab support services. Coordinate the working lab environment daily and oversee all stock items in and near the labs including but not limited to glassware, lab coats, PPE, consumables. Occasionally support / coordinate waste removal from labs, ensuring use of waste streams with appropriate third-party vendors. Act as the liaison for escorting third-party vendors to customer lab staff for maintenance and/or repairs visits. Meet regularly with key stakeholders (lab staff, service providers, management) to identify, review and resolve issues in a timely manner and/or escalate as necessary. Regularly engage with the customer and PerkinElmer staff to ensure quality and compliance within the laboratory. Collaborate with customer line safety reps to ensure a high level of safety is maintained in the lab. Provide updates and timely communication to lab users on service work requests. Provide area walkthrough for new members of customer staff and visitors. Once certified, provide coordination of a 5S (Sort, Set in Order, Shine, Standardize, Sustain) lean service. Required to cross-train and provide back-up to other lab support areas. Complete relevant paperwork according to principles of Good Documentation Practice. Subject Matter Expert (SME) on various support needs across different buildings/floors/locations. | 1/12/2024 |
| 862 | Coating Place Verona, WI QC Analytical Chemist - FP Team (1st Shift) Bachelor’s degree in Chemistry or related field. Exp: 1+ years |
1st Shift Position 8:00am - 4:30pm, Mon - Fri The primary purpose of the QC Analytical Chemist is to provide support to the Production and Formulations Departments by analyzing pharmaceutical and/or cleaning samples. Support will be provided by analyzing samples using various procedures including, but not limited to, internal procedures, specifications, and analytical methods; compendial monographs, client procedures, and miscellaneous protocols. The QC Analytical Chemist is expected to understand basic internal procedures and conduct analyses with some supervision after training is complete. In addition, support is provided by ensuring the essential job functions of this position are completed as part of the daily and/or weekly schedule. | 1/12/2024 |
| 863 | Codexis Redwood City, CA Bioprocess Development Downstream Research Associate III Master’s degree in Biochemistry, Biological Science, Chemical or Biomolecular Engineering, or related discipline. Exp: 0-3 years |
The Bioprocess Development Downstream Research Associate III is responsible for designing, performing, and analyzing experiments to establish, understand, and optimize enzyme purification processes. The Research Associate will also be responsible for communicating technical data and contributing to tech transfer activities for external manufacturing of cutting-edge enzymes for nucleic acid synthesis. This position will be based on-site in Redwood City. | 1/12/2024 |
| 864 | Codexis Redwood City, CA Process Development, Research Associate II BS or equivalent in Chemical Engineering, Biology, Biochemistry or relevant scientific field. Exp: 1 year |
The Process Development Research Associate II will join the Process Chemistry group which is part of the R&D department. Successful candidates will be a part of a dynamic and enthusiastic team responsible for development, scale up and tech transfer of the ECO Synthesis™ platform. The individual will be working with a high performing team with day-to-day laboratory workflows and operations to help with design, optimization, and analysis of ECO Synthesis™ technology. The position is an on-site role located at our Redwood City facility full time. | 1/12/2024 |
| 865 | Cognate Bioservices Seattle, WA Research Associate I B.S. in either animal science or similar discipline preferred. Exp: 6-12 months |
In the Research Associate role, you have the responsibility of performing a variety of animal procedures to support company and client research projects. This includes setting up study forms, preparing procedure rooms, and labeling and shipping samples. You will also perform various procedures, such as administering drugs through different routes (oral, SC, IP, IM, IV), collecting blood/tissue samples, and performing grafting techniques. In addition to these tasks, you will operate and maintain laboratory equipment (e.g., isoflurane machine). The Research Associate will be responsible for accurate data entry. To ensure the success of the research projects, it is critical that you maintain accurate study records and assist in maintaining lab and facility inventories. As part of your role, you will be expected to complete study reports and perform routine animal health-related tasks such as changing cages or supplying food as needed. Your attention to detail and ability to follow procedures carefully will be essential to ensure the accuracy and reliability of your research results. Lastly, you may need to perform health rounds and treatments on weekends, holidays, and occasional evenings. | 1/12/2024 |
| 866 | Cognate Bioservices S. San Francisco, CA Research Study Technician I Associate degree (A.A./A.S.) in animal or laboratory science or related discipline. Bachelor's (B.A./B.S.) Degree preferred. Exp: six to twelve (6-12) months |
We are seeking a Research Study Technician I for our Insourcing Solutions Department located in South San Francisco, CA. In this role you will observe, monitor, and document the health and physical environment within the Charles River Accelerator & Development Labs (CRADL) animal facility. Conduct in vivo experiments in rodents for multiple clients to support research programs. Collaborate with the veterinary staff to ensure that the health and welfare of laboratory animals are maintained in compliance with local, state, federal and institutional guidelines, and regulations. You will handle routine handling, restraint, identification (including ear notching, tagging) and sexing of common laboratory animals. Ability to distinguish various common laboratory animal strains in accordance with standardized genetic nomenclature and phenotype identification. You will also perform technical functions required by research protocols such as assist with dilution and dosing calculations; dosing administrations (PO, SQ, IP, IM, and IV); blood collections (Submandibular, Cardiac); basic necropsy and tissue collection; tumor measurement and body weights. Assist Vet Techs and Veterinarians with follow-up checks, treatments and procedure if needed. Perform health surveillance sample collection procedures. Actively interact with research staff to provide technical assistance. | 1/12/2024 |
| 867 | Cognate Bioservices Mattawan, MI Research Technician - Pharmacokinetics & Acute Toxicology 1 1 Bachelor’s/Master’s. Exp: 1+ years |
We are seeking an experienced Research Technician for our Pharmacokinetics & Acute Toxicology Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 1/12/2024 |
| 868 | Cognate Bioservices Mattawan, MI Research Analyst I - Immunochemistry Bachelor's degree (BA/BS). Exp: 0+ years |
We are seeking an Research Analyst I for our Immunochemistry at the site located in Mattawan, MI. The following are responsibilities related to the Research Analyst I: The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked immunosorbent assay (ELISA), to measure large molecules and their immune responses. The main types of assays include Pharmacokinetic (PK) assays to measure drug and Immunogenicity assay to measure anti-drug antibodies (ADA) and neutralizing antibodies (NAb). Other assay types also performed are branched DNA (bDNA) and cell-based assays. An array of platforms are used to support these assays that include spectrophotometer, Meso Scale Discovery (MSD), Luminex and Gyrolab. Utilizing these platforms/assays, the teams are responsible for the method development, validation and routine sample analysis in both the regulated and non-regulated space of non-clinical and clinical studies. | 1/12/2024 |
| 869 | Cognate Bioservices Newark, DE Molecular Technologist-1 Sequencing Associates Degree in Microbiology or related discipline required. Bachelors Degree preferred. Exp: 0-3 years |
Charles River Labs is seeking a Molecular Technologist for our Microbial Solutions site located Newark, DE. This position is Monday - Friday 10:00am to 6:30pm. The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping. Ensure adherence to regulatory requirements and GMP compliance. | 1/12/2024 |
| 870 | Bausch & Lomb Greenville, SC Microbiology Technician III 2nd Shift BS in Biology, Microbiology or related life science. Exp: 1+ years |
Execute microbiological testing in support of but not limited to Environmental/Water/Bioburden monitoring, Media and lab supplies preparation, Sterility Testing and Microbial Identification. Conducts tests for in-process and finished products as well as raw materials using aseptic techniques. Compliance with all applicable procedures and practices to include local and global SOP’s, product test procedures, safety, USP, ISO, GMP, and applicable governmental regulations. | 1/2/2024 |
| 871 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 872 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 873 | Bausch & Lomb Rochester, NY Lab Technician IV AAS in Chemistry, or related field. Exp: 1-5 years |
Monitor product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 1/2/2024 |
| 874 | Bausch & Lomb Rochester, NY Chemist I BS in Chemistry, or related field. Exp: 1-3 years |
The Chemist is a member of the Global Quality organization. This person is responsible to monitor product quality by performing tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 1/2/2024 |
| 875 | Bausch & Lomb Tampa, FL Chemistry Technical III B. S. in Chemistry preferred, Minimum B.A. in Chemistry or related science. Exp: 1-3 years |
Perform pharmaceutical GMP wet chemistry and instrumental analysis of raw material, in-process, finished product and stability samples in the quality control chemistry laboratory in accordance with all applicable FDA/EP/JP regulations. Assume the responsibility for the GMP, ISO, and Environmental Health and Safety procedure awareness, and compliance within the respective area. | 1/2/2024 |
| 876 | Bausch & Lomb Tampa, FL Microbiology Technician III Bachelor’s degree in microbiology, Biology, or equivalent Life Science required. Exp: 1-2 years |
Perform routine and non-routine microbiological testing and environmental monitoring (EM) in support of sterile manufacturing operations. | 1/2/2024 |
| 877 | Baxter Round Lake, IL Quality Lab Associate I - Stability Bachelor’s degree in Chemistry or biological science with analytical chemistry laboratory coursework. Exp: 0-1 years’ |
The position may be responsible for analytical testing, validation/verification, and/or transfer of test methods supporting parenteral products. The position will be in the Round Lake, IL Stability Laboratories within Product Quality serving multiple global businesses. This role is essential for supporting the global commercial product teams and/or product development teams. The position may collaborate with multiple functions. The individual in this position must: 1) Optimally demonstrate working technical knowledge and skills to support a variety of projects within the relevant discipline with minimal assistance. 2) Display basic technical understanding of related teams. 3) Conduct routine/ experiments with assistance. | 1/3/2024 |
| 878 | Baxter Marion, NC Associate I, Quality Lab Master’s Degree in Natural Sciences: Chemistry preferred. Exp: 0-3 years |
Conduct qualitative and quantitative chemical analysis on raw materials, solutions, and components following approved Standard Operating Procedures and test methods in an accurate and timely manner. Ability to work under minimum supervision while meeting deadlines. | 1/3/2024 |
| 879 | Baxter Marion, NC Quality Associate I - Plastics (8th Shift: 7pm-7am) Bachelor's degree preferred. Exp: 0+ years |
Responsible for providing Quality support and oversight via direct staff supervision or process/area responsibilities. Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Baxter quality practices. | 1/3/2024 |
| 880 | Baxter Marion, NC Quality Lab Associate I - Micro ID B.S. degree in Microbiology, Biology, or related science. Exp: 0-2 years |
Responsible for reading plates for EM, Bioburden, and special project testing and recording test results. Performs additional microbiological testing as required. | 1/3/2024 |
| 881 | Baxter Marion, NC Quality Associate I (3rd Shift: 10pm-7am) Bachelor's degree strongly preferred. Degree in engineering or life science preferred. Exp: 1+ years |
Responsible for working with the manufacturing departments to address defects with the finished products. | 1/3/2024 |
| 882 | Baxter Marion, NC CAPA Associate I Bachelor's degree preferred(in science or engineering preferred). Exp: 1+ years |
Will be an Investigation Owner and/or CAPA Owner and is responsible for developing and performing the investigation, identifying the root cause(s) of the event, and detailing the results of the investigation. The CAPA I will likely assist in identifying the appropriate actions to mitigate or eliminate the root causes, and in determining an Effectiveness Plan for the actions (including efficiency criteria and timeframe). | 1/3/2024 |
| 883 | Baxter Marion, NC Quality Lab Associate II - Endotoxin Master’s Degree in biological sciences. Exp: 0-3 years |
Conduct microbiological analysis on raw materials, solution, and water samples following approved Standard Operating Procedures in an accurate and timely manner. | 1/3/2024 |
| 884 | Becton Dickinson Tempe, AZ Manufacturing Engineering II Master’s degree in a technical field. Exp: one to three years |
This is a manufacturing engineering position for the Vascular Graft and Covered Stent Graft production facility. This position is responsible for development of process improvements and validations of Vascular Graft and covered Stent Graft production processes. This position is also responsible for the transfer of newly developed products to production. | 1/3/2024 |
| 885 | Becton Dickinson Columbus, NE Manufacturing Unit Process Engineer Bachelors Degree in an engineering discipline or equivalent experience. Exp: no experience |
This position is responsible for supporting the manufacturing operation. This individual will develop and implement improved methods of manufacturing, procedures, and processes that result in improved efficiencies, yields, machine operations, and quality. Provides technical support to the development group for the implementation of new products or processes. | 1/3/2024 |
| 886 | Becton Dickinson Grayson; Covington, GA Microbiology Lab Tech BS in Biological Science. Exp: 1-3 years |
The Laboratory Technician is responsible for manufacturing various bacterial antigens, antisera, Treponema product line, Myco product line, Bactrol product line, purified proteins and various solutions including but not limited to buffers, reagents growth media etc. to the finished bulk product stage. | 1/3/2024 |
| 887 | BeiGene Hopewell, VA Purification,Technician I AS/BS/BA in science related field. Exp: 1+ years |
The Purification Manufacturing Technician I position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. | 1/3/2024 |
| 888 | BeiGene Hopewell, VA Cell Culture, Technician II AS/BS/BA in science related field. Exp: 1+ years |
The Cell Culture Manufacturing Technician II position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. | 1/3/2024 |
| 889 | Berg Framingham, MA Research Associate Bachelor’s degree in Biology, Chemistry, Biochemistry, or a closely related field of study. Exp: One (1) year |
Assist in ligand binding assay method development (MSD, ELISA) and provide technique and application support for immunoassays transferred to downstream users. Test antibody quality for purity (SDS-PAGE), specificity (Western Blot, ELISA), and concentration (Nanodrop, BCA). Conduct assay performance validation. Perform protein analysis (SDS/native-PAGE, Western Blot, and Immunoprecipitation). Develop experiment protocols and prepare SOPs. Perform laboratory experiments carefully and troubleshoot to solve problems. Meticulously document experiment results in laboratory notebooks and databases timely. Analyze, summarize, and present experimental results to managers and other team members. Prepare experiment and project reports as required. Order and stock laboratory supplies for a continuous and consistent workflow. | 1/4/2024 |
| 890 | Bethyl Laboratories, Inc. Montgomery, TX Lab Associate BS, Bachelor of Science, or related degree. Exp: 1+ years |
In this position you will support all company mammalian cell culture needs, including both production and research and development, in support of our antibody development activities. In this position you will assist with all tasks in the cell culture core. These include, but are not limited to, maintaining cells and carrying out transient transfections for expression and purification of recombinant proteins and antibodies; culturing hybridoma cell lines for antibody production; and maintaining a cell bank of over 125 different human and rodent cell lines, processing them for flow cytometry, FFPE cell pellets and cell lysate. The successful candidate is detail-oriented, highly motivated, and willing to learn new skills. Bethyl Laboratories is nimble, market-focused and growing. If you are looking for the opportunity to be first, fast, and flexible, come join us! | 1/4/2024 |
| 891 | BGI San Jose, CA LC/MS Research Associate - Small Molecule B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
San Jose Mass Spec Lab of BGI Americas is seeking an exceptional and motivated research associate with competitive compensation. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up metabolomics and lipidomics capability in SJMS lab, 4) to support other departments when needed. A candidate with metabolomics/lipidomics LC-MS experience is a plus; a candidate with small molecule sample prep experience is a plus. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for metabolomic or lipidomics analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and working with biofluids is a plus. | 1/4/2024 |
| 892 | BGI San Jose, CA LC/MS Research Associate - Proteomics B.S. degree with biochemistry/chemistry major or related field. Exp: 0-2 years |
BGI Americas San Jose Mass Spec (SJMS) center is seeking an exceptional and motivated research associate to join our Proteomics department at our San Jose facility. The main responsibility of this position includes, but not limited, to support the SJMS production team 1) to turn around routine customer and research projects, 2) to maintenance and operate LC-MS instrument, 3) to assist lab manager to build up additional proteomics capability in SJMS lab, 4) to support other departments when needed. An ideal candidate will need to demonstrate that they are capable of consistently following Standard Operational Procedures (SOPs) to consistently perform sample preparation procedures for proteomics and biologics characterization analysis. A candidate with hands-on experience in HPLC, Orbitrap mass spec and, working with biofluids is a plus. | 1/4/2024 |
| 893 | BioFire Diagnostics Hazelwood, MO Mechanical Engineer Master’s Degree in Mechanical Engineering. Exp: 1+ year |
Assists in the definition, proof of concept, development, implementation and/or support of technical or business solutions by performing specific tasks within the scope of the assigned activity. Identifies issues and uses problem-solving tools to formulate the necessary activities to provide successful solutions. Ensures quality of deliverables by following the appropriate design practices and departmental procedures for design control and regulatory compliance. Creates appropriate documentation such as technical communications, reports, meeting notes and other relevant technical documentation within the role’s function. Prioritizes activities within the scope of the assignments to ensure schedules or quality of work is successfully achieved. Ability to define, review and check product Bill of Materials (BOM) structures, assembly instructions and test procedures. Works with internal department and project specific teams | 1/4/2024 |
| 894 | BioFire Diagnostics Hazelwood, MO Lab Technician - Media Tech Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 1/4/2024 |
| 895 | BioFire Diagnostics Salt Lake City, UT Laboratory Technologist - QC I/II Associate degree or higher in a Life Science or related field. Exp: Technologist I - 6 months |
QC Technologist I works in a cGMP environment performing quality control testing for commercial and diagnostics products. Responsibilities include conducting testing of reagents and IVD materials as well as personnel swabs. Responsibilities include working with Manufacturing, Technology Transfer and other departments for data collections and validations for new product QC qualifications, organization of quality-controlled materials used for QC testing and learning new techniques or workflow as required by new product lines. QC Technologist I is also responsible for gathering and filling out quality documents pertaining to quality control testing, generation of Non-Conformance Report (NCR) when necessary and Temporary Change Order (TCO) application. QC Technologist II will be responsible for software-assisted product release (e.g., Pouch QC Web releases). This position will work in a laboratory setting and perform a variety of scientific techniques, including spectrophotometry, PCR, pipetting, etc | 1/4/2024 |
| 896 | BioFire Diagnostics Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. The LT-I will receive general instruction on routine work, perform lab duties under supervision, and receive training and additional instruction for new tasks as needed. | 1/4/2024 |
| 897 | BioFire Diagnostics Salt Lake City, UT Lab Technologist I - Oligo, Night Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
***SIGN ON BONUS OFFERED*** $500 on first paycheck $500 after 6 months of employment BioMerieux is seeking a Lab Technologist I to join our swing shift team that manufactures Oligonucleotides. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments. | 1/4/2024 |
| 898 | BioFire Diagnostics Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months' |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. The position requires basic laboratory technical skills, organizational skills, attention to detail, critical thinking, troubleshooting and problem-solving, and a dedication to the mission and goals of the department and bioMérieux. A Research Associate I may receive general or detailed instruction and direct supervision on general work, new procedures, and assignments | 1/4/2024 |
| 899 | BioFire Diagnostics Salt Lake City, UT Lab Technologist I - Oligo, Day Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
Sunday - Tuesday from 6:00 AM - 6:00 PM + every other Wednesday Thursday - Saturday from 6:00 AM - 6:00 PM + every other Wednesday ***SIGN ON BONUS OFFERED*** $300 on first pay check $300 after 6 months of employment We are seeking a Lab Technologist I to join our team. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments Strong pipetting skills, attention to detail, organization, and familiarity with cGMP are desired. | 1/4/2024 |
| 900 | Biogen Research Triangle Park, NC Associate II, QC Microbiology B.S. Degree. Exp: 1 1/2 - 2 years |
Schedule: this position will work 4-day, 10-hour shift Friday-Monday from 8 AM to 6 PM. The Associate II, Quality Control is responsible for supporting key functional, tactical, and operational aspects of the QC Microbiology group at the Biogen manufacturing facility. | 1/4/2024 |
| 901 | Biogen Research Triangle Park, NC Manufacturing Associate III Bachelor’s Degree (STEM preferred). Associate’s Degree. Exp: BS: 6 months; AS: 1 year |
Manufacturing Associates perform processing steps and manufacturing support activities in our facilities in Research Triangle Park (RTP). These teams are the backbone of our operations – each person playing a critical role in delivering our therapies to the patients who need them. This position will be in our Parenteral Filling area, and our teams operate across the following units: | 1/4/2024 |
| 902 | Biogen Research Triangle Park, NC Manufacturing Associate (Recent Grad/Entry Level) – Upstream & Downstream Bachelor’s Degree (STEM preferred) OR Associate’s Degree OR Military training & experience and are soon to transition. Exp: Entry-Level |
This requisition represents multiple open positions in our RTP Manufacturing organization. The Talent Acquisition team continually assesses all applicants that apply through this posting and will reach out to the selected candidates to discuss current and future opportunities. | 1/4/2024 |
| 903 | Biogen Research Triangle Park, NC Associate II, QA - Swing Shift Bachelor’s degree preferably in a field of science or biotechnology. Exp: 0-2 years |
The Quality Assurance Associate II is responsible for contributing to the oversight of key strategic, tactical, and operational aspects within Quality Assurance at the Biogen Research Triangle Park (RTP) facility. Activities include but are not limited to: review of GMP raw data for compliance, review of GMP documentation to support batch disposition, review/approval of GMP procedures, protocols and reports, GxP Quality systems-related training, identifying gaps in existing Quality systems and proposing solutions to site management. The QA Associate will perform all duties in a manner consistent with site and corporate policies, cGMP, safety, environmental and human resources policies and procedures and also adhere to all regulatory licenses and regulations, interfacing with key Quality and manufacturing customers, and coordination of investigations impacting the RTP site. The QA Associate may participate in internal compliance audits; assess and approve discrepancies from site, corporate, and regulatory guidance. The QA Associate will also ensure compliance with training policies. Please note that this is a Swing Shift position and will work a traditional 2-2-3 Manufacturing Rotation from 12pm to 12am, on a 12hr/shift schedule. There is a 10% pay differential for this position. | 1/4/2024 |
| 904 | BioLegend Pittsburgh, PA Associate Lab Technologist Bachelor's degree in a life science discipline such as Biology, Chemistry, or Medical Technology. Exp: 0-3 year |
Our team is seeking an Associate Lab Technologist to join us in our efforts to serve patients and families around the world. | 1/5/2024 |
| 905 | BioLegend Pittsburgh, PA Research Clinical Laboratory Scientist Bachelor’s Degree in life sciences. Exp: 1-2 years |
The research clinical laboratory scientist will assist in the validation and performance of clinical laboratory tests for the diagnosis, treatment, and prevention of disease within humans. | 1/5/2024 |
| 906 | BioLegend Lafayette, CO Associate Scientist Bachelor's Degree in Life Sciences. Exp: 0-3 years |
Revvity has a rewarding and exciting opportunity for an Associate Scientist for our Synthetic Manufacturing laboratory. The Associate Scientist position will perform primary tasks in an ISO 9001:2015 laboratory in Lafayette, CO. Key responsibilities for this position include a wide array of duties related to the manufacturing, processing, and packaging of RNA and DNA oligonucleotides. This includes synthesis, cleaving, quality and quantity determination, purification, inventory control, and order packaging. The position will require the ability to learn and to troubleshoot various aspects of manufacturing chemistry in multiple laboratories. | 1/5/2024 |
| 907 | LGC Biosearch Technologies Middleton, WI Associate Production Scientist, Comp Cells Associate degree in relevant life sciences field (molecular biology, microbiology, biochemistry, etc.). Exp: 1+ years |
The Associate Production Scientist will manufacture competent cells for the Company’s various product lines. The position may expand to also support manufacture of additional product lines and development of new products, applications and businesses. This position is regularly based out of the company's site in Middleton, WI, with standard hours of operation Monday-Friday (8am-5pm). | 1/5/2024 |
| 908 | LGC Biosearch Technologies Petaluma, CA Associate Engineer, Facilities Services 4 Year Degree in Mechanical Engineering, Electrical Engineering or similar. Exp: 1+ Year |
The Associate Engineer will function as an integral part of LGC’s Engineering team and will help provide strategic vision and technical support to ensure that the facilities/utilities/equipment for LGC Biosearch’s manufacturing sites are designed and operating efficiently and safely. The primary purpose of this role is to provide engineering support and design expertise for Biosearch’s Petaluma and Novato manufacturing facilities. This individual will be involved in the design and implementation of process improvements and system maintenance. This role will support the design, engineering, commissioning, and qualification of new or modified utility equipment systems and/or GMP manufacturing process instrumentation. | 1/5/2024 |
| 909 | Biosero San Diego, CA Mechanical Design Engineer Bachelor’s degree in Bioengineering, Mechanical Engineering, or comparable field. Exp: 1 year |
We are looking for driven Mechanical Design Engineer to join our Engineering Team and help us design world-changing laboratory automation systems and associated hardware products. In this role, you will also assist the applications and sales teams in the conceptualization of automation workcells, generate the bill of materials for projects and products, work with the procurement team and vendors to ensure all fabricated components are ordered and tracked, and generate assembly drawings and instructions for the Automation Team to build projects. | 1/5/2024 |
| 910 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, RNA Synthesis Bachelor’s in Chemistry, Biochemistry, or a related field. Exp: 0-3 years |
· Design, synthesis, purification, and analysis of chemically modified oligonucleotides · Improve upon and/or develop new synthetic methods and processes to expand the current capabilities. · Utilize analytical instrumentation such as UV-Vis spectroscopy, HPLC, and/or LC-MS for the analysis of both crude and purified synthetic products. Effectively troubleshoot synthetic/process issues and independently find solutions. · Improve upon and/or develop new methods and automation for the downstream processing of synthetic oligonucleotides and their subsequent analysis/purification and annealing into siRNA duplexes. · Analyze, interpret, and organize analytical data to present to team members.· | 12/27/2023 |
| 911 | Alnylam Pharmaceuticals Cambridge, MA Associate Scientist II, Protein Sciences BS/MS degree. Exp: 0-1 years |
We are seeking an associate scientist-II to join our protein sciences group within Medicinal Chemistry to help with production, protein chemical conjugation and development efforts. The candidate must be independent, goal oriented, technically competent, and able to efficiently work across multiple projects. We are searching for enthusiastic, innovative, and highly motivated individuals, with scientific background in protein expression, purification, protein conjugation and analytical techniques, who are comfortable working in a fast-paced entrepreneurial environment. This position is onsite and will be located at 675 W. Kendall St. Cambridge, MA 02142We are seeking an associate scientist-II to join our protein sciences group within Medicinal Chemistry to help with production, protein chemical conjugation and development efforts. The candidate must be independent, goal oriented, technically competent, and able to efficiently work across multiple projects. | 12/27/2023 |
| 912 | Alphazyme Jupiter, FL Formulation and Order Fulfillment Technician Associates degree in life science discipline such as Molecular Biology, Biochemistry or Biotechnology. Exp: 1+ years |
Maravai LifeSciences is seeking a #MiracleMaker to join our Order Fulfillment team as a Formulation and Order Fulfillment Technician. As a Formulation and Order Fulfillment Technician you will support Alphazyme’s maintenance and production of inventory necessary for fulfilling customer demands, which includes all activities related to maintaining the responsible lab area, and assists with supporting internal demands and the management of relevant formulation and fulfillment processes through executing protocols. | 12/27/2023 |
| 913 | Alstem Richmond, CA Research Associate B.S. or M.S. degree in Biochemistry, Molecular Biology or related discipline. Exp: 1 year |
ALSTEM is looking for a highly organized and energetic Research Associate with a B.S or M.S. degree to join its scientific team. The candidate will be responsible to work as a team at all levels which will include but will not be limited to product testing and QC, and custom service projects following SOPs and protocols to support customer workflows. | 12/27/2023 |
| 914 | Alveo Technologies Alameda, CA Scientist I BA/BS degree in Biochemistry, Molecular Biology, Microbiology or related field. Exp: 1-3 years |
Alveo Technologies is looking for a Development and Verification Scientist I to support ongoing V&V efforts of projects in disease detection. The successful candidate will assist in planning and executing protocols / conducting experiments at the bench to meet objectives. The candidate should be able to review, understand and follow the instructions, protocols and SOPs provided by the R&D and Manufacturing departments. | 12/27/2023 |
| 915 | Amarex Clinical Research Ann Arbor, MI Lab Technician I Associate’s degree in a physical science. Exp: 1+ years |
NSF is looking for a motivated candidate who enjoys working hands-on and on their feet to be in the Exposures or Preparations Lab as a Technician I. This position is perfect for someone looking to get lab experience and have the potential to learn and grow within a certification company. This role is to perform laboratory procedures in an accurate and timely manner and continue to expand skill base while under supervision. Depending on the circumstance, potential for flexible schedules and/or part-time if someone is in school obtaining their degree and would like this experience. | 12/27/2023 |
| 916 | Amarex Clinical Research Ann Arbor, MI Lab Technician I Associate’s degree in a physical science. Exp: 1+ years |
NSF is looking for a motivated candidate who enjoys working hands-on and on their feet to be in the Exposures or Preparations Lab as a Technician I. This position is perfect for someone looking to get lab experience and have the potential to learn and grow within a certification company. This role is to perform laboratory procedures in an accurate and timely manner and continue to expand skill base while under supervision. Depending on the circumstance, potential for flexible schedules and/or part-time if someone is in school obtaining their degree and would like this experience. | 12/27/2023 |
| 917 | AmbioPharm North Augusta, SC Quality Control Chemist I Bachelor’s Degree in Chemistry or life sciences. Exp: 1-2 years |
Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments. Perform Quality control raw material/ release/ stability testing. Support routine analytical testing using KF, FTIR, UV and HPLC. Adapt, maintain, and operate analytical instrumentation. Perform method transfer and validation activities with minimal supervisor guidance. Conduct all quality QC chemical tests. Involve in procedure review and propose modifications and updates. Conduct various analytical testing procedures as per QC SOPs | 12/27/2023 |
| 918 | Amide Tech Cambridge, MA Research Associate / Senior Research Associate - Peptide Chemistry BS or MS degree or equivalent experience in chemistry, chemical engineering, biochemistry, or related field. Exp: 1+ years |
Amide is seeking an exceptional individual to join our growing team as a Research Associate/Technician. The successful candidate will be a key contributor to various research projects and be responsible for executing laboratory experiments, analyzing and reporting results, and working within a larger team on a regular basis. Applicants should be team players able to excel in a fast-paced, collaborative environment. | 12/28/2023 |
| 919 | Amneal Pharmaceuticals Brookhaven, NY Production Engineer Bachelors Degree (BA/BS) Engineering discipline or Master Degree (MS/MA) Engineering discipline. Exp: less than one year |
The Production Engineer plans and designs methods to improve production processes. Reviews existing processes and develops solutions to increase productivity or reduce costs. Ensures compliance with approved production methods and quality standards. | 12/28/2023 |
| 920 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist I Bachelors Degree (BA/BS) in Chemistry or related field. Exp: 1+ years |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 12/28/2023 |
| 921 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist I Bachelors Degree (BA/BS) Microbiology or related field. Exp: 1+ years |
The QC Chemist I (internally titled “Scientist I, Quality Control”) is an entry-level role responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, to clearly document activities performed during testing and to calculate and report results on applicable specification documents. | 12/28/2023 |
| 922 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS). Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 923 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS) in Chemistry or related science discipline. Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 924 | Amneal Pharmaceuticals Brookhaven, NY QC Chemist II Master Degree (MA/MS) in Chemistry or related science discipline. Exp: 1+ years |
The QC Chemist II (internally titled “Scientist II, Quality Control”) is responsible for performing testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculating and reporting results on applicable specification documents, participating in method transfer activities within departments or between facilities or organizations. Provides feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. | 12/28/2023 |
| 925 | AnaSpec Fremont, CA Synthesis Chemist I BS or above in Chemistry, Organic Chemistry, or related disciplines. Exp: 1-3 years |
The Synthesis Chemist I will perform peptide production and conduct in-process testing using Good Laboratory Practices (GLP). As a member of the Synthesis department, the Synthesis Chemist I will work closely with the Purification, QC, and Sales & Business Development departments. | 12/28/2023 |
| 926 | AnaSpec Fremont, CA QC Chemist Bachelor's degree in Chemistry or science related field. Exp: 1+ years |
This position is responsible for performing analytical testing for various product lines, such as peptides, dyes, and unusual amino acids and ensures that the products are evaluated in a timely manner and meet all procedural requirements. | 12/28/2023 |
| 927 | AnaSpec Fremont, CA GMP Manufacturing Chemist Bachelors in chemistry, organic chemistry, biochemistry. Exp: 1+ years |
The GMP Manufacturing Chemist will be responsible for supporting all GMP upstream and downstream peptide manufacturing related processes. The GMP Manufacturing Chemist will ensure prioritization, and proper documentation of projects. This individual will work closely with GMP downstream lead and GMP upstream lead. The GMP Manufacturing Chemist is also responsible for ensuring that the assigned tasks are completed in a timely manner. | 12/28/2023 |
| 928 | Ansh Labs Webster, TX Scientist Master’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: 1 year |
As a key member of the Manufacturing or R&D Department, this individual will provide critical scientific skills to assist in the development and scale-up of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays, Lateral Flow assays and micro fludics based immunoassays). | 12/28/2023 |
| 929 | Ansh Labs Webster, TX Jr. Scientist Bachelor’s degree in Biological/Chemical Sciences/Biotechnology or related area. Exp: one year |
As a key member of the Manufacturing, Research & Development and Quality Control departments, this individual will provide critical scientific skills to assist in the development, scale-up and QC testing of immunodiagnostic products on various platforms (microtiter based ELISA, magnetic particle based immunoassays). | 12/28/2023 |
| 930 | Applied Medical Rancho Santa Margarita, CA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 0+ years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 12/29/2023 |
| 931 | Applied Medical Rancho Santa Margarita, CA CAPA Quality Engineer I Bachelor’s degree in an Engineering or Science, Technology, Engineering, and Mathematics (STEM) field or related education and experience. Exp: 0+ years |
Collaboration is a fundamental part of our organization's culture and is essential to our continued success. As such, the successful candidate for this position is expected to work on-site, enabling them to engage fully with colleagues and contribute to cross-functional initiatives. Therefore, the ability to work collaboratively and contribute to a positive and supportive team environment is a key requirement for this role. | 12/29/2023 |
| 932 | Argonaut Manufacturing Services Carlsbad, CA Bioprocess Technician II/III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Bioprocess Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. | 12/29/2023 |
| 933 | Argonaut Manufacturing Services Carlsbad, CA Formulation Technician II/III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Formulations Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance | 12/29/2023 |
| 934 | Argonaut Manufacturing Services Carlsbad, CA Manufacturing Technician II or III Level II: Requires a bachelor's degree in a related field. Exp: 1 year |
The Manufacturing Technician is responsible for executing all processes in production while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which could apply. Under the general direction of the lead technician and the overall direction of the supervisor, this position shall be responsible for the hands-on execution of all activities in the production area. The Manufacturing Technician is expected to fully participate in both departmental projects and any quality working teams which may be applicable. existing procedures. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. This role is 100% on-site, Monday - Friday, 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. This role is 12:00 pm - 8:30 pm with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. | 12/29/2023 |
| 935 | Arraystar Rockville, MD Lab Assistant - Molecular Biology Bachelor’s degree in a relevant biological field. Exp: 1-2 years’ |
Perform routine molecular biology lab duties such as DNA and RNA extraction, gel electrophoresis, solution and buffer preparation, and etc. Perform and document all test procedures with accuracy, consistency and timeliness in accordance with laboratory SOPs and regulatory guidelines. Assist with the generation and updating of laboratory SOPs. Perform basic lab maintenance tasks such as ordering lab supplies, and keeping detailed lab records. Communicate with clients to obtain/verify information of their projects, orders or requests. | 12/29/2023 |
| 936 | Artiva Biotherapeutics San Diego, CA Manufacturing Associate (Temporary) Bachelor’s degree in relevant science or engineering discipline. Exp: 1 years |
The Manufacturing Associate will support manufacturing of Artiva’s off-the-shelf cell therapy platforms in our new, state of the art, cGMP facility. The successful candidate will develop, adhere to, and optimize written procedures (SOPs) related to GMP facility operations, monitor equipment and facilities, and will play a key role in the manufacturing of cell therapies internally at Artiva. The ideal candidate will demonstrate in-depth knowledge of cGMP compliance and will be a self-starter and have the ability to work independently to achieve corporate objectives. This is a temporary position and is located at our corporate headquarters in San Diego, CA. | 12/29/2023 |
| 937 | Astute Medical Salt Lake City, UT Research Associate I Bachelor's degree in a scientific discipline. Exp: six months' |
The Research Associate I (RA I) works to meet deadlines in a dynamic environment and has the temperament to operate proactively and collaboratively in a team in support of research and development activities. Tasks will focus on molecular and microbiological experiments and procedures (e.g., nucleic acid extraction, serial dilution, PCR, bacterial and fungal culture, etc.) with associated collection, analysis, verification and recording of data in accordance with established protocols and work instruction documents, regulations, safety requirements, and the quality system. Work is primarily collaborative and requires the ability to communicate and coordinate with peers and supervisor(s) effectively and respectfully. | 12/29/2023 |
| 938 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field, or hold an Associate’s degree and have exceptional lab experience. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 12/29/2023 |
| 939 | Astute Medical Hazelwood, MO B-Lab Technician - Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 940 | Astute Medical Hazelwood, MO Lab Technician - Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 941 | Astute Medical Hazelwood, MO Lab Technician-Media Lab Bachelor’s degree in a scientific field required. Biology/Chemistry preferred. Exp: One year |
This is a 3rd shift position. The primary purpose of this position is the timely preparation, delivery, and set-up of quality, complex chemical media to Card Production., being current on training including curriculum procedures, work station organization and cleaning, establishing a safe work environment, housekeeping and maintenance functions in the production department. | 12/29/2023 |
| 942 | Astute Medical Salt Lake City, UT Template Control Laboratory Technologist I B.S. in chemistry, biology, or a related field, or hold an Associate’s degree and have exceptional lab experience. Exp: 6 months |
The Template Control Laboratory Technologist (LT) works with a team that formulates DNA and RNA template control components to support the company’s in vitro diagnostic products’ research and development, manufacturing, validations, and quality control efforts. The LT-I will use established methods and techniques to maintain the lab’s DNA and RNA template inventory, perform template manipulations and verification including diluting, aliquoting, mixing, quantitative PCR, quantitative RT-PCR, and FilmArray analysis, perform template and control mix formulations, and dispense template and control mixes to dependent departments in accordance with the company’s quality system. | 12/29/2023 |
| 943 | Astute Medical Salt Lake City, UT Lab Technologist I - Oligo, Day Shift Bachelor’s Degree (BS), or working toward a degree. Chemistry, BioChemistry, and Biology preferred. Exp: 1+ years |
We are seeking a Lab Technologist I to join our team. Lab Technologists are responsible for performing a wide variety of laboratory tasks and production processes. This includes operating and troubleshooting HPLCs, DNA Synthesizers, LC/MS, liquid handling robots, and UV/Vis Spectrometry. Lab Technologists works on assignments that are routine in nature where ability to recognize deviation from accepted practice is required. Normally receives general instructions on routine work, detailed instructions on new assignments Strong pipetting skills, attention to detail, organization, and familiarity with cGMP are desired. | 12/29/2023 |
| 944 | Atalanta Therapeutics Boston, MA Associate Scientist II, Oligonucleotide Chemistry Master’s degree in Chemistry or related scientific discipline. Exp: 0-2 years |
Atalanta Therapeutics is seeking a motivated Associate Scientist to join the Chemistry team to assist with the preparation of oligonucleotides for drug discovery. The Associate Scientist will work as part of a team on various projects that are critical in advancing our research and development efforts, using specialized equipment to produce high-quality compounds and analyzing data to facilitate process optimization. This individual will deliver oligonucleotides for research experiments, help maintain and troubleshoot equipment, and collaborate with cross-functional teams in a cutting-edge laboratory environment. Successful candidates will have strong analytical and problem-solving skills with an eagerness to learn and contribute to a dynamic team environment. | 12/29/2023 |
| 945 | Atalanta Therapeutics Boston, MA Associate Scientist II/Senior Associate Scientist, In Vivo Pharmacology Master’s degree. Exp: 0-2 years |
Atalanta is seeking a highly skilled and motivated Associate/Senior Associate Scientist to join the in vivo pharmacology group to support Atalanta’s drug discovery programs. This individual will have extensive hands-on experience in performing survival surgeries (stereotaxic or direct intraparenchymal injection preferred), pharmacological administration, brain and tissue collection, and in processing CNS tissue and molecular analysis to assess target gene and protein expression. We are seeking candidates who thrive in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The Associate/Senior Associate Scientist will be responsible for assay development and execution of experiments to determine the biodistribution, pharmacodynamic properties and efficacy of oligonucleotides in research and preclinical studies supporting multiple drug discovery programs and platform discovery research. | 12/29/2023 |
| 946 | August Bioservices Nashville, TN Manufacturing Technician I/II/III - Formulation & Component Prep BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician– Component Preparation and Formulation will operate a variety of processing and packaging equipment to prepare components for aseptic filling to include bulk formulation of aqueous and non-aqueous based products, order and receive components, dispense and formulate raw materials, manage sterilized components, operate various equipment used in the formulation process, and perform cleaning operations for process equipment and the GMP ISO 8 areas. | 12/29/2023 |
| 947 | August Bioservices Nashville, TN Manufacturing Technician I/II/III – Filling, Lyophilization, & Terminal Sterilization BS or BA or equivalent in a biological, chemical science, engineering, or degree in another discipline. Exp: One year or more |
August Bioservices is hiring Filling/Manufacturing Associates at various position levels to work in the new aseptic manufacturing facility located in Nashville, TN. The Manufacturing Technician – Filling, Lyophilization, and Terminal Sterilization will use proper aseptic technique while performing tasks in aseptic manufacturing areas to include syringe and vial filling operations with an automated line in an RABS environment as well as routine and non-routine aseptic interventions through RABS glove ports. The technician II level will operate filling and auto loading equipment, and freeze dryers using automated control systems. The Technician will be responsible for unloading of autoclaves, performing cleaning operations for process equipment and the GMP ISO 8 areas, management of sterilized components, and coordinating with maintenance as needed. | 12/29/2023 |
| 948 | AxoGen Vandalia, OH QC Histology Technician Associate degree in chemistry, biology, or a science/technical related field required (Bachelor’s degree preferred). Exp: 1+ years |
The Quality Control (QC) Histology Laboratory Technician will support QC Histological testing by conducting a variety of laboratory tasks. He/she will also be responsible for routine laboratory operations including maintenance, solution and media preparation, routine testing, ordering supplies, and laboratory housekeeping. The QC Histology Technician will be required to handle biohazardous materials. The successful candidate will carry out testing and evaluations according to established procedures, document results, and detail any testing observations. He/she may be responsible for incoming materials release, in process testing, and release testing. He/she will also contribute to writing reports and documenting laboratory standard operating procedures (SOPs). The successful candidate will be responsible for cleaning, disinfecting, and managing inventory of lab equipment other related duties as assigned. | 12/29/2023 |
| 949 | Bardy Diagnostics Plymouth, MN Engineer I - R&D Disposables (Hybrid) BS in Mechanical, Plastics, Biomedical Engineering or a related field, MS preferred. Exp: 0 - 1 year |
What you'll be doing Document engineering concepts. Create, modify, and maintain design documentation per company procedures. Assist in the design and building of basic tooling, test fixtures and assembly equipment. Build prototypes and models and may operate machine tools. Understand customer needs through literature review, customer interviews, direct observation, competitive analysis, prototype evaluation, and clinical/simulated use studies. Write technical reports based on design verification analysis/testing for design changes and product design activities. Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis, and data analysis. Identify, investigate, and solve engineering problems. | 12/29/2023 |
| 950 | Uptake Medical Johnson City, TN Quality Control Chemist - 2nd Shift Minimum 2-year Associates Degree or 4-year BS Degree in Science. Exp: 0 - 5 years’ |
The QC Chemist 1 is responsible for assisting in supporting Quality Control Laboratory personnel as it pertains to the sampling of raw materials, purified water system, in-process materials and finished products. | 12/18/2023 |
| 951 | Uptake Medical Johnson City, TN Associate Scientist Bachelor’s degree in Chemistry or other related discipline. Exp: 0-2 years |
Crown Laboratories, Inc. is currently recruiting for an Associate Research Scientist. The Associate Research Scientist is responsible for assisting the Research Scientist and the R&D department in the development of new products from concept to commercialization to support company growth. | 12/18/2023 |
| 952 | Wugen St. Louis, MO Associate Scientist: CMC Process Development MS Degree in biology or related field. Exp: 1+ years |
Join a fast-paced startup based in St. Louis with the opportunity to help drive process development activities of novel therapies for treating rare diseases. The associate scientist role is part of the CMC department, and will focus on executing experiments in flow cytometry. | 12/18/2023 |
| 953 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab (1st Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 12/18/2023 |
| 954 | Abbott Sturgis, MI Assistant Chemist I, Analytical Lab (1st Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
An Assistant Chemist I is responsible for testing the necessary raw ingredient, in process, and finished product as prescribed in the various quality procedures and assuring specifications and quality guidelines are met. The incumbent is responsible for producing the highest quality results while operating within the constraints of the manufacturing schedule and safety guidelines. They are responsible for maintaining good manufacturing practices and good laboratory practices. The chemist I is responsible for developing positive relations with other chemists and operators from other departments that interact with the laboratory. The incumbent is also responsible for providing timely feedback to the chemist following them, their lead chemist, and their supervisor as to the status of their area of responsibility. | 12/18/2023 |
| 955 | Abbott St. Paul, MN Clinical Engineer-2 Associates Degree. Exp: 1 year |
Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. Under general supervision, responsible for designing new products and processes and improving and maintaining existing products. May execute less complex projects. | 12/18/2023 |
| 956 | Abbott Irving, TX Associate Mechanical Engineer BS Mechanical Engineering. Exp: 0-2 years’ |
Individual contributor that works under limited supervision. Designs mechanical and electromechanical products and systems by developing and testing specifications and methods. | 12/18/2023 |
| 957 | Abbott Sturgis, MI Assistant Microbiologist I (2nd Shift, Tues-Sat) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment Product testing, Environmental testing, Raw ingredient testing Documentation, Project work, Troubleshooting Media preparation/general lab work: Housekeeping Communication, Teamwork | 12/18/2023 |
| 958 | Abbott Sturgis, MI Assistant Microbiologist I (3rd Shift) - Sturgis, MI Plant Science related Associates Degree or Science related Bachelor’s Degree. Exp: AS: 1 year; BS: 0+ years |
Apply high quality scientific techniques in the microbiological analysis of raw ingredients, in-process production samples, finished product testing and environmental monitoring, to ensure that all products manufactured are fit for use Be able to work with fellow microbiologist, with a high degree of motivation, attention to important details with clear communication to all team members. This is important due to the high degree of responsibility and working within a small group where each person is relied upon highly Prioritize tasks to efficiently be completed with the most accurate results, and to communicate clearly and work together in a team environment Product testing, Environmental testing, Raw ingredient testing Documentation, Project work, Troubleshooting Media preparation/general lab work: Housekeeping Communication, Teamwork. | 12/18/2023 |
| 959 | Abbott St. Paul, MN Manufacturing Engineer I Bachelors of Science degree in Electrical Engineering, a related field or equivalent. Exp: 0-3 years |
This position works out of our St Paul, MN location in the Electrophysiology Medical Device division. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. We are seeking a Manufacturing. Engineer I. This position will design and develop manufacturing processes and support production and service activities in order to meet daily production schedules while enhancing productivity, cost and product quality. Product lines supported are comprised of electronic systems used in our medical devices to better the lives of patients around the globe. | 12/18/2023 |
| 960 | Abeona Therapeutics Cleveland, OH Manufacturing Associate MS in scientific discipline. Exp: 1-2 years |
Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 12/20/2023 |
| 961 | Abeona Therapeutics Cleveland, OH Manufacturing Associate MS in scientific discipline. Exp: 1-2 years |
Abeona is looking for a Manufacturing Associate to join our team in Cleveland, OH. The successful candidate will be responsible for Manufacturing initiatives supporting multiple product pipelines. The candidate will be an integral part of a fast-paced group responsible for the manufacture of retroviral vector, autologous gene-corrected cell therapies, and clinical AAV gene therapies. Responsibilities will include executing protocols and manufacturing clinical material across multiple products as well as supporting process optimization work and document generation. The ideal candidate will have experience in production of biologics in a controlled cGXP setting. Strong aseptic and cell culture technique as well as collaborative work in a team is an integral part of this position. | 12/20/2023 |
| 962 | Analytical Biological Services Wilmington, DE Biorepository Technologist I (In-Sourced) Associate’s Degree in a medical or biological science is required. Bachelor’s Degree preferred. Exp: 1+ years |
Primary duties and responsibilities of the Biorepository Technologist I (In-Sourced) included but are not limited to: -Receive biospecimens including frozen, fixed, or fresh solid and liquid samples -Coordinate with shipping and receiving department to ensure all shipments are appropriately tracked -Coordinate with internal clinical study team to ensure sample and data accuracy -Communicates by written and verbal methods with related departments to assure samples arrive in the appropriate lab -Record sample quality concerns and provide feedback to collection site or central lab -Document sample information in laboratory database from source documents -Accession samples and appropriate data in the laboratories electronic data management system -Pull samples from inventory when requested by scientists for internal projects -Report and reconcile study data for management teams across departments -Provide Data management with scheduled monthly inventory reports and inventory reports upon Data managers request in a timely manner. -Upload monthly inventory reports to LIMS Labmatrix. -Organize and audit existing inventory QC and QC of sample location and data integrity -Ensure compliance with best practice guidelines, laboratory and EHS protocols, company standards and policies, standard operating procedures (SOP), and industry regulations. -Other duties as assigned | 12/20/2023 |
| 963 | Analytical Biological Services Wilmington, DE Cell Culture Scientist BS or BA or higher degree in biological sciences. Exp: 1+ years |
- The position involves maintenance of cell culture lines to include thawing, expanding, harvesting and freezing lines. - Strict quality control guidelines of all products coming from cell culture must be monitored and adhered to. - Proper and aseptic maintenance of cell culture and production laboratory is required. - The Scientist must be able to effectively communicate with team members and clients of our progress with products and services and be able to respond quickly and accurately to client inquiries and requests. - Record keeping, excellent organizational skills and the ability to multitask are a must. | 12/20/2023 |
| 964 | Absorption Systems Baltimore, MD Research Assistant undergraduate with a Life Sciences degree. Exp: entry-level |
We are seeking Research Assistants to join our Baltimore, MD clinical team! As a Research Assistant, you will be responsible for a variety of clinical research activities, ensuring that established protocols are followed, maintaining study protocol integrity, monitoring participant's status and safety, and playing a significant role in the training of clinical staff. We are conveniently located on the University of Maryland BioPark campus and provide paid parking for all employees. We have 12-hour day shifts, night shifts, and weekend shifts available. If you're seeking an entry-level role in Research, please apply. | 12/20/2023 |
| 965 | Abveris Portland, OR Manufacturing Associate Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 12/20/2023 |
| 966 | Abveris Portland, OR Manufacturing Associate - Gene Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. The Manufacturing Associate, Gene Production, will produce various DNA and plasmid products, focusing on molecular and cellular biology, as well as running analytic techniques in the high-throughput/highly-automated lab according to established SOPs, along with working with sensitive equipment and following good manufacturing practices. Candidates must also be a team player, neat and highly organized, able to work in a cleanroom environment and foster safe work practices. The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. | 12/20/2023 |
| 967 | Abveris South San Francisco, CA Manufacturing Associate, NGS TE Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations Team in South San Francisco. The Manufacturing Associate, NGS TE will perform basic molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture of variety of custom oligonucleotide products. The ideal candidate will be able to work independently, be very neat and organized, have the ability to follow established SOPs and complete manufacturing batch records to contribute to the daily production schedule. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. The Manufacturing Associate will be responsible for the production of custom gene based products and/or various intermediates according to established SOPs and complete manufacturing batch records to contribute to the daily production schedule. They will uphold standards as defined by the manufacturing process, work on continuous improvement and have good time management resulting in efficiency, and work in a safe manner. | 12/20/2023 |
| 968 | Abveris Portland, OR Manufacturing Associate - Reagent Production Associates or Bachelors degree in Biology, chemistry or related field is desirable. Exp: 1+ years |
We are looking for motivated, enthusiastic individuals to join our Twist Bioscience Operations team in Wilsonville, OR. Shift: Tuesday-Saturday (3:00pm-11:30pm PST) The Manufacturing Associate will perform basic reagent handling, chemistry and molecular biology workflows in a highly automated, high-throughput manner and will be responsible for the manufacture and analysis of a variety of custom DNA based intermediates and products across Twist Bioscience’s proprietary process workflow to meet the Twist production forecast and timelines. The ideal candidate will be driven and will do what it takes to keep manufacturing on track in a fast paced start-up environment. | 12/20/2023 |
| 969 | Abveris South San Francisco, CA Associate Engineer Bioinformatics, Biopharma Libraries BS or MS in Computer Science, Bioinformatics, or related scientific/engineering field. Exp: 0 - 1 years |
Twist Biopharma is seeking an Associate Bioinformatics Engineer to develop and integrate workflows, analyses, and computational tools involved in the production and research of antibodies and proteins. While you have a broad interest in biotech and related scientific technologies, you also understand that computer science resources must be utilized to reach the scale required for our most complex solutions. The ideal candidate has computational/software/bioinformatics experience, and a basic knowledge of biology, DNA, antibody development, or protein sciences. He or she is comfortable with Python and JavaScript and will assist in the development of cutting-edge machine-learning applications, databases, and reports using modern tools, software development techniques, and coding best practices. | 12/20/2023 |
| 970 | Abveris South San Francisco, CA Research Associate II, Process Development Research Associate: BA. Research Associate II: MSc. Exp: RA: 0-2 years; RAII: 0-2 years. |
The Research Associate II will interface between R&D and Operations to establish new processes at scale for DNA-based products in manufacturing. You will develop and support the production team’s custom DNA-based applications and assays for synthetic biology including high-throughput probe generation through robust experimental design. The ideal candidate will be driven and will do what it takes to keep manufacturing on track and constantly improving in a fast-paced startup environment. | 12/20/2023 |
| 971 | Associates of Cape Cod East Falmouth, MA Quality Control Analyst I B.S. degree in a relevant scientific discipline. Exp: 0-2+ years |
In this role you will perform chemical and/or biological assays of commercial product raw materials, production intermediate and bulk samples, finished product, environmental monitoring samples, process and cleaning validation samples. Assays are qualitative, quantitative and investigational in nature and are performed in compliance with cGMP, ACC SOPs, and FDA Analyst has working knowledge of relevant QC techniques, policies and procedures to perform QC tasks and document results. Analyst receives minimal supervision on routine assignments and detailed instructions on new assignments. | 12/20/2023 |
| 972 | Adaptimmune Therapeutics Philadelphia, PA Quality Analytical Science and Technology Associate Scientist Bachelor’s degree in molecular biology, biomedical sciences or related specialties. Exp: 1+ years |
The purpose of this role is primarily to perform scientific work to support the Quality Control and Analytical Science and Technology team of analytical method and assay validations of Adaptimmune’s T-cell platform analytics. An Associate Scientist is broadly expected to support the team with the following duties. | 12/22/2023 |
| 973 | Adare Pharmaceuticals Philadelphia, PA Analytical QC Chemist I Bachelor’s degree in chemistry, Biology, biochemistry, or related scientific field. Exp: 0-2 years’ |
The Analytical Chemist II is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures. | 12/22/2023 |
| 974 | Admera Health South Plainfield, NJ Associate Scientist I/II Bachelor’s degree in Biological Sciences or M.S. in Biological Sciences. Exp: BS: 1-3 years; MS: 1 year. |
Responsibilities: • Preparing solutions and reagents for performing assays on the bench. • Perform Next Generation Sequencing-based genomic assays on different workflows (few listed below): o RNAseq o Whole Genome Sequencing o Whole Exome Sequencing | 12/22/2023 |
| 975 | Aimmune Therapeutics Dublin, OH Chemistry Technician BS in Related Science. Exp: 0-5 years |
Position Summary: The Technician position may undertake performance and documentation of routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods and/or basic laboratory techniques, functions and equipment. To conduct specific procedures and tests both within and outside of the laboratory requiring the use of applied knowledge and practical skills learned from on-the-job experience; modify or adapt techniques to fit special needs or problems; to calculate data from routine tests to final results and to evaluate such results for accuracy where expected findings are not precisely defined, but sufficient guidelines exist for reference; to assist with and occasionally perform specialized and non-routine tests and assays, and to maintain records of such work; to coordinate and plan assigned work with other technicians and scientists. This position requires the following schedule pattern: Tuesday - Saturday 7:00am - 3:30pm OR Thursday - Monday 7:00am – 3:30pm | 12/22/2023 |
| 976 | Aimmune Therapeutics Leonia, NJ Chemist B.S. in chemistry preferred. Exp: 1+ years |
Position Summary: The Chemist position is responsible for performing routine laboratory procedures in a quality control laboratory. Duties are performed under general supervision. Must be familiar with basic laboratory equipment and techniques. Responsibilities are focused on less complex testing and support functions. | 12/22/2023 |
| 977 | Aimmune Therapeutics Dublin, OH Quality Technician undergraduate degree in closely related science preferred (i.e. Microbiology, Chemistry, Biology, et al.) Exp: 1 year |
Position Summary: This position performs and documents routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods, and/or basic laboratory techniques, functions and equipment. The position conducts specific procedures and tests within the laboratory requiring the use of applied knowledge and practical skills learned from on-the-job experience; modify or adapt techniques to fit special needs or problems; to calculate data from routine tests to final results and to evaluate such results for accuracy where expected findings are not precisely defined, but sufficient guidelines exist for reference; to assist with and occasionally perform specialized and non-routine tests and assays, and to maintain records of such work; to coordinate and plan assigned work with other technicians and scientists. | 12/22/2023 |
| 978 | Aimmune Therapeutics Bayport, NY Associate Technical Services Scientist/Specialist (TAG - Bayport, NY) Bachelor’s degree in Science, Chemistry, Chemical Engineering or in a related field required. Exp: 1+ years |
The Associate Technical Services Scientist/Specialist works within our Technical Applications Group (TAG) and will assist in formulating nutritional supplement products in various forms in support of manufacturing by collecting, evaluating, analyzing and summarizing data, address manufacturing issues, evaluate new technologies and/or ingredients and seek cost savings. Adherence to Standard Operating Procedures (SOP’s) and current Good Manufacturing Practices (cGMP’s) in this role is required. This position will work onsite Monday through Friday at Nestle Health Science’s manufacturing site in Bayport, NY (Long Island area). | 12/22/2023 |
| 979 | Aimmune Therapeutics Mechanicsburg, PA Controls Technical Specialist I | $2,000 Sign On Bonus Eligible Associate’s Degree in a technical discipline Exp: 1+ years |
At Nestlé Purina PetCare, we’re a “safety first” culture, driven by a zero accident, zero defect, zero waste mentality. As a Controls Technical Specialist I, you’ll be responsible for troubleshooting, maintaining and enhancing the accuracy, reliability and system control’s data credibility of PLC and PC-based automation systems. In this role, you will oversee PLC upgrades and wiring modifications on production equipment and work directly with our maintenance team to troubleshoot and support production line modifications. As a Controls Technical Specialist I at our Mechanicsburg facility, you will enjoy competitive pay, $2,000 sign-on and retention bonus, premium pay, up to 5% quarterly bonus, $500 Lifestyle Spending each year, full health benefits, 401k match, generous PTO, excellent maternity/paternity leave and so much more! | 12/22/2023 |
| 980 | Aimmune Therapeutics Flagstaff, AZ Associate Staff Engineer Bachelor’s Degree in Engineering or related field. Exp: 1+ year |
As an Associate Engineer, you will support the development of factory masterplans to align with Nestlé Purina long-term business objectives. You will have the opportunity to leverage your leadership skills while working with cross-functional teams at the corporate and factory levels. You will assist with delivering high value through technical scope development with supported justification, while adhering to project standards and strategies. Additionally, you will work on project submittal requirements and ensure quality while working closely with Nestlé Purina stakeholders. | 12/22/2023 |
| 981 | Aimmune Therapeutics Solon, OH Product Development Associate BS or MS degree in Food Science, Food Engineering, Chemical Engineering, Packaging Science, Packaging Engineering, Mechanical Engineering, or related Exp: 0-3 years |
You will work hands-on the with our Pilot Plants and Factories, and Manufacturing facilities to deliver on the Innovation & Renovation (I&R) business objectives. You will dig into recipe (re)formulation, rapid pro-typing, and manage vendor relationships/interactions. You will help to build consumer insights and be the face of our products in cross-functional settings with commercial teams like Marketing, Sales, Finance. | 12/22/2023 |
| 982 | Alkermes Wilmington, OH QC Analyst I Bachelor of Science degree in Chemistry or related scientific field. Exp: 1+ years |
The QC Analyst I performs testing of samples submitted to the laboratory in a cGMP compliant manner, as well as according to approved written procedures. The QC Analyst I may be required to write or revise SOPs, analytical procedures, or other analytical documentation at the discretion of quality control supervisory staff. | 12/22/2023 |
| 983 | Alkermes Wilmington, OH Temp-QC Analyst-Microbiology Wilmington, OH, United States Bachelor's in science, preferably in Biology / Microbiology / Biotechnology or Biochemistry, required. Exp: 1+ year |
QC Analyst I must have broad knowledge of microbiology techniques within the laboratory required for the routine support of the microbiology laboratory operations. In this role the Analyst will be a fully functional member of the team responsible for testing and data entry for finished product, in-process samples, stability samples, clinical materials and raw material release in a cGMP regulated environment | 12/22/2023 |
| 984 | Alkermes Wilmington, OH QC Analyst I/II Bachelors Degree in Chemistry. Exp: 0-2 years |
The position requires the individual to perform routine/non-routine physical, chemical, and in-vitro assays of clinical, commercial, process and cleaning validation samples, and process development samples to support Manufacturing. Performs physical and/or chemical analyses of product to ensure stability. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. | 12/22/2023 |
| 985 | Alkermes Wilmington, OH Temp-Manufacturing Associate-Bulk-2nd Shift Associates degree or higher in a science/technical discipline. Exp: 0-1 year |
Perform all necessary operation activities in bulk manufacturing. These activities include but are not limited to the following: Equipment Cleaning, Equipment Set-up, Equipment/Automation Operation, and Batch Processing. Reads and follows detailed written SOPs / Procedures and detailed documentation of operations according to cGMP. Performs sample collection, equipment/process monitoring, and minor maintenance. Maintain individual training proficiency through individual Learning Management System. Other responsibilities include SOP writing and review of cGMP documentation. | 12/22/2023 |
| 986 | Alkermes Wilmington, OH Manufacturing Associate-Bulk 2nd Shift Associates degree or higher in a science/technical discipline. Exp: 1+ year |
Perform all necessary operation activities in bulk manufacturing. These activities include but are not limited to the following: Equipment Cleaning, Equipment Set-up, Equipment/Automation Operation, and Batch Processing. Reads and follows detailed written SOPs / Procedures and detailed documentation of operations according to cGMP. Performs sample collection, equipment/process monitoring, and minor maintenance. Maintain individual training proficiency through individual Learning Management System. Other responsibilities include SOP writing and review of cGMP documentation. | 12/22/2023 |
| 987 | Alkermes Wilmington, OH Process Engineer I/II/Lead-Filling Process Engineer I: BS degree in Engineering or technical discipline. Exp: 0-2 years |
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Scale-up and transfer formulations/processes to production facility, design and recommend equipment purchases, write and execute qualification/validation protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process/equipment improvements (utilizing Change Control system) to reduce waste and increase process reliability. Support of manufacturing management in periodic review of existing and new revisions to manufacturing documentation in regard to, but not limited to, Operability, Technical accuracy (technical reviews), Compliance, Process Robustness. Perform process and equipment evaluation (FMEA, etc) to identify risks and weaknesses in new and current processes, Write or revise SOPs and other GMP documentation in support of new or changed manufacturing processes in cooperation with appropriate manufacturing personnel, Assure the resolution of deviations, corrective actions, action items from Change Control systems, and any audit non-compliance items. Develop and implement SOPs in support of new and upgraded processes, Develop and implement effective training of manufacturing personnel related to technical transfer and process upgrades, represent manufacturing on process design teams, Champion projects as they move into and through the manufacturing areas, Provide regular updates to manufacturing management on the status and issues involved in projects. | 12/22/2023 |
| 988 | Alliance Pharma Malvern, PA Associate Scientist I- Immunoassay BA/BS or higher. Exp: 1-2 years |
• Prepare reagents, standards, and control samples • Analyze samples using various techniques specific to department • Perform method validation or qualification • Operate analytical equipment • Maintain analytical equipment • Ensure lab area is clean and inspection ready at all times • Remove lab waste • Record tasks in accordance with Good Documentation Practices (GDP) • Understand and apply regulatory requirements; GLP, GCP, 21CFR Part 11 • Follow applicable SOPs and procedural documents • Review and evaluate data results | 12/22/2023 |
| 989 | Alliance Pharma Malvern, PA Assistant Scientist II BA/BS or higher. Exp: 1-2 years |
Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Operate analytical equipment · Maintain analytical equipment · Ensure lab area is clean and inspection ready at all times · Remove lab waste · Record tasks in accordance with Good Documentation Practices (GDP) · Learn and apply regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Learn how to review and evaluate data results · Other tasks as assigned | 12/22/2023 |
| 990 | Prominex San Diego , CA Research Associate I/II Master’s degree in Science Exp: 0-2 years |
We are looking for an enthusiastic and dedicated Research Associate to implement and execute analytical and scientific experiments to drive Product Development. Demonstrates high degree of organization and planning and the ability to apply scientific principles to plan out and execute experiments involving a variety of laboratory methods. This individual demonstrates technical proficiency, high degree of organization and planning and the ability to apply scientific principles. | 12/12/2023 |
| 991 | RayzeBio Indianapolis, IN Microbiologist BS/MS in Biology, Microbiology, or other Life Science related field. Exp: up to five years |
Reporting to the Asst. Manager of Microbiology, the Microbiologist will help support the establishment of a new Environmental Monitoring/Microbiology laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Microbiologist will be providing support for the commissioning, qualification, and validation of cleanroom environments and equipment and the associated environmental monitoring program. Upon establishment of the laboratory and program, the position will support the environmental monitoring and microbiological release testing of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 12/13/2023 |
| 992 | RayzeBio Indianapolis, IN Radiopharmaceuticals Production Operator (I/II) Associate’s or Bachelor’s Degree in a STEM field is preferred. Exp: 1 – 4 years’ |
The Radiopharmaceuticals Production Operator will be an integral part of bringing RayzeBio’s innovative drug products to patients in need. As the Production Operator, you will play an active role in daily operations, striving to ensure each batch is right the first time and that the production area is kept in order at our manufacturing site in Indianapolis IN. You will be responsible for the production of RayzeBio drug products, strictly complying with good manufacturing practice and aseptic requirements. Additionally, you will be the front line in ensuring compliance with radiation safety requirements on the production floor. As RayzeBio expands the production site and its portfolio of new products, you will support validation work for future company initiatives, and support management with internal projects and new hire training. The Radiopharmaceuticals Production Operator will report directly to the Production Manager. Operator level will be evaluated with experience and qualifications. | 12/13/2023 |
| 993 | RayzeBio Indianapolis, IN Quality Control Chemist BS/MS in Chemistry, Science, or relevant field. Exp: up to five years |
Reporting to the Sr. Manager of Quality Control, the Quality Control Chemist will help support the establishment of a new Quality Control laboratory which supports RayzeBio’s Radiopharmaceutical manufacturing facility in Indianapolis. The Quality Control Chemist will be responsible and/or providing support for the installation, commissioning, qualification, and validation of analytical and radiochemical equipment for the QC lab. Upon establishment of the laboratory and program, this position will utilize a wide range of analytical and radiochemical analyses to support the advancement and release of novel targeted radiopharmaceuticals from the R&D phase through clinical development to GMP commercial radiopharmaceutical production. Specifically, the quality control chemist will support the release of manufactured radiopharmaceuticals to support RayzeBio’s clinical and commercial programs. | 12/13/2023 |
| 994 | MacroGenics Rockville, MD Research Associate II Master’s degree in a scientific discipline. Exp: 0+ years |
The Research Associate II / Associate Scientist I position will support preclinical development of MacroGenics antibody-drug conjugates (ADC) through cell line engineering and molecular biology support. This position will independently develop and engineer cell lines, and conduct cell-based, molecular, and biochemical assays which contribute to the ADC research and development pipeline. | 12/13/2023 |
| 995 | MacroGenics Rockville, MD Animal Health Technician I Bachelor’s degree in scientific discipline. Exp: 0+ years |
The Animal Health Technician I is responsible for executing animal care duties and responsibilities that enable us to support rapid advancement of preclinical programs. | 12/13/2023 |
| 996 | Rockland Immunochemicals Pottstown, PA Associate Scientist/Scientist I, Molecular Biology Bachelor’s degree in biological sciences, biochemistry, or a closely related scientific field. Exp: 1-2 years |
Responsibilities include: RNA and DNA amplification and digestion (for transfection or transformation) as well as immunofluorescence assays, antibody validation (SDS, WB, Analytical SEC) Purification and characterization of recombinant protein targets using AKTA, ion exchange, affinity and size exclusion chromatography. Perform laboratory experiments independently or with other team members, including immunoassays, column production, affinity chromatography, and product handling Bacterial and mammalian expression of recombinant proteins, protein characterization including but not limited to: SDS page, western blot, dot blot, ELISA, Immunofluorescence Candidate is expected to perform basic mammalian cell culture Maintain laboratory space, equipment, and inventory in an appropriate and professional manner Lab housekeeping and solutions and materials restocking. Present data and final report suitable to deliver to clients Perform other duties as assigned | 12/13/2023 |
| 997 | Rockland Immunochemicals Pottstown, PA Associate Scientist, Quality Control Bachelor’s degree in biochemistry, pharmacology, molecular biology, cancer biology, or related field or associate degree in similar field. Exp: 1+ years |
Rockland Immunochemicals is a worldwide leader in the development and commercialization of antibodies and antibody based tools. To further enable innovative biomarker development for drug discovery and diagnostic applications, we also offer highly customized solutions to meet basic, applied and clinical research demands. We are seeking a talented and highly motivated team player as an addition to our Quality Control Department. Join the group and apply your experience in the QC environment. | 12/13/2023 |
| 998 | Toxikon Madison, WI Research Lab Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
Labcorp Drug Development is the leading global Clinical Research Organization. We have an exciting career opportunity for an Analyst on our BioAnalytical team in Madison, WI. The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 12/15/2023 |
| 999 | Toxikon Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 1000 | Toxikon Greenfield, IN Research & Development Scientist Minimum of Bachelors in an appropriate scientific field. Exp: 1+ years |
Scientific Knowledge and Technical Expertise: Technical expertise in one or more of the following scientific disciplines is desired: Cell Culture and Cell-Based Potency Assays ELISA Statistics/Biostatistical experience pertaining to biopotency assays and/or In Vivo Relative Potency Assays. Virology qPCR Flow Cytometry Additional experience in Western blotting, Capillary IsoElectric Focusing, Capillary Electrophoresis, UV Spectroscopy and HPLC/ UHPLC is a plus. | 12/15/2023 |
| 1001 | Toxikon Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 1002 | Toxikon Greenfield, IN Research Assistant I-Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 12/15/2023 |
| 1003 | Toxikon Research Triangle Park, NC Cytogenetics Technologist - 2nd Shift Bachelor's degree in Biology, Chemistry, Medical Technology or a related science. Exp: 1+ years |
Are you an experienced Medical Lab Professional? Are you looking to embark on a new challenge in your career, or start your career in Medical Lab Science? If so, LabCorp wants to speak with you about exciting opportunities to join our team as a Cytogenetics Technologist in RTP, NC. In this position you will work in a fast paced, customer focused, and challenging environment, and will be a part of our overall mission at LabCorp: "Improving Health, Improving Lives". Integrated Oncology, a LabCorp Specialty Testing Group, provides reference anatomic pathology, hematopathology and molecular pathology testing services to hospitals, health systems and independent oncology practices. Integrated Oncology is focused on providing world class solutions to better the lives of patients living with cancer. The schedule for this position will be 2nd Shift (Tuesday-Saturday 1pm-9:30pm) | 12/15/2023 |
| 1004 | Toxikon Greenfield, IN Laboratory Scientist Mammalian Cell Culture BA/BS in biology, molecular biology, microbiology, immunology, or a related field. Exp: 1+ years |
As a Laboratory Scientist, you will analyze samples for various compounds and components, run assays, perform mammalian cell culture, flow cytometry and perform data analysis and QC data in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 12/15/2023 |
| 1005 | Trevigen Minneapolis, MN Advanced Research Associate, QC Bioassay Master’s degree om the biological sciences or equivalent. Exp: 0 to 2 years |
The Bioassay Quality Control department provides team members the opportunity to practice and learn a variety of laboratory techniques. This position is responsible for performing protocol-defined bioassays on proteins and antibodies to demonstrate the activity of a product. The position requires experience with ELISAs, PCR, Western Blotting, and cell culture, including maintenance of cell lines and isolation of primary cells for use in the bioassays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. | 12/15/2023 |
| 1006 | Trevigen Minneapolis, MN Research Associate, Molecular Biology Master’s degree in Molecular Biology or equivalent. Exp: 0-2 years |
The responsibilities of this position are to assist the protein product development team in the area of recombinant protein expression. This includes the preparation of eukaryotic expression vectors, cell culture, and screening procedures. The successful candidate will perform various techniques such as DNA preps, sub-cloning, mammalian and insect cell culture, transfections, Western blotting, ELISA, and flow cytometry. They will also prepare buffers and reagents, assist in cleaning and maintenance of the laboratory and equipment, and perform other general lab duties as assigned. | 12/15/2023 |
| 1007 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in Biology, Biotechnology, Biochemistry or equivalent required. Exp: 0 to 2 years |
In this position you will build custom made-to-order kits for our rapidly growing Luminex product line, including qualification of assay components, formulation of intermediates, and preparation for packaging. | 12/15/2023 |
| 1008 | Trevigen Waltham, MA Medical Laboratory Technologist Bachelor of Science Degree in a chemical, physical or biological science. Exp: six months |
This position is responsible for performing high-complexity CLIA testing in day-to-day operations of the laboratory. | 12/15/2023 |
| 1009 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0-2 years |
The responsibilities of this position are to prepare conjugated proteins, antibodies, enzymes and microparticles for both manufacturing and research. In addition, this position will be responsible for the preparation and testing of other chemistry related reagents for company personnel. Perform additional duties as assigned. | 12/15/2023 |
| 1010 | Trevigen Minneapolis, MN Research Associate Bachelor’s degree in the biological sciences or equivalent. Exp: 0 to 2 years |
The responsibilities of this position are production, bottling, and packaging of stem cell and gene therapy medias. Perform QC testing and analysis of some cell culture media. Perform cell culture of multiple cell lines. Production of components for additional stem cell, and non-stem cell kits. Skills used include cell culture, high attention to detail, strong communication and organizational skills. This will be a Tuesday through Saturday work schedule. | 12/15/2023 |
| 1011 | Trevigen Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 12/15/2023 |
| 1012 | Tyber Medical Bethlehem, PA Quality Engineer /Senior Quality Engineer Bachelor’s degree from a four-year college or university in a related field of study. Exp: one year |
The Quality Technician organizes and runs the routine analysis of the Quality Control Department. This job is essential in ensuring the Quality Control Department meets its goals of efficiency and customer satisfaction. This individual is responsible for conducting inspection and testing procedures during manufacturing processes and receiving inspection processes to ensure the products comply with requirements. | 12/15/2023 |
| 1013 | Universal Cells Seattle, WA Research Associate II, Gene Editing MS degree. Exp: 0-2 years |
The primary purpose of the Research Associate II position is to assist with gene editing of pluripotent stem cells. This position will work primarily in a laboratory setting in collaboration with other Scientists and Research Associates. | 12/15/2023 |
| 1014 | Vala Sciences San Diego , CA Research Associate (RA)/Senior Research Associate (SRA) – Assay Development and iPSC Maintenance B.S. or M.S. in Molecular/Cell Biology, Biochemistry, Neuroscience, Bioengineering, or related. Exp: 1+ years |
We’re seeking an RA or SRA to join our dynamic assay development and induced pluripotent stem cell (iPSC) research team. The successful candidate will execute validated assays for contract research projects and assist in management and maintenance of iPSC lines. Additionally, you will work with senior scientists in the Neurobiology and Cardiology groups to plan and perform experiments for assay development to support Vala’s internal and contract research projects. You will maintain differentiated iPSC cell cultures for live cell assays using Vala’s Kinetic Image Cytometry (KIC) technology, as well as perform IF staining to assist in development of reproducible and optimized assays. You may perform differentiation of iPSC to different cell types, such as neurons, astrocytes, microglia and cardiomyocytes. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 12/15/2023 |
| 1015 | Vala Sciences San Diego , CA Research Associate (RA)/Senior Research Associate (SRA) – iPSC Manufacturing B.S. or M.S. in Cell/Molecular Biology, Biochemistry, Neuroscience, or related field. Exp: 1-2 years |
The successful candidate will manage iPSC lines and their differentiation to different cell types, like cardiomyocytes, microglia, neurons, and astrocytes. These differentiated iPSC lines will be used for internal R&D projects, commercial research contracts, and manufacture for sale. You will evaluate and validate differentiated cell lines with biomarker detection methods like ICC or flow cytometry, and investigate and characterize cellular function using Vala’s live-cell fluorescent imaging technology. You will work in a close-knit, fast-paced team environment and adapt readily to changing needs as projects and technologies evolve. | 12/15/2023 |
| 1016 | VaxCyte San Carlos, CA Associate Scientist II, Upstream Development for Protein Development and Manufacturing MS in Biology, Chemical Engineering or Chemistry/ Biochemistry. Exp: 0-2+ years |
Vaxcyte is seeking a talented and energetic Associate Scientist I/II, to join the Upstream Process Development group within the Protein Development and CMC team. Vaxcyte is developing a multi-valent conjugate vaccine, based on a novel carrier protein produced using the XpressCFTM platform. This is an exciting opportunity to join a team aiming to establish a new fermentation development lab and pilot plant at Vaxcyte. | 12/15/2023 |
| 1017 | Vector Laboratories Newark, CA Technical Application Scientist II Master’s degree in Biology, Chemistry or related life science field required. Exp: 1+ years |
The Technical Support Scientist’s primary responsibility will be to provide product and application expertise, insight and troubleshooting assistance for all Vector Laboratories’ reagents to researchers across the life sciences fields and to our distributors worldwide. Also, as a member of the commercial team, the Technical Support Specialist will help in the generation of technical material and marketing content to support promotional activities and campaigns, as well as represent the company at conferences, meetings and vendor shows as required. The successful candidate will be self-motivated, a creative thinker and a problem solver who enjoys direct interaction with people. Candidate will be a team player with strong communication, organizational, and time management skills. Previous experience in a technical support role in a life science company would be beneficial. This position reports to the Sr Director, Commercial Operations. The ideal candidate for this position will be a collaborative problem solver, working to find the best possible solution to the client’s questions and needs. The candidate should embrace opportunities to learn more about our existing and upcoming products, as well as what our competitors are releasing. This is a collaborative, team, environment. To apply for this position, please email your resume and cover letter to: talent@vectorlabs.com. | 12/15/2023 |
| 1018 | VGXI Conroe, TX UPSTREAM MANUFACTURING PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three Years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for upstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Upstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 12/15/2023 |
| 1019 | VGXI Conroe, TX DOWNSTREAM MANUFACTURING PROCESS TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three Years |
Responsible for manufacturing revolutionary clinical and commercial nucleic acid based pharmaceuticals by interfacing with manual and automated production systems and controls in cGMP manufacturing environment while maintaining areas in a state of compliance with internal quality systems. Follows standard operating procedures to operate production equipment for downstream operations. Maintains records, process and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for proficiency in assigned functional area: Downstream Manufacturing. Understands and applies biological, chemical and mechanical principles and techniques. | 12/15/2023 |
| 1020 | VGXI Conroe, TX QUALITY CONTROL TECHNICIAN Bachelor’s or Associate's degree or equivalent from college or technical school. Exp: one to three years |
The Quality Control Technician is responsible for in-process and release testing of products manufactured at VGXI. Responsibilities also include environmental monitoring of the production areas and raw material quarantine and release. Set-up, organization, and day-to-day operations of a Quality Control Lab are also required. | 12/15/2023 |
| 1021 | Viant Medical Brimfield, MA Quality Engineer Minimum of Associate’s Degree in Engineering or related technical field, with Bachelor’s Degree preferred. Exp: 0-3 years |
The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for medical device manufacturing/operations in accordance with applicable Regulatory and Standards requirements for compliance. | 12/15/2023 |
| 1022 | Vividion Therapeutics San Diego , CA Research Associate I/II, Proteomics B.S. in Chemistry- or Biology-related field. Exp: 1-4 years |
Vividion Therapeutics is seeking a highly motivated Research Associate to help support the operation of our cutting-edge proteomics platforms. The successful candidate will have a high level of organization and attention to detail. The role will involve techniques such as cell culture, in vivo tissues processing, high throughput screening on an automated system, and protein chemistry or chemical biology. This position will help discover novel small-molecule ligands of protein targets through the execution of screens using our novel mass spectrometry-based proteomics platforms. | 12/15/2023 |
| 1023 | WaVe Life Sciences Cambridge, MA Research Associate II BS/MS in biology, biochemistry, cellular/molecular biology or related discipline. Exp: 1+ years |
Wave seeks a highly motivated biologist to join its research team in Cambridge, Massachusetts to support a rapidly expanding RNA-editing platform. This is an ideal position for an individual who is interested in working with cutting edge technologies and who thrives in a team-oriented, fast-paced, and cross-disciplinary biotech environment. The candidate should have strong technical skills, and will be responsible for designing, executing, and analyzing experiments as a member of team focused on advancing therapeutic programs and discovery research platforms. | 12/15/2023 |
| 1024 | Frontage Exton, PA Associate Scientist/Scientist, BCGT Analytical Development Master's degree in, Molecular Biology, Cell Biology, or a related field. Exp: 1-2 years |
We seek a highly skilled Associate Scientist/Scientist to join our dynamic Molecular and Cell Biology team. This role will focus on developing analytical methods supporting biologics, cell, and gene therapy modalities. The ideal candidate will possess a deep understanding of tissue culture, cell line maintenance, cell-based assays, and proficiency in molecular approaches such as DNA/RNA extraction and PCR techniques. | 12/15/2023 |
| 1025 | Frontage Exton, PA Associate Scientist Bachelor’s or master’s degree in molecular biology, cell biology, biochemistry, or a related field. Exp: 1+ years |
The Cell-based Assay Core Lab, based at our Exton headquarters, stands as a premier provider of diverse cell-based assays. These include potency assays, neutralizing antibodies assays, EliSpot, virus plaque assay, TCID50 Assays etc. We are seeking a candidate with a fundamental understanding of Cell Biology, Biochemistry, and Molecular Biology. The ideal candidate should be highly organized, self-motivated, enthusiastic about learning, and capable of managing multiple projects concurrently. | 12/15/2023 |
| 1026 | Frontage Exton, PA Associate Scientist/Scientist – Protein Biochemist BS Degree or MS Degree. Exp: 1 year |
This is a bench scientific position for a competent and hardworking scientist with experience in protein purification and/or labeling of protein reagents. The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc. He/she will be responsible for the quality of final product, record keeping and interacting with end user. The position will require excellent communication skills, and basic computer skills. | 12/15/2023 |
| 1027 | Frontage Concord, OH Laboratory Research Technician – Full time /Concord Ohio Educational Requirements: High School/GED or above (AS & BA/BS). Exp: entry-level |
Individuals in this position support evaluation of the safety and/or toxicity of pharmaceutical and biotechnology products by ensuring the health and welfare of research animals. | 12/15/2023 |
| 1028 | Frontage Hayward, CA Research Assistant-ADME BS in biology, biochemistry and other related fields. Exp: 0-3 years |
We are looking for a highly-motivated Research Assistant to develop and conduct biochemical and cellular assays to evaluate potential therapeutics. Experience in cell line development, ELISA, PBMC biomarker, cell culture, cellular assays, gene expression is desirable. Prior experience in ADME assays including metabolite stability, drug transporter, CYP450, PPB and measurements of physicochemical properties is preferred. The candidate needs to be proficient in assay design, trouble-shooting, data analysis and working with 96-w & 384-w plate-based assays. The candidate needs to have a good understanding of drug discovery processes and experience in a discovery project is preferred. This position requires working with an interdisciplinary team of DMPK scientists, analytical chemists and pharmacologists. | 12/15/2023 |
| 1029 | Frontage Hayward, CA Research Associate-Bioanalytical M.S. degree in related scientific discipline or B.S degree. Exp: BS: 1+ years; MS: 0-3 years. |
1)Execute established protocols and methods to assay small molecule compounds, their metabolites, and impurities in various chemical and biological samples. 2)Perform data analysis on LC/MS and HPLC instruments, with the ability to identify and troubleshoot inconsistencies as needed. 3) Perform analytical, pharmacokinetic/pharmacodynamic, metabolism data analysis. 4) Conduct basic method development and validation studies. 5) Conduct trouble-shooting and instrument maintenance of LC/MS. 6) Present and discuss data internally and externally. 7) Write reports under supervision. | 12/15/2023 |
| 1030 | PCI Pharma Services Bedford, NH QA Associate I - Operations Bachelor’s Degree in a relevant scientific discipline preferred. Exp: 0-2 years |
The Quality Associate I - Operations is responsible to provide QA support real-time for GMP Manufacturing of drug product. Responsibilities include providing QA on the Floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed. Real time continuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phase appropriate GMP manufacture of drug products. | 12/4/2023 |
| 1031 | PCI Pharma Services Philadelphia, PA Process Engineer I Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout | 12/4/2023 |
| 1032 | PCI Pharma Services Philadelphia, PA Process Engineer I-2nd Shift Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout.**This is a second shift position. Hours are: 4pm to 12 Midnight, Monday to Friday** | 12/4/2023 |
| 1033 | PCI Pharma Services Philadelphia, PA Process Engineer I-Wkends AM Bachelor's Degree in mechanical, packaging engineering, or in a related field of study. Exp: 1-5 years |
We are looking for a dedicated process engineer to provide technical leadership for new product launches and lead continuous improvement activities. You will also identify and mitigate packaging issues for existing business through strong engineering and process improvement methods. All activities are focused around technical and operational support to production, maintenance, and support staff to include but not limited to: process improvement, equipment modification, optimization, safety, quality improvement, and increasing throughput. The process engineer will achieve this through delivery of tracking, analysis of metrics and project management. The ideal candidate will have a strong understanding and utilization of good engineering practices with the usage of lean six sigma techniques. The process engineer will also provide excellent organizational and leadership skills to determine staffing projections, equipment needs, equipment purchase, equipment installation, component layout, and line layout***This is a weekend position 6am to 6pm Friday, Saturday, and Sunday.** | 12/4/2023 |
| 1034 | PCI Pharma Services Rockford, IL Package Testing Engineer Bachelors degree in engineering and/or related discipline. Exp: 0-2 years |
The Package Testing Engineer supports PCI’s mission to provide industry-leading experience to clients, developing and commercializing solutions to optimize the delivery of lifesaving medicines and support better health outcomes for patients around the world. Reporting to the Principal Package Testing Lead, a successful Package Testing Engineer would utilize engineering skills and technical insights to evaluate, develop, test, and qualify effective packaging systems for PCI’s clients. Under the guidance of the Principal Associate, utilizing practical packaging development knowledge, effective report writing, and hands-on assembly skills, the Package Testing Engineer would support PCI’s Package Testing Services, commercial sales efforts as well as the successful commercialization of awarded packaging projects. In addition to the primary role of package testing, the incumbent would support package design and on-site prototyping projects as needed. Package Testing Engineer would support the workflows and reliability of the on-site Package Testing Lab and regularly coordinate projects with external partners. The Package Testing Engineer may engage clients, consultants, vendors, and suppliers directly to aid in the successful design and implementation of new packaging systems and products. | 12/4/2023 |
| 1035 | PCI Pharma Services Rockford, IL Serialization Engineer Bachelor's Degree in a related field. Exp: 1-5 years |
Serve as primary technical expert and principal designer/developer for all global major packaging line serialization design and integration efforts. Work closely with suppliers and internal colleagues to identify and specify complex line connectivity requirements and translate to comprehensive interface solutions specifications and delivery. | 12/4/2023 |
| 1036 | PharPoint Research Durham or Wilmington, NC Quality Assurance Auditor Bachelor’s degree (B.A./B.S.) or equivalent in a scientific, computer, or related discipline. Exp: 1-2 years’ |
Performs project and non-project quality assurance duties at PharPoint Research. Responsible for carrying out quality initiatives at the company, including but not limited to SOPs and training, computer systems validation, and Quality Management System. | 12/4/2023 |
| 1037 | PolyPeptide Group Torrance, CA Production Chemist I BS in Chemistry, Biochemistry, Biology or related science field. Exp: 1+ years |
Production Chemist is responsible for completing tasks & assignments in accordance with established processes & methodologies; synthesize peptides, intermediates, & processing from initial stage. | 12/4/2023 |
| 1038 | Poseida Therapeutics San Diego, CA Quality Control Analyst Bachelor’s degree in Life Sciences or related discipline. Exp: 1+ years |
Poseida Therapeutics, Inc. is seeking an outstanding candidate to join our Quality Control team. The Quality Control Analyst I will be a member of a dynamic team that ensures the safety of our products at various points during the manufacturing process by performing environmental monitoring, raw material and final product testing. As well as working cross-functionally with individuals and departments within the Pilot Plant Facility. | 12/4/2023 |
| 1039 | Kriya Therapeutics Morrisville, NC GMP Facilities Engineer Bachelor's degree in Engineering or related field. Exp: 1-3 years |
The GMP Facilities Engineer will be responsible for overseeing the facility's alarm response, deviation, change control, and CAPA management, ensuring compliance with Good Manufacturing Practices (GMP) in a biotech manufacturing environment. This individual will also play a crucial role in managing the Computerized Maintenance Management System (CMMS) and participation in project teams by serving as the representative of the facilities group. | 11/27/2023 |
| 1040 | Krystal Biotech Pittsburgh, PA Bioprocess Engineer Bachelor’s degree, preferably in life sciences. Exp: 1+ years |
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing. | 11/27/2023 |
| 1041 | Krystal Biotech Pittsburgh, PA Manufacturing / Bioprocess Support Technician BS Degree in Biology, Engineering or related field is preferred. Exp: Entry Level |
Krystal Biotech, Inc is seeking a highly motivated Bioprocess Support Technician to support the growing Manufacturing team in Pittsburgh, PA. This role will perform a wide range of duties to support manufacturing processes in a GMP environment. | 11/27/2023 |
| 1042 | LakePharma
LakePharma
LakePharma
Camarillo, CA Microbiologist I Bachelor’s degree in Microbiology, Science or related field. Exp: 0-3 years |
Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Quality Control Microbiologist I performs quality activities in support of product production and releases. The position performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing, trending and reporting results. | 11/28/2023 |
| 1043 | LakePharma
LakePharma
LakePharma
Lebanon, NJ Analytical Chemist I Bachelor’s degree in Chemistry or Chemical engineering. Exp: 1-2 year |
MAJOR DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Perform routine testing related to compendial monographs and general chapters; Saponification/Hydroxyl/Acid/Iodine Value, IR/UV analysis, Assays GC/HPLC analysis, ICP-MS analysis, Atomic Absorption spectrometry, etc. Perform measurements, computations, tabulation, and analyze results related to the testing conducted. Under the supervision of more experienced analysts, perform basic non-routine instrumental analysis and wet chemistry analysis in response to customer inquiries and projects as required. This may include but not limited to developing methods and performing method validation and verifications. Operate and maintain/calibrate laboratory equipment as per manufacturer’s recommendations and company’s Preventive Maintenance program. Maintain laboratory records related to all testing activities assuring that they are accurate and up to date. Perform other related duties as assigned. Perform all analysis and lab related duties as per cGMP. | 11/28/2023 |
| 1044 | Liquidia Morrisville, NC Manufacturing Technician B.S. degree. Exp: 0-2 year’s |
We are looking for a hands-on and experienced Manufacturing Technician. In this role, you will perform routine running of manufacturing equipment to support production and R&D efforts. Furthermore, you will provide feedback to engineering and scientific staff on process performance and ideas for process improvement. | 11/29/2023 |
| 1045 | Lygos Berkeley, CA Process Engineer B.S. in Chemical Engineer, Bioengineering, or related Engineering discipline. Exp: 1-2 years |
We are seeking a motivated Process Engineer to join our growing organization. As a key member of the pilot fermentation facility at Lygos, you will report to the Director of Fermentation and work closely with another Process Engineer on the team to support day to day operations of our pilot scale fermentations. You will support the fermentation team in maintenance and repair of fermentation equipment and contribute to the development of automation tools for the team. | 11/29/2023 |
| 1046 | Lyra Therapeutics Watertown, MA MSAT Engineer I/II Bachelor’s Degree (Engineering Preferred). Exp: 1+ years |
Our team is growing, and we are currently recruiting a Manufacturing Sciences and Technology (MSAT) Engineer I/II to support pharmaceutical operations at the Waltham and Watertown, MA sites. The focus of this position is to ensure manufacturing equipment and processes are operating as intended to meet the requirements for drug product manufacturing. This position will play a key role in delivering results in a fast paced, highly collaborative, and dynamic environment. The position will assist in the startup of a combination drug-device product from new product launch through commercial production. This involves process development, commercial process validations, technology transfers, as well as being accountable for commercial production. | 11/29/2023 |
| 1047 | Masy Biosciences Charleston, SC Environmental Monitoring Technician - 2nd Shift Bachelor’s degree preferred. Exp: 0-2 years |
The Environmental Monitoring Technician I is accounable for results in a fast-paced environment. The Level I Technician follows applicable SOPs and cGMPs to perform environmental monitoring for the facility, and may also perform simple, routine basic interpretation of environmental monitoring (EM) results, typically under supervision. This position is also responsible for hazardous waste and sanitation/cleaning of the Microbiology laboratory. The position requires strong leadership behaviors of the Alcami core competencies and non-negotatiables, as well as the functional competencies of this profile | 11/29/2023 |
| 1048 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 1st Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 1049 | Masy Biosciences Morrisville, NC QC Data Review Specialist - Chemistry Master’s degree in Chemistry, Biology, or related field. Exp: 1+ years |
The Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance-oriented training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies included in this position profile. Business needs and deadlines will require employee to perform work duties outside of standard work hours on occasion. | 11/29/2023 |
| 1050 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 2nd Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 1051 | Masy Biosciences Charleston, SC Pharmaceutical Manufacturing Technician - 3rd Shift Associate’s degree preferred. Exp: 1-2 years |
The Manufacturing Technician I is accountable for results in a fast-paced environment and assists with the manufacturing of drug products (parenteral or solid dosage) for commercial distribution and clinical trials. The Manufacturing Technician I assists with the operation of manufacturing processing equipment by following standard operating procedures (SOPs) and batch records in accordance with regulatory agencies and current Good Manufacturing Practices (cGMPs). The Manufacturing Technician I employs acceptable techniques while working in manufacturing environments, including PPE gowning. The Manufacturing Technician I works collaboratively to support other manufacturing areas as required. The position requires superior leadership behaviors of the Alcami core competencies and non-negotiables, as well as expertise in functional competencies for the role. | 11/29/2023 |
| 1052 | Meridian Life Science Memphis, TN Lab Production Associate Bachelor’s or Master’s degree from an accredited institution with a relevant scientific discipline such as Chemistry, Biology, Biochemistry, Molecula Exp: 1+ years |
The Lab Production Associate position is responsible for performing assigned manufacturing and laboratory support activities according to company policies, SOPs, and quality regulations. The position will be responsible for performing upstream and downstream bioprocessing procedures to support the commercial manufacturing of native antigens, recombinant proteins, antibodies, and blockers. Upstream processes include tissue culture, cell bioreactors, fermentation, virus propagation, cell and virus bank production, and buffer/media preparation. Downstream unit operations include harvest, clarification, chromatography, centrifugation, TFF (UF/DF), filtration, formulation, and fill-finish. The candidate will be required to maintain an assigned lab area and perform equipment and lab cleaning procedures. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO1345 regulations. | 11/30/2023 |
| 1053 | Meridian Life Science Memphis, TN Research Associate Bachelor’s degree from an accredited institution in a relevant scientific discipline such as Biology, Chemistry, Biochemistry, Molecular Biology etc. Exp: 1+ years |
The Research Associate will be responsible for providing hand-on support, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The candidate will be expected to perform routine laboratory duties following company SOPs, protocols, and regulations. The role will assist with the execution of experiments under direct supervision of their supervisor performing experimental procedures, analytical procedures, analyzing data, and generating analysis reports. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. The Research Associate will be responsible for providing hand-on support, within our Technical Operations and Development department, to drive the improvement and growth of our immunological reagent offerings including recombinant proteins, native antigens, antibodies, blockers, and custom manufacturing. The candidate will be expected to perform routine laboratory duties following company SOPs, protocols, and regulations. The role will assist with the execution of experiments under direct supervision of their supervisor performing experimental procedures, analytical procedures, analyzing data, and generating analysis reports. The candidate will be responsible for performing routine laboratory maintenance and lab management duties including maintaining sufficient supply of reagents, cleaning and disinfecting of laboratory equipment, cleaning lab area, environmental monitoring, and filling out proper paperwork. The candidate must be able to execute assigned procedures in a fast-paced and results-oriented environment satisfying quality standards in accordance with customer satisfaction, cost, schedule, and ISO13485 regulations. | 11/30/2023 |
| 1054 | Myriad Genetics San Diego, CA Lab Tech II BS in Molecular Biology or related discipline. Exp: 1-2 years |
Execute high throughput preparations and dispenses of simple and complex reagents (enzyme formulations, primer combinations, large volume solutions) for our clinical lab using a variety of automated dispensing platforms; Assist in the receiving, handling, and monitoring of quantities and testing quality of raw materials and finished products; Assist in document manufacturing activities and quality control results; Auditing, stocking and equipment maintenance tasks | 11/30/2023 |
| 1055 | NAMSA Northwood, OH Microbiology Technologist Bachelor degree. Exp: no experience |
• May perform routine test article/product preparation and execute routine testing and perform routine calculations per NAMSA SOPs and work instructions. • Accurately collects and records raw data in logbooks and on worksheets. • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable. If needed, the Associate will respond in accordance with criteria outlined in Standard Operating Procedures. • May be required to perform required specific testing as applicable. • May be required to operate specified laboratory equipment. • May perform Environmental Monitoring, clean and disinfect cleanroom suites (required as applicable). • Other duties as assigned | 11/30/2023 |
| 1056 | NAMSA Northwood, OH LC-MS Chemist Master’s degree in chemistry or a related scientific field. Exp: no experience |
• Operates and maintains a variety of chromatographic and spectroscopic systems such as LC, LC/MS/MS, and GCMS to analyze biological and chemical elements as directed by assays or study protocols. • May order and/or stock supplies subject to approval. Maintain ancillary records (logbooks, worksheets). • Conduct routine studies independently according to work instructions. May be requested to conduct more involved studies. Routes all excursions or unusual testing occurrences to management. • Participate in the improvement of documents, test systems, quality systems, and workflow. | 11/30/2023 |
| 1057 | NAMSA Minneapolis, MN Laboratory Technician– Talent Pool An Associate or Bachelor degree in related scientific field is required. Exp: 1+ years |
• Conducts sample preparation for Sponsor materials as directed by study protocols for in vivo and in vitro biocompatibility assays and pharmacology, toxicology and analytical studies. • Performs the extraction process on prepared samples in accordance to ISO, USP and JMHLW regulations as directed by study protocols for biocompatibility assays. • Receives and logs Sponsor materials for testing. Completes chain of custody documentation for test article tracking. • Prepares and maintains sterile glassware for the sample preparation process. Processes glassware through washer, autoclave and depyrogenation oven as needed. • Operates, cleans and maintains incubators, autoclaves, hoods and other equipment routinely utilized. • Maintains an efficient and clean work area by organizing and restocking the sample preparation lab as needed. | 11/30/2023 |
| 1058 | NantKwest Culver City, CA Associate, Quality Control Bachelor’s degree in a life sciences discipline. Exp: 1+ years |
The Quality Control Associate in the Quality Control department is responsible for ensuring the timely execution of Quality Control Analytical assays in support of product release across all of ImmunityBio’s oncology and vaccine product platforms. This position will train on and perform a variety of molecular biology, and/or chemistry assays including but not limited to cell culture, ELISA, qPCR, HPLC, icIEF, CE-SDS techniques and/or Compendial test methods in the evaluation of product quality. | 11/30/2023 |
| 1059 | Nexelis Valencia, CA Laboratory Assistant Bachelor's degree in science preferred. Exp: 1+ years |
Process samples as required by each protocol. Assist laboratory technologists with sorting, processing, storage, and retrieval of medical specimens. | 12/1/2023 |
| 1060 | Nexelis Ithaca, NY Associate Scientist, LCMS (Sign on Bonus Offered) Bachelor’s Degree, Chemistry and/or Biology preferred. Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 12/1/2023 |
| 1061 | Nexelis Ithaca, NY Associate Scientist Sample Preparation (Sign on bonus offered) Bachelor's Degree required. Exp: 1+ years |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments, and the preparation of solutions and reagents. | 12/1/2023 |
| 1062 | Nexelis Ithaca, NY Associate Scientist Sample Preparation (Sign on bonus offered) Bachelor's Degree required. Exp: 1+ years |
Responsible for routine sample preparation duties inclusive of troubleshooting routine experiments, and the preparation of solutions and reagents. | 12/1/2023 |
| 1063 | Nexelis Indianapolis, IN Laboratory Assistant Bachelor's Degree Some CAP/CLIA lab locations may require a BS in chemistry, biology, or medical laboratory technology degree Required. Exp: 6 months |
Responsible for performing a variety of routine testing procedures to obtain data for use in clinical trials research. | 12/1/2023 |
| 1064 | Nexelis Ithaca, NY Associate Scientist, LCMS (Sign on Bonus Offered) Bachelor’s Degree, Chemistry and/or Biology preferred. Exp: 1 year’s |
The Scientist Core LC/MS (Liquid Chromatography/Mass Spectrometry) employs liquid chromatographic separation techniques and mass spectrometric analysis for data collection. In addition to instrument operation, the Scientist LC/MS is responsible for some associated instrument maintenance, documentation in accordance with SOPs and regulations, and data processing in a manner which meets company quality best practices, objectives, and timelines. | 12/1/2023 |
| 1065 | Nexelis Austin, TX Laboratory Associate Associate degree Required or equivalent. Exp: 0–1-year |
Perform routine packaging and filling procedures with accuracy, consistency, and timeliness. Provide routine documentation and review of work performed in a timely manner. | 12/1/2023 |
| 1066 | Noble Life Sciences Sykesville, MD Research Technician Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1 year |
Description 1. Compliance: Perform assigned tasks and responsibilities under the direction of the Scientist(s) and/or the Study Director(s) and in accordance with relevant study protocols, regulations, and Standard Operating Procedures (SOPs). 2. Training: Ensure personal training is documented according to Noble SOPs prior to the performance of associated procedures. 3. Procedure Preparation: Label tubes and other supplies needed for collecting and processing specimens. Prepare reagents needed for collection or processing of specimens. 4. Performance of Procedures: Process various blood and tissue samples. Maintain quality, safety, and/or infection control standards. Perform procedures using various instrumentation according to Noble SOPs. 5. Documentation: Maintain lab notebooks and document experimental procedures and associated data. Assist in writing deviations and preparing responses to quality assurance audits related to duties performed. 6. Laboratory Maintenance: Take ownership of assigned laboratories. Coordinate with the inventory manager to stock assigned labs as needed. Maintain inventories of assigned cold storage units. Maintain the laboratories in a clean and organized manner. Prepare shipment packages as directed. 7. Collaborate: Collaborate with and assist other research technicians, research associates, study directors, study coordinators, and scientists across various departments. 8. Any other relevant duties as assigned. | 12/1/2023 |
| 1067 | Noble Life Sciences Sykesville, MD Jr. Research Associate Bachelor’s degree in biological sciences, biomedical engineering, or a related field. Exp: 1 year |
Ensure all necessary supplies needed to conduct the associated projects as specified by the protocols and/or SOPs are stocked. Print labels and label sample collection tubes and other laboratory reagents. Prepare data forms required to conduct the project as specified by the protocol and/or SOP. Assist in processing various blood and tissue samples. Assist in the preparation of samples using a variety of laboratory procedures for testing with various laboratory equipment. Conduct various laboratory procedures and operate analytical equipment. Maintain quality, safety, and/or infection control standards. Maintain the laboratories in a clean and organized manner after completion of procedures. Maintain lab notebooks and document experimental procedures and associated data. | 12/1/2023 |
| 1068 | Oakwood Labs Solon, OH Quality Control Chemist- Pharmaceuticals Bachelor's degree in Chemistry, Biochemistry, Biology, or related field. Exp: One to four years' |
We are adding to our Quality Control Chemistry Staff. We are currently seeking individuals to: Perform analytical testing of raw material, in-process product, final product release and stability testing. Clear documentation of test activities in approved worksheets and laboratory notebooks. Execute mathematical calculations as outlined in test methods. Assess data to determine if the material tested meets specifications. Peer review of quality control data. Participate in investigational testing and assist with root cause analysis. Create and review SOP’s and author Change Controls. Other general lab related duties as necessary | 12/1/2023 |
| 1069 | Oakwood Labs Oakwood Villiage, OH Chemist Bachelor’s degree in chemistry, biology, or related discipline. Exp: entry level |
Oakwood Laboratories is looking to add to their Analytical Chemistry Team! This is an excellent entry level opportunity for those interested in working at a technology-based pharmaceutical company. There will be on the job training rotations in the research and development lab and the quality control chemistry lab. You will gain hands-on experience analyzing and interpreting data for excipients, polymers, active ingredients, and finished pharmaceuticals utilizing advanced analytical instrumentation. You will work as part of small multi-disciplinary technical teams on both immediate and sustained release drug development projects in various stages of development including early proof of concept, supporting pharmacokinetic and clinical studies, technical transfer activities, and supporting commercial product manufacturing. You will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development | 12/1/2023 |
| 1070 | Pacific BioLabs Hercules, CA Microbiology Laboratory Analyst I/II An undergraduate or AA degree in a science-related field (e.g., Microbiology, Biological Sciences). Exp: 0-3+ years |
PBL has immediate openings for full or part time Microbiology Laboratory Analysts in the Microbiology Services Department. The Microbiology Laboratory Analyst will report to Microbiology Management and will contribute to general laboratory testing, sample management, and laboratory maintenance. The Microbiology Laboratory Analyst is expected to participate with the team to meet Microbiology Services Department goals and perform routine laboratory duties as directed. | 12/1/2023 |
| 1071 | Pacific BioLabs San Francisco Bay Area, CA Quality Assurance Specialist I Associate or B.S. in Chemistry, Biology, Microbiology, or equivalent experience required. Exp: 0-2 years |
Pacific BioLabs has immediate openings for full time Quality Assurance Specialist I in the Quality Assurance Department. The QA Specialist I will report to the Chief Quality Officer or designated individual. The Quality Assurance Specialist I is responsible for assisting management with the maintenance of the Quality Systems. The QA Specialist I must be sensitive to the demanding regulatory compliance requirements attending to the operation of a pharmaceutical testing laboratory. This job also requires the ability to demonstrate a high commitment to interpersonal relations. Work must be performed in compliance with Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Quality System Regulations (QSR), ISO quality management system requirements, and other necessary regulatory requirements (e.g. OSHA, EPA, CDC, USDA, OLAW, etc.) as required by the task at hand, as well as any additional duties as assigned by the Chief Quality Officer. | 12/1/2023 |
| 1072 | Patheon Middleton, WI Entry Level Chemist Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 0 to 1 years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 1073 | Patheon St. Louis, MO Scientist I, Electrophoresis Analytical Development Bachelor in Molecular Biology / Chemistry / Biochemistry / Chemical Engineering, or a related field. Exp: no experience |
Responsible for developing or transferring analytical methods to support biopharmaceutical process development. You will work within an interdisciplinary team of scientists where you will learn and supply your skills and ideas to projects. | 12/1/2023 |
| 1074 | Patheon Cincinnati, OH R&D/Mfg Scientist I Associate’s or Bachelor’s degree in physical science; Chemistry or Biology preferred. Exp: 1+ years |
As a Laboratory Team Member, you will coordinate with your supervisor and collaborate with colleagues in diverse groups to assure that critical timelines are met. You will have the opportunity to collaborate with your peers within the laboratory and those in other departments such as formulations, operations, project management and quality assurance on a regular basis. You will perform analytical methods for elaborate testing for validated and experimental methods and other tests as needed to support lab operations. You will participate in the validation of analytical test methods when additional resources are required. | 12/1/2023 |
| 1075 | Patheon Cincinnati, OH Scientist I, Formulation & Process Development Minimum Bachelor of Science (BS) in science/engineering related field. Exp: 1+ years |
Supports execution for the development of new formulations and manufacturing processes of solids, liquids, and semi-solid dosage forms. Increase and develop knowledge regarding drug toxicology, pre-clinical – phase III, scale-up, and registration. Connect with technical leads, supervisors and project team peers (analytical and project management) on the progress and timely completion of activities and critical milestones. | 12/1/2023 |
| 1076 | Patheon Burlington, MA Labs FSP Associate Scientist - Raw Materials GMP Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1 year |
This position will work with others in Quality Control, Analytical Development teams, Quality Assurance, Manufacturing and CROs to support routine QC testing for Raw Materials for the manufacturing of Gene therapy products. The Analyst will specifically support the Raw material and gene therapy program pipeline (as needed) including but not limited to Project Management of the raw material program and development of testing strategies. | 12/1/2023 |
| 1077 | Patheon Middleton, WI Associate Scientist (Sunday -Thursday or Tuesday - Saturday) Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Possesses an understanding of laboratory procedures and under general supervision can conduct complex analysis. Performs a variety of routine sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices for stability and analytical testing. Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory guidelines. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 1078 | Patheon Middleton, WI Associate Scientist - Mass Spec Bachelor's degree or equivalent and relevant formal academic / vocational qualification. Exp: 1+ years |
Performs a variety of routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or biological matrices. Follows validated or experimental analytical procedures with periodic direct supervision. Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications. | 12/1/2023 |
| 1079 | Charles River Laboratories Mattawan, MI Research Analyst I - Formulations 1 Bachelor’s/Master’s degree in a relevant field. Exp: no experience |
We are seeking a Research Analyst I for our Test Material Control/Formulations Department site located Mattawan, MI. A Research Analyst I - Test Material Control (TMC)/Formulations is responsible for: preparing, sampling, and dispensing formulated test material according to applicable Standard Operating Procedures (SOPs) and GxP guidelines. The individual in this role: completes projects on time while maintaining quality and efficiency; communicates effectively with management, internal customers, and team members; assists others with their duties; and may assist with troubleshooting formulation issues. The pay range for this position is $23.50/hr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. The shift is for the weekend, Friday to Monday 6 AM-2:30 PM but will train for the first 12 weeks Monday-Friday 6 AM-2:30 PM. When you work Saturday or Sunday there will be a 10% shift differential. | 11/20/2023 |
| 1080 | Charles River Laboratories Worcester, MA Research Technician I Bachelor’s preferred (B.S) or equivalent in animal or life science or related discipline. Exp: 6 months |
We have an exciting opportunity for a Research Technician I (Tuesday through Saturday hours) at our Discovery site located in Worcester, MA. This position collects and records data with minimal supervision in the performance of studies. You will be be part of a team that is responsible for handling and restraining animals, clinical observations, sample collection, monitoring food consumption, animal husbandry, and performing accurate data collection and reporting. After training, you will administer test substances by various basic methods. | 11/20/2023 |
| 1081 | Charles River Laboratories South San Francisco, CA Research Technician II - In Vitro B.S. or A.S. degree in a Life Science discipline, such as biology, veterinary science, or a related field. Exp: 1 - 2 years |
We are looking for a highly motivated Research Technician II - In Vitro (Rodent Facility) to join our Insourcing Solutions team located in South San Francisco, CA. | 11/20/2023 |
| 1082 | Charles River Laboratories Cleveland, OH Research Analyst I- Bioanalytical Bachelor’s degree (BA/BS). Exp: no experience |
We are seeking a Research Analyst I for our Bioanalytical Chemistry Team at our Safety Assessment site located in Cleveland, OH. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP’s and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 11/20/2023 |
| 1083 | Charles River Laboratories Mattawan, MI Research Analyst I - Bioanalytical 1 Bachelor’s degree (BA/BS). Exp: no experience |
We are seeking an experienced Research Analyst for our Safety Assessment site located in Mattawan, MI. Bioanalytical Chemistry supports the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies including preclinical safety evaluations, pharmacokinetic/pharmacodynamic studies, and clinical trials. Staff participate in the development and validation of quantitative LC/MS/MS methodology, sample analysis, and interpretation and reporting of data utilizing validated hardware and software systems. This includes the development of sample extraction techniques, rapid LC separations, and employment of laboratory robotics to enhance delivery time of bioanalytical data. Staff are also knowledgeable in the application of GxP's and applicable SOPs, along with adhering to study protocols to accurately document methods, procedures, and results for inclusion into study reports and regulatory documents. | 11/20/2023 |
| 1084 | Charles River Laboratories Mattawan, MI Analytics Associate I Bachelor’s degree (Mathematics, Statistics, or Computer Science preferred). Exp: 0-2 or more years |
SALARY: The hourly rate for this position is $27.00. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. SCHEDULE: Monday - Friday, 8:00am - 4:30pm *flexible start and end time after 1-3 months of training We are seeking an experienced Analytics Associate for our Biostatistics Team at our Mattawan, MI site. An Analytics Associate is responsible for producing custom tables with statistical analyses using established systems and / or standardized code, to be completed in an accurate and timely manner consistent with the direction provided by the study director. | 11/20/2023 |
| 1085 | Charles River Laboratories Durham, NC Research Technician I Bachelor’s degree (B.A./B.S.) or equivalent in animal science or related discipline. Exp: 1+ years |
We are seeking a Research Technician I for our Discovery site located Durham. The following are responsibilities related to the Research Technician I: • Perform routine research activities as assigned, including in vivo-based screens. • Perform dosing of laboratory animals, animal husbandry. • Prepare & verify dosing solutions for administration. • Ensure that all individual study supplies are on-site & prepared in a timely manner. • Perform equipment maintenance. • Review protocol with manager to insure proper study execution. • Prepare & organize study data, study folders & data forms; perform data collection and entry. • Review study report, gives feedback on the accuracy of the materials & methods section; report data to more senior staff. | 11/20/2023 |
| 1086 | Hemacare Mattawan, MI Research Technician - Pharmacokinetics & Acute Toxicology 1 1 Bachelor’s/Master’s degree. Exp: no experience |
We are seeking an experienced Research Technician for our Pharmacokinetics & Acute Toxicology Team located in Mattawan, MI. A Research Technician is responsible for: administering substances to animals, performing husbandry duties, including cleaning/transporting caging and providing food and water; performing clinical observations of animals to determine morbidity/mortality; collecting and handling data and specimens; euthanizing animals and assisting veterinarians, management, and other company personnel with animal care, study-related tasks, and process improvement initiatives. | 11/20/2023 |
| 1087 | Hemacare San Diego, CA Husbandry Technician I B.S. in either animal science or life sciences preferred. Exp: one (1) year |
We are looking for a Husbandry Technician I (Rodent Facility) to join our Insourcing Solutions team located in San Diego, CA. | 11/20/2023 |
| 1088 | Hemacare Cambridge, MA Animal Support Technician I B.S. in Animal Science, Biology, or Biological Science. Exp: 6+ months’ |
We are seeking an Animal Support Technician to join our Insourcing Solutions team, located in Cambridge, MA. | 11/20/2023 |
| 1089 | Integra LifeSciences Plainsboro, NJ Manufacturing Engineer Bachelor's degree in Engineering (Mechanical Engineering, Pharmaceutical Engineering, Chemical Engineering, Biomedical Engineering). Exp: 0-2 years |
The Manufacturing Engineer will play a key role in the support of manufacturing operations, process scale–up, and manufacturing improvement activities. They will oversee projects to evaluate, analyze, and improve existing processes, support the development of new manufacturing processes, implement statistical process controls, analyze and trend existing process parameters, improve manufacturing yields, reduce scrap, and error proof manufacturing processes. | 11/21/2023 |
| 1090 | Integra LifeSciences Boston, MA QC Analyst I, Analytical - 2nd Shift Bachelor’s Degree in the biological or chemical sciences or equivalent. Exp: 1-3 years’ |
The QC Analyst I, Analytical – 2nd Shift, will be responsible for performing quality control Analytical laboratory testing of in-process, finished goods, validation studies, and adherence to all applicable regulations, policies, and procedures purchased components, manufactured sub-assemblies and final product. Must have working knowledge of U.S. Food and Drug Administration regulations, ISO 13485, and other applicable regulatory agencies as they pertain to laboratory testing. | 11/21/2023 |
| 1091 | MEDTOX Burlington, NC Research Associate I, Lab Automation Bachelor’s degree in chemistry, computer science, or an equivalent scientific discipline. Exp: 1+ years |
The Research Associate I-Lab Automation will be part of the Research and Development team that supports automation efforts in robotic liquid handling and data analysis. In this role, you will use mass spectrometry and other analytical technologies, provide assay development and validation support and assist in training and orientation of personnel as assigned. | 11/22/2023 |
| 1092 | MEDTOX Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 1093 | MEDTOX Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 1094 | MEDTOX Greenfield, IN Research Assistant I-Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/22/2023 |
| 1095 | MEDTOX Indianapolis, IN Analyst - BioAnalytical Lab, 2nd shift Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday | 11/22/2023 |
| 1096 | MEDTOX Madison, WI Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Precipitation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 11/22/2023 |
| 1097 | MEDTOX Madison, WI Research Lab Analyst Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. This position is a day shift with a flexible start time. | 11/22/2023 |
| 1098 | Merck West Point , PA B63 Associate Specialist, Engineering Bachelor’s Degree in Science or Engineering. Exp: 1+ years |
The Polysaccharide Vaccine (PV) Technical Operations team is seeking a highly motivated individual to fill an open position to support the start-up, process qualification, and successful licensure of new bulk vaccine manufacturing facility, Building 63, at West Point. The Associate Specialist, PV Technical Operations is responsible for technical support for bulk vaccine manufacturing unit operations while actively supporting, participating in, and embracing an empowered team culture. In this role, the Associate Specialist will work as an individual contributor as well as a team member within a cross-functional group that includes West Point Operations, Quality, Automation, Deviation Management, Global Technical Operations, Research and Development Division, and others. | 11/22/2023 |
| 1099 | Merck Elkton, VA Associate Manufacturing Science & Engineering Specialist Bachelor degree or higher in engineering, science, or business fields. New graduates or anticipated Fall 2023 graduates are also encouraged to apply. Exp: entry level |
At our Company's campus in Elkton, Virginia, we have an entry level position available to support and sustain our manufacturing processes. The manufacturing facility is located in the Shenandoah Valley along the Shenandoah River and the Blue Ridge Mountains a short distance from the University of Virginia and James Madison University. The successful candidate will have the opportunity to apply their enthusiasm and technical skills as a member of a multidisciplinary team supporting the operation of pharmaceutical, biopharmaceutical, and vaccine product manufacturing facilities. Depending on interests, education, experience, and skills, successful candidates will be matched with positions across the Elkton campus and may have the opportunity to participate in developmental rotations across functional areas. | 11/22/2023 |
| 1100 | Merck West Point , PA Off-Shift Specialist, Engineering Bachelor’s Degree in Science or Engineering. Exp: 1-3 years |
We are seeking a highly motivated individual to fill an open off-shift position to support the start-up, process qualification, and successful licensure of new bulk vaccine manufacturing facility, Building 63, at West Point. The Specialist, Operations is responsible for technical support for bulk vaccine manufacturing unit operations while actively supporting, participating in, and embracing an empowered team culture. In this role, the Specialist will work as an individual contributor as well as a team member within a cross-functional group that includes West Point Operations, Quality, Automation, Deviation Management, Global Technical Operations, MRL, and others. | 11/22/2023 |
| 1101 | Merck Rahway, NJ Specialist, Process Engineer - Oral Solid Dosage, Clinical Manufacturing Bachelor’s degree in Chemical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field. Master’s degree in Chemical Engineering, Ch Exp: BS: 1 year; MS: 0 years |
The Formulation, Laboratory, and Experimentation (FLEx) Center is a multi-modality (small molecule, biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey. The Process Engineer role at the Specialist level will serve as a leader in the FLEx Oral Solid Dosage GMP Clinical Manufacturing facility. This role will support formulation and process development, scale-up activities, quality investigations, change management and authoring GMP standard operating procedures and protocols in support of oral solid dosage clinical drug product operations. This individual will collaborate closely with the formulation scientists, engineers, quality representatives, and other team members to ensure the quality of the clinical supplies, the scientific rigor of the processes, and ultimately to enable the flexibility and speed of our Company's pipeline. The role is based in New Jersey and reports to the Oral Solid Dosage Process Lead of the FLEx GMP facility within Pharmaceutical Operations and Clinical Supply. | 11/22/2023 |
| 1102 | Merck Kenilworth and Rahway, NJ Associate Scientist, Biologics Process Research & Development BS (or expected completion by May 2024) in Chemical/Biochemical/Biomedical Engineering, Biotechnology, Biochemistry, Microbiology, Structural biology, Exp: 1+ years |
In April 2020, our Company announced plans to consolidate our New Jersey campuses into a single New Jersey headquarters location in Rahway, NJ in 2023 and 2024. Therefore, this role will be temporarily based in Kenilworth and exact timing of the departmental move to Rahway, NJ will be communicated at a future date. Our Research Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we partner to deliver the next medical breakthrough. Biologics Process Research & Development (BPR&D) within our company's Research Laboratories in our Research Division is on a mission to rapidly deliver diverse biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies. To achieve this, we work closely with colleagues in Discovery, Pre-clinical, Early Development, Analytical, Formulation, and Commercial Manufacturing while providing a diverse and inclusive environment for all. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies. Examples include investments for development of continuous manufacturing, green and sustainable processes, and proprietary technology platforms. We actively publish and engage with the scientific community to influence the field. BPR&D includes three lab-facing technical functional areas: Process Cell Sciences (PCS), Upstream Process Development (UPD) and Downstream Process Development & Engineering (DPDE). This job posting covers opportunities for all three functional areas. We are actively looking for highly motivated people with a passion for innovation and interest in contributing to one or more of the three technical functional areas mentioned above. As an Associate Scientist in BPR&D you will work with a highly collaborative team of scientists and engineers to design, develop and execute robust processes in support of early- to late-stage biological products. You will apply rigorous scientific principles to solve challenging problems focused on developing the best processes to deliver life-changing medicines to patients worldwide. You will also have an opportunity to contribute to additional areas of interest such as biophysical, process, economic and/or multivariate modeling as we are committed to leveraging digital ways of working to enhance our ability to design robust processes. | 11/23/2023 |
| 1103 | PerkinElmer Annapolis, MD Chemical Media Buffer Technician Associate Degree in a chemistry, biology, or other relevant discipline. Exp: 1+ years |
Responsibilities: Perform FACS (Fluorescence-activated cell sorting) machine QC daily. Tasks include but are not limited to emptying sheath waste, refilling sheath tank and running daily test cycle. Perform preventative maintenance on the DNA sequencing machines. Task is performed 3 times weekly. Tasks include emptying and refilling buffer trays, rinsing and drying critical parts and contacting respective end-users with any issues or material orders. Check ViCell reagents and cups in all locations twice a week. Track levels of remaining ViCell reagents and cups and inform Lab Consumable Supplies when more needs to be ordered. Check volumes and fill Multitron and Stability chamber carboys 3x per week. (Mobile phase solutions for HPLC). Distribute distilled water for incubators daily. Deliver RODI (reverse osmosis deionized) and USP water to designated Labs. Distribute FBS from central stock to appropriate locations once per week; monitor central stock and track usage to inform when the reordering process needs to occur. | 11/24/2023 |
| 1104 | Sanofi Waltham, MA mRNA Senior Research Associate - Vaccine Bachelors in a related field (e.g., Cell Biology, molecular biology, biochemistry, etc.). Exp: 1-3 years |
As a part of the Discovery biology group at Sanofi's mRNA Center of Excellence (CoE), our team leads the development and implementation of high-throughput screening techniques to aid in the development of our next generation mRNA vaccines. Our team functions transversally and as such gets to work alongside all of the other R&D groups to achieve our goal of advancing our mRNA platform to the next generation. | 11/24/2023 |
| 1105 | Sanofi Framingham, MA Research Associate, Gene Therapy - Genomic Medicine Bioanalytics BS in biological sciences or related field. Exp: 1 – 3 years |
The Sanofi Genetic Medicine Unit CMC organization is responsible for the design and optimization of gene and cell therapy manufacturing processes and platforms. A key function of this group is to establish operational excellence in the manufacturing of Sanofi’s emerging portfolio of gene therapy products. The bioanalytical group provides analytical testing to support in process, release, and stability testing, as well as development activities for process optimization and life cycle management from early to late-stage clinical entry. The Research Associate is responsible for executing test methods under control of established procedures. Additional functions will include interpretation of data, preparation of test documentation, and management of analytical databases. We are looking for a candidate that is capable of learning quickly with the goal of executing analytical methods and managing assigned test schedules, with excellent communication skills. The position is primarily located in Framingham, MA but will be moving to Waltham, MA in Q4, 2022 | 11/24/2023 |
| 1106 | Sanofi Waltham, MA Senior Research Associate, Genomic Medicine Unit - Cell Culture Process Development Master’s degree in biological science or engineering discipline. Exp: 1+ years |
The Genomic Medicine Unit (GMU) CMC group at Sanofi is dedicated to the establishment of best in class manufacturing platforms to support development of life-changing advanced cell and gene therapy products, including recombinant AAV vectors, lentiviral vectors and cell therapy products. This organization encompasses vector and cell line engineering, upstream and downstream process development, analytics, and clinical manufacturing support. The cell culture process development group is responsible for viral vector production optimization and development of next generation production platforms to support high dose therapeutic products. The group is seeking a motivated Senior Research Associate to join the team | 11/24/2023 |
| 1107 | Sanofi Framingham, MA Senior Research Associate - QC, Genomic Medicine Bioanalytics - CT Master’s degree in Biology/Biochemistry or related discipline. Exp: 1+ years |
This position resides within the Genomic Medicine Unit (GMU), a part of Sanofi’s CMC Development organization. The GMU Analytical Development group has the overall responsibility to establish phase appropriate control strategies and to develop, qualify, and validate robust analytical methods to support release and characterization testing of different cell therapy candidates. The group supports cGMP-compliant in-process Quality Control (QC) support of cGMP Manufacturing cutting edge methods such as flow cytometry. The selected candidate will execute rapid turnaround cGMP testing of in-process materials. In addition, contribute to method improvement, qualification, and drug product testing prior to going to clinical trials. The candidate will work with the team to facilitate these goals. This group will be in Framingham working onsite. This position will be a rotating morning shift (9am-7pm), 4 days per week, and will be required to work two weekends a month | 11/24/2023 |
| 1108 | Sanofi Waltham, MA Senior Associate Scientist, Genome Engineering-NGS, Genomic Medicine Unit Master’s Degree. Exp: 1 year |
We are seeking a Sr. Associate Scientist to be part of a team focused on next generation sequencing in genome and cellular engineering in the Genomic Medicine Unit. The successful candidate will play a key supporting role in application of genome editing technology as an approach for treatment of cancer, rare blood and/or rare genetic diseases. | 11/24/2023 |
| 1109 | Sanofi Waltham, MA Senior Research Associate - Pilot Plant Operator Waltham, MassachusettsSenior Research Associate - Pilot Plant Operator Waltham, Massachusetts MS in a related discipline. Exp: 1+ years |
The gene therapy development and manufacturing group in Sanofi is responsible for the design and optimization of viral vector manufacturing processes and platforms. A key function of this group is to establish operational excellence in the manufacturing of gene therapy materials and products, through the development and implementation of robust and safe manufacturing practices, capable of supporting program needs, that are aligned with Sanofi internal standards and evolving regulatory expectations The manufacturing operations team is responsible for the safe and compliant execution of established manufacturing procedures to meet aggressive program deliverables. The team is responsible for “transfer-in” of manufacturing operations from development, as well as manufacturing of product to support internal program needs and external technology transfers for early and late-stage clinical gene therapy products. The Senior Research Associate will be responsible for executing upstream and operations under control of established manufacturing procedures and cross training of junior staff as needed. | 11/24/2023 |
| 1110 | Sanofi Framingham, MA Senior Manufacturing Technician Associate’s degree or Bachelor's degree. Exp: AS: 1-3 years; BS: 1-2 years |
This is a 12-hour, rotating position for within our Downstream Manufacturing team at our 8 NYA facility. 8 NYA is an integrated, continuous, biomanufacturing facility (ICBF). The facility is operated by Upstream, Downstream and Support Service groups which support a 24/7 large-scale therapeutic protein manufacturing facility housing multiple products. Initial job responsibilities will include supporting a diverse range of manufacturing related activities during plant start-up from Operational Commissioning/Shakedown through process validation (PV) and commercial operations. The Senior Manufacturing Technician will be responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMPs. | 11/24/2023 |
| 1111 | Invitrogen St. Louis, MO Scientist II, Process Development Master’s degree or foreign degree equivalent in Chemistry, Biology, Biochemistry, Chemical Engineering, or a related field of study. Exp: 1+ years |
DUTIES: Works with a variety of chromatography techniques including reverse phase, size exclusion, affinity, and ion exchange chromatography. Assists with the design of experimental plans based on defined deliverables. Conducts semi-routine and moderately complex tasks and sample analysis to support process development. Functions as a process subject matter expert in a cGMP environment. Assists with preparing protocols, reports, and test methods. Maintains and ensures safe laboratory environment and work practices. Executes, records, and evaluates experimental data appropriately, including the writing and revising of process development reports and technology transfer protocols as needed. | 11/24/2023 |
| 1112 | Invitrogen St. Louis, MO Scientist I, Electrophoresis Analytical Development Bachelor in Molecular Biology / Chemistry / Biochemistry / Chemical Engineering, or a related field. Exp: no experience |
Responsible for developing or transferring analytical methods to support biopharmaceutical process development. You will work within an interdisciplinary team of scientists where you will learn and supply your skills and ideas to projects. | 11/24/2023 |
| 1113 | Invitrogen St. Louis, MO Biopharmaceutical Production Technician II Bachelor’s degree in Biology, Biochemistry or Chemistry (or related) Exp: 1+ year |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He/She will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 11/24/2023 |
| 1114 | Invitrogen St. Louis, MO Formulation Technician I (Day Shift) Associates in a relevant scientific field or bachelor’s degree in Biology, Biochemistry or Chemistry preferred. Exp: AS: 1-3 years; BS: 0+ years |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. They will be responsible for following Current Good Manufacturing Practices (cGMPs) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. We're currently hiring Biopharmaceutical Technicians and Buffer & Media Technicians on Day and Night shifts (12/hour shifts either 6:00AM-6:30PM or 6:00PM-6:30AM on a rotating schedule of a 2/2/3). Minimum base pay is $21/hour (plus built-in overtime). Base pay can vary per education, experience and position level. | 11/24/2023 |
| 1115 | Invitrogen St. Louis, MO QC Scientist I Bachelor’s degree in STEM field preferred. Exp: no experience |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 1116 | Invitrogen St. Louis, MO QC Scientist I - Environmental Monitoring Bachelor’s degree in STEM field preferred. Exp: no experience |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale! Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 1117 | Invitrogen St. Louis, MO Scientist I, QC Microbiology (4x10 Days; Wed - Sat) Bachelor’s degree required in a scientific field, preferably a Microbiology or Biology. Exp: 0 - 2 years |
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. | 11/24/2023 |
| 1118 | Jordi labs Mansfield, MA Senior Chemist 1 - Must be local to Mansfield, MA Masters of Science in Chemistry Exp: 1+ years |
Job Summary: Candidate will be responsible for Reports Preparation; preparing technical reports summarizing findings related to mass spectroscopy (LCMS, GCMS, PYMS) and chromatography methods (HPLC, GC), Designing Analyses; designing and implementing analytical strategies to help resolve complex, real world analytical problems including material failures, deformulations and quantitation, Performing Analysis; direct or perform mass spectroscopy or chromatographic analyses including overseeing method development and performing existing methods, Discussing Results; skilled at discussing analytical data and would be able to communicate in simple terms the results from a series of analytical tests. This would include helping other team members with interpretation as well as discussing results with customers. | 11/24/2023 |
| 1119 | Stryker Portage, MI Entry-level Electrical Design Engineer, R&D Bachelor's degree in Electrical Engineering or related discipline. Exp: 0+ years |
At Stryker we are dedicated to improving lives, with a passion for researching and developing new medical device products. As an engineer at Stryker, you will be proud of the work that you will be doing, using cutting-edge technologies to make healthcare better. Here, you will work in a supportive culture with other incredibly talented and intelligent people, creating industry-leading medical technology products. You will also have growth opportunities as we have a culture that supports your personal and professional development. | 11/13/2023 |
| 1120 | Acrotech Biopharma Dayton, NJ CHEMIST A BS/MS in a Scientific field. Exp: 1-3 years’ |
The Chemist will perform a variety of testing to assess the strength, identity and purity of finished product, which are mainly oral solids and/or raw materials. The Chemist will work as a member of a team to effectively plan and develop/validate new methods (for Assay, Dissolution, Residual solvents, and Related compounds tests) to execute analytical testing and/or test using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 11/14/2023 |
| 1121 | Acrotech Biopharma Durham, NC ASSISTANT SCIENTIST BA/BS in Chemistry, Pharmaceutical Sciences or related field. Exp: 0+ years |
Capable of performing test methods for complex formulations under general oversight and documenting those experiments per cGMP requirements. Must be able to calculate, organize, and communicate results via standard data templates and reports. Experience in a cGMP laboratory and testing inhaled product (e.g. MDI and DPI) samples is preferred. Must possess good organizational skills, a commitment to quality work, and good oral and written communication skills, and work effectively as part of a team. | 11/14/2023 |
| 1122 | Acrotech Biopharma Dayton, NJ CHEMIST A BS with Chemistry is one of the subjects would be preferable. Exp: 1-3 years |
Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% - 100% of their work at the bench level. | 11/14/2023 |
| 1123 | Repligen Auburn, MA Applications Engineer I Bachelor’s degree in engineering. Exp: 1-2 years |
Responsibilities Working closely with commercial team, convert customer conceptual design into a product solution that meets customer applications need Guide customer in selection of various raw materials that aligns with business preferred raw material Generate finish product cost estimates Product setup in ERP system which includes but not limited to creating Item Master, manufacturing router and Bill of materials. Initiate / Approve Engineering Change Orders for raw materials and finished products Travel required <10 % of time to visit industry events and customer visit | 11/14/2023 |
| 1124 | Cel-Sci Baltimore & Elkridge, MD Validation Technician B.S. in science or engineering or a related discipline or 2-year degree. Exp: BS: 0+ years; AS: 1 to 2+ years |
The Validation Technician is responsible for supporting validation activities of GMP equipment and systems. Assists in specifying and selecting equipment. Maintains all records related to qualification and validation. Prepares validation reports, suggests, and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Technician reports to the Validation Engineer. | 11/14/2023 |
| 1125 | Cel-Sci Baltimore & Elkridge, MD Validation Engineer B.S. in a related discipline. Exp: 1 to 5+ year |
The Validation Engineer is responsible for the regulation and support of equipment and systems. Assists in equipment selection, specification, and negotiating fees. Maintains all records related to qualification and validation. Works on projects where data analysis requires evaluation of defined factors to broad concepts. Utilizes independent judgment within broad parameters to determine an appropriate solution. Prepares validation reports, suggests and assists in determining specifications, and makes recommendations for modifications as necessary. The Validation Engineer reports to the Validation Supervisor. | 11/14/2023 |
| 1126 | Cel-Sci Elkridge, MD Manufacturing Process Technician BS/BA Degree in a related field or AA Degree in a related field. Exp: BS: 0+ years; AS: 1+ years |
The Manufacturing Process Technician contributes to the manufacturing team and participates in the manufacture of LI under GMP, and in process development and facilities operations and maintenance. The Manufacturing Process Technician reports directly to Supervisor of Manufacturing. | 11/14/2023 |
| 1127 | Cogent Professionals Indianapolis, IN Cellular Biologist/Biochemist BS - Biology, Cell/Molecular Biology, Biochemistry or related field or MS. Exp: 1-3 years |
We currently have a role available for a Cellular Biologist/Biochemist with industrial pharma experience. Job duties include, but are not limited to: Developing methods and assays, running assays efficiently, and recording and interpreting data. Strong cell culture (pre-clinical/mammalian) and aseptic technique skills needed. Ability to present data and summarize conclusions in written and oral forms. Utilizing Western blots, gel electrophoresis, MS and other biochemistry/molecular biology techniques. | 11/14/2023 |
| 1128 | Cogent Professionals San Diego, CA Entry-level Pharma Chemist BS-Chemistry or related field. Exp: 0-2 years |
We currently have a role available for an Entry-level Pharma Chemist. Job duties include, but are not limited to: Receiving and managing routine and daily orders. Weighing and preparing samples for storage and shipping. Sharing best practices and improvement opportunities. Working with laboratory automation (i.e. Hamilton, Tecan, etc.). Clearly documenting all laboratory duties. Keeping lab space clean and safe. | 11/14/2023 |
| 1129 | Cogent Professionals Pasadena, CA Molecular Biologist/Biochemist BS-Biology, Molecular/Cell Biology, Biochemistry, or related field. Exp: < 1 year |
We currently have a role available for a Molecular Biologist/Biochemist. Job duties include, but are not limited to, the following: Cell culture on a moderate scale and plating 96-well plates. Prepare reagents for automated liquid handling system. Preliminary analysis of data to verify completeness and accuracy. Some biochemistry background would be highly desirable, including Western Blot. Knowledge of liquid handling robots would be a plus (Tecan). Thorough documentation of experimental procedures via eLN (Benchling), reports, and technical documents. Compliance with all electronic notebook, safety, and quality SOPs is a must. Willingness to prepare and communicate technical presentations as needed. | 11/14/2023 |
| 1130 | Cogent Professionals Pasadena, CA Synthetic Chemist BS-Chemistry, Organic Chemistry, or related field or MS. Exp: BS: 1-3 years; MS: 0-1 years |
We currently have roles available for skilled Synthetic Chemists with industrial pharma lab experience. Job duties include, but are not limited to, the following: Synthesis of small molecules and proficiency in synthetic organic chemistry. Understanding standard unit operations (e.g., reaction set up, work up, flash column purification, isolation, and characterization), along with demonstrated technical problem-solving ability, is a must. Synthesis of peptides using automated peptide synthesizers and solution chemistry. Purification using preparative RP-HPLC, flash chromatography, FPLC, SEC, or equivalent. Bioconjugation of peptides/proteins using standard techniques. Strong expertise running and interpreting NMR, HPLC, and LC-MS data. Thorough documentation of experimental procedures via eLN, reports, and technical documents. Compliance with all electronic notebook, safety, and quality SOPs is a must. Willingness to prepare and communicate technical presentations as needed. | 11/14/2023 |
| 1131 | Debut Biotechnology San Diego, CA Research Associate - Downstream Process Development Bachelors/Masters degree in Chemistry, Chemical Engineering, or related subject. Exp: 0-2 years |
Debut Biotechnology is seeking a Research Associate in downstream process development for small molecule purification. You will assist in the development of robust & scalable downstream processes, and support pilot-scale process operations to maximize product yield. This individual should have familiarity with phenomena that can be leveraged for purification on a molecular level, as well as those that can be applied for physical material separations. As such, those with backgrounds in chemistry & chemical engineering are strongly encouraged to apply. Research Associate II and Senior Research Associate level candidates will also be considered. The successful candidate will work closely with the internal members of the downstream process development team, as well as the cross-functionally with fermentation scientists, pilot plant associates, biologists, chemists, and engineers. | 11/15/2023 |
| 1132 | Dicerna Pharmaceuticals Clayton, NC Filling Technician I - AP - Days AAS degree in a related field preferred. Exp: one (1) year |
The Position Filling of insulin & media preparations under aseptic conditions & operation of inspection equipment in order to achieve production goals | 11/16/2023 |
| 1133 | Dicerna Pharmaceuticals Clayton, NC Manufacturing Process Technician I - FP - NIGHTS AAS degree or military training preferred. Exp: six (6) months |
The Position Operate Assembly/Packaging manufacturing equipment in order to achieve production goals. | 11/16/2023 |
| 1134 | Dicerna Pharmaceuticals West Lebanon , NH Manufacturing Technician Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. We offer both day and night shift positions (schedule below). With the growth of our site, we are seeking night shift suppport. Day Shift (7:00am-7:00pm) : Sun-Tuesday everyother Wedneday Thur-Saturday everyother Wednesday Night Shift (7:00pm-7:00am- includes 15% shift differential): Sunday-Tuesday everyother Saturday Wednesday-Friday everyother Saturday | 11/16/2023 |
| 1135 | Dicerna Pharmaceuticals West Lebanon , NH Manufacturing Technician - Night Shift Bachelors’ Degree in a science discipline. Exp: zero (0) years’ |
This position has primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. With the growth of our site, we are seeking night shift support. We offer the following shift schedules that include a 15% shift differential: 7:00pm-7:00am (everyother week has 8-hours built in overtime): Sunday-Tuesday and everyother Saturday Wednesday-Friday and everyother Saturday | 11/16/2023 |
| 1136 | DxTerity Rancho Dominguez, CA Laboratory Technician/Scientist Molecular Biology, Lab Operations S. or M.S. in chemical, biological or clinical laboratory science, or medical technology from an accredited institution. Associate degree in a laborat Exp: 1-3 years |
Purpose of the Position: Testing biological specimens in molecular biology laboratory environment, including high throughput workflows, analyzing the results, and preparing them for reporting. | 11/17/2023 |
| 1137 | DxTerity Rancho Dominguez, CA Research Associate B.S. or M.S Degree in Biochemistry, Molecular Biology or a related field. Exp: 1-3 years |
DxTerity, a patient-centric genomics company located in Los Angeles, CA is looking to hire a Research Associate to join our Research and Product Development team. Responsibilities include: development of molecular diagnostic test kits, reagents and procedures in a team environment. Perform experiments independently after receiving general direction from supervisor. Make detailed observations, analyzes data and interpret results. Prepare technical reports, summaries, protocols and quantitative analyses. Maintain and develop skills in molecular biology and company technology through reading of internal reports and scientific literature. Support the achievement of project objectives and time schedules while meeting ISO and FDA regulatory and design control requirements. | 11/17/2023 |
| 1138 | Etubics Culver City, CA Associate, Quality Control Bachelor’s degree in a life sciences discipline. Exp: 1+ years |
The Quality Control Associate in the Quality Control department is responsible for ensuring the timely execution of Quality Control Analytical assays in support of product release across all of ImmunityBio’s oncology and vaccine product platforms. This position will train on and perform a variety of molecular biology, and/or chemistry assays including but not limited to cell culture, ELISA, qPCR, HPLC, icIEF, CE-SDS techniques and/or Compendial test methods in the evaluation of product quality. | 11/17/2023 |
| 1139 | Fluxergy Irvine, CA Manufacturing Engineer Bachelors or Masters degree in Mechanical Engineering or equivalent engineering degree. Exp: 1 to 3 years |
About the Role Are you a passionate and experienced Manufacturing Engineer ready to take on exciting challenges in the world of manufacturing and process engineering? Do you thrive in a dynamic, cross-functional environment where your skills can make a real impact? If so, we have the perfect opportunity for you! | 11/17/2023 |
| 1140 | Fluxergy Irvine, CA R&D Mechanical Engineer - Product Development Bachelor or master's in mechanical engineering, Biomedical Engineering, Bioengineering preferred. Exp: 1-4 years |
About the Role Would you enjoy taking the latest version of our flagship product from the design stage – all the way to a successful FDA 510K submittal - then commercialization? Does the idea of using your engineering skills to help decentralize traditional laboratory infrastructure sound like a cause you can get behind? If you answered ‘yes’ to both questions above, apply today! Your resume will be reviewed within days - everyone who applies will hear back from us. | 11/17/2023 |
| 1141 | Forbius Montreal, Quebec, CA Sample Manager and Biobank Coordinator Bachelor’s degree (B.Sc.) in Biochemistry, Cell Biology, Life Sciences or a related field. Exp: one (1) year |
We are currently looking for a multi-skilled Sample Manager and Biobank Coordinator to join our growing team in Montréal. In collaboration with our preclinical, translational and clinical teams, the incumbent will be in charge of sample management associated to our preclinical and clinical programs. | 11/17/2023 |
| 1142 | Free Think Technologies Branford, CT Analytical Scientist? Bachelor’s or master’s degree in chemistry, chemical engineering, or related scientific field. Exp: 0-6 years’ |
We are seeking a full-time Analytical Scientist to work in our laboratories in Branford, Connecticut. KEY RESPONSIBILITIES INCLUDE, BUT ARE NOT LIMITED TO Perform analytical measurements including HPLC/UPLC, GC, KF and dissolution testing Ensure all work performed complies with company standard operating procedures Develop and maintain technical expertise through continuing professional education and training | 11/17/2023 |
| 1143 | Fujifilm Diosynth College Station, TX Quality Control Cell Biology Analyst I Undergraduate degree in Biology or science related field; OR AAS in biology or science related field.Undergraduate degree in Biology or science relate Exp: BS: 0+ years; AAS: 1 year |
Summary The Cell Biologist I, under general direction, will be responsible for performing routine and non-routine quantitative and qualitative analysis of samples submitted to the Quality Control (QC) Laboratory. | 11/17/2023 |
| 1144 | Fujifilm Diosynth College Station, TX Quality Control - Microbiology Analyst I Bachelor of Science or Associate of Science degree preferably in Biochemistry, Chemistry, Biology or related field. Exp: 0+ years |
Summary: The Microbiology Analyst I will be responsible for assisting the QC microbiological aspects of cGMP compliance and testing at the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. | 11/17/2023 |
| 1145 | Haemonetics Clinton, PA Manufacturing Engineer Automation I Bachelor's Degree Engineering Exp: 0-2+ years |
This position is responsible to develop and implement changes to product design and/or to the manufacturing process to achieve significant quality, or cost improvements. Requires participation in new product development and existing programs, working with other business units to identify design-for-manufacturability issues and ensuring these issues are addressed prior to release.in a timely manner. | 11/17/2023 |
| 1146 | Haemonetics Clinton, PA Manufacturing Engineer I Bachelor's Degree Engineering; Master's Degree Engineering. Exp: 0-3+ years |
This position is responsible to develop and implement changes to product design and/or to the automation and manufacturing process to achieve significant quality, or cost improvements. Requires participation in new product development programs, working with other business units to identify design-for-manufacturability issues, ensuring these issues are addressed prior to release, and mentoring engineers. | 11/17/2023 |
| 1147 | Pace Analytical Lenexa, KS Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 1148 | Pace Analytical Mt. Juliet, TN Scientist 1 - RadChem Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 1149 | Pace Analytical Mt. Juliet, TN Scientist 1 Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 1150 | Pace Analytical Mt. Juliet, TN Environmental Scientist - Entry Level Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: Entry Level |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 1151 | Pace Analytical Lenexa, CA Scientist 1 - Chemistry, Biochemistry Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 1152 | Pace Analytical Mt. Juliet, TN Chemist (Scientist 1) Shift Differential Offered! Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 1153 | Pace Analytical Ormond Beach, FL Chemist (Scientist 1) Bachelor’s degree in Chemistry/ Biochemistry or a closely related field. Exp: 1+ years |
Join us as a Scientist I, where you’ll put your love of science to work performing and overseeing projects within the wet chemistry department of our environmental testing laboratory. | 11/17/2023 |
| 1154 | InVivo Biosystems Eugene, OR Lab Technician I - Zebrafish Husbandry Associates or Bachelor degree in Biology or related field preferred. Exp: one year |
This is a collaborative, team-based role with the responsibility to support transgenic and phenotyping client and grant-funded projects. On any given day you may perform zebrafish husbandry, general laboratory upkeep for zebrafish and c. elegans research. As you will be joining a growing biotech company, a passion for science, a positive outlook, and an ability to work in a dynamic environment are a must. | 11/17/2023 |
| 1155 | Ionetix Lansing, MI Mechanical Engineer (Lansing, MI) Bachelor’s degree in mechanical engineering. Exp: 1+ years |
Ionetix Corporation is seeking a Mechanical Engineer to design, develop, prototype, test and release mechanical and electromechanical designs of cyclotrons, automated chemistry systems, and related products. | 11/17/2023 |
| 1156 | Ionetix Sarasota, FL Site Production Technician (Sarasota, FL) A degree in a science field such as chemistry, microbiology, pharmaceutical, medical technology. Exp: 1+ years |
Ionetix is seeking a full-time Site Production Technician in Sarasota, Florida. This position will operate the cyclotron and purification unit to manufacture and release PET products, fully integrating the tracer production at the point of imaging. | 11/17/2023 |
| 1157 | Vigene Biosciences Rockville, MD Quality Control Associate - Environmental Monitoring B.S in Biology or related field. Exp: 1-2 years |
At Charles River Laboratories, we are looking for a highly motivated and energetic candidate to join our growing business in the CMO industry. The QC Analyst I will perform microbiological testing, static and dynamic viable and non-viable monitoring of classified clean room areas to support planned or in process manufacturing processes. This position, as well as all positions in the Charles River team will require demonstration of Charles River DNA “Characteristics and Behaviors” (Care, Lead, Own and Collaborate). | 11/17/2023 |
| 1158 | Boston Scientific Arden Hills, MN Quality Engineer I - Electrical Bachelor's degree or higher in Electrical Engineering. Exp: 1+ years |
The Electrophysiology (EP) Design Quality Assurance team is looking for an engineer to evaluate manufacturing and design changes. EP has a broad portfolio of capital equipment used in the field to support ablation and diagnostic procedures. The EP Design Quality assurance team is growing, and the timely evaluation of design changes is key to maintaining a robust EP Capital Equipment portfolio to reduce potential safety and quality issues. This role provides visibility across the Research and Design organization. The selected candidate will collaborate with Manufacturing, Product Complaints, Regulatory, and Field Servicing engineering. This is a significant role for an entry-level engineer with opportunities to grow into Computer Programming, Cybersecurity, Risk, or Electrical Design. The selected candidate will be mentored by a Senior Electrical Engineer. | 11/17/2023 |
| 1159 | BioPharmGuy Anywhere, US Contract Data Work some college Exp: 0 yrs |
We are looking for someone to help confirm mailing addresses in our directory. Mostly Googling. Can do work any time, any place. Must be able to accept payment via PayPal or Venmo. If interested, send a message through the contact form. Thanks! | 11/6/2023 |
| 1160 | Covance Greenfield, IN Research Assistant I - Cell Based and Immunology Team BS/BA degree in science or related field. Exp: 1+ years |
Executes basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 1161 | Covance Greenfield, IN Research Assistant I - Protein Chemistry BS/BA degree in science or related field. Exp: 1+ years |
If you have a passion for science and working in a dynamic and fast paced lab with a cohesive team, the Research Assistant position will take you to the next level in your career. We have an excellent opportunity for someone to join our Protein Chemistry team in Greenfield, IN. In this role you will learn to execute basic Biotechnology laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 1162 | Covance Greenfield, IN Research Assistant I BS/BA/BSc degree in science or related field. Exp: 1+ years |
Executes basic Molecular BioA (Mol BioA) laboratory procedures under the oversight of experienced personnel. | 11/6/2023 |
| 1163 | Covance Indianapolis, IN Research Assistant I BS/BA degree in science or related field. Exp: 1+ years |
Analyzes biological or chemical samples and/or develops/validates methodologies for various compounds and components in compliance with standard operating procedures (SOPs) and regulatory agency guidelines. | 11/6/2023 |
| 1164 | Covance Indianapolis, IN Analyst - BioAnalytical Lab, 2nd shift Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1+ years |
The Analyst is focused on the extraction of biological samples (Protein Preciptation, Liquid-Liquid, SLE/SPE) in various matrices to support clinical and preclinical trials as well as the operation of Chromatographic and Mass Spectrometry instrumentation (Waters/Shimadzu LC, AB Sciex MS). Ideal candidates will also be versed in the operations of various LIMS systems (Nautilus, Watson, IDBS eWorkbook), however, this is not required and training will be provided based on other skills and experience. Schedule: This is a 2nd shift position (2:00pm-10:30pm) scheduled Monday through Friday. | 11/6/2023 |
| 1165 | Covance Indianapolis, IN Research Assistant II Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field. Exp: 1-2 years |
As a Research Assistant II in Bioanalytical Services you will be part of a cohesive team and conduct routine analysis on biological and chemical samples in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines for multiple studies. | 11/6/2023 |
| 1166 | Dexcom Mesa, AZ Process Engineer I Bachelor’s degree in a technical discipline. Exp: 0-2 years |
In this role, you will use sound and proven engineering principles to assist in designing and developing processes and requirements. The projects and activities will focus on Dexcom’s sensor technology. Working as a member of a technology team, you will collaborate with other engineers, management, and operators. This position will lead efforts to prove out manufacturing and automation processes to achieve design requirements specified by R&D, and explore and evaluate new technologies and concepts through analysis, prototyping, fixture design, and experimentation. This position will transfer and scale up new products from R&D. Involvement may begin from feasibility at vendors to full scale manufacturing. | 11/7/2023 |
| 1167 | Exact Sciences Madison, WI Clinical Laboratory Scientist - Tuesday - Friday, 8:00pm - 6:30am Bachelor's degree in a chemical, physical, biological or clinical laboratory science or medical technology from an accredited institution. Exp: 1+ years |
The Clinical Laboratory Scientist I performs laboratory analysis on clinical specimens using established laboratory procedures. The Clinical Laboratory Scientist I duties will include but are not limited to; processing of specimens, performance of moderate, and highly complex analytical testing, establishing, performing and documenting quality assurance, quality control, equipment maintenance, and accurately documenting all work performed under the direction of the Laboratory Medical Director. As a Clinical Laboratory Scientist I, you will recognize and resolve problems using good laboratory practices. Training: Monday - Friday, 7:00am - 3:30pm for the first 4 weeks Location: 650 Forward Drive and 145 E. Badger Road | 11/7/2023 |
| 1168 | ICON plc. San Antonio, TX Laboratory Assistant Bachelor’s degree (preferred). Exp: 1 year |
Duties: • Monitoring samples/Troubleshooting discrepancies. • Consolidating created samples/containers (i.e. slides, blocks, reports, etc.) • Searching and retrieving documents and samples. • Performing data entry/Monitoring e-mails and various correspondences. • Checking that slides/blocks are properly barcoded and labeled. • Assisting the pathologists with the technical/clerical work. | 11/7/2023 |
| 1169 | ICON plc. San Antonio, TX Laboratory Assistant Bachelor's degree (preferred). Exp: 1 year |
Duties: • Monitoring samples/Troubleshooting discrepancies. • Consolidating created samples/containers (i.e. slides, blocks, reports, etc.) • Searching and retrieving documents and samples. • Performing data entry/Monitoring e-mails and various correspondences. • Checking that slides/blocks are properly barcoded and labeled. • Assisting the pathologists with the technical/clerical work. | 11/7/2023 |
| 1170 | Eli Lilly Cambridge, MA Chemist/Sr Chemist - RNA Therapeutics BSc or MSc in Organic Chemistry or related field. Exp: 1+ years |
The successful candidate for this Chemist/Senior Chemist position will have a strong research track record in synthetic organic chemistry, be analytically minded, embrace data-driven decision making, and have experience in oligonucleotide chemistry and or bioconjugation. He/she will provide key technical knowledge and collaborate within a multidisciplinary team to support the development of next-generation RNA based therapeutics. | 11/8/2023 |
| 1171 | Eli Lilly Cambridge, MA Biologist - Cell Biologist Neurodegeneration BS and/or MS. Exp: 1+ Years |
The Cell Biologist position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. The primary responsibility will be culturing iPSC derived motor neurons as a cellular model of Amyotrophic Lateral Sclerosis to support the development of therapeutic agents. | 11/8/2023 |
| 1172 | Eli Lilly Cambridge, MA Biologist –Cell Biologist/Biochemist Neurodegeneration BS and/or MS. Exp: 1+ years |
The Cell Biologist/Biochemist position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. The primary responsibility of the role will be to develop and optimize cellular models of neurodegenerative disease as a platform for therapeutic development. The role will be focused on the biology of aggregate prone proteins such as TDP-43, synuclein or tau. | 11/8/2023 |
| 1173 | Eli Lilly Cambridge, MA Biologist –Biomarker Development Neurodegeneration BS and/or MS. Exp: 1+ years |
The Biomarker Development position will be within the Proteostasis Group, which is part of the larger Neurodegeneration division. In order to effectively diagnose and treat neurodegenerative diseases the identification and measurement of biomarkers is vital. The primary responsibility for this role will be the identification, development and optimization of assays which will support biomarker discovery for neurodegenerative disorders, such as ALS, Parkinson’s Disease and Alzheimer’s Disease. | 11/8/2023 |
| 1174 | Eli Lilly Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree. Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 11/8/2023 |
| 1175 | Eli Lilly Pasadena, CA Chemist / Biochemist Undergraduate degree in chemistry, biochemistry, chemical engineering. Exp: 0+ years |
The team at Protomer is working on responsive biotherapeutics that can be controlled using small molecule modulators. Protomer team is based in Pasadena and the research labs are located in Pasadena. We are currently expanding the team to advance several programs, including glucose sensing insulins (GSIs), and are looking for a research associate with experience in biochemistry, synthesis, bioconjugations, and purification/characterization of therapeutic compounds of interest. The ideal candidate will have a bachelor’s or master’s degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a team player in a fast-paced research setting. The applicant will be responsible for assisting Protomer’s senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively participate and present in team meetings and is expected to contribute to the team’s progress and success. | 11/8/2023 |
| 1176 | Eli Lilly Boston, MA Engineer, Downstream Process Development - Akouos M.S in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an entry level Engineer with a background in AAV vector purification technologies and gene therapy downstream process development. The successful candidate will actively participate in downstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 11/8/2023 |
| 1177 | Organogenesis Canton, MA Production Associate I-Collagen A Biotech certificate, Associate's degree, Bachelor's degree in Biology or a related science discipline is strongly preferred. Exp: 1+ years |
The Production Associate I - Collagen performs activities involved in the production of Collagen These activities include, but are not limited to, protein purifications, filtrations, and titrations in the production of high quality, purified, sterile collagen for both internal and external customers. This position requires working in a regulated area under the direct supervision of a team leader or departmental supervisor. | 11/8/2023 |
| 1178 | Organogenesis Canton, MA Production Associate I Bachelor’s degree or Biotech certificate. Exp: 1+ years |
The Production Associate will perform all activities involved in one of the following areas: the aseptic processing of a living product; the production of ICL and FortaFlex Products; or activities associated with HTP Product under the direct supervision the Manager. This role will support the Manufacturing Team by performing the tasks that will assure the safe and timely processing of our products, working in a Class 100/ISO 5, Class 10K/ ISO 7 and/or Class 100K/ISO 8 cleanroom. Sunday-Thursday schedule or Monday-Friday schedule, approximately 7:30am-4:00pm. Some weekend and holiday work required. | 11/8/2023 |
| 1179 | Meridian Medical Technologies Rocky Mount , NC MS&T Associate Process Engineer Bachelor’s degree. Exp: zero to one years |
As an Associate MS&T Engineer, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will make it easy to manage difficult issues and help in establishing consensus between teams. | 11/8/2023 |
| 1180 | Meridian Medical Technologies Rochester, MI Chemist / Microbiologist Master’s degree. Exp: 1+ years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to patients. Your understanding of Quality Control instruments will help us meet their accuracy specifications against established standards. You will also be relied on for setting requirements for the transfer of methodology from R&D. As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. | 11/8/2023 |
| 1181 | Meridian Medical Technologies Andover, MA QC Technician (2nd Shift) Biotechnology Certificate/Associate Degree. Exp: 0-2 years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control team. You will support commercial manufacturing and QC testing labs by managing sample lifecycle including bulk sample receipt, aliquot, labeling, delivery, and storage of QC test samples. Sample types may include release test, backups, retains, reference material, assay controls, and stability. You will support and maintain the retain program as required by CFR regulations. Monitoring of environmental chambers is also critical to the storage of the above sample types. Your contribution to the Quality Control Sample Operations team will help Pfizer provide safe drugs to patients. | 11/8/2023 |
| 1182 | Meridian Medical Technologies Rocky Mount , NC QC Chemistry Lab Analyst I Bachelor’s degree. Exp: 0+ years |
Your prior work experience and ability to apply your breadth of knowledge will help you adapt the standard methods and procedures. You will help us identify required delivery and process improvements that drive increased efficiency, throughput and quality. You will arrive at decisions on which methods and procedures are the best fit for different work situations. | 11/8/2023 |
| 1183 | Meridian Medical Technologies Rocky Mount , NC Manufacturing Quality Engineer- Quality Distribution Bachelor's Degree. Exp: 0 to 1 year |
You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies. As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues. | 11/8/2023 |
| 1184 | Meridian Medical Technologies Kalamazoo, MI QC Laboratory Analyst II (1st Shift) Bachelor’s degree in Chemistry, Biochemistry or related science. Exp: 0-1 years |
You will be a member of Pfizer’s dedicated and highly effective quality assurance and control team. You will be responsible for analyzing chemical, biological or microbiological products to support our quality programs. You will also be relied on for setting requirements for the transfer of methodology from R&D. You will be developing and applying your knowledge of procedures, techniques, tools, materials and equipment. Your receptiveness to new ideas will enhance the team’s ability to achieve goals and targets. You will follow standard procedures to complete tasks and identify process issues or problems that involve direct application of your skills/knowledge. | 11/8/2023 |
| 1185 | Meridian Medical Technologies Sanford, NC QC Senior Associate Scientist - Method Transfer and Validation BS/BA Degree in Science/related field. Exp: 0 years |
You will be a member of Pfizer’s dedicated and highly effective Quality Control Team at Sanford, NC. Key responsibilities in QC Method Transfer and Validation (MTV) are performing tasks/activities associated with analytical method qualification, validation, verification and transfer. Specific activities include authoring/executing/review of protocols and reports associated with analytical method qualification/validation/transfer to support Pfizer’s quality programs. You will be responsible for participating in method transfer/validation activities to support Demo, Engineering, CTM (Clinical Trial Material), product/process validation and commercial batches manufactured at Pfizer. Additional responsibilities will include driving continuous improvement/Operational Excellence/innovative implementations and represent QC MTV on cross functional teams. Key responsibilities in this role include executing method transfer activities (verification, co-validation, validation, qualification) in the QC laboratory. Other responsibilities may include testing support, SOP revision, LIMS review etc. | 11/8/2023 |
| 1186 | Regeneron Tarrytown, NY Process Development Associate II, Analytics BS Exp: 0 – 2 years |
Regeneron's Preclinical Manufacturing & Process Development (PMPD) Analytics group is seeking a laboratory Scientist or Engineer interested in the analytical characterization of biopharmaceuticals. In this role, you will conduct analytical experiments that support manufacturing process development and research activities in a fast-paced laboratory setting. | 11/09/2023 |
| 1187 | Regeneron Tarrytown, NY Process Development Associate II, Cell Culture Development (PMPD) BS or MS in Chemical Engineering or Bio-related Engineering Exp: 0-3 years |
The Cell Culture Development Group within Preclinical Manufacturing and Process Development (PMPD) is looking for a motivated person to work as part of the medium and feed development team on projects for mammalian cell culture process medium optimization. In this role, you will perform studies at small scale to develop cell culture medium that improves cell growth, cell productivity, and/or product quality to support the extensive Regeneron clinical pipeline. | 11/09/2023 |
| 1188 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associate to support biobanking operations and sample data processes. | 11/09/2023 |
| 1189 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associate to support biobanking operations and sample data processes. | 11/09/2023 |
| 1190 | Regeneron Tarrytown, NY Sample Management Associate BS degree Exp: 0-4 years |
Regeneron’s Sample Management Group, located in Tarrytown, NY, is seeking a highly motivated Sample Management Associateto support biobanking operations and sample data processes. | 11/09/2023 |
| 1191 | Regeneron Tarrytown, NY Associate Scientist, Therapeutic Antibody Early Discovery BS or MS degree Exp: 0-5+ years |
Regeneron's Therapeutic Antibody Immunoscreening group is looking for a highly motivated Assoc Scientist to join our team. In this role you will contribute to the identification of potential therapeutic antibodies, in-vitro characterization and selection process of the lead molecules in early discovery stage. | 11/09/2023 |
| 1192 | Regeneron Tarrytown, NY Process Development Associate I, Bioreactor Development (1 of 3) Undergraduate degree. Exp: 0-3+ years |
Regeneron's Bioreactor Scale-Up and Development (BSD) team, a group within our Preclinical Mftg and Process Development (PMPD) organization, and which provides the link between small scale cell culture development and manufacturing, is seeking a Process Development Associate I. In this role you will assist the reagent productions to support pipeline and assay development needs for research groups and critical reagents to support GMP lot release. BSD performs cell culture up to 500 L scale and studies to support process transfer to manufacturing. | 11/09/2023 |
| 1193 | Steris Mentor, OH Quality Engineer Bachelor's Degree (In engineering or related technical field). Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 1194 | Steris Conroe, TX Quality Technician Associate's Degree in Engineering General or Science. Exp: (1) year |
The Quality Technician is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. The Quality Technician supports manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final QC product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances. They work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. | 11/09/2023 |
| 1195 | Steris Mentor, OH Mechanical Engineer Bachelors degree in Mechanical Engineering. Exp: one year |
The Mechanical Engineer will join a fast-paces Infection Prevention Technologies R&D team developing new Sterilizers. You will interact with other engineering disciplines and cross functional team member during the development lifecycle phases from concept development through final release. The mechanical engineering position will utilize problem solving techniques and engineering principals such as statics, machine design, thermodynamics, heat transfer, material selection and fabrication to develop solutions for medical equipment. You will be involved in 3D Modeling, Design Controls documentation, Design Verification Testing and hands-on prototyping while developing new and innovative solutions for our customers. *This position is located onsite in Mentor, Ohio with eligibility for a hybrid work schedule. | 11/09/2023 |
| 1196 | Steris Eden Prairie, MN Quality Engineer Bachelor's Degree in Engineering General or Science. Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 1197 | Steris St. Louis, MO Microbiologist Bachelor degree required, with a focus in Biology or Microbiology areas required. Exp: 0-5 years |
Are you interested in contributing to a healthier and safer world? The Associate Scientist (Microbiologist) is an entry level position that is responsible for supporting new product development through innovative research and through developing technical expertise in STERIS's Infection Prevention Technology product segments, including surface disinfectants and cleaners. The Associate Scientist, with the appropriate training and guidance, will work in the lab supporting the new product development team, operations and quality to enhance the sophistication and compliance of new, unique infection prevention solutions to meet the customer’s varying unmet needs. | 11/09/2023 |
| 1198 | Steris Arlington, VA Medical Equipment Integration Technician Associate's degree in Electronics, mechanical or similar degree. Exp: one year |
Are you mechanically and technology inclined with a knack for hands-on work and love to travel? Do you enjoy working independently and thrive in a fast-paced environment where you provide an exceptional customer experience? If you want to work for a great company where you will have the opportunity to advance your career, join our growing team as an Integration Technician specializing in installing Operating Room systems to integrate all equipment, audio/visual systems, and hardware and software solutions. ***This position requires overnight travel, up to 85% of the time, Monday - Friday*** This is a remote based customer facing position. To support and service our customers in this assigned territory candidates must be based out of one of the following states: Virginia. | 11/09/2023 |
| 1199 | Steris Montgomery, AL Quality Engineer Bachelor’s Degree (Engineering or related technical field). Exp: 1-5 years |
The Quality Engineer is responsible for maintaining and improving the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role supports complaint/CAPA investigations, supplier quality improvement, operations production and process controls, and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. | 11/09/2023 |
| 1200 | BioDuro Irvine, CA Associate Scientist/Scientist, Analytical Development (Small Molecules) BS degree in Chemistry or related scientific discipline. Exp: 0-3 years’ |
The Associate Scientist/Scientist, Analytical Development independently performs analytical development activities and tasks to support formulation development and drug product manufacturing. The Associate Scientist/Scientist facilitates and assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. Responsible for performing advanced experiments and general laboratory duties. | 10/31/2023 |
| 1201 | BioDuro Irvine, CA Process Engineer BS degree in Engineering or Chemical Engineering preferred. Exp: 0-3 years’ |
The Process Engineer, under direct supervision, performs various duties related to optimization and analysis of production processes, new products, commercial process support and new product technology transfers. | 10/31/2023 |
| 1202 | BioDuro Irvine, CA Associate Scientist, Formulation Development BS in Chemistry or related field required. Exp: 1 year |
The Associate Scientist, Formulation Development, assists in the design and development of drug delivery systems and dosage forms. | 10/31/2023 |
| 1203 | Biomerics Salt Lake City, UT Process Engineer II Engineering Degree needed. Exp: 1-3 years |
The Process Engineer II will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities must be documented according to design control requirements in a design history file (DHF).P: The Process Engineer II may be an individual contributor in a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team. | 10/31/2023 |
| 1204 | Biomerics Winston-Salem, NC Manufacturing Engineer I or II Engineering degree. Exp: 0-5 years’ |
The ME will be expected to lead high-impact projects. The ME is expected to lead change, contribute new ideas, and find innovative methods to accomplish goals. Work with tooling/outside suppliers/in-house personnel performing analysis of situations or data and develop an in-depth evaluation of various factors. Acts independently and exercises judgment within broadly defined practices and policies. Determines methods and procedures for new assignments. The ME will be expected to have the ability to get things done through people who do not report to them. The ME will also need to have the ability to work through adverse situations while building and maintaining good personal relationships. | 10/31/2023 |
| 1205 | Biomerics Salt Lake City, UT Process Engineer II Engineering Degree needed. Exp: 1-3 years |
The Process Engineer II will be responsible for supporting and improving the manufacturing of class II medical and surgical devices in a dynamic, customer-focused organization. You will be expected to work with customers to understand product and process specifications, develop manufacturing processes, and build and test devices to those specifications. All activities must be documented according to design control requirements in a design history file (DHF). The Process Engineer II may be an individual contributor in a small cross-functional team comprising engineering, operations, and quality members to provide process and manufacturability input to designs throughout the product development process. You will support verification, validation, and regulatory submissions of these devices, then lead the transfer of the products to production and ensure a smooth transition to the production engineering team | 10/31/2023 |
| 1206 | Biomerics Salt Lake City, UT Lab Technician I - II Lab Technician I typically requires an associate or bachelor’s degree. Lab Technician II typically requires a bachelor’s degree in chemistry or a rela Exp: 1+ years |
Performs analytical and functional testing. Maintains glassware by picking up, cleaning, washing, sterilizing, and distributing. Keeps laboratory supplies ready by inventorying stock, placing orders, and verifying receipts. Keeps equipment operating by following operating instructions. Troubleshoots breakdowns maintains supplies, performs preventive maintenance, and calls for repairs—documents information by maintaining daily logs and equipment record books. Resolves problems by examining and evaluating data; select corrective steps. | 10/31/2023 |
| 1207 | PSC Biotech Remote Job, CSV Engineer I - Remote Job Bachelor’s degree in Computer Science, Engineering, or a related field. Exp: 1-3 years |
We are hiring motivated and passionate entry to junior level Computer Systems Validation Engineers to join our team. The successful candidate will have excellent communication and interpersonal skills, strong analytical and problem solving skills, and a strong drive to learn. While this is a remote position, candidates in Midwest and/or Pacific Time Zones are preferred. | 11/01/2023 |
| 1208 | PSC Biotech York, PA Manufacturing Associate I Associates Degree in Life Sciences/Liberal Arts field preferred. Exp: 1-3 years |
This position is responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMP/ISO requirement and standards as defined in FDA and EU applicable Regulations. With general supervision the individual will perform routine and critical manufacturing operations, including but not limited to work functions in aseptic and non-aseptic filling, equipment prep, cleaning dissolution and formulation activities. The individual may provide support in other departments within the company, including but not limited to, engineering, warehouse and facilities. The incumbent is also responsible and accountable for the execution of the PSC BioTechnique mission, “to maintain the integrity and professionalism of our products and services while enabling steady growth and development”. | 11/01/2023 |
| 1209 | Biotium Fremont, CA Chemistry Technician I (CHEMISTRY) B.S. or M.S. degree in Chemistry. Exp: 1+ years |
Under the direct supervision from a senior chemist, perform chemical purifications using chromatography including preparative HPLC or gravity chromatography; carry out chemical synthesis using standard protocols; carry out chemical analyses using modern instruments including analytical HPLC, LC-MS, TLC, UV/Vis and fluorescence spectrophotometry. | 11/02/2023 |
| 1210 | Biotium Fremont, CA Research Associate I, BIOSCIENCE B.S. or M.S. in Biology, Molecular Biology, Biochemistry or a related field. Exp: 1+ years |
Under supervision from Biotium scientists, perform biological testing of fluorescent dyes and related reagents. Perform production and quality control testing of assay kit components following standardized protocols. | 11/02/2023 |
| 1211 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, Research Technologies BS degree in Molecular Biology, Cellular Biology, Biochemistry, or a closely related field. Exp: one year |
ShapeTX is seeking a highly motivated Research Associate/Senior Research Associate (RA/SRA) to join our Research Technologies Team. This is an excellent opportunity for a motivated individual with demonstrated molecular biology expertise to contribute to the advancement of our RNAfixTM technology. In this multifaceted position, you will be at the forefront of developing innovative gene therapy payload designs for ShapeTX's disease programs, with responsibilities encompassing independent cloning of plasmids and constructs, employing techniques such as PCR, plasmid ligation, bacterial transformation, and DNA/RNA isolation. You will also play a pivotal role in evaluating novel payloads through tissue culture and transfection-based experiments while maintaining meticulous lab organization and communicating results effectively within our dynamic research environment. This role presents a unique chance to join the critical core of our Research Technologies Team within a rapidly growing biotechnology startup, offering substantial opportunities to contribute to groundbreaking biological applications addressing serious human diseases. | 11/02/2023 |
| 1212 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, AAV Purification - Cell, Assay, and Vector Engineering BS/MS in molecular/cellular biology or other relevant scientific discipline. Exp: 1-5 years |
ShapeTX is looking for a highly motivated individual with a strong passion for learning to join the growing Research team as Research Associate/Senior Research Associate, AAV Purification - Cell, Assay, and Vector Engineering. In this role, the successful candidate will purify and characterize AAV to support the early research pipeline and ShapeTX’s novel RNAfixTM and RNAskipTM technology platforms. The candidate will conduct exploratory research to develop novel AAV purification methods in addition to routine purifications. An ideal candidate will have demonstrated AAV/viral purification experience or broad recombinant protein purification experience a collaborative spirit, and a desire to work in a fast-paced startup environment. | 11/02/2023 |
| 1213 | Shape Therapeutics Seattle, WA Research Associate/Senior Research Associate, Virus Production and Engineering BS/MS in molecular/cellular biology or other relevant scientific discipline. Exp: 1/3 years |
ShapeTX is looking for a highly motivated individual with a strong passion for learning to join the growing Research team as a Research Associate/Senior Research Associate, Virus Production and Engineering. In this role, the successful candidate will generate AAV to support the early research pipeline and ShapeTX’s novel RNAfixTM and RNAskipTM technology platforms. An ideal candidate will have broad cell culture experience, an understanding of molecular biology techniques, a collaborative spirit, and a desire to work in a fast-paced startup environment. | 11/02/2023 |
| 1214 | Boston Analytical Salem, NH Quality Assurance Specialist I Bachelor’s degree in a related science discipline. Exp: 0-1 years |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. | 11/02/2023 |
| 1215 | Boston Analytical Salem, NH Analytical Chemist Bachelor’s degree in Chemistry or a related science discipline is required. Exp: 0-2 years |
The Analytical Chemist I conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products using HPLC, GC, Dissolution, AA, UV-Vis, Wet Chemical Analysis and Method Development. | 11/02/2023 |
| 1216 | Boston Analytical Salem, NH QC Microbiologist BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The QC Microbiologist conducts quantitative and qualitative analysis of pharmaceutical products according to FDA, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include analysis of pharmaceutical products through compendial methods and client specific test protocols. | 11/02/2023 |
| 1217 | Boston Analytical Salem, NH Microbiologist - Environmental Monitoring BA or BS degree in Microbiology or related science discipline. Exp: 0-2 years |
The EM Microbiologist conducts quantitative and qualitative analysis of pharmaceutical industries Environment according to FDA, ISO, cGMP and Boston Analytical, Inc. Standard Operating Procedures. Duties will include Sampling of pharmaceutical industries through ISO standards and client specific test protocols. | 11/02/2023 |
| 1218 | Boston Analytical Framingham, MA Offsite EM Technician Associates degree preferred. Science classes or an associates degree in a scientific discipline is preferred. Exp: 0+ years |
The Offsite Environmental Monitoring Technician will perform Environmental Monitoring (EM) of pharmaceutical cleanrooms and the associated spaces on a daily basis according to FDA, cGMP and Boston Analytical's/Client Standard Operating Procedures. The position is primarily in the Framingham, MA area. | 11/02/2023 |
| 1219 | Boston Institute of Biotechnology Southborough, MA Research Associate - Downstream Process Development BS degrees in biology, biochemistry, biomedical/biochemical engineering, or related fields. Exp: ≤1 year |
A Research Associate I is an entry level position for Bachelor’s degree with no prior experience and reports to a scientist level or above on relevant projects. The individual is responsible for routinely setting up, operating, and maintaining the downstream lab equipment under direct supervision. | 11/03/2023 |
| 1220 | Boston Institute of Biotechnology Southborough, MA Research Associate - Upstream Process Development BS degree in Biochemical Engineering or related field of study. Exp: 0-2 years |
Responsibilities 1. Set up, execute, and monitor microbial and mammalian cell culture production in fermenters and bioreactors. 2. Collect, record, and report experimental data. 3. Provide updates to a team lead on a regular basis. 4. Maintain all notebooks and documentation according to department standards. 5. Write SOPs, and batch records. 6. Ability to work well in a team environment and independently as required. 7. Ensure and promote safe environmental and laboratory practices. 8. Order supplies as needed. 9. Prepare solutions and buffers. 10. Maintain lab space and equipment. | 11/03/2023 |
| 1221 | Boston Institute of Biotechnology Southborough, MA Research Associate - Analytical Development Bachelor’s or Master’s degree in Biology, Chemistry, Pharmaceutical Sciences, or a related/relevant discipline. Exp: Entry Level |
The Research Associate role within Analytical Development is an entry level position for individuals with a Bachelor’s or Master’s degree. Responsibilities include developing analytical methods for biologics characterization, characterizing samples from process development, and supporting subsequent clinical and/or commercial GMP manufacturing. | 11/03/2023 |
| 1222 | BostonGene Waltham, MA Research Associate, Molecular Biology & Next Generation Sequencing Bachelor’s (B.S.) degree in biology, clinical laboratory science, medical technology, or related discipline. Exp: 0-2 years |
BostonGene is seeking a highly motivated Research Associate to join our R&D team in our laboratory located in Waltham, MA. This candidate will support BostonGene’s state-of-the-art primary next-generation sequencing (NGS), adjunct analytical platforms, and automated analysis pipelines. The candidate will be expected to develop proficiencies in NGS support protocols, such as RNA and DNA isolation from tissue, cell-free DNA isolation from plasma, Whole Exome and RNA-Seq library preparation, qPCR, Molecular Biology techniques, and other sample QC techniques | 11/03/2023 |
| 1223 | Boundless Bio San Diego, CA Research Associate, HTS Screening, Drug Discovery BS/MS in biology related field. Exp: 1 year |
As a Research Associate at Boundless Bio, you will play a significant role in helping us transform exciting extrachromosomal DNA (ecDNA) discoveries into cancer medicines of the future. You will contribute to the process of developing robust, miniaturized high-throughput assays designed to enable drug discovery programs supporting multiple ecDNA-directed targets. This will involve broad application of biochemical and cellular assays across a range of formats to enable screening and SAR campaigns in support of our drug pipeline. These efforts will make an important contribution to the Boundless Bio drive for innovation in targeting difficult to treat cancers. | 11/03/2023 |
| 1224 | BPS Bioscience San Diego, CA Research Scientist I - Cell Biology M.S Exp: 1+ years |
BPS Bioscience Inc. is a leading provider of recombinant proteins, assay kits, lentiviruses, and recombinant cell lines for drug discovery. We are currently seeking a diligent and highly motivated scientist to join our cell biology group to assist in production and new product development. | 11/03/2023 |
| 1225 | BroadPharm San Diego, CA QC Chemist Bachelor or MS degree in Analytical Chemistry or Organic Chemistry is required. Exp: 1-4 years |
BroadPharm is a fast-growing biotech company which specializes in providing high purity PEG products and customer services worldwide. We are seeking a highly motivated QC Chemist to join our expanding team. The ideal candidate would already have 1+ year of working experience with HPLC, MS, and NMR. The position will work closely with the production team and regulatory manager in addition to the current QC staff. | 11/03/2023 |
| 1226 | Cabaletta Bio Philadelphia, PA Sr. Research Associate/Associate Scientist Molecular Biology M.S. degree in Life Sciences or closely related discipline. Exp: 1 -2 years |
Reporting to the Associate Director, Molecular Biology group, we are seeking an experienced and motivated Senior Research Associate or Associate Scientist. Under scientific and technical supervision, the candidate will design and produce molecular constructs that could be utilized for vector development and protein production. The individual will focus and work along for manufacturing small and large scale LVV gene therapy vectors across various preclinical programs and disease areas. The position offers growth into additional areas such as cell biology and molecular biology, immunology, and cell therapy. The position involves both technical and operational responsibilities. | 11/03/2023 |
| 1227 | Bayer Berkeley, CA Associate Electric Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 11/03/2023 |
| 1228 | Bayer Pittsburgh, PA Manufacturing Associate II - O'Hara M-TH 5:30am-3:50pm Associate's Degree Exp: 1+ years |
This advanced position exists to provide experienced resources to assemble and support the various medical device manufacturing processes. It also provides a supporting role in the way of quality control in combination with advanced assembly, performed in a timely manner to meet quality and productivity goals of the department. This role will also assist the process coordinator or group lead in any training or cross training efforts as needed. The role will also interact between many departments to transmit information and recommend solutions to design, process and quality problems/non-problems. Leadership, a positive attitude and willingness to support teamwork is key! This role provides mentorship and support to the Manufacturing Production floor personnel in any way possible! This position will incorporate both Assembly and Quality inspections and requires more than one years’ experience at Bayer or in a position with related work experience | 11/03/2023 |
| 1229 | Bayer Luling, LA Chemical Production Engineer Bachelor’s of Science degree in Chemical Engineering, including May 2024 B.S. Chemical Engineering graduates. Exp: Up to 3 years |
The Chemical Production Engineer provides support to plan, coordinate, and execute technical activities needed to support manufacturing operations. Also, ensures the safe, efficient, productive, and environmentally sound manufacture of active ingredients or intermediates. | 11/03/2023 |
| 1230 | Bayer Berkeley, CA Associate Electrical Engineer M.S. Degree in Electrical Engineering or related discipline. Exp: 0-1 years |
Exciting and challenging electrical engineering opportunity where each day is different. Tasks would include evaluating electrical capacity, emergency power readiness, equipment maintenance, alternative sustainable energy solutions, and component electrical ratings analysis. Interact with cross-functions including Quality, Production, Procurement, Investment Management, Research and Development at the at the local, regional, and global levels as well as external vendors, and CA state supplier. | 11/03/2023 |
| 1231 | Abcam Waltham, MA Laboratory Technician - Proteins Associate's degree. Exp: one year |
Abcam is looking for a Lab Technician to join our team in Waltham MA, working to support the Protein Science team in the development of standalone recombinant products at Abcam. The goal of this product line is to deliver outstanding products to our customers and help Abcam achieve our aim of being the most influential company in life sciences by helping advance global understanding of biology and causes of disease, which, in turn, will drive new treatments and improved health. | 11/03/2023 |
| 1232 | Abcam Eugene, OR Research Associate - Biochemical Assay Design Bachelor's degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 1+ years |
Abcam, a leading life sciences company, is seeking a motivated and detail-oriented individual to join our team as a Research Associate - Biochemical Assay Design in our Eugene, Oregon location. If you are passionate about advancing research in the life sciences and possess a strong background in biochemical assays, we encourage you to apply. | 11/03/2023 |
| 1233 | Agilent Carpinteria, CA Histology Laboratory Assistant Bachelors in biological sciences preferred. Exp: 1+ years |
The position will support the tissue procurement department and will include tasks and documentation to move new donor samples through incoming quality control to delivery of qualified samples to internal teams. This laboratory assistant position will have duties both in the lab and at the desk. | 11/03/2023 |
| 1234 | Bio Marin Pharmaceutical San Rafael, CA Research Associate (Temporary) Master’s degree in a scientific discipline or equivalent. Exp: 1 to 3 years |
We are searching for a talented and highly motivated Research Associate II to develop assay methods that will provide safety and efficacy data on experimental therapeutics entering clinical studies. The candidate will be responsible for the development of assays for diverse drug modalities, which may include gene therapies, monoclonal antibodies, oligonucleotides, biologics, and small molecules, with guidance from a Scientist in the Assay Strategy and Development group. The ideal candidate should have experience developing and optimizing bioanalytical methods, analyzing and interpreting experimental results, and communicating conclusions to other scientists. The successful candidate will participate in programs that range from exploratory in vitro and animal studies to non-clinical efficacy and safety studies and clinical trials. You will be responsible for developing new methods, evaluating novel technologies, conducting translational research internally at the BioMarin Research Center and externally in partnership with contract research organizations, and communicating results to cross-functional teams. This position offers a unique opportunity to interact with scientific and business colleagues across many functional areas, including Research, Translational Sciences, Regulatory Affairs, and Clinical Sciences. This RA II position will report to a Scientist in the Assay Strategy and Development group and will have the opportunity to advance our most promising pipeline programs to treat rare genetic diseases. | 11/03/2023 |
| 1235 | Bio Marin Pharmaceutical San Rafael, CA Research Associate II, Molecular Medicine, Translational Sciences Master’s degree in Biology, Chemistry, or like field. Exp: 0-2 yr |
The Molecular Medicine Group within the Translational Sciences Department at BioMarin Pharmaceutical is seeking a Research Associate II to help drive understanding of the underlying mechanisms for successful treatment with recombinant Adeno Associated Viral (rAAV) gene therapy and antisense oligo (ASO) modalities. The ideal candidate has a flexible mindset, natural curiosity and motivation to understand biology at the molecular and biochemical levels. The Molecular Medicine group aims to creatively apply the complete molecular and cellular toolkit to understand the contributing mechanisms of action or effect, in collaboration with colleagues across the company. We are positioned to help solve technically challenging questions that present as unexpected findings and/or have cross-program impact. We are currently particularly interested identifying early indicators and mechanisms that modulate the magnitude, durability and variability of expression of our gene therapy candidate(s). We work with cross-functional teams to develop and evaluate nucleotide integration capabilities for safety assessments. The Molecular Medicine group strives to improve technologies to enable analysis on small samples with definitive results, including at the single cell and nuclei level. The group collaborates with the entire set of Translational Sciences functions to understand the molecular and cellular actions of our therapeutics in preclinical experiments through clinical delivery to our patients. As our expanding clinical stage pipeline evolves, this RAII will have the opportunity to contribute to molecular investigations on a variety of therapeutic modalities and the genetic diseases that BioMarin strives to treat. This position will be primarily laboratory focused. The Research Associate II will be responsible for the design and execution of technically complex experiments to support multiple projects, with strategic input and guidance from Molecular Medicine and Translational Sciences leadership. S/he will provide quantitative data analysis, interpretation of results, and contribute to technical reports and scientific papers. S/he will evaluate existing complex methods and technologies, develop new solutions, and collaborate across functions to solve technical problems. The Molecular Medicine team values learning agility, open communication skills, willingness to support others’ experiments, and ability to trouble-shoot experiments on multiple platforms. The SRAII al | 11/03/2023 |
| 1236 | Bio Marin Pharmaceutical San Rafael, CA Research Associate II, Assay Strategy and Development (Temporary) Master’s degree in a scientific discipline or equivalent. Exp: 1 to 3 years |
We are searching for a talented and highly motivated Research Associate II to develop assay methods that will provide safety and efficacy data on experimental therapeutics entering clinical studies. The candidate will be responsible for the development of assays for diverse drug modalities, which may include gene therapies, monoclonal antibodies, oligonucleotides, biologics, and small molecules, with guidance from a Principal Scientist in the Assay Strategy and Development group. The ideal candidate should have experience developing and optimizing bioanalytical methods, analyzing and interpreting experimental results, and communicating conclusions to other scientists. The successful candidate will participate in programs that range from exploratory in vitro and animal studies to non-clinical efficacy and safety studies and clinical trials. You will be responsible for developing new methods, evaluating novel technologies, conducting translational research internally at the BioMarin Research Center and externally in partnership with contract research organizations, and communicating results to cross-functional teams. This position offers a unique opportunity to interact with scientific and business colleagues across many functional areas, including Research, Translational Sciences, Regulatory Affairs, and Clinical Sciences. This RA II position will report to a Principal Scientist in the Assay Strategy and Development group and will have the opportunity to advance our most promising pipeline programs to treat rare genetic diseases. | 11/03/2023 |
| 1237 | Bristol-Myers Squibb Phoenix, AZ Associate, QC Microbiology Operations Bachelor’s Degree in a scientific field preferred. Exp: 0-2 years’ |
2nd Shift- 2pm.-10:30pm. Position: EG 70-Associate, QC Microbiology Operations Location: Phoenix, AZ At Bristol Myers Squibb, we are inspired by a single vision – transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease – and one of the most diverse and promising pipelines in the industry – each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference. | 11/03/2023 |
| 1238 | Bristol-Myers Squibb Devens , MA Manufacturing Associate II, Cell Therapy (12-hour shifts) Bachelors in relevant science or engineering discipline. Exp: 1+ years |
BMS Cell Therapy Manufacturing seeks an Associate II within Manufacturing that brings enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are searching for enthusiastic, and innovative individuals with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. | 11/03/2023 |
| 1239 | Bristol-Myers Squibb Devens , MA Bioprocess Associate (Night Shift) B.S., in science, engineering, biochemistry or related discipline, or its equivalent is desired but not required. Exp: 1+ years |
The Bioprocess Associate assists in the execution of commercial manufacturing processes according to established electronic work instructions and production records for the manufacture of therapeutic proteins in accordance with current Good Manufacturing Practices (cGMPs). *This is a rotating night shift position (5pm-5am), therefore eligible for a 20% shift differential. | 11/03/2023 |
| 1240 | Advanced Cell Diagnostics Minneapolis, MN Research Associate Bachelor’s degree. Exp: 0-2 years |
We are seeking an Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/23/2023 |
| 1241 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate Master’s degree in a related field. Exp: up to 2 years |
We are seeking an Advanced Research Associate for Bio-Techne’s Protein Purification department in Minneapolis. Our group supports 5000 different protein products used in academic research, pharmaceutical research, and all facets of biological science including: neurodegenerative diseases, stem cell research, glycobiology, developmental biology, etc. This individual will collaborate with many different departments to support the manufacturing processes of our products and contribute to the ongoing development of our growing and evolving portfolio. This position provides a potential for growth and career advancements within the company. This is a fantastic opportunity for an individual to gain problem solving and troubleshooting experience in a collaborative lab environment. This position also provides continuous learning and development, flexible working hours, and the ability to learn and apply a variety of lab techniques every day. | 10/23/2023 |
| 1242 | Advanced Cell Diagnostics Minneapolis, MN RA - Advanced Research Associate Master’s degree. Exp: 1+ years |
Position Summary In this role, you would be responsible for the development and execution of QC test method validations for a variety of products, utilizing a wide variety of laboratory techniques. This position also assists in troubleshooting investigations and process improvement projects. As an Advanced Research Associate, you will also participate in cross-functional teams focused on new product introduction. | 10/23/2023 |
| 1243 | Advanced Cell Diagnostics Minneapolis, MN RA - Research Associate Bachelor’s degree in a related field. Exp: up to 3 years |
Position Summary: This position is responsible for participating in the development of Bio-Techne's various product lines. You will follow standard operating procedures to manufacture these products and will contribute to the ongoing development of new and existing products to help advance Bio-Techne's evolving portfolio. | 10/23/2023 |
| 1244 | Advanced Cell Diagnostics Minneapolis, MN Advanced Research Associate, Mammalian Cell Culture Bachelor’s degree in a biological science. Exp: 0 to 2 years |
POSITION SUMMARY This position is responsible for performing small scale cell culture to produce GMP and non-GMP recombinant proteins for growth in various types of bioreactor systems, reviewing previous batch records to optimize growth conditions for recombinant protein production, media and supplement preparation, and additional duties as assigned. This position requires a Sunday through Thursday workweek. | 10/23/2023 |
| 1245 | Advanced Cell Diagnostics Minneapolis, MN Research Associate - Protein Purification Development Bachelor’s degree in Biology or related field. Exp: up to 5 years |
Position Summary: We seek a highly motivated and creative individual to join our protein purification development team. Our team is responsible for the development of Bio-Techne's various product lines, with a focus on the high-quality recombinant protein products. You will participate in the development and optimization of protein purification procedures for recombinant proteins expressed in various cell lines (E. coli, baculovirus, and mammalian). In addition, you will also assist with initial, small-scale production for release of newly developed proteins and redevelopment of existing products to help advance Bio-Techne's evolving portfolio. This is a great opportunity to gain experience with cutting-edge biotech development/manufacturing processes & practices while working in a collaborative laboratory environment. | 10/23/2023 |
| 1246 | Advanced Cell Diagnostics Minneapolis, MN Research Associate, Analytical QC B.S. degree in Biochemistry, Chemistry, Biology, or a related field. Exp: 0 - 2 years |
Position Summary: As the Research Associate, Analytical Quality Control Analyst you will perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include concentration determination, SDS-PAGE with densitometry, endotoxin assay, PCR, HABA, conductivity, total organic carbon and other testing as assigned. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis, and communication of results within the department and across different groups. Other duties include instrument calibration and maintenance, record keeping, and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity, and team building across the QC Department or the entire company. Perform additional duties as assigned. | 10/23/2023 |
| 1247 | Akouos Boston, MA Engineer, Downstream Process Development - Akouos M.S in Biochemistry, Chemical Engineering, Bioengineering or related discipline. Exp: 1+ years |
The Process Development group at Akouos is seeking an innovative Engineer to provide hands-on development support for the manufacturing of AAV-based gene therapy vectors. The ideal candidate for this position is an entry level Engineer with a background in AAV vector purification technologies and gene therapy downstream process development. The successful candidate will actively participate in downstream process development, scale-up, process optimization, and process tech transfer for GMP manufacturing. The successful candidate will thrive in a collaborative, scientifically stimulating, and fast-pace work environment. | 10/25/2023 |
| 1248 | Akouos Indianapolis, IN Chemist- Nucleic Acid Synthesis Bachelor's and/or Master's degree Exp: 1+ years |
The Lilly Genetic Medicines Team is looking for collaborative creative and energetic problem solvers to join a multidisciplinary team at the front edge of innovation. You will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to complement and enable core capabilities and help drive the revelation and development of RNA-based clinical candidates. Do you have an aptitude for innovative approaches and modalities in discovery and development focused on identifying impactful therapies for the patient? We want you on our team! | 10/25/2023 |
| 1249 | Akouos Branchburg, NJ Engineer - Technical Services/Manufacturing Science BS degree in Chemistry, Microbiology, Biochemistry or related science, or BS in Chemical Engineering or related engineering discipline. Exp: 0-3 years |
This position is responsible for the technical support of manufacturing operations. This position will interact with the engineering, manufacturing, validation, quality assurance, quality control and regulatory departments. Interaction may be required with other Lilly site / contract producers of Lilly products. Knowledge of cell culture, purification and support systems used in the manufacturing of biotech products is required. Spreadsheet experience is required. Database experience a plus. | 10/25/2023 |
| 1250 | Alexion Pharmaceuticals Cambridge, MA Associate Scientist Masters Degree Exp: 1-2 years |
The Genomic Medicine group at Alexion Pharmaceuticals, AstraZeneca Rare Disease, has an outstanding opportunity for an Associate/Senior Associate position within the Genomic Medicine Group. We seek a highly motivated, curious, and detail-oriented individual with strong technical and problem-solving skills that would like to join our Rare Neurological and Rare Neuromuscular disorders team. The candidate will contribute to data generation, collaborate in discovering high-quality drug candidates, and will help build data packages to advance programs to IND. | 10/25/2023 |
| 1251 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist, Biology Master’s degree in Biology Exp: 1-2 years |
We are seeking a dedicated and innovative Senior Associate Scientist or Scientistto join our Genomic Medicine group at Alexion, AstraZeneca Rare Disease. The successful candidate will be a key member of the Alexion Genomic Medicine Cardiology team. The group’s mission is to discover and deliver transformational genomic medicines to patients with rare genetic cardiomyopathies. We are looking for a candidate with a background in cellular and molecular biology. In this role, you will be mainly responsible for developing and implementing a range of molecular and functional assays to assess the disease process, discover new medicines, and evaluate their therapeutic potential using human induced pluripotent stem cell derived cardiomyocytes (HiPSC-CMs). Additionally, you will be part of cross-functional teams and state of the art technology cores, and your scientific contributions will help advance Alexion’s preclinical programs to the clinic. | 10/25/2023 |
| 1252 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist, Biology Master’s degree in Biology Exp: 0-2 years |
We are seeking a dedicated and innovative Senior Associate Scientist to join our Genomic Medicine group at Alexion, AstraZeneca Rare Disease. The successful candidate will be a key member of the Alexion Genomic Medicine Cardiology team. The group’s mission is to discover and deliver transformational genomic medicines to patients with rare genetic cardiomyopathies. We are looking for a candidate with a background in molecular biology and experience with mammalian cell culture. In this role, you will be responsible for developing and performing molecular and immunoassays in samples collected from cells or mammalian in vivo models. With the support of cross-functional teams and state of the art technology cores, your scientific contributions will help advance our preclinical programs to the clinic. | 10/25/2023 |
| 1253 | Alexion Pharmaceuticals Cambridge, MA Senior Associate Scientist Master's Degree in cell biology and/or disease biology, pharmacology. Exp: 1-2 years |
We are searching for a dedicated and innovative Senior Associate Scientist to enhance our genomic medicine within Alexion, AstraZeneca Rare Disease. The chosen candidate will assume a pivotal role as a valuable member of the Alexion Genomic Medicine Cardiology team. Our mission revolves around pioneering genomic treatments for patients facing rare genetic cardiomyopathies. We are particularly interested in applicants with a robust background in pharmacology and disease biology. In this position, you wil |