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6027 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
| Job Information | Description | Date Added | |
| 1 | Foundation Medicine Cambridge, MA Pathology Research Assistant BS/BA in biology or biochemistry Exp: 0-2 years |
This is a great opportunity for a dedicated, recent graduate looking to gain more experience in molecular genetics as well as the broader functionality of a genomics laboratory committed to advancing the field of precision medicine. As you prepare for the next steps in your career, you will work directly with the pathology team and will assume the following duties: Participate in research projects, led by either the pathologist or yourself, focusing on various aspects of cancer genomics and immunohistochemistry through data gathering, data analysis, figure creation and writing manuscripts. Participate in projects, led by either the pathologist or yourself, focusing on quality improvement/quality assurance of laboratory operations and workflow through team collaboration with data gathering, data analysis, generation of metrics, internal presentations and/or manuscript synthesis and submission. | 2/5/2019 |
| 2 | Gene Dx Gaithersburg, MD DNA Sequencing Lab Technician BS/BA in biology or biochemistry Exp: 0-2 years |
This position is for an entry level DNA technician position in our laboratory. The job involves following basic protocols for PCR, gel electrophoresis, and Sanger sequencing. The Technician will be trained to use the various robots and instruments used to automate our PCR and sequencing workflows. At times technicians will be working as part of a team but would also be responsible for a good amount of individual work. Our work is clinical in nature and is repetitive, so this position absolutely requires someone who is very focused, meticulous, and willing to see that there are small things to learn every day. Implement the standard operating procedures for specimen handling and processing, test analysis, reporting of results to team leads, supervisors and test managers, and record-keeping | 2/5/2019 |
| 3 | Hikma Columbus, OH Scientist I, QC Aero Star 2nd Shift BS in chemistry or related Exp: 1+ years lab experience |
To perform routine, work-flow processes within the quality control laboratory to meet customer requirements by supporting the testing of raw materials and finished products while ensuring regulatory compliance standards and release times are met. | 2/8/2019 |
| 4 | Dexcom Mesa, AZ Quality Inspector 1 HS diploma/GED Exp: 6 months QC inspector experience |
The incumbent is responsible for performing a variety of quality control (QC) related work functions that include performing visual, functional and dimensional inspection and testing of raw materials, component piece parts, in-process materials, and review of lot history records in accordance with documented specifications and/or procedures. Prepares accurate documentation of QC inspection results including accepted and non-conforming materials. Scanning and archiving of Receiving Inspection Reports for the department. | 1/30/2019 |
| 5 | MilliporeSigma St. Louis, MO Associate scientist BS/BA degree in chemistry, chemical engineering or related life science. Exp: 6+ months lab experience |
Perform Quality Control activities in support of GMP products, including routine testing and peer review of raw materials, intermediate and final products, and stability samples. Essential job functions include ensuring quality through adherence to GMP requirements. Assure adequately trained to perform tasks/assignments. Perform routine assays in accordance to applicable GMP requirements, processes and/or unit operations. Clean-up equipment and working areas during and after operations. Provide complete and accurate records consistent with quality guidelines and GDP requirements. | 1/31/2019 |
| 6 | ERT Rochester, NY Associate Biostatistician MS in statistics Exp: 1+ years |
Essential duties/responsibilities as an associate biostatistician include: Develop SAS and R programs for statistical analysis in conjunction with the Senior Biostatistician. Test, maintain, and execute SAS and R programs to perform statistical analysis including central tendency analysis, categorical analysis, and concentration-QTc analysis for data from both TQT studies and early clinical studies, in close consultation with the Senior Biostatistician. Prepare tables, figures, and listings for statistical analysis as outlined in the statistical analysis plan. Assist in post-processing data activities including data QC, completing IIRV reports, and cardiologist consistency checks. | 2/1/2019 |
| 7 | Eurofins West Point, PA Upstream Process Development Spectrophotometry Scientist BS or MS in chemsitry, biochemistry, chem engineering or related Exp: 0-2 years |
Upstream Process Development Spectrophotometry Scientist responsibilities include, but are not limited to, the following: In-line light scattering studies to support the tech transfer of sterile drug product processes between manufacturing sites. Develop lab based methods for the real time determination of formulation homogeneity during the filling process of The client’s alum adjuvant vaccine products Ready instrumentation for use in the field at manufacturing facilities Scope may include transfer of manufacturing processes from The client facilities to external third party manufacturing organizations, both domestic and international Work with engineering groups at the manufacturing facilities to ensure the instrumentation can be effectively coupled to the process equipmen | 2/1/2019 |
| 8 | Eurofins Bothell, WA Trace Metals Scientist BS/BA in science or chemistry Exp: 1 year analytical chemistry |
This position is an entry level analytical preparation position. The Associate Scientist performs a majority of sample preparation and light analysis of dietary supplement and environmental samples for trace metals determinations. The associate scientist interprets and manages data using LIMS, Access and Excel, ensuring that data meets all established QA/QC criteria and is made available to the Project Manager within specified time frames. | 2/1/2019 |
| 9 | Eurofins Durham, NC Sterility Microbiologist BS/BA in biology, chemistry, or related Exp: 1-3 years lab experience |
Microbiologist responsibilities include, but are not limited to, the following : Performs laboratory testing on a variety of product samples, including bulk vaccine, filled vaccine, and media. Will initially be assigned to support the microbiology testing laboratories. o The emphasis is on microbiological methods, such as sterility, bacteriostasis/fungistasis, Neomycin potency, Mycoplasma, and Mycobacteria. o Cell culture propagation and maintenance procedures, and/or microbiological laboratory procedures o Authors standard operating procedures (SOPs) for the performance of laboratory methods | 2/1/2019 |
| 10 | Celegene Bothell, WA Manufacturing Associate I BS in science or engineering Exp: 0-2 years in cGMP manufacturing |
The primary focus of the role will be cellular therapeutic manufacturing at JuMP during process transfers, routine production, and technology improvements. The key deliverables for this role are (1) helping to establish the JuMP manufacturing operations and (2) completing production assignments with a high quality and timely output. | 1/22/2019 |
| 11 | Celegene Warren, NJ Associate Bioengineer II BS or MS in biochemical, chemical, or biomedical engineering or cell biology Exp: BS: 1-3 years, MS: 0-2 years |
With minimal supervision, design and execute/implement characterization experiments of moderate complexity Critically analyze and interpret data using statistical methods. Apply fundamental scientific knowledge to projects and problems in a positive manner. Perform data analysis and summarize experimental results Interact with Process Development and Analytical Development teams to advance projects Author technical documents for interdepartmental use. Organize, record and maintain experimental data Convey data analysis and interpretation to supervisor and colleagues with clarity and high level of accuracy. Ensure proper operation and perform routine maintenance of all laboratory equipment Assist other staff to complete all laboratory tasks as necessary Maintain a safe workplace in accordance with company and OSHA policies/procedures | 1/22/2019 |
| 12 | Celldex Needham, MA Associate Scientist BS in biological sciences Exp: 1-3 years mammalian cell culture |
The Associate Scientist is part of a team working to develop mammalian cell culture (CHO) for the manufacture of recombinant proteins (transient and stable expression). The Associate Scientist will be responsible for maintaining mammalian cell lines for the production of research and pre-clinical products and ensuring scale-up to pilot plant manufacturing under cGMP. | 1/22/2019 |
| 13 | Cellectis New York, NY Research Associate, Immuno-Oncology BS/MS in biology or related Exp: 1+ years lab experience |
Cellectis is seeking a highly self-motivated Research Associate to join its Immuno-Oncology (IO) group focused in the development of innovative cellular therapies for cancer treatment. Ideal candidates are self-driven, dynamic, and preferably skilled in the following techniques: cell culture (cell lines and primary cultures), cell-based and immunological assays (cytotoxicity, ELISA, Antigen-dependent proliferation), lentiviral transduction, multicolor flow cytometry. Candidates must be able to keep detailed documentation of daily experiments and should be able to perform data analysis with minimal supervision. The successful candidate should be able to excel in a fast-moving, goal-oriented environment aiming to make a change in immunotherapy. | 1/22/2019 |
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| 16 | Clinipace Morrisville, NC Pharmacovigilance Specalist BS in life science, nursing/pharmacy Exp: 1-2 years |
The Pharmacovigilance Specialist (PVS) primary responsibility is SAE case management. This includes but is not limited to: initial case disposition, confirmation of case disposition with Medical Monitor (MM)/Safety Physician PV (SP PV), MM, receipt of adverse event data, data entry, source document data extraction, draft narrative development, follow-up management and reporting according to regulatory requirements. All activities will be in accordance with Clinipace and/or client SOPs, ICH Guidelines and local regulatory requirements. | 1/23/2019 |
| 17 | Coda South San Francisco, CA Research Associate, Neurobiology BS in neuroscience, or biological sciences Exp: 1-2 years research experience |
We are looking for a highly motivated and dynamic candidate for the role of Research Associate, Cell Biology / Electrophysiology. This individual will work under the guidance of a scientist to support characterization of our engineered ligand-gated ion channels using electrophysiology assays in the lab. The ideal candidate is open-minded, trainable, and enthusiastic about research. Responsibilities include cell culture, solution preparation, data analysis and presentation, and general lab maintience | 1/23/2019 |
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Cogent Professionals is searching for two (2) organic synthesis chemists for one of our Indianapolis, IN area pharmaceutical laboratories. Responsibilities include the ability to prepare multi-step organic syntheses reactions, bench chemistry, documentation, and ability to maintain high level of productivity in lab settings. | 1/23/2019 |
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Under the direction of the Senior Manufacturing Quality Engineer, the Manufacturing Quality Engineer I will be assigned product accounts and be responsible for collaborating with Program Managers, Manufacturing Engineers and other departments to analyze customer ECO’s and ensure effective implementation to the production floor through proper use of the Cogmedix ECO process. As part of the ECO Process and new proposal review, support the management of the customer BOM structure, creation of part numbers and structuring of Supplier Relationships and costs. Define PP/PA/Phantom, Commodity codes, documentation packages commodity and Work Instruction evaluation. Promptly respond to manufacturing floor issues, taking appropriate action within the Cogmedix Quality System and continually building strong rapport with customers and suppliers. Generate process validation/qualification documentation (e.g., validation protocols, IQ/OQ/PQ) and implement protocols and completion of reports. | 1/23/2019 |
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| 24 | Conmed Utica, NY Quality Assurance Lab Technician I AAS in science Exp: 0-3 years in lab |
Decontaminate and evaluate returned Customer Complain Products by performing visual, functional, electrical, mechanical, and chemical testing, when appropriate. Provide evaluation results/reports for complaint files per procedural requirements. | 1/24/2019 |
| 25 | Conmed Largo, FL Manufacturing Engineer I BS in engineering or equivalent Exp: 1-3 years in manufacturing environment |
Under supervision perform a variety of engineering work in planning and design of tools, equipment, machinery, processes, etc. and oversee the installation, operation, maintenance of such equipment, etc. Implement changes, alterations, modifications and repair based on engineering project requests, etc. Perform process validations and qualify vendors, suppliers, components, etc. | 1/24/2019 |
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| 27 | Myriad RBM Austin, TX RBM Research Associate (manufacturing) BS or AS Exp: 0-5 years |
Myriad RBM is looking for a self-motivated individual to fill a Research Associate-Manufacturing position in our Austin facility. In this position you will be responsible for planning, performing, and evaluating the process of manufacturing reagents and propose experiments within a project(s) to provide valid and needed information. Conduct assigned experiments and assists in their designs. Manufacture reagents required for the testing of samples, including but not limited to coupling of antibody to beads, biotinylation of antibody for detection, testing of minipool and simplex reagents, batching and qualification of new lots of batched reagents, and troubleshooting problematic reagents. | 1/24/2019 |
| 28 | Covance Wilmington, NC Contracts Specalist I Bachelors or university-level law degree (UK/EU) Exp: 0-2 years |
Perform the following, with occasional guidance from line management or more experienced colleagues: daily tracking, negotiation and approval of Site Agreements and Site Agreement templates (as applicable) for clinical study teams; timely updating of the departmental Site Agreement Management System (“SAMS”) or any other system required for use on a particular study. Manage assigned studies with careful compliance with internal processes and procedures, or otherwise according to specified Sponsor requirements. Performs contract administration functions including: assisting with obtaining approvals on authorization forms as required; maintaining a contract tracking system to report contract status updates and signing status; providing notice of all executed contracts to the appropriate team members along with contract values; and scanning and filing executed contracts in the shared electronic storage area in a timely manner for access by other staff members. | 1/24/2019 |
| 29 | Covance Leeds, Un Project Coordinator I (Project Management Academy) University/college degree related to health profession/sciences Exp: 0 years |
Project expertise for CTMS reporting, study metrics, risk management regarding communication, coordination, and eTMF quality. Able to co-ordinate and manage support across large global study. Applies therapeutic knowledge to daily activities of the clinical trial, brings new knowledge to the team, drives best practices in coordination, communication and documentation. Primary responsibility for the coordination and completion of all administrative functions in support of the project manager. | 1/24/2019 |
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| 31 | CryoLife Kennesaw, GA Quality Assurance Speacialist I BS in life sciences or related Exp: 1+ years preferred |
Establish and maintain Quality Systems that comply with regulations and standards. Review all records associated with the production of medical device products. Reduce waste and variability in processes. Ensure that all areas identified as “Principal Responsibilities” are accomplished in an efficient and professional manner. | 1/25/2019 |
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We are seeking a qualified individual to join us as a Validation Engineer at our Menlo Park facility. This position will support and coordinate Validation activities which may include manufacturing equipment, utility systems, facilities, laboratory instruments, and software within the company's GMP facility. Job responsibilities include the following: Perform commissioning, qualification, and validation activities for facility, utility, equipment, and software; including developing project plans, preparing protocols, addressing discrepancies, and developing technical reports, Author and execute IQ, OQ, and PQ qualifications and summary reports, Develop and/or participate in generating validation lifecycle documentations, such as impact assessments, URS, FS, TM, etc. Work with Quality, Operations, Manufacturing and Quality Control to establish, develop, communicate, and maintain all GMP equipment in validated state; this includes but is not limited to manufacturing equipment, facilities, computer systems, and laboratory instrumentation. | 1/25/2019 |
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The Clinical Research Associate will perform all types of site visits including Site Selection, Initiation, Monitoring, and Close-out, as well as drug accountability and other monitor activities to assure adherence to Good Clinical Practices (ICH GCP), SOPs, and study protocols. As the Clinical Research Associate you will ensure selected study sites have adequate qualification resources and facilities/equipment, have provided eligible subjects and qualified investigators. | 1/17/2019 |
| 34 | Biotechne Centennial, CO SRM/Content Management Associate BS in biological sciences Exp: 0 years |
The Content Management Associate will manage scientific product data displayed on the Novusbio.com website. (S)he will help to create content that effectively markets scientific products on Novusbio.com. (S)he must have a basic back ground in science as well as being technically savvy in Excel. The Content Management Associate must be able to communicate with all areas of the company including Marketing, IT, Customer and Technical Service. | 1/17/2019 |
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Individual will use lentiviral vectors to genetically modify freshly isolated T lymphocytes, expand modified T cell cultures, and characterize cultures using standard immunological assays including flow cytometry. Data from experiments will be compiled and presented to functional teams, and used to inform future experiment/project design. | 1/18/2019 |
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bluebird bio’s Oncology Discovery Team is looking to add an Associate Scientist to its Research and Discovery group. This group identifies and develops novel strategies that enhance anti-tumor T cell activity through synthetic biology and genetic engineering. This new position will serve a critical function by providing laboratory level support to project leads with a focus on cellular and molecular immunology. As a team member, the successful candidate will use their proficiency in several immunological techniques (e.g. FACS, ELISA, western blot, qPCR, etc.) to help drive exploratory science, make recommendations on next steps and facilitate the transition to drug product. | 1/18/2019 |
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We are seeking a Process Development Associate to contribute to our newly created Process Development group in Berkeley. The ideal candidate will participate in the Process Development efforts and interact closely with functional group leaders, scientists and research associates to transfer the technology from discovery to pre-clinical development. This hands-on role will involve design and execution of the experiments for process development, optimization, scale-up, and tech transfer, and will help manage the technology transfer to a CMO/CRO. | 1/19/2019 |
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We are seeking a Research Associate to join our Immune Cell Engineering team in Berkeley. The ideal candidate will interact closely with functional group leaders, scientists and research associates to drive discovery and development of new therapeutics in pre-clinical development. Responsibilities include mammalian cell culturing, immune cell biology based assay development and implementation, and coordinating experiments with other researchers | 1/19/2019 |
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| 44 | Bausch Health Bothell, WA Electrical Engineer I, Energy-Based BS in EE required Exp: 1-2 years |
The successful candidate will implement conceptual/product designs for performance, innovation, reliability, and cost. S/He will not only conceptualize solutions, but follow through with detailed design supervision, prototyping, testing, supplier management, and documentation. S/He should have strong written and verbal communication skills and openness to working in a team environment. Specifically, to assist the Energy-Based Devices department in the R&D of current/future devices, which are based on electromagnetic and mechanical energy (i.e. RF, Optical, Lasers, and Ultrasound). | 1/8/2019 |
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| 47 | Berg Framingham, MA Lab Operations Specialist I – Precision Medicine AS or BS in Project management or life sciences Exp: 0-2 years |
Reporting to the Chief Precision Medicine Officer, the entry level Laboratory Operations Specialist will process laboratory specimens (aliquoting and accessioning) along with maintain operational activities within the precision group. Process laboratory specimens, including transporting specimens within the lab, centrifugation and aliquoting and labeling specimens. Identify problems with specimen types, missing information, etc. | 1/12/2019 |
| 48 | Berg Framingham, MA Research Associate I – Functional Lipidomics BS in chemistry, biochemistry or related Exp: 0-2 years |
BERG is seeking a highly motivated individual to join our “Omics” group, reporting to the Chief Precision Medicine Officer. The candidate will join a team responsible for biomarker discovery/validation in multiple disease areas, including neurodegenerative diseases, diabetes, obesity, and cancer, using state-of-the-art quantitative lipidomics platforms. The successful candidate is a highly motivated individual with experience in lipid analysis, lipidomics, or small molecule analysis using LC-MS/MS platforms. | 1/12/2019 |
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| 52 | Alcami Charleston, SC Assistant Scientist I Analytical BS in science Exp: 0-2+ years |
The Assistant Scientist I Analytical is accountable for performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Assistant Scientist I may also be required to work on method development/method validation projects. Typical types of testing includes: assays (potencies, related substances, residual solvents, metals, etc.), rate of release (dissolution), moisture content, identification and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, AA and IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by the company). The role will work on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors. | 1/2/2019 |
| 53 | Allcells Alameda, CA Quality Control Specialist I/II BS in science or technology Exp: 1+ years |
The QC Specialist is responsible for supporting the release of commercial products. Their primary responsibility is to perform routine in-process and final product flow cytometry analysis, CD34+ enumeration (ISHAGE) and immunophenotyping of raw tissue lots in accordance with required release timelines while ensuring compliance with internal procedures and specifications. | 1/2/2019 |
| 54 | Amgen Thousand Oaks, CA Engineer – Technical Investigator MS Exp: 0 years |
The Engineer – Technical Investigator will support technical investigations of Level 2 and 3 complaints associated with product design and / or usability issues, and support trend and consolidated investigations using data analytics. S/he performs root cause analysis to identify the failure mode for mechanical and/or electromechanical medical devices and associated product components such as packaging, returned due to product complaint using root cause analysis tools and processes. Additional equipment such as CT scanners, FTIR material analysis and Instron tensile test machines may be used. S/he supports trend investigations through the review of manufacturing batch records, evaluation of returned product, product reserve sample inspections, and review of complaint histories and trends. Upon completion of these activities, s/he will support authoring final reports in accordance with established procedures, which may include data collection and statistical analysis of the data. S/he will own CAPA’s in support of identifying design solutions based on root cause and will also support cross functional ideation of design solutions. The Engineer – Technical Investigator maintains close interaction with the engineering and quality functions to contribute to product improvement. | 1/3/2019 |
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| 56 | Amicus Philadelphia, PA Associate Scientist, Bio-Reagent Development - Gene Therapy BS or MS Exp: BS: 2+ years of wet lab experience, MS: 0-2 years of wet lab experience |
This position will be responsible for the expression and purification of enzymes and antibodies required as bio-reagents for the evaluation of gene therapy-based protein products. Duties include collaboration with Therapeutic Target Leads to identify required Bio-reagents, collaboration with Molecular Biology Core and Protein Expression Analysis teams for required DNA constructs, expression and purification of bio-reagents, sceening of commercial antibodies against targets of interest, selection of target epitopes for antibody production, tracking progress of multiple bio-reagent projects and prioritization of parallel projects to ensure timely delivery, and analysis and presentation of results to larger scientific group This position will be responsible for the expression and purification of enzymes and antibodies required as bio-reagents for the evaluation of gene therapy-based protein products. Duties include collaboration with Therapeutic Target Leads to identify required Bio-reagents, collaboration with Molecular Biology Core and Protein Expression Analysis teams for required DNA constructs, expression and purification of bio-reagents, sceening of commercial antibodies against targets of interest, selection of target epitopes for antibody production, tracking progress of multiple bio-reagent projects and prioritization of parallel projects to ensure timely delivery, and analysis and presentation of results to larger scientific group This position will be responsible for the expression and purification of enzymes and antibodies required as bio-reagents for the evaluation of gene therapy-based protein products. Duties include collaboration with Therapeutic Target Leads to identify required Bio-reagents, collaboration with Molecular Biology Core and Protein Expression Analysis teams for required DNA constructs, expression and purification of bio-reagents, sceening of commercial antibodies against targets of interest, selection of target epitopes for antibody production, tracking progress of multiple bio-reagent projects and prioritization of parallel projects to ensure timely delivery, and analysis and presentation of results to larger scientific group | 1/3/2019 |
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| 58 | Antech Diagnostics Portland , OR Specimen Processor HS diploma required, 2-4 year degree preferred Exp: 1+ years of experience |
The Specimen Processor receives and prepares samples for laboratory analyses and tests. Prepares samples on slides or other testing format, records required information and sends to appropriate specialty lab area. Duties will include: Receives and prepares samples for laboratory analyses and tests to diagnose various pet and other animal illnesses, injuries and diseases in support of veterinarian animal treatment. Assists other lab personnel with specimen storage and ensures Turn Around Times (TAT's) are met. | 1/4/2019 |
| 59 | Antech Diagnostics Ottawa, Ca Laboratory Generalist AS/BS in science or veterinary technician Exp: 1 year clinical lab experience |
As a Laboratory Generalist you will perform laboratory testing that helps veterinarians diagnose and treat pets across the United States. You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: Hematology, urinalysis, chemistry/endocrinology | 1/4/2019 |
| 60 | Antech Diagnostics Mississauga, Ca Laboratory Generalist AS/BS in science or veterinary technician Exp: 1 year clinical lab experience |
As a Laboratory Generalist you will perform laboratory testing that helps veterinarians diagnose and treat pets across the United States. You will be using automated analyzers, microscopes and other laboratory diagnostic tools to perform analyses and tests that diagnose animal illnesses, injuries and diseases in support of veterinarian animal treatment. You will be responsible for setting up and running lab tests, and reading and releasing results according to SOPs (Standard Operating Procedures). You can expect to specialize in one or more of the following areas: Hematology, urinalysis, chemistry/endocrinology | 1/4/2019 |
| 61 | Antech Diagnostics Fountain Valley, CA Lead Laboratory Technician BS Exp: 1-2 years in clinical or production lab |
The Lead Laboratory Tech you will support the Serology work flow providing guidance and training, and jumping on the bench to ensure quality work is completed on time. The Lead Technician will assist in leading the team through the shift while encouraging an atmosphere of teamwork, integrity, and respect. | 1/4/2019 |
| 62 | Applied Medical Rancho Santa Margarita, CA Specialist I,II/Engineer I,II BS in Engineering, Physical ,or Biological Sciences Exp: 1+ years in medical industry |
As a Specialist I/II or Engineer I/II on the Regulatory Affairs(RA)/Quality Systems(QS) Team, you will be responsible for working within the framework of a team and performing the following activities: Monitor and ensure conformance through the understanding of standards and regulations, Manage projects to maintain and improve the quality system by establishing or updating procedures, Participate in internal and external audits, Interprets existing and emerging regulations, standards and guidance documents, Act as a liaison to internal and external customers, and Identify and implement systems within RA/QS. | 1/4/2019 |
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| 67 | Siemens East Walpole, MA Laboratory Technician - Reagent Mfg Antibody/ Purification Lab BS Exp: 0 |
This position in the Walpole Conjugate Manufacturing Organization is responsible for the manufacture of immunoassay components used in ADVIA Centaur systems diagnostic products. | 1/7/2019 |
| 68 | Siemens Tarrytown, NY Biochemist 1 BS Exp: 0-2 yrs |
Participate in research, experimentation, and analysis for product and process development of immunoassays by following standard operating procedures and/or protocols. Requires experience in preparing electronically generated documents necessary to summarize semi-complex technical data. This position involves handling potentially bio hazardous materials from human and animal sources. | 1/7/2019 |
| 69 | Abbott PLEASANTON, CA MANUFACTURING ENGINEER I BS Exp: 1-2 years |
At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 99,000 of us are working to help people live not just longer, but better, in the more than 150 countries we serve. | 1/7/2019 |
| 70 | SUN PHARMA Princeton, NJ Regulatory Associate BS Exp: 1-2 years |
This is an immediate opening (for temporary position, possible extension) at Sun Pharma, Princeton, NJ location as a Regulatory Affairs Associate. Work closely with Regulatory Affairs Manager and Regulatory Affairs Associates to ensure the compliance and completion of assigned activities and provide regulatory strategic input and compliance with FDA regulations, guidance, and applicable industry guidelines to internal and external stakeholders, and ensure the implementation. | 1/7/2019 |
| 71 | Sutro Biopharma, Inc. South San Francisco, CA Research Associate, Protein Expression, Conjugation & Analytics BS/MS Exp: 1-3+ years |
Sutro Biopharma, Inc. is looking for an energetic and talented individual to join the multidisciplinary Protein Biochemistry group within the Research Department. You will be working to understand and improve the performance of our core technologies including in vitro biochemical protein synthesis, site specific antibody drug conjugation by designing and executing experiments on transcription, translation, protein folding, conjugation and analysis. You will participate in cross-functional teams to perform multiple projects. Responsibilities extend from protein expression, protein-small molecules conjugation, protein-protein conjugation and characterization. The successful candidate will design and validate protein expression and conjugation methods appropriate to the scale, number-of-samples, and required purity level for the given project, and will implement appropriate assays to characterize products and to better understand the technology and process.Sutro Biopharma, Inc. is looking for an energetic and talented individual to join the multidisciplinary Protein Biochemistry group within the Research Department. You will be working to understand and improve the performance of our core technologies including in vitro biochemical protein synthesis, site specific antibody drug conjugation by designing and executing experiments on transcription, translation, protein folding, conjugation and analysis. You will participate in cross-functional teams to perform multiple projects. Responsibilities extend from protein expression, protein-small molecules conjugation, protein-protein conjugation and characterization. The successful candidate will design and validate protein expression and conjugation methods appropriate to the scale, number-of-samples, and required purity level for the given project, and will implement appropriate assays to characterize products and to better understand the technology and process. | 1/7/2019 |
| 72 | Hikma Cherry Hill, NJ Quality Lab Associate I - Micro BS/BA Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. | 1/8/2019 |
| 73 | Hikma Cherry Hill, NJ Chemical Process Operator I BS Exp: 1 yr |
Using company procedures and guidelines, the Chemical Process Operator I is responsible for a limited spectrum of duties within the department. This may include but is not restricted to: weighing, mixing, equipment cleaning, tank cleaning, tank movement and PM activities, etc. | 1/8/2019 |
| 74 | Adaptive Biotechnologies Seattle, WA Research Associate I BS in biology, molecular biology, immunology, etc Exp: 1-5 |
A Research Assocaite I will be working with other researchers and computational biologists to develop/optimize PCR-based assays for transition into service lab and/or kits. Responsible for next-gen DNA sequencing library preparation and loading, reviewing and analyzing data, and execution of detailed experimental plans. | 12/19/2018 |
| 75 | Adaptive Biotechnologies Seattle, WA Research Assistant BS in biological science Exp: ~1 |
As a Research Assistant, you will perform regular upkeep and lab maintence, properly stock lab with necessary consumables, prepare and track aliquots of reagents, perform DNA extractions, PCR/ddPCR/qPCR experiments, and work with others including the environmental health and safty officer in biological and chemical safety. | 12/19/2018 |
| 76 | Adaptive Biotechnologies Seattle, WA Production Associate II (Sun-Thu, 8am-5pm) BS in Medical Technology or Chemical/Physical/Biological Sciences Exp: 1-2 |
The Production Associate II position will be responsible for processing client samples using high throughput DNA sequencing technology. This role will work within a team of other Laboratory Technicians in a fast-paced, high production setting to process research and clinical diagnostic samples. | 12/19/2018 |
| 77 | ADMA Biologics Boca Raton, FL Quality Assurance Specialist I AS minimum, BS prefered Exp: 1-3 |
As a QA Specialist I you will perform a wide variety of QA activities to ensure compliance with regulatory requirements and provide support to manufacturing and QC. Additional responsibilities include revewing cGMP documents, and conducting investigations related to manufacutred products and intermediate lot releases. | 12/19/2018 |
| 78 | Bio-Techne Flowery Branch, GA Manufacturing Technician Min. 2-year technical degree plus 1 year experience, or equivalent combo of education/experience Exp: ~1 |
In this position you will primarily be responsible for manufacture of cell culture products in a controlled environment using aseptic technique, media preperation, equipment inspection, and steam-sterilization. Other responsibilities include maintaining parts and equipment, maintaining supply stock, and cleaning of the manufacturing area. | 12/19/2018 |
| 79 | Bio-Techne Newark, CA Associate Scientist BS or MS in molecular biology, biochemistry, cell biology Exp: 1+ |
Individual will perform various RNAscope-based assays to support new product development and optimization, clinical assay development and validation, and provide customer service. As a Associate Scientist, you will be expected to design and conduct experiments independently, and to record, analyze, and present results to senior staff. | 12/19/2018 |
| 80 | Bio-Techne Minneapolis, MN Research Associate BS or MS Exp: BS: 0-5 years, MS: 02-years |
Responsibilities as a Research Associate include the application of molecular biology techniques to clone and express recombinant antibodies/proteins of interest, build and modify prokaryotic/eukaryotic expression vectors, and perform protein analysis and purification. Experience working with mammalian cell culture and DNA cloning are a plus but not required. | 12/19/2018 |
| 81 | AGC Biologics Bothell , WA Contract Development Associate AA or BS in life science or engineering Exp: 0-3 years |
This is an opportunity for a Contract Development Associate I to join the Upstream Process Development group. The primary responsibility of this position 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. | 12/21/2018 |
| 82 | Agios Pharmaceuticals Cambridge, MA Research Associate/Sr. Research Associate, Cell Metabolism BS or MS Exp: BS: Required 1+ years, MS: 0+ years |
Agios Pharmaceuticals is searching for a dynamic Research Associate/Sr. Research Associate to join our growing Cell Metabolism team. You will be responsible for the design and execution of metabolomics and targeted LCMS experiments to support drug discovery efforts in cancer metabolism, immuno-oncology, and rare genetic disorders. You will have the ability to work cross-functionally as a contribution member to project teams. This role will be primarily lab focused supporting multiple aspects of our pre-clinical pipeline | 12/21/2018 |
| 83 | Agios Pharmaceuticals Cambridge, MA Associate/Sr. Associate, Regulatory Information Management, RegOps BA or BS Exp: 1+ years in biotech/pharma |
Agios Pharmaceuticals is searching for a dynamic Associate/Sr. Associate Regulatory Information Management to be responsible for the maintenance, tracking and archive of Regulatory Information. The person in this role will also be responsible for maintaining and distributing reports to stakeholders to ensure compliance with Health Authority activities. The ideal candidate shall become proficient in a specialized regulatory information management (RIM) system which they will use for the majority of their work activities. | 12/21/2018 |
| 84 | Ajinomoto Bio-Pharma Services San Diego, CA Manufacturing QA Assistant BS in life sciences or equivalent strongly prefered Exp: 0-2 years |
he MQA Assistant ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. This individual has the ability to work independently, within prescribed guidelines, and as a team member. This position promotes a cGMP environment and follows SOP’s. Multiple positions avalible. | 12/21/2018 |
| 85 | Ajinomoto Bio-Pharma Services San Diego, CA Drug Product Manufacturing Assistant - Formulations BS in life sciences or equivalent strongly prefered Exp: 0-2 years |
The Drug Product Formulations Manufacturing Assistant is responsible for execution of routine production and manufacturing procedures to support processes and ensure compliance with regulatory requirements. The Manufacturing Assistant will work with the Drug Product team to ensure the successful completion of various cGMP activities. The Manufacturing Assistant will learn and demonstrate proficiency in both the technical aspects as well as the quality systems which govern cGMP manufacturing. Duties include visual inspection of tanks and bulk drug substances, preperation of media/buffers/solutions as needed, preparation of material to be sterilized, and accurate documentation of batch records. Multiple positions avalible. | 12/21/2018 |
| 86 | Pace Analytical Maplewood, MN Regulatory Data Specialist BS Exp: 0-1 yrs |
Candidate will work on regulatory documents related to health care regulations. This person will review documents, enter data, and convert documents to new formatting. Must have organizational skills, attention to detail, and an interest to be outside of the lab. Assist in document management of health care product labels and technical regulatory forms. Review and correct formatting within documents. Create templates for electronic filing conversions to new format - follow outline for headers, fonts, and other specifics. Bachelor's degree in a scientific field . 0-1 years of professional experience. Strong computer skills- Word, publishing. Attention to detail. Ability to multitask | 12/19/2018 |
| 87 | Pace Analytical Eagan, MN Chemical Technician Associates degree in applied science or related field required. Bachelor's degree in chemistry or biology preferred Exp: 0-2 yrs |
The main function of a chemical technician is to conduct chemical and physical laboratory tests to assist scientists in making qualitative and quantitative analyses of solids, liquids, and gaseous materials. Perform routine and quantitative and qualitative chemical analytical tests, using techniques such as chromatography, spectroscopy, physical and chemical separation techniques, and microscopy Perform routine calculations and determinations on tests and evaluating physical characteristics Perform product stability tests to evaluate color and other product attributes Use standard laboratory glassware and knowledge of general laboratory equipment Maintain, clean, and sterilize laboratory instruments and equipment Write technical reports or prepare graphs and charts to document experimental results Basic knowledge of chemical composition, structure and properties of substances and of the chemical processes and transformations that they undergo Strong attention to detail Excellent time management skills Knowledge of Microsoft Excel 7 | 12/19/2018 |
| 88 | Pace Analytical Port Allen, LA Quality Assurance Associate Associates Degree in Chemistry or related field. Bachelor's degree in Chemistry or other science preferred Exp: 0-6 months |
Responsibilities Promptly perform reports and records all Quality Control procedures and test results in a precise and accurate manner Applies Good Laboratory Practices to accurately record and file all raw test data, including pertinent paperwork Communicates results and dispositions to Prouction, QA and Supervisor as requires. Reports all problems regarding procedures, equipment, products, raw materials specifications etc to the QC Supervisor or designate, as well as other QC Chemists Maintains inventroy status of reagents and equipment in order to keep the lab at full operational capacity. Maintains a clean, safe and orderly work environment and assures smooth operation of the QA Laboratory by communication, planning and preparation in support of other shifts. Qualifications Associates Degree in Chemistry or related field. Bachelor's degree in Chemistry or other science preferred Experience working in a quality control setting at a chemical manufacturing facility a plus Up to 6 months of relevant work experience Basic computer skills Must have the ability to don a respirator Must be able to life and carry 50 pounbs Have the ability to bend, squat down and reach above your head Ability to climb stairs and ladders | 12/19/2018 |
| 89 | Pace Analytical Oakdale, MN Analytical Chemist I Four-year degree in Chemistry, Materials Science or Physics Exp: 0 yrs |
We are actively seeking candidates to support our Laboratory operations in our Oakdale, Minnesota Facility. The ideal candidate is one who will thrive working in a highly dynamic, team oriented environment; sharing the common goal of providing reliable data to our clients that can be used to improve the safety and effectiveness of materials produced and used in pharmaceutical and medical device products. Responsibilities Job Responsibilities: Perform routine laboratory activities in support of testing medical devices, pharmaceutical products and raw materials, utilizing appropriate instrumentation Support method transfer and validation activities within operational area with supervision and support from laboratory supervisors, principal staff, and/or senior staff Support the process of compiling, analyzing, interpreting, and documenting results Assist with laboratory investigations Participate in quality, cGMP, safety, method and technique training appropriate for their area Qualifications Requirements: Four-year degree in Chemistry, Materials Science or Physics; Previous laboratory work experience desirable Ability to adhere to Good Documentation Practices within a cGMP environment Keen attention to detail and adherence to Standard Operating Procedures Demonstrated ability to work independently Ideal candidate is self-guided, motivated, and possesses a strong sense of initiative Ability to excel in a fast-paced work environment Ability to multi-task and be flexible with changing priorities | 12/19/2018 |
| 90 | Pace Analytical Fort Dodge, IA Microbiology Lab Analyst BS in Microbiology or a related science Exp: 0-3 yrs |
The Microbiology Lab Analyst will support product development and continued product improvement by independently conducting experiments related to cell culture, bacteriology, and virology. Responsibilities Perform testing, including: Cell culture, both primary and continuous cell lines Viral/Bacterial Titrations Viral/Bacterial Re-isolations Serum neutralization assays Perform viral neutralization assays PCR, RT-PCR, Q-PCR Hemagglutination Assay Hemagglutination Inhibition Assay Immunofluorescences Assay Growth Kinetics Studies Optimization Studies ELISA Western Blot Embryonated egg work Schedule and perform maintenance of instruments/equipment Evaluate new laboratory equipment Contribute to troubleshooting activities Prepare SOPs/working procedures Perform data analysis and organization of data for use in reports, etc. Comply with quality systems and standards Use proper safety equipment and follow appropriate safety procedures Qualifications BS in Microbiology or a related science New graduates will be considered 0-3+ years of related lab experience Preferred: Emphasis in microbiology and aseptic techniques Experience working in a GMP lab setting | 12/19/2018 |
| 91 | Pace Analytical Greenfield, IN Lab Analyst - Formulation BS in Chemistry or a related science Exp: 0-3 yrs |
This candidate will perform testing using traditional laboratory techniques for proteins and enzymes. They will be supporting product development and continued product improvement. Responsibilities Perform basic lab testing, including: Conduct and/or Develop basic to advanced formulations Conduct optimization studies Conduct transfer studies Perform stability studies Contribute to troubleshooting activities Perform data analysis and organization of data for use in reports, excel, etc. Comply with quality systems and standards Use proper safety equipment and follow appropriate safety procedures Qualifications BS in Chemistry or a related science New graduates will be considered 0-3+ years of related lab experience | 12/19/2018 |
| 92 | PerkinElmer Austin, TX Associate Lab Technologist Associate or B.S. degree in Life Sciences Exp: 0-3 yrs |
The Associate Lab Technologist will perform standard operating procedures applying basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment, and record keeping necessary to manufacture and test Food and Feed Safety products. Follow detailed instructions for assigned tasks or project with direct supervision. Core Duties and Responsibilities: Execute product manufacturing according to established procedures, record the data, interpret results and validate the quality of the data. Perform in-process and/or final quality control testing and accurately document all results. Perform lab calculations needed to make solutions from powder or from stock solutions. Support general lab functions, setup, calibration and maintenance of equipment. Production records will be reviewed by senior production staff or supervisor. Perform transactions using ERP or equivalent system. Accurate and reliable inventory management participation. Achieve high productivity while maintaining all quality standards. Organize and prioritize work to ensure on-time delivery. Periodically review and discuss your priorities with supervisor. Critically think about the manufacturing process and suggest improvements to maintain high quality standards. Actively participate in process improvement projects. Adherence to ISO guidelines and the PerkinElmer quality policy. Actively participate in maintaining a safe, clean, and functional work environment. Responsible for the completion of all tasks assigned daily; this may require more than 40 hours in some work weeks. Additional Responsibilities: Work may involve the handling of hazardous or biological materials. Must have adequate training to safely handle these materials and work safely under laboratory rules and SOPs. May include labeling, dispensing, packaging of reagents and final product. Participate in the investigation, recording and implementation of product deviations or CAPA systems. Participate in transfer and implementation of new products into the production lab. Other duties as assigned. Qualifications: Associate or B.S. degree in Life Sciences, or related scientific discipline with 0-3 years of job related experience. Knowledge, Skills & Abilities: Familiarity with common equipment such as plate readers, centrifuges, balances, and liquid transfer equipment Experience or knowledge of assays such as ELISA and Lateral Flow. Pipette reproducibly. Basic lab and computer skills. Attention to d | 12/19/2018 |
| 93 | Physical Sciences Inc. Boston, MA CHEMIST/CHEMICAL ENGINEER BS/MS Exp: 0-2 yrs |
Physical Sciences Inc., located just north of Boston in Andover, has a career opportunity for a Chemist or Chemical/Materials Engineer interested in developing and scaling up materials production from laboratory/batch processes to pilot-scale/continuous processes. The applicant we seek must also have materials characterization expertise, which drives the scale-up process success criteria. Experience with wet chemistry laboratory procedures and related analytical techniques is essential. Hands on experience with hardware assembly for chemical processes is preferred. Applicant must have a BS or MS degree in Chem Eng, Chemistry or Materials Science and 0 to 2 years’ experience. Excellent written and verbal communication skills are a must, as is superior analytical capability. US Citizenship is required. | 12/19/2018 |
| 94 | Bio-Techne Centennial, CO Antibody Purification Research Associate BS Exp: 0-2 yrs |
Novus Biologicals, a Bio-Techne Brand, is seeking a full-time Research Associate to join our antibody cpurification team. The responsibilities of this position are to perform routine antibody purification and quality control testing, meeting all deadline and quality metrics. Record all information on production worksheets and update production logs as necessary. This is a dead-line driven position requiring a motivated individual to keep up with demand while still producing consistent and high quality products according to specific SOPs. Excellent attention to detail, the ability to multi-task and perform repetitive tasks in a fast-paced lab environment are a must. Send a cover letter along with your resume describing how your skills and experience relate to this position. Key Responsibilities: Perform antibody purification in strict accordance to SOPs Must be able to produce a consistent and high-quality product Record all antibody production information on worksheets for data analysis Provide support to technical services department with scientific feedback Must be self-motivated and able to work in a team environment towards a common goal Must be willing to take constructive feedback, learn from mistakes and work towards the goal of producing high quality products in a timely fashion. | 12/19/2018 |
| 95 | Bio-Techne Minneapolis, MN Research Associate BS/MS Exp: 0-5 yrs |
The responsibilities of this position are to apply general molecular biology skills to clone and express recombinant antibodies and other proteins of interest. Prepare DNA at various scales. Build and modify prokaryotic and eukaryotic expression vectors. This position involves using cell culture to evaluate expression of antibodies. Experience in basic immunology is a plus but not required. Use various basic techniques, including assays, to test and validate antibodies and proteins. Perform additional laboratory duties as assigned. Key Responsibilities: Molecular biology techniques including DNA isolation, PCR, and cloning Expression of recombinant antibodies and other proteins Protein analysis using SDS-PAGE, Western Blot, and ELISA Small-scale protein purification of immunogens and controls Mammalian cell culture techniques Written and electronic record-keeping of experimentation Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance to the job. Performs additional duties as assigned. | 12/19/2018 |
| 96 | Rapid Micro Biosystems Lowell, MA Research Scientist BS Exp: 0-2 yrs |
We are seeking a Research Scientist for the R&D Microbiology group based in Lowell. The ideal candidate will have solid independent laboratory research experience and excellent academic credentials. The candidate will have the opportunity to work closely with our highly skilled scientists and engineers on a variety of cross functional projects in developing new applications, technologies and products for rapid microbial enumeration assays. The candidate must be well-versed with general microbiology laboratory techniques such as aseptic technique, culturing methodologies, microbial testing methods for bioburden and environmental monitoring, pipetting, autoclaving, and surface disinfection. Familiarity with word processing and data spreadsheet software, such as MS Office (particularly MS Word, MS PowerPoint and MS Excel) is required. Experience working with Biosafety Level 2 organisms is required. Good writing and oral presentation skills are required. Must be well-organized, enthusiastic, dependable, hard-working and able to operate in a fast-paced environment. Experience in an ISO or GMP/GLP qualified lab environment and an understanding of statistical analysis a plus. Experience in experimental design desirable. | 12/19/2018 |
| 97 | 4DMT Emeryville , CA Analytical Development Associate BS Exp: 0-5 |
As an Analytical Development Associate, your responsibilities include routine analytical testing in support of manufactoring and process development, assistance in assay development, and the execution of qualification assays under senior supervision. Associate should be able to make experimental observations, and review data for presentations/reports. Experience with basic laboratory techniques required. | 12/19/2018 |
| 98 | Masimo Irvine, CA CAPA Engineer - Quality BS Engineering Exp: 1-2 years |
The CAPA Engineer is responsible for Corrective and Preventive action (CAPA) activities and the management of the CAPA process and workflow in accordance with Company procedures. This position will interface with individuals at all levels of the organization to facilitate and document investigations, communicate CAPA status, and to ensure consistency and completeness in the documentation for each CAPA file. | 11/14/2018 |
| 99 | Nevro Redwood City, CA Technical Support Specialist BS Engineering Exp: 1+ years |
The position requires good listening, verbal and written communication skills to accurately present technical information to our non-technical customers. Good organizational and multi-tasking skills is a must to succeed in this high paced environment. Successful candidates will need to have a good technical background with good problem solving skills. The primary responsibility will be to troubleshoot and resolve active implantable medical devices issues by means of communication with the patients, doctors and field representatives, and simultaneously document the communication in approved system. | 11/15/2018 |
| 100 | Nirmidas Biotech Palo Alto, CA Research Associate BS/MS Biology, Chemistry Exp: 1+ years |
Reporting to the Director of Research and Development or Project Lead Scientist, you will contribute to our in-vitro diagnostic assay development and NIR and IR platform building. Candidates will be expected to participate and assist in the development of platforms and programs in support of current and future NIR and IR diagnosis and imaging products. Qualified applicants must have the desire and flexibility to work in a fast-paced startup environment. The ideal candidate will design experiments, qualify reagents, conduct quality control protocols, maintain instruments, draft protocols and standard operating procedures. The candidate is expected to be detail oriented, possess strong trouble-shooting skills and is a team player. | 11/15/2018 |
| 101 | KBI Pharma Durham, NC Research Assistant - Automation BS Life Science Exp: 0-2 years |
Assist with and support execution of routine procedures within the analytical development labs. | 11/8/2018 |
| 102 | KBI Pharma Durham, NC Research Assistant BS/MS Chemistry, Biochemistry Exp: 0 years |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 11/8/2018 |
| 103 | Freudenberg Medical Carointeria, Ca Manufacturing Quality Engineer BS Exp: 1-3 years |
Medical device quality experience required in ISO13485 and ISO14971 | 10/27/2018 |
| 104 | GlaxoSmithKline Warren, NJ Research & Development Consumer Healthcare BS/MS Sciences Exp: Less than 1 year |
Are you an analytical graduate who wants a career with real purpose? On our tailored development program within R&D (Consumer Healthcare), you’ll make consumers’ lives easier through our targeted scientific efforts all over the globe. Working through four rotations (each nine months long), you’ll gain the knowledge and skills to move quickly into more senior positions within the R&D function. | 10/31/2018 |
| 105 | GlaxoSmithKline Research Triangle Park, No GMS Quality Associate BS Engineering Exp: Less than 1 year |
Are you a capable engineering graduate with the skills to develop robust, leading-edge manufacturing technologies? If so, you could help create the systems we need to make treatments that save lives. | 10/31/2018 |
| 106 | Hikma Cherry Hill, NJ Manufacturing Specialist BS Sciences Exp: 0-3 years |
Assist the shift lead in a hands-on approach to overseeing production activities including, filling, sterilization, component and equipment prep, and compounding. Completes quality systems activities including commitments, deviations, DCEs, and SOP revisions as necessary. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing recommendations. Interprets manufacturing policies, procedures, and programs | 11/1/2018 |
| 107 | Hikma Cherry Hill, NJ Quality Lab Associate I - Micro BS Microbiology/Biology Exp: 0-2 years |
Perform functions within the Microbiology Laboratory and/or conduct critical microbiological analysis on test articles from all stages of the manufacturing process from incoming raw materials to finished goods. The duties also include equipment maintenance and LIMS management. | 11/1/2018 |
| 108 | Immucor, Inc. Norcross, GA Medical Laboratory Technologist II BS Lifesciences Exp: 1-3 years |
The Medical Technologist is responsible for performing laboratory testing (including potency, specificity, reactivity and hemagglutination assays) and chemical evaluations (including protein, absorbance, chloride, osmolality, and pH) of Immucor products according to approved Standard Operating Procedures (SOP’s) within defined timeframes. | 11/1/2018 |
| 109 | Noven Miami, FL Assoc Research Scientist - Skin Group MS Exp: 0-3 yrs |
Perform in vitro human skin flux studies including HPLC/GC sample analysis to support the formulation feasibility and development of transdermal patch products; innovate to continuously update or develop the skin lab methods | 10/18/2018 |
| 110 | OncoSec Pennington, NJ Research Assistant BS in a relevant biological discipline Exp: 1-3 yrs |
Supports R&D team efforts on preclinical projects with an emphasis on validating novel immune-oncology therapeutic candidates. The successful candidate will conduct bench experiments for various projects under the guidance of R&D scientists. | 10/18/2018 |
| 111 | Ocular Therapeutix, Inc. Bedford, MA Manufacturing Engineer I, Process Validation BS in Engineering, preferably Chemical Exp: 1 yr |
The Manufacturing Engineer I, Process Validation shall assist with diverse commercial product and new product development projects in the manufacturing organization, and all facility related engineering projects and ongoing maintenance. Assists with transfer of clinical manufacturing to Technical Operations and provides technical support for process performance. The position is set in a dynamic, fast-paced start-up environment and shall require the individual to work on a broad range of tasks. | 10/18/2018 |
| 112 | Ortho Dermatologics Clearwater, FL Microbiologist BS in Biology/Microbiology or related Life Sciences Exp: 1-3 yrs |
Acts as the Subject Matter expert on tasks related to the quality of products tested within the Microbiology laboratory with minimal oversight. | 10/18/2018 |
| 113 | Organogenesis CANTON, MA Quality Control Analyst I/II - QC Materials BS Exp: 1-5 yrs |
The QC Analyst I/II performs quality activities in support of material inspection, testing coordination, collation, review, and dispositioning. The position has interaction with other internal departments, including Apligraf Production, FortaFlex Production, Cell Culture, Materials, and Logistics. The position also has interactions with external entities including contractors and suppliers. The QC Analyst I/II performs a wide variety of activities to ensure compliance with applicable regulatory requirements by inspecting, coordinating testing, trending, and reporting results. | 10/18/2018 |
| 114 | Pace Analytical Greenfield, IN Lab Analyst - Formulation BS in Chemistry or a related science Exp: 0-3 yrs |
This candidate will perform testing using traditional microbiological techniques for proteins and enzymes. They will be supporting product development and continued product improvement. | 10/18/2018 |
| 115 | Pace Analytical Greenfield, IN Lab Analyst - Formulation BS in Chemistry or a related science Exp: 0-3 yrs |
This candidate will perform testing using traditional microbiological techniques for proteins and enzymes. They will be supporting product development and continued product improvement. | 10/18/2018 |
| 116 | Pace Analytical Eagan, MN Entry-Level Chemist BS in Chemistry, Chemical Engineering, or related field Exp: 0 yr |
The Entry-Level Chemist will report to the Lead Chemical Engineer as they prepare samples, complete testing, record data, and analyze results. | 10/18/2018 |
| 117 | Pace Analytical Maplewood, MN Document Control Coordinator BS Exp: 0-1 yr |
This candidate will be responsible for: maintaining the division’s Certificate of Analysis (CoA) database, data entry of test results, data analysis, technical writing, and report writing. | 10/18/2018 |
| 118 | Pace Analytical St. Paul, MN Quality Engineer Assistant BS in Chemistry or related science Exp: 1-2 yrs |
Candidate will work with Quality Assurance as a Quality Engineer Assistant to ensure compliance of manufacturing processes in a GMP environment. This person will serve as reviewer and/or approver for required documentation in a pilot plant setting. This position is very project orientated, so the QE Assistant can expect every day to be different with changing responsibilities and priorities. | 10/18/2018 |
| 119 | Pace Analytical Maplewood, MN Chemist Entry-Level - HPLC BS in Chemistry or related science Exp: 1-2 yrs |
Candidate will perform analytical testing to support product development on pharmaceutical patches. Analytical lab experience is necessary, specifically with HPLC. | 10/18/2018 |
| 120 | Pace Analytical Pompano Beach, FL Environmental Technician BS in Chemistry or related science Exp: 1-2 yrs |
Responsible for providing sampling services to clients in the wastewater and air groups. Provides assistance to Environmental Technicians I and II through training and project management. Provides revenue through billable labor and equipment rental for Field Department. | 10/18/2018 |
| 121 | MilliporeSigma Rockville, MD Associate Scientist II, In-Vitro Cytogenetics BS/MS Exp: 0-3 yrs |
The In Vitro Cytogenetics Department performs a variety of assays or tests required to characterize product or material safety. The AS II conducts pre-designed assays, make scientific observations, maintain detailed workbooks and ensure all documentation fulfills generally accepted professional/industry standards. | 10/13/2018 |
| 122 | MilliporeSigma Sheboygan Falls, WI Associate Production Scientist (Evening Shift) BS/BA in chemistry, biochemistry, biology, chemical engineering Exp: 1 yr |
MANUFACTURE OR EVALUATE PRODUCTS ACCORDING TO ESTABLISHED PROTOCOLS, PROVIDE TECHNICAL SUPPORT TO OTHERS AND PERFORM OPERATIONS IN SUPPORT OF THE GROUP AND DEPARTMENT. | 10/13/2018 |
| 123 | MilliporeSigma Madison, WI Validation Specialist BS in an Engineering discipline, or Life Science Exp: 1-3 yrs |
In the role of Validation Specialist, you will also be interacting cross-functionally with Manufacturing, Project Management, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance. | 10/13/2018 |
| 124 | MilliporeSigma Billerica, MA Associate Scientist Downstream Process Development BS in biotechnology, biochemistry, or engineering Exp: 1-3 yrs |
Responsible for development of downstream processes and GLP Tox drug substance production, which includes, protein purification, nano-filtration, UF/DF, and biochemical and biophysical characterization of proteins. | 10/13/2018 |
| 125 | MilliporeSigma Billerica, MA Associate Scientist- Immuno-Oncology Biomarkers BS/MS Exp: 1 yr |
The associate scientist works within the laboratory from the Immuno-Oncology Biomarker group focusing on the development of PD biomarkers, target engagement, and whole blood assays. The incumbent will require a background in cell biology, immunology, and/or oncology. | 10/13/2018 |
| 126 | MilliporeSigma Rockville, MD Associate Scientist II, Immunoassay BA/BS Exp: 1-3 yrs |
The Associate Scientist II (ASII) will perform safety testing required to manufacture clinical and commercial products. The ASII is required to make scientific observations, maintain detailed workbooks/ documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of BioReliance services, technical principles and applications. | 10/13/2018 |
| 127 | MilliporeSigma Madison, WI Production Chemist/Scientist BS in Chemistry, Biochemistry, Chemical Engineering Exp: Entry Level |
Position primarily involves the safe and efficient manufacturing of API’s according to cGMP requirements | 10/13/2018 |
| 128 | NAMSA Northwood, OH Chemist MS Exp: 1 yr |
May perform USP and EP monograph testing activities using wet chemical and analytical instrumentation. | 10/13/2018 |
| 129 | Myriad Austin, TX RBM Research Associate (Manufacturing) BS Exp: 0-5 yrs |
In this position you will be responsible for planning, performing, and evaluating the process of manufacturing reagents and propose experiments within a project(s) to provide valid and needed information. | 10/13/2018 |
| 130 | Myriad Austin, TX Quality Assurance Specialist - Archivist BS Exp: 0-2 yrs |
Under indirect supervision, organizes, maintains, and preserves a specified print and/or non-print archival collection. Develops policy and/or procedure and directly manages the acquisition, disposition, and safekeeping of archival materials. | 10/13/2018 |
| 131 | MolecularMD Portland, OR Clinical Medical Histology Technician (CMHT) BS/BA in Histology, Biology, Chemistry, or a related science Exp: 1 yr |
The Clinical Medical Histology Technician (CMHT) is responsible for standards, practices, and procedures commonly used in immunohistochemical (IHC) testing assays, new test development and implementation, new instrument integration into Histopathology workflows, as well as instrument and assay performance monitoring. The CMHT prepares tissue sections for routine and complex histological procedures, records and analyzes data, recognizes trends, compares data sets for equivalency, evaluates assay control material for acceptance, and completes data reports. Relying on experience and knowledge of Histopathology and IHC processes, the employee in this position exercises good judgment to plan and accomplish goals. This position works to support the MolecularMD strategic goals as well as Histopathology department goals of timely and accurate work, achievement of client deliverables, and excellent customer service | 10/13/2018 |
| 132 | Nevro Redwood City, CA Technical Support Specialist BS Exp: 1 yr |
The position requires good listening, verbal and written communication skills to accurately present technical information to our non-technical customers. Good organizational and multi-tasking skills is a must to succeed in this high paced environment. Successful candidates will need to have a good technical background with good problem solving skills. The primary responsibility will be to troubleshoot and resolve active implantable medical devices issues by means of communication with the patients, doctors and field representatives, and simultaneously document the communication in approved system. | 10/13/2018 |
| 133 | Nektar San Francisco, CA Clinical Biosample Associate II BS Exp: 1 yr |
Performs biomarker and pharmacokinetic/immunogenicity sample tracking using advanced Microsoft Excel skills: generating reports and trackers, collaborating with internal and external partners for clarification and escalation of issues to the clinical team. Performs tracking of images using advanced Microsoft Excel skills, generating reports and trackers, collaborating with internal and external partners for clarification and escalation of issues to the clinical team. Maintains sample and image collection instructions for sites to ensure clarity, quality and compliance. Responsible for tracking and management of document versions aligned with protocols and amendments. Reviews laboratory and imaging manuals, associated forms and labels. Provides training support for investigators/site teams for proper collection techniques, time point requirements and sample/image handling to ensure viability and data reliability. Supports escalation of sample and imaging management concerns during the execution of the study. Ensures all issues are documented, advises on mitigation and remediation, escalates issues and drives to closure in support of team goals and timelines. Actively maintains status updates for routine reporting to study team. Demonstrates good communication and interpersonal skills; leverages those competencies to ensure continuous progress, moving issues to resolution. Displays strong written and oral communication skills. Works with all levels of staff and management to resolve issues and update on progress. Able to work with large and small teams to achieve business goals with professionalism and poise. | 10/13/2018 |
| 134 | MedImmune Frederick, MD QC Analyst-Operations BS Exp: 0-5 yrs |
Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. | 10/7/2018 |
| 135 | MedImmune Frederick, MD Quality Control Analyst-Operations BS Exp: 0-5 yrs |
Responsible for conducting raw materials, in process, finished product and stability testing according to standard operating procedures. | 10/7/2018 |
| 136 | MedImmune Gaithersburg, MD R&D Associate II MS Exp: 1 yr |
The successful candidate will conduct sample testing for immunoassays with a focus on operation of the GyroLab automated immunoassay platform. The successful candidate will also be responsible for the manufacture and qualification of critical reagents to support immunoassay workflows. | 10/7/2018 |
| 137 | MedImmune Frederick, MD Validation Technician- Operations BS in Engineering or Technical Field Exp: 0-3 yrs |
Conducts the validation plans and processes for facilities, laboratory equipment, utility systems and process equipment. | 10/7/2018 |
| 138 | MedImmune Gaithersburg, MD Pilot Production Technician I/II BS Exp: 0-2 yrs |
The technician is responsible for the operation of equipment according to established Standard Operating Procedures and Master Production Records for the manufacture of therapeutic proteins and vaccines in accordance with Current Good Manufacturing Practices (cGMP’s) | 10/7/2018 |
| 139 | MedImmune Gaithersburg, MD Research Associate I/II BS/MS Exp: 0-2 yrs |
The successful candidate will carry out analytical testing and method development using Electrophoresis, Chromatography, and Mass Spectrometry techniques in support of early and late stage development of biopharmaceutical products, such as humanized monoclonal antibodies, and recombinant proteins. Industry internship experience is a plus. The candidate will make detailed experimental observations, review and analyze data, interpret experimental results, and summarize data for presentations and reports. The candidate will author SOPs, protocols, reports and other relevant documentation. | 10/7/2018 |
| 140 | Medtronic Northridge, CA Verification Engineer MS in Engineering or Science-related discipline Exp: 1 yr |
Under general supervision, candidate works independently on moderately complex verification testing assignments. Candidate will develop and validate test methods, both manual and automated. Candidate will work cross-functionally to ensure proper test coverage of design requirements. | 10/7/2018 |
| 141 | Laboratory Corporation of America San Diego, CA QA Analyst - Laboratory Compliance BS/BA in Medical Technology Exp: 1-2 yrs |
Provides leadership in the areas of quality assurance, quality control, quality related training, and standardization compliance within the laboratory. This position is also responsible for project management activities as they relate to identified areas within the laboratory requiring standardization to improve the quality and/or efficiency of operations. | 10/7/2018 |
| 142 | Medtronic North Haven, CT Manufacturing Engineer MS Exp: 0 yr |
The Manufacturing Engineer (Supplier Reliability) responsibilities include but not limited to provide technical and subject matter expert support to the Supplier Development & Improvement Program. This includes collaborating and working with Quality Engineering, Global Sourcing, Global Supplier Excellence, manufacturing sites and other team members to improve quality and service with our suppliers. | 10/7/2018 |
| 143 | Medtronic North Haven, CT Associate Industrial Engineer BS in Industrial or Systems Engineering Exp: 0-2 yrs |
This position provides industrial engineering support for New Product Development initiatives in Medtronic’s Surgical Innovations business unit. This role will support the portfolio of Surgical Innovations projects being led by the R&D centers in North Haven, Shanghai, Woburn, and Trevoux. Team is focused on creating innovative analytic solutions & data visualization to influence and drive sound business decisions related to product life-cycle management, manufacturing strategy, and extended value stream capacity planning. | 10/7/2018 |
| 144 | Medtronic North Haven, CT Associate Materials Engineer BS Exp: 0 yr |
The Associate Materials Engineer responsibilities include but are not limited to support various manufacturing sites for Medtronic devices. This includes working with Seniors Engineers and participating in cost savings, redesigns, manufacturing process improvements, tooling replacement projects and resolving production issues related to metal and/or plastic components. | 10/7/2018 |
| 145 | Cantel Plymouth, MN Research Associate (Chemist) BS in chemistry Exp: 1-3 yrs |
Develop expertise in the operation maintenance, calibration, performance verification, and application of analytical instruments | 10/7/2018 |
| 146 | Medpace Cincinnati, OH Clinical Research Associate-Cincinnati Entry Level BS in a health or science related field Exp: 1 yr |
Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff.Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff.Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol; Communication with the medical site staff including coordinators, clinical research physicians, and their site staff. | 10/7/2018 |
| 147 | Viant Brimfield, MA Design Engineer BS Exp: 0-3 yrs |
Initiates, directs and manages the design, development, constructing and modification of products and processes from conception to implementation. Works closely with other departments to coordinate design engineering activities. Reviews, initiates or approves engineering drawings, layouts, changes orders and specifications. | 10/7/2018 |
| 148 | Viant Orchard Park, NY Manufacturing Engineer BS in Engineering/technical field Exp: 0-4 yrs |
Execute configuring items/BOMs/Routings to support CS and Operations. | 10/7/2018 |
| 149 | Medtronic Portsmouth, NH Supplier Quality Engineer MS Exp: 0 yr |
This position has the responsibility to perform Quality Engineering functions including inspection and testing, procedure writing, statistical analysis of quality data, supplier qualification and performance monitoring and reviewing and approving design changes, | 10/7/2018 |
| 150 | Medtronic North Haven, CT Test Engineer (2nd Shift) BS Exp: 1 yr |
Author Test Reports and route documents for approval (strong writing skills); Create quality and safety related documentation to support validity of test. | 10/7/2018 |
| 151 | MedImmune Gaithersburg, MD R&D Associate I/II - Analytical Sciences MS in Chemistry, Biochemistry, or related field Exp: 0-2 yrs |
The successful candidate will carry out analytical testing and method development using Electrophoresis, Chromatography, and Mass Spectrometry techniques in support of early and late stage development of biopharmaceutical products, such as humanized monoclonal antibodies, and recombinant proteins. The candidate will make detailed experimental observations, review and analyze data, interpret experimental results, and summarize data for presentations and reports. The candidate will author SOPs, protocols, reports and other relevant documentation. | 10/7/2018 |
| 152 | Merit Medical Systems, Inc., South Jordan, UT Technician III BS Exp: 1 yr |
Performs non-routine technical assignments of substantial variety and complexity. | 10/7/2018 |
| 153 | Merieux NutriSciences Mississauga, ON QA Analyst I BS Exp: entry-level |
Perform basic chemical and physical analyses, and sensory evaluation on food and non-food samples. | 10/7/2018 |
| 154 | Merit Medical Systems, Inc., South Jordan, UT R&D Biocompatibility Engineer I BS in Biomedical Engineering or related field Exp: 1 yr |
Performs biological safety related tasks and assists with biomaterials characterization and analysis in our R&D environment. | 10/7/2018 |
| 155 | Pfizer Groton, CT Technical Associate, Comparative Medicine BS/BA Exp: 1 yr |
The Technical Associate’s primary responsibility is to provide basic husbandry, handling, restraint and health surveillance of laboratory animals in compliance with local regulatory requirements. This individual will also provide daily record keeping of common laboratory species, their environments, and provide basic technical assistance (i.e., restraint, injections, blood collection) to other technicians and researchers. Other more specialized functions, depending on interest and aptitude may be assigned in the areas of technical and research services. | 10/7/2018 |
| 156 | Pfizer Groton, CT Associate Scientist, Process Chemistry BS in Chemistry Exp: 0-5 yrs |
We are seeking an Associate Scientist in synthetic organic chemist to join the Process Chemistry group within Chemical Research and Development (CRD) in Groton. CRD, as part of Worldwide R&D in Pharmaceutical Sciences, is responsible for the development of process technology for the production of active pharmaceutical ingredients (API). CRD scientists engage in all facets of development from small scale synthesis in support of Discovery programs, to the development of the commercial synthetic route. CRD scientists partner with manufacturing specialists for API synthesis in kilo-lab and pilot plant facilities, as well as provide support for technology transfer to Pfizer manufacturing sites and third party facilitie | 10/7/2018 |
| 157 | Pfizer St Louis, MO Associate Scientist, Gene Therapy Purification Process Development BS in a biological or engineering discipline Exp: 0-2 yrs |
The successful candidate will have a Bachelor’s degree in Chemical Engineering, Chemistry/Biochemistry, or Biology, and have a working knowledge of biochemistry and related analytical chemistry, preferably in chromatography, centrifugation, precipitation, and filtration design principles. This position requires the design and execution of experiments using the aforementioned technologies and the ability to evaluate and clearly reporting the results to laboratory colleagues and other affected functional areas. | 10/7/2018 |
| 158 | Pfizer Andover, MA Associate Scientist, Formulation BS in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, Pharmacy, Biochemistry or equivalent Exp: 0-3 yrs |
This position will be part of Pharmaceutical Research and Development. The incumbent will participate in the development of parenteral formulation for biologics modalities such as monoclonal antibodies, antibody drug conjugates, proteins, vaccines, and viral vectors for genomic therapeutics. This position will be responsible for performing analytical characterization of candidate molecules by using various biophysical and biochemical characterization techniques. Furthermore this position will assist in developing processes for drug product manufacturing, responsible for data compilation, data presentations and report writing. | 10/7/2018 |
| 159 | Pfizer Chapel Hill, NC Associate Scientist, QC Microbiology, Gene Therapy BS in microbiology, biochemistry, biology or related field Exp: 0-2 yrs |
The qualified candidate will join the Analytical R&D Quality Control & Microbiology organization to enable development of gene therapy products in Chapel Hill, NC. The qualified candidate will be responsible for applying GMP microbiological (bioburden, LAL, PCR, etc.) and biochemistry (UV, pH, HPLC, etc.) methods in the assessment of product quality and detection of impurities. This group also performs micro method qualifications and Environmental Monitoring (EM) of Drug Substance and Drug Product facilities. | 10/7/2018 |
| 160 | Pfizer McPherson - Hospira, KS Supplier Quality Coordinator BS Exp: 1 yr |
The primary function of this position is to support operations relating to the supplier quality program. The Supplier Quality Coordinator is responsible for the maintaining/managing supplier management systems, tracking/completion of supplier related documentation and maintaining/reporting supplier metrics. | 10/7/2018 |
| 161 | MethodSense Morrisville, NC Quality Assurance Associate BS Exp: 1-3 yrs |
Assist or lead in the maintenance of Quality Management System (QMS) | 10/7/2018 |
| 162 | MESO SCALE DIAGNOSTICS, LLC. Gaithersburg, MD Research Associate I BS in life sciences, cellular and molecular biology, protein sciences or related field Exp: 1 yr |
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). Some degree of professional latitude, creativity and self management is expected. | 10/7/2018 |
| 163 | Micropoint Bioscience, Inc. Santa Clara, CA Quality Control Associates MS in chemistry, biology, or related scientific field Exp: 0 yr |
These positions are responsible for participating as team members in a laboratory environment for finished product/or development programs focused on the goal of testing and releasing the immunoassays found in Micropoint's in-vitro diagnostic products for point-of-care (POC) testing. | 10/7/2018 |
| 164 | Merck & Co., Inc. West Point, PA ASSOCIATE SCIENTIST BS/MS in Chemical Engineering, Material Science and Engineering, Pharmaceutical Sciences, or a related discipline Exp: 0 yr |
The position is for an Associate Scientist, Engineering in Pharmaceutical Commercialization Technology (PCT). This group is responsible for pharmaceutical process and technology development for oral solid dosage drug products. PCT’s process development ownership begins as products enter Phase IIb and continue through regulatory filings, process validation, and the first few years of commercial launch. The group’s work is facilitated by a network of commercialization sites, which are currently located in Ireland and Puerto Rico. Coupled with our pilot plant in West Point, PA, these sites form the foundation of Merck’s oral solid dosage development and commercialization capabilities. | 10/7/2018 |
| 165 | Mission Phrmacal Boerne, TX Associate Formulator BS in Pharmaceutical Sciences, Chemistry, Engineering or equivalent Exp: 6 months |
Works with a multi-disciplinary team in developing, designing, testing and preparing stability and clinical batches for a variety of pharmaceutical and nutraceutical products. Contributes as part of a multi-disciplinary development team, learning how to design formulations and testing plans, developing manufacturing processes, and preparing stability and clinical batches for a variety of pharmaceutical and nutraceutical products. Assists in seamless technology transfer of processes between pilot plants and into final commercial manufacturing plants. Design and optimize various formulation and filling unit operations including active ingredient dissolution or dispersion, mixing, emulsification, blending, tableting, coating, and bottle/tube filling. Assists in the execution of pilot to commercial scale fill/finish manufacturing process. Communicate with material and equipment vendors to source equipment and project specific materials. Prepare the scientific content in regulatory documents, manufacturing instructions, and SOPs. | 10/7/2018 |
| 166 | Miltenyi Biotec Sunnyvale, CA Manufacturing Associate BS in biological science or related discipline Exp: 1-3 yrs |
As a member of the Miltenyi Biotec Manufacturing team, you will have the exciting opportunity to participate in both the manufacture and process development of T-cells and multiple other cell therapy products within a GMP environment. The unique duties of this position will primarily consist of manufacturing primary human cells including activities that involve graft engineering for cellular therapies as well as supporting the development of scalable cell culture processes. Furthermore, you will be responsible for completing successful qualifications and ongoing support procedures for clean room operations and assisting in the development, writing, and review of SOPs, material specifications, standard manufacturing procedures, batch records and other GMP documentation. | 10/7/2018 |
| 167 | Miltenyi Biotec Gaithersburg, MD Document Control Specialist BS in the life sciences Exp: 1-2 yrs |
As a member of the Lentigen Technology team, you will have the opportunity to support the Quality Assurance systems by means of creating, tracking, and maintaining high quality technical documentation. Furthermore, you will be responsible for ensuring records are organized and maintained, and support the implementation of quality systems in compliance with GMP regulations and company policies. Overall, your keen ability to support the maintenance of quality systems and processes will help power Lentigen Technology’s continued success. | 10/7/2018 |
| 168 | MilliporeSigma Rockville, MD Associate Scientist BS/BA/MS/MA Exp: 0-3 yrs |
The Associate Scientist I and Associate Scientist II conducts pre-designed assays, make scientific observations, maintain detailed workbooks and ensure all documentation fulfills generally accepted professional/industry standards. The Rockville, MD location performs a wide variety of assays or tests required to characterize product or material safety. | 10/7/2018 |
| 169 | MilliporeSigma Milwaukee, WI Packaging Engineer BS Exp: 1-2 yrs |
Packaging Engineer | 10/7/2018 |
| 170 | MilliporeSigma NA, IL Production Scientist Associate BA/BS in the field of Chemistry, Biochemistry, Analytical Chemistry Exp: 1-3 yrs |
To perform routine and non-routine chemical manufacture, following established protocols and procedures; to accurately prepare complete and legible records; to provide lab support and to maintain equipment. | 10/7/2018 |
| 171 | MilliporeSigma Sheboygan Falls, WI Associate Process Engineer BS in Chemical & Biologigal Engineering Exp: 0-4 yrs |
CONDUCT PROCESS ENGINEERING ACTIVITIES ASSOCIATED WITH NEW MANUFACTURING PROCESSES OR IMPROVING EXISTING MANUFACTURING PROCESSES. JOB RESPONSIBILITIES WILL INCLUDE STATISTICAL PERFORMANCE OF PROCESSES AND PROCESS EQUIPMENT IN ORDER TO ENSURE MINIMUM VARIABILITY OR PRODUCT QUALITY FROM DEVELOPED SYSTEMS. | 10/7/2018 |
| 172 | MilliporeSigma Rockville, MD Associate Scientist 1 - Cell Biologist BA/BS Exp: 0 yr |
Responsible for having a basic knowledge of lab policies and assays | 10/7/2018 |
| 173 | MilliporeSigma Rockville, MD Quality Specialist I (US Biologics) Data Audits BS Exp: 0-1 yr |
PERFORMS A VARIETY OF TASKS IN SUPPORT OF SPECIFIC AREAS OF THE QUALITY SYSTEM IN ONE OR MORE OF THE FOLLOWING GROUPS WITHIN THE QUALITY ASSURANCE DEPARTMENT: QA DATA AUDITS (DATA AND REPORT REVIEWS), QA CLIENT SERVICES (CLIENT, SUPPLIER, AND INTERNAL AUDITS), OR QA TECHNICAL SERVICES (VALIDATION AND ASSAY DOCUMENTATION REVIEWS). | 10/7/2018 |
| 174 | MilliporeSigma Carlsbad, CA Manufacturing Technician 2 - Buffer Media/Mfg Team BS Exp: 1-3 yrs |
The Tech positions will be the primary entry point for GMP Manufacturing of biologics at the Carlsbad site. Differentiation on Tech level will be based on experience levels in GMP Manufacturing at both the Carlsbad site and at external locations. These positions do not have supervisory responsibility. | 10/7/2018 |
| 175 | Merck & Co., Inc. Rahway, NJ METROLOGY SPECIALIST MS in Chemistry , Biochemistry, or closely related sciences Exp: 1 yr |
The candidate will be involved in overseeing the lifecycle of the lab instrumention covering acquisition and installation, performance or coordination of routine maintenance, computer system validation, and regulated systems retirement. | 10/7/2018 |
| 176 | Moderna Cambridge, MA (Contract) Associate I, Quality Control BS Exp: 1 yr |
The individual in this role will perform cGMP QC sample management activities for QC Chemistry, Microbiology, Bioassay. Analytical Development and Drug Product Development labs. Also, this individual may support special projects as assigned. | 10/7/2018 |
| 177 | MicroVention® TERUMO Aliso Viejo, CA Engineer I, Process Development BS/MS in Engineering or equivalent Exp: 0-3 yrs |
The Process Development Engineer I creates and/or supports projects focused on developing systemic changes within the Equipment Engineering group. Leads and/or supports execution of projects related to equipment maintenance objectives. Evaluates, initiates, and creates improved engineering and project systems for equipment maintenance procedural issues. Provides engineering support in areas of equipment calibration, preventative maintenance, and installation/operational qualification. | 10/7/2018 |
| 178 | MicroVention® TERUMO Aliso Viejo, CA Engineer I/Engineer II (EIT) BS in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Industrial Engineering, Chemistry or other related discipline Exp: 0-2 yrs |
The Engineer I (EIT) supports development of medical device products with work including writing or verifying specifications, designing new products, fixtures, test processes, equipment and specifying raw materials to ensure the concepts and/or prototypes meet their requirements. | 10/7/2018 |
| 179 | LakePharma Hayward, CA Associate Scientist, Process Development MS in biochemistry, chemical engineering or related field Exp: 1 yr |
The position focusing on CHO cell culture and continuous harvesting process | 9/29/2018 |
| 180 | KBI Biopharma Durham, NC Manufacturing Associate I/II-Upstream BS Exp: 0 yr |
Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities | 9/29/2018 |
| 181 | KBI Biopharma Durham, NC Manufacturing Associate-Upstream (temp to hire) BS Exp: 0 yr |
Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP’s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities | 9/29/2018 |
| 182 | Syneos Health, Inc. NA, MN Quality Control Analyst I BS/MS in any Life Sciences Exp: 0-3 yrs |
Perform supportive activities for general lab readiness, laboratory equipment qualification and method transfers. | 9/29/2018 |
| 183 | Syneos Health, Inc. NA, IL Clinical Research Assistant BS Exp: 1-5 yrs |
Coordinates assigned clinical research studies;Identify potential research subjects through IRB approved practices. | 9/29/2018 |
| 184 | Syneos Health, Inc. NA, MN QA Specialist II MS in Life Sciences Exp: 0-2 yrs |
Support site GMP activities through basic record review, quality system support and regular interaction with site personnel. | 9/29/2018 |
| 185 | Syneos Health, Inc. NA, MO Bench Scientist I BS Exp: 1 yr |
The scientist filling this position will work within a highly-matrixed team setting on a variety of modalities including vaccines, viral constructs, therapeutic proteins, and monoclonal antibodies | 9/29/2018 |
| 186 | Syneos Health, Inc. NA, NC Pharmaceutical Process Technic BS/MS in Chemistry Exp: 0-2 yrs |
Performs a variety of chemical analysis and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, finished product and stability samples in accordance with cGMP, GLP, DEA and company policies and procedures. Assists in writing and performing method validations and method transfers. Assists in process validations. Conducts equipment validations IQs, OQs, PQs, and MQs, if necessary. Provides assistance and technical support to other groups with chemical testing needs and performs troubleshooting of analytical methods and instrumentation. | 9/29/2018 |
| 187 | Syneos Health, Inc. Chicago, IL Document Specialist BS Exp: 1-2 yrs |
Assists in the completion of activities regarding quality control, compliance, investigational product release for clinical studies and/or data collection; including working with functional areas to ensure assigned activities are completed per plan. | 9/29/2018 |
| 188 | LI-COR, Inc. Lincoln, NE Sr. Synthetic Chemist, Clinical R&D MS in Chemistry Exp: 1-3 yrs |
Independently develop protocols, applications, and products. Identify product opportunities consistent with corporate goals. Independently plan and execute experiments, and review results with supervisor. Write reports, technical documents, and application notes. Develop synthetic routes and analytical methods. Perform syntheses and purifications at bench scale (milligram to kilogram) of chemical products for Research and Development, clinical trials and commercial use. Analyze compounds produced and maintain documentation of experimental results. Prepare and present scientific posters at national meetings. Mentor others in the group. | 9/29/2018 |
| 189 | Leidos COLUMBIA, MD Quality Control Inspector/Auditor MS Exp: 0-2 yrs |
The successful candidate will use their experience to help this program achieve critical mission success by supporting a quick reaction capability production environment as a quality control professional. | 9/29/2018 |
| 190 | Leidos JACKSONVILLE, NC Research Assistant – Audiology BS in a hearing, psychology or acoustics field Exp: 0-2 yrs |
Provide planning and coordination support for the Hearing Conservation Research Program | 9/29/2018 |
| 191 | Leidos FREDERICK, MD Research Technician (NCI) BS Exp: 0 yr |
Isolating DNA and RNA from tumor tissue and in vitro cell cultures on a large scale | 9/29/2018 |
| 192 | Leidos SAN DIEGO, CA Research Assistant BS in a relevant social science field (e.g., psychology, sociology, epidemiology, public health, economics) Exp: 1 yr |
The Research Assistant will work collaboratively with the full research team, including Principal Investigators, research scientists, data analysts and subject matter experts. Under direct supervision, this role will support a variety of research projects, including health promotion evaluations, clinical treatment interventions, and epidemiological investigations, designed to promote the behavioral and psychological health and readiness of military personnel and their families. | 9/29/2018 |
| 193 | Luitpold Pharmaceuticals, Inc. NORRISTOWN, PA Clinical Research Associate BS Exp: 1 yr |
Assist with Administration of clinical research projects: site and investigator recruitment, collecting investigator documentation, site management, site monitoring, preparing and maintaining proper status reports of activities at investigative sites through the duration of a clinical trial and completing other technical tasks to completion. | 9/29/2018 |
| 194 | PharmaForce, Inc NEW ALBANY, OH Document Control Coordinator BS Exp: 0-1 yr |
This position is a member of the Document Control Group. The Document Control Group is responsible for controlled documents associated with the manufacture of safe, pure, effective and sterile pharmaceuticals in accordance with company SOPs, policies and cGMPs. The Document Control group provides support to other departments as needed and is critical in maintaining production schedules and meeting company goals. The Document Control Coordinator will participate in all aspects of the Document Control Process. This includes all elements of the document lifecycle such as editing, reviewing, tracking, issuing, and filing of controlled documentation as per applicable Standard Operating Procedures. The Document Control Coordinator works under the direct supervision of senior management in Quality Assurance and senior members of the Document Control Group. This position will include significant travel between each of the Pharmaforce facilities. | 9/29/2018 |
| 195 | Lonza Houston, TX Quality Control Analyst I BS in Biology Exp: 1-2 yrs |
Performs Quality Control assays for Product Release and Stability Studies in compliance with Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs). Being familiar with cell culture and cells assays. Skill set includes, but is not limited to flow cytometry. | 9/29/2018 |
| 196 | Lonza Walkersville, MD Research Associate I MS in Life Sciences or related discipline Exp: 1-2 yrs |
Execute virus media development projects. Data analysis and report writing. Troubleshoot problems in manufacturing and QC for virus media. | 9/29/2018 |
| 197 | Lonza Rochester, NY Production Engineer BS in Chemical Engineering Exp: 1 yr |
Provide technical coverage and troubleshooting of plant processes;Improvement and optimization of existing operations | 9/29/2018 |
| 198 | LifeSensors Malvern , PA Entry Level Scientist BS/MS in biological sciences Exp: 0-2 yrs |
We are seeking individuals who are passionate about research, bring out of the box thinking and take bold steps to develop innovative technologies with applications in the ubiquitin research field. Successful candidates will have basic knowledge of biochemistry and molecular biology techniques, in particular experience with, protein expression and purification and cloning. Knowledge of the ubiquitin proteasome pathway is desired. | 9/29/2018 |
| 199 | Liquidia Technologies Morrisville, NC Associate/Senior Associate Scientist/Engineer, Manufacturing Sciences MS in chemical engineering, material science, polymer chemistry, or related discipline Exp: 0-2 yrs |
Assist the Liquidia manufacturing team with various tasks and projects. | 9/29/2018 |
| 200 | Manus Bio Cambridge, MA Research Assistant, Molecular Biology BS/MS in Bioengineering, Molecular Biology, Biochemistry, or similar discipline Exp: 1 yr |
We are seeking a motivated individual for a research assistant position that will specialize in molecular biology and natural product discovery. | 9/29/2018 |
| 201 | Magenta Cambridge, MA RESEARCH ASSOCIATE/SENIOR RESEARCH ASSOCIATE, IMMUNOLOGY/STEM CELL BIOLOGY BS/MS Exp: 1-5 yrs |
The successful candidate will be an integral member of a team involved in multiple projects focused on developing novel therapeutics to improve stem cell transplantation. The position requires experience working with , tissue culture, flow cytometry, and experience in assay development and optimization. | 9/29/2018 |
| 202 | LSNE Madison, WI QC Chemist I BS in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area Exp: 0-5 yrs |
This position will have responsibility for supporting all activities in the Quality Control Laboratory. This includes the testing of R&D samples, in-process samples, finished product samples, stability samples, and raw materials. This may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 9/29/2018 |
| 203 | LSNE Manchester, NH QA Associate I - Document Control BS Exp: 1 yr |
Manage, coordinate, and maintain CGMP documentation, procedures, and records to ensure only controlled copies are reviewed, approved, issued, distributed, and archived. | 9/29/2018 |
| 204 | LSNE Manchester, NH QA Specialist I - Operations MS Exp: 1-5 yrs |
Review all records associated with the manufacturing of a product lot for completeness and accuracy to ensure qualified specifications, parameters, and controls have been met and/or all deviations from such have been adequately and timely addressed. | 9/29/2018 |
| 205 | LSNE Manchester, NH QC Microbiology Technician BS Exp: 0-1 yr |
Conducts sampling of incoming raw materials, product environments, and/or facility clean utilities, as per approved procedures and submits these samples to the appropriate testing facility for documented and controlled results. Applies material / system status labels, as indicative of testing status and/or results obtained. Assists with lab maintenance and inventory. | 9/29/2018 |
| 206 | LSNE Manchester, NH QA Associate I - Ops BS Exp: 0-2 yrs |
QA Associate I - Ops | 9/29/2018 |
| 207 | Lung Biotechnology Silver Spring, MD QA Specialist I - Documentation BS in Biological Sciences, Chemistry or related discipline Exp: 1 yr |
Utilizing your knowledge of fundamental theories, principles, and concepts as the Quality Assurance (QA) Specialist I, you will be contributing to all relevant documentation areas to support the QA team meet its functional deliverables as outlined in the cGMP and organizational standard operating procedures (SOP). | 9/29/2018 |
| 208 | Lung Biotechnology RTP, NC Research Associate / Senior Research Associate - Cell Biology BS/MS in Biology, Cell or Molecular Biology, Biomedical Sciences or related field Exp: 1 yr |
Conduct and assist in research efforts to develop novel cell and cell-based products for treating pulmonary hypertension and other lung diseases. | 9/29/2018 |
| 209 | MDxHealth Irvine, CA Clinical Laboratory Scientist I/II BS/MS Exp: 1 yr |
The Clinical Laboratory Scientist I (CLS I) performs a variety of both routine and complex clinical laboratory tests in accordance with established processes and procedures. These require professional level of knowledge to properly execute and analyze results, especially where results are abnormal or atypical. Responsible for compliance to all applicable regulations including but not limited to the Food and Drug Administration, ISO and State and Federal requirements. | 9/29/2018 |
| 210 | Marker Gene Technologies, Inc. Eugene, OR Laboratory Technician-Biology BS in cell biology, biochemistry, biology molecular biology or a related science field Exp: 0-3 yrs |
The position will be based in Eugene, Oregon. The successful candidate will support laboratory staff by performing routine cell culture, running cell assays, preparing media and buffers, and maintaining laboratory supplies and glassware. Additionally the successful candidate will play a role in the development and production of new products | 9/29/2018 |
| 211 | Masimo Irvine, CA Regulatory Affairs Specialist II BS/MS in Engineering or Life Sciences Exp: 1-3 yrs |
Regulatory Affairs is responsible for obtaining and documenting our mission-critical, domestic regulatory clearances for Masimo’s amazing innovative products. The individual will be the sole RA representative on various project teams for new products. For each project, the individual will provide regulatory input on, for example, design, labelling, and clinical testing issues. Thus, the individual must work closely with Engineering and Marketing team members to understand the technology, marketing and clinical application of each new product. | 9/29/2018 |
| 212 | Medtronic North Haven, CT Associate Manufacturing Engineer BS in Chemical, Mechanical, or Bio-Medical Engineering Exp: 0 yr |
The Associate Manufacturing Engineer is responsible for providing daily support of multiple product families with specific regard to product quality, product cost, process improvements, safety, and customer feedback. Areas of responsibility include chemical, polymer extrusion, textile, and bio-medical processes. Duties include managing and/or participating in cross functional teams to accomplish project specific goals. This person will be mentored to become the resident expert on production equipment and processes, plus play a supporting role for new products transitioning from R&D into manufacturing production. Key responsibility will be to insure efficient product processing while maintaining established quality/cost/safety standards. | 9/29/2018 |
| 213 | Medtronic Plymouth, MN Design Assurance Engineer MS Exp: 0 yr |
Develops, coordinates and conducts technical reliability studies and evaluations of engineering design concepts and design of experiments (DOE) constructs. | 9/29/2018 |
| 214 | Medtronic North Haven, CT Manufacturing Engineer MS Exp: 0 yr |
The Manufacturing Engineer is responsible for providing daily support of finished good level suture manufacturing with specific regard to safety, product quality, service, process improvement, and customer feedback. Duties include participating in cross functional teams to accomplish project specific goals, root cause analysis, and developing and implementing robust corrective and preventive action plans. This person will be mentored to become the resident expert on assembly, packaging, and automated production equipment and processes, to develop strong project management skills, and to lead teams of his/or her peers. | 9/29/2018 |
| 215 | Medtronic Santa Rosa, CA Process Develoment Engineer MS in Engineering Exp: 0 yr |
You will be involved in process innovation with emphasis on improving quality, reducing process variation, reducing cycle time and cost down initiatives. You will perform analysis and provide recommendations on process improvements. You will participate in Equipment and Process Development, Process Characterization and Process Qualification to support new product introduction. You will utilize functional excellence in process development including Design Reliability & Manufacturability (DRM) and Cell Operating System (COS) methodologies. | 9/29/2018 |
| 216 | Medtronic North Haven, CT Product Engineer MS Exp: 0 yr |
The Product Engineer will prioritize daily production activities, improvements, scheduling and production tracking. The Position is in a fast-paced, and collaborative environment that is supportive of program initiatives and compliant with the company’s best practices, Tenets and Philosophy. | 9/29/2018 |
| 217 | Medtronic Louisville, CO Supplier Quality Engineer MS Exp: 0 yr |
As Supplier Quality Engineer you will have responsibility and authority to collaborate with suppliers to ensure product specifications are met. Recommend, plan and lead corrective and preventive actions for continuous improvement with suppliers under general supervision. Work with Suppliers and purchasing to ensure that supplier management files are maintained according to established requirements to include the development and management of supplier control plans. | 9/29/2018 |
| 218 | Medtronic NA, MN Associate Manufacturing Engineer-Welding Engineering BS Exp: 0-1 yr |
Frequent use and application of laser welding technical standards, principles, theories, concepts, and techniques. Capable of learning and performing all required competencies in the laser welding functional area. Basic understanding of mechanical testing and failure modes of laser welds. Can evaluate and identify critical laser weld inputs and outputs, & design and analyze an appropriate DOE (full factorial, minitab). Basic understanding of heat balance, flow, tooling, and equipment development. | 9/29/2018 |
| 219 | Viant Orchard Park, NY Senior Engineering Technician BS Exp: 0-3 yrs |
The primary purpose of this position is to perform semi-standardized or semi-prescribed assignments requiring judgmental and problem solving skills. Selects or adapts standard procedures ore equipment. Receives initial instruction, equipment requirements, and technical advice from supervisor or engineer. | 9/29/2018 |
| 220 | Laboratory Corporation of America Santa Fe, NM Cytogenetics Technician - Entry Level BA/BA in Biology or relatable life science Exp: 0 yr |
This position will include various wet lab procedures, troubleshooting, quality control, and microscope analysis. | 9/29/2018 |
| 221 | Laboratory Corporation of America Westborough, MA Molecular Technician - QC BA/BA in Biological/Chemical sciences Exp: 0-1 yr |
The QC Technician will be responsible for reagent preparation and testing for use in a high throughput clinical testing laboratory. The Westborough molecular genetics laboratory provides high-throughput carrier screening and diagnostic testing for genetic conditions. | 9/29/2018 |
| 222 | Laboratory Corporation of America Burlington, NC QA Coordinator BS in a life science field Exp: 1-2 yrs |
Works to ensure lab generated data meets acceptance criteria. Performs review of QC certification data. Will be resposible for assisting the area supervisor with all training paperwork, all competency assessments, inventory tasks as assigned, managing employee procedure review info, annual SOP review, LEAD training, Safety module employee review, monthly sign off of equipment logs, equipment PMs, periodic CE updates for employees, audits/inspection, and other duties as assigned by the supervisor. | 9/29/2018 |
| 223 | Laboratory Corporation of America Seattle, WA QA Analyst BS/BA in Medical Technology Exp: 1-2 yrs |
Provides leadership in the areas of quality assurance, quality control, quality related training, and standardization compliance within the laboratory. This position is also responsible for project management activities as they relate to identified areas within the laboratory requiring standardization to improve the quality and/or efficiency of operations. | 9/29/2018 |
| 224 | Illumina Madison, WI Associate Production Scientist BS/MS Exp: 0-5 yrs |
We are seeking a talented, driven protein production professional to join our dynamic team and contribute to the production and process optimization of novel proteins and molecular biology reagents. In this position, you will be responsible for leading in the production of a wide variety of proteins utilizing processes associated cell lysis, filtration, chromatography, and purity and contamination screening. You will participate in team-driven purification process development and improvement and be expected to contribute to an inquisitive scientific environment. | 9/21/2018 |
| 225 | Syneos Health, Inc. NA, CA Lab Technician (Wet Lab) BS in Biology, Chemistry, Biochemistry, Molecular Biology or a related field Exp: 1-3 yrs |
The Lab Technician will be a critical member in the lab to help take the Company’s Single Molecule Sequencing Platform from an advanced proof of principle to an operational laboratory instrument. He or she will ensure that labs have the necessary supplies for their research and must be detail oriented and keep exceptional notes. The candidate will should also have excellent troubleshooting and problem solving skills, along with experimental design experience. | 9/21/2018 |
| 226 | Syneos Health, Inc. NA, CA Quality Analyst I BS/MS in biological or chemical sciences or equivalent Exp: 0-1 yr |
Perform aseptic sampling Pilot Plant critical utilities and controlled environment; Perform general laboratory maintenance activities such as cleaning, inventory, and ordering of laboratory supplies. | 9/21/2018 |
| 227 | Syneos Health, Inc. NA, NJ Quality Coordinator BS/BA Exp: 1 yr |
File Organization and Management (set up / organize training files, historical files (including archiving)); Staff Meeting Management and meeting minutes. | 9/21/2018 |
| 228 | Syneos Health, Inc. NA, FL Lab Tech/Lab Rsch Asst. BS Exp: 1-2 yrs |
Effectively communicates with all clinical trials research coordinators. Exhibits a high responsibility to attention, organization and detail. Analytical, reasoning, reading skills and multitasking skills are essential. Accurately processes research samples strictly following study protocols and study lab manuals. | 9/21/2018 |
| 229 | Syneos Health, Inc. NA, CA Scientist I/II (Assay Dev) BS in Biological/Life Sciences, Chemistry, Biochemistry or related field Exp: 1-3 yrs |
After introduction to work processes, begins to organize, conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. Assumes responsibility for the accuracy, quality, and timeliness of experimental results. Summarizes experimental results, and reviews conclusions with supervisor/project leader. Communicates results of experiments. Keeps supervisor/project leader informed of project status, particularly of significant findings and results in critical problem areas. Performs work according to established internal safety guidelines and procedures, and as specified by appropriate external regulatory agencies (e.g., OSHA). Analyzes and interprets experimental data using various data analysis software and/or applying quantitative methods. Uses technical writing skills to produce reports and documents. May present findings at internal meetings. Assumes accountability for electronic lab notebook documentation, ensuring experimental methods and results are recorded timely, accurately and consistently, and according to established formats. Participates in routine lab maintenance, lab safety, ISO, and QSR implementation. | 9/21/2018 |
| 230 | Syneos Health, Inc. NA, CA Process Technician BS in Biology, Chemistry, Biochemistry, Molecular Biology, Mechanical Engineering or a related field Exp: 1-3 yrs |
The Lab Technician will be a critical member in the lab to help take the Single Molecule Sequencing Platform from an advanced proof of principle to an operational laboratory instrument. He or she will ensure that labs have the necessary supplies for their research and must be detail oriented and keep exceptional notes. | 9/21/2018 |
| 231 | Syneos Health, Inc. NA, MN Quality Control Analyst I BS/MS in any Life Sciences Exp: 0-3 yrs |
Perform supportive activities for general lab readiness, laboratory equipment qualification and method transfers. Conduct critical biological test methods including samples generated for in-process, drug substance and stability. | 9/21/2018 |
| 232 | Irvine Scientific Santa Ana , CA R&D SCIENTIST I MS in a Biological/Chemical/Life Science Exp: 0-2 yrs |
Perform cell culture experiments for development of cell biology and embryology research, product development, technical product support, and/or process improvements. | 9/21/2018 |
| 233 | Ionis Pharmaceuticals, Inc. Carlsbad, CA Senior Research Associate BS/MS in Chemistry, Biochemistry, or related field Exp: 1 yr |
We are looking for a motivated and creative scientist to join our oligonucleotide/medicinal chemistry groups. Duties include production of synthetic oligonucleotides, equipment maintenance and troubleshooting of instrumentation. The successful candidate has the ability to complete assignments and meet deadlines and time schedules. May research and implement new methods and technologies to enhance operations. Other duties as assigned. | 9/21/2018 |
| 234 | Medical Diagnostic Laboratories LLC Hamilton, NJ Research Associate MS in biochemistry, molecular biology or related field Exp: 1 yr |
The successful candidate will contribute to the work of a multi-disciplinary community of scientists, supporting the development of novel therapeutics. | 9/21/2018 |
| 235 | Invivotek, LLC Hamilton, NJ Research Associate BS in Life Sciences Exp: 1-2 yrs |
We are seeking a motivated and talented Research Associate to develop and perform in vivo and in vitro bioassays on mice and rats. The Research Associate should have excellent skills in basic rodent procedures. Rodent surgery skills are a plus. Experience with biochemical and tissue culture techniques is a plus. Excellent communication and computer skills and motivation to learn new assays are essential. Ability to work in a highly interactive and multidisciplinary team environment. | 9/21/2018 |
| 236 | Medical Diagnostic Laboratories LLC Hamilton, NJ Serology Technician BS in Biology, Chemistry, or related science field Exp: 9 months |
Perform manual Enzyme Linked Immunosorbent Assay (ELISA) and automated ELISA tests using DSX Automated Processor on patient serum samples. | 9/21/2018 |
| 237 | Medical Diagnostic Laboratories LLC Tampa, FL Certified Medical Technologist BS in Medical Technology, Biology, Microbiology or related Science field Exp: 1-3 yrs |
MDL specializes and performs Polymerase Chain Reaction (PCR) with a larger menu of testing available in the field of infectious disease. Our main theme of research is in the field of Gynecology, Infectious Diseases, Infectious Arthritis, Tick-borne Diseases, Mycology, and Chronic Fatigue Syndrome (CFS). | 9/21/2018 |
| 238 | IQVIA Research Triangle Park, NC Laboratory Associate 2 BS in biology or chemistry Exp: 1 yr |
Perform a wide variety of routine and complex testing procedures to obtain data from client specimens. Provide documentation and review of work performed in a timely manner. | 9/21/2018 |
| 239 | IQVIA NA, NA Clinical Research Associate (GFR-L) Regional Travel BS in a health care or other scientific discipline Exp: 1 yr |
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation | 9/21/2018 |
| 240 | Just Biotherapeutics Seattle, WA Associate Scientist, Media Development BS in Biology, Molecular Biology, Biochemistry or related field Exp: 0-3 yrs |
Develop and test cell culture media formulations using analytical and cell culture models; Develop and apply new methods to advance cell culture media technology. | 9/21/2018 |
| 241 | Just Biotherapeutics Seattle, WA Associate Scientist, Protein Expression BS Exp: 0-5 yrs |
Development of stable, clonal cell lines for the expression of therapeutic proteins; Technology development to improve productivity of cell lines/processes | 9/21/2018 |
| 242 | Juno Therapeutics Bothell, WA Manufacturing Associate BS in relevant science or engineering discipline Exp: 0-4 yrs |
The primary focus of the Manufacturing Associate role will be cellular therapeutic manufacturing at JuMP during process transfers, routine production, and technology improvements. | 9/21/2018 |
| 243 | Juno Therapeutics Bothell, WA Associate Engineer, Process Engineering MS in biotechnology/ bioprocess engineering Exp: 1 yr |
Process development, optimization and scale up of biotechnological processes (USP and DSP) to produce proteins for our reagents | 9/21/2018 |
| 244 | KEW, Inc Cambridge , MA HISTOLOGY LABORATORY TECHNOLOGIST BS/MS in biological science or other related discipline Exp: 1-4 yrs |
This individual will utilize their experience in order to perform all testing consistent with established procedures and quality standards and processes within the laboratory. | 9/21/2018 |
| 245 | KEW, Inc Cambridge , MA MOLECULAR LABORATORY TECHNOLOGIST BS in science?related field Exp: 1-5 yrs |
The scope of this role will include routine sample prep and processing through our workflow in accordance with our established Technical Operating Procedures. | 9/21/2018 |
| 246 | KBI Biopharma Durham, NC Research Associate/Sr. Research Associate BS/MS in chemistry, biochemistry or related area Exp: 0-2 yrs |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 9/21/2018 |
| 247 | KBI Biopharma Durham, NC Data Reviewer/Scientist I MS in chemistry, biochemistry or related area Exp: 0 yr |
Perform data review for contract services projects, including analytical and formulations programs for monoclonal antibodies, recombinant proteins, peptides, and small molecules in a variety of dosage form such as liquids and lyophilized powders and suspensions for injection, topical gels, and other novel delivery systems. | 9/21/2018 |
| 248 | KBI Biopharma Louisville, CO Research Associate BS Exp: 0-2 yrs |
Responsible for method development of analytical test methods and product characterization. | 9/21/2018 |
| 249 | KBI Biopharma Durham, NC Data Reviewer BS/MS in chemistry, biochemistry or related area Exp: 0-2 yrs |
Perform data review for contract services projects, including analytical and formulations programs for monoclonal antibodies, recombinant proteins, peptides, and small molecules in a variety of dosage form such as liquids and lyophilized powders and suspensions for injection, topical gels, and other novel delivery systems. | 9/21/2018 |
| 250 | KBI Biopharma Durham, NC Process Development Associate-Upstream BS/MS in Chemical Engineering, Biotechnology or related area Exp: 0-2 yrs |
This person will lead and assist in cell culture and harvest of mammalian cell lines (mainly CHO variants) in support of process development, scale-up, and technology transfer to cGMP manufacturing. | 9/21/2018 |
| 251 | KBI Biopharma The Woodlands, TX Cell Based Assay Associate - Quality Control MS in the Life Sciences (biology, immunology, medical technology) Exp: 1 yr |
This individual will conduct cell culture and bioassays in support of product characterization and potency assessment. Requirements of the position include execution and documentation of experimental protocols, and assisting in the qualification and validation of methods. | 9/21/2018 |
| 252 | KBI Biopharma Boulder, CO Manufacturing Associate I/II BS/BA Exp: 0 yr |
Coordinate and perform cGMP manufacturing operations for biopharmaceutical products. Ensure the effective use of material, equipment and personnel while making products with the highest quality. | 9/21/2018 |
| 253 | Kashiv Pharma Bridgewater, NJ R&D Scientist I / II MS in Analytical Chemistry or related Exp: 0-2 yrs |
A Scientist will be a key technical resource responsible for independently developing methods, generating reliable and interpreting data, using analytical instrument that include HPLC, UPLC, GC, UV/Vis, Mass spectrometer, dissolution apparatus and particle analyzer. You will be expected to develop a close working relationship with Technical personnel at all levels within the organization to provide technical support needed in meeting R&D milestones and goals. | 9/21/2018 |
| 254 | Kashiv Pharma Bridgewater, NJ Scientist I - AR&D MS in Analytical Chemistry or related Exp: 0-2 yrs |
A Scientist will be a key technical resource responsible for independently developing methods, generating reliable and interpreting data, using analytical instrument that include HPLC, UPLC, GC, UV/Vis, Mass spectrometer, dissolution apparatus and particle analyzer. You will be expected to develop a close working relationship with Technical personnel at all levels within the organization to provide technical support needed in meeting R&D milestones and goals. | 9/21/2018 |
| 255 | KVK Tech, Inc. Newtown, PA Topical Formulation Associate MS in Chemistry, Biochemistry or Pharmaceutical Sciences Exp: 1-3 yrs |
Person exhibits aptitude in assisting in the development of topical product pharmaceutical formulations, as well as meeting timelines for the department. | 9/21/2018 |
| 256 | KVK Tech, Inc. Newtown, PA Analytical Chemist BS/MS Exp: 1-4 yrs |
Perform analytical testing of raw materials, in-process materials, stability samples, finished products and product development products using different analytical techniques. | 9/21/2018 |
| 257 | KVK Tech, Inc. Newtown, PA QC Document Reviewer BS in Chemistry or a related field Exp: 1 yr |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. | 9/21/2018 |
| 258 | KVK Tech, Inc. Newtown, PA Quality Control Microbiologist BS in Microbiology or related disciplines Exp: 1 yr |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. | 9/21/2018 |
| 259 | KSQ Therapeutics Cambridge , MA Associate Scientist, Immuno-Oncology BS/MS in biology or related discipline Exp: 0-3 yrs |
Assist in querying novel pathways and mechanisms for immunological therapeutic intervention; Support of in vivo animal model experiments. | 9/21/2018 |
| 260 | KSQ Therapeutics Cambridge , MA Senior Associate Scientist/Scientist, Pharmacology BS Exp: 0-3 yrs |
This person will contribute to in vivo pharmacology efforts to support the advancement of our pre-clinical Oncology and Immuno-Oncology small and large molecule pipeline. We are looking for motivated and team-oriented individuals who want to contribute to our growing company. | 9/21/2018 |
| 261 | KSQ Therapeutics Cambridge , MA Associate Scientist/ Scientist, Oncology Drug Discovery BS Exp: 0-3 yrs |
This person will contribute to cell biology and translational efforts for our drug discovery pipeline. This skilled scientist will characterize novel cancer pathways and develop assays for drug targets. She/he must be driven and flexible with the broad number of in vitro, in vivo, and biomarker activities associated with cancer drug discovery. | 9/21/2018 |
| 262 | KSQ Therapeutics Cambridge , MA Associate Scientist/Scientist: Target Discovery BS/MS in cell biology, molecular biology, or a related field Exp: 0-4 yrs |
This person will employ cutting-edge functional genomics technology to identify and validate novel targets in oncology and immuno-oncology. | 9/21/2018 |
| 263 | NemaMetrix Inc. Salt Lake City, UT Genetics Laboratory Technician II BS in Biology or related field Exp: 1 yr |
Manage and maintain appropriate record keeping and related documentation of laboratory work | 9/21/2018 |
| 264 | LATITUDE San Diego, CA Research Associate BS in Chemistry, Pharmaceutical Sciences or Biochemistry Exp: 1-5 yrs |
A successful candidate will possess proficiency in a variety of analytical chemistry techniques including HPLC. | 9/21/2018 |
| 265 | Lampire Biological Laboratories Everett, PA Molecular Biologist BS/MS in Molecular Biology, Immunology, Biochemistry or related scientific field Exp: 1-3 yrs |
Seeking a highly motivated Research Associate I/II with a background in Molecular Biology to assist in the development of new technologies including CRISPR genome engineering and recombinant antibody generation. The successful candidate will be responsible for learning, researching and implementing recombinant DNA approaches to support research team needs, as well as designing work-flows, and assay developmen | 9/21/2018 |
| 266 | Lampire Biological Laboratories Everett, PA Small Animal Technician BS in Life Sciences or equivalent Exp: 1 yr |
The primary responsibility of this individual is to maintain the overall health and well-being of the rabbits including cage and facility maintenance. This would include the feeding and watering of rabbits, administering treatments, as well as swapping, cleaning, disinfecting, and sanitizing all animal housing units and animal facilities. | 9/21/2018 |
| 267 | LakePharma Hayward, CA Associate Scientist, Process Development MS in biochemistry, chemical engineering or related field Exp: 1 yr |
The candidate will provide support to the Process Development group. | 9/21/2018 |
| 268 | LakePharma Belmont, CA Associate Scientist/Scientist BS in Life Sciences or equivalent Exp: 1 yr |
Hybridoma generation, screening, characterization, and maintenance. | 9/21/2018 |
| 269 | Medtronic North Haven, CT Associate Industrial Engineer BS in Industrial or Systems Engineering Exp: 0-2 yrs |
This position provides industrial engineering support for New Product Development initiatives in Medtronic’s Surgical Innovations business unit. This role will support the portfolio of Surgical Innovations projects being led by the R&D centers in North Haven, Shanghai, Woburn, and Trevoux. Team is focused on creating innovative analytic solutions & data visualization to influence and drive sound business decisions related to product life-cycle management, manufacturing strategy, and extended value stream capacity planning. | 9/16/2018 |
| 270 | Medtronic Irvine, CA Process Engineer BS/MS in an engineering discipline Exp: 0-2 yrs |
Supports the manufacture of Medtronic Neurovascular products to ensure operations core metrics of safety, quality, product availability, cost, and organizational excellence. Provides manufacturing floor support, contributes technical expertise, and leads implementation of manufacturing improvements to assigned product lines. | 9/16/2018 |
| 271 | Medtronic Danvers, MA Materials Engineer MS in an engineering discipline Exp: 1 yr |
Provide engineering support in the concept, prototyping, clinical evaluation, process/equipment development and production scale up of new products and components from R&D, Supply Chain, manufacturing transfers and business acquisitions. Provide engineering support in product transfers from R&D to Manufacturing. Provide engineering support in product line transfers from outside facilities to internal manufacturing in Massachusetts. Provide engineering support in product line transfers from current manufacturing to outsourced manufacturing vendors. Provide engineering support scale up of component manufacturing for other businesses within Medtronic. Provide engineering support for development and scale up of low cost manufacturing for legacy product lines. Define equipment, process, material and operator specifications for manufacturing. Approach all engineering activities with the objective to reduce variability in operator, materials, machines and manufacturing processes to improve profitability at the Danvers site. | 9/16/2018 |
| 272 | Medtronic Tempe, AZ Product Engineer MS in Electrical Engineering or equivalent discipline Exp: 1 yr |
This position is with the Released Integrated Circuits (IC) Product Engineering group. This group is responsible for ICs in multiple technologies as they transition from Product Development through obsolescence. There is a tremendous focus on quality and reliability since many of these ICs will be used in Implantable Medical Devices. The group conducts product monitoring ensuring stable supply to our customers and leads cost improvement projects through yield improvements, and cost reduction activities. Additionally, the group also monitors and supports root cause analysis of field returns and product non-conformances to drive product improvements. | 9/16/2018 |
| 273 | Medtronic North Haven, CT Assoc Post-Market Quality Specialist BS in Science, Engineering, Nursing or related field Exp: 0-2 yrs |
The Associate PMV Analyst is responsible for monitoring, tracking, and trending product complaints in order to assure compliance with worldwide regulations and standards. Duties include intake and closure of complaint files and in-depth trend analysis. The candidate must have excellent customer service skills, an analytical mind, and the ability to evaluate and disseminate information from a global perspective. This entry level position requires and eye for detail and excellent organizational skills. | 9/16/2018 |
| 274 | Medtronic Goleta, CA Associate Quality Systems Specialist - Brain Neurosurery BS in Engineering, Quality/Regulatory, or Life Sciences Exp: 1 yr |
The Associate Quality System Specialist is responsible for participating in the development, documentation, maintenance, and improvement of the business’s Quality Management System, including quality policies, processes, procedures and controls that monitor system performance and ensures conformance to established standards necessary to maintain quality of products and sustainable customer satisfaction. The incumbent also will facilitate and participate in the Corrective and Preventive Action (CAPA) and Product Experience (PE) Systems as well as coordinate all audits activities as necessary at MNS in accordance with FDA QSR, ISO 13485, MDD and Canadian Medical Device Regulations. | 9/16/2018 |
| 275 | IDEXX Westbrook, ME Associate Scientist, Cell Culture MS in Biology, Biology or Life Sciences Exp: 1 yr |
You will join a highly energetic group of scientists engaged in the upstream processes of cell culture to produce antigens and antibodies used in in-vitro diagnostic applications. | 9/16/2018 |
| 276 | ICON All US locations, Al Senior Clinical Research Associate BS in life science or related discipline Exp: 1 yr |
As a Senior Clinical Research Associate at ICON, you will work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV, ensuring adherence to applicable regulations and principles of ICH-GCP. We pride ourselves on our supportive company culture, where we work as one team to achieve industry-leading results. | 9/16/2018 |
| 277 | ICON North Wales, PA Clinical Research Associate (II/Sr) BS in life science or related discipline Exp: 1 yr |
You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. | 9/16/2018 |
| 278 | ICON Brentwood, TN CRA II/Senior CRA BS in life science or related discipline Exp: 1 yr |
You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. | 9/16/2018 |
| 279 | ICON Home Based, Ho Clinical Research Associate BS in life science or related discipline Exp: 1 yr |
You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. | 9/16/2018 |
| 280 | ICU med San Clemente, CA R&D Engineer BS in Mechanical, or in a similar technical engineering discipline Exp: 0-2 yrs |
The R&D Engineer is responsible for developing and implementing new products through adherence to established design control processes and good engineering and documentation practices. The key responsibility of this position is the design, development, and improvement of product lines to ensure their efficiency and reliability. The incumbent will be heavily involved with plastics, polymers, molding, medical disposables, plastics engineering, and solid modeling. The R&D Engineer will be expected to interface with customers and suppliers on high-volume disposable medical device design. | 9/16/2018 |
| 281 | Immunomedics Morris Plains, NJ Cell Culture Technologist, Upstream Process & Manufacturing Sciences BS in biology or related discipline Exp: 0-3 yrs |
The Cell Culture Technologist, Upstream Process and Manufacturing Sciences is responsible for participating in the operation of mammalian cell culture processes under cGLP conditions. | 9/16/2018 |
| 282 | Immunomedics Morris Plains, NJ Quality System Specialist BS in Biology/Chemistry Exp: 1-3 yrs |
The Quality Management System Specialist executes daily activities and maintains focuses on the Change Control, CAPA and Risk Management systems. | 9/16/2018 |
| 283 | Immunomedics Morris Plains, NJ Quality Control Analyst-Stability BS in chemistry, biology, pharmaceutical science or related degree Exp: entry-level |
The QC Analyst performs routine sampling, testing, and data reporting and performs support activities such as purchasing, receiving, and general laboratory maintenance as assigned by management. May coordinate with external suppliers of testing services. | 9/16/2018 |
| 284 | Imbed Bio Madison, WI Production Technician, Medical Device Manufacturing BS Exp: 1-4 yrs |
We are looking for a highly motivated Production Technician with experience working in chemical or biological laboratories. Technician will assist Manufacturing team in production of medical devices. Successful candidate will work within a high-energy, small, focused team environment and maintain a strong sense of shared responsibility and shared reward to make work fun and interesting | 9/16/2018 |
| 285 | iFyber Ithaca, NY Research Technician: Microbiology BS in the biological sciences Exp: 1 yr |
The person in this position will support a variety of programs that will require experience and/or the ability to pick up bench skills related to microbiology. | 9/16/2018 |
| 286 | iFyber Ithaca, NY Research Technician: Chemistry BS in the biological sciences Exp: 1 yr |
The person in this position will support a variety of programs that will require experience and/or the ability to pick up bench skills related to chemistry. | 9/16/2018 |
| 287 | Illumina San Diego, CA Mfg/Ops Quality Engineer 1 BS in an engineering or scientific discipline Exp: 0-3 yrs |
This position will have direct interaction with Manufacturing operations and Lifecycle Management group to support manufacturing sustaining activities. The position may have responsibility of Sustaining Quality support for more than one manufacturing area. Knowledge/experience with microarrays and DNA sequencing is preferred. | 9/16/2018 |
| 288 | Illumina San Diego, CA Equipment Engineer 1 BS in Electrical or Mechanical Engineering preferred or related discipline Exp: 1-3 yrs |
The Equipment Engineer I will be responsible for integration, implementation, service and maintenance of laboratory equipment. This will include automation and instrumentation in support of a Clinical, Research and various GxP Laboratories. This includes installation, configuration and repair of equipment, integrating equipment with information systems and validation and verification of the equipment in accordance with CLIA, cGMP and/or GLP guidelines. Responsible for preparing maintenance and operation protocols for licensed Clinical Laboratory Scientist review while following the manufacturers and the Equipment Quality system documents. The Equipment Engineer will trouble-shoot problems with equipment and conduct or coordinate required repairs and complex maintenance tasks. The Equipment Engineer will provide input regarding the selection of new equipment and support of new processes as it pertains to the site infrastructure. | 9/16/2018 |
| 289 | Illumina San Diego, CA Associate Scientist 1 BS/BA in Chemistry, Biochemistry or Material Sciences Exp: 1-3 yrs |
We are looking for a Associate Scientist 1 with experience in Chemistry, Biochemistry, and/or Materials Science to join the Chemistry and Materials group within Consumables Development Department. As a successful candidate you will work in a dynamic, team-oriented environment to create genomic analysis consumable devices that enable leading-edge medical research. You will be a key contributor within integrated and multidisciplinary teams developing new, and improving existing nucleic acid sequencing and sample preparation technology platforms. | 9/16/2018 |
| 290 | Illumina San Diego, CA Supplier Quality Engineer 1/2 BS in Engineering, Life Sciences, or related field Exp: 0-3 yrs |
This position is responsible for Supplier Quality activities that improve, monitor and measure Illumina’s compliance with the Quality System Regulations, Illumina Quality policies, FDA regulations and ISO standards as well as Illumina product quality for current operation and compliance objectives. | 9/16/2018 |
| 291 | Illumina San Diego, CA Research Associate 1 – Reagents Development BSc/MS in Biochemistry, Molecular Biology, Chemistry, Bioengineering, or related disciplines Exp: 1-2 yrs |
As a Research Associate 1 at Illumina, you will work in a dynamic, collaborative environment and help the reagents/assay team in the development of core platform consumables to create cutting edge and robust new products. You will work in a fast-paced environment with multi-disciplinary teams, design and execute experiments, analyze data and communicate results and progress. Your work on reagent formulation, characterization, stability optimization and workflow development will enable project teams to make critical decisions during a product development cycle. | 9/16/2018 |
| 292 | Illumina San Diego, CA Associate Scientist I - IVD Development MS Exp: 1 yr |
As an Associate Scientist within Illumina’s Clinical Genomics Product Development organization, you will work as part of a multi-disciplinary team to ensure clinical products meet their stated claims, continuously meet global regulatory standards, meet customers’ expectations, and remain competitive in the markets they serve. | 9/16/2018 |
| 293 | Illumina San Diego, CA Integration Research Associate - 1 BS in Bioengineering, Chemical Engineering, Biochemistry, Analytical Chemistry, Biology Exp: 0-2 yrs |
As a Research Associate 1 you will work in a dynamic, team-oriented environment and help improve genomic analysis tools used in cutting edge research. Working with Illumina’s Chemistry Development, Consumables, Software, Field, and Engineering teams, you will be responsible for investigating and resolving system level platform issues and supporting system verification and validation activities for planned platform changes. | 9/16/2018 |
| 294 | Incyte Wilmington, DE Drug Safety Coordinator BS in a science or healthcare related discipline Exp: 1 yr |
Drug Safety Coordinator | 9/16/2018 |
| 295 | InBios International, Inc. Seattle, WA Research Associate I BS in a biological science Exp: 1-2 yrs |
A successful candidate will enjoy working in a fast-paced environment and exhibit excellent interpersonal skills, the flexibility to adapt to changing priorities, and a firm scientific foundation to understand ongoing diagnostic R&D and associated studies. | 9/16/2018 |
| 296 | Impel NeuroPharma Seattle, WA CLINICAL TRIAL ASSOCIATE BS in a science, health, or related field Exp: 1-3 yrs |
This (in-house) position will provide support for all clinical activities, ensuring the successful planning, execution and completion of clinical trials as well as support for setting up and smooth running of a clinical operations department. | 9/16/2018 |
| 297 | Inovio Plymouth Meeting, PA Clinical Trial Associate - Plymouth Meeting BS/MS in Biology, Immunology, Bioengineering, Cell or Molecular Biology Exp: 0-1 yr |
Sets-up and maintain Trial Master File (TMF) including project documentation files, investigator files, study books, and project databases on more complex projects | 9/16/2018 |
| 298 | Inova Diagnostics, Inc. San Diego, CA Chemist I- MTS BS/BA in the biological, chemical or related sciences Exp: 0-1 yr |
Assists technical support with investigation of complaints according to established procedures. Assists with the design changes of current products according to established procedures by improving or developing new procedures. Major development activities include assistance with process validation, equipment validation and evaluation of vendor samples. | 9/16/2018 |
| 299 | Inova Diagnostics, Inc. San Diego, CA Chemist I- Bioflash BS/BA in the biological or related sciences Exp: 1-2 yrs |
Participates in the preparation of autoimmune diagnostic products, utilizing the Bioflash technology platform, following established procedures. Major duties include Bioflash bead and reagent preparation activities and the preparation of controls and conjugates for the Bioflash product lines. | 9/16/2018 |
| 300 | Inova Diagnostics, Inc. San Diego, CA Chemist I- Research & Development BS/BA in the biological or related sciences Exp: 0-1 yr |
Assists with the development of new or improved autoimmune diagnostic assays according to established procedures. Major research and development duties include assistance with reagent formulation and optimization of existing formulations. Additional duties involving organizing and facilitating timely progress and completion of projects will be assigned. | 9/16/2018 |
| 301 | Inova Diagnostics, Inc. San Diego, CA Chemist I- IFA Slides Manufacturing BS/BA in the biological or related sciences Exp: 0-1 yr |
Assists with preparation of autoimmune diagnostic Immunofluorescence Assay (IFA) cell culture slide products according to established procedures. Major duties include mammalian cell culture, immunofluorescence cell suspension and slide preparation activities. | 9/16/2018 |
| 302 | Intuity Medical, Inc. Fremont, CA Chemistry Technician - Temporary BS in chemistry, biochemistry, life science or related discipline Exp: 1 yr |
Responsible for executing assigned experiments and tasks to support the development of Intuity Medical new blood glucose monitoring system. Under the direction of senior staff, the chemistry technician works independently and within cross-functional teams to carry out project tasks related to reagent formulation, method development and validation, feasibility study, material evaluation, selection and validation, stability study as well as performance testing of built cartridges and meters. | 9/16/2018 |
| 303 | intrexon Davis, CA LABORATORY OPERATIONS TECHNICIAN BS in biology Exp: 1-2 yrs |
The Laboratory Operations Technician will be responsible for providing a range of services to support intrexon’s AgBio Division. As the foundation of research operations, lab support is critical to processes in all labs and this position will interact with scientists across all functions. | 9/16/2018 |
| 304 | intrexon South San Francisco, CA RESEARCH ASSOCIATE I OR II, RATIONAL STRAIN ENGINEERING BS in molecular biology, microbiology, genetics, chemical engineering or a related field Exp: 1-3 yrs |
We are seeking a talented Research Associate (level determined by candidate experience), Rational Strain Engineering for our Industrial Products Division (IPD) located in South San Francisco. The candidate will have strong molecular/microbiology biology skills and familiarity with micro-cultivation of microorganisms. Appropriate candidates will have strong background in synthetic biology and microbiology and thrive in a dynamic team environment. | 9/16/2018 |
| 305 | intrexon South San Francisco, CA RESEARCH ASSOCIATE I OR II, STRAIN ENGINEERING BS in molecular biology, microbiology, or a related field Exp: 0-3 yrs |
We are seeking a talented Research Associate (level determined by candidate experience), Strain Engineering for our Industrial Products Division (IPD) located in South San Francisco. The Research Associates will be key players in our high throughput strain construction operations. | 9/16/2018 |
| 306 | Integrity Bio, Inc. Newbury Park, CA Research Associate BS in biochemistry, analytical chemistry, biological sciences, or related Exp: 1-5 yrs |
Assemble study designs, perform laboratory experiments, organize data, and analyze results under minimal supervision. | 9/16/2018 |
| 307 | Integrity Bio, Inc. Newbury Park, CA Manufacturing Associate/ Sr. Associate BS Exp: 1-3 yrs |
Manufacturing Associate will be responsible for the manufacture of pre-clinical/clinical products | 9/16/2018 |
| 308 | Integrity Bio, Inc. Newbury Park, CA Quality Assurance Associate I BS Exp: 1 yr |
Formatting of documents, publishing, completing change control process; Document upload into training system and course creation. | 9/16/2018 |
| 309 | Integra LifeSciences Austin, TX LABELING ASSOCIATE BS Exp: 1-3 yrs |
Support strategic product launches and ongoing maintenance of existing products by coordinating the collection, creation, approval, and implementation of core product labeling, surgical techniques and instructions for use (IFU) | 9/16/2018 |
| 310 | Integra LifeSciences Mansfield, MA QUALITY ENGINEER BS in Engineering or related technical/scientific field Exp: 1 yr |
The position will support improvements of existing products as part of the design change process, support supply chain concerns as well as design related aspects of product and process transfers between manufacturing sites. This position will have responsibility for executing base business design change projects to ensure the highest levels of product quality to the end customer. | 9/16/2018 |
| 311 | Integra LifeSciences Boston, MA QA SPECIALIST BS Exp: 1-3 yrs |
Writes and revises operating procedures; Conducts training for staff at all levels as it relates to quality systems. | 9/16/2018 |
| 312 | Intuitive Sunnyvale, CA Project Engineer BS in Biomedical, Electrical, Mechanical Engineering, or Computer Science Exp: 1-3 yrs |
The Project Engineer (PE) will support the Training Technologies staff in all facets of product lifecycle management including new product development, ongoing product improvement, product launches and customer and sales support. These projects relate to the core technologies in simulation and remote collaboration. The Project Engineer will support the concurrent operations of the Training Technology projects. The Project Engineer will support the collection and translation of customer feedback into prioritized product enhancement ideas for development and help create market requirements. The PE will support development of product training and product marketing collateral and will provide assistance to customers and fields sales. | 9/16/2018 |
| 313 | Syneos Health NA, PA Quality Analyst I BS/MS in biological or chemical sciences or equivalent Exp: 0-1 yr |
Perform aseptic sampling Pilot Plant critical utilities and controlled environment | 9/16/2018 |
| 314 | GSK Conshohocken, PA Plant Engineer (Mechanical) BS in Engineering Exp: 1-3 yrs |
Mechanical and utility system operational authority for the biopharmaceutical process facility. Plans and implements the operation, modifications to, and maintenance of mechanical and utility systems (HVAC, Boilers, Chillers, Cooling Towers, Purified Water Systems, Compressed Air/Gas, CIP Skids) and their distribution. Also responsible for the maintenance and improvement of broader site architecture and facilities. | 9/8/2018 |
| 315 | GSK St Louis, MO QC Chemist BS/BA Exp: 1 yr |
The main purpose of this job is to perform routine analytical testing on raw materials, finished goods, stability and other samples as needed. It is also important to participate in OOS, investigations, audits, and cross functional improvement teams to provide analytical expertise. | 9/8/2018 |
| 316 | GSK Collegeville, PA Medicinal Chemist MS Exp: 0-5 yrs |
This individual will plan and implement efficient synthetic routes to complex molecules of interest both independently and under guidance, applying state of the art purification, and characterization techniques for lead optimization and SAR generation. | 9/8/2018 |
| 317 | GSK Rockville, MD Biopharmaceutical Manufacturing Associate II BS Exp: 0 yr |
Performs all production operations in the area of assignment within the Rockville Manufacturing facilities. Support Start-up/changeovers/tech transfer activities and perform production operations in areas assigned. Duties include: preparation of buffers and medias and other solutions, following written procedures and batch records. Operate process equipment such as tanks, CIP/SIP skids, agitators, filtration devices, autoclaves, glass washers, integrity testing and other small equipment following a high standard of GMP compliance and SOP and BRs as written. | 9/8/2018 |
| 318 | GSK Marietta, PA Process Equipment Engineer BS in Engineering Exp: 1 yr |
This role will provide technical expertise within the Formulation, Filling and Lyophilization value stream, to lead troubleshooting exercises and implement continuous improvement projects to achieve business objectives for supply, quality, EHS and cost. | 9/8/2018 |
| 319 | Gilead Sciences, Inc. Foster City, CA Research Associate, Medicinal Chemistry BS/MS degree in Chemistry. Exp: 0 yr |
As Research Associate, you will participate in an integrated research team aimed at discovering and synthesizing novel chemical entities for various targets. Under the guidance of an experienced Research Scientist you will be responsible for planning, designing and executing multi-step synthesis pathways toward key target molecules, followed by purification and compound characterization. Communication of results, methods and conclusions to departmental colleagues is essential. Collaboration with colleagues across disciplines, participation in project team meetings, and contribution toward creative problem solving are all encouraged. | 9/8/2018 |
| 320 | Gilead Sciences, Inc. Oceanside, CA Sr Res Assoc I - Protein Purification Process Development MS Exp: 0 yr |
Gilead Sciences is seeking a Sr Research Associate I with experience in protein purification process development to support operations at our biologics development and manufacturing site in Oceanside California. | 9/8/2018 |
| 321 | Ginkgo BOSTON, MA Research Associate - NGS BS/MS in biology, biochemistry, bioengineering, molecular biology, or related fields Exp: 1 yr |
Operate high-throughput semi-automated NGS processes (DNA and RNA seq) | 9/8/2018 |
| 322 | Ginkgo BOSTON, MA Research Associate - Protein Engineering BS/MS in biology, biochemistry, bioengineering, molecular biology, or related fields Exp: 1 yr |
Enzyme purification and characterization; Data analysis; Automate protocols. | 9/8/2018 |
| 323 | Genscript Piscataway, NJ Analytical Biochemist MS in Molecular Biology, Biochemistry or Chemistry Exp: 6 months |
To independently perform essential biochemical screening and analytical experiments, and interpret analytical data in accordance with the relevant SOPs. | 9/8/2018 |
| 324 | FUJIFILM Diosynth Biotechnologies U.S.A., Inc. Morrisville, NC Associate Scientist, Analytical Methods Transfer BS Exp: 1 yr |
The Analytical Methods Transfer group is seeking an energetic Associate Scientist with protein chemistry experience to become an integral member of a high performing method transfer team supporting protocol based activities including technical transfer of methods from donor labs as well as training of colleagues for internal transfer, and qualification, validation and verification of methods. The successful candidate will primarily execute biochemistry based techniques such as UPLC/HPLC (SEC, IEX, RP, glycan, affinity, etc), capillary electrophoresis (icIEF, CE-SDS), gel electrophoresis, western blot, plate based assays and spectrophotometry (SoloVPE) for the characterization and testing of recombinant protein pharmaceuticals. | 9/8/2018 |
| 325 | FUJIFILM Diosynth Biotechnologies U.S.A., Inc. College Station, TX Analytical Development – Technician II BS in Biology, Biotechnology, Biochemistry, Analytical Chemistry, or other related field Exp: 0 yr |
Routinely follow established analytical protocols and SOPs to produce highly reproducible results； Assist with preparations of buffer solutions and perform other lab duties related to methods development. | 9/8/2018 |
| 326 | FUJIFILM Diosynth Biotechnologies U.S.A., Inc. College Station, TX Associate Scientist – Upstream Process Development MS in Chemistry, Biology, Life Sciences or related field Exp: 1 yr |
Assist in the development, optimization, and scale-up of cell- and virus/viral vector-based processes including cell banking, adherent and suspension cell culture, cell counting and metabolite analysis. | 9/8/2018 |
| 327 | Charles River Woburn, MA Laboratory Technician II BS in biochemistry, chemistry or related discipline Exp: 1-3 yrs |
In this position, the Laboratory Technician II will perform analytical methods independently as specified in standard in-house SOPs and Client Test Methods and other written procedures. Under direct supervision, perform method development work as assigned. In addition, perform reagent preparation and laboratory maintenance/monitoring, prepare reagents and test samples, and analyze data and report results of experiments and procedures. For both GMP and R&D grade routine testing, generate analytical data and technical report(s) on-time with respect to internal and client deadlines and maintain a weekly schedule to ensure all timelines are met. May be required to co-ordinate laboratory functions such as updating of sample-tracking databases and maintenance of consumable or HPLC column inventory(s). Must comply with all pertinent regulatory standards regarding environs, equipment and testing services. Make detailed observations and maintain clear, detailed, accurate and timely documentation of all laboratory work. Perform assay and equipment troubleshooting under guidance from senior members of the group. Compose high quality written reports such as deviation reports and change control documentation under guidance. Review and edit SOPs, protocols and testing documentation. | 9/8/2018 |
| 328 | Charles River Mattawan, MI Veterinary Assistant - Office of Animal Care BS Exp: 0-2 yrs |
A Veterinary Assistant is responsible for: providing animal care and welfare compliance in the form of basic medical treatments and emergency response as directed by staff veterinarians; assisting the veterinary staff in general husbandry oversight of all laboratory animals in accordance with Institutional Animal Care and Use Committee (IACUC) policies, and animal welfare standards and regulations by Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC), United States Department of Agriculture (USDA), and Public Health Service – Office of Laboratory Animal Welfare (PSH-OLAW); and performing assigned basic technical and administrative functions within the guidelines/requirements outlined in a protocol or Standard Operation Procedure (SOP) in order to support the evaluation of a test article. | 9/8/2018 |
| 329 | Charles River Mattawan, MI Research Associate - Bioanalytical MS/BS/BA Exp: 0-2 yrs |
The Research Associate in Bioanalytical is responsible for: following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. | 9/8/2018 |
| 330 | Charles River Spencerville, OH Formulations Technician I BS Exp: 0-1 yr |
The Formulations Technician will prepare routine test article/substance dosage solutions and/or suspensions in accordance with Standard Operating Procedure (SOP) and Good Laboratory Practice (GLP) guidelines under direct supervision, and may serve as primary technician on studies that tend to be routine, less complex studies. In a typical day, you will perform standardized preparation procedures and calculations, ensure record keeping is consistent and correct, complete documentation for the use of all test articles and vehicles/reagents to ensure consistency and correctness, and receive incoming test articles/substances and reagents. You will also be expected to ensure formulations samples are collected, packaged, and shipped properly and on time, as well as ensure the test articles from assigned completed studies are returned to the sponsor or reassigned to another protocol. Additionally, you will respond to Quality Assurance (QA) audits of preparation procedures and calculations on assigned studies, ensure data sheets are complete and submit them for review, assist in reviewing data, prepare labels and samples, maintain cleanliness and general appearance of the laboratory, ensure the laboratory is stocked and assist in maintaining current inventory of reagents, test articles, vehicles, and samples, utilize appropriate Quality Control (QC) procedures/measures to help verify the accuracy and correctness of data prior to submission to internal QA, and perform all other related duties as assigned. | 9/8/2018 |
| 331 | Charles River Mattawan, MI Research Associate - Test Material Control BS/MS Exp: 0-6 months |
The Research Associate in Test Material Control (TMC) 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. | 9/8/2018 |
| 332 | Gritstone Oncology Cambridge, MA RESEARCH ASSOCIATE/SENIOR RESEARCH ASSOCIATE, NGS AND MOLECULAR BIOLOGY BS/MS Exp: 1 yr |
The primary role of the RA/SRA is to be responsible for execution of next-generation sequencing laboratory workflows to support scientific research objectives at Gritstone Oncology | 9/8/2018 |
| 333 | GreenLight Biosciences Medford, MA Research Associate (I/II/III/Senior) and/or Postdoctoral Engineer – Process Development BS/MS in Chemical Engineering, Biological Engineering, Molecular Biology, Biochemistry or equivalent Exp: 0-5 yrs |
The successful candidate will be involved in high throughput screening of strains/cell free reactions, and/or process development of commercially relevant fermentations/cell free reactions in 10 mL to 150 L reactors. The successful candidate will work hands-on in small teams to execute fermentation/cell free bioprocessing and other associated bioprocess unit operations with a high degree of excellence, in a fast-paced environment. A high degree of flexibility, creativity and initiative is essential for success. Strong technical, organization, communication, documentation, inter-personal, and trouble shooting skills are essential. | 9/8/2018 |
| 334 | GRAIL Menlo Park, CA Clinical Project Assistant BS/BA in Life Science or related discipline Exp: 1 yr |
The Clinical Project Assistant will provide key support to the GRAIL Clinical Operations group in clinical trial conduct for diagnostic product development. The key accountability includes the coordination of activities associated with the setup and management of a clinical trial in compliance with SOPs, regulations, and ICH/GCP guidelines. | 9/8/2018 |
| 335 | GRAIL Menlo Park, CA Process Monitoring Associate BS/BA in Molecular Biology or a related field Exp: 1 yr |
The Process Monitoring Associate will assist in monitoring Clinical Lab assay activities to sustain high quality data generation and resolution of production assay issues. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multi-task, be flexible with tasks and schedules, and the ability to work independently in a team environment. | 9/8/2018 |
| 336 | GRAIL Menlo Park, CA Research Associate 2 MS in Molecular Biology, Biochemistry, or relevant disciplines Exp: 0-2 yrs |
GRAIL is seeking a Research Associate 2 who will be responsible for planning and execution of experiments and data analysis with the guidance of scientists and senior lab members. The ideal candidate is a detail-oriented, strong team player with hands-on experience in NGS assay development and genomic data analysis. | 9/8/2018 |
| 337 | Gore Flagstaff, AZ Industrial Engineer- BS in supply chain, industrial engineering, systems engineering, or business analytics Exp: 1 yr |
In this role, you will support medical-device manufacturing operations, drive improvement projects, and partner with manufacturing and engineering teams to manage projects and execute on initiatives that support key business priorities. You will build influential relationships with manufacturing teams across multiple shifts, establishing a strong partnership with all manufacturing support functions, including engineering, planning, internal suppliers, quality assurance, maintenance, health and safety, and finance. You will also collaborate with other industrial engineers across the organization to share best practices and establish IE functional excellence. | 9/8/2018 |
| 338 | Goodwin Biotechnology Inc. Plantation, FL Upstream Manufacturing Associate BS in biological or physical science Exp: 1-2 yrs |
Assists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. | 9/8/2018 |
| 339 | AURIS Redwood City, CA Test and Automation Engineer BS/MS in mechanical, biomedical, or similarly related engineering field Exp: 0-3 yrs |
As an Instruments and Accessories Test Engineer, you will contribute to the development of various instruments and accessories used with a robotic platform for surgical applications, focusing on design support, testing, automation, and analyzing instruments and accessories. This position reports to the Test Engineering Department Lead. | 9/8/2018 |
| 340 | Guardant Health Redwood City, CA Research Associate, Technology Development BS/MS in Molecular Biology, Genetics, Biochemistry, Bioengineering or related field Exp: 0-5 yrs |
As a Research Associate supporting product and technology development, you will work with members within the team and interface with multiple teams including process engineering, clinical operations, research operations, IVD team members, and bioinformatics. You will be hands on in the lab and be required to design, implement, and validate new technologies related to liquid biopsy sequencing assays for the early detection, treatment, and monitoring of all cancer types. | 9/8/2018 |
| 341 | Hemacare Corporation Van Nuys , CA Research Associate I BS in Biological Sciences Exp: 1 yr |
This position is responsible for the evaluation of human blood products for manual or automated cell isolations, product manufacturer, and cell culture. Perform QC testing and create a certificate of analysis (COA) for products manufactured. Record isolation details on a processing worksheet using good documentation practices. Operate flow cytometer and basic lab equipment. | 9/8/2018 |
| 342 | Medtronic Portsmouth, NH Supplier Quality Engineer MS Exp: 0 yr |
This position has the responsibility to perform Quality Engineering functions including inspection and testing, procedure writing, statistical analysis of quality data, supplier qualification and performance monitoring and reviewing and approving design changes, | 9/8/2018 |
| 343 | Medtronic North Haven, CT Test Engineer (Instrumentation Lab) BS in Engineering, Science or Technical discipline Exp: 1 yr |
A new product development team for the Surgical Innovation business in Medtronic’s Minimally Invasive Therapies Group (MITG) Business Unit is seeking a Test Engineer. The Test Engineer shall support test activities to best meet the project’s requirements. This position will be a part of a R&D Systems Engineering team and will interface with cross-functional team members. | 9/8/2018 |
| 344 | Medtronic Miami Lakes, FL Quality Engineer MS Exp: 0 yr |
Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. | 9/8/2018 |
| 345 | Medtronic Plymouth, MN Associate Process Development Engineer BS in Engineering Exp: 1 yr |
Partners with Design Engineering to identify Design for Manufacturability and Assembly targets; Creation and execution of process characterization and validation protocols. | 9/8/2018 |
| 346 | Medtronic Brooklyn Center, MN Assoc Manufacturing Engineer MS Exp: 1 yr |
The Associate Manufacturing Engineer is responsible for the evaluation, analysis, and implementation of projects driving cost reduction of manufacturing processes that provide implantable components to finished devices. This position interacts closely with the Operations team as well as several engineering disciplines such as Process Development, Quality, Reliability Engineering, and Regulatory Affairs. Additionally, this position requires problem solving skills and technical knowledge (Lean, DMAIC) and the ability to manage complex projects to a successful and timely conclusion. | 9/8/2018 |
| 347 | Medtronic Northridge, CA Chemist/Materials Engineer MS in Materials Science, Chemistry, Physical Chemistry, Polymer Chemistry, Biochemical/Chemical Engineering or related discipline Exp: 0 yr |
We are looking for a Scientist/Engineer with a strong foundation in chemistry, materials science and/or polymer science to join our team. In collaboration with internal and external partners/vendors, the candidate will plan, initiate and execute studies aimed at improving the biocompatibility of existing continuous glucose sensors and developing various chemistries for next generation sensor technology platforms. Strong organizational and communication skills are required to collaborate with other staff and complete required activities in a timely manner. The individual must be able to handle multiple competing priorities in a fast-paced environment. | 9/8/2018 |
| 348 | Medtronic Fridley, MN Quality Systems Specialist MS Exp: 0 yr |
This position will be primarily responsible for supporting the development, documentation, maintenance and improvement of the site Quality Management System. This position will work closely with Quality Systems leadership (Process Area Leads) and Subject Matter Experts (Process Owners) to ensure the Quality System and processes are efficient, and compliant to internal and external requirements. | 9/8/2018 |
| 349 | Hovione East Windsor, NJ Associate Quality Assurance Specialist BS in Chemistry/Science of Chemical Engineering Exp: 1-2 yrs |
The Quality Assurance Associate Specialist promotes high quality standards and a continuous improvement culture within the Quality area of the New Jersey site in order to ensure that these are aligned with applicable quality regulations and the company's high quality standards. This role provides support in achieving the department objectives and supports the cGMP programs (i.e. validation, qualification, stability, and environmental control). | 9/8/2018 |
| 350 | Hovione East Windsor, NJ Analytical Chemist BS in Chemistry, Pharmacy or related field Exp: 1 yr |
The Analytical Chemist will provide analytical support to all projects guaranteeing that development analytical tasks are accomplished within the time frame defined and according with the scope and GMP requirements. | 9/8/2018 |
| 351 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in the field of Engineering, preferably Chemical Engineering Exp: 1-2 yrs |
The Process Technician will support the installation and qualification of a GMP continuous tablet manufacturing line, highly automated, with Process Analytical Technology enabled control. This position will also support the development and manufacturing activities for drug product and formulation development projects. | 9/8/2018 |
| 352 | Hovione East Windsor, NJ QC Analyst (QC) MS Exp: 1 yr |
The Quality Control Analyst will be responsible for carrying out analytical testing on Raw Materials, In-Process Materials and Finished Products; and for providing technical support as required by management. | 9/8/2018 |
| 353 | Hovione East Windsor, NJ Quality Control Peer Reviewer BS in Chemistry or related field Exp: 1-2 yrs |
The Quality Control Peer Reviewer performs all activities within Quality Control in compliance with Corporate Operating Procedures (COP), Standard Operating Procedures (SOP), Internal Operating Procedures (IOP), and Federal Food and Drug Administration (FDA), International Conference on Harmonization (ICH), Occupational Safety and Health Administration (OSHA), and Environmental Protection Agency (EPA) requirements. They will also perform QC peer reviewing on all relevant records and analytical data in accordance with Operating Procedures (COP), Standard Operating Procedures (SOP), and Internal Operating Procedures (IOP). They will carry out the analytical review of QC analyses, LIMS authorization of analytical tests and QC release of raw materials, in-process controls, packaging materials, intermediates, and environmental tests | 9/8/2018 |
| 354 | HemoSonics, LLC Durham, NC Quality Associate BS Exp: 1-3 yrs |
Will be resonsible for reviewing manufacturing records for accuracy and completeness to ensure compliance as well as timely release. | 9/8/2018 |
| 355 | Hill-Rom Skaneateles Falls, NY Optics Engineer I BS in Optical Engineering or Imaging Science Exp: 0-2 yrs |
This role will provide optical engineering support to the product development teams tasked with the design of new products within R&D. This role will ensure effective resolution to design related issues with Welch Allyn products, develop product changes to grow the business, ensure compliance with product related standards, and implement continuous improvements in the design of existing products. | 9/8/2018 |
| 356 | Hill-Rom Skaneateles Falls, NY Welch Allyn Engineer I Manufacturing BS in relevant Engineering discipline Exp: 0-2 yrs |
As an Engineer I in the Manufacturing Engineering Department you will support several manufacturing assembly lines within the Final Assembly Dept. You will partner with cross-functional operations team members (i.e. Production Supervisor, Quality Assurance Engineer, and Materials Planning) to effectively identify, investigate and resolve manufacturing process related issues. In addition, you will drive continuous improvement initiatives in support of departmental, site and corporate objectives for Safety, Quality, Delivery, Productivity, and Cost performance. | 9/8/2018 |
| 357 | Hikma Pharmaceuticals PLC Cherry Hill, NJ Quality Lab Assoc I (EM) BS/BA in Microbiology or Biology Exp: 0-2 yrs |
Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. | 9/8/2018 |
| 358 | Hikma Pharmaceuticals PLC Cherry Hill, NJ Qual Lab Assoc II-Chem MS in Chemistry, or Biological Sciences Exp: 0-3 yrs |
Perform functions of the Chemistry Laboratory and conduct chemical and physical analyses on pharmaceutical products through all stages of the manufacturing process from incoming components and raw materials to finished goods and stability. Execute process and cleaning validation and/or test method validation under the direction of supervision. Write/revise standard operating procedures, forms and exception reports. The duties also include equipment maintenance and LIMS management | 9/8/2018 |
| 359 | Charles River Malvern, PA Sample Processing and Materials Technician BS/BA Exp: 1-3 yrs |
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 activities related to log in, sample processing, storage, shipping of stored materials and client support. | 9/3/2018 |
| 360 | Charles River Malvern, PA Technician I Mammalian Cell Banking BS/BA Exp: 0-2 yrs |
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 cell banking and vaccine preparation activities. | 9/3/2018 |
| 361 | Charles River Malvern, PA Technician I Microbial Cell Banking BS/BA Exp: 0-2 yrs |
Under direct supervision, responsible for performing basic daily laboratory and clean room tasks as they relate to the operations performed within the Microbial Cell Banking group of the Manufacturing department. | 9/3/2018 |
| 362 | Charles River Mattawan, MI Research Technician 1 - Animal Services BS/BA Exp: 0-2 yrs |
A Research Technician 1 is responsible for providing humane care to all laboratory animals and to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound | 9/3/2018 |
| 363 | Charles River Frederick, MD Research Associate I BS/BA Exp: 0-2 yrs |
Assist scientific staff by working under general guidance/supervision on basic scientific support, report development, regulatory compliance, and research. | 9/3/2018 |
| 364 | Charles River Worcester, MA Associate Scientist BS/BA Exp: 1-3 yrs |
This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices. The position is hands-on, working in close cooperation with and under the guidance of more senior staff members in a fast-paced environment where a commitment to teamwork, quality data and speed is essential. | 9/3/2018 |
| 365 | Charles River King of Prussia, PA Technician II Cell Culture BS in biology or related discipline Exp: 1-2 yrs |
Perform daily laboratory tasks and interpret data related to cell culture and media preparation. | 9/3/2018 |
| 366 | Ferring Pharmaceuticals Parsippany, PA Technician, QC Micro BS/MS in Biology or other related Exp: 1 yr |
To perform laboratory QC Microbiological testing for in-process and finished product, water sampling testing, and routine and batch processing environmental monitoring in aseptic classified cleanrooms. | 9/3/2018 |
| 367 | Emergent BioSolutions Gaithersburg, MD Associate Scientist-Temporary BS Exp: 1 yr |
The Associate Scientist will develop and perform ELISA and other immunological assay procedures to advance early stage concepts within the Company including review of technical procedures and study protocols, writing portions of study reports and completion of data analyses by manual methods as well as electronic methods to meet the evolving needs of the Company. | 9/3/2018 |
| 368 | Emergent BioSolutions Baltimore, MD Analyst I,Training BS Exp: 0-2 yrs |
Provide oversight and support of document and records management in Document Control using company procedures and regulations. Provide support for Global Document Management System project (Veeva). | 9/3/2018 |
| 369 | Emergent BioSolutions , MD Associate, Tech Transfer Process-TEMP BS in Chemical Engineering, Biology, Chemistry, or a related field Exp: 1 yr |
The Tech Transfer Process (TTP) Associate will support process validation activities as a member of the Manufacturing Science & Technology (MS&T) Team. S/He will have the opportunity to work on multiple projects ranging from process development studies through process performance qualifications. Two key responsibilities of the TTP Associate are data entry and assisting with the preparation of technical documents (e.g., batch records; protocols; reports). The TTP Associate may also have the opportunity to perform benchtop testing in a process development lab. The ideal TTP Associate will have GMP experience, preferably in process validation, and can demonstrate exceptional attention detail. | 9/3/2018 |
| 370 | Foundation Medicine Cambridge, MA Laboratory Operations Assistant I BS in a Biological or Life Science Exp: Entry level |
This position may include equipment maintenance and reagent preparation in addition to other tasks in a highly complex clinical diagnostic laboratory. | 9/3/2018 |
| 371 | Foundation Medicine Morrisville, NC Laboratory Operations Assistant BS in biological science Exp: 0-1 yr |
The Laboratory Assistant will be responsible for laboratory documentation and quality control activities in the Accessioning, Histology and IHC laboratories. Data verification will be performed both on paper documentation and in LIMS and other computer systems. The assistant will also be responsible for performing miscellaneous laboratory duties | 9/3/2018 |
| 372 | Fluke Corporation Everett, WA Manufacturing Engineer- Thermography BS in Mechanical Engineering, Manufacturing Engineering, Manufacturing Engineering Technology or equivalent Exp: 0-2 yrs |
As a Manufacturing Engineer with Fluke Electronics you will be tasked with analyzing, developing, implementing and maintaining methods, manufacturing operation sequences, specifications, and equipment requirements for production/assembly of new and existing products. Assist new product introduction to manufacturing and released product support. Through these activities metrics will improve in such areas as safety, quality, cost, and productivity to name a few. | 9/3/2018 |
| 373 | GeneDx Gaithersburg, MD DNA Sequencing Technician BS in Biology, Biochemistry, or related-field Exp: 1-3 yrs |
A GeneDx DNA Sequencing Lab Technician in the Sanger Sequencing Laboratory performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 9/3/2018 |
| 374 | GeneDx Gaithersburg, MD Laboratory Applications Specialist BS in Biology/Biochemistry/Genetics/Engineering Exp: 1 yr |
The Lab Application Specialist/Automation Specialist will work with robotics and automation systems in our DNA sequencing labs. The successful candidate will be a member of the Bioinformatics department, with a focus on genomics and high throughput sequencing. Responsibilities will include projects ranging from technical support to workflow development for several robotic platforms, such as Hamilton, Caliper/Perkin Elmer, Beckman, Qiagen, etc. | 9/3/2018 |
| 375 | GeneDx Gaithersburg, MD MicroArray Lab Technician BS in Biology, Biochemistry, or related-field Exp: 0-1 yr |
A GeneDx MicroArray Lab Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 9/3/2018 |
| 376 | GeneDx Gaithersburg, MD Bioinformatics Developer/Engineer BS Exp: 1 yr |
The Bioinformatics Developer/Engineer supports the development of assays and clinical data analysis tools for the BioReference-GenPath division, which currently includes somatic tumor sequencing and reproductive carrier screening. | 9/3/2018 |
| 377 | GeneDx Gaithersburg, MD Product Development Associate BS/MS Exp: 1-2 yrs |
The GeneDx Product Development Associate plans and coordinates product test development, launch, and marketing functions. | 9/3/2018 |
| 378 | FUJIFILM COLLEGE STATION, TX Virology Technician II BS in Biology, Chemistry, Molecular Biology or related Exp: 0-2 yrs |
Perform basic laboratory work in BSL 2 Laboratory; Perform cell culture and cell passage with minimal assistance;Perform cell culture and cell passage with minimal assistance. | 9/3/2018 |
| 379 | FUJIFILM COLLEGE STATION, TX Virology Associate MS in Biology, Biotechnology, Biochemistry, or other related field Exp: 1 yr |
The Virology Associate will be involved in the growth of both adherent and suspension cells, the creation of cell and virus banks, virus expansion and cultivation, and the use and development of assays to titer and identify virus and monitor expression of gene of interest with moderate supervision. | 9/3/2018 |
| 380 | FUJIFILM COLLEGE STATION, TX Quality Control Microbiology Analyst II MS in Biochemistry, Chemistry, Biology or related field Exp: 1 yr |
Performs QC microbiological aspects of cGMP compliance and testing. | 9/3/2018 |
| 381 | FUJIFILM COLLEGE STATION, TX Quality Control Chemist – Technician I BS Exp: 0-2 yrs |
Assist with raw material release; Helps prepare monthly metrics for raw material release as needed. | 9/3/2018 |
| 382 | FUJIFILM COLLEGE STATION, TX Environmental Monitoring Technician – Temporary BS Exp: 0-2 yrs |
Function as primary shift technician for environmental monitoring. | 9/3/2018 |
| 383 | FUJIFILM COLLEGE STATION, TX Downstream Manufacturing Technician III MS in Biology, Microbiology, Chemistry, Biochemistry, Engineering or other related field Exp: 1 yr |
The Downstream Manufacturing Technician III will work directly with a range of purification technologies including: filtration technologies (TFF and depth), chromatographic separations (Single Use GE AKTA systems), viral inactivation following aseptic techniques and procedures in a cGMP environment. | 9/3/2018 |
| 384 | FUJIFILM COLLEGE STATION, TX Cell Biology Analyst I BS in Biology or science related field Exp: 0-2 yrs |
Assist with quality control analytical testing of samples provided to the QC laboratory. | 9/3/2018 |
| 385 | Frontage Labs. Exton, PA Associate Scientist, Analytical Services-CMC BS in Chemistry or related discipline Exp: 1-2 yrs |
Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines | 9/3/2018 |
| 386 | Fresenius Kabi Skokie, IL ASSOCIATE SCIENTIST/SCIENTIST BS in Chemistry or related field Exp: 0-3 yrs |
We currently have an opportunity for an Associate Scientist or Scientist, Analytical Development who will conduct all aspects of Analytical Development including method development, experimentation, and record keeping, including developing and implementing methods that meet project needs. | 9/3/2018 |
| 387 | Fresenius Kabi Wilson, NC ASSOCIATE SCIENTIST (PRODUCT TESTING) MICROBIOLOGY BS Exp: 1-2 yrs |
This position reports to the supervisor for the functional area to which they are assigned, and has no direct reports. The Associate Scientist position works closely with other departments, such as Operations, Validation, Product Development, Quality Systems, Product Release and Chemistry to assure the support of the Microbiology department on various projects, studies and routine tasks. The individual holding the position of Associate Scientist shall be responsible for coordinating the timely completion of routine and project testing. This person will also be responsible for coordinating the timely completion of routine and special finished product testing and environmental issues. They will assist with the training of Production and Quality Control personnel in microbiological tests and methods. | 9/3/2018 |
| 388 | Fresenius Kabi Wilson, NC ASSOCIATE SCIENTIST (DATA REVIEW) - MICROBIOLOGY BS/BA Exp: 1-2 yrs |
The Associate Scientist Data Reviewer is responsible for the review of all test results and supporting laboratory data associated with raw materials, in-process materials and final product for microbial assessment according to cGMP and company specifications. | 9/3/2018 |
| 389 | Fresenius Kabi Wilson, NC ENVIRONMENTAL MONITORING ANALYST BS/BA Exp: 1-2 yrs |
The Quality Control Environmental Monitoring Technician is responsible for day-to-day activities required to perform monitoring of aseptic areas and controlled environments. | 9/3/2018 |
| 390 | Fresenius Kabi Melrose Park, IL TECH TRANSFER SPECIALIST BS in physical science, engineering Exp: 1-3 yrs |
The individual is responsible for independently or as part of a project team, planning, designing, tracking and implementing effective project technical support systems as well as facilitating multiple technical transfer activities (e.g., protocols, batch records, operating procedures, training materials, etc.) to achieve a successful transfer of products. The position will support multiple sites within North America and Europe and reports into the Director of Production and Technology Transfers. | 9/3/2018 |
| 391 | GE Healthcare Marlborough, MA Associate Engineer, R&D Systems Engineering BS in Chemical, Mechanical, Electrical Engineering Exp: 1-3 yrs |
Prototype, design, develop and document next generation products, including both bioprocess equipment and consumable single-use products such as in GE’s Xcellerex, WAVE, and Ready-To-Process product lines | 9/3/2018 |
| 392 | GE Healthcare Wauwatosa, WI Quality Assurance Specialist BS in technical field Exp: 1 yr |
This role is responsible for providing manufacturing and/or engineering process support in accordance with documented procedures and practices. Responsible for the development, implementation, improvement and continuous reinforcement of established Quality Assurance fundamental practices that are utilized in the local business. | 9/3/2018 |
| 393 | GenomeDx Biosciences San Diego, CA Sample Processor I - Procurement BS Exp: 1 yr |
The Sample Processer’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the GenomeDx internal and external customers, including the Chief Commercialization Officer, VP of Sales, VP of Marketing, Sales Team, Operations Team and Medical Staff in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor. | 9/3/2018 |
| 394 | GenomeDx Biosciences San Diego, CA Sample Processor I - Accessioning BS Exp: 1 yr |
The Sample Processer’s primary responsibility is to provide front-line support in the procurement of record of loan (ROL) material and manage chain-of-custody of samples received. This individual must support the GenomeDx internal and external customers, including the Chief Commercialization Officer, VP of Sales, VP of Marketing, Sales Team, Operations Team and Medical Staff in the routine functions to ensure client satisfaction and appropriate records and materials management are consistently maintained. This individual must work with staff to employ a team approach. Manages patient orders with or without samples and oversees special projects assigned by their supervisor | 9/3/2018 |
| 395 | Genomatica San Diego, CA Senior/Research Associate, Quantitative Small-Scale BS/MS in biology-related science and engineering Exp: 0-5 yrs |
The position is based on San Diego, CA and a title will be Senior/Research Associate working in Quantitative Small Scale (QSS) team under Systems Bioengineering group. The successful candidate will implement custom-designed microbial cultivation assays for quantitative physiology studies in an information-rich and precise way and involve in developing experimental platforms for high-throughput quantitative strain evaluation. | 9/3/2018 |
| 396 | GenMark Diagnostics Carlsbad, CA Manufacturing Process Engineer I BS in Engineering Exp: 1-2 yrs |
The Process Engineer will be responsible to drive stable, reliable production processes for new manufacturing processes recently transferred to production. Under minimal supervision, the Process Engineer will develop and characterize manufacturing processes, including surface treatment (i.e. plasma, CO2 cleaning) and precision dispensing of fluids and adhesives. This position will be instrumental in creating and maintaining process input and output specifications, perform capacity analyses, troubleshoot, test, and support for existing products and new product lines. | 9/3/2018 |
| 397 | GENEWIZ South Plainfield, NJ QA Associate BS in Life Sciences Exp: 1 yr |
Interact with all personnel levels and departments to help ensure full compliance with organizational, state, federal and other laws and guidelines | 9/3/2018 |
| 398 | GENEWIZ South Plainfield, NJ Associate Scientist I, NGS BS in Biological Sciences Exp: 1 yr |
Prepare amplified template libraries for high-throughput sequencing; Carry out DNA sequencing on next-generation DNA analyzers. | 9/3/2018 |
| 399 | Generation Bio Cambridge, MA Contractor - Research Associate, Upstream Process Development BS/MS in Chemical engineering, Bioengineering, Biotechnology Exp: 0-3 yrs |
The successful candidate would report directly to Lead Scientist in the group and will assist in the optimization of our development processes in the path toward clinical manufacture. | 9/3/2018 |
| 400 | Genentech Oceanside, CA BIOPROCESS MANUFACTURING TECHNICIAN, PRODUCTION SERVICE BS in Life Sciences or Engineering Exp: 1 yr |
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for being proficient in one functional area. Understands and applies biological, chemical and mechanical principles and techniques. | 9/3/2018 |
| 401 | Genentech Oceanside, CA BIOPROCESS MANUFACTURING TECHNICIAN, UPSTREAM (NIGHT SHIFT) BS in Life Sciences or Engineering Exp: 1 yr |
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for being proficient in one functional area. Understands and applies biological, chemical and mechanical principles and techniques. | 9/3/2018 |
| 402 | Genentech Oceanside, CA BIOPROCESS MANUFACTURING TECHNICIAN, DOWNSTREAM (NIGHT SHIFT) BS in Life Sciences or Engineering Exp: 1 yr |
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media/buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). Responsible for being proficient in one functional area. Understands and applies biological, chemical and mechanical principles and techniques. | 9/3/2018 |
| 403 | Genoptix Carlsbad, CA Pathology Services Associate I- TEMPORARY BS Exp: 1 yr |
The Pathology Services Associate I works with laboratory technicians, technologists and a team of physicians to ensure quality and timely diagnostic test results are delivered to clinicians/oncologists and their patients. The primary purpose of the position is to provide support for the Hematopathology departments by preparing reports, and performing quality review of reports. | 9/3/2018 |
| 404 | Cyprotex US, LLC Watertown, MA Entry Level Scientist BS/MS Exp: Entry Level |
The successful candidate will actively participate in experimental design, performing experiments, and troubleshooting, as well as performing data analysis and interpretation. The ideal candidate will be independent, self-motivated, collaborative and able to multitask effectively while frequently under pressure to meet tight deadlines. | 8/25/2018 |
| 405 | Cyprotex US, LLC Watertown, MA Associate Scientist BS Exp: 1-2 yrs |
Cell Culture experience with immortalized cell lines. (Primary cell experience a plus). Responsible for planning and conducting high and low throughput toxicology screens, processing data to a high quality of standards, and within specified time frames. | 8/25/2018 |
| 406 | Charles River Mattawan, MI Research Associate - Molecular Imaging BS/MS Exp: 0-2 yrs |
The Research Associate position is responsible for: quantifying, characterizing, synthesizing and/or modifying chemical entities according to applicable Standard Operating procedures (SOPs), established methods and/or GxP regulations. The individual in this role demonstrates proficiency in the use of applicable analytical and biochemistry instruments and laboratory techniques, and contributes to the team by completing assigned projects on time, contributing to process improvement initiatives, and communicating effectively with team members and customers. | 8/25/2018 |
| 407 | Charles River Mattawan, MI Research Associate - Test Material Control BS/MS Exp: 0-6 months |
The Research Associate in Test Material Control (TMC) 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. | 8/25/2018 |
| 408 | Charles River Mattawan, MI Laboratory Operations Assistant - Office of Animal Care - Intern BS Exp: 0-2 yrs |
The Laboratory Operations Assistant position is responsible for facilitating and/or directly conducting administrative departmental functions and other miscellaneous functions, as assigned. | 8/25/2018 |
| 409 | Charles River Charleston, SC Lab Testing Technician BS/BA in Biology or related field Exp: 1-2 yrs |
Performs Biological testing to support Manufacturing of products. Prepares and monitors tests and paperwork to support documentation, GMP and FDA requirements. Documents activities and demonstration of proficiency in SOPs. Demonstrates proficiency of techniques and competency of various production operations. | 8/25/2018 |
| 410 | Charles River Mattawan, MI Clinical Laboratory Assistant - Clinical Pathology BS/MS Exp: 0 yr |
A Clinical Laboratory Assistant is responsible for: managing sample containers, data, and communications for accurate and timely tracking and disposition of samples and data; or, for processing blood samples for multiple species of animals. Individuals in this role use effective communication and interpersonal skills in a collaborative team environment. | 8/25/2018 |
| 411 | Charles River Newark, DE Molecular Technologist BS/BA in Microbiology or related discipline Exp: 0-3 yrs |
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. | 8/25/2018 |
| 412 | Charles River Mattawan, MI Research Associate - LBA Development MS/BS/BA Exp: 0-2 yrs |
The Research Associate position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. | 8/25/2018 |
| 413 | C. R. Bard, Inc. Tempe, AZ Manufacturing Engineer I BS in engineering Exp: 0-2 yrs |
This position is responsible for process improvements (i.e. LEAN) and validation of Vascular Graft and covered Stent Graft manufacturing processes. This position is also responsible for the transfer of newly developed products to manufacturing. | 8/25/2018 |
| 414 | C. R. Bard, Inc. Covington, GA Regulatory Affairs Specialist II BS in a scientific discipline Exp: 1-3 yrs |
The Regulatory Affairs Specialist is responsible for implementation of regulatory strategies including domestic and international submissions and other support of product project team. | 8/25/2018 |
| 415 | C. R. Bard, Inc. Woburn, MA QC Technician / Sr. QC Technician BS in Chemistry, Bio-Chemistry, or Microbiology Exp: 1-2 yrs |
Under the general supervision of the QC Technical Supervisor, the QC Technician / Sr. QC Technician will perform chemical assays on finished goods and incoming raw materials used in the production of products according to official compendium and BD Interventional Surgery test methods. | 8/25/2018 |
| 416 | C. R. Bard, Inc. Covington, GA Regulatory Affairs Specialist I BS Exp: 1-3 yrs |
The position of Regulatory Affairs Specialist is responsible for the development and support of China FDA product registrations with International Business Center (IBC) contacts in China. The candidate requires a working knowledge of the products and relevant Chinese regulations and guidance documents. | 8/25/2018 |
| 417 | Cytovance Oklahoma City, OK OPERATIONS ENGINEER BS in an applicable engineering discipline Exp: 0-5 yrs |
The Operations Engineer is responsible for equipment, facility, and utility (EFU) lifecycle management. This includes managing the specification, procurement, installation, and commissioning of new EFU assets; contributing to the development of calibration, maintenance, operation, and cleaning procedures; providing technical support to end user, quality, and maintenance personnel; and managing the decommissioning of EFU assets to be retired. The Operations Engineer is quality-centered and follows company standard operating procedures (SOPs) geared toward FDA and other applicable regulations and in-line with current good manufacturing practices (cGMPs). | 8/25/2018 |
| 418 | Cytovance Oklahoma City, OK QS&C SPECIALIST BS Exp: 1-3 yrs |
Takes an active role in assisting with the development, execution and management of the Quality Compliance Team. A QS & C Specialist assists the Compliance Team in the identification and resolution of quality issues and regulatory concerns. | 8/25/2018 |
| 419 | Cytovance Oklahoma City, OK QC ASSOCIATE BS in Life Sciences/Chemistry Exp: 0-4 yrs |
The QC Associate will participate in the entire range of quality control analytical activities: assay performance, qualification/validation of assays and laboratory equipment, and transfer of standard protein characterization methods. Duties will be carried out in accordance with quality standards and procedures set by the company and applicable government agencies. | 8/25/2018 |
| 420 | CytomX Therapeutics, Inc. South San Francisco, CA Research Associate 2/Sr Research Associate, Upstream Process Development MS in Biochemistry, Molecular Biology, or Cell Biology Exp: 0-3 yrs |
Candidates must have experience in a cell culture process development setting, including operation of stirred-tank bioreactors and associated instruments. Advanced troubleshooting and data analysis skills are highly desired. | 8/25/2018 |
| 421 | Dexcom, Inc. San Diego, CA Research Associate 1 BS/BA Exp: 1-2 yrs |
Incumbent provides technical support for material and process development related to DexCom’s sensor technology platforms. | 8/25/2018 |
| 422 | Dexcom, Inc. San Diego, CA Process Development Engineer 1 BS/MS in Mechanical Engineering, Bioengineering or equivalent Exp: 0-2 yrs |
As a member of the R&D Process team this engineer will lead efforts to understand current and future needs of our manufacturing and automation processes, explore and evaluate new technologies and concepts for meeting those needs, and rapidly demonstrate feasibility of such technologies through rigorous modeling, analysis, prototyping, experimentation, and other risk identification and mitigation activities. | 8/25/2018 |
| 423 | Dendreon, Inc. Seal Beach, CA Quality Specialist I - Supplier Quality BS Exp: 1 yr |
The Quality Specialist I, Supplier Quality is responsible for performing a wide variety of Supplier Quality activities to ensure compliance with applicable regulatory requirements. | 8/25/2018 |
| 424 | DJO Global Dallas, TX Quality Systems Specialist BS/BA Exp: 1 yr |
Utilizing a basic knowledge of engineering and problem-solving principles, this position is responsible for a variety of more routine activities regarding the designing, implementation, and maintenance of quality assurance protocols and methods to ensure external safety, quality and compliance with the Company standards and government regulations. | 8/25/2018 |
| 425 | DynoSense San Jose, CA QA Engineer BS in Computer Science, Engineering or a related subject Exp: 0-2 yrs |
Develop test plan, test cases, test scenarios based on Users Stories and product’s design description to meet business requirements and technical specifications | 8/25/2018 |
| 426 | DURECT CORPORATION Cupertino, CA Technical Support Specialist BA/BS in Science Related Field Exp: 6 months- 2 yrs |
The Technical Support Specialist will serve as the liaison to our customers and international distributors on the use of ALZET and IPRECIO pumps an ancillary products. | 8/25/2018 |
| 427 | Dr. Reddy’s Laboratories Ltd. Shreveport, LA Formulation Scientist BS in Pharmaceutical sciences / technology Exp: 0-2 yrs |
Identify the Quality Target Product Profile, Critical Quality Attributes, Critical Material Attributes and Critical Process Parameters to arrive at robust formulation strategy. | 8/25/2018 |
| 428 | Edwards Lifesciences Draper, UT Supplier Quality Engineer I, Quality Assurance BS Exp: 1-2 yrs |
This person will be responsible for supporting supplier quality vendor management, audits, and improvements while supporting continued Quality System improvements. In this position you will support activities sustaining quality engineering within Receiving Inspection, Manufacturing, and Product Verification as applied to supplier related issues. | 8/25/2018 |
| 429 | Editas Medicine Cambridge, MA Research Associate I/II - Stem Cell Biology BA in Cell or Molecular Biology or relevant field Exp: 1-2 yrs |
The successful candidate will work as part of a team to aid in developing novel CRISPR/Cas9 technologies to be used as therapeutics. This stimulating role will be in exploratory CRISPR/Cas9 platform development in an entrepreneurial and fast-paced environment. The successful candidate will have strong stem cell culture experience and molecular biology skills and be able to independently design and interpret results. The position requires flexibility, creativity, and the ability to work effectively in a multi-disciplinary team, as well as excellent written and verbal communication skills, and a capacity for creativity and innovation to achieve company goals. | 8/25/2018 |
| 430 | Editas Medicine Cambridge, MA Clinical Operations Associate BS in a biomedical, life science, or related field Exp: 1-2 yrs |
We are seeking a Clinical Operations Associate (COA) with a keen attention to detail who can both prioritize and handle multiple tasks effectively in a fast-paced Research and Development (R&D) environment. The COA is responsible for assisting the study team in running the day to day operational activities of clinical studies. Under the guidance of Clinical Operations management, the individual will coordinate, track, and manage daily activities for multiple clinical studies to support both the internal project team and the CROs. | 8/25/2018 |
| 431 | Editas Medicine Cambridge, MA Process Development Associate BS/MS in life sciences Exp: 1-3 yrs |
This new role on the Technical Development and Manufacturing team provides a unique opportunity to contribute to Editas’ efforts to develop safe and effective cellular therapies using CRISPR-based gene editing technologies. We are seeking a talented and highly-motivated individual to perform experiments that generate data to guide development of processing methods and standard operating procedures (SOPs) for the preparation of cellular therapies for translational clinical studies. Candidate must be experienced with aseptic technique and be versatile to assist in the development of processes for autologous or normal donor cellular products derived from different lineages of cells (T cells, HSCs, etc.). | 8/25/2018 |
| 432 | Editas Medicine Cambridge, MA Research Associate I/II - Stem Cell Biology BA in Cell or Molecular Biology or relevant field Exp: 1-2 yrs |
The successful candidate will work as part of a team to aid in developing novel CRISPR/Cas9 technologies to be used as therapeutics. This stimulating role will be in exploratory CRISPR/Cas9 platform development in an entrepreneurial and fast-paced environment. The successful candidate will have strong stem cell culture experience and molecular biology skills and be able to independently design and interpret results. The position requires flexibility, creativity, and the ability to work effectively in a multi-disciplinary team, as well as excellent written and verbal communication skills, and a capacity for creativity and innovation to achieve company goals. | 8/25/2018 |
| 433 | Emergent BioSolutions Rockville, MD Manufacturing Associate I-TEMP BS/BA in Biology, Chemistry, or related discipline Exp: 0-2 yrs |
Job activities include the preparation of equipment and components for aseptic filling operations, performing visual inspection of filled vials, vial labeling, vial packaging and distribution of filled vials as per GMP regulations. | 8/25/2018 |
| 434 | Emergent BioSolutions Rockville, MD Analyst I, QC Bioassay BS Exp: 0-2 yrs |
You will excel in an environment characterized by respect, innovation and growth opportunities. Here, you will join passionate professionals who advance their scientific, technical and professional skills to develop products designed-to protect life. | 8/25/2018 |
| 435 | Emergent BioSolutions Rockville, MD Analyst I, Document Control BS Exp: 0-2 yrs |
Provide oversight and support of document and records management in Document Control using company procedures and regulations. Provide support for Global Document Management System project (Veeva). | 8/25/2018 |
| 436 | Lilly Branchburg Park, NJ Engineer -Plant-HVAC BS in Chemical, Mechanical Engineering or related engineering discipline Exp: 0-5 yrs |
This position is responsible for the “front line” support of senior engineers involved in operating, maintaining and upgrading HVAC system used to support biotech manufacturing facilities. These systems will including air handlers, chillers, cooling towers, exhaust systems and the associated support and controls equipment. This position will interact with various team members on Process Teams, including Engineering, Facilities, Manufacturing, validation, and quality assurance and other Lilly Sites as required. Knowledge of HVAC and building management systems (BMS) or appropriate training is required. | 8/25/2018 |
| 437 | Lilly San Diego, CA Biologist-Protein Engineering BS in biochemistry, biotechnology, or a related discipline Exp: 1 yr |
Your role will include design and execution of mRNA and/or yeast library selections that should result in discovery of clinical drug candidates. You will also be responsible for designing and implementing novel chemical reactions that can be incorporated in mRNA library design. One of your main responsibilities will include evolving the current display/panning practices towards innovative functional-based selection processes. | 8/25/2018 |
| 438 | Lilly Indianapolis, IN Associate-Search & Evaluation-Oncology BS in life science and/or pharmaceutical Exp: 1-4 yrs |
Support leading the identification, evaluation and tracking of opportunities of interest, and maintain accurate records of activity through use of in-house caseload management information systems | 8/25/2018 |
| 439 | Lilly Branchburg Park, NJ Engineer-Plant-Critical Utilities Exp: 0-5 yrs |
This position is responsible for the “front line” support of senior engineers involved in operating, maintaining and upgrading critical utility system used to support biotech manufacturing facilities. These systems will include purified water, water for injection, clean steam, clean dry, air and other systems as required in the manufacturing process. | 8/25/2018 |
| 440 | Envigo Princeton, NJ Analyst, Immunoassay BS Exp: 0-1 yr |
Responsible for all aspects of validation, sample analysis and data preparation in support of pre-clinical and clinical studies. Ensure all work is conducted in accordance to GLP/GCP regulations. | 8/25/2018 |
| 441 | Enzymatics. Frederick, MD Production Associate Scientist BS in Molecular Biology, Biochemistry, chemistry or related Life Sciences field Exp: 1-3 yrs |
Responsible for manual/automated production/assembly in compliance with relevant regulations and Standard Operating Procedures. | 8/25/2018 |
| 442 | Enzo Ann Arbor, MI Associate Manufacturing Scientist BS Exp: 1 yr |
With assistance from senior scientists or management, this position is responsible for protein and/or antibody production, purification of recombinant proteins and/or antibodies, and testing product specificity and quality through variety techniques including, but not limited to SDS-PAGE electrophoresis, Western Blotting, enzyme-immunoassays and cell-based assays. As part of manufacturing team, this position will share matrixed responsibilities with team members to meet reagent production goals. | 8/25/2018 |
| 443 | Exosome Diagnostics Waltham, MA Laboratory Technologist BS/MS in biological sciences or clinical laboratory sciences Exp: 0-2 yrs |
Perform complex molecular biology procedures at the Cambridge facility under the supervision of the Clinical Laboratory Director. | 8/25/2018 |
| 444 | Exelixis, Inc. Alameda, CA Temporary Clinical Supplies Specialist I MS/MA Exp: 1 yr |
The Clinical Supply Specialist is responsible for supporting multiple clinical programs working closely with the Clinical Supplies project leads. The selected candidate will independently coordinate clinical supply activities for clinical studies in support of development programs. The activities include review of clinical study protocols, design of clinical labels, preparation of packaging and labeling requests, management of depot and site shipments, monitoring study drug inventory levels, and assist in supply planning and forecasting. | 8/25/2018 |
| 445 | Exelixis, Inc. Alameda, CA Assistant Research Scientist II (PK) MS Exp: 1 yr |
The successful and highly motivated candidate will support the in vivo pharmacology research program and contribute to the multidisciplinary research team by designing and executing in vivo studies to determine pharmacokinetics and pharmacodynamics relationships and efficacy of optimized leads. | 8/25/2018 |
| 446 | Exelixis, Inc. Alameda, CA Organic/Analytical Chemist (Temp) BS/MS Exp: 0-2 yrs |
Seeking a temporary analytical and/or QC chemist to assist our medicinal chemistry drug discovery team. The ideal candidate will be experienced in the analysis and characterization of small molecule compounds. | 8/25/2018 |
| 447 | FivePrime South San Francisco, CA Research Associate II, Protein Chemistry BS in Biochemistry, Protein Sciences, or related fields Exp: 0-4 yrs |
The successful candidate will be responsible for learning and implementing the operation, maintenance, and optimization of Five Prime’s automated high-throughput protein expression system as a member of a cross-functional team supporting early target discovery efforts within Research. The candidate must be self-motivated, detail oriented and thorough, and capable of working both independently and in a team environment. | 8/25/2018 |
| 448 | Ferring Pharmaceuticals Parsippany, NJ Validation Specialist BS in Engineering or related field Exp: 1-5 yrs |
Responsible for preparing and executing commissioning, qualification, and validation studies for new facilities, processes, and equipment as well as assisting in maintaining the facility, processes, and equipment in a validated state. | 8/25/2018 |
| 449 | Brammer Bio Lexington, MA Manufacturing Associate IV, Downstream BS in Life Sciences Exp: 1-3 yrs |
The Manufacturing Associate 4 (MA4) exhibits a level of technical expertise and experience in viral vector or biological manufacturing. The incumbent will play a vital role in the start-up of the Lexington manufacturing facility performing complex activities outside of routine manufacturing operations to commensurate with their experience and training. | 8/16/2018 |
| 450 | Catalent San Diego, CA Pharmaceutical Chemist II-III (Solid Dose) BS/MS Exp: 1-4 yrs |
The Chemist II will be developing the use of innovation and creativity in exploring alternative approaches to problem solving. The individual may be required to assist in the creation and/or revision of company SOPs. | 8/16/2018 |
| 451 | Cibus US LLC San Diego, CA Research Associate - Product Development BS/MS in Plant Pathology, Plant Science, Plant Breeding and Genetics, or related field Exp: 1-2 yrs |
Primary responsibilities include conducting disease tolerance and screening assays on various crop species from the laboratory research environment to growth-chamber/greenhouse research environment. | 8/16/2018 |
| 452 | Cibus US LLC San Diego, CA Breeding & Development Associate/Sr. Associate – Product Development BS/MS in Plant Pathology, Plant Science, Plant Breeding and Genetics, or related field Exp: 0-2 yrs |
Develop breeding populations and carry out germplasm improvement activities in the greenhouse and field including pollination, phenotypic characterization, seed harvest, MAS, sample submission and data collection and analysis. | 8/16/2018 |
| 453 | Cibus US LLC San Diego, CA Research Associate – Cell Culture Automation BS in cellular or molecular biology, plant biology or a related field Exp: 0-2 yrs |
The position will help to run and maintain an automated platform supporting Cibus’ patented RTDS™ gene editing technology. The successful applicant will be expected to assist with all aspects of the automated workflow including maintaining plant cell cultures, operating a robotic system, and data mining and analysis. Responsibilities will involve initiating experiments, sample monitoring and management, image analysis, running and troubleshooting the automation platform, data retrieval, processing, analysis and reporting. | 8/16/2018 |
| 454 | Cibus US LLC San Diego, CA Research Associate - Technology Development BS in Biological Sciences or in a related discipline Exp: 1-2 yrs |
Mange multiple molecular biology projects simultaneously across several different fields, with an emphasis on RNA based methods is desired | 8/16/2018 |
| 455 | ChemPacific Corp Baltimore, MD Chemist MS in Chemistry or Organic Chemistry Exp: 1 yr |
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. | 8/16/2018 |
| 456 | Cheminpharma LLC Branford, CT Associate scientist, Medicinal/Synthetic chemistry BS/MS in synthetic chemistry Exp: 0-5 yrs |
The successful candidate will be an experienced chemist with state of art knowledge of synthetic organic chemistry, and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members and external customers. | 8/16/2018 |
| 457 | Charles River Wilmington, MA Laboratory Technician I BS in biological sciences or related discipline Exp: 0-2 yrs |
Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Perform within the MDX laboratory to process and interpret internal and external samples by performing PCR testing (to include Taqman based PCR on 96 well and 384 well platforms) using aseptic technique. Reconcile customer paperwork with submission documentation to ensure accuracy. Make detailed observations and maintain documentation of all laboratory work. Analyze data and report testing results with respect to department turnaround time. | 8/16/2018 |
| 458 | Charles River Reno, NV Research Assistant I (Laboratory Sciences) BS in laboratory science or related discipline Exp: 0-2 yrs |
This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 8/16/2018 |
| 459 | Charles River Skokie, IL Research Assistant I BS Exp: 0-2 yrs |
Responsible for performing moderately complex laboratory work in collaboration with departmental staff. | 8/16/2018 |
| 460 | Charles River Malvern, PA Technician I Cell Culture BS in biological sciences or related discipline Exp: 0-1 yr |
Under direct supervision, perform basic daily laboratory tasks as they relate to cell culture and media preparation in the Cell Culture group. | 8/16/2018 |
| 461 | Charles River Mattawan, MI Report Coordinator Associate - Report Services BS/MS Exp: 0-2 yrs |
The Report Coordinator Associate is responsible for: coordinating the reporting processes to produce quality, on-time reports; providing support for assigned Study Director(s); and prioritizing his/her workload. Good communication skills and the ability to adhere to deadlines are necessary for success. | 8/16/2018 |
| 462 | Charles River Ashland, OH Clinical Pathology Technician I BS in animal or life science or health-related discipline Exp: 1 yr |
Performs technical laboratory activities in support of client studies or procedures. Performs analysis of data for quality and completeness and determines if results are as expected. Records data in compliance with company and regulatory policies and standards to meet quality and accuracy requirements. Prepare study materials and study books prior to clinical pathology bleeding days. Operate basic to moderately complex analyzers (e.e., hematology and co-ag analyzers) and process toxicokinetic samples. Assist in the performance and review of study ordered parameters and computer input of raw data. | 8/16/2018 |
| 463 | Charles River South San Francisco, CA Research Associate BS/BA Exp: 0-3 yrs |
We are seeking Research Associate candidates that are early in their careers and are highly motivated, enthusiastic and possess a passion for learning. This individual will work closely with more senior colleagues to contribute to the establishment and delivery of discovery bioanalytical (small Molecule) services from our new location. This position is ideally suited to recent graduates who enjoy a fast-paced and collegial environment. The individual in this position will be responsible for working hands-on and under the direction of more senior staff in a dynamic environment where teamwork, data quality, innovation and speed are valued. | 8/16/2018 |
| 464 | AGC Biologics Bothell, WA Environmental Health & Safety Specialist BS in Occupational Safety and Health or Environmental-related discipline Exp: 1-5 yrs |
The role will be focused on assisting the facility in ensuring that operations are carried out in accodance with Federal, state, and local regulatory requirements, as well as company EH&S policies and procedures. | 8/16/2018 |
| 465 | Clinipace Worldwide Morrisville, NC Pharmacovigilance Specialist BS Exp: 1-2 yrs |
The Pharmacovigilance Specialist (PVS) primary responsibility is SAE case management. This includes but is not limited to: initial case disposition, confirmation of case disposition with Medical Monitor (MM)/Safety Physician PV (SP PV), MM, receipt of adverse event data, data entry, source document data extraction, draft narrative development, follow-up management and reporting according to regulatory requirements. | 8/16/2018 |
| 466 | Clinipace Worldwide home based, ho Clinical Research Associate II BS Exp: 1 yr |
The Clinical Research Associate II monitors investigational sites to ensure subject safety and provides high quality data review and reporting in compliance with the Clinipace and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (ICH) guidelines, ISO14155, and other applicable regulations. Builds, manages and supports site relationships while serving as liaison between the Sponsor and assigned sites. | 8/16/2018 |
| 467 | Clinilabs Inc. New York, NY Clinical Research Coordinator BS Exp: 1-2 yrs |
The Clinical Research Coordinator (CRC) is primarily responsible for coordinating the operational aspects of ongoing clinical projects to ensure that the clients’ goals of time, cost, and quality are met. The CRC may serve as the primary contact with the client to ensure appropriate communications, project budget management, and meeting of timelines. The CRC may also serve as the project lead responsible for directing internal teams in the execution of the protocol and ensuring that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained on the protocol. | 8/16/2018 |
| 468 | Clinilabs Inc. New York, NY Quality and Regulatory Compliance Associate BS Exp: 1 yr |
The Quality and Regulatory Compliance Associate is responsible to support strategies for Quality System processes and supporting technology, and ensuring the integrity, consistency, and harmonization of these processes and systems for Clinilabs. | 8/16/2018 |
| 469 | ICON home based, ho Clinical Research Associate - Home-Based BS in a life science or related discipline Exp: 1 yr |
You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. | 8/16/2018 |
| 470 | ICON Farmingdale, NY Medical Technologist II - Molecular - (Per Diem) BS in Medical Technology Exp: 1 yr |
The Medical Technologist in the Molecular Lab will perform genetic and molecular biology laboratory procedures involving traditional techniques such as PBMC, isolation of DNA and RNA, PCR, RT-PCR, Real-Time PCR, and other molecular techniques (knowledge of Illumina MiseqDx NGS and Luminex 200 are strongly desired). | 8/16/2018 |
| 471 | ICON home based, ho Clinical Research Associate (I/II/Sr) BS in a life science or related discipline Exp: 10-12 months |
You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. | 8/16/2018 |
| 472 | Complete Genomics San Jose, CA Manufacturing Associate 1 (Temp) BS in Molecular Biology or related field Exp: 1-2 yrs |
The successful candidate will be responsible for developing and executing standard work procedures on a wide range of molecular biology techniques related to Next Generation Sequencing | 8/16/2018 |
| 473 | Cold Genesys, Inc. Santa Ana, CA Clinical Trial Associate BS Exp: 1 yr |
Coordinating with investigator sites to ensure compliance with protocol and maintenance of patient safety | 8/16/2018 |
| 474 | Cogent Professionals San Diego, CA Chemist BS in Chemistry Exp: 0-2 yrs |
The positions will focus on implementing and utilizing state-of-the art automation, analytical and preparative scale chromatographic systems to deliver high quality compounds for drug discovery in the first in-class Automated Life Sciences Studio facility located in La Jolla, CA. | 8/16/2018 |
| 475 | Cochlear Centennial, CO Document Control Specialist BS Exp: 1 yr |
To be successful in this role, you’ll be able to efficiently maintain the document control portion of Cochlear Americas’ standard operating procedures (SOPs) and marketing submissions in MasterControl. You’ll work collaboratively across various departments to create, maintain, and update job title specific training matrices along with Cochlear employee infocards. Additionally, you will be responsible for document retrieval, monitoring delinquent training assignments, and reporting on document control metrics. | 8/16/2018 |
| 476 | CoreRx Clearwater, FL QUALITY CONTROL INSPECTOR BS/BA Exp: 1-2 yrs |
Adherence to all company procedures. Perform sampling of in-process and raw materials. Release of materials. Manage the retain program. Perform weekly cycle audits. Check in-process work. Oversight of environmental monitoring and water systems. Perform cleaning verifications. | 8/16/2018 |
| 477 | Cardinal Health Chicago, IL Regulatory Affairs Specialist (FDA & EU) BS Exp: 1-3 yrs |
Regulatory Affairs (FDA & EU) is responsible for planning, coordinating and implementing regulatory strategies for products that require government approval. This position will be responsible for preparation, submission and maintenance of domestic and international regulatory applications and filings including 510(k)s, Technical Files, Summary Technical Documents and Design Dossier submissions. | 8/16/2018 |
| 478 | Conagen Bedford, MA Research Associate - Microbial Synthetic Biology MS in metabolic engineering, molecular biology, molecular genetics, synthetic biology, or other related field Exp: 1 yr |
We are currently seeking a scientist to support projects related to metabolic engineering of plant and microbial secondary metabolites. This position will focus on microbial metabolic engineering and the candidate is expected to have a strong background in metabolic engineering, molecular biology, genetics, and ideally synthetic biology. Strong technical, organizational, and communication skills are essential. | 8/16/2018 |
| 479 | Conagen Bedford, MA Research Associate – Automation BS/MS in biology, biotechnology or related fields Exp: 1 yr |
The successful candidate will support and develop automation solutions related to the genetic engineering and screening of industrial microbes. | 8/16/2018 |
| 480 | CONMED Corporation Atlanta, GA Engineer, Quality I BS Exp: 1-3 yrs |
Provide Quality Engineering support to all functions for the design, procurement, assembly, test, manufacturing, validation, and distribution of medical devices, processes, and quality systems. | 8/16/2018 |
| 481 | Crown Bioscience San Diego, CA Research Associate - In Vivo BS Exp: 1-2 yrs |
Manipulation and handling of mice in a lab setting; Ear tagging, shaving, and measuring body weights of mice. | 8/16/2018 |
| 482 | Counsyl South San Francisco, CA Manufacturing Associate BS in Molecular Biology or related field Exp: 1 yr |
The Manufacturing Associate is an enthusiastic, self-motivated person with great communication skills who can support Manufacturing and Clinical Operations through the manufacture and quality control testing of in house prepared reagents. As a Manufacturing Associate you will be heavily involved in the manufacture and testing of bulk reagents and assay plates. | 8/16/2018 |
| 483 | Counsyl South San Francisco, CA Clinical Laboratory Scientist I BS/BA in Medical Technology, Biological Sciences, Molecular Biology, or related field Exp: 0-2 yrs |
We currently seek to hire a full-time Clinical Laboratory Scientist to assist in sample processing & analysis in our highly-automated laboratory. You will Interact and communicate with laboratory staff to ensure efficient work flow within our state-of-the-art laboratory. | 8/16/2018 |
| 484 | Covance Madison, WI Research Assistant - Study Technician Pathology BS in life sciences Exp: 0 yr |
As a Study Technician (Research Assistant) - Pathology, you will perform basic necropsy or histology tasks on a variety of laboratory models. While ensuring compliance with the appropriate SOPs, GLPs, and regulatory guidelines, | 8/16/2018 |
| 485 | Covance Greenfield, IN Study Technician DART/Necropsy BS in Life Sciences, Associate degree in Laboratory Animal Technology Exp: 0-2 yrs |
Perform advanced necropsy laboratory procedures including but not limited to: dissection, tissue collection/preservation, fresh tissue trimming, sample collection, data entry, tissue weights, coordinate unscheduled activities, prosection, perfusions, assay specific requirements, CSF collection, and electronic QC, in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines. Will perform administrative roles within department. Knowledgeable of inter-site processes and procedures and can identify gaps for process excellence. Serve as a resource for others in an area of specific focus. Must know correct anatomic terms. | 8/16/2018 |
| 486 | Covance Indianapolis, IN Medical Technologist I BS in Medical Technology or Clinical Laboratory Science or other life science Exp: 1 yr |
Perform assigned clinical laboratory testing accurately and in a timely manner. | 8/16/2018 |
| 487 | Covance Indianapolis, IN Medical Technologist II - Vaccines and Novel Immunotherapeutics BS in a chemical, physical or biological science Exp: 1 yr |
The Medical Technologist II - Vaccines and Novel Immunotherapeutics performs established procedures for clinical testing as required in all assigned laboratory disciplines and is responsible for analyzing specimens whose results are reported to the sponsor. | 8/16/2018 |
| 488 | Covance mutiple, mu Research Assistant - Study Technician Animal Operations BS in Life Sciences Exp: 0 yr |
As a Research Assistant (Study Technician) in our Madison, WI In-Life department, you will monitor the research animals’ health and welfare using your experience in animal observation and your experience working with sample collections. | 8/16/2018 |
| 489 | Covance Nashville, TN Clinical Research Assistant BS Exp: 1 yr |
Perform CRF review, query generation and resolution against established data review guidelines, under direct supervision on Covance or client data management systems, as assigned by management | 8/16/2018 |
| 490 | Covance Madison, WI Analyst BioA BS/BA in chemistry or related scientific field Exp: 1 yr |
Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. | 8/16/2018 |
| 491 | Crown Bioscience San Diego, CA Research Associate - In Vivo BS Exp: 1-2 yrs |
Manipulation and handling of mice in a lab setting； | 8/16/2018 |
| 492 | CooperSurgical Los Angeles, CA Laboratory Technician 1 BS in a chemical, life, (Biology [Cell, Molecular, Development, Genetics]), or clinical lab sciences discipline Exp: 1 yr |
This position involves using the latest single-cell technologies to screen for chromosomal abnormalities via next generation sequencing. | 8/16/2018 |
| 493 | CooperSurgical Houston, TX Research Associate/ Technician BS/MS in Biology or related science Exp: 1 yr |
Performs complex molecular-based procedures on research samples. Analyzes research results and provides diagnoses. Performs other research tasks associated with research for the organization. | 8/16/2018 |
| 494 | BioMarin NOVATO, CA RESEARCH ASSOCIATE BS/MS in the Pharmaceutical Sciences, Biochemistry, Biophysical Chemistry or related discipline Exp: 0-2 yrs |
Perform routine and semi-routine analysis of drug product formulations using chromatographic (reverse phase, size exclusion and ion exchange HPLC), spectrophotometric (UV, CD, florescence), calorimetric (DSC, ITC), microscopy and standard wet chemistry techniques. | 8/12/2018 |
| 495 | BioLegend San Diego, CA Product Development Associate I - Tissue Culture BS in Biology, Biochemistry, Chemistry, or Science Exp: 1 yr |
The Product Development Associate I position is an important member of the New Clones Team, which develops new antibody-producing cell lines for BioLegend products. The position is responsible for basic tissue culture responsibilities. This is a great opportunity to enhance your knowledge in the biotechnology industry and to be part of BioLegend, a fast growing company that will provide you with the skills and experience necessary to thrive in the Biotech Industry. | 8/12/2018 |
| 496 | BioLegend San Diego, CA Product Development Associate I - Purification BS in Biology, Biochemistry, Chemistry, or Science Exp: 1 yr |
The Product Development Associate I position is an important member of the New Clones Team, which develops new antibody-producing cell lines for BioLegend products. The position is responsible for basic purification responsibilities. This is a great opportunity to enhance your knowledge in the biotechnology industry and to be part of BioLegend, a fast growing company that will provide you with the skills and experience necessary to thrive in the Biotech Industry. | 8/12/2018 |
| 497 | BioLegend San Diego, CA Quality Control Associate (Cell Biology) BS Exp: 6 months |
The Quality Control Associate will function as an integral member of the Cell Biology-Quality Control group within the Molecular Immunology department. The primary job functions for this position include polyclonal antibody purification, affinity gel products manufacturing, quality control of cell biology for polyclonal and monoclonal antibodies and associated products, troubleshooting and communicating with supervisors regarding any quality control or manufacturing related problems, and keeping all documentations up to date. | 8/12/2018 |
| 498 | BioLegend San Diego, CA Production Associate I/II/III BS in Biochemistry, Molecular Biology, or related Biological Science area Exp: 1 yr |
The Production Associate will participate in producing recombinant proteins of cytokines, growth factors, hormones, and enzymes from bacterial to mammalian expression systems and will be involved in general lab duties such as maintaining lab supplies and inventory management. | 8/12/2018 |
| 499 | BioLegend San Diego, CA Research Associate - Hybridoma BS in Cell Biology, Immunology or related discipline Exp: 1 yr |
Primary responsibilities include animal work, buffer preparation, mammalian cell line handling, preparation and maintenance of materials used for hybridoma selection. Additional responsibilities include hybridoma screening via ELISA and Western Blot. | 8/12/2018 |
| 500 | BioLegend San Diego, CA Manufacturing Associate Purification (Finished Good and Bulk Processing) BA/BS in Biology, Biochemistry or related field Exp: 6 months |
The Manufacturing Associate will be an important member of our Finished Goods Inventory/Bulk Inventory team that supplies purified bulk antibodies for finished goods and custom bulk orders. This position will be responsible for performing all essential functions related to FGI and bulk antibody processing, including verifying specifications and sales order information, reviewing available inventory, adjusting concentration, performing buffer exchange if necessary and endotoxin assays. These materials will support customers in the areas of Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. This position will also interact with external groups including Planning, Bottling, Customer Service, Marketing and Internal Sales. This is a great opportunity to enhance your knowledge in the biotechnology industry. | 8/12/2018 |
| 501 | Biotechne San Marcos, CA Manufacturing Chemist III BS in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 yrs |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 8/12/2018 |
| 502 | Biotechne Wallingford, CT Engineer BS in Engineering or Physics Exp: 0-5 yrs |
Work in a small team of engineers developing internal production processes and commercial products for the life sciences instrumentation market. Our technology platform comprises software, instruments, consumable micro-fluidic cartridges and immunoassays. Our initial development phases require clever application of engineering, physics, instrumentation, control systems, data processing algorithms, firmware and software to achieve robust repeatable reliable biological measurements. | 8/12/2018 |
| 503 | Boston Analytical Salem, NH Microbiologist BS/BA in Microbiology or related science discipline Exp: 0-2 yrs |
The 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. | 8/12/2018 |
| 504 | Boston Analytical Salem, NH Quality Assurance Specialist BS Exp: 0-3 yrs |
The Quality Assurance Specialist supports the QA Lead and the company’s quality program by auditing chemists analytical data, routine work, protocols and reports. | 8/12/2018 |
| 505 | Boston Analytical Salem, NH Lab Technician – Microbiology BS in Microbiology or related scientific discipline Exp: 0 yr |
The Lab Technician in the Microbiology Lab will perform routine laboratory tasks and assist laboratory personnel according to FDA, cGMP and Boston Analytical’s Standard Operating Procedures. | 8/12/2018 |
| 506 | Boston Analytical Salem, NH Analytical Chemist II BS in Chemistry or a related discipline Exp: 1-5 yrs |
The Chemist 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. | 8/12/2018 |
| 507 | Boehringer Ingelheim Fulton, MO Clinical Data Management Associate BS in Biology Exp: 0-2 yrs |
Data Entry Associate will enter clinical research data into a clinical trial management system(s). The work is transcribed both from paper documents as well as from an electronic system. Data Entry Associates assist Clinical Data Management team in all tasks related to study start up to closure. | 8/12/2018 |
| 508 | C3J Therapeutics, Inc. Marina del Rey , CA Research Associate I/II BS/MS in Molecular Biology, Microbial Pathogenesis, Microbial Genetics, Virology or related field Exp: 1 yr |
The candidate will support the overall program goals and strategy of the group which include significant laboratory activities, such as phage engineering and characterization, protein expression and preclinical evaluation of phage therapy efficacy in relevant animal models. The candidate will have broad molecular and cell biology experience. Previous experience with virology and viral vector construction (phage or mammalian viruses) will be considered a plus. Excellent verbal, presentation, and written communication skills are essential and the capability to effectively work in a team environment is required. | 8/12/2018 |
| 509 | Bryllan LLC Brighton, MI Pharmaceutical Production Technician BS in Life Sciences or Engineering Exp: 0-2 yrs |
Formulation, Aseptic Filling, and Packaging. The Production Technician ensures a clean, safe workplace and quality production of drug product adhering to current Good Manufacturing Practices. (CGMP's). | 8/12/2018 |
| 510 | Brammer Bio Alachua, FL Specialist, Manufacturing BS Exp: 1 yr |
The position is expected to execute and provide on-the-floor oversight of all fill finish department manufacturing processes while strictly adhering to standard operating procedures, cGMP regulations, environmental health and safety guidelines, and any other regulation which could apply. The incumbent will demonstrate skills of a drug product specialist, which include: developing process understanding of primary work areas (formulation, filtration, filling, autoclave, capping, inspection, cleaning, isolator knowledge, etc.), executing activities on the manufacturing floor in accordance with schedule, oversight of fill finish manufacturing activity, participation in all departmental manufacturing and support functions, and providing a moderate level of troubleshooting. In addition, the specialist is expected to: | 8/12/2018 |
| 511 | Brammer Bio Alachua, FL Technician, Plant Maintenance Mechanic BS Exp: 1 yr |
The Technician, Maintenance: A motivated self-starter with high levels of initiative. Responsible for supporting and maintaining the Alachua site for GMP clinical manufacturing facility and utility systems, including: HVAC, PCW, RO, Pre-Treatment of water systems, Compressed Gases, and other building systems. Respond to utility and equipment related alarms and maintenance issues during manufacturing campaigns. Identify areas of potential to improve operational performance and compliance. Responsible to uphold safety procedures and safe practices. Provide technical support and troubleshooting for facility support equipment. Responsible for providing maintenance support for new facility equipment, installations and modifications to existing equipment. Documents all work in SAP and equipment log books. Participates in the 'On-Call' duties of providing 24/7 Maintenance suppo | 8/12/2018 |
| 512 | Brammer Bio Cambridge, MA Manufacturing Associate III BS in Life Sciences Exp: 1-3 yrs |
The Manufacturing Associate 4 is an associate with a moderate level of technical expertise and experience. An MA4 may perform complex activities outside of routine manufacturing operations commensurate with their experience and training. An MA4 participates in the day to day operation of a cGMP compliant Manufacturing facility. Responsibilities include performing basic to complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls under limited supervision. Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities. The MA 4 must be technically capable with a good theoretical comprehension of general biopharmaceutical manufacturing equipment, principles and processes and have a good understanding of current GMP and safety standards and be able to apply this knowledge in a GMP manufacturing environment during performance of routine activities. | 8/12/2018 |
| 513 | Brammer Bio Cambridge, MA Manufacturing Science & Technology Associate MS Exp: 0-2 yrs |
MST Associate role in the Analytics Laboratory within the Manufacturing Sciences and Technology (MST) Department to support the development, validation and execution of cell-based, nucleic acid-based, protein-based and chemistry-based assays that support quality control of cell and gene therapy products under development and manufacturing. | 8/12/2018 |
| 514 | Brammer Bio Cambridge, MA Document Specialist III BS in Life Sciences Exp: 1-3 yrs |
The document specialist 3 is an associate with a moderate level of expertise and experience with general biopharmaceutical manufacturing equipment, principles and processes and has a good understanding of current GMP and safety standards. The DS3 collaborates with subject matter experts and technical specialists to plan, develop, author, edit, format, illustrate, update, and create new standard operating procedures and other related documentation such as PBRs, logbooks, job aids and technical reports in support of the cGMP compliant Manufacturing facility. Responsibilities include maintaining established documentation design and quality standards, using performance tools (Human Performance) and managing documentation workflows to meet departmental needs. Additional responsibilities may include administrative duties to manage and process controlled documents for the manufacturing facility. | 8/12/2018 |
| 515 | Brammer Bio Cambridge, MA Document Specialist I BS in Life Sciences Exp: 1-3 yrs |
The document specialist 1 is an associate with a minimal level of expertise and experience with general biopharmaceutical manufacturing equipment, principles and processes and has a good understanding of current GMP and safety standards. The DS1 collaborates with subject matter experts and technical specialists to plan, develop, author, edit, format, illustrate, update, and create new standard operating procedures and other related documentation such as PBRs, logbooks, job aids and technical reports in support of the cGMP compliant Manufacturing facility. Responsibilities include maintaining established documentation design and quality standards, using performance tools (Human Performance) and managing documentation workflows to meet departmental needs. Additional responsibilities may include administrative duties to manage and process controlled documents for the manufacturing facility. | 8/12/2018 |
| 516 | Brammer Bio Cambridge, MA Associate - Molecular, Quality Control BS in Life Sciences Exp: 1-3 yrs |
This position will work in the GMP compliant QC Laboratories to qualify, and conduct cell-based, nucleic acid-based, protein-based, and chemistry-based assays that support quality control of biopharmaceutical products being developed and manufactured. Will perform routine assays and testing including PCR, real time PCR, agarose gel electrophoresis, SDS-PAGE, immuno blotting, ELISAs, immunocytochemistry, and infectivity and reporter gene based cell assays using insect or mammalian cell lines. Functions also involve maintenance of cell lines used in the QC laboratories, maintenance (routine and preventive operation) of equipment, and preparation and purification of commonly used biological reagent and chemical supplies. The incumbent will be expected to technically interpret, write controlled documents and reports, and review data produced by self and participate in laboratory investigations. Will interact with other departments to ensure that sample flow, supply chain, and equipment disposition are correctly maintained. | 8/12/2018 |
| 517 | Bristol-Myers Squibb Syracuse, NY ASSISTANT SCIENTIST BS in Biological Sciences or related field Exp: 0-3 yrs |
Perform laboratory analysis of samples, using aseptic technique, following established procedures and in full compliance with official compendial, health authority regulations, and established BMS policies. Conduct qualification of methods and/or other laboratory studies, according to scientific protocols. Maintains accurate records of work performed and documents results, according to Good Documentation Practices and established procedures as well as perform data entry into LIMS. Assist with review of worksheets and laboratory data as assigned. Assists in the investigation of OOS results in areas of assigned responsibility. Operates and maintains laboratory instruments, while ensuring the reliability of instrumentation through proper maintenance, with ability to troubleshoot minor issues. Must analyze, evaluate, and interpret data, notifying clients of results, and assisting to resolve issues, if applicable. Identify opportunities for workflow and procedural improvements. | 8/12/2018 |
| 518 | Bristol-Myers Squibb Devens, MA Associate, QC Microbiology BS in Biological Sciences or related field Exp: 0-2 yrs |
Perform routine utility monitoring and in-process testing in accordance with SOPs, safety, and cGMP guidelines to support the release and stability of finished products, raw materials, in-process materials, and various components. | 8/12/2018 |
| 519 | Catalent Woodstock, IL Microbiologist BS in Microbiology or Biological Sciences Exp: 1-4 yrs |
The Microbiologist, reporting to the Microbiology Lab Manager, will be instrumental in performing microbiological analyses, water sampling (DI water and WFI), in-process bioburden testing of raw materials and bulk product, final product endotoxin and sterility testing, investigating out-of-limit or out-of-specification test results, and providing lab support for validation and business development activitie | 8/12/2018 |
| 520 | Catalent Woodstock, IL Validation Engineer BS in Mechanical or Chemical Engineering Exp: 1 yr |
The Validation Engineer will be instrumental in the design, schedule, execution, and evaluation of scientifically and statistically sound qualification experiments. These experiments define and demonstrate that critical Cleaning, Controls, Equipment, Facilities, Processes, and Utilities function in a consistent and repeatable manner, in accordance with a host of regulations and policies affecting final product integrity. | 8/12/2018 |
| 521 | Catalent Madison, WI Associate, cGMP Biomanufacturing BS/BA in Biotechnology, or related field Exp: 0 yr |
As an Associate, cGMP Biomanufacturing you will be part of a group that is responsible for current Good Manufacturing Practices (cGMP) production activities, including Master/Working Cell Bank production, Upstream cell culture, Downstream protein/mRNA purification, and/or Fill/Finish. | 8/12/2018 |
| 522 | Catalent Madison, WI Assistant Scientist, Analytical Development - Formulation BA/BS/MS in Biotechnology Exp: 1-3 yrs |
The Assistant Scientist, Analytical Development - Formulation position will perform a variety of laboratory procedures to support Analytical Development. The Assistant Scientist, Analytical Development - Formulation will perform daily work assignments accurately and in a timely and safe manner. The Assistant Scientist, Analytical Development - Formulation will independently evaluate, select and apply standardized scientific and techniques; assignments have clear and specified objectives, and require the investigation of a limited number of variables. This position relies on limited experience and exercises judgment within defined procedures and practices in making minor adaptations and modifications. | 8/12/2018 |
| 523 | Catalent Kansas City, MO Associate Scientist BS in life sciences Exp: 0-3 yrs |
The main activities will be to provide and report data, as required by project contracts within the Biologics Department. The data may be used for submission in Regulatory packages, release and stability testing of clinical and animal trial dose forms and in support of development projects. | 8/12/2018 |
| 524 | Catalent Madison, WI Chemist BS in Chemistry or other relevant discipline Exp: 1-5 yrs |
The Chemist will be responsible for testing raw materials, in-process, finished product, and stability samples as well as investigating out of specification test results. | 8/12/2018 |
| 525 | Catalent San Diego, CA Pharmaceutical Process Engineer I BS in Engineering Exp: 0-3 yrs |
Set up and operation of small scale and pilot scale pharmaceutical manufacturing equipment; Evaluation of drug product formulation processes and procedures;Execution of demonstration batches prior to cGMP productions. | 8/12/2018 |
| 526 | Caris Life Sciences Phoenix, AZ Quality Assurance Specialist BS Exp: 1-3 yrs |
This position is responsible for assisting in maintaining regulatory compliance to all applicable regulatory requirements and the occurrence management system in accordance with regulatory requirements. | 8/12/2018 |
| 527 | Cancer Genetics, Inc. Rutherford, NJ Microdissection Technician BS in medical science-related field Exp: 1 yr |
Under the general supervision of the Microdissection / Histology Supervisor and Medical Director, the Microdissection Technician is responsible for the day-to-day performance of solid tumor H&E screening and microdissection procedures. | 8/12/2018 |
| 528 | Cell Signaling Technology, Inc. Danvers, MA Cell Signaling Technology, Inc. BS in Biological Sciences or related field Exp: 1 yr |
The mission of the VSC is to provide a single source of well-characterized, high quality cells and lysates to the Product Development organization to enable accelerated product development cycle times. Additionally, the VSC serves as a center of innovation for the culture, treatment, lysis, and storage of cell lines. These team members are expected to continuously evaluate leading edge technologies and techniques, and to sponsor their implementation in their work. | 8/12/2018 |
| 529 | Cayman Chemical Company Ann Arbor, MI Quality Assurance Assistant BS in Life Sciences Exp: 1-3 yrs |
Ensures any products that are not qualified internally have batch-specific data provided by the supplier;Manages vendor data, assuring it is stored for easy retrieval by Tech Support and others. | 8/12/2018 |
| 530 | Cayman Chemical Company Ann Arbor, MI QC Chemist - Chemistry BS in Chemistry Exp: 1-3 yrs |
Conducts method development, material and final product qualifications ; working with moderate independence;Working knowledge in many analytical areas including wet chemistry, gas and liquid chromatography, IR and UV spectrometry. | 8/12/2018 |
| 531 | Champion Oncology, Inc. Rockville, MD Research Technician I, Study Services BS/MS in biology, pharmacology, or related field Exp: 1 yr |
Support in vivo oncology studies in mice as a member of the Study Services Team. | 8/12/2018 |
| 532 | Ceva Lenexa, KS Bioreactor Technician BS/MS in Medical Process Engineering, Biochemical Engineering, Biotechnology Engineering, Microbiology, Biology, Virology, Biochemistry or equivalent Exp: 1-3 yrs |
The Bioreactor Technician will work directly with a range of scientific, technologies and equipment supporting the production of biological processes in vaccine preparations. The Bioreactor Technician is responsible for direct involvement into manufacturing processes, trouble-shooting equipment issues, and involvement in optimizing existing processes to achieve the highest process quality, yield and efficiency. The candidate must be willing to work cohesively in a team environment to solve manufacturing issues across the entire Ceva Biomune Campus. The Bioreactor Technician will apply both microbial and engineering principles and concepts to new and existing manufacturing processes. The incumbent will work cross-functionally with Maintenance, Engineers, and Scientists; on the operational floor to develop and support optimal manufacturing workflows following aseptic technique and cGMP procedures. The Bioreactor Technician will work directly with a range of technologies and equipment including microscopes, centrifugation, roller bottles, cell cubes, bioreactors, filtration skids. The Technician will work directly with cell culture and viral propagation techniques, buffer and equipment preparations, cell culture and bioreactor operations, bacterial and fermentation operations, and inactivation methods following aseptic technique and cGMP procedures | 8/12/2018 |
| 533 | Ceva Lenexa, KS GIPI Technician I BS/MS in Microbiology, Virology, Biochemistry or equivalent Exp: 1-2 yrs |
Assist in the development of laboratory based state-of-the-art and cost effective biological production, quality control, and analytical techniques to facilitate production from laboratory to industrial scales for new and existing products | 8/12/2018 |
| 534 | Biocare Medical, LLC. Pacheco, CA Lab Services Laboratory Assistant BS Exp: 1-2 yrs |
Work as part of Lab Services team to provide support for all routine Histology and IHC work pertaining to delivery of CAP/CLIA and GLP-like oriented lab services offered to external partners, including BioPharma, Academia, and Oncology Research Centers. | 8/5/2018 |
| 535 | BioAssay Systems Hayward, CA SCIENTIST - ASSAY DEVELOPMENT BS in biochemistry, chemistry or biology Exp: 1-2 yrs |
This position will entail developing novel assays kits and performing service projects. The assay kit development will utilize colorimetric, fluorescent and luminescence methods for both liquid based assays and paper based test strip formats. This candida | 8/5/2018 |
| 536 | Bioclinica Melbourne, FL Clinical Research Coordinator BS in a health-related field Exp: 1 yr |
The CRC I plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned research projects. The CRC I follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff | 8/5/2018 |
| 537 | Bioclinica Melbourne, FL Clinical Research Coordinator I BS in a health-related field Exp: 1 yr |
The CRC I plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned research projects. The CRC I follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff | 8/5/2018 |
| 538 | Ajinomoto Althea, San Diego, CA DRUG PRODUCT MANUFACTURING ASSISTANT BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. | 8/5/2018 |
| 539 | Ajinomoto Althea, San Diego, CA DRUG SUBSTANCE MANUFACTURING ASSOCIATE II – DOWNSTREAM BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
Althea is currently seeking a Drug Substance Manufacturing Associate II – Downstream responsible executing the day to day responsibilities related to the Drug Substance Manufacturing Downstream group under the guidance of Althea's established procedures a | 8/5/2018 |
| 540 | Baxter Marion, NC Quality Lab Assoc I Chemistry BS in Micro and Biology Exp: 0-2 yrs |
Conduct critical biological, chemical and physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision. | 8/5/2018 |
| 541 | Baxter Marion, NC QLA I-Microbiology Lab BS in Microbiology or Biological Science Exp: 0-2 yrs |
Perform sampling to support the Environmental Monitoring Program; Use laboratory instrumentation and computer systems to collect and record data. | 8/5/2018 |
| 542 | Baxter Round Lake, IL Engineer II, Data and Validation BS Exp: 1-3 yrs |
Interacts with manufacturing facilities globally to define information flows and dashboards. Interacts with global complaints handling process. Publishes monthly and ad-hoc reports. Conducts investigations into specific complaints and manufacturing event | 8/5/2018 |
| 543 | Baxter Marion, NC Quality Lab Assoc. I (Micro EM) BS in Microbiology or Biological Science Exp: 0-2 yrs |
Conduct microbiological analyses on raw materials, in-process and finished products; Collect samples related to Environmental Monitoring program at Baxter manufacturing area. | 8/5/2018 |
| 544 | BioLegend San Diego, CA Quality Control Associate- Flow Cytometry BS in a field of Life Sciences Exp: 1 yr |
The primary responsibilities include performing experiments (e.g. cell culture, cell preparation and flow cytometry testing), analysis and reporting of data, maintaining accurate documentation, use internal company databases for product filing and retriev | 8/5/2018 |
| 545 | BioLegend San Diego, CA Manufacturing Associate - Legendplex BS in Biology, Chemistry, or other relevant discipline Exp: 1 yr |
The Manufacturing Associate will be working closely with the manufacturing lead and others on the team to ensure the timely production of high quality multiplex bead-based immunoassay products. The primary responsibilities for this position are performing | 8/5/2018 |
| 546 | BioLegend San Diego, CA Manufacturing Associate - Chemistry BS in Biology, Chemistry, or other relevant discipline Exp: 1 yr |
The main responsibility for this position will be to assist in the large-scale manufacturing of magnetic nanoparticles conjugated with proteins such as streptavidin and antibodies according to established Standard Operating Procedures (SOPs). Other duties | 8/5/2018 |
| 547 | BioLegend San Diego, CA Research Associate Cell Biology BS Exp: 1 yr |
The Research Associate position in Cell Biology group will support the development of new antibody and ancillary products. This position will play an integral role in antibody characterization for applications such as Western Blotting, immunofluorescence | 8/5/2018 |
| 548 | BioLegend San Diego, CA Research Associate - Immunoassay BS in Immunology or other relevant biology discipline Exp: 1 yr |
The Immunoassay Associate will work closely with an experienced scientist on the product development team within the group and will be responsible for developing cutting edge research products utilizing bead-based sandwich immunoassay and flow cytometry t | 8/5/2018 |
| 549 | BioLegend San Diego, CA Manufacturing Associate-Purification BS in Biology, Biochemistry, Chemistry, or Science Exp: 1 yr |
This position will be an individual contributor role within the Purification Team and will be responsible for performing all essential functions related to antibody purification. Essential tasks for this position include: following Standard Operating Pro | 8/5/2018 |
| 550 | BioLegend San Diego, CA Research Associate Cell Analysis BS in a Life Sciences related field Exp: 1 yr |
This position will actively participate in all stages of the development, optimization and validation of new products, including antibodies, proteins, and other probes for various research fields. The primary responsibilities include performing experimen | 8/5/2018 |
| 551 | Biogen Research Triangle Park, NC Associate II, Knowledge and Content Management BS/BA Exp: 1-3 yrs |
The Corporate Quality Knowledge and Content Management team is responsible for developing and delivering the strategies, methods and tools used to identify, capture, manage, store, and deliver all information assets (knowledge, content, and records) relat | 8/5/2018 |
| 552 | Biogen Research Triangle Park, NC Associate Sci II/Engineer I, Protein Formulation and Process Development MS Exp: 0-2 yrs |
As a member of Biogen’s Drug Product development team, the candidate will be responsible for providing formulation and process development support for injectable protein drug product development programs. Planning, executing, and communicating results fro | 8/5/2018 |
| 553 | BiopharmX Menlo Park, CA RESEARCH ASSOCIATE BS/BA/MS in Cell Biology or related field Exp: 1-2 yrs |
The employee will be responsible for the scientific/technical aspects of assigned preclinical studies, including animal handling, cell culture, general biochemical techniques, such as western blotting and ELISA. The position’s primary purpose is to assist | 8/5/2018 |
| 554 | BioMarin NOVATO, CA RESEARCH ASSISTANT/ASSOCIATE BS in biological science, chemistry, chemical engineering, or biological engineering degree Exp: 1-3 yrs |
The Research Assistant/Associate is involved with the design of protein purification processes suitable for manufacturing therapeutic proteins or gene therapy vectors, and with the transfer of those processes to manufacturing facilities. The Assistant/Ass | 8/5/2018 |
| 555 | BioMarin SAN RAFAEL, CA RESEARCH ASSOCIATE I / II - VECTOR BIOLOGY, GENE THERAPY MS Exp: 1 yr |
Successful candidates will join a dynamic interdisciplinary group which will develop and commercialize the major gene therapeutics for several genetic diseases. | 8/5/2018 |
| 556 | Bio-Technical Resources Manitowoc , WI ASSISTANT RESEARCH SCIENTIST, MICROBIOLOGY/MOLECULAR BIOLOGY BS/BA in microbiology or molecular biology Exp: 6month-1 yr |
Bio-Technical Resources is seeking an Assistant Research Scientist to work with supervision as a microbiologist and molecular biologist as part of a team developing new strains for the production of antibiotics, enzymes, metabolites, and proteins. | 8/5/2018 |
| 557 | Bio-Technical Resources Manitowoc , WI ASSISTANT RESEARCH SCIENTIST, ANALYTICAL SUPPORT BS/BA in analytical chemistry, biochemistry, or chemical engineering Exp: 1 yr |
Bio-Technical Resources is seeking an Assistant Research Scientist to work with supervision as an analytical research assistant supporting teams developing fermentation and biotransformation processes for the production of antibiotics, enzymes, proteins, | 8/5/2018 |
| 558 | Bio-Techne Boston, MA Research Associate 1 BS/MS in Biological Sciences Exp: 0-3 yrs |
We seek a protein biochemist who will contribute to the ongoing research and development of products including complex assay systems, post-translationally modified proteins and peptides, and recombinant enzymes. The successful candidate will have previous | 8/5/2018 |
| 559 | Bio-Techne San Jose, CA Manufacturing Associate BS Exp: 1-5 yrs |
This individual will work with other members of the production team as well as a multidisciplinary team of engineers and scientists to support our consumables production demand. | 8/5/2018 |
| 560 | Bio-Techne Woburn, MA Research Associate BS/MS in Biological Sciences or related discipline Exp: 0-2 yrs |
This is a fast-growing life sciences location focused on transforming cell separation and cell therapy manufacturing workflows though our disruptive QuickGelTMtechnology. This Research Associate position will provide technical and logistical support for o | 8/5/2018 |
| 561 | Bio-Techne Minneapolis, MN Technical Service Associate BS in Biological Sciences, Biochemistry or equivalent Exp: 0-2 yrs |
Answers and documents in CRM incoming customer inquiries by phone, email, and LiveChat on product techniques & procedures and performs simple trouble-shooting. Communicate to obtain all pertinent information relating to inquiry. Communicate adequate infor | 8/5/2018 |
| 562 | Bio-Techne Minneapolis, MN Research Associate 1/2 BS in Biology or related biological science Exp: 0-6yrs |
As a Research Associate in the QC Immunoassays group your responsibilities will be to perform Luminex assays and Qkit ELISA assays to check for quality performance of product, maintain accurate documentation of results, and maintain assay database. You wi | 8/5/2018 |
| 563 | Bio-Techne San Jose, CA Process Engineer MS in a Chemistry, Automation, Science or Engineering-related discipline Exp: 1 yr |
The successful applicant will support and engage with members of the Consumables Manufacturing/ Production team, as well as a multidisciplinary team of engineers and scientists, to support the production of microfluidic devices incorporating chemically mo | 8/5/2018 |
| 564 | Bio-Techne Minneapolis, MN Manufacturing Associate 1 BS in biochemistry, chemistry, biology, microbiology, or equivalent Exp: 0-2 yrs |
As a Manufacturing Associate at Bio-Techne you will be processing retail bottling of antibodies and protein, as well as capping and labeling of antibodies and proteins. You will be responsible for special and bulk bottling for retail customers. Additional | 8/5/2018 |
| 565 | Biorasi Aventura, FL Clinical Trial Assistant BS in biomedical sciences or related scientific discipline Exp: 1-2 yrs |
Support Clinical Trial Manager (CTM) in preparing and/or reviewing study-related documents (e.g., Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, and CRF Completion Guidelines). | 8/5/2018 |
| 566 | Bio-Rad Woodinville, WA QC Chemist I BA/BS in Life Sciences Exp: 0-2 yrs |
The QC Chemist I position will perform activities related to the review and release of in-process batch records for Quality Control. | 8/5/2018 |
| 567 | Bio-Rad Irvine, CA Research Assoc III BS/MS Exp: 1-3 yrs |
Plans and performs moderate to complex experiments to support development of new quality control products for use with in vitro diagnostic infectious disease assays and helps facilitate timely completion of multiple projects following established mileston | 8/5/2018 |
| 568 | Bio-Rad Hercules, CA Manufacturing Chemist (Chemist I) BS/BA in Biology, Cell Biology, Micro Biology, Biochemistry, Chemistry Exp: 0-2 yrs |
The Manufacturing Chemist will support NGS and droplet manufacturing of Bio-Rad's RainDance product line. Work will focus on all aspects of manufacturing. The Manufacturing Chemist will be expected to plan and perform the manufacturing of reagents and c | 8/5/2018 |
| 569 | Bio-Rad Woodinville, WA Quality Engineer I BS Exp: 0-2 yrs |
The Quality Engineer I works both collectively with a team and individually to administer, evaluate, maintain, modify and improve quality method, processes and programs that support products that are manufactured and distributed. | 8/5/2018 |
| 570 | Bio-Rad Pleasanton, CA Research Assoc I - Temp BS/MS in molecular biology, biochemistry or related fields Exp: 1-2 yrs |
Verification and Validation of droplet digital biology products, including but not limited to assays, reagents, consumables, instruments and software. | 8/5/2018 |
| 571 | Bio-Rad Hercules, CA Research Associate I BS in Chemistry or the Life Sciences. Exp: 1 yr |
Assists R&D scientists in new product development and product improvement activities | 8/5/2018 |
| 572 | Biotronik Lake Oswego , OR Quality Systems Specialist BS in Biosciences or Healthcare related field Exp: 1 yr |
The right candidate will support activities associated with compliance to FDA regulations and policy, and HIPAA requirements as well as other associated regulatory concerns. You’ll be part of a dynamic team that functions cohesively to ensure that all reg | 8/5/2018 |
| 573 | bluebird bio Cambridge, MA Associate Scientist, T cell Gene Editing BS/MS in cell biology, immunology or related discipline Exp: 1 yr |
Develop and optimize protocols for T cell gene editing, including: megaTAL delivery methods, culture conditions, scale up, and multiplexing | 8/5/2018 |
| 574 | Ajinomoto Althea, Inc San Diego, CA DRUG SUBSTANCE MANUFACTURING ASSOCIATE II – DOWNSTREAM BS in a life science discipline Exp: 0-2 yrs |
Althea is currently seeking a Drug Substance Manufacturing Associate II – Downstream responsible executing the day to day responsibilities related to the Drug Substance Manufacturing Downstream group under the guidance of Althea's established procedures and policies. The position works under the guidance of experienced team members in support of the technical transfer and integration of processes into the Drug Substance Manufacturing Downstream department. The position will be exposed to chromatography and TFF (UF/DF) systems employed during manufacturing campaigns. | 7/29/2018 |
| 575 | Ajinomoto Althea, Inc San Diego, CA DRUG PRODUCT MANUFACTURING ASSISTANT - MULTIPLE OPENINGS ON 1ST AND 2ND SHIFT BS in a life science discipline Exp: 0-2 yrs |
The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements | 7/29/2018 |
| 576 | Aprecia East Windsor, NJ Analytical Development Chemist Exp: 0 yr |
This position is responsible for performing routine testing of raw materials, intermediates, and finished product to support product development. Works with minimal supervision to assist in analytical method development and pre-validation. Interacts extensively with Product Development and Quality functions to proactively deliver Analytical Development supports and to leverage analytical sciences to characterize and understand formulations and novel 3DP (three-dimensional printing) manufacturing processes. In addition, this position is also responsible for writing protocols, development reports, and SOPs (standard operating procedures); training others on analytical techniques; being familiar with USP/NF (United States Pharmacopeia/National Formulary) analytical procedures; and maintaining an understanding of cGMPs (current Good Manufacturing Practices) and ICH (International Conference on Harmonization) guidelines. | 7/29/2018 |
| 577 | Arcturus Therapeutics Ltd. San Diego, CA Research Associate I, RNA Production BS Exp: 1 yr |
The successful candidate will be responsible for leading and carrying out required lab activities for RNA targets including cloning and production of plasmid constructs, developing and executing biochemical assays, producing and purifying RNA, and supporting process development for clinical RNA manufacture. This individual will prepare detailed standard operating procedures for technology transfer. The RA I will work with a team of highly motivated scientists in the RNA Science, RNA production and analytical sciences group. This individual will support project leads, key internal and external stakeholders, and Arcturus’ research leadership to advance development projects. | 7/29/2018 |
| 578 | ArcherDx Boulder, CO Regulatory Affairs Associate BS/BA Exp: 1-3 yrs |
The Regulatory Affairs Associate, reporting to the Regulatory Affairs Manager, will help develop, implement and maintain the Regulatory Processes within the Quality Management System (QMS), including creation and maintainenance of the documentation associated with filing for high risk medical device for the US and OUS submissions. | 7/29/2018 |
| 579 | Arrowhead Pharmaceuticals, Inc Madison, WI Process Chemist BS/MS Exp: 1-5 yrs |
The successful candidate will be tasked with developing and scaling methods for the manufacturing of oligonucleotides to support toxicological testing of investigational drug substances. | 7/29/2018 |
| 580 | Arthrex, Inc. Naples, FL Clinical Research Assoc - Data Assistance BS Exp: 1 yr |
Assists the study team in running the day to day operational activities of clinical studies. Assist in the development and maintenance of Electronic Trial Master File (eTMF) and Electronic Data Capture (EDC). | 7/29/2018 |
| 581 | Assurex Mason, OH Lab Tech I BS/MS Exp: 0-1 yr |
At Assurex The Laboratory Technologist I is responsible for specimen processing, test performance and reporting of test results according to laboratory procedures. This position reports to the Laboratory Manager. | 7/29/2018 |
| 582 | Associates of Cape Cod, Inc. Falmouth, MA QUALITY CONTROL ANALYST I BS Exp: 0-2 yrs |
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. | 7/29/2018 |
| 583 | Atreca Redwood City, CA RESEARCH ASSOCIATE, PROTEIN BIOCHEMISTRY BS in molecular biology, biochemistry or related discipline Exp: 1-6 yrs |
In this position, the successful candidate will apply her/his skills and expertise in protein biochemistry to assist in purifying protein targets bound by Atreca antibodies so that they may be identified using protein sequencing techniques. These methods include immunoprecipitation, chromatography and other protein biochemistry techniques. | 7/29/2018 |
| 584 | Astellas Pharma Marlborough, MA Manufacturing Associate 1 BA Exp: 0-2 yrs |
The position performs duties with appropriate supervision and according to standard operating procedures. The position participates in technical investigations of process deviations to ensure production proceeds as scheduled and also assists in laboratory maintenance duties. | 7/29/2018 |
| 585 | Astellas Pharma Marlborough, MA Research Associate II, Assay Development MS in cell or molecular biology or related discipline Exp: 0-2 yrs |
The Research Associate 2, Assay Development will support assay development activities by performing cell culture and wet lab experiments, analyzing data, and drafting protocols and reports. This individual will collaborate closely within the team and across functional groups (R&D/QC) to advance pipeline programs. | 7/29/2018 |
| 586 | Astellas Pharma Marlborough, MA Stem Cell Research Associate BA/BS Exp: 1-2 yrs |
We are seeking an energetic and driven Stem Cell Research Associate to join our team to design and implement cell and molecular biology laboratory research in the lab and work directly with preclinical disease models. | 7/29/2018 |
| 587 | AstraZeneca Mount Vernon, IN Formulation Process Engineer / Sr. Process Engineer MS Exp: 0 yr |
You will be responsible for providing technical support for process manufacturing, including investigation and correction of process-related problems and deviations from standards. | 7/29/2018 |
| 588 | AstraZeneca Coppell, TX Microbiologist I BS in microbiology, chemistry Exp: 1-2 yrs |
Perform and document routine tasks related to sample processing and assays using written operating procedures, standard laboratory methods and/or basic laboratory techniques, functions and equipment. | 7/29/2018 |
| 589 | Assembly Biosciences Groton, CT Associate Scientist, Drug Substance Process Development BS/MS Exp: 1-5 yrs |
The selected candidate for Drug Substance Process Developmentwill play a pivotal role in the development of processes for the production of human commensal bacteria suitable for formulation as Drug Product. It is expected that the individual will also work closely with the Drug Product formulations team to coordinate the transfer of formulations and processes, facilitate phase-appropriate scale-up, provide analytical support and lead troubleshooting activities. | 7/29/2018 |
| 590 | Avid Bioservices Tustin, CA Research Associate/Sr. Research Associate, Upstream Cell Culture Process Development MS in Biological Science Exp: 1-2 yrs |
We are seeking a Research Associate/Sr. Associate, Process Development who is interested in pursuing a career in developing biologics and pharmaceutical agents. The Sr. Research Associate ("RA") will assist process development in developing and optimizing scalable processes with improved product yield and reduced costs for manufacturing systems. In addition, the Sr. RA may assist with the maintenance of production equipment and may research and implement new methods and technologies to enhance process operations. | 7/29/2018 |
| 591 | Avid Bioservices Tustin, CA Quality Assurance Specialist BS in a Science discipline Exp: 0-1 yr |
The Quality Assurance Specialist is an individual contributor who solves a variety of issues following cGMP regulations and company standards. | 7/29/2018 |
| 592 | Avid Bioservices Tustin, CA Downstream Research Associate/Sr. Associate, Process Development BS Exp: 0-2 yrs |
The Research Associate provides laboratory support for Process Development and performs a range of activities (while the Sr. position performs at a senior level). The employee may be assigned various tasks within the department to complete. | 7/29/2018 |
| 593 | Avid Bioservices Tustin, CA Associate Specialist, Quality Assurance BS/BA Exp: 0-2 yrs |
The Quality Assurance Associate Specialist is an individual contributor who solves a variety of issues following cGMP regulations and company standards. | 7/29/2018 |
| 594 | Avedro Burlington, MA Associate Research Scientist BS/MS in a scientific or biomedical discipline Exp: 0-2 yrs |
This highly motivated candidate will work within a small multidisciplinary project team, helping to support a focused research effort into phototherapy processes to treat the eye. This individual will also be responsible for conducting laboratory-based research, including implementing and executing experimental assay protocols with a focus on timely and accurate results. Accurate and timely recording of data in lab notebooks and electronic files will be a priority. | 7/29/2018 |
| 595 | Bellicum Pharmaceuticals, Inc. Houston, TX Manufacturing Associate BS in chemistry or biological sciences or equivalent Exp: 0-1 yr |
Participates in the production of life saving gene-modified cellular product for Bellicum | 7/29/2018 |
| 596 | Bellicum Pharmaceuticals, Inc. Houston, TX Assay Development Associate MS in the life sciences or related discipline Exp: 1 yr |
The successful candidate will work with the other team members to support the development, characterization, and tech transfer of analytical assays to other teams. The selected candidate will be highly independent and self-motivated, and will make detailed observations, analyze data, summarize and interpret results. In addition to the primary responsibilities, the candidate will be responsible for maintaining laboratory equipment and space. | 7/29/2018 |
| 597 | Danaher Timonium, MD Manufacturing Process Engineer BS in Manufacturing or Mechanical Engineering or related discipline Exp: 1 yr |
Control manufacturing and engineering specifications for the plant; Implement ICR’s/ECR’s; Maintain plant ISO procedures. | 7/29/2018 |
| 598 | Danaher Miami, FL Manufacturing/Process Engineer BS in an Engineering Discipline Exp: 1 yr |
The Senior Manufacturing Engineer supports the development, implementation and maintenance of manufacturing methods, techniques, processes, and tooling on fabricated parts, components, subassemblies, and final products. Interfacing as appropriate with Development, Quality, Manufacturing, Purchasing and suppliers, the incumbent assists with coordinating the release of new and enhancements to existing products; participates in design reviews, inspections and MRB processes; aids the development product structures; provides technical support for internal and external suppliers; participates in the resolution of technical issues; and ensures manufacturing documents are created, updated and in compliance with company standards, ISO and GMP as required. | 7/29/2018 |
| 599 | Danaher Belleville, IL Product Development Test Engineer BS in an engineering, engineering technology, or science field Exp: 0-2 yrs |
The successful candidate will be an integral member of the R&D team for product enhancements and new product development. This is a hands-on position. Responsibilities include: Test plan development, testing execution, evaluation of test results, limited fabrication, Mechanical and electrical assembly, troubleshooting, and full functional testing including software. As your knowledge and understanding of our products grow you will be expected to provide recommendations for product improvements ranging from function and reliability to improved manufacturability. | 7/29/2018 |
| 600 | Danaher Ames, IA Compliance Chemist BA/BS in a Physical Science, Chemistry Exp: 0-2 yrs |
Maintain programs and policies in place to ensure legal and regulatory compliance with National and International chemical regulations. Provide support for corporate compliance and key objectives through continuous improvement and other corporate policies. | 7/29/2018 |
| 601 | Danaher Chaska, MN Supplier Quality Analyst I BS Exp: 0-2 yrs |
The Supplier Quality Analyst ensures suppliers deliver quality product on an on-going basis, while developing supplier capability for future needs. This includes supplier selection & approval, material qualification, material control and supplier development activities. The individual will be responsible for assisting in investigations of nonconforming materials to understand the root cause of failure. The person plans, coordinates, and reports on material projects and supplier performance. The individual must demonstrate sound technical ability and decision making to achieve the desired results. The person will represent QA on development, manufacturing and product improvement projects. | 7/29/2018 |
| 602 | Baxter Round Lake, IL Assoc II, Research MS in a scientific or engineering Exp: 0-2 yrs |
Effectively contribute solid technical knowledge to a variety of projects related to process development with minimal assistance.Display basic technical understanding of process development.Conduct routine/non-routine research and design experiments with minimal assistance. | 7/29/2018 |
| 603 | Baxter Marion, NC Quality Lab Assoc I Chemistry BS in Micro and Biology Exp: 0-2 yrs |
Conduct critical biological, chemical and physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision. | 7/29/2018 |
| 604 | Baxter Round Lake, IL Engineer II BS in Engineering Exp: 1-3 yrs |
Responsible for designing, developing, implementing and evaluating optimal, cost-effective projects and technologies. In addition to providing technical support and service to these areas, the incumbent may also perform the following functions: supervising, requisitioning, defining, initiating, specifying, documenting and training. | 7/29/2018 |
| 605 | Baxter Mountain Home, AR Quality Assoicate I BS Exp: 1-2 yrs |
Responsible for providing supervisory support to Quality Manager. Supervises the product and process testing, calibration, release, documentation, complaint reduction required by: Corporate specifications, Plant Standard Operating Procedures, FDA regulations, ensure compliance with GMP/QSRs and all applicable ISO and Country Standards, and Corporate/Plant goals. | 7/29/2018 |
| 606 | Baxter Mountain Home, AR Quality Associate BS Exp: 1-2 yrs |
Responsible for providing supervisory support to Quality Manager. Supervises the product and process testing, calibration, release, documentation, complaint reduction required by: Corporate specifications, Plant Standard Operating Procedures, FDA regulations, ensure compliance with GMP/QSRs and all applicable ISO and Country Standards, and Corporate/Plant goals. | 7/29/2018 |
| 607 | Baxter Mountain Home, AR Assoc I, Quality Lab BS in Chemistry or a related physical science Exp: 0-2 yrs |
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. | 7/29/2018 |
| 608 | Axsome Therapeutics, Inc. New York City, NY Clinical Trials Assistant BS in a biological or physical life science or a nursing degree or equivalent Exp: 1 yr |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. | 7/29/2018 |
| 609 | Avomeen ANN ARBOR, MI QUALITY ASSURANCE SPECIALIST BS Exp: 0-3 yrs |
Manage laboratory accreditation applications and renewals including DEA licensing and ISO registration; Perform and review internal audits of the laboratory quality program. | 7/29/2018 |
| 610 | Avomeen ANN ARBOR, MI ANALYTICAL CHEMIST BS/MS in Chemistry Exp: 0-5 yrs |
Learn techniques spanning across the entire spectrum of analytical chemistry from wet chemistry to HPLC, NMR, Mass Spectrometry, FTIR, GC and GC-MS. | 7/29/2018 |
| 611 | Bausch Health Companies Inc. Rochester, NY Technician IV, Lens Compatibility & Stability BS Exp: 1 yr |
Support the development of new lens and lens care products. Support testing of currently marketed products. | 7/29/2018 |
| 612 | BERG, LLC Framingham, MA Research Associate I - Neurology BS/MS in biology, biochemistry, neuroscience or a related field Exp: 1-2 yrs |
Assist in the characterization of novel diagnostic biomarkers and therapeutic targets for Alzheimer’s and Parkinson’s disease using standard molecular biology techniques | 7/29/2018 |
| 613 | BERG, LLC Framingham, MA Research Associate I/II - Immuno-Oncology BS/MS in biology, immunology, or a related field Exp: 1-3 yrs |
The Research Associate I/II will report to the Immuno-Oncology Program Leader and will contribute to the development of novel therapeutics in cancer and other disease areas with focus on understanding the mechanism of action of lead compounds within the immune system. | 7/29/2018 |
| 614 | Alcami Wilmington, NC Assistant Scientist II BS in Pharmaceutical Sciences, Chemistry or equivalent Exp: 1-2 yrs |
The Assistant Scientist II is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Analytical Assistant Scientist II may also assist with method development/method validation projects. Typical types of testing: assays (potencies, related substances, residual solvents, metals etc.), rate of release (dissolution), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). 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. | 7/22/2018 |
| 615 | Alcami Germantown, WI Analytical Chemist BS in chemistry or related field Exp: 0-2 yrs |
The Analytical Chemist I is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of active pharmaceutical ingredients development or pharmaceutical manufacturing. This position may also be required to work on method development/method validation projects. Typical types of testing include: assays (potencies, related substances, residual solvents, metals etc.), moisture content, identification, and various other wet chemistry based measurements. HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations, UV, DSC, TGA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by Alcami). | 7/22/2018 |
| 616 | Aldevron Fargo, ND Lab Tech III - GMP Source BS in Life Sciences (Biology, Chemistry, Biotech) Exp: 0-2 yrs |
As a Lab Technician, you will be responsible for the detailed, thorough cleaning, line clearance, and segregation of GMP-Source production areas and associated equipment while wearing appropriate gowning. You will assist with training of other lab technicians and writing and completing Standard Operating Procedures. You will completing necessary equipment and facility control task requirements (like laboratory water sampling, and pH and conductivity calibration), along with other assigned duties. | 7/22/2018 |
| 617 | Aldevron Fargo, ND In-Process Quality Assurance Specialist BS in a Life Sciences discipline Exp: 1-2 yrs |
In this role, you will support Aldevron's quality assurance programs, processes and facilities by ensuring compliance with regulatory, internal and client requirements in the manufacture of products. You will act as quality representative on the floor during manufacturing operations | 7/22/2018 |
| 618 | Align Technology San Jose, CA Clinical Development Research Associate BS/MS Exp: 1 yr |
Responsible for gathering, analyzing, and generating global clinical evidence for both the Ortho and GP channels. Support of development of regulatory clinical evaluations, as well as clinical summaries for submissions to regulatory bodies. Additional duties include reviewing existing literature and providing summaries for cross-functional teams to use, clinical evidence gap analysis, and publication planning and development. | 7/22/2018 |
| 619 | Alexion New Haven, CT Development Associate I, Downstream Process Development BS in Biochemistry, Chemistry, Chemical Engineering or related discipline Exp: 0-2 yrs |
The Development Associate I is responsible for performing assigned experimental tasks to support the development and optimization downstream purification processes for Alexion’s biotherapeutic molecules and will be expected to accurately follow written procedures and contribute to laboratory tasks under supervision. The Development Associate I will collaborate regularly with scientific staff in other Research & Development groups. | 7/22/2018 |
| 620 | Abbott Scarborough, ME Technical Services Support Specialist BS/BA Exp: 1-2 yrs |
Under basic direction and supervision, the scope of this position is responsible for addressing customer calls and emails relating to product inquiries, opinions/suggestions and complaints concerning a variety of the company's products, using professional concepts, technical knowledge, and company’s strategies, tactics, and policies and procedures formulated in association with management, with the objective of satisfactorily addressing the customer's inquiry or complaint. | 7/22/2018 |
| 621 | Abbott Santa Rosa, CA Confirmations Laboratory Technician II BS in chemistry, analytical chemistry or related field Exp: 1 yr |
The GC/LC Lab Technician II will be responsible for processing batches of data compiled from the extractions of drugs of abuse in the Confirmation Laboratory. | 7/22/2018 |
| 622 | Abbott San Diego, CA Production Chemist II MS/MA in Chemistry or Biological Sciences Exp: 0-2 yrs |
Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. | 7/22/2018 |
| 623 | Abbott San Diego, CA Production Chemist 1 BA/BS Exp: 0-5 yrs |
Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. | 7/22/2018 |
| 624 | Abbott San Diego, CA Laboratory Technician II BA/BS Exp: 0-4 yrs |
Under close supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP, under the direction of senior staff. | 7/22/2018 |
| 625 | Abbott Pomona, CA Quality Control Technician II BS/BA in chemistry or biology Exp: 1-2 yrs |
To support QC functions within our Drugs of Abuse test manufacturing facility. The position will primarily focus on incoming, in-process and final QC testing, labeling, document inspection results and enter raw material inventory data to ensure the quality and functionality of manufactured products. | 7/22/2018 |
| 626 | AlloSource Centennial, CO Operations Processing Technicians BS Exp: 1 yr |
The Operations Production Technician (OPT) is responsible for safely and aseptically processing human tissue and cell products, and decontaminating, sterilizing reusable equipment and supplies. The OPTs perform responsibilities according to SOPs, WIs, equipment specifications and product specifications. Depending on the product/process, the OPT may utilize various tools, equipment, machinery, and chemicals. This position works in a Controlled Work Area (CWA). | 7/22/2018 |
| 627 | AlloSource Centennial, CO Research Associate BS/MS in Biology, or similar field Exp: 0-1 yr |
The Research Associate is an entry level role that works under direct supervision and executes studies to assist product development/characterization. Frequently uses and applies technical standards, principles, theories, concepts and techniques while contributing to the completion of milestones associated with specific R&D projects. Provides solutions to a variety of technical problems of small to moderate scope and complexity. Interacts within the department and with Marketing and Sales, Operations and Regulatory, will also engage in cross functional contact as well as outside vendor contacts on routine matters. | 7/22/2018 |
| 628 | Alkermes Waltham, MA Lab Technician, Small Molecule Drug Product Process Development BS in an Engineering discipline Exp: 0-2 yrs |
This position will manage the small molecule drug product process development laboratory and pilot plant, as well as aid in the execution of batch and continuous drug product unit operations. The position will also support implementation of new equipment and continuous process unit operations. Experience with control systems and skid build out is strongly desired. The candidate is expected to show a strong lab presence, a commitment to continuous learning, attention to detail, organizational skills, and electronic notebook record keeping | 7/22/2018 |
| 629 | Alkermes Waltham, MA Contract Research Associate II BS in Chemistry, Biochemistry, Biotechnology, Chemical Engineering or related field Exp: 0-1 yr |
A Research Associate in the Formulation Development Group will participate in the development of both liquid and lyophilized protein formulations to support formulation development from initial screening through commercialization. | 7/22/2018 |
| 630 | Alkermes Waltham, MA Research Associate II, Analytical Development MS in Chemistry, Analytical Chemistry, Biochemistry, Pharmaceutical Science, or related field Exp: 0-3 yrs |
Alkermes is currently seeking a talented and motivated scientist for a temporary position in the process analytical technology (PAT) group in Analytical Development. The successful candidate will actively contribute to the PAT method development. | 7/22/2018 |
| 631 | Alkahest, Inc. San Carlos, CA RESEARCH ASSISTANT / RESEARCH ASSOCIATE (IN VIVO) BS Exp: 1 yr |
This person will be involved in establishing, validating, and implementing methodologies in Alkahest’s laboratories and is thus pivotal to the company’s mission. | 7/22/2018 |
| 632 | ATEC SPINE Carlsbad, CA Design Engineer BS in mechanical or biomedical engineering Exp: 1-4 yrs |
Designs and develops implants and instruments utilizing SolidWorks; Assists in the development of new products and manufacturing processes and/or serves as a member of a development team. | 7/22/2018 |
| 633 | Ajinomoto Althea, Inc. San Diego, CA TEMPORARY ENVIRONMENTAL MONITORING ASSISTANT BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
The Environmental Monitoring Assistant is responsible for supporting manufacturing at Ajinomoto Althea, Inc through performing routine, process specific, and event response environmental monitoring. The Environmental Monitoring Assistant will require an understanding of aseptic technique, continuously exhibit proper clean room behavior, and adhere to cGMPs. | 7/22/2018 |
| 634 | Ajinomoto Althea, Inc. San Diego, CA SR. DRUG PRODUCT MANUFACTURING ASSISTANT BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
Althea is currently seeking a Sr. Drug Product Manufacturing Assistant responsible for implementation of semi-routine production and manufacturing procedures to optimize processes and regulatory requirements. | 7/22/2018 |
| 635 | Ajinomoto Althea, Inc. San Diego, CA SR. QC ASSISTANT – CHEMISTRY BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
Althea is currently seeking a Sr. Quality Control Assistant - Chemistry, to be responsible for conducting routine analysis of raw materials, in process and final product under moderate supervision. The Sr. QC Assistant - Chemistry may focus in a specialized area and provide routine analysis and testing according to standard operating procedures in any of the following areas: in process and finished formulations, cleaning samples, and perform qualifications and transfers of methods. | 7/22/2018 |
| 636 | Ajinomoto Althea, Inc. San Diego, CA MQA ASSISTANT BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
The QA Assistant is performing a wide variety of routine and semi-routine activities pertaining to assuring compliance with Quality Assurance (QA) requirements and applicable regulatory requirements, including assisting with audits and documentation review. | 7/22/2018 |
| 637 | Ajinomoto Althea, Inc. San Diego, CA FACILITIES ENGINEER I BS Exp: 0-3 yrs |
Althea is currently seeking a Facilities Engineer I to provide engineering support to facility and utility systems supporting biopharmaceutical manufacturing, including aseptic filling operations. The Facilities Engineer I diagnoses and repairs facility and utility systems, and completes GMP-related documentation including corrective and/or preventive actions, change controls, deviations, and address of audit observations. This position is also responsible for maintaining a safe work environment in compliance with OSHA and other local, state, and federal regulatory agencies. | 7/22/2018 |
| 638 | Ajinomoto Althea, Inc. San Diego, CA DRUG SUBSTANCE MANUFACTURING ASSOCIATES I /II – DOWNSTREAM BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
The position works under the guidance of experienced downstream team members in support of the successful technical transfer and integration of processes into the Drug Substance Manufacturing Downstream department. The position will become proficient with chromatography and TFF (UF/DF) systems employed during manufacturing campaigns. Compliance with established Good Manufacturing (GMP) procedures, safety, and regulatory regulations is required. The position aligns daily actions with company goals and Althea’s cultural values. | 7/22/2018 |
| 639 | Ajinomoto Althea, Inc. San Diego, CA DRUG PRODUCT MANUFACTURING ASSISTANT - FORMULATIONS BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
This position is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. | 7/22/2018 |
| 640 | AMPAC Fine Chemicals Rancho Cordova, CA Analytical Scientist MS in Chemistry or related field Exp: 1 yr |
Candidate will assist with assigned tasks such as method development, transfer and validation; provide analytical support to the research and development group to meet project goals; select appropriate methods and techniques in performing experiments; collaborate with analytical personnel to help develop routine analytical methods; work cross functionally to achieve target goals and proactively seek out potential solutions to issues. | 7/22/2018 |
| 641 | Amneal Pharmaceuticals Branchburg Township, NJ Validation Engineer BS/MS in Pharmaceutical or Biomedical Engineering or Chemical Engineering. Exp: 1 yr |
The validation engineer is responsible to perform validation and conducting development studies. This role is also responsible for monitoring, and analyzing to assist in improvising pharmaceutical systems and processes. | 7/22/2018 |
| 642 | Amicus Therapeutics Cranbury, NJ Associate Scientist, Biochemistry MS Exp: 0-2 yrs |
This position will be responsible for the characterization of enzymes expressed in mammalian and prokaryotic cell systems. This resource will apply a wide knowledge of protein quantitation and analysis techniques both in vitro and in cell-based models, especially related to enzymology, to characterize protein products. This position will share responsibility for propagation of prokaryotic and mammalian cell lines and purification of enzyme products using established protocols. | 7/22/2018 |
| 643 | Ambry Genetics Corporation Aliso Viejo, NJ Automation Technologist BS in a life sciences field: Biology, Bioengineering, Molecular Biology or related field Exp: 0-1 yr |
The primary duties of this position are to assist other Automation Team members in assay automation development, as well as support the Clinical Laboratory by aiding in recovery and troubleshooting validated laboratory instruments. This position also plays a role in designing, optimizing, validating, maintaining, and troubleshooting automation tools for our clinical diagnostic assays. | 7/22/2018 |
| 644 | ANAPTYSBIO, INC. San Diego, CA Clinical Trials Assistant BS Exp: 1-3 yrs |
As a Clinical Trial Assistant (CTA) you will assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support. | 7/22/2018 |
| 645 | ARL Bio Pharma, Inc. Oklahoma City, OK Laboratory Technician - Analytical Lab BS Exp: 0-2 yrs |
Under general supervision, the Laboratory Technician is responsible for working collaboratively with Chemists and performing integral support tasks to ensure overall efficient testing of samples. | 7/22/2018 |
| 646 | ARL Bio Pharma, Inc. Oklahoma City, OK Laboratory Technician - Chemistry Lab BS Exp: 0-2 yrs |
This position is responsible for maintaining the cleanliness of the laboratory, the organization of supplies, reagents and standards. Additionally, this position is responsible for the daily calibration and/or verification of the balances and pH meter. The employee will have basic knowledge of commonly used laboratory concepts, practices, procedures and instrumentation and will perform limited tests under supervision. | 7/22/2018 |
| 647 | EAG Columbia, MO Associate Scientist I, Analytical Chemistry MS in chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field Exp: 0-2 yrs |
We are looking for an Assistant Scientist to join our Product Chemistry group. This position is responsible for conducting analysis and experimentation on substances in the laboratory with minimal supervision and using prescribed procedures (protocols, standard operating procedures, methods, etc.). Completes work for research and development, CGMP and/or GLP studies, and documents and reports data in a timely manner according to regulatory guidelines. | 7/22/2018 |
| 648 | EAG Columbia, MO Associate Scientist I, Method Development & Validation MS in chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field Exp: 0-2 yrs |
The Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). | 7/22/2018 |
| 649 | EAG Columbia, MO Associate Scientist I, Residue Chemistry & Field Programs MS in chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field Exp: 0-2 yrs |
The Associate Scientist conducts analysis and experimentation on substances in the laboratory with minimal supervision and using prescribed procedures (protocols, standard operating procedures, methods, etc.). Completes work for research and development, and GLP studies, and documents and reports data in a timely manner according to regulatory guidelines. | 7/22/2018 |
| 650 | EAG Columbia, MO Associate Scientist I, Stability & Batch Release MS in chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field Exp: 0-2 yrs |
The Associate Scientist position is an intermediate-level professional position involved in somewhat complex day-to-day activities in a laboratory setting under prescribed processes (protocols, standard operating procedures, methods, etc.). | 7/22/2018 |
| 651 | EAG Columbia, MO Associate Scientist I, Biotech MS in chemistry, biochemistry, biology, chemical engineering, pharmaceutical sciences, or other directly related field Exp: 0-2 yrs |
EAG Laboratories is looking for an Associate Scientist to join our fast growing Biotech team which provides a comprehensive range of biopharmaceutical services from analytical physic-chemical characterization to routine release and stability testing utilizing well-established techniques including HPLC, capillary electrophoresis, light scattering, ELISA, cell bioassays and mass spectrometry. | 7/22/2018 |
| 652 | Avantor Solon, OH Quality Control Technician BS in Chemistry, Biology, or Microbiology Exp: 1-3 yrs |
Responsible for testing of raw materials and finished products in the Quality Control laboratory. | 7/22/2018 |
| 653 | Antech Diagnostics Phoenix, AZ Laboratory Generalist BS Exp: 1 yr |
As a Laboratory Generalist you will perform laboratory testing that helps veterinarians diagnose and treat pets across the United States. | 7/22/2018 |
| 654 | WuXi AppTec Philadelphia, PA Laboratory Technician II, QC/Analytical BS/MS in Biological Sciences or other science-related major Exp: 1-3 yrs |
Performs basic and next-level Analytical 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). Completes Test Methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs and thoroughly documents Research & Development activities as required. Performs daily work activities with minimal supervision. | 7/1/2018 |
| 655 | WuXi AppTec Philadelphia, PA Laboratory Technician, Environmental Monitoring BS in Microbiology or Biology Exp: 1 yr |
Responsible for performing sampling and testing in support of manufacturing and validation activities. Works in a team environment with various laboratory staff. Performs assays according to and in compliance with current Good Manufacturing Practices (cGMPs), Code of Federal Regulations (CFR) and Standard Operating Procedures (SOPs). Under direct supervision, completes batch records and other required documentation and performs laboratory maintenance duties according to cGMPs, CFR and SOPs. | 7/1/2018 |
| 656 | WuXi AppTec Philadelphia, PA Technical Writer, Sterility Assurance BS in the Life Sciences Exp: 1-2 yrs |
This position is responsible for investigative writing, performing root cause analysis, developing appropriate corrective and preventative action for deviations, developing protocols for qualification of sterility levels, and periodic reporting for microbiology and sterility assurance. Additional responsibilities include ownership of change controls, laboratory protocols, and providing a technical resource for topics around microbiology and process improvements. | 7/1/2018 |
| 657 | WuXi AppTec Philadelphia, PA Laboratory Technician II, Virus Production BS in Biological Sciences or science related field Exp: 1-2 yrs |
Performs assays according to testing records 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 supervision, completes test methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. | 7/1/2018 |
| 658 | WuXi AppTec Plainsboro, Nj Associate Scientist MS Exp: 0 yr |
Works on assignments with a diverse team of scientists to facilitate all aspects of performing in vitro screening and running an HTS laboratory | 7/1/2018 |
| 659 | WuXi AppTec Philadelphia, PA Technical Operations Specialist I BS Exp: 1 yr |
The Documentation Specialist will generate and/or review Manufacturing related technical documents and manage timely closure of these documents. This includes but is not limited to Non-Conforming Event (NCE) investigations, CAPAs, Change Controls (CC), Batch Records (BR), Technical Transfers (TT), Final Reports (FR), and Standard Operating Procedures (SOP). | 7/1/2018 |
| 660 | WuXi AppTec Philadelphia, PA Quality Control-Flow Cytometry Specialist MS in Biological Sciences or other science-related major Exp: 0-1 yr |
Sufficient scientific training and competence to perform basic and moderate complexity Flow Cytometry and/or Cell Based Assay according to, and in compliance with, current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). As part of standard work, completes assigned Test Methods, assay development, other required documentation and general laboratory duties according to relevant cGMP, CFR and/or PTC guidelines and SOPs. Performs daily work activities with minimal supervision. | 7/1/2018 |
| 661 | Zymergen San Francisco, CA RESEARCH ASSOCIATE, MICROBIAL GENOME ENGINEERING BS/MS Exp: 0-2 yrs |
The Research Associate will help create new technologies, bring in cutting edge protocols, and improve existing Zymergen protocols to provide newer and better workflows to our microbe engineering Factory. At Zymergen, the Research Associate will work together with other scientists, automation engineers, and software engineers to develop protocols for DNA cloning and microbial strain engineering, and then enable their use in high throughput workflows. | 7/1/2018 |
| 662 | Accelerate Diagnostics Tucson, AZ Research Associate BS in Microbiology, strongly preferred; however, studies in Biochemistry, Molecular Biology, or related field of study Exp: 1 yr |
The ideal candidate will be a motivated self-starter with experience in the following areas: microbiology, biochemistry, and/or molecular biology. The successful candidate will be responsible for the day-to-day execution of experiments supporting assay development. | 7/1/2018 |
| 663 | Absorption Systems Exton, PA Associate Scientist – Bioanalysis BS/MS in chemistry, biochemistry or related discipline Exp: 1-3 yrs |
The position is a bench chemist level position with primary duties in preparing and analyzing samples from biological matrices using LC-MS/MS as the primary analytical instrumentation. | 7/1/2018 |
| 664 | Acelity L.P. Inc. San Antonio, TX Clinical Support Specialist BS in Nursing or other clinical science Exp: 1 yr |
The Clinical Support Specialist champions product safety through the clinical call center that provides 24/7/365 clinical support and education to internal and external customers including nights, weekends and holidays under the leadership and direction of the Sr. Manager of Global Safety. | 7/1/2018 |
| 665 | Accurus Biosciences Richmond, CA Research Associate BS/MS in Biology Exp: 0-3 yrs |
The primary responsibilities of this position include DNA cloning, plasmid DNA preparation, mammalian cell culture, transient transfection and stable cell line generation, analysis of cell surface protein expression or antibody binding by FACS, cell-based functional assays, and general lab maintenance. | 7/1/2018 |
| 666 | Adare Pharmaceuticals, Inc. Vandalia, OH QC ANALYST - CONTRACT BS in Chemistry or related field Exp: 1-3 yrs |
The QC ANALYST performs physical and chemical testing of intermediate and finished products according to written procedures. | 7/1/2018 |
| 667 | Adaptive Biotechnologies Corp. Seattle, WA Production Associate I / II / III (Tue-Sat, AM) BS in Biology, Molecular Biology, Immunology or Medical Technologist Exp: 1 yr |
The Production Associate I/II/III positions will be responsible for processing client samples using high throughput DNA sequencing technology. This role will work within a team of other Laboratory Technicians in a fast-paced, high production setting to process research and clinical diagnostic samples. Candidates must have a minimum of 1 years’ experience working with human samples in a certified lab. | 7/1/2018 |
| 668 | Adaptive Biotechnologies Corp. Seattle, WA BSM Specialist I BS in a biological related field or the equivalent Exp: 1 yr |
The BSM Specialist I position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support the sample management activities for the regulated laboratory that provides services for research, clinical projects, and diagnostic testing. | 7/1/2018 |
| 669 | Adaptive Biotechnologies Corp. Seattle, WA Biological Sample Management (BSM) Associate II BS in biology or a related field Exp: 1 yr |
The BSM Associate II position will join the Biological Sample Management (BSM) group at Adaptive Biotechnology’s Seattle laboratory. The primary function of this role is to support sample management and chain of custody for Adaptive’s immunosequencing services that includes research, clinical projects, and diagnostic testing. | 7/1/2018 |
| 670 | Adaptive Biotechnologies Corp. Seattle, WA Production Associate I / II / III (Mon-Fri, AM) BS in Biology, Molecular Biology, Immunology or Medical Technologist Exp: 1 yr |
The Production Associate I/II/III positions will be responsible for processing client samples using high throughput DNA sequencing technology. This role will work within a team of other Laboratory Technicians in a fast-paced, high production setting to process research and clinical diagnostic samples. Candidates must have a minimum of 1 years’ experience working with human samples in a certified lab. | 7/1/2018 |
| 671 | Adaptive Biotechnologies Corp. Seattle, WA Production Associate I / II / III (Sun-Thu, PM) BS in Biology, Molecular Biology, Immunology or Medical Technologist Exp: 1 yr |
The Production Associate I/II/III positions will be responsible for processing client samples using high throughput DNA sequencing technology. This role will work within a team of other Laboratory Technicians in a fast-paced, high production setting to process research and clinical diagnostic samples. Candidates must have a minimum of 1 years’ experience working with human samples in a certified lab. | 7/1/2018 |
| 672 | Acumed Hillsboro, OR Quality Engineer - Medical Device BS in an engineering or science discipline Exp: 1-3 yrs |
The Quality Engineer 1 (QE1) is responsible for providing Quality Assurance support to product development and manufacturing to increase product quality, reliability, and process capability. Participates on teams responsible for identifying, documenting, assessing, correcting and presenting quality issues using risk analysis and root cause analysis tools. Supports quality of new products being released to the market through participation in the product development process to ensure product and process conformance to global standards (including FDA and ISO 13485). | 7/1/2018 |
| 673 | Acorda Chelsea, MA Manufacturing Associate BSin Physical or Chemical Sciences (life sciences) or related Engineering field Exp: 1-3 yrs |
The Manufacturing Associate performs routine and complex operations for the GMP production of pharmaceutical products. This individual operates in accordance with environmental, health, safety, and cGMP guidelines. This individual is responsible for the hands on execution of production activities as they relate to spray drying, capsule filling, and blister packaging operations of manufactured products. | 7/1/2018 |
| 674 | Acorda Chelsea, MA Document Control Specialist Temp BS Exp: 0-3 yrs |
Responsible for performing various administrative tasks in support of the Quality Assurance department and its clients including but not limited to SOP review, supporting the QA Archive, Electronic Document Management System (EDMS), and GxP Training Program. Participates in independent and team projects as defined by the department manager. | 7/1/2018 |
| 675 | ADMA Biologics Boca Raton, FL Analyst-Validation BS in Science or Engineering Exp: 1-3 yrs |
To provide validation support to Immuno-therapy Production, Quality Control and Plant Engineering. Assisting with portfolio tracking and status updates. Assist risk management teams with examinations, audits, and real-time responses. Coordinate independent validation, reviewing results from third parties. Prepare reports, summaries, and/or analysis of validations to present performance metrics. | 7/1/2018 |
| 676 | Adello Biologics i Chicago, IL QC Analyst III - HPLC MS in Biochemistry, Biotechnology, Biology Exp: 1-2 yrs |
The Quality Control Scientist III will be responsible for analytical testing and data verification supporting both late-stage clinical and commercial biosimilar products in cGMP-compliant laboratories, and will also be expected to be engaged in continuous improvement initiatives to drive efficiency and effectiveness of Adello’s Quality Systems. A strong background in protein chemistry will be essential to perform and troubleshoot techniques, with a focus on HPLC. A demonstrated ability to collaborate across multiple departments to drive timely resolution of projects, laboratory investigations, and process improvements is also required. | 7/1/2018 |
| 677 | Adello Biologics i Chicago, IL Assistant I , Manufacturing BS in a Biotechnology, Biology or Chemistry Exp: 0-2 yrs |
The Assistant I, Manufacturing is a regular employee in a full-time non-exempt position at Adello Biologics, LLC, in Chicago, IL, this employee will be responsible for the manufacturing of Biotechnology products for clinical and commercial human use. Employee employs aseptic techniques while working in controlled and classified environments, some of which require complete aseptic gowning. Must comply with Adello policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and any other government requirement. | 7/1/2018 |
| 678 | Advanced Cell Diagnostics, Inc. Newark, CA Associate Scientist/ Research Associate BS/MS in molecular biology, biochemistry, cell biology or related field Exp: 1 yr |
Perform RNAscope-based assays to support new product development and optimization, clinical assay development and validation, and provide customer service. Help with managing and organizing marketing materials and collaboration projects. You must be willing to learn new techniques quickly and adapt to shifting priorities in a fast-paced growing environment. | 7/1/2018 |
| 679 | Advanced Cell Diagnostics, Inc. Newark, CA Associate Scientist MS in molecular biology, biochemistry, cell biology or related field Exp: 1-2 yrs |
You will be a key member of the ACD Service Department, performing RNAscope assay services for industrial, pharmaceutical, and academic clients. You will also have the opportunity to work closely with scientists and investigators from a broad customer base. | 7/1/2018 |
| 680 | Advanced Cell Diagnostics, Inc. Newark, CA Product Specialist BS/MS in life sciences Exp: 1-3 yrs |
Serve as subject matter expert for new product development, collecting VOC, scientific literature search | 7/1/2018 |
| 681 | Aduro Biotech, Inc. BERKELEY, CA Research Associate – Chemistry BS/MS in Chemistry Exp: 0-3 yrs |
As a Research Associate / Senior Research Associate in Chemistry, the candidate will participate in an integrated project team geared towards solving the challenges that face drug discovery. Working under the supervision of an experienced Scientist, the person will be expected to produce high quality compounds that will address known issues to advance into further pharmacological assessment. | 7/1/2018 |
| 682 | B. Braun Medical Irvine, CA QC Chemistry Associate II BS/BA Exp: 1-2 yrs |
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. | 7/1/2018 |
| 683 | B. Braun Medical Irvine, CA QC Process Control Assoc I BS Exp: 1-2 yrs |
Under supervision, responsible for performing in-process inspections, process monitoring, quality support and investigations/resolution. Process monitoring includes AQL sampling, performing line clearances and line control. Provide quality support by performing tasks as assigned by Process Control Management. | 7/1/2018 |
| 684 | Aerie Pharmaceuticals Irvine, CA Regulatory Affairs Specialist - PVG BS/BA in chemistry, biology or pharmacology Exp: 0-3 yrs |
The Regulatory Affairs Specialist supports the creation, revision and review of various documents associated with clinical research and meeting the regulatory requirements of US Food and Drug Administration (FDA) and other international and regional governing bodies and Health Authorities (HAs). The documents may be submitted to support clinical development, registration, and regulatory compliance of Aerie’s drug products, worldwide. This position supports also Aerie’s post marketing pharmacovigilance (PVG) and promotional activities, as needed. | 7/1/2018 |
| 685 | Agilent Technologies, Inc. Boulder, CO Manufacturing Chemist BS in chemistry, biology, biochemistry, science or equivalent Exp: 1 yr |
As a Manufacturing Associate, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification. Your proficiency in analytical testing and immunohistochemistry applications will be required to perform | 7/1/2018 |
| 686 | Agilent Technologies, Inc. Santa Clara, CA Product Support Engineer BS in Science/Engineering or equivalent Exp: 1 yr |
Primary responsibilities for this role are to provide post-sales support and to develop the support strategy for new products. | 7/1/2018 |
| 687 | Agilent Technologies, Inc. Carpinteria, CA Research Assistant BS in the biological sciences. Exp: 1-3 yrs |
The primary role of the Research Assistant will be to execute studies that help validate the performance of immunohistochemical (IHC) assays in the Companion Diagnostics business area. | 7/1/2018 |
| 688 | Alan Laboratories, CA Chemistry Lab Technician BS Exp: 0 yr |
To conduct formulation preparation or analytical test in direct support of the drug development team, including writing documents and reports. Responsible for the maintenance of lab instrumentation and general lab duties. | 7/1/2018 |
| 689 | Alcami Wilmington, NC Quality Specialist II MS in Chemistry, Biology, or related field Exp: 1 yr |
The Quality Specialist II is accountable for driving results in a fast-paced environment by effectively performing activities of some variety and complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and processes inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance training as needed. The Quality Specialist II 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. | 7/1/2018 |
| 690 | Alcami Charleston, SC Process Engineer I BS in Engineering, Pharmacy or Chemistry Exp: 0-2 yrs |
The Process Engineer I (Sterile) for our parenteral site in Charleston, SC is accountable for driving results in a fast-paced environment by providing technical support for the manufacturing facility, including, troubleshooting validated processes, process deviations and investigations, transfers of new processes and technologies into the site and preparation of documentation to support validation and process transfer activities.. 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. | 7/1/2018 |
| 691 | Alcami Wilmington, NC Associate Scientist MS in Pharmaceutical Sciences, Chemistry or equivalent Exp: 0-2 yrs |
The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also be required to work on method development/method validation projects. For this psotion HPLC and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include: titrations UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company). 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. | 7/1/2018 |
| 692 | Agios Pharmaceuticals Cambridge, MA Research Associate/Sr. Research Associate, DMPK-Bioanalytical BS/MS in Chemistry, Analytical Chemistry, Pharmaceutical Sciences or Biotechnology Exp: 0-3 yrs |
Assist to method development and qualifications for drug candidates and biomarkers in biological matrix using LC-MS/MS | 7/1/2018 |
| 693 | Agenus Lexington, MA Research Operations Assistant BS Exp: 1-2 yrs |
The candidate will support the Agenus’ mission through implementation and management of the company’s policies, procedures and operational workflows. | 7/1/2018 |
| 694 | Vir Biotechnology San Francisco, CA Research Associate (Contract) BS/MS in Chemistry or Chemical Engineering or a similar discipline Exp: 1 yr |
You will be working in our analytical laboratory using diverse analytical methodologies as needed. These methods will initially be HPLC, cIEF, SDS-PAGE gel, UV/SPEC, pH, and other routine lab functions as needed. As a key member of Vir’s core lab services group, you will have the chance to learn about modern testing methods for biotechnology products while implementing state of the art methods to measure critical product attributes of our MAb portfolio while being exposed to a broad range of activities both inside and outside of the laboratory. | 6/24/2018 |
| 695 | West-Ward Pharmaceutical Corp. Bedford, OH SCIENTIST I BS in chemistry or closely related field Exp: 0-2 yrs |
Provide chemistry laboratory support and work with more senior R&D scientists performing duties such as, but not limited to, preparing formulations, analyzing samples, developing analytical methods and conducting pre-validation studies. Responsibilities primarily involve working in the lab with supervision. | 6/24/2018 |
| 696 | West-Ward Pharmaceutical Corp. Cherry Hill, NJ Quality Lab Assoc I (EM) BS/BA Degree in Microbiology or Biology Exp: 0-2 yrs |
Perform functions within the Microbiology Laboratory related to Environmental Monitoring of controlled production areas. The duties also include equipment maintenance and LIMS management. | 6/24/2018 |
| 697 | Waters Corporation Taunton, MA Senior Chemist MS in chemistry Exp: 0-6 yrs |
This person will work closely with QC, Synthesis Department, Chemistry R&D, as well as other departments to ensure smooth manufacturing operations. | 6/24/2018 |
| 698 | Waters Corporation Golden, CO Chemistry Technician BS/BA in Chemistry or Science related field Exp: 1 yr |
Responsible for manufacturing and production of products to meet customer delivery expectations / delivery dates | 6/24/2018 |
| 699 | X-Chem Waltham, MA Research Associate – High-Throughput Chemistry BS/MS in Chemistry or a related subject Exp: 1-4 yrs |
A track record of success in organic synthesis, particularly in the areas of reaction optimization or library synthesis. | 6/24/2018 |
| 700 | WuXi AppTec Marietta, GA Associate Laboratory Technician BS Exp: 1 yr |
This position is responsible for processing samples for assigned tests in compliance with GLP, GMP and ISO standards. | 6/24/2018 |
| 701 | WuXi AppTec Marietta, GA Laboratory Technician BS Exp: 1-2 yrs |
Perform job specific tasks in compliance with applicable Regulations, International Standards, and WuXi AppTec Policies and Standard Operating Procedures. | 6/24/2018 |
| 702 | WuXi AppTec Plainsboro, NJ Technical Support Specialist I BS Exp: 1-2 yrs |
Responsible for first level day to day onsite support of users and systems (regulated and non-regulated). | 6/24/2018 |
| 703 | WuXi AppTec Plainsboro, NJ Technical Editor/Writer I BS Exp: 1-2 yrs |
Assists in preparing the following:Study protocols and research reports for submission to government agencies and sponsors. | 6/24/2018 |
| 704 | WuXi AppTec San Diego, CA Research Associate I BS in a life science or related field Exp: 0-2 yrs |
The ideal candidate will work under supervision of a research scientist to support research projects involving genome editing, molecular cloning, and biochemical/cell-based assays. | 6/24/2018 |
| 705 | WuXi AppTec Plainsboro, NJ Associate Scientist III (LC/MS Operator) BS in a Chemical, Pharmaceutical, Biological discipline or equivalent Exp: 1-2 yrs |
Primarily responsible for performing highly complex scientific analyses by operating LC/MS/MS instruments for quantitative drug analyses and data review. | 6/24/2018 |
| 706 | WuXi AppTec San Diego, CA Research Associate II BS in the life sciences Exp: 1-2 yrs |
We’re seeking highly skilled and motivated Research Associates to help advance HD Biosciences’ immuno-oncology team to complete client-based projects and experiments. | 6/24/2018 |
| 707 | Zymo Research Irvine, CA Technical Manufacturing and QC Associate BS in Biochemistry, Microbiology, Genetics, Immunology, Virology, Molecular Biology or related field. Exp: 1-2 yrs |
Assist in the manufacturing of various chemicals, buffers, and other product-related components to ensure consistent product performance. Responsible for conducting quality control tests on various chemicals, buffers, and other product-related components. | 6/24/2018 |
| 708 | Zymergen San Francisco, CA SENIOR RESEARCH ASSOCIATE/SCIENTIST I, METABOLIC MODELING BS in chemical engineering, bioengineering, or a related field Exp: 1-2 yrs |
This person will be responsible for carrying out metabolic (flux-balance analysis) and fermentation models for existing projects and new client engagements under consideration by business development. These models are used to calculate maximum theoretical yields of products as well as expected performance in fermentation (using either our internal process or our client’s process). This person will be responsible for running models using tools developed internally by the modeling team, evaluating the model results under different parameters and assumptions, and summarizing results for delivery to internal stakeholders. They will also be involved in onboarding and curating new metabolic models. | 6/24/2018 |
| 709 | Zymergen San Francisco, CA ENGINEER I/II, ENGINEERING MS Exp: 1 yr |
The Fermentation Engineering group is hiring experienced engineers provide support for new project onboarding and validation into standard operations. | 6/24/2018 |
| 710 | Zymergen San Francisco, CA RESEARCH ASSOCIATE I-III, ANALYTICAL CHEMISTRY - PRODUCTION BS/BA in chemistry, biology, engineering Exp: 0-2 yrs |
The Research Associate will be joining a growing team as one of the core members. Will assist to make critical measurements used to evaluate fermentations and high throughput processes under development. The Research Associate will participate in continuously improving measurement quality and efficiency in collaboration with the development, production and engineering teams. The hire will communicate frequently with strain and process developers to help them understand assay requirements and to interpret data. | 6/24/2018 |
| 711 | Zymergen San Francisco, CA RESEARCH ASSOCIATE I-III, DNA/PLASMID/STRAIN MANUFACTURING BS in molecular biology, microbiology, biology, chemistry, engineering Exp: 1 yr |
This Research Associates position will be responsible for either the DNA, Plasmid or Strain manufacturing processes within Production. The Research Associate will run a diversity automated workflows in a high-throughput environment. We need members of the Production team to be thoughtful, meticulous, well-organized, energetic, collaborative, and fully engaged in the execution of the workflows. | 6/24/2018 |
| 712 | Zymergen San Francisco, CA RESEARCH ASSOCIATE II/III, GENOME SEQUENCING MS in Biology, Computer Science, Bioinformatics or related field Exp: 1 yr |
This role is for a Research Associate who will have primary responsibility for preparing libraries for both Pacific Biosciences long read sequencing and operating the sequencer. As time permits this individual will carry out other types of sequencing and research. The work of this Research Associate will aid essential Research and Development and contribute meaningfully genome-on-boarding. Over time this role will grow to include method development work, computational work and presentations. | 6/24/2018 |
| 713 | Zymergen San Francisco, CA RESEARCH ASSOCIATE I/II, STRAIN BANKING BS in biology, chemistry, engineering Exp: 0-2 yrs |
The Research Associate will assist in supporting a number of cell banking activities working with a diversity of microbes following standardized operating procedures (SOPs). | 6/24/2018 |
| 714 | Yumanity Cambridge, MA BS-MS Research Associate – Medicinal Chemistry BS/MS in synthetic organic chemistry Exp: 0-4 yrs |
This lab-based chemist will be a key part of an interdisciplinary team of scientists and will be involved in the synthesis, purification, and characterization of novel drugs in the areas of neurodegenerative disease. | 6/24/2018 |
| 715 | Abbiotec, Inc. San Diego, CA Research Associate, Monoclonal Antibody Production, Part-time BS in Cell Biology Exp: Entry-level- 5 yrs |
The position requires being technically competent in the field of monoclonal antibody production. The individual will carry out monoclonal antibody production by hybridoma technology for our contract research projects and in-house development projects. | 6/24/2018 |
| 716 | ADP LLC UNION CITY, CA Automation Technician BS Engineering or technical training Exp: 1-3 yrs |
Work with engineers to build automated equipment to print;Test equipment to verify design intent;Work with engineers to resolve design issues. | 6/24/2018 |
| 717 | ADP LLC UNION CITY, CA Chemist 2 MS Exp: 1-2 yrs |
Participate in the development, maintenance and improvement of high sensitivity immunoassays using LSPR and/or magnetic bead and chip-based technology | 6/24/2018 |
| 718 | AB SCIENCE Home-based , Ho Clinical Research Associate MS Exp: 1-2 yrs |
Performance of monitoring activities of all assigned clinical studies in accordance with regulations, SOPs and Good Clinical Practices guidelines: | 6/24/2018 |
| 719 | 4D Molecular Therapeutics Emeryville, CA RESEARCH ASSOCIATE, ANALYTICAL DEVELOPMENT BS in Biochemistry, Chemistry, or Related Discipline Exp: 0-3 yrs |
The Research Associate will be responsible for the execution of routine testing in support of process development and routine manufacturing, and will contribute to the development of analytical assays for characterization of therapeutic products. The successful incumbent will need to make experimental observations, review and analyze data for presentations and reports, and will share maintenance responsibilities such as reagent preparation, material ordering, and general lab upkeep. | 6/24/2018 |
| 720 | 3M Maplewood, MN Sr. Synthetic Chemist MS in Chemistry Exp: 1 yr |
Typical development activities will take place in the lab, working directly with application development engineers. | 6/24/2018 |
| 721 | 3M Indianapolis, IN Product Development Acoustical Test Engineer BS in an engineering or science discipline Exp: 1 yr |
Performs testing and evaluation of hearing protectors and/or communications products in accordance with hearing protection industry standards and regulations, which includes working with human test subjects and acoustical manikins | 6/24/2018 |
| 722 | 3M Red Wing, MN Technical Writer BS Exp: 1 yr |
The person hired for this position will be responsible for designing and writing technical documentation for products such as user manuals, repair manuals, parts lists, exploded assemblies of product, technical reference materials, technical translations, release notices and update instructions, technical publications, etc. Clearly and accurately addresses the information needs of the applicable audience, while also editing work for other writers. | 6/24/2018 |
| 723 | 3M Flemington, NJ Process Engineer BS/MS in a science or engineering discipline Exp: 1 yr |
Leads projects and programs to improve safety, environmental performance, productivity, and overall operational efficiency of the equipment using Lean Principles and Six Sigma Tools | 6/24/2018 |
| 724 | 3M Maplewood, MN Product Assurance Engineer BS/MS in a science or engineering discipline Exp: 1 yr |
The person hired for the position of Product Assurance Engineer will focus on electronic hardware products in our device reprocessing business. This position will lead and support projects that positively impact product service, performance, and quality. This individual will work closely with plant and division Manufacturing Engineers, plant manufacturing personnel, division Product Assurance personnel, and component Suppliers, and will report directly to the Device Reprocessing Hardware Quality Manager. | 6/24/2018 |
| 725 | 10x Genomics Pleasanton, CA Production Associate I/II BS/MS in Molecular Biology, Analytical Chemistry, Chemical Engineering, or equivalent Exp: 0-5 yrs |
Execute production operations according to defined procedures and ensure the integrity and quality of our products | 6/24/2018 |
| 726 | Abcam Burlingame, CA Research Associate, IVD BS in biochemistry, pathology, cell and molecular biology, immunology or other Life Sciences Exp: 1 yr |
This position will contribute to the development and validation of qualified reagents and generate data to support IVD products. Protocols and associated data may include immunohistochemistry (IHC), western blots, ELISA or other immunoassays, immunofluorescence or others as required. In addition, this position will be expected to complete scientific and technical tasks on aggressive timelines and to work as part of a team on varied tasks with changing priorities. | 6/24/2018 |
| 727 | Abcam Burlingame, CA Research Associate - Custom Antibody Development BS in Biological Sciences Exp: 1 yr |
The position is primarily responsible for the screening and characterization of monoclonal antibodies. The successful candidate will play a hands-on role in the company’s use of a wide variety of analytical assays such as ELISA, flow cytometry, Octet, and HTRF. He or she will partner closely with other team members within the group, assisting with every step of antibody development. The candidate will make observations, analyze data, and interpret results with full supervision. | 6/24/2018 |
| 728 | Abbott Irving, TX Associate Quality Professional, Labeling BS in Life Science,Engineering,or closely related discipline Exp: 0 yr |
Conduct quality-related activities to deliver consistent,high quality documents,services,products and processes. | 6/24/2018 |
| 729 | Abbott Temecula, CA Associate Product Quality Analyst BS Exp: 0-2 yrs |
Analyzes customer complaints to determine which are regulatory reportable and coordinates activities with internal, field, and end use customers. Responsible for adherence to Good Manufacturing Practices (GMPs) and proper complaint handling per the Code of Federal Register (CFR) and other governmental regulations. Communicates event investigation results via regulatory reports and written communications, as appropriate | 6/24/2018 |
| 730 | Abbott Des Plaines/Abbott Park, IL Technician Quality BS Exp: 0-2 yrs |
Completes assigned daily activities; workload; scheduling; and constraints independently. Provides technical expertise to complex projects / product and investigations as required. Strives to become the technical expert within work area. | 6/24/2018 |
| 731 | Abbott Atlanta, GA Quality Engineer I - Post Market Investigations BS in Engineering, applicable Technical Field Exp: 1-2 yrs |
Conduct and document complaint investigations on returned product per department complaint handling procedures | 6/24/2018 |
| 732 | Abbott Santa Clara, CA Quality Engineer MS Exp: 0-2 yrs |
Provide Process/Quality Engineering support on quality system improvements. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products. | 6/24/2018 |
| 733 | Abbott Tipp City, OH Assistant Chemist I (12 Rotating Night Shift) BS in Chemistry, Biology, Math, or closely related technical field Exp: 1 yr |
Performance of analytical testing on raw ingredients, packaging commodities, in-process product, finished product, and plant utilities per current methodology. This includes testing for release of product to manufacturing for further processing, filling, and finishing. This also includes planning, sampling, testing, audit of records and release of sample materials. | 6/24/2018 |
| 734 | Regeneron Rensselaer, NY QA Validation Specialist BS/BA in Engineering, Chemistry, or Life Sciences Exp: 1 yr |
Validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures. | 6/17/2018 |
| 735 | Regeneron Tarrytown, NY Research Associate MS in Biochemistry Exp: 1-3 yrs |
The qualified individual will be responsible for performing a variety biochemical and biophysical assays to characterize protein biologics to support late-stage development and commercialization efforts. | 6/17/2018 |
| 736 | Regeneron Tarrytown, NY Process Development Engineer - Bioreactor Scale-Up and Development BS/MS in Chemical Engineering, Biochemical Engineering, or Biochemistry Exp: 0-2 yrs |
We are seeking a Process Development Engineer to work in the Bioreactor Scale-Up and Development group within Pre-Clinical Manufacturing and Process Development. This person will be primarily involved in developing clinically-enabling bioreactor processes intended for use in cGMP manufacturing. | 6/17/2018 |
| 737 | SBI Palo Alto,, CA Customer & Technical Support Representative (CSR/TSR) BS in a life sciences field. Exp: 1-2 yrs |
The ideal candidate will have a B.S. degree in the life sciences and will support an existing group of customer support personnel taking telephone orders from customers, logging into a CRM system, printing packing slips, sales orders, and shipping documentation, and assist with packaging of life science reagents for shipment to worldwide customers. This position will also provide support to the Commercial Team. This is a fast-paced position requiring attention to detail, technical knowledge of life sciences (as telephone conversations with customers will require technical understanding of SBI's products and service offerings, and some technical support), and an ability to multi-task with tight deadlines. | 6/17/2018 |
| 738 | Takeda Brooklyn Park, MN Manufacturing Associate I BS in a scientific or engineering discipline Exp: 0-1 yr |
The Manufacturing Associate performs and documents cGMP activities to support upstream and downstream production areas and operations . This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating/ revising cGMP documents and other assignments as directed. | 6/17/2018 |
| 739 | Takeda Cambridge, MA Research Associate, Analytical Development BS in chemistry, biology, pharmacy, engineering or related pharmaceutical science Exp: 0 yr |
Responsible for executing basic/routine experiments under supervision. This position also assists in the planning of basic experiments and experiments and performs specialized/complex experiments with assistance from supervisor as appropriate | 6/17/2018 |
| 740 | Takeda Cambridge, CA Senior Research Associate, Analytical Development MS in chemistry, biology, pharmacy, engineering or related pharmaceutical science Exp: 0 yr |
Responsible for executing basic/routine experiments under limited supervision. This position also plans basic experiments and experiments and performs specialized/complex experiments with assistance from supervisor as appropriate. | 6/17/2018 |
| 741 | Tanvex Biopharma San Diego, CA Research Associate, Biology BS in biochemistry, molecular and cell biology, or related scientific discipline Exp: 0-3 yrs |
The Research Associate is responsible for executing experimentation related to the biological characterization of company’s products, from method development and sample testing to method qualification/transfer/validation in order to support of pipeline projects. This position is responsible for designing and conducting a set of scientific experiments which contribute to project objectives, applying a variety of biochemical, biological, and immunological techniques to support process development, impurity analysis, formulation development, and quality control. Candidate will demonstrate effective application of scientific principles including: antigen/receptor binding, Fc receptor binding, PK assays, functional biological assays (i.e., cell adhesion, proliferation, and cytotoxicity). | 6/17/2018 |
| 742 | Tanvex Biopharma San Diego, CA Research Associate, Analytical Chemistry BS in chemistry, biochemistry, chemical/biochemical engineering or related disciplines Exp: 0-3 yrs |
The Research Associate in our Analytical Chemistry group is responsible for providing analytical support for process development of pipeline projects. This position is responsible for analytical method development, validation and testing of recombinant protein therapeutics. Candidate conducts routine sample analysis to support process development as well as detailed protein physicochemical characterization using a variety of analytical techniques (HPLC, CE, spectroscopy, MS and others). Candidate provides critical analytical support in R&D and QC settings for samples from various process scales and is responsible for analytical method transfer to QC department as needed. | 6/17/2018 |
| 743 | TE Connectivity Ltd Campbell, CA MFG & PROCESS DVL ENGINEER I BS in Engineering or Manufacturing field Exp: 1-3 yrs |
The Manufacturing & Process Development Engineer I is a technical position responsible for providing manufacturing engineering knowledge, skill, and experience to handle such tasks as: generating documentation, implementing DFM (design for manufacturability), lean manufacturing, process capability analysis, and yield / efficiency improvements. | 6/17/2018 |
| 744 | TE Connectivity Ltd Winston Salem, NC Manufacturing Engineer BS/MS in Mechanical, Electrical or Manufacturing Engineering Exp: 1-3 yrs |
They act as the binding element between product development and manufacturing engineering, ensuring the effectiveness and efficiency of this critical interface. They support Product Development in the optimization of designs and piece parts for manufacturability by realizing sample tooling/products/prototypes. They also design, develop, and qualify tooling and processes to meet TE quality and production standards, document all processes and tooling in applicable TE systems, support supply chain to verify supplier compliance and capability, initiate and implement programs to continuously improve quality, cost and cycle time and adhere to all appropriate specifications, regulatory requirements and customer requirements. | 6/17/2018 |
| 745 | TE Connectivity Ltd Winston Salem, NC PRODUCT ENGINEER BS in Engineering Exp: 1-3 yrs |
Provide on-going technical support, including review of changes, resolution of quality problems related to design and redesign projects to address issues of cost or manufacturability. Experience with 8-D’s and other root cause analysis tools is a plus. | 6/17/2018 |
| 746 | Transcriptic Menlo Park, CA Operations Associate (Third Shift) BS Exp: 1 yr |
In this position, you will execute client assays on our automated platform, help generate and collect data supporting reproducibility and quality control on our robotics system, and assist in developing and implementing tools to increase operational efficiency. This includes coordinating new instrument installation, performing instrument maintenance and assisting with assay transfer within the organization. | 6/17/2018 |
| 747 | Tris Pharma, Inc. Monmouth Junction, NJ Product Development R&D Scientist MS in Pharmaceutical Sciences/Pharmaceutics/Industrial Pharmacy or related science field Exp: 1 yr |
Product Development R&D Scientists perform pre-formulation and formulation development activities, prepares formulation batches for compatibility studies, stability studies, Pilot batches and Pivotal batches, perform maintenance of Research and Development (R&D) equipment/instruments. | 6/17/2018 |
| 748 | Two Pore Guys Santa Cruz, CA RESEARCH ASSOCIATE - NANOPORE BS in Chemistry, Biochemistry, Biology or related field Exp: 0-2 yrs |
The Research Associate I will be responsible for the execution of a wide variety of diagnostic assays on 2PG’s hand-held nanopore device. The incumbent will perform established assays, as well as contribute to the development of new assays with industry partners. | 6/17/2018 |
| 749 | UCB Raleigh, NC Medical Writing Specialist BS Exp: 0-1 yr |
Provide support to writing functions to ensure timely, high-quality deliverables in compliance with Standard Operating Procedures (SOPs), FDA, EMEA, ICH, and national and local regulations, as applicable | 6/17/2018 |
| 750 | United Therapeutics Corporation Silver Spring, MD QA Specialist I - Documentation BS in Biological Sciences, Chemistry or related discipline, or equivalen Exp: 1 yr |
Utilizing your knowledge of fundamental theories, principles, and concepts as the Quality Assurance (QA) Specialist I, you will be contributing to all relevant documentation areas to support the QA team meet its functional deliverables as outlined in the cGMP and organizational standard operating procedures (SOP). | 6/17/2018 |
| 751 | Utah Medical Midvale, UT Quality Control Engineer BS Exp: 1 yr |
Responsible for the day-to-day activities of the QA inspection function. Conducts internal audits. Participates as assigned in an engineering capacity on product/process improvement teams. | 6/17/2018 |
| 752 | Unum Therapeutics Cambridge, MA Contract Associate Scientist, Process Development MS Exp: 1-3 yrs |
Working within the process development group, you will assist in the development and optimization of closed system clinical scale manufacturing processes to support ongoing Phase I/II cancer immunotherapy trials. | 6/17/2018 |
| 753 | Vedanta Cambridge, MA Contract - Process Development Associate Engineer BS in Chemical Engineering, Bioengineering, Microbiology, or related field. Exp: 1-4 y r s |
The candidate will set up and be responsible for the execution of process development experiments, including medium development, generation and characterization of cell banks, small scale fermentation, and scale-up. | 6/17/2018 |
| 754 | Vedanta Cambridge, MA Contract - Research Associate, Bioinformatics BS/MS Exp: 1 yr |
The RA will perform bioinformatics analysis of next-generation sequencing data. The principal activities will include bacterial isolate genome assembly, open reading frame prediction, functional pathway analysis, and metagenomic analysis of microbial communities. Analyses will also involve the implementation of statistical algorithms to infer taxonomic or functional associations among sample groups to support ongoing clinical and pre-clinical programs. The job title and level will correspond to the experience and skills of the selected candidate. | 6/17/2018 |
| 755 | Vertex Boston, MA Temporary Scientific Associate II BS in materials science, chemical engineering, mechanical engineering, or related field Exp: 0-3 yrs |
Participate in planning and execution of experiments；Maintain a clear, concise, and accurate record of experiment；Operate and troubleshoot laboratory instruments。 | 6/17/2018 |
| 756 | Vertex Boston, MA Temporary Scientific Associate II, Analytical Development BS in the physical sciences or engineering Exp: 0- 4 yrs |
As a member of the Analytical Development team, this role will support the drug development programs at Vertex. | 6/17/2018 |
| 757 | Vertex Boston, MA Temporary Quality Associate BS Exp: 0-3 yrs |
The Quality Associate executes activities within the Quality archive and preparing and distributing CMC documentation ensuring alignment with department and corporate goals and compliance with all regulatory requirements. | 6/17/2018 |
| 758 | Vertex Boston, MA Medical Writing Scientist MS Exp: 1-4 y r s |
Prepare routine clinical regulatory documents, including clinical study protocols, clinical study reports, and investigator’s brochures, and sections of regulatory submissions | 6/17/2018 |
| 759 | Vividion Therapeutics, Inc. San Diego, CA Research Associate, Biology (Temporary) BS in Chemistry- or Biology-related field Exp: 1-4 yrs |
This position will be responsible for maintenance and expansion of cell lines to support screening activities, cell-line inventory management, and use of lab automation to assemble assay-ready compound plates. | 6/17/2018 |
| 760 | Vividion Therapeutics, Inc. San Diego, CA Research Associate, in vivo Pharmacology BS/MS Exp: 1-3 yrs |
Execute pharmacokinetic / pharmacodynamic, target engagement, efficacy, ormechanism of action studies to support pre-clinical and discovery programs. | 6/17/2018 |
| 761 | Viracor-IBT Lee's Summit, MO Laboratory Technician or Clinical Laboratory Scientist I, II or III BS/BA in biological, physical, chemical or clinical laboratory science Exp: 1 yr |
The Laboratory Technician is primarily responsible for performing laboratory tests and analyses under the direction of a lab supervisor or scientist including specimen management, specimen pipetting, instrument operation/maintenance, data entry and specimen storage with a high degree of proficiency. Follow Standard Operating Procedures (SOPs). Ensure all laboratory equipment and work areas are clean, sterile, and in proper working order. May be responsible for calibration of instruments. Conducts routine tasks as directed. Closely supervised with little latitude for independent judgment. | 6/17/2018 |
| 762 | Thermo Fisher Scientific St. Louis, MO QC Technician 1 (Environmental Monitoring) BS Exp: 1-3 yrs |
You will be joining a team that plays a role in ensuring the production of quality products. In this role, you will be responsible for performing a variety of duties to support manufacturing at the STL site, including environmental monitoring, testing of process gases and water sampling. Other responsibilities may include drafting/revising procedures and reports, authoring deviation investigations, and evaluation of data. | 6/17/2018 |
| 763 | Thermo Fisher Scientific Fremont, CA Formulations Scientist I BS Exp: 0-2 yrs |
The Formulations Scientist I will manufactures products for the Bulk Formulations team and complete associated cGMP documentation. Work with chemicals and biologicals to manufacture reagents, calibrators, and controls for IVD use. Participate in process improvement projects. | 6/17/2018 |
| 764 | Thermo Fisher Scientific Fremont, CA Scientist I, Molecular Controls BS Exp: 0-2 yrs |
The Scientist will manufacture and test molecular controls by following standard operating procedures (SOPs) and current good manufacturing/documentation practices (cGMP and cGDP). | 6/17/2018 |
| 765 | Thermo Fisher Scientific South San Francisco, CA Scientist I, Manufacturing Sciences BS in the Biological Sciences or Chemistry Exp: 1 yr |
The Scientist I, Manufacturing Sciences will perform Antibody Detection Preproduction processes. | 6/17/2018 |
| 766 | Thermo Fisher Scientific South San Francisco, CA Quality Engineer (entry level) BS in Chemistry, Biology, or Engineering Exp: 1 yr |
Create, maintain and evaluate product/process trends, designing and/or participating in process and product improvement plans | 6/17/2018 |
| 767 | Thermo Fisher Scientific Fremont, CA QC IA, QC Engineer/Scientist I BS/BA in Chemistry, Biochemistry, or Bioscience Exp: 0-2 yrs |
Performs routine testing of bulks, components and finished kits according to established quality control procedures using different instrument platforms. | 6/17/2018 |
| 768 | Thermo Fisher Scientific South San Francisco, CA Scientific Engineer 1, Systems Engineering BS/MS in Bioengineering, Engineering or related field Exp: 1-2 yrs |
The responsibilities will include working on projects related to real-time qPCR platforms that lead to new applications and performance improvements. The projects include applications for existing as well as new product platforms. Duties will include, but not limited to, running experiments on various qPCR and sample preparation platforms, designing assays and experiments, collecting, analyzing, and presenting data, drafting new liquid handler scripts to improve workflows. | 6/17/2018 |
| 769 | The Weinberg Group Washington, DC Regulatory Specialist MS Exp: 1 yr |
Understands the client’s problem; conceptualizes how to solve it and achieve task objectives;Contributes scientific and innovative thinking. | 6/17/2018 |
| 770 | Theravance Biopharma South San Francisco, CA Research Assistant - Research Associate I, Medicinal Chemistry BS/MS in Chemistry Exp: 1-2 yrs |
As a member of the Theravance Biopharma medicinal chemistry team, you will be responsible for the design and synthesis of a variety of new small molecule candidates on one of our exciting interdisciplinary drug discovery programs. We offer a stimulating, challenging and productive discovery environment with a strong commitment to developing the medicinal chemistry skills of our people. | 6/17/2018 |
| 771 | West Pharmaceutical Services, Inc. Exton , PA Associate Design Engineer BS in mechanical engineering or other relevant principle Exp: 0-3 yrs |
The Tooling Design Department is an essential component in Engineering and Operations. The team’s objective is to continue the support in designing tools the manufacturing facilities require for production. In parallel, the team also provides innovative solutions and services to the tooling group and other departments within the company, where possible, to assist with meeting company goals and objectives. | 6/17/2018 |
| 772 | West Pharmaceutical Services, Inc. Exton , PA Associate QA BS Exp: 0-3 yrs |
Provide oversight, coordination or actions related to West’s change control program. Create, review, coordinate and complete actions to ensure that the changes are in accordance with current regulation, standards, West policies & procedures. Maintain the change control and notification history, records & documentation to demonstrate compliance to regulations & requirements. Coordinate customer notification process. Support processes for maintaining Supplier Quality, as well as supporting and performing internal & external audits. | 6/17/2018 |
| 773 | Terumo Medical Corporation Elkton, MD NPD Quality Engineer I BS in engineering, life sciences Exp: 1-3 yrs |
As part of a project team and with the assistance of the manager, the NPD QE I will be responsible for developing sound Design History File deliverables, including, but not limited to, Quality Plans, Supplier Qualification Strategies/Quality Agreements, Manufacturing Quality Plan, Design Verification protocols and reports, and conducting Design History File Verifications at the end of each design control phase. In addition, the NPD QE I will actively participate in design characterization, risk management activities, and design and process validation. | 6/17/2018 |
| 774 | Regeneron Rensselaer, NY Associate Quality Engineer / Quality Engineer (Med Device) BS/MS in Engineering Exp: 0-2 yrs |
Provide Quality Assurance guidance and ensure compliance in the support of combination device development life cycles. | 6/10/2018 |
| 775 | Regeneron Tarrytown, NY Research Associate - Biologics LIMS Database Management BS/BA in biochemistry, chemistry, or related field Exp: 1 yr |
The Protein Development group is looking for a highly organized person to manage our protein, peptide, and small molecule compounds data base. This person will be responsible for distributions, uploading new lots received, and organizing current lots in stored locations, while updating the LIMS database. | 6/10/2018 |
| 776 | Regeneron Tarrytown, NY Bioanalytical Analysis Associate I BS/MS Exp: 0-2 yrs |
An entry level Bioanalytical Analysis Associate (BAA) that executes experiments under the direct supervision of a supervisor/manager. Performs routine technical tasks requiring minimal decision making capabilities. Possesses a knowledge of the basic principles of immunoassays obtained through academic training or relevant industry experience. | 6/10/2018 |
| 777 | Regeneron Tarrytown, NY Research Associate - RNAseq BS Exp: 1-2 yrs |
We are looking for a Research Associate -RNAseq, who is responsible for running NGS library construction for RNAseq and Illumina sequencing. | 6/10/2018 |
| 778 | Regeneron Tarrytown, NY Research Associate I-II, Immunology & Inflammation BS Exp: 1-4 yrs |
Conducts experiments, predominantly of basic immunology and basic lab techniques. Troubleshoots methodological and technical issues, interprets experimental data and literature, and communicates results to supervisor, department, or project team. Helps create a safe, effective, and efficient working environment. | 6/10/2018 |
| 779 | Regeneron Tarrytown, NY Research Associate II/III (Formulations Development) MS in Chemistry, Biochemistry, Biology, Chemical Engineering or related field Exp: 0-2 yrs |
Research Associates in the Formulation Development Group participate in the development of both liquid and lyophilized protein formulations to support formulation development from initial screening through commercialization. | 6/10/2018 |
| 780 | Semma Therapeutics Cambridge, MA Process Development, Senior Research Associate BS/MS in biology, bioengineering, process science or related field Exp: 1-3 yrs |
The full-time role will focus on process development for producing stem cell derived pancreatic islets, including stem cell culture, directed differentiation at pilot and bioreactor scale, and downstream processing. Under supervision of senior scientists, the research associate will work with our process development teams and internal and external manufacturing groups to develop and implement processes for manufacturing Semma's first cell therapy product. | 6/10/2018 |
| 781 | Synthetic Genomics, Inc. La Jolla, CA Sr. Research Associate, Bioinformatics MS in Bioinformatics, Computer Science, Statistics, Genomic Sciences, Molecular Biology, Genetics, Microbial Ecology or a related field Exp: 1-3 yrs |
The Bioinformatician will be part of the SGI-DNA with primary focus on tool development, improvement and maintenance to support the business of DNA synthesis. The successful candidate will be responsible for the development of machine-learning models for the analysis of DNA synthesis datasets, DNA synthesis design tools, and NGS data analysis pipelines. These analysis pipelines and applications will be based on existing tools and algorithms as well as newly developed solutions tailored to address specific business goals. This role requires strong programming skills, experience with NGS analysis tools, and expertise in classical machine-learning and deep-learning frameworks. | 6/10/2018 |
| 782 | Sinclair Research Auxvasse, MO Study Coordinator BS Exp: 6 months |
Study Coordinator | 6/10/2018 |
| 783 | Siemens Cypress, CA Application Engineer – Customer Champion BS/MS Exp: 1-5 yrs |
The Customer Champion will work in the pre and post production environment, and acts as the liaison between the customers and the NX development teams to resolve customer software defects. | 6/10/2018 |
| 784 | Siemens Norwood, MA Biostatistician 1 BS/MS in biostatistics, statistics, mathematics or related field Exp: 0-2 yrs |
Conducts statistical studies to generate data and insights used to innovate, plan and support improved healthcare. Prepares analysis plans to ensure the best statistical methods are developed and utilized. Writes specifications for files, consistency checks, tables, and calculations used to collect and analyzes data from a variety of sources. Interprets analyses and prepares exhibits for reports and presentations. Interfaces with non-technical users to assist with data interpretation and understanding of results. Reports directly to the Director of Biostats and Data Management. | 6/10/2018 |
| 785 | Siemens Hoffman Estates, IL Quality Engineer 1 BS Exp: 1-3 yrs |
This role is responsible for all aspects of Post Market Surveillance for Molecular Imaging medical devices. | 6/10/2018 |
| 786 | Siemens Buffalo Grove, IL Quality Technician BS in Engineering Exp: 1-2 yrs |
This person will work within the manufacturing QA team and will be responsible for addressing problems/issues that occur in our manufacturing production work cell environment that affect the established quality, FPY, delivery, or efficiency levels. Problems may be product, process, and/or supplier related. They will participate in various problem solving techniques; help identify the root cause of the problem; and help to ensure the necessary corrective actions are put in place to prevent the issue from occurring in the future. This person will be involved in problem solving techniques to solve issues from inception through closure. | 6/10/2018 |
| 787 | Smith & Nephew Mansfield, MA Quality Assurance Engineer 1 BS in Engineering or technically related field Exp: 1-3 yrs |
Reporting into the Quality Department, this role has responsibility for Quality related actions in support of New Product Development (NPD, Design Quality). Works collaboratively with project team members to develop and manage project plans. Champion design control and risk management activities for assigned projects. Evaluate risk and verification implications for purposed post launch design changes. Continuously improve Design Control procedures and maintain procedural compliance. | 6/10/2018 |
| 788 | Smith & Nephew Memphis, TN Packaging Project Engineer 1 BS In Packaging Engineering /Science or a related technical area Exp: 0 yr |
Researches, identifies and pilots new technologies and methodologies to improve packaging designs and processes. Proposes solutions and opportunities to management for review. | 6/10/2018 |
| 789 | SNBL USA Everett, WA Veterinary Technician BA/BS Exp: 6-12 months |
The Veterinary Technician position works primarily under direct supervision. Veterinary Technicians perform various duties to facilitate and support the work and research of the Veterinarians, Study Directors, and clients by completing a variety of animal health activities in the areas of medicine, surgery, and drug therapy. At SNBL USA we work with many different animal models: non-human primates, rats, mice, guinea pigs, rabbits, swine and canine. As a team, the vet services staff is responsible for the treatment of all on-site ill and injured animals, and for the fulfillment of the preventive medicine program as determined by the Attending Veterinarian. | 6/10/2018 |
| 790 | SNBL USA Everett, WA Research Associate - Scientific Services BS/BA in a scientific discipline Exp: 6-12 months |
In this position your main focus will be working directly with the research animals and performing the technical procedures per the study protocols. At SNBL USA we work with many different animal models: non-human primates, rats, mice, guinea pigs, rabbits, swine and canine. In this position you are given many growth opportunities by learning and perfecting multiple technical procedures, working with different animal models, operating laboratory equipment, collecting specimens and data in compliance with GLP standards. | 6/10/2018 |
| 791 | Solid Biosciences Cambridge, MA Associate Scientist, Upstream Process Development - Weekend Shift BS in Chemical Engineering, Biochemical Engineering, Biochemistry or equivalent related fields Exp: 1 yr |
This individual will join a dynamic and motivated team to develop and characterize unit operations in support of a mid to late stage viral vector program, as well as tech transfer of the process to the clinical/commercial manufacturing team. The successful candidate will support experiments supporting development, characterization, scale-up, and transfer of the upstream manufacturing processes. They will also be responsible for evaluation and implementation of new and existing technology. | 6/10/2018 |
| 792 | Solid Biosciences Cambridge, MA Process Engineer I MS in life sciences, engineering, or equivalent Exp: 0 yr |
This position will provide engineering support for tech transfers to contract manufacturing organizations (CMOs) and provide technical support for ongoing manufacturing operations through process monitoring, troubleshooting, and process improvements. | 6/10/2018 |
| 793 | Soligenix, Inc. Princeton, Nj Clinical Trial Assistant BS Exp: 6 months |
The Clinical Trial Assistant (CTA) will support the in-house activities of the clinical project team to ensure timely start-up and smooth maintenance of operational and regulatory requirements of clinical studies from study initiation through study closeout. | 6/10/2018 |
| 794 | SomaLogic Boulder, CO Research Associate I/II BS/MS in a chemical, physical, or biological science Exp: 0-4 yrs |
We are seeking a talented Research Associate I/II to characterize SOMAmer® reagents (protein affinity reagents comprised of modified ssDNA). You will work in a fast-paced, team-oriented research group testing and documenting the protein binding specificity of SOMAmer reagents. The qualified applicant will contribute to a deeper understanding and more extensive validation of a cutting edge, multiplexed proteomic assay at an exciting local biotechnology company | 6/10/2018 |
| 795 | SomaLogic Boulder, CO Laboratory Associate I/II BS in chemical, physical, biological science, or clinical laboratory science Exp: 0-5 yrs |
The primary role of this position is to perform daily testing of patient samples using robotic liquid handling systems. Level commensurate with experience. | 6/10/2018 |
| 796 | Spherotech, Inc. Lake Forest, IL Quality Control Associate BS in Chemistry or related field Exp: 1 yr |
Duties include final product inspection, documentation, Quality Control testing etc. | 6/10/2018 |
| 797 | Spinal Elements Carlsbad, CA Product Development Engineer BS in mechanical or biomedical engineering Exp: 1-3 yrs |
The Product Development Engineer needs limited supervision and is primarily responsible for the development of new and/or the improvement of existing spinal implants and instruments. They will create designs, models and drawings utilizing SolidWorks. The design of medical devices is a highly regulated field, and the incumbent will be responsible for the creation and maintenance of design documentation. Additionally, they will work to support the associated Planning, Manufacturing, Quality Control, and Regulatory review for their project. | 6/10/2018 |
| 798 | Springfield Clinic Springfield, IL Medical Technologist - Lab BS Exp: 1 yr |
Under the direct supervision of the appropriate Lab Manager, the Medical Technologist is responsible for a variety of laboratory tests in microbiology, clinical chemistry, hematology, serology, coagulation and urinalysis. | 6/10/2018 |
| 799 | Spectrum Pharmaceuticals Irvine, CA Clinical Trials Assistant BS in life science Exp: 1-2 yrs |
Provide support to the Clinical Trial Managers and Clinical Research Associates in Clinical Trial conduct via preparation, distribution, and tracking of study supplies, mass mailings, copying, data entry, etc. | 6/10/2018 |
| 800 | SRI Menlo Park, CA Research Associate I/II - Neurobiology BS in Biological Sciences or related field Exp: 1 yr |
The Center for Neuroscience has an opening for a Research Associate to support research in sleep and circadian neurobiology. The primary duties for this role include management of in vivo resources, genotyping, and meticulous record keeping. Other duties include scoring EEG records, histology, immunohistochemistry, assistance with surgeries, behavioral assays, and other general lab work (e.g., preparing solutions, maintaining equipment & supplies). | 6/10/2018 |
| 801 | Starkey Hearing Technologies Eden Prairie, MN Regulatory Affairs Engineer I BS/MS in Science or Engineering Exp: 1 yr |
This position is responsible for supporting all Regulatory affairs for medical devices and hearing related products. This position will work with various departments across the organization such as Sales and Marketing to the Product Development group with guidance from senior regulatory personnel throughout the product lifecycle. This position is responsible to support activities that keeps Starkey current with changes to medical device regulations. This position is also responsible for creating and maintaining the technical files for all medical devices and hearing related products. | 6/10/2018 |
| 802 | STERIS Saxonburg, PA Supervisor, Production I BS Exp: 1-3 yrs |
Supervises all the activities of production personnel engaged in all facets of the manufacturing function during assigned shift. Assumes authority for personnel actions and oversees most day to day operations to a group of professionals or skilled operational and technical employees. Relies on extensive experience and judgment to plan and accomplish goals and assist the Production Manager in the processing of Customer products. Contributes to the performance management of shift personnel and addresses issues pertaining to training, wages, hiring and terminating. | 6/10/2018 |
| 803 | Stratos Genomics Seattle, WA Scientist/Research Associate—Molecular Biology/Nanotechnology BS/BS/MS in molecular biology, biochemistry, bioengineering, or related field Exp: 1-5 yrs |
Candidates will be involved in developing and optimizing the nanopore-based detection platform for our novel DNA sequencing technology, Sequencing by Expansion. The position primarily involves hands-on laboratory work as individual contributors and as a part of a development team. The Research Associate will work directly with founding Technical and Scientific Officers, Scientists, and Research Associates in a dynamic start-up biotech environment. | 6/10/2018 |
| 804 | Stratos Genomics Seattle, WA SCIENTIST/RESEARCH ASSOCIATE—MOLECULAR ENGINEERING BS/BS/MS in chemistry, chemical engineering, organic chemistry or related field Exp: 1-5 yrs |
Candidates will be involved in developing and optimizing synthesis protocols for our novel DNA sequencing technology, Sequencing by Expansion. | 6/10/2018 |
| 805 | Stryker Corporation Fremont, CA Packaging R&D Engineer BS in Packaging or Industrial Engineering Exp: 1 yr |
As a Packaging R&D Engineer at Stryker Neurovascular, you will be required to have strong attention to detail, high level of service and responsibility in managing a high and varied workload from internal and external clients and be comfortable working to tight timelines. Skills at prioritization, multi-tasking, and excellent written and verbal communication is needed to excel. When faced with issues, you will use your knowledge and quick thinking to solve problems while building quality into all aspects and ensuring compliance to all requirements. You may also be called upon to perform IFU/eIFU (Instructions For Use) development and demonstrate knowledge through delivery of high quality documentation (SOPs, technical literature and work instructions). | 6/10/2018 |
| 806 | Stryker Corporation Lake City, UT Industrial Engineer BS Exp: BS |
In this position, you will be responsible for identifying and leading value improvement and waste elimination projects that drive plant and company performance improvements while promoting the development and advancement of the lean culture within the plant. | 6/10/2018 |
| 807 | Stryker Corporation Mahwah, NJ Sterilization Engineer BS in Biology, Microbiology, or a closely related life science. Exp: 0 yr |
As a Sterilization Engineer you will apply cGLP, cGMP, ANSI, AAMI, ISO, FDA, EPA, and USP guidelines to the bioburden, cytotoxicity, bacterial endotoxin, and biocompatibility analysis of orthopaedic implants and surgical instruments. In this role you will actively support new product development activities. | 6/10/2018 |
| 808 | Stryker Corporation Phoenix, AZ Engineer, Post-Market Quality BS in an engineering or science field Exp: 0-2 yrs |
Reprocessing of single-use medical devices (SUDs) is the practice of inspecting, cleaning, function testing, sterilizing and packaging so that they can be clinically and safely used again. | 6/10/2018 |
| 809 | Stryker Corporation Township, PA Quality Engineer (Operations) BS in Engineering or related field Exp: 1-3 yrs |
As an Engineer, Advanced Quality you will lead engineering activities in the development of orthopedic implants and instruments to ensure the highest level of product and process quality. You will also be responsible for providing guidance to the New Product Development teams to ensure compliance to the company’s quality system and external standards. | 6/10/2018 |
| 810 | Synlogic, Inc. Cambridge, MA Process Development Engineer BS in biology, bio-chemical engineering Exp: 0-3 yrs |
We are currently seeking a highly motivated and enthusiastic Process Development Engineer to contribute to operation and development of fermentation and downstream processes for manufacturing of our engineered probiotics. | 6/10/2018 |
| 811 | Synthego Redwood City, CA Research Associate, Morning Shift BS in Biology, Chemistry, or a similar field Exp: 1-3 yrs |
You will be assisting scientists in the operation of our services and the manufacturing of our products so that everything runs smoothly and customers get what they need. | 6/10/2018 |
| 812 | Synthetic Genomics, Inc. La Jolla, CA Sr. Research Associate, Bioinformatics MS in Bioinformatics, Computer Science, Statistics, Genomic Sciences, Molecular Biology, Genetics, Microbial Ecology or a related field. Exp: 1-3 yrs |
The Bioinformatician will be part of the SGI-DNA with primary focus on tool development, improvement and maintenance to support the business of DNA synthesis. The successful candidate will be responsible for the development of machine-learning models for the analysis of DNA synthesis datasets, DNA synthesis design tools, and NGS data analysis pipelines. These analysis pipelines and applications will be based on existing tools and algorithms as well as newly developed solutions tailored to address specific business goals. | 6/10/2018 |
| 813 | Pionyr Immunotherapeutics, Inc. San Francisco , CA Research Associate – Protein Sciences BS/MS in a life sciences discipline Exp: 1 yr |
Development of biosensor (SPR or BLI) based assay platforms for screening/characterization of antibody binding and specificity | 6/3/2018 |
| 814 | Plexxikon Berkeley, CA Regulatory Associate BS Exp: 1-2 yrs |
Regulatory Associate | 6/3/2018 |
| 815 | Poseida Therapeutics, Inc. La Jolla, CA Process Development Associate MS Exp: 1 yr |
This is a lab-based position that will involve hands-on development of clinical manufacturing processes for selecting, gene-modifying and growing T cell subsets. This position will interface with our Research and Development team as well as with outside Contract Manufacturing Organizations. | 6/3/2018 |
| 816 | Precision Medicine Group Oakland, CA Associate Research Statistician - Health Economics MS Exp: 1-3 yrs |
As an Associate Research Statistician you will develop and implement your advanced research skills across a broad portfolio of evidence synthesis and decision modeling research projects. You will collaborate with project teams to execute analytical work, as well as contribute to the development of the department as a whole. | 6/3/2018 |
| 817 | Precision Medicine Group Chicago, IL Medical Writer BS in biomedical or related life sciences discipline Exp: 1 yr |
You will research, write, and develop medical content for a variety of promotional resources including; evaluating and identifying supporting documentation, organizing and annotating references. | 6/3/2018 |
| 818 | Precision Medicine Group Redwood City, CA Research Associate - Clinical Trials (Lab) BS in Life Sciences, Cell or Molecular Biology or related field Exp: 0-2 yrs |
The Research Associate performs and conducts independently novel non-cell and cell based immunoassays for complex scientific projects. | 6/3/2018 |
| 819 | Progenra Inc. Malvern , PA Research associate BS/MS in a life science Exp: 1-10 yrs |
Research associates will be expected to apply focused expertise to projects supporting the development of screening assays, and to the discovery and evaluation of compounds active in the various screens. Candidates should have demonstrated proficiency in molecular biology or biochemistry and be willing to contribute to the company product and intellectual property development as exemplified by scientific articles, patents, and internal publications. Research associates are, in addition, expected to present their data in company settings and, if appropriate, at external meetings and in the literature. | 6/3/2018 |
| 820 | Progenra Inc. Malvern , PA Scientist/Senior Scientist, Medicinal Chemistry BS/ MS in organic/medicinal chemistry Exp: 0-10 yrs |
As a medicinal chemist you will apply state of the art synthetic chemistry, structural and computational approaches to discover and synthesize novel medicines for a variety of diseases including immuno-oncology, inflammation and neurodegenerative diseases. Research Scientist will independently plan and implement efficient synthetic routes for target compounds and apply state of the art purification and characterization techniques, conduct research with the drug discovery team to develop SAR, analyze the data and write laboratory reports. | 6/3/2018 |
| 821 | Prometheus Laboratories Inc. San Diego, CA Bioengineering Associate II MS Exp: 0-2 yrs |
Assists with the development and transfer of diagnostic assays and analytical methods. | 6/3/2018 |
| 822 | Pulmatrix, Inc. Lexington, MA Engineering Associate // Senior Engineering Associate BS/BA/MS in Chemical Engineering, Biomedical Engineering, or related field Exp: 1-5 yrs |
Support development and optimization of engineered particle inhaled dosage forms. Specific methods may include bench and pilot-scale spray drying | 6/3/2018 |
| 823 | Pulse Biosciences, Inc. Hayward, CA Manufacturing Engineer BS in engineering, manufacturing, industrial engineering, or a related discipline Exp: 1-3 yrs |
The Manufacturing Engineer is responsible for manufacturing engineering, production, product support, and servicing to achieve world-class results. Responsible for manufacturing engineering and production of both durable and disposable products. | 6/3/2018 |
| 824 | Pyramid Laboratories, Inc. Costa Mesa, CA Environmental Monitoring Technician BS in chemistry, microbiology or related technical discipline Exp: 1-3 yrs |
Under general supervision, perform various microbiological related activities for a cGMP compliant Fill/Finish operation. Ability to apply standard practices, techniques, procedures and criteria, is necessary. Must be able to summarize findings and prepare or assist in the preparation of reports, documents, records, etc., for assigned tasks. | 6/3/2018 |
| 825 | Q-STATE BIOSCIENCES, INC Cambridge, MA RESEARCH ASSOCIATE-TISSUE CULTURE BS in biology, chemistry, or a related field Exp: 1 yr |
The laboratory technician will work closely with Q-State’s scientific and management teams to perform studies in a high quality and scientifically rigorous fashion. | 6/3/2018 |
| 826 | Quanterix Corporation Lexington, MA Manufacturing Technician I BS in chemistry, biochemistry or biological/natural sciences Exp: 1-3 yrs |
The Reagent Manufacturing Technician role spans a broad range of activities within the manufacturing operations team at Quanterix. The Reagent Manufacturing Technician is primarily responsible for meeting manufacturing schedule requirements within a fast-paced manufacturing operation. The process responsibilities range from complex protein conjugations to diluent formulation and filling and kitting activities to support a diverse assay menu. | 6/3/2018 |
| 827 | QPS, LLC Newark, DE Associate Scientist - BA BS Exp: 0-2 yrs |
The Associate Scientist will work in the Bioanalytical Department of QPS, LLC. Principal responsibilities of the Associate Scientist may include: working under the direction of a Principal Investigator to perform wet lab experiments; sample preparation by various extraction methods; and analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations. | 6/3/2018 |
| 828 | QPS, LLC Fargo, ND Associate Scientist - DTRL BS Exp: 0-2 yrs |
The principal responsibilities of the Associate Scientist in QPS Dermal/Transdermal Laboratory may include: conducting in vitro absorption and release testing; sample preparation for analytical analysis; assisting in analytical conduct; and recording study results and observations. | 6/3/2018 |
| 829 | QPS, LLC Newark, DE Specialist, Sample Coordination - BA BS in Biology, Pharmacology, Chemistry, Biochemistry, Toxicology or related discipline Exp: 0-2 yrs |
The Specialist, Sample Coordination provides a vital link between QPS’ clients and its scientific staff, and is responsible for handling and recording all samples sent to QPS to ensure compliance with FDA regulations, GLPs and QPS Standard Operating Procedures. | 6/3/2018 |
| 830 | Regeneron Tarrytown, NY Research Associate - Bioassay Development and Antibody Screening MS in biology or a related field Exp: 1 yr |
The candidate should expect 70-80% of benchwork, involving but not limited to cell culture work, FACS, common molecular biology (eg. cloning) and biochemistry (eg. ICC and WB) techniques. The rest will be mainly on data recording (ELN) data analysis/organization. There will also be numerous chances for both intragroup and intergroup presentations. | 6/3/2018 |
| 831 | Regeneron Tarrytown, NY Temp - Associate I, Clinical Logistics BS Exp: 1 yr |
The Clinical Logistics Associate I provides support to the Clinical Logistics group and IP distribution process for one or more clinical trials. Activities are performed on time, within budget and with good quality, in compliance with Regulatory Authorities’ regulations / guidelines and Regeneron SOPs / WPDs. Contributes to ongoing process improvement initiatives. This role applies to internally sourced studies and/or CRO/Partnered studies. Interacts with clinical trial managers, as well as staff from quality, clinical compliance, and IOPS (CMC, external manufacturing, stability). | 6/3/2018 |
| 832 | Regeneron Tarrytown, NY Flow cytometry Operator/Specialist BS Exp: 0-4 yrs |
The Research Flow Cytometry Core in the Therapeutic Proteins Department provides service to members of the Research Department, the various Therapeutic Focus Areas and many of the research projects throughout Regeneron. The primary responsibility will be to perform sorting experiments for the research staff. Other responsibilities include maintenance of analytical instruments that are located in the various buildings on Regeneron’s campus. Will also be responsible for data analysis using various flow cytometric software programs. | 6/3/2018 |
| 833 | Regeneron Tarrytown, NY Research Associate I/II (Protein Biochemistry) BS in biochemistry or related field Exp: 0-2 yrs |
This is a permanent laboratory position in a protein biochemistry group involved in the characterization of critical protein reagents to support protein therapeutic pre-clinical testing and release testing. | 6/3/2018 |
| 834 | Regeneron Tarrytown, NY Research Associate, Ophthalmology MS Exp: 1-2 yrs |
The Ophthalmology Research Group is seeking a motivated and collaborative individual to be responsible for molecular and cell biological laboratory work and perform animal studies to support a range of ongoing projects. Experience with molecular cloning techniques, including plasmid design and construction, DNA manipulation, RNA isolation, PCR, sequence analysis is required. This individual will also be responsible for execution of biological experiments necessary to develop animal models and deliver experimental therapeutic reagents. Experience with mammalian cell and tissue culture is also necessary. | 6/3/2018 |
| 835 | Regeneron Tarrytown, NY Temp Process Development Associate/Engineer 1 BS/MS Exp: 0-4 yrs |
A laboratory scientist or engineer with a sound understanding of the principles and techniques used in modern analytical sciences. The ideal candidate is motivated by a dynamic, fast paced environment and a collegial team-oriented approach. He/she will execute routine analytical experiments with minimal guidance, in support of process characterization efforts within the department. | 6/3/2018 |
| 836 | Regeneron Tarrytown, NY Research Associate II-IV, Infectious Diseases MS in Microbiology, Immunology, Molecular Biology, Medical Technology or a related field Exp: 0-4 yrs |
Regeneron is seeking a highly qualified candidate for a Research Associate for infectious disease target discovery, assay development and monoclonal antibody evaluation and selection. | 6/3/2018 |
| 837 | QIAGEN Germantown, MD QC Associate Scientist II BA/BS Exp: 1 yr |
Responsible for testing of raw materials, bulks, components and kits in compliance with cGMP and all applicable government regulations and relevant Standard Operating Procedures. | 6/3/2018 |
| 838 | QIAGEN Beverly, MA Protein Purification Technician I BS Exp: 1-2 yrs |
The Protein Purification Technician I performs assigned manufacturing and process development duties in a ISO 13485 environment. | 6/3/2018 |
| 839 | PharmaForce, Inc. HILLIARD, OH QA Operations Associate I BS Exp: 1 yr |
This position is responsible for ensuring the overall Quality in their assigned areas through the execution of site policies and procedures, programs and work instructions. Ensures all processes and products meet specifications and that products are produced in accordance with GMP requirements. | 6/3/2018 |
| 840 | READCOOR, INC. Cambridge, MA Research Assistant BS in Molecular Biology, Biochemistry, Biomedical Engineering or related Biological Sciences Exp: 1-2 yrs |
We are seeking scientists to help us develop the most advanced fluorescent in situ sequencing (FISSEQ) platform in the industry. We are looking for candidates that want to play an integral role in transforming the way science and medicine approaches RNA sequencing. You will develop techniques in cells and tissue that improve our understanding of molecular interactions between enzymes, cellular environment, hydrogels and surfaces to tackle challenges of molecule immobilization, amplification and detection. Candidates will also be part of a multidisciplinary team that designs, builds, and tests a custom sequencing device tailored to FISSEQ applications. | 6/3/2018 |
| 841 | Sekisui Diagnostics San Diego, CA QC Technician II, Temporary Contract BS Exp: 0-1 yr |
To perform routine QC techniques by adhering and following written procedures under general supervision. | 6/3/2018 |
| 842 | Roche Branchburg, NJ LAB TECH OPS (Quality Control - Chemistry) BS Exp: 0-2 yrs |
Perform testing for raw materials, intermediates and finished kits as required to meet Operations goals and objectives with direction as appropriate. | 6/3/2018 |
| 843 | Roche Branchburg, NJ LAB TECH OPS BS Exp: 0-2 yrs |
Perform testing for raw materials, intermediates and finished kits as required to meet Operations goals and objectives with direction as appropriate. | 6/3/2018 |
| 844 | RTI Surgical Marquette, MI Engineer BS in Engineering Exp: 0-3 yrs |
This position is responsible for support to the design team with task responsibility. This will involve modeling and detailing instrument prints, contributing individually and within cross-functional design teams, and general project support. They will be a self-starter, have a hands-on approach in performing their work duties, and be able to work independently. This position will help RTI Surgical maximize the amount of patients served while maintaining a high level of quality and safety. | 6/3/2018 |
| 845 | Sanofi Inc. Allston, MA Quality Control Analyst II MS in Life Sciences discipline Exp: 1 yr |
This individual will report to the QC shift Supervisor in the Allston Quality Control laboratory and will contribute to general operations and testing of the QC Microbiology laboratory. | 6/3/2018 |
| 846 | Sanofi Inc. Framingham, MA Quality Engineer Associate BS Exp: 0-3 yrs |
The Quality Engineer Associate will support the Quality Engineering function at the Framingham Biosurgery site. This person will be directly involved in internal auditing, product and process investigations, including root cause analysis and technical report writing and reviewing. This individual will participate in risk management activities and external audits on an as needed basis. This Quality engineer associate will work with Manufacturing, Manufacturing Technical Support, Facilities/Engineering, Package Engineering, Validation, Quality Control and Quality Assurance personnel. | 6/3/2018 |
| 847 | Sanofi Inc. Framingham, MA Research Associate (Bioassay Development) MS Exp: 0-2 yrs |
This position is within the Analytical Development group which develops, validates, and transfers analytical methods used for characterization and release of protein therapeutics. We are seeking a highly motivated individual to participate in developing and validating molecular and cell-based analytical methods. This individual will participate in testing of pre-clinical and clinical materials using these methods. Additionally, this job is within a cGMP setting and requires excellent verbal and written communication across several departments. | 6/3/2018 |
| 848 | Sanofi Inc. Meriden, CT Analytical Formulations Professional MS/MA in Chemistry, Biology, Pharmacy, Biomedical, Biotechnology Exp: 1-3 yrs |
The candidate will be responsible for the routine characterization of process intermediates and active pharmaceutical ingredients using a wide variety of biophysical and biochemical methods. This work supports a number of programs including annual strain change, yield improvement, formulation development, comparability studies, and deviation investigations. Candidate will be required to follow standard operating procedures, execute development and stability studies according to protocols, and perform small scale drug product fills by hand. The incumbent will also perform data entry to maintain the databases. The incumbent will be expected to participate on cross-functional teams and will report to the Manager, Senior Scientist. | 6/3/2018 |
| 849 | Sarepta Therapeutics Cambridge, MA Translational Development, Clinical Research Associate I BS in Biochemistry, Immunology, Cell Biology or related field Exp: 1-2 yrs |
The RA will support the transfer of clinical samples from collaborators and CROs to Sarepta and third party storage facilities. He/She will work closely with the Clinical Research Manager and Associate Director to facilitate the training of international biopsy surgical sites and distribution of training materials. Additionally, he/she will take on a role in tracking training documentation across studies/research protocols. The candidate must exercise discretion and judgment in handling confidential information and will follow FDA regulations, ICH guidelines and GCP in all tasks. Strong organizational skills are required, as well as the ability to balance changing priorities. The role may involve occasional travel to oversee clinical sites or vendors | 6/3/2018 |
| 850 | SCIEX Atlanta, GA Field Service Technician BS/BA in Life Sciences, Chemistry, Engineering Exp: Entry level |
Service Technician is responsible for developing the knowledge and skills to support the maintenance, installation and triage repair of Sciex products at both internal and external 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 competencies are developed. | 6/3/2018 |
| 851 | Seattle Genetics Bothell, WA Research Associate II/III, Formulations and Drug Product Sciences MS in pharmaceutical sciences, chemistry, biochemistry, biological sciences or a related discipline Exp: 0-2 yrs |
The ideal candidate will be proficient in performing analytical assays for protein samples. Candidates with analytical chemistry, analytical sciences and protein chemistry background are encouraged to apply. | 6/3/2018 |
| 852 | Seattle Genetics Bothell, WA Quality Control Analyst I/II BA/BS Exp: 1 yr |
This position is located within the Quality Control (QC) department and is responsible for daily laboratory operations and conducting routine and non-routine sampling and analysis of samples for microbiology methods such as environmental monitoring, clean utilities monitoring, bioburden and endotoxin, and analytical methods in accordance with standard operating procedures (SOPs) in a cGMP compliant QC laboratory. | 6/3/2018 |
| 853 | Novartis Morris Plains, NJ Associate Scientist, QC BA/MS in biology, chemistry, biochemistry, microbiology or other related science Exp: 0-5 yrs |
Perform micro/EM testing such as environmental monitoring, gram stain, sterility, en-dotoxin, and mycoplasma. | 5/27/2018 |
| 854 | Novavax Gaithersburg, MD Quality Control Analyst II/III - HPLC BS in Biology, Molecular Biology, Biochemistry, Chemistry, Life Sciences, or other related discipline Exp: 1-3 yrs |
Qualified individuals will be responsible for performing assay qualification and validation as well as analytical testing on in-process samples, drug substance and drug product for release and in support of stability studies.ﾠ | 5/27/2018 |
| 855 | Novavax Gaithersburg, MD Quality Control Analyst II/III BS in Biology, Molecular Biology, Biochemistry, Chemistry, Life Sciences, or other related discipline Exp: 1-3 yrs |
Qualified individuals will be responsible for performing assay qualification and validation as well as analytical testing on in-process samples, drug substance and drug product for release and in support of stability studies.ﾠ | 5/27/2018 |
| 856 | Novavax Gaithersburg, MD Quality Assurance Specialist I/II, Materials (Temporary Assignment) BS Exp: 0-2 yrs |
The QA Specialist, Quality Operations, is responsible for support of GMP compliance with a focus on raw material release through provision of critical review, organization, and Quality oversight of records generated during receipt, testing, and disposition of materials intended for useﾠin GMP manufacturing. | 5/27/2018 |
| 857 | Novavax Gaithersburg, MD Process Development Associate I (IPC) BS/MS in chemistry, biological science, or related field Exp: 1 yr |
Sample testing, experimental documentation and data analysis in a regulated setting;Provide analytical support for process development of vaccine products using analytical techniques, such as UV-Vis spectroscopy, BCA, SDS-PAGE, Western Blot, RP-HPLC, sandwich ELISA immunoassay. | 5/27/2018 |
| 858 | Novavax Gaithersburg, MD Formulation Development Associate I (Temporary Assignment) BS in Pharmaceutics, Chemistry, Biology or equivalent Exp: 0-2 yrs |
Development of liquid formulations forﾠ protein nanoparticle based vaccines through logical screening of excipients | 5/27/2018 |
| 859 | Novavax Gaithersburg, MD Bioprocess Associate I BS Exp: 1-2 yrs |
Main function will be to perform the day to day activities in the Solutions Preparation Area: preparation of buffers, preparation of cell culture media/feeds, calibration of pH and conductivity meters/probes, transport of glassware, scheduling equipment maintenance, etc., to support all of process development. | 5/27/2018 |
| 860 | Oncotherapy Solutions Seattle, WA Research Associate I in biochemistry, cell and molecular biology MS in Biological Sciences or related discipline Exp: 1 yr |
seeking a highly motivated and creative research associate to characterize and test drug conjugatesﾠin-vitroﾠas well as analyze tissue and blood samples from outsourcedﾠin-vivoﾠstudies. | 5/27/2018 |
| 861 | OncoSec Medical Pennington, Nj Research Associate BS Exp: 0-2 yrs |
Supports the R&D group on preclinical projects, with a focus on validating novel immune- oncology therapeutic candidates. As part of this directive, the successful candidate will conduct bench research for various discovery projects. | 5/27/2018 |
| 862 | Ora Andover, MA Clinical Trial Associate BS Exp: 1 yr |
Assists project managers in clinical conduct of ophthalmic clinical trials. Serves as point of contact for investigator sites and ensures compliance with protocol and overall clinical objectives. As a member of the clinical operations team, relies on instructions and pre-established SOPs to perform the functions of the job while working under supervision of a supervisor or manager. Performs day-to-day activities under the guidance of the clinical project managers.ﾠ Placement at the CTA I, CTA II or Sr. CTA level will be determined based on the candidateﾒs qualifications. | 5/27/2018 |
| 863 | Noven Miami, FL Regulatory CMC Specialist, TEMP MS Exp: 1-3 yrs |
Provide Regulatory CMC support to marketed and investigational products.ﾠ Provide regulatory assessment and author post-approval regulatory filings for CMC changes for marketed products.ﾠ Provide Regulatory CMC guidance and author IND amendments, NDAs and DMFs for new drugs in development.ﾠﾠ | 5/27/2018 |
| 864 | Novo Nordisk West Lebanon, NH QA Specialist? BS Exp: 1 yr |
This position will reviews manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will assist in the internal audit program and be a QA presence on the manufacturing floor. | 5/27/2018 |
| 865 | Osiris Therapeutics? Columbia, MD MANUFACTURING COMPLIANCE ASSISTANT ? BIOSURGERY BS Exp: 1-2 yrs |
The Manufacturing Compliance Assistant will be responsible for assuring all manufacturing processes are conducted and documented in compliance with current GMP/GTP and safety regulations, AATB requirement. | 5/27/2018 |
| 866 | Organogenesis CANTON, MA Quality Control Analyst I/II - Microbiology BS in microbiology, biology or a related scientific discipline Exp: 6 months- 2 yrs |
The QC Analyst I/II - Microbiology performs quality activities in support of product production and releases. The QC Analyst I/II communicates with internal departments at Organogenesis and with outside contacts including contractors and suppliers. The QC Analyst I/II performs a wide variety of activities to ensure compliance with applicable regulatory requirements by conducting testing and reporting results. This individual works in Microbiology environment. | 5/27/2018 |
| 867 | Novozymes Davis, CA Research Associate, Biofuel Yeast Strain Engineering MS in Molecular Biology, Biochemistry, Microbiology or related discipline Exp: 1 yr |
The researcher will be responsible generating yeast strains for biofuels applications. The candidate will support the development of techniques to improve strain building and screening processes including automation of high throughput processes.ﾠ | 5/27/2018 |
| 868 | Novozymes Davis, CA Senior Quality Control Analyst/Quality Control Analyst BS in Microbiology or related field Exp: 0 yr |
As a QC analyst, you will leverage your skill set to execute studies in accordance to written procedures while maintaining accurate up-to-date records of all work performed. Focus and attention to detail are a must as you will work cross-functionally to resolve issues impacting key areas. | 5/27/2018 |
| 869 | Nuventra Pharma Sciences Durham, NC Archivist and Validation Specialist BS Exp: 0-2 yrs |
Responsible for qualifying new systems, maintaining the qualified state of existing systems including computerized systems and equipment | 5/27/2018 |
| 870 | Nuventra Pharma Sciences Durham, NC Quality Assurance Specialist BS Exp: 0-2 yrs |
To assist in quality review of documents (Format and quality based on company SOPs);Support ongoing quality programs and initiatives, and other duties as assigned. | 5/27/2018 |
| 871 | Nuventra Pharma Sciences Durham, NC Pharmacokineticist MS in pharmaceutical sciences Exp: 1-2 yrs |
Contribute to or conduct non-compartmental and compartmental pharmacokinetic analysis using Phoenix WinNonlinﾮ.Contribute to or conduct PK/PD analysis and population PK modeling and simulation using industry standard software tools. | 5/27/2018 |
| 872 | Osmotica Pharmaceutical Marietta, GA Process Development/Validation Scientist?-?Pharma Technology? BS in Engineering, Pharmacy or a scientific discipline Exp: 1-3 yrs |
The incumbent is responsible for supporting Technology Transfer of pharmaceutical dosage forms and drug delivery systems for new and existing chemical entities according to approved plans/protocols.ﾠ The Process Development/Validation Scientist is responsible for developing, organizing, leading development activities on the shop floor and performing validation activities. ﾠThe Process Development/Validation Scientist also performs related technical writing functions, including Standard Operating Procedures.ﾠ The incumbent is also responsible for operating laboratory process and testing related equipment in the Pharmaceutical Sciences Laboratory. | 5/27/2018 |
| 873 | Miltenyi Biotec Cambridge, MA Regulatory Affairs Associate BS in life sciences or chemistry Exp: 1-3 yrs |
As a member of the Miltenyi Biotec Regulatory Affairs Team, you will be responsible to support all company regulatory objectives to ensure that products meet worldwide regulatory requirements on all aspects of product approval and post-marketing compliance. I | 5/27/2018 |
| 874 | Otsuka Pharmaceutical Princeton, NJ Packaging Engineer BS in Engineering, Business or related field Exp: 1-4 yrs |
The Packaging Engineer is a technical resource responsible for assisting in the day-to-day operations ensuring the timely packaging of Otsukaﾒs products. The positionﾒs key responsibilities are the support of Otsukaﾒs product portfolio including package and device development, component specifications and graphic arts related activities. | 5/27/2018 |
| 875 | Otsuka Pharmaceutical Princeton, NJ Associate Scientist Technical Services BS/MS Exp: 0-2 yrs |
The Scientist/Sr. Scientist will be responsible for various activities under the direction of the manager or Director of Sterile Dosage Technologies.ﾠ These include performing process development/scale-up studies, participating in the manufacture of cGMP clinical lots, and transfer of processes to clinical or commercial manufacturing facilities for new drug candidates or existing commercial products.ﾠ ﾠ | 5/27/2018 |
| 876 | Pace Analytical Services Eagan, MN Entry-Level Chemist BS in Chemistry Exp: 0-2 yrs |
The Entry-Level Chemist willﾠprepare samples, complete testing, record data, and analyze results. | 5/27/2018 |
| 877 | Pace Analytical Services Maplewood, MN Microbiology Lab Analyst BS in Microbiology or related science Exp: 1-3 yrs |
This candidate will perform microbiological testing as part of a quality group that deals with food safety and food safety products.ﾠWork is performed in a fast-paced lab setting. | 5/27/2018 |
| 878 | Pace Analytical Services St. Paul, MN Quality Engineer Assistant BS in Chemistry or related science Exp: 0-2 yrs |
Candidate will work with Quality Assurance as a Quality Engineer Assistant to ensure compliance of manufacturing processes in a GMP environment. This person will serve as reviewer and/or approver for required documentation in a pilot plant setting. This position is very project orientated, so the QE Assistant can expect every day to be different with changing responsibilities and priorities. | 5/27/2018 |
| 879 | Pace Analytical Services Maplewood, MN Regulatory Specialist BS in Chemistry, Biology, Environmental Science, or related science Exp: 1-2 yrs |
Candidate will work to ensure compliance of medicalﾠdevices with electronic labeling regulations. This person will review documents, collect data, enter data, and assist in process improvement. This is a non-lab position. | 5/27/2018 |
| 880 | Pace Analytical Services Maplewood, MN Formulation Chemist BS in Chemistry, chemical engineering, or other science Exp: 1 yr |
The Chemist willﾠfor the develop, formulate, and test pharmaceuticalﾠproducts. | 5/27/2018 |
| 881 | PAION Cambridge, MA Quality Assurance Associate GMP BS Exp: 0-3 yrs |
QA support to all other departments within PAION;Assist in the maintenance and management of PAION's QMS;Batch review for API, bulk and packed/labelled material and co-ordination and control of certification/release process together with QPs.QA support to all other departments within PAION;Assist in the maintenance and management of PAION's QMS;Batch review for API, bulk and packed/labelled material and co-ordination and control of certification/release process together with QPs. | 5/27/2018 |
| 882 | Paragon Bioservices Baltimore, MD Quality Control Analyst I/II - Environmental Monitoring BS in a Life Sciences discipline Exp: 1-4 yrs |
This role is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring and microbiological testing to support Phase I/II GMP manufacturing. Works in a fast-paced environmental supporting the quality control department of a CMO for manufacturing of biologic bulk drug substance, sterile finished drug product, and fill/finish. | 5/27/2018 |
| 883 | PBL Assay Science Piscataway, NJ R&D Scientist BS/MS in biological sciences Exp: 1 yr |
ﾠThe R&D Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes assay development strategy and aids in the transfer of the assays to the Manufacturing department for final commercialization. The R&D Scientist is also responsible for development of custom assays and reagents for clients. | 5/27/2018 |
| 884 | PBL Assay Science Piscataway, NJ Senior Scientist BS/MS in biological sciences Exp: 1-4 yrs |
The Senior Scientist is responsible for the hands-on development of immunoassays, such as ELISAs and cell-based assays, for commercial production. This individual plans and executes assay development strategy, and oversees multiple product transfers to the Manufacturing department for final commercialization. The Senior Scientist is also responsible for development of custom assays and reagents for clients. | 5/27/2018 |
| 885 | Penumbra Alameda, CA QA Engineering Specialist BS Exp: 1 yr |
As a Quality Assurance Engineering Specialist at Penumbra, you will support quality engineering activities designed to ensure that all processes, products and systems meet the highest standards of quality and compliance with domestic and international regulations. | 5/27/2018 |
| 886 | Penumbra Alameda, CA Regulatory Specialist BS in biology, neuroscience, chemistry or biomedical engineering Exp: 1 yr |
Support the preparation of submissions to gain approvals for clinical research, export, and commercial distribution around the world. | 5/27/2018 |
| 887 | Perrigo Allegan?, MI Assistant Scientist / Associate Scientist - Analytical R & D BS in Chemistry or Pharmaceutical Sciences Exp: entry levelﾠ |
The individual will be responsible for development of assay, impurities, dissolution, water content, and physical characterization methods for liquid and solid oral drug products. There is an expectation of both direct hands-on laboratory work as well as, depending on level of experience, mentoring/training of colleagues. | 5/27/2018 |
| 888 | Personalis Menlo Park, CA Laboratory Assistant BS in Molecular Biology or related field Exp: 0-2 yrs |
Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. | 5/27/2018 |
| 889 | Pfenex San Diego, CA Research Technician , Analytical Sciences BS in molecular biology, biochemistry or related scientific fields Exp: 1 yr |
As a member of the Analytical team, the research technician will conduct analytical experiments, analytical methods and document results for product development.ﾠ | 5/27/2018 |
| 890 | Pfenex San Diego, CA Associate Scientist, Analytical Science- Product Development BS in Biochemistry or related subjects Exp: 1-3 yrs |
As an Associate Scientist 1, you will be responsible for developing and implementing protein biochemistry analytical methods for microbial strain screening and biological product characterization. The individual will work with senior scientific staff to design and implement analytical biochemistry protocols, including routine PAGE/Western, SDS-CGE, ELISA and HPLC for characterization of recombinant proteins from a microbial expression system. The individual will work within project timelines and in a team structure that interfaces with different research and development departments. | 5/27/2018 |
| 891 | Pharmaforce SHIRLEY, NY Q.C. Microbiologist I? BS Exp: 0-2 yrs |
The QC Microbiologist I will perform microbial testing and environmental monitoring according to current guidance and established procedures for analysis of samples in the Quality Control Microbiology and Environmental Monitoring Laboratories. | 5/27/2018 |
| 892 | Pharmaforce NEW ALBANY, OH R&D Formulation Chemist I Exp: 1-2 yrs |
Responsible for formulation and process development activities associated with parenteral drug product development. Participates in scale-up of manufacturing process. | 5/27/2018 |
| 893 | LabConnect? Johnson City , TN Laboratory Information Systems Coordinator 2 yrs college Exp: 0 yr |
LIS Coordinator, Laboratory Information Systems assists with test builds, utilizing the LabConnect system and partner laboratory LIMS. S/he performs duties associated with day-to-day tasks as assigned by Data Specialists. | 05/21/18 |
| 894 | LabConnect? Johnson City , TN Data Coordinator-Early Development Services Bachelors in Science/Computers Exp: 0 yr |
The Data Coordinator is responsible for supporting EDS data quality via digital form mapping and validation, assisting EDS team members with data quality issues handling, and supporting the Data Manager with special projects related to data quality. All activities ensure quality deliverables on time to EDS clients. | 05/21/18 |
| 895 | LabConnect? Cambridge, MA Clinical Trials Contract Coordinator Bachelors Exp: 1-3 yrs |
his unique associate level position will be responsible for vendor contract coordination and various aspects regarding the procurement to payment process with our biopharmaceutical client. This position falls within business operations. | 05/21/18 |
| 896 | Moderna Cambridge, MA Sr./Research Associate, Delivery Innovation BS/BA Exp: 0-2 yrs |
Research Associate/Sr. Research Associate who will be responsible for the preparation and characterization of mRNA-containing nanoparticles within a dynamic and highly interdisciplinary environment.ﾠ | 5/20/2018 |
| 897 | Moderna Cambridge, MA Sr./Research Associate, In Vivo Pharmacology, Moderna Oncology MS in a biological science Exp: 1 yr |
The successful candidate will primarily work with in vivo tumor models and be responsible for validating the in vivo pharmacology and therapeutic utility of novel mRNA therapeutics.ﾠ Applicants should be great team members and have a track record of independent research accomplishments. | 5/20/2018 |
| 898 | Moderna Cambridge, MA Sr. Research Associate , Potency Assay Development MS Exp: 0-2 yrs |
The individual will participate in the development and performance of cellular and biochemical potency assays to support advancement of Modernaﾒs mRNA clinical development candidates. | 5/20/2018 |
| 899 | MilliporeSigma St. Louis, MO Scientist, Production Associate Sr? BS/BA in chemistry, biochemistry, biology, chemical engineering or related life science Exp: 1 yr |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 5/20/2018 |
| 900 | MilliporeSigma Milwaukee, WI Scientist, Production Associate BS/BA in chemistry, biochemistry, biology, chemical engineering or related life science Exp: 1 yr |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 5/20/2018 |
| 901 | MilliporeSigma Milwaukee, WI Production Scientist Associate BA/BS in the field of Chemistry, Biochemistry, Analytical Chemistry Exp: 1-3 yrs |
To perform routine and non-routine chemical analysis, following established protocols and procedures; to accurately interpret results and to prepare complete and legible records; to provide lab support and to maintain equipment. | 5/20/2018 |
| 902 | MilliporeSigma Burlington?, MA Lab Tech III BS Exp: 1 yr |
Your primary area of focus would be to perform extractions and then subsequent NVR, TOC, FTIR, and RP-HPLC testing and peer review for Extractables and Leachables studies in a GMP environment.ﾠ A secondary area of focus will be on assisting with sample preparations and performing lab maintenance activities such as glassware cleaning, hazardous waste disposal, and order receipt. | 5/20/2018 |
| 903 | MilliporeSigma Sheboygan Falls, WI Scientist, Production Associate (Quality Control) BS/BA in chemistry, biochemistry, biology, chemical engineering or related life science Exp: 1 yr |
Analyzeﾠproducts according to established protocols, provide technical support to others and perform operations in support of the group and department. | 5/20/2018 |
| 904 | Medtronic Northridge, CA Verification Engineer MS in Engineering or Science-related discipline Exp: 1 yr |
Under general supervision, candidate works independently on moderately complex verification testing assignments. Candidate will develop and validate test methods, both manual and automated. Candidate will work cross-functionally to ensure proper test coverage of design requirements. | 5/20/2018 |
| 905 | Medtronic Irvine, CA Medical Writer (Bilingual ? Chinese/English) MS Exp: 0 yr |
The Medical Writer [Bilingual - Chinese (Cantonese/Mandarin) and English] role in our Medical Affairs organization supports the Global Neurovascular business unit. The bilingual (Chinese/English) Medical Writer will be focused on developing clinical, scientific, and regulatory documents for the China FDA along with some responsibilities for other global markets. | 5/20/2018 |
| 906 | Medtronic Santa Rosa, CA R&D Engineer-Heart Valve Frame Design MS Exp: 0 yr |
Design and development of transcatheter heart valves, manufacturing processes, and test methods used in the manufacturing and design characterization of medical device implants in a regulated environment. Activities will include Nitinol heart valve frame design, methods/process development, tooling design/fabrication, equipment design/fabrication, qualification, validation, project management, failure analysis, regulatory submission, and documentation. Supports development projects in multi-functional project teams. | 5/20/2018 |
| 907 | Medtronic Santa Rosa, CA Supplier Quality Engineer MS Exp: 0 yr |
In this exciting roleﾠSupplier Quality Engineer, you will have responsibility forﾠsupplier management activity working with external suppliers and internal teams to assure that our products exceed the requirements and expectations of patients, physicians, regulatory agencies and the business. | 5/20/2018 |
| 908 | nanostring Seattle, WA Associate International Regulatory Affairs Specialist BA/BS/MS Exp: 0-2 yrs |
Creates, evaluates and completes International regulatory projects consistent with the company goals. Successful candidate is responsible for assembling regulatory submissions and international dossiers to non-EU territories.ﾠ | 5/20/2018 |
| 909 | nanostring Seattle, WA Manufacturing Research Associate I (Sun thru Thurs) BS Exp: 0-2 yrs |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. | 5/20/2018 |
| 910 | nanostring Seattle, WA Manufacturing Research Associate I (Mon thru Fri) BS Exp: 0-2 yrs |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. | 5/20/2018 |
| 911 | NantKwest San Diego, CA Research Associate?(Cell Culture Technician)? BS in Biology, Biochemistry, Immunology or a related field Exp: 1-3 yrs |
TheﾠResearch Associateﾠ(Cell Culture Technician)ﾠwill assist scientist/senior research associate for the culturing, plating, distribution, maintenance, and banking of cell culture lines. Important aspects of this role include excellent organization skills, flexibility, and the ability to thrive in an efficient, highly interactive, goal-oriented team environment, and working with minimal supervision. | 5/20/2018 |
| 912 | Nanosyn Santa Clara, CA Research Associate, Synthetic Organic or Medicinal Chemist BS/MS in synthetic organic chemistry, medicinal chemistry, or closely related field Exp: 0-5 yrs |
Develop and implement synthetic routes for production of arrays of synthetic compounds | Perform labor |
| 913 | Natera Austin, TX Quality Assurance Specialist BS in Life Sciences, Engineering, Software or equivalent Exp: 1 yr |
This is an entry-level position to assist the Quality Department in continuous compliance and improvement.ﾠ | 5/20/2018 |
| 914 | Natera San Carlos, CA Clinical Laboratory Associate I BS/BA in a biological science or similar field of study Exp: 0-2 yrs |
Clinical Laboratory Associate I to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. | 5/20/2018 |
| 915 | Natera San Carlos, CA Clinical Laboratory Associate I (Temporary) BS/BA in a biological science or similar field of study Exp: 0-2 yrs |
Clinical Laboratory Associate I (Temporary) to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. | 5/20/2018 |
| 916 | Navitor Pharmaceuticals Cambridge, MA Research Associate/Senior Research Associate BS/BA in Biochemistry/Biophysics, Cell Biology or related discipline Exp: 1-2 yrs |
We are seeking highly motivated, energetic and committed individuals to join our interdisciplinary team and actively contribute to advancing our drug discovery programs from discovery to proof- of-concept. You will build your experience in early discovery projects using cell-based and biochemical/biophysical approaches to support small-molecule discovery activities and advance our cutting-edge programs that target the mTORC1 pathway. | 5/20/2018 |
| 917 | Nemametrix? Murray, UT Genetics Laboratory Technician II BS in Biology or related field Exp: 1 yr |
You will be reporting to the Transgenics Supervisor working among a team,ﾠto deliver custom transgenics to our clients, in a timely manner, using established procedures. ﾠThe sophisticated nature of the work requires attention to detail and high-functioning knowledge of current genetic techniques. The ability to work independently according to schedule is balanced with the need to collaborate extensively with colleagues to ensure that we consistently meet or exceed our clientsﾒ expectations. | 5/20/2018 |
| 918 | Nemametrix? Murray, UT Molecular Biologist Laboratory Technician II BS in Biology or related field Exp: 1 yr |
You will be reporting to the Molecular Biology Supervisor working among a team, to deliver custom transgenics to our clients, in a timely manner, using established procedures.ﾠ The sophisticated nature of the work requires attention to detail and high-functioning knowledge of current molecular biology techniques.ﾠ The ability to work independently according to schedule is balanced with the need to collaborate extensively with colleagues to ensure that we consistently meet or exceed our clientsﾒ expectations. | 5/20/2018 |
| 919 | Nemametrix? Eugene, OR Zebrafish Technician BS in Biology or related field Exp: 1 yr |
Microinjections of zebrafish embryos.Fluorescent imaging of zebrafish embryos.Harvest DNA of zebrafish embryos. | 5/20/2018 |
| 920 | , Exp: |
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| 921 | Nelson Laboratories Salt Lake City, UT Validation Specialist BS/BA Exp: 1 yr |
Responsible for preparing, executing and finalizing test method validations, equipment, system and utility IQ, OQ and PQs as well as maintain control charts. ﾠAlso, required to maintain the re-qualification schedule per the current validation master plan schedule. | 5/20/2018 |
| 922 | Neogen Pleasantville, IA QC Technician/ Document Control BS Exp: 1-2 yrs |
The main responsibility will be to setup a quality control program and testing for products and materials. Other responsibilities include but are not limited to, calculating and summarizing data using scientific equations, set up and perform studies on components, record test results on standardized forms and write reports detailing procedures, file and maintain retention storage of all product components and reagents. | 5/20/2018 |
| 923 | Neogen Lexington, KY QC Chemist BS Exp: 1-2 yrs |
The selected candidate will be responsible for performing instrument/method troubleshooting as well as validation, qualification, calibration, and preventative maintenance, and performing investigations on out-of-specification results. The selected candidate will participate in QA functions of the QCU including document review, room and equipment log review, room cleaning approvals, and other quality functions as assigned by the Director of AS Quality Systems. | 5/20/2018 |
| 924 | Neogen Lansing, MI Lateral Flow Chemist BS Exp: 1-2 yrs |
Lateral Flow Chemist | 5/20/2018 |
| 925 | Neogen Lexington, KY QA/QC Technician BS Exp: 1-2 yrs |
This position is part of the Quality Control Department within the Life Science group. Duties performed with this position include preparing and/or assaying components to be included in Neogenﾒs ELISA Drug Detection and Life Science test kits and verifying conformity to specifications for release. | 5/20/2018 |
| 926 | Nephron Pharmaceuticals Corporation West Columbia, SC Microbiologist I BS in Biology, Microbiology or Life Science Exp: 1 yr |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. | 5/20/2018 |
| 927 | Nephron Pharmaceuticals Corporation West Columbia, SC Quality Specialist BS Exp: 1-3 yrs |
Responsible to assure compliance with FDA regulations in the areas of non-conformance investigations, planned deviations, or corrective and preventive actions (CAPAﾒs) at Nephron Pharmaceuticals Corporation. | 5/20/2018 |
| 928 | NGM Biopharmaceuticals South San Francisco, CA Research Associate ? Nonclinical Safety BS/MS degree in life sciences Exp: 1-2 yrs |
This is a highly dynamic role with responsibility to support programs across NGMﾒs research and development portfolio.ﾠ | 5/20/2018 |
| 929 | Nordson Corporation Chippewa Falls, WI Design Engineer MS in engineering in a field related to polymers, polymer rheology, or flow modeling Exp: 1-3 yrs |
The Design Engineer will be responsible for a broad range of activities that support product design, new product development and technical sales.ﾠ | 5/20/2018 |
| 930 | Nordson Corporation Eagan, MN Regulatory Affairs Specialist BS Exp: 1-3 yrs |
Responsibilities include implementing regulatory plans, completing regulatory deliverables for medical devices and supporting customers with product registrations. ﾠ | 5/20/2018 |
| 931 | Novan Morrisville, NC Assistant Scientist, Chemistry Development BS in chemical engineering, chemistry, or related discipline Exp: 0-5 yrs |
The Assistant Scientist, Chemistry Development will be responsible for assisting with and conducting chemistry development manufacturing.ﾠ Additional responsibilities will include performing routine cleaning and preventative maintenance, where appropriate, on manufacturing equipment up to approximate 5 kg scale, preparing for chemistry development manufacturing activities, and maintaining an inventory of raw materials and consumables. | 5/20/2018 |
| 932 | Novartis Fort Worth, TX Labeling Specialist II BS Exp: 1 yr |
Collaborate with R & D, Regulatory and Global Graphics Designers to create labeling for medical products.ﾠ | 5/20/2018 |
| 933 | Novartis Lake Forest, CA Engineer (Research) BA/BS in Engineering? Exp: 0 yr |
Execute Global Medical Affairs vitreoretinal strategic tactics (lab studies part of the Phase IIIB/IV study plan).ﾠ | 5/20/2018 |
| 934 | Novartis Fort Worth, TX QA Operations Analyst I BS Exp: 1 yr |
Responsible for completing product attribute and particulate inspections, manufacturing batch record review, line audits, and product sampling to ensure products are manufactured in compliance with corporate, regulatory and industry standards. Functions as primary contact for QA operations team, escalating issues to supervisors as needed. Participates in development and implementation of quality projects and supports department initiatives. | 5/20/2018 |
| 935 | Novartis Morris Plains, NJ Associate Scientist Bioanalytics BA in Cell biology Immunology, Molecular biology, virology, biochemistry, microbiology or other related science Exp: 0-5 yrs |
Perform Bioanalytical testing in support of clinical and commercial release strategies.ﾠ | 5/20/2018 |
| 936 | MedImmune Gaithersburg, MD R&D Associate II or Associate Scientist I - Gene Therapies MA in Cell Biology or relevant scientific discipline? Exp: 1 yr |
The main duties for the ideal candidate are to help build gene- and stem cell-based approaches to support MedImmuneﾒs pipeline projects. This candidate will be responsible for optimizing and testing viral vectors for transduction efficiency, sustainability, safety and manufacturability. You will also be responsible for maintenance and differentiation of pluripotent stem cells. You will plan and execute experiments on the bench. In addition, you will be working in a multidisciplinary matrix environment to design strategies towards clinically relevant strategies. | 5/13/2018 |
| 937 | Medpace Dallas, TX Clinical Research Associate-Dallas Entry Level BS in a health or science related field Exp: 1 yr |
Conductﾠqualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol | 5/13/2018 |
| 938 | Medtronic Irvine, CA Assoc Manufacturing Engineer BS in Engineering Exp: 1 yr |
Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. | 5/13/2018 |
| 939 | Medtronic New Haven, CT Clinical Research Specialist MS Exp: 1 yr |
Serve as Clinical Affairs representative on assigned project teams and/or PDP teams to develop clinical strategies that support corporate and departmental objectives. Provide clinical and technical feedback to product development teams during project team meetings.ﾠ | 5/13/2018 |
| 940 | Medtronic Mansfield, MA R-D Engineer MS Exp: 0 yr |
Designs, develops, analyzes, troubleshoots and provides technical skills during research and/or product development. | 5/13/2018 |
| 941 | Medtronic Northridge, CA Product Engineer MS Exp: 0 yr |
This position will be responsible for developing test methodology to conduct material, component and device level testing to ensure products meet specifications and regulatory requirements. The engineer will conduct verification and validation activities inclusive of creating protocols, testing per approved protocols, and documentation activities in accordance with applicable development and regulatory requirements. The engineer will collaborate with design colleagues to ensure designs are capable of meeting performance targets while supporting multiple projects within the product development group. | 5/13/2018 |
| 942 | Medtronic Boulder, CO Quality Systems Engineer MS Exp: 0 yr |
Oversee and manage the operational aspects of ongoing projects and serve as liaison between project management, planning, project team, and line management. | 5/13/2018 |
| 943 | Medtronic Northridge, CA Medical Affairs Safety Clinical Research Specialist MS Exp: 1 yr |
ﾠCoordinate activities related to safety assessment, report management, safety committees, system and process development, policy review and implementation, and management review.ﾠ Contribute to accurate and timely reports for study teams and management, including resolution of action items.ﾠ Maintain documentation consistent with Medtronic standards, guidelines and policies. Execute continuous improvement projects, perform other duties and ad hoc projects as assigned in support of the Clinical Research department.ﾠﾠ | 5/13/2018 |
| 944 | Meridian Bioscience Cincinnati, OH Validations Engineer I BS in Chemistry, Biochemistry, Microbiology or Engineering Exp: 1 yr |
Responsible for day to day performance and documentation of validation studies assigned to the Validations Department. Execution of equipment qualifications (IQ, OQ, PQ), test method validation, raw material qualifications, specification validations (characterization studies), and process validations (PPQ). Will run the validation activities in Production Departments when appropriate and secondarily provide troubleshooting and problem-solving support for production related problems. | 5/13/2018 |
| 945 | MESO SCALE DIAGNOSTICS, LLC Gaithersburg, MD Research Associate I BS in life sciences, cellular and molecular biology, protein sciences or related field Exp: 1 yr |
A Research Associate I (RA I) is responsible for carrying out reagent and assay development activities in the laboratory, under supervision, working to achieve development project goals including data analysis and assay qualification. This is a laboratory position performing protein-based immunoassays on a routine basis with relatively high throughput (3-10 plates per day). ﾠSome degree of professional latitude, creativity and self management is expected. | 5/13/2018 |
| 946 | MethodSense Morrisville, NC Quality Assurance Associate BS Exp: 1-3 yrs |
We are seeking a Quality Assurance Associate to work closely with the MethodSense Executive Team and Project Managers to assist with the maintenance of clientﾒs Quality Management Systems, supporting client Regulatory solutions, and the implementation and maintenance of client technology solutions on a contract basis. | 5/13/2018 |
| 947 | MQA Laboratories Concord, CA Lab Technician for Microbiology & Environmental Monitoring BS in microbiology or related science Exp: 1 yr |
looking for laboratory technicians to perform environmental monitoring functions at client facilities and microbiology testing in the microbiology lab.ﾠ | 5/13/2018 |
| 948 | ?MicroVention Aliso Viejo, CA Regulatory Affairs Specialist BS in Science, Engineering or Medical Technology Exp: 1-3 yrs |
The Specialist, Regulatory Affairs is responsible for obtaining regulatory approvals in U.S. and ensures compliance to agency requirements including ISO, local, state and/or federal requirements | 5/13/2018 |
| 949 | ?MicroVention Aliso Viejo, CA Engineer I/Engineer II (EIT) BS in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Industrial Engineering, Chemistry or other related discipline Exp: 0-2 yrs |
This 24-month rotational program is designed to train new Engineers on various aspects of MicroVention Terumo technology, procedures, and processes.ﾠ All candidates will be assigned a Mentor, as well as an Advisor to oversee their program succession, and will be provided with additional classroom training.ﾠﾠ | 5/13/2018 |
| 950 | ?MicroVention Aliso Viejo, CA Industrial Engineer I BS/MS in Industrial Engineering or a related field Exp: 1-3 yrs |
The Industrial Engineer I will support the manufacturing of products for medical devices with work including Operational systems development, process flow, Operational needs and Process efficiencies.ﾠ | 5/13/2018 |
| 951 | MRIGlobal Gaithersburg, MD Associate Scientist - GHSD RDT&E-RV MS Exp: 0 yr |
The successful candidate will join a team of researchers actively conducting genomics-based research in infectious disease diagnostics, bio-surveillance, microbiology, virology, and microbial forensics for a variety of government and industrial clients. | 5/13/2018 |
| 952 | Miltenyi Biotec? Cambridge, MA Regulatory Affairs Associate BS in life sciences or chemistry Exp: 1-3 yrs |
As a member of the Miltenyi Biotec Regulatory Affairs Team, you will be responsible to support all company regulatory objectives to ensure that products meet worldwide regulatory requirements on all aspects of product approval and post-marketing compliance. In addition, you will act as a regulatory liaison for medical and clinical research groups to keep the regulatory affairs department apprised of research progress. Overall, you will be a key contributor to the continued success of all submissions to North American regulatory agencies. | 5/13/2018 |
| 953 | MilliporeSigma? Madison, WI Production Scientist (Chemist)? BS in Chemistry, Biochemistry, Chemical Engineering, or equivalent Exp: Entry Level |
Kilo Lab and Pilot Plant manufacturing of APIs and intermediates;Demonstrate proper lab safety practices, and work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines. | 5/13/2018 |
| 954 | MilliporeSigma? Billerica, MA Associate Scientist, Analytical Chemistry BS Exp: 1 yr |
The purpose of this position is to contribute to the overall success of our drug discovery pipeline by helping perform purification of small molecules and several physicochemical assays. | 5/13/2018 |
| 955 | MilliporeSigma? St. Louis, MO Associate Scientist? BS/BA in chemistry, biochemistry, biology, chemical engineering or related life science Exp: 6 months |
Manufacture or evaluate products according to established protocols, provide technical support to others and perform operations in support of the group and department. | 5/13/2018 |
| 956 | MilliporeSigma? Sheboygan Falls, WI Scientist, Production Associate BS/BA in chemistry, biochemistry, biology, chemical engineering or related life science Exp: 6 months |
Analyzeﾠproducts according to established protocols, provide technical support to others and perform operations in support of the group and department. | 5/13/2018 |
| 957 | MilliporeSigma? Madison, WI Associate Production Scientist BS in Chemistry, Biochemistry, Chemical Engineering, or equivalent Exp: Entry Level |
Position primarily involves the safe and efficient manufacturing of APIﾒs according to cGMP requirements. | 5/13/2018 |
| 958 | MilliporeSigma? Sheboygan Falls, WI Scientist, Production Associate BS/BA/MS in chemistry, biochemistry, biology, chemical engineering or related life science Exp: 1-5 yrs |
Primary responsibilities will focus on conducting thermal analyses and calorimetry experiments to address safety needs for bulk manufacturing in large-scale plant equipment. Other responsibilities will include generating technical reports and executing preventative maintenance on equipment. | 5/13/2018 |
| 959 | MilliporeSigma? Billerica, MA Associate Scientist, Medicinal Chemistry BS Exp: 1 yr |
The Associate Scientist will contribute to the achievement of drug discovery project goals through the synthesis of target molecules by applying modern organic synthetic methods and following best medicinal chemistry practicesﾠ | 5/13/2018 |
| 960 | Moderna therapeutics Cambridge, MA (Contract) Research Associate, Process Development BS in Chemical Engineering, Chemistry, Biochemical Engineering, Biochemistry or closely related field Exp: 0-2 yrs |
The primary responsibilities for the Research Associate, Process Development will be to support the Process Development team to develop and scale-up messenger RNA therapeutics. The scientist/engineer will be involved in clinical study enabling scale-up and pilot production of mRNA. The position will partner closely with Process Sciences and Production teams, and the candidate must be able to work in a multi-disciplinary environment. | 5/13/2018 |
| 961 | Moderna therapeutics Cambridge, MA (Contract) Associate I, Quality Control, Chemistry BS Exp: 1 yr |
The individual in this role will perform routine testing of raw materials and samples for mRNA products (in process, release and stability) manufactured at the Moderna facility. Also, this individual may support special projects as assigned.ﾠ He/she will participate in troubleshooting assays and equipment and may support investigations for OOS and other non-conforming results. | 5/13/2018 |
| 962 | Moderna therapeutics Norwood, MA Associate I, Quality Control Stability BS Exp: 1 yr |
Reporting to the Senior Manager of Quality Control, the Quality Control Stability Associate will be responsible for supporting GMP stability testing programs and Quality Systems, including the maintaining of stability databases, performing data trending and statistical analyses, creation and review of SOPﾒs, stability protocols and reports in accordance with current GMP, FDA, EU and ICH guidelines and regulations. This individual will also support the implementation and functionality of stability related processes, equipment and systems at both the Cambridge, MA and Norwood, MA locations. | 5/13/2018 |
| 963 | Moderna therapeutics Norwood, MA (Contract) Technical Writer, Manufacturing BS Exp: 1-2 yrs |
The individual in this role will be part of a cohesive team responsible for producing high quality mRNA-based medicines for evaluation in human clinical trials.ﾠ The Manufacturing Support Technical Writing team member uses knowledge of cGMP regulations and biopharmaceutical production processes to create and revise standard operating procedures, batch records, specifications, forms and other critical documentation. They will work directly with subject matter experts to ensure content accuracy, improve efficiency and documentation practices. | 5/13/2018 |
| 964 | Moderna therapeutics Norwood, MA (Contract) Support Specialist, Manufacturing MS Exp: 0-2 yrs |
The individual in this role will be part of a cohesive team responsible for producing high quality mRNA-based medicines for evaluation in human clinical trials.ﾠ The Manufacturing Support Specialist team member uses knowledge of cGMP regulations and biopharmaceutical production processes to assist in investigations, document generation and improvement initiatives within manufacturing operations or other departments as needed. They will work directly with subject matter experts to ensure content accuracy, improve efficiency and documentation practices. | 5/13/2018 |
| 965 | Moderna therapeutics Cambridge, MA Research Associate/Engineer I, Process Development BS in Chemical Engineering, Biochemistry, or a related field of science Exp: 0-2 yrs |
The candidate will work under supervision to develop fermentation and purification processes for plasmid DNA and enzymes. The incumbent with work closely with members of molecular biology, cell line development, mRNA process development, and analytical development teams to optimize the upstream and downstream unit operations and deliver high quality raw materials for mRNA synthesis. | 5/13/2018 |
| 966 | Moderna therapeutics Cambridge, MA Associate Engineer, Manufacturing Sciences and Technology MS in Biochemical engineer, Chemical engineer, or Biochemistry Exp: 0-2 yrs |
This position is part of Modernaﾒs Manufacturing Science and Technology (MST) team responsible for ensuring the robust technology transfer and technical support of our mRNA platform in cGMP Manufacturing.ﾠ The individual will work closely within MST, and with Process Development, Manufacturing, Regulatory, and Quality, to ensure all aspects of technology transfer and technical support are successfully executed. | 5/13/2018 |
| 967 | Momenta Cambridge, MA QA Associate (Contractor) BS in life sciences Exp: 1-5 yrs |
We are currently seeking a QA Associate, Contractor to assist with developing and maintaining Momentaﾒs quality assurance programsﾠwith primary responsibilityﾠfor quality oversightﾠof Momenta's equipment management system.ﾠﾠAmong other responsibilities, thisﾠincludes review and approval of equipment qualification packages, performing periodic validations, and guiding the user community in following applicable SOPs and regulations.ﾠ | 5/13/2018 |
| 968 | MyoKardia South San Francisco, CA Research Associate I/II BS in molecular biology, cell biology pharmacology or related discipline Exp: 1-2 yrs |
Cell culture of cell lines, primary mammalian lines, iPSCs, and differentiation of cardiomyocytes derived from iPSC | 5/13/2018 |
| 969 | MyoKardia South San Francisco, CA Scientist I - Pharmacology MS in physiology, pharmacology, biochemistry, or related discipline Exp: 0-2 yrs |
Work with pharmacology colleagues to gain an understanding of primary and secondary pharmacology mechanisms, biomarkers, translational potential, and safety for discovery- and development-stage programs | 5/13/2018 |
| 970 | MPI Research Mattawan, MI Research Associate (Intern) - Analytical MS/BS/BA Exp: 0-2 yrs |
This position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and/or GxP regulations. This individual proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement communicating effectively with others. initiatives, and demonstrates | 5/13/2018 |
| 971 | MPI Research Mattawan, MI Research Assistant 1/Research Associate 1 - Pathology Services - Tissue Trimming - 2nd Shift BS Exp: 0-2 yrs |
This position is responsible for performing the technical functions in tissue trimming including soft tissue, bones, and measuring fixed organ weights, as well as for performing technical support functions, as necessary. It is expected to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. | 5/13/2018 |
| 972 | MPI Research Mattawan, MI Research Assistant 1/Research Associate 1 - Pathology Services - Necropsy BS Exp: 0-2 yrs |
This position is responsible for performing the technical functions in necropsy including the handling and euthanize of multiple species of animals, collection of tissue and blood samples, and the proper preservations of specimens, as well as for performing technical support functions, as necessary. It is expected to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. | 5/13/2018 |
| 973 | MPI Research Mattawan, MI Research Assistant 1/Research Associate 1 - Pathology Services - Histology BS Exp: 0-2 yrs |
This position is responsible for performing the technical functions in histology including tissue processing, tissue embedding, microtomy, slide staining, and microscopic review, as well as for performing technical support functions, as necessary. It is expected to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. | 5/13/2018 |
| 974 | MPI Research Mattawan, MI Research Assistant 1/Research Associate 1 - Clinical Pathology BS Exp: 0-2 yrs |
This position is responsible for performing assigned basic support functions in the Clinical Pathology Laboratory setting. Functions include Set-up, Processing, Sample Management, and/or administrative functions as outlined in a protocol or appropriate Standard Operating Procedures (SOPs). | 5/13/2018 |
| 975 | Myriad? Salt Lake City, UT Quality Assurance Engineer BS in Engineering, Life Science, other technical discipline Exp: 0-3 yrs |
The Quality Engineer (QA ﾖ Quality Systems) will assist the Quality Manager (Quality Systems) with activities in support of Myriadﾒs Quality Management System (QMS) | 5/13/2018 |
| 976 | Labcorp Shelton, CT Laboratory Supervisor I - FISH BS/BA Exp: 1-3 yrs |
Assigns, oversees, and reviews the work of employees. Directs all phases of work, quality, service, and costs; and performs tests or assays as required. | 5/6/2018 |
| 977 | Labcorp Westborough, MA Laboratory Technician - DNA Extraction BS/BA in Biology, Chemistry, or related scientific discipline Exp: 0-2 yrs |
The Extraction Technician will be responsible for extracting DNA from a myriad of sample types for molecular genetics testing. 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 and Southern Blot analysis to test for specific genetic diseases such as cystic fibrosis, spinal muscular atrophy and Fragile X syndrome to name just a few. | 5/6/2018 |
| 978 | Labcorp Englewood, CO Quality Analyst BS/BA in Medical Technology Exp: 1-2 yrs |
Provides leadership in the areas of quality assurance, quality control, quality related training, and standardization compliance within the laboratory. This position is also responsible for project management activities as they relate to identified areas within the laboratory requiring standardization to improve the quality and/or efficiency of operations. | 5/6/2018 |
| 979 | Labcorp Burlington, NC Lab Supervisor BS/BA Exp: 1-3 yrs |
Assigns, oversees, and reviews the work of employees. Directs all phases of work, quality, service, and costs; and performs tests or assays as required. | 5/6/2018 |
| 980 | Labcorp San Diego, CA Lab Supervisor I - Microbiology BS/BA in Microbiology or Biology Exp: 1-3 yrs |
Assigns, oversees, and reviews the work of employees during assigned work hours; Directs all phases of work, quality, service, and costs;Performs tests or assays as required. | 5/6/2018 |
| 981 | Labcorp San Diego, CA Clinical Laboratory Technician - Sequenom BS in Biology, Chemistry, or other related scientific discipline Exp: 0-2 yrs |
Under supervision of licensed personnel, the Technician will assist with routine and specialty clinical laboratory testing responsibilities and provide general support for all aspects of the operation of the clinical laboratory while following established policies and procedures. | 5/6/2018 |
| 982 | LakePharma Hayward, CA Associate Scientist, Process Development? MS in biochemistry, chemical engineering or related field Exp: 1 yr |
The candidate will provide support to the Process Development group.ﾠ | 5/6/2018 |
| 983 | LakePharma Worcester, MA Cell Culture Associate Scientist? BS Exp: 0-5 yrs |
The employee will be responsible for executing hands-on laboratory work in cell culture including planning and executing shake flask, bench scale bioreactor, bench scale purifications and large scale bioreactor experiments. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. | 5/6/2018 |
| 984 | LakePharma Hopkinton, MA Associate Scientist, Assay Services? BS in Biology or related field Exp: 1-3 yrs |
Perform Cell-based and Enzyme-based assays and related procedures using manual and automated liquid handling equipment | 5/6/2018 |
| 985 | LakePharma Worcester, MA Associate Scientist / Scientist, Molecular Biology? BS/MS in Biology or related field Exp: 0-3 yrs |
The employee will be responsible for executing projects within the laboratory, writing study/research plans, and summarizing data to clients and colleagues via technical reports. The position requires a drive to provide outstanding customer service by maintaining regular communications with clients, meeting or exceeding quality and timeline expectations. ﾠ | 5/6/2018 |
| 986 | LATITUDE San Diego, CA Research Associate BS in Chemistry, Pharmaceutical Sciences or Biochemistry Exp: 1-5 yrs |
Seekingﾠa Research Associate to carry out individual drug formulation development projects for our clients. LATITUDE utilizes its extensive experience and proprietary technologies to solve issues of insolubility, instability, poor absorption and otherﾠformulation challenges over a range of dosage forms for both external clients and internal programs. A successful candidate will possess proficiency in a variety of analytical chemistry techniques including HPLC. This is a salaried, full-time position at our San Diego location. | 5/6/2018 |
| 987 | Lampire Biological Laboratories? Coopersburg, PA Manufacturing Technician BS Exp: 1-2 yrs |
To collect, process and package various abattoir sourced animal blood and/or tissues at the Coopersburg Lab and/or off-site abattoir/vendor locations as need to support production requirements. | 5/6/2018 |
| 988 | Lampire Biological Laboratories? Coopersburg, PA Cell Culture Technician BS Exp: 0-2 yrs |
Candidate will be responsible for scheduling, preparing, and performing cell culture and cell banking activities such as Hybridoma development and growing of monoclonal cells in culture, and to document activities accurately, with the goal of providing consistent, high quality products and services to our customers with complete, accurate documentation. | 5/6/2018 |
| 989 | Lampire Biological Laboratories? Everett, PA Molecular Biologist BS/MS in Molecular Biology, Immunology, Biochemistry or related scientific field Exp: 1-3 yrs |
The successful candidate will be responsible for learning, researching and implementing recombinant DNA approaches to support research team needs, as well as designing work-flows, and assay development. | 5/6/2018 |
| 990 | Lampire Biological Laboratories? Everett, PA Small Animal Technician BS in Life Sciences or equivalent Exp: 1 yr |
The primary responsibility of this individual is to maintain the overall health and well-being of the rabbits including cage and facility maintenance. This would include the feeding and watering of rabbits, administering treatments, as well as swapping, cleaning, disinfecting, and sanitizing all animal housing units and animal facilities. | 5/6/2018 |
| 991 | Lampire Biological Laboratories? Pipersville, PA Purification Technician BS Exp: 0-2 yrs |
Purification of normal, secondary antibodies, and custom mono and polyclonal antibodies with the goal of providing consistent, high quality products and services to our customers with complete, accurate documentation. | 5/6/2018 |
| 992 | LI-COR Lincoln, NE Sr. Chemist, Clinical R&D MS in Chemistry? Exp: 1-3 yrs |
Independently develop protocols, applications, and products. Identify product opportunities consistent with corporate goals. Independently plan and execute experiments, and review results with supervisor. Write reports, technical documents, and application notes. Develop synthetic routes and analytical methods. Perform syntheses and purifications at bench scale (milligram to kilogram) of chemical products for Research and Development, clinical trials and commercial use. Analyze compounds produced and maintain documentation of experimental results. Prepare and present scientific posters at national meetings. Mentor others in the group. Keep laboratory notebooks, attend project and group meetings, and perform other job-related duties as required. | 5/6/2018 |
| 993 | LI-COR Lincoln, NE QC Specialist I BS/BA in life sciences, molecular biology, chemistry, or a related field Exp: 1 yr |
Responsible for independent implementation of protocols, test scripts, documentation, process audits and test methodologies that ensure stringent testing of assigned reagents to achieve a quality reagent product. Requires strict documentation procedures, and good laboratory skills.ﾠ Will be required to compile and legibly document results in the form of a work instruction or report.ﾠ Requires strong interpersonal and technical skills to work effectively and efficiently with other departments to resolve problems and to achieve a quality reagent product that results in customer satisfaction. The QC Specialist I position requires experience in analytical methods used to test chemical material or biologics. | 5/6/2018 |
| 994 | Lexicon Pharmaceuticals? Basking Ridge, NJ Drug Safety Specialist BA/BS Exp: 1-2.5 yrs |
The Drug Safety Specialist will be responsible for providing drug safety and pharmacovigilance support for ongoing clinical trials and marketed products across a variety of therapeutic areas and indications. This position will be responsible for the accurate and timely entry of safety data into the safety database. | 5/6/2018 |
| 995 | LifeSensors Malvern , PA Entry Level Scientist BS/MS in biological sciences or related Exp: 0-2 yrs |
We are seeking individuals who are passionate about research, bring out of the box thinking and take bold steps to develop innovative technologies with applications in the ubiquitin research field. | 5/6/2018 |
| 996 | Leidos? RESTON, VA Junior Engineer BS in an engineering Exp: 0-2 yrs |
The Junior Engineer will support ground transportation-related work for contracts with the U.S. Department of Transportation (U.S. DOT), State Departments of Transportation (DOTs), and the National Highway Traffic Safety Administration (NHTSA).ﾠ | 5/6/2018 |
| 997 | Leidos? Walkersville, MD Validation Specialist II BS in sciences or engineering Exp: 1 yr |
Responsible for supporting the Validation Engineers. | 5/6/2018 |
| 998 | Leidos? ATLANTA, VA Maintenance Technician BA Exp: 0-2 yrs |
rovide subject matter expertise in workgroups for replacement of customer systems Interface e.g. (Sensaphone, Computerized Maintenance Management System, and Ventilators) and perform as the strategic liaison with the appointed representative within Program for the development of the management tool for the accountability of Maintenance tools and systems.ﾠ Provide research and analysis with vendors, site personnel, customer IT Support, customer Quality Control Unit, customer Team Room, and customer Leadership that manages the Chemical Package program. | 5/6/2018 |
| 999 | Leidos? SPRINGFIELD, VA Process Improvement Engineer/Specialist BS Exp: 0-3 yrs |
Applies process improvement, reengineering methodologies, and best practice principles to design and implement process modernization and improvements. Assists with analysis, evaluation, and assessment leading to development of recommendations for system and process improvements, optimization, development, and/or operations sustainment efforts for IT systems, software, and processes. Coordinates and manages analysis evaluations and quality assessments for proper implementation of programs, systems specifications, and quality standards. Establishes performance measures, monitors and analyzes performance metrics to identify and implement performance based improvements. Works closely with senior engineers/specialists or task leads. | 5/6/2018 |
| 1000 | Leidos? Bethesda, MD Junior Systems Engineer (Level 0) - TS/SCI w/ Polygraph BS Exp: 0 yr |
The selectee will, under the leadership of Senior Personnel, provide technical expertise to aid the Government in the overall certification of cryptographic products for ground/airborne/satellite communications including those making up Space Systems of Systems, a collection of task-oriented or dedicated systems creating more security functionality than the individual components | 5/6/2018 |
| 1001 | Luminex Northbrook, IL MANUFACTURING ASSEMBLY ASSOCIATE II? BS Exp: 1 yr |
The Manufacturing Assembly Associate II is responsible for the building of plastic parts into a medical device cassette for use by Engineering R&D, Clinical Studies and Product Sales.ﾠTheﾠ process of building may be done manually with simple tools, fixtures and/or automated equipment.ﾠAny process control points will be processed similarly to the build process.ﾠAdditionally, this position involves the maintenance and/or calibration of equipment used for the manufacturing of product under the company quality system.ﾠ | 5/6/2018 |
| 1002 | Lygos Berkeley, CA Molecular Biology: Research Assistant I, II, III BS in molecular biology (or related field) Exp: 0-6 yrs |
The successful applicant will work as part of a collaborative team to engineer microbial strains for improved production of bio-based chemicals. The position will involve the construction of combinatorial strain libraries, measurement and analysis of strain performance, and the development and application of assays to improve enzyme properties or interrogate cellular conditions. Research objectives are milestone driven. | 5/6/2018 |
| 1003 | MannKind Danbury, CT Sr. Research Associate MS Exp: 1-3 yrs |
The responsibilities for this position will include preparing and analyzing formulations to characterize drug substances and prototype drug products. Analysis includes characterization of physical and chemical properties, including but not limited to evaluation using HPLC and aerodynamic particle size distribution. | 5/6/2018 |
| 1004 | PharmaForce COLUMBUS, OH QC Microbiologist I BS in Microbiology, Biology, or equivalent Life Science Exp: 1 yr |
This position in the Microbiology Laboratory will be primarily responsible for performing, coordinating and tracking the microbiological testing for in-process and finished products as well as monitoring of controlled manufacturing facilities and utility systems. | 5/6/2018 |
| 1005 | PharmaForce NEW ALBANY, OH R&D Formulation Chemist I BS in Pharmaceutical Science, Chemistry, Chemical Engineering or equivalent Exp: 1-2 yrs |
Responsible for formulation and process development activities associated with parenteral drug product development. Participates in scale-up of manufacturing process. | 5/6/2018 |
| 1006 | Marin Biologic Laboratories? Novato, CA Research Associate BS/MS in cell biology, molecular biology, biochemistry, immunology or a related scientific discipline Exp: 1-6 yrs |
Successful candidates will participate in and develop competencies in a wide variety of techniques in the fields of cell and molecular biology, biochemistry and immunology and will be able to develop independence to manage multiple projects. Additionally, successful candidates demonstrate collaborative and professional skills used in client services. | 5/6/2018 |
| 1007 | LSNE Contract Manufacuring Bedford, NH Specialist I - MTS BS in life sciences or related discipline Exp: 1 yr |
The Manufacturing Technical Specialist's primary responsibility is to provide technical (scientific), GMP, regulatory, and quality/compliance knowledge, as well as client support for the company's aseptic and non-aseptic manufacturing processes including pharmaceutical form/fill/finish and medical device manufacturing. The position will assist in the technical transfer of client processes, generate batch records and reports for technical studies, and provide Quality System support via the ownership of deviations, CAPAs, change controls, and excursion investigations. The position also develops, edits, and completes additional GMP documentation (e.g., SOPs, material specifications, training documentation) related to manufacturing operations and client specifications. The Manufacturing Technical Specialist actively participates and provides input and feedback for the LSNE Safety Program to meet health and safety regulations and OSHA requirements. | 5/6/2018 |
| 1008 | LSNE Contract Manufacuring Bedford, NH Scientist I - Process Development BS/MS in biology, biochemistry, chemistry, biotechnology, chemical engineering or closely related Exp: 0-3 yrs |
The Scientist I position will perform a variety of tasks in support of all Process Development activities. | 5/6/2018 |
| 1009 | LSNE Contract Manufacuring Bedford, NH QC Chemist I BS in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area Exp: 0-3 yrs |
This position will have responsibility for supporting all activities in the Quality Control Laboratory. This includes the testing of in-process samples, finished product and stability samples and raw materials. This may also include assisting in the performance of instrument validations, cleaning validations, and method qualifications as deemed appropriate by management. | 5/6/2018 |
| 1010 | LSNE Contract Manufacuring Bedford, NH QA Associate I - Document Control BS Exp: 1 yr |
Manage, coordinate, and maintain CGMP documentation, procedures, and records to ensure only controlled copies are reviewed, approved, issued, distributed, and archived. | 5/6/2018 |
| 1011 | LSNE Contract Manufacuring Bedford, NH Engineer I - MTS BS in Engineering or related discipline Exp: 1-2 yrs |
The Engineer I - MTS position will define relevant operational/technical standards and practices for LSNE sites that produce medical devices as well as the site and identify and drive implementation of improvements to maximize throughput and capacity utilization. The role will interface with other LSNE functions as well as external clients to implement new processes and technologies into LSNE GMP manufacturing. | 5/6/2018 |
| 1012 | Marker Gene Technologies Eugene, OR Laboratory Technician-Biology BS in cell biology, biochemistry, biology molecular biology or a related science field Exp: 0-3 yrs |
The successful candidate will support laboratory staff by performing routine cell culture, running cell assays, preparing media and buffers, and maintaining laboratory supplies and glassware. Additionally the successful candidate will play a role in the development and production of new products | 5/6/2018 |
| 1013 | MacroGenics? Rockville, MD Product Safety Coordinator BS in Life Sciences, Nursing, Pharmacy, or related field Exp: 0 yr |
This is an individual contributor position responsible for assisting in the management of adverse event reports. The incumbent in this role will support pharmacovigilance activities including but not limited to: adverse event data entry into the safety database; reconciliation of the safety database with clinical databases, exchanging safety information with business partners and other vendors; and providing general administrative support. | 5/6/2018 |
| 1014 | Masimo? Irvine, CA ?Algorithm Engineer (Biomedical Optics) MS in Biomedical Engineering Exp: 1-3 yrs |
Key individual contributor in the development of next generation sensors/tools and improvement in existing products/tools | |
| 1015 | Maverick Therapeutics Brisbane, CA Bioinformatics Associate (Research Associate) or???Bioinformatics Analyst (Sr. Research Associate) BS/MS in Bioinformatics, Computational Biology, or a related field Exp: 1 yr |
The successful candidate will work closely with both Discovery and Development groups and will provide support through building data visualization tools/UIs, building and maintaining databases, analyzing NGS and proteomic dataset, QCing data sources, and providing additional bioinformatics support across all company projects. | 5/6/2018 |
| 1016 | MedImmune Gaithersburg, MD R&D Associate II/ Associate Scientist I MS Exp: 1 yr |
Test API and final drug substance and drug product according to written procedures following cGMP practices | 5/6/2018 |
| 1017 | MedImmune Gaithersburg, MD R&D Associate I/II BS/MS in Biochemistry, Chemical Engineering, or related field Exp: 0 yr |
Develop and characterize downstream processes for the manufacture of biopharmaceuticals (monoclonal antibodies and other proteins) in late stage clinical development through commercial launch. | 5/6/2018 |
| 1018 | MedImmune Frederick, MD QA Specialist II - ATS BS/MS in Science/Engineering Exp: 0-4 yrs |
You will be responsible for assuring the quality of commercial and clinical products manufactured at the facility.ﾠ | 5/6/2018 |
| 1019 | MedImmune Gaithersburg, MD Research Associate II/ Associate Scientist I - Analytical MS Exp: 1 yr |
Test API and final drug substance and drug product according to written procedures following cGMP practices | 5/6/2018 |
| 1020 | MedImmune Gaithersburg, MD R&D Associate I/II - Analytical Sciences BS/MS in Chemistry, Biochemistry or related field Exp: 0-2 yrs |
The successful candidate will carry out analytical testing and method development using Electrophoresis, Chromatography, and Mass Spectrometry techniques in support of early and late stage development of biopharmaceutical products, such as humanized monoclonal antibodies, and recombinant proteins. The candidate will make detailed experimental observations, review and analyze data, interpret experimental results, and summarize data for presentations and reports. The candidate will author SOPs, protocols, reports and other relevant documentation. | 5/6/2018 |
| 1021 | Medical Diagnostic Laboratories Hamilton, NJ Research Associate BS Exp: 1-2 yrs |
ﾠThe successful applicant will become a core member of a highly interactive team of senior and junior scientists who bring with them an expertise in lipid biology, drug-discovery, pharmacology, assay development, liver lipid biology, and mouse models of liver disease. | 4/29/2018 |
| 1022 | Invivotek Hamilton, NJ Research Associate BS in Life Sciences Exp: 1-2 yrs |
Perform in vivo assays and other bioassays in mice for validation of potential drug development targets and to characterize pharmacological compounds. | 4/29/2018 |
| 1023 | Medical Diagnostic Laboratories Hamilton, NJ Histotechnician BS Exp: 0-2 yrs |
Perform histology tasks such as embedding, cutting, staining, and cover-slipping of slides for microscopic examination. | 4/29/2018 |
| 1024 | IQVIA Durham, NC Epidemiology Research Associate - RWI BS Exp: 1 yr |
As a member of the Injury Surveillance and Analytics (ISA) Team, assist in data analytics, including data management, quality, and organization as well as project management of research related to sports injuries and player health. Responsibilities include contributions to development of study questions and substantive contributions to ad-hoc and scheduled reports (analysis and writing), data collection and management, creation of datasets using complex existing data sources, and ownership of client deliverables.ﾠ | 4/29/2018 |
| 1025 | Jazz Pharmaceuticals i Palo Alto, CA Clinical Trial Coordinator BS Exp: 1 yr |
As the Clinical Trials Coordinator, you will work as an integral member of Jazz Pharmaceuticalsﾒ Clinical Operations Team, providing administrative support of our clinical trials. You will work on all phases of clinical trials that are in the JPI product development pipeline.ﾠ | 4/29/2018 |
| 1026 | Juno Therapeutics Bothell, WA QC Associate II - Microbiology? BS Exp: 1 yr |
The primary focus of the QC Associate I/II role will be to perform GMP testing and environmental monitoring to support lot release and in-process testing.ﾠ | 4/29/2018 |
| 1027 | Juno Therapeutics Bothell, WA Manufacturing Associate? BS Exp: 0-4 yrs |
The primary focus of the Manufacturing Associate role will be cellular therapeutic manufacturing at JuMP during process transfers, routine production, and technology improvements. | 4/29/2018 |
| 1028 | Juno Therapeutics Seattle, WA Research Associate/Sr. Research Associate, Analytics - Protein Sciences? BS Exp: 1-3 yrs |
The primary focus of this role will be to purify and analyze recombinant proteins. Successful candidates will demonstrate understanding of basic biochemistry principals and working knowledge of protein purification and analysis. Demonstrated ability to follow protein purification protocols and deliver reagents under specified timelines is required.ﾠ | 4/29/2018 |
| 1029 | Juno Therapeutics Seattle, WA Research Associate, Cell Sciences BS Exp: 0-3 yrs |
The candidate will be a member of the Cell Sciences team working to support Junoﾒs expression function.ﾠ The job will require the candidate to play different roles within the group, as need dictates.ﾠ The focus will be on establishing and maintaining expression cell lines, with the objective of supplying research groups with critical reagents.ﾠﾠ | 4/29/2018 |
| 1030 | Juno Therapeutics Seattle, WA Research Associate, Analytical Technologies BS Exp: 1-3 yrs |
This individual will join an innovative, interdisciplinary team focused on the advancement of current analytical methods and maintaining a state-of-the-art flow cytometry facility. This individual will also be required to support colleagues in a cross-functional environment through the performance of routine analytical testing. | 4/29/2018 |
| 1031 | Juno Therapeutics Bothell, WA Validation Associate? BS in an engineering or science discipline Exp: 0-2 yrs |
This entry-level role allows for development within Validation and the Manufacturing Sciences organization, and is initially responsible for the execution of equipment qualification (IQ/OQ/PQ, requalification) protocols and completing execution summary reports with high quality and timely output.ﾠ This role will be exposed to all facets of Validation at Juno Therapeutics and the Associateﾒs scope of responsibilities is expected to grow over time as their skills develop.ﾠ This role reports through site GMP Validation. | 4/29/2018 |
| 1032 | Jounce Therapeutics Cambridge, MA Clinical Trial Associate BS/BA Exp: 1 yr |
The successful candidate will assist with daily clinical trial execution activities and assist in the coordination of documentation associated with the conduct of investigational clinical studies in accordance with Food and Drug Administration (FDA) Regulations, Good Clinical Practice (GCP), and company standard operating policies and procedures. | 4/29/2018 |
| 1033 | KBI Biopharma? Boulder, CO Research Associate - Particle Characterization BS/BA in Chemical Engineering, Chemistry, Biochemistry or related field Exp: 0-2 yrs |
Responsible for executing laboratory preparation activities and protocol execution in Particle Characterization Core Facility laboratories. | 4/29/2018 |
| 1034 | KBI Biopharma? Durham, NC Manufacturing Associate-Upstream BS Exp: 0 yr |
Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOPﾒs and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding, harvesting, counting and freezing; product seeding; growth system maintenance; labeling, packaging and freezing of product; and culture media preparation. Follow specific techniques and operations while demonstrating an understanding of cGMPs and how they apply to specific responsibilities | 4/29/2018 |
| 1035 | KBI Biopharma? Durham, NC Manufacturing Associate I/II-Downstream BS Exp: 0 yr |
Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. | 4/29/2018 |
| 1036 | KBI Biopharma? Durham, NC Research Associate/Sr. Research Associate? MS in chemistry, biochemistry or related area Exp: 0 yr |
Responsible for executing experimental protocols and performing elementary data analysis in biopharmaceutical development laboratories. | 4/29/2018 |
| 1037 | Kashiv Pharma, LLC. Bridgewater, NJ Facilities Engineer BS/MS in Engineering Exp: 1-3 yrs |
The Facility Engineer will ensure that all safety standards are followed. Maintenance and inspections will be done to guarantee that cGMP standard are being followed. Performs routine inspections of the equipment and . Monitoring of the BMS system and coordinating the PM schedule and maintenanceﾠactivity. | 4/29/2018 |
| 1038 | NemaMetrix Eugene, OR Zebrafish Technician BS/MS in biology or a related field Exp: 1 yr |
Perform molecular biology assays such as PCR, HRMA, Restriction Enzyme digestion, and gel electrophoresis. | 4/29/2018 |
| 1039 | NemaMetrix Murray, UT C. elegans Laboratory Technician II BS in Biology or related field Exp: 1 yr |
You will be reporting to the Transgenics Supervisor working among a team,ﾠto deliver custom transgenics to our clients, in a timely manner, using established procedures. ﾠThe sophisticated nature of the work requires attention to detail and high-functioning knowledge of current genetic techniques. The ability to work independently according to schedule is balanced with the need to collaborate extensively with colleagues to ensure that we consistently meet or exceed our clientsﾒ expectations. | 4/29/2018 |
| 1040 | NemaMetrix Murray, UT Molecular Biologist Laboratory Technician II BS in Biology or related field Exp: 1 yr |
You will be reporting to the Molecular Biology Supervisor working among a team, to deliver custom transgenics to our clients, in a timely manner, using established procedures.ﾠ The sophisticated nature of the work requires attention to detail and high-functioning knowledge of current molecular biology techniques.ﾠ The ability to work independently according to schedule is balanced with the need to collaborate extensively with colleagues to ensure that we consistently meet or exceed our clientsﾒ expectations. | 4/29/2018 |
| 1041 | KSQ Therapeutics Cambridge, MA Associate Scientist/ Scientist, Oncology Discovery BS Exp: 0-3 yrs |
This person will contribute to cell biology and translational efforts for our discovery pipeline. This skilled scientist will characterize novel cancer pathways and develop assays for drug targets. She/he must be driven and flexible with the broad number of in vitro, in vivo, and biomarker activities associated with cancer discovery.ﾠ | 4/29/2018 |
| 1042 | KVK Tech Newtown, PA Topical Formulation Associate MS in Chemistry, Biochemistry or Pharmaceutical Sciences Exp: 1-3 yrs |
Person exhibits aptitude in assisting in the development of topical product pharmaceutical formulations, as well as meeting timelines for the department. | 4/29/2018 |
| 1043 | KVK Tech Newtown, PA Analytical Chemist BS/MS Exp: 1-4 yrs |
Perform analytical testing of raw materials, in-process materials, stability samples, finished products and product development products using different analytical techniques. | 4/29/2018 |
| 1044 | KVK Tech Newtown, PA QC Document Reviewer BS in Chemistry or a related field Exp: 1 yr |
The QC Data Review Specialist will be responsible for GMP review and comment on laboratory raw data, procedures and reports to ensure methods, protocols and other procedures were properly followed, results are analytically accurate and correct, and that all documentation meets GMP standards. | 4/29/2018 |
| 1045 | KVK Tech Newtown, PA Quality Control Microbiologist BS in Microbiology or related disciplines Exp: 1 yr |
Executes the activities of QC Microbiology Laboratory by following approved microbiological and chemical test procedures and ensure their delivery in an accurate and timely manner following proper safety precautions. Also provide QC microbiology support to the Aseptic Manufacturing and validation process. | 4/29/2018 |
| 1046 | KVK Tech Newtown, PA Sample Management Associate BS/BA Exp: 0 yr |
Sample Management Associate provides support to Sample Coordinator and performs administrative tasks in the Sample Management Department. Follows SOPs, and fulfills laboratory requests with minimum direct supervision. | 4/29/2018 |
| 1047 | LabCorp Burlington, NC Technologist Trainee ?BA/BS degree in Biology, Chemistry, Medical Technology, or other related science Exp: 1-3 yrs |
We are is seeking an enter level Technologist to join our Mass Spectrometry team in Burlington, NC! Assays performed in our department utilize a variety of scientific techniques, including Performs tests and analyses according to established procedures in designated technical department. Position may perform various techniques including EIA, IFA, and other non-automated and automated procedures. | 4/29/2018 |
| 1048 | LabCorp Burlington, NC Cytogenetics Technologist / Technologist Trainee BS/BA in Biology or relatable life science Exp: 1 yr |
The Integrated Genetics Division is seeking a Cytogenetics Technologist or Technologist Trainee to join their Cytogenetics team in the Microarray Group! Assays performed in the Cytogenetics Department utilize a variety of scientific techniques, including specimen culturing, PCR, fragment analysis, and gel electrophoresis. | 4/29/2018 |
| 1049 | LabCorp Burlington, NC Technologist BA/BS degree in Biology, Chemistry, Medical Technology, or other related science Exp: 1-3 yrs |
Receive specimens for testing | 4/29/2018 |
| 1050 | LabCorp San Antonio, TX QA Analyst BS/BA in Medical Technology Exp: 1-2 yrs |
Provides leadership in the areas of quality assurance, quality control, quality related training, and standardization compliance within the laboratory. This position is also responsible for project management activities as they relate to identified areas within the laboratory requiring standardization to improve the quality and/or efficiency of operations. | 4/29/2018 |
| 1051 | Grifols? RTP, NC INTERN-Clinical Development BS in Life Sciences or Biomedical Sciences Exp: NA |
This summer internship will provide a student the opportunity to support the Clinical Development Department and provide input into monitoring and management of clinical studies. | 4/29/2018 |
| 1052 | Grifols? Clayton, NC INTERN - Purification - Manufacturing BS in Chemical Engineering or Industrial Engineering Exp: NA |
The Purification Manufacturing intern will work to improve annual production capacity for Thrombate and HyperImmune products, which compete for same resources (equipment, space, FTEs), ﾠby identification of most efficient campaigning and scheduling schemes and through the identification of process solutions to overcome bottlenecks. | 4/29/2018 |
| 1053 | Ginkgo BOSTON, MA Test Team Padawan ? High-Throughput Screening (1 year paid internship) BS/MS in chemistry, bioengineering, chemical engineering or related fields Exp: NA |
Run and QC HTS operations including: transformation, cultivation, sample extraction, high-throughput assays and analytics. | 4/29/2018 |
| 1054 | Ginkgo BOSTON, MA Test Team Padawan (1 year paid internship) BS/MS in chemistry, bioengineering, chemical engineering or related fields Exp: NA |
Run and QC unit operations associated with strain testing including: cultivation, sample extraction, assays and analytics. | 4/29/2018 |
| 1055 | Ginkgo BOSTON, MA Process Engineering Padawan (1 year internship) BS in chemical engineering or biotechnology Exp: NA |
Assist with design and execution of laboratory and pilot scale experiments leading to definition of commercially viable processes that leverage Ginkgo's engineeredﾠorganisms. | 4/29/2018 |
| 1056 | Insmed Bridgewater, NJ Summer Intern - Pharmacovigilance BS/MS Exp: NA |
The intern will be assigned goals and objectives that will support the strategic business plan of the team.ﾠIntern will have responsibility to support PV scientific and operational topics for new and existing Insmed pharmaceutical products. | 4/29/2018 |
| 1057 | Insmed Bridgewater, NJ Summer Intern - Manufacturing BS/MS Exp: NA |
The Process Development Intern will have responsibility to support process development, process characterization, scale-up, technology transfer activities, and new and existing pharmaceutical products. | 4/29/2018 |
| 1058 | GE Erie, PA GE Transportation Engineering Intern BS/MS Exp: NA |
The GE Transportation Summer 2018 Internship Program encourages college students to explore their professional interests. Engineering students can experience rotations in design, software development, product testing or commercial operations to attain professional experience in the engineering field as a pipeline for our Edison Engineering Development Program (EEDP). | 4/29/2018 |
| 1059 | GE NA, AN Environmental, Health, & Safety Intern - GE Aviation - Fall BS/MS Exp: NA |
The Environmental Health and Safety department fosters and EHS culture that promotes the safety and wellness of our employees; protects the environment; ensures compliance; delivers value to our business, customers and communities; enhances GEﾒs reputation and distinguishes us as a socially responsible company. | 4/29/2018 |
| 1060 | GE NA, AN Summer 2018 Engineering Intern BS/MS Exp: NA |
Perform design and analysis of offshore drilling equipment, pressure relief valves, Hydril and Vetco diverters, gas handlers, handling tools for oil & gas, power-gen and industrial process industries | 4/29/2018 |
| 1061 | GenScript Piscataway, NJ Analytical Biochemist MS in Molecular Biology, Biochemistry or Chemistry Exp: 6 months |
To independently perform essential biochemical screening and analytical experiments, and interpret analytical data in accordance with the relevant SOPs. | 4/20/2018 |
| 1062 | GigaGen South San Francisco, CA Research Assistant BS Exp: 1-3 yrs |
GigaGen seeks a talented, highly motivated Research Assistant to work alongside PhD-level scientists on research funded by a $50 million co-development deal with Grifols, plus Phase II SBIR grants from the NCI and NIAID. This project involves high-throughput discovery and development of therapeutic antibody drug candidates from human and mouse immune repertoires. The work involves significant cell culture work, including a bioreactor and flow cytometry. | 4/20/2018 |
| 1063 | Gore Flagstaff, AZ Medical Device Reliability Engineer BS in engineering Exp: 1 yr |
The job will require establishing product reliability tests, performing appropriate analyses and tasks to ensure the product will reliably meet its requirements.ﾠ The qualified candidate will be expected to provide leadership and guidance to other engineers to establish a reliability competence that will meet the needs for development, manufacturing, and field performance of devices.ﾠ This engineering position will support new product development of products in structural heart applications. | 4/20/2018 |
| 1064 | Graybug Vision Baltimore, MD Research Associate BS/MS in chemical engineering, biomedical engineering, pharmacology and pharmaceutical sciences, chemistry, materials science, or other related fields Exp: 0-3 yrs |
The Research Associate will be an integral part of the Research Department. The successful candidate will be expected to perform research studies and prepare scientific reports to support pre-IND and IND activities. | 4/20/2018 |
| 1065 | Grifols Clayton, NC Aseptic Filling Technician I/II BS in Biology, Chemistry, Biochemistry, Engineering, Pharmaceutical Technology, Business, Teaching or a related Exp: 1 yr |
Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals | 4/20/2018 |
| 1066 | Grifols San Diego, CA Quality Specialist 1 BS Exp: 0-2 yrs |
Responsible for ensuring compliance with applicable domestic and international standards and regulations through audits and systematic maintenance of effective quality systems. ﾠEnsures that deadlines are met on time and within budget. ﾠLimited interface with other departments and business or marketing partners. Work independently with supervision and exercise judgment within the defined procedures and practices to determine appropriate actions. ﾠ | 4/20/2018 |
| 1067 | Grifols Clayton, NC Assistant / Associate Biologist BS in biology, chemistry or related field Exp: 6-12 months |
The incumbent is responsible for performing complex laboratory analysis of plasma and plasma products in a GMP laboratory. Responsibilities include sample accessioning, sample preparation, reagent preparation, testing, result calculation, as well as quality control of assays and equipment.ﾠ | 4/20/2018 |
| 1068 | Grifols Clayton, NC Label Verification Technician? BS in Biology, Chemistry, Biochemistry, Engineering, Pharmaceutical Technology, Business, Teaching or a related Exp: 1 yr |
The Label Verification Technician's primary responsibility is to perform a variety of tasks (i.e. operate labeler machine, inspect labels for accuracy, etc.) related to the labeling of packaged biological products. | 4/20/2018 |
| 1069 | Grifols Clayton, NC Assistant / Associate Chemist? BS/BA in chemistry or related? Exp: 6 months |
Performs chemical testing of moderate to advanced complexity within a Quality Operations Laboratory in a safe, accurate, and efficient manner following established written procedures while maintaining complete and accurate records of the work and results. This testing is required for the release of raw materials, in-process materials, and final containers.ﾠ | 4/20/2018 |
| 1070 | Guardant Health Redwood City, CA Research Associate, Technology Development BS/MS in Molecular Biology, Genetics, Biochemistry, Bio-engineering?or related field Exp: 0-5 yrs |
As a Research Associate supporting product and technology development, you will work with members within the team and interface with multiple teams including process engineering, clinical operations, research operations, IVD team members, and bioinformatics. You will be hands on in the lab and be required to design, implement, and validate new technologies related to liquid biopsy sequencing assays for the early detection, treatment, and monitoring of all cancer types.ﾠ | 4/20/2018 |
| 1071 | Guardant Health Redwood City, CA Clinical Trial Assistant BS in biology-related field or equivalent Exp: 1 yr |
TheﾠClinical Trial Assistant (CTA)ﾠis primarily responsible for the coordination of activities associated with the setup and management of clinical studies under the direction of, or as delegated by a member of the Clinical Trial team. Responsibilities will range from clinical study coordination to data entry projects and general office work. | 4/20/2018 |
| 1072 | Health Decisions Inc. Durham, NC In-House Clinical Research Associate BA/BS Exp: 1-2 yrs |
We are seeking anﾠIn-House Clinical Research Associateﾠ(IHCRA) in our Durham Headquarters to remotely manage and support site activities for the delivery of clinical studies in accordance with the Task Order, protocol, standard operating procedures, ICH guidelines and all applicable regulatory requirements.ﾠ | 4/20/2018 |
| 1073 | High Point Clinical Trials Center? High Point, NC CLINICAL RESEARCH COORDINATOR BS Exp: 1 yr |
Supports the conduct of research studies at the clinical research center The Clinical Research Coordinator (CRC)ﾒs primary responsibility is the protection of subject safety. The CRC is the client liaison to the internal and external operational teams ensuring that studies are conducted in compliance the protocol, ICH and GxP. | 4/20/2018 |
| 1074 | Hovione NA, NJ Quality Control Peer Reviewer BS in Chemistry or related field Exp: 1-2 yrs |
The Quality Control Peer Reviewer performs all activities within Quality Control in compliance with Corporate Operating Procedures (COP), Standard Operating Procedures (SOP), Internal Operating Procedures (IOP), and Federal Food and Drug Administration (FDA), International Conference on Harmonization (ICH), Occupational Safety and Health Administration (OSHA), and Environmental Protection Agency (EPA) requirements. They will also perform QC peer reviewing on all relevant records and analytical data in accordance with Operating Procedures (COP), Standard Operating Procedures (SOP), and Internal Operating Procedures (IOP). They will carry out the analytical review of QC analyses, LIMS authorization of analytical tests and QC release of raw materials, in-process controls, packaging materials, intermediates, and environmental tests. | 4/20/2018 |
| 1075 | ICON? North Wales, PA CRA I (Clinical Research Associate) BS Exp: 10-12 months |
Weﾠsupportﾠour CRAsﾠwith manageable sites & protocols, a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and eligible for the annual performance bonus. Additionally, we have cutting edge technology to ensure better outcomes. | 4/20/2018 |
| 1076 | ICON? Home Based, Ho Clinical Research Associate - Any Therapeutic Area - Remote, US BA/BS Exp: 1 yr |
Weﾠsupportﾠour CRAsﾠwith manageable sites & protocols, a strong benefits package that includes a comprehensive health plan, retirement plans, competitive pay, vacation, and eligible for the annual performance bonus. Additionally, we have cutting edge technology to ensure better outcomes. | 4/20/2018 |
| 1077 | ICON? Houston, TX Validation Specialist II BS Exp: 1 yr |
This person will be providing testing support specializing in test script writing, execution, and documentation.ﾠ | 4/20/2018 |
| 1078 | IDEAYA Biosciences South San Francisco, CA Senior Research Associate/Research Scientist, Molecular and Cell Biology MS/MA Exp: 1-3 yrs |
This individual will play a key role in validating drug targets and running cellular assays using siRNA and small-molecule drug candidates. | 4/20/2018 |
| 1079 | IDEXX Westbrook, ME Biostatistician MS in Biostatistics, Statistics, Epidemiology, Engineering Exp: 1-4 yrs |
As aﾠBiostatisticianﾠat IDEXX, you will be contributing to sound experimental structures, statistical analysis plans, and statistical analyses for prospective, retrospective, and observational studies for clinical trials and studies utilizing our patient health data. | 4/20/2018 |
| 1080 | IDEXX Westbrook, ME Associate Scientist ? Cell Culture MS in Biology, Biology or Life Sciences? Exp: 1 yr |
Perform the functions and related tasks of antigen (native and recombinant) and monoclonal antibody production and other cell culture activities. | 4/20/2018 |
| 1081 | Immucor Grand Rapids, MI Medical Technologist I , CLIA Lab BS in Medical Technology or Molecular Biology Exp: 1-3 yrs |
As a CLIA Laboratory Technician, you will ensure that complex diagnostic assays are performed under appropriate regulatory requirements and are CLIA and CAP compliant. In addition, you will facilitate test sample intake, reconcile shipping records, determine sample acceptability, reconcile problem samples, contact provider to resolve issues, and document contact and resolution. | 4/20/2018 |
| 1082 | ImmunoGen? Waltham, MA ENGINEER II? MS in Chemistry, Chemical Engineering, Biochemistry, Pharmaceutical Sciences, or a related field Exp: 0-2 yrs |
ImmunoGen is seeking an experienced and talented professional to join the department of Analytical & Pharmaceutical Sciences (APS) and play an important role in advancing ImmunoGenﾒs key development programs through both early and late-stage development with commercialization of our Antibody Drug Conjugates (ADCs). The Development Associate II will work with other internal developmental functionalities (e.g., Cell Line and Upstream Engineering, Process Science and Engineering, etc.) to perform high throughput purification and related analytical testings of development samples of therapeutical antibodies to advance various key developmental projects. | 4/20/2018 |
| 1083 | Immunomedics Morris Plains, NJ Pharmaceutical Manufacturing Technologist BS in biology, chemistry, or related discipline Exp: entry levelﾠ |
We areﾠseeking a Pharmaceutical Manufacturing Technologist to be responsible for the manufacturing of clinical products in compliance with current Good Manufacturing Practice (cGMP) and Standard Operating Procedures (SOPs). | 4/20/2018 |
| 1084 | Immunomedics Morris Plains, NJ Quality Control Microbiology Technician BS in microbiology, biology, or other relevant scientific discipline Exp: 0-3 yrs |
Responsible for performing microbiological testing of cGMP controlled areas, pharmaceutical grade water, and in-process materials in compliance with cGMP guidelines and SOPs | 4/20/2018 |
| 1085 | InBios International? Seattle, WA research associate I? BS in a biological science Exp: 1 yr |
The research associate will work alongside a team to provide for daily R&D needs while also qualifying reagents under development.ﾠ A successful candidate will enjoy working in a fast-paced environment and exhibit excellent interpersonal skills, the flexibility to adapt to changing priorities, and a firm scientific foundation to understand ongoing diagnostic R&D and associated studies. | 4/20/2018 |
| 1086 | InBios International? Seattle, WA research associate-ELISA BS in a biological science Exp: 1 yr |
The research associate will work alongside a team to provide for daily R&D needs while also qualifying reagents under development.ﾠ A successful candidate will enjoy working in a fast-paced environment and exhibit excellent interpersonal skills, the flexibility to adapt to changing priorities, and a firm scientific foundation to understand ongoing diagnostic R&D and associated studies. | 4/20/2018 |
| 1087 | Indivio Richmond, VA NA Regulatory Operation Associate BS Exp: 1-3 yrs |
The Associate will support projects assigned to GRO submission staff across functional departments based on business needs across NA. The primary focus of this position will be to support North American and specific regions in the Australasia markets.ﾠ | 4/20/2018 |
| 1088 | ?InGeneron Houston, TX Life Sciences Research Associate MS Exp: 1 yr |
Under the direction of the Chief Scientific Officer, you will assist in the conduct of research and preclinical studies involving adult human stem cells. This includes planning, conducting and directing a variety of experiments and assisting in daily activities for research projects.ﾠ | 4/20/2018 |
| 1089 | OmniPod Insulin? Billerica, MA Associate Systems Engineer, Design Verification BS in Engineering Exp: 1-5 yrs |
The Associate Systems Engineer, Systems Design Verification, will be integral in the technical design and development of Insuletﾒs products by supporting all phases of the Design Verification Process.ﾠ The person in this position will be required to design, execute and report on engineering tests, for characterization and Design Verification, as well as participate in the documentation and resolution of product development issues.ﾠ This role requires a strong engineering background with the ability to fully understand Design Verification principles. | 4/20/2018 |
| 1090 | IntegenX Pleasanton, CA Research Associate BS in Molecular Biology, chemistry or equivalent disciplines Exp: 1-5 yrs |
Contributes to Assay Development including assay optimization and methods development to achieve robust genomic test performance on challenging clinical samples. | 4/20/2018 |
| 1091 | Integra LifeSciences Cordova, TN Quality Assurance Specialist BS/BA/MSin math, science, engineering or related technical field Exp: 1 yr |
Conduct release and closure reviews of product history records for accuracy and completeness to ensure adherence to Integra Life Sciences policies and procedures, both at site and global levels, cGTP and FDA regulations, andAATB Standards. | 4/20/2018 |
| 1092 | Intrexon South San Francisco, CA Research Associate I or II, Fine Chemicals BS in molecular biology, biochemistry, or related field Exp: 1 yr |
Yeast transformations;Molecular biology;Work in partnership with team members to support their needs;Develop and improve workflows, including developing and implementing automation where appropriate. Operate with a sense of urgency. | 4/20/2018 |
| 1093 | Integer Holdings Corporation Chaska, MN QUALITY ENGINEER? BS in Engineering Exp: 0-2 yrs |
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. | 4/20/2018 |
| 1094 | ?Integrity Bio Newbury Park, CA Quality Assurance Associate I BS Exp: 1 yr |
Formatting of documents, publishing, completing change control process;Document upload into training system and course creation;Annual document review including generation of list of documents due, issuing and tracking completion, document revision. | 4/20/2018 |
| 1095 | Intrexon South San Francisco, CA Research Associate, Screening Operations BS in biochemistry, chemical or biological engineering, genetics, molecular biology, microbiology, or a related field Exp: 1 yr |
The Research Associate, Screening Operations will be responsible for the execution of high throughput screens for microbial strain development. The candidate will have strong molecular/microbiology biology skills and familiarity with micro-cultivation of microorganisms. Practical experience using liquid handling robots and knowledge of biostatistics is preferred. | 4/20/2018 |
| 1096 | GE NA, NA Fall 2018 Engineering Co-op/Intern BS/MS Exp: NA |
GE Oil & Gas Early Identification (EID) assignments provide students with opportunities to work with experienced leaders in the following areas: Subsea Systems, Drilling & Surface, Turbomachinery, Downstream & Unconventionals, Measurement & Control, and Pipeline Solutions. In addition to challenging projects, these assignments provide interns & co-ops the opportunity to build leadership and functional skills through workshops, training, and networking activities. | 4/20/2018 |
| 1097 | Genentech Vacaville, CA INTERN - PHARMA TECHNICAL OPERATIONS - MANUFACTURING SCIENCES BS/MS in Biological Sciences (eg. biochemistry, genetics, bioinformatics) and Engineering Exp: NA |
Working with engineers and specialists to learn the science behind the purification unit operations of the manufacturing process and to support technology transfer | 4/20/2018 |
| 1098 | Genentech South San Francisco, CA INTERN - PHARMA TECHNICAL OPERATIONS - FACILITIES AND ENGINEERING BS/MS in Engineering Exp: NA |
Dynamic environment providing service support of instruments in the Drug Substance manufacturing areas.ﾠﾠ | 4/20/2018 |
| 1099 | GENEWIZ South Plainfield, NJ Intern, Next Generation Sequencing? BS Exp: NA |
Assist with Next Generation Sequencing lab and office work as directed | Receive and l |
| 1100 | GENEWIZ South Plainfield, NJ Bioinformatics Intern BS/MS in Life Sciences, Bioinformatics or Engineering Exp: NA |
Process raw NGS data including but not limited to de-multiplexing FASTQ generation, adaptor trimming, and data QC | 4/20/2018 |
| 1101 | Genomic Health Redwood City, CA Clinical Operations Intern BS in health care, genomics, clinical trial management and/or diagnostics. Exp: NA |
The Clinical Operations intern will work closely with Clinical Operations staff to support the management of clinical studies for the development and commercialization of novel assays which lead to improved treatment decisions for oncology patients. This position will also support department projects and initiatives, as assigned.ﾠ | 4/20/2018 |
| 1102 | Ginkgo Bioworks? BOSTON, MA Automation Padawan BS/MS Exp: NA |
Developing automated experimental workflows for genetic engineering processes, strain cultivation, sample preparation, and multi-omics analysis | 4/20/2018 |
| 1103 | Ginkgo Bioworks? BOSTON, MA Fermentation Padawan BS/MS in chemical engineering, microbiology, or related field Exp: NA |
We are looking for highly talented and motivated students, excited to tackle the ambitious challenge of transitioning multiple organisms from microtiter plates to bench-scale fermentation, and up through scale-up to commercial manufacturing. | 4/20/2018 |
| 1104 | Ginkgo Bioworks? BOSTON, MA Summer Internship BS in bioengineering, microbiology, plant science, or related fields Exp: NA |
We are looking for highly talented and motivated students to join us. Key areas of expertise include enzymatic pathway discovery and engineering, biochemical assay development, host strain engineering, bioinformatics, and microbial plant colonization. | 4/20/2018 |
| 1105 | GNS Healthcare? Cambridge, MA Intern, Health Economics and Outcomes Research MS in epidemiology, health economics, public health, statistics, or related area Exp: NA |
GNS Healthcare is seeking a talented and highly motivated intern to support the Health Economics and Outcomes Research team. The role will be responsible for projects related to HEOR work. | 4/20/2018 |
| 1106 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Rensselaer, NY 3rd shift Quality Control Chemistry Analyst BS in biology, chemistry, or other related degree Exp: 0-10 yrs |
Routine testing to support analytical laboratory;Using multiple analytical methods including HPLC, Spectrophotometer, analytics, pH, raw materials. | 4/13/2018 |
| 1107 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC West Point, PA High Throughput Process Development Scientist BS in Biology, Cell Biology, Bio/chemical Engineering, or related science Exp: 1 yr |
Execute high throughput process development (HTPD) experiments with BSL-1 and BSL-2 biological agents and viruses.ﾠ These experiments may include the screening of conditions for one or more of the following: cell culture, bioreactor, chromatography, precipitation, and conjugation/cross-linking chemistry. | 4/13/2018 |
| 1108 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC West Point, PA GC Scientist with Empower E BS in biochemistry, chemistry, or other related degree Exp: 1 yr |
Support the analytical testing for development of biologics;Chemical labeling of biological samples, GC, and data analysis.Accurately perform existing analytical procedures, ensure analytical results are of high quality, and ensure all work is documented in a clear, concise and timely manner. | 4/13/2018 |
| 1109 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC West Point, PA ELISA Scientist BS in biology, chemistry, or other related degree Exp: 6 months |
Performing Second Scientist Review of notebooks | Keeping inven |
| 1110 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC West Point, PA Downstream Process Development BS in Chemistry, Biochemistry, Bio/chemical Engineering, or related science Exp: 0-2 yrs |
Perform lab-scale downstream processing of vaccine products and process intermediates;Perform assays on vaccine products, process intermediates, and related experimental samples using biochemical/analytical tests. | 4/13/2018 |
| 1111 | Fresenius Kabi Warrendale, PA MANUFACTURING ENGINEER BS in engineering or related discipline Exp: 1-3 yrs |
We currently have an opportunity for aﾠManufacturing Engineer in our Warrendale, PAﾠmanufacturing facilityﾠto provide manufacturing process development support for hardware manufacturing systems. | 4/13/2018 |
| 1112 | Fresenius Kabi Boston, MA ASSOCIATE SCIENTIST BS in biological sciences Exp: 1-2 yrs |
Perform routine testing of in-process and finished product samples. Monitor environmental conditions in the production and lab areas. Summarize environmental monitoring and product test results. Provide project support to Scientist and Lead Scientist. Prepare media and reagents and equipment. | 4/13/2018 |
| 1113 | GE Fayetteville, NC Biomedical Technician I BS in Electrical Engineering, Biomedical Engineering, Mechanical Engineering, or related field Exp: 1 yr |
Responds to service calls to evaluate, diagnose, and perform repair and planned maintenance (PM) on customersﾒ basic biomedical equipment. Drives customer satisfaction through service excellence. | 4/13/2018 |
| 1114 | GE Norwich, NY Project Engineer BS in Mechanical, Electrical, Aeronautical or other Engineering field Exp: 1 yr |
As a Project Engineer, you will work closely with Senior Engineers and lead New Product Development (NPD) of engineering projects for the Power Generation and Sensor team on projects involving high speed permanent magnet alternators and other similar machines, power electronics and regulators, temperature sensors, and probes. | 4/13/2018 |
| 1115 | GE HOUSTON, TX Quality Engineer (Completions & Wellbore Intervention)? BS in Engineering or Applied Science Exp: 1-3 yrs |
This position is responsible for evaluating the manufacturing processes to determine root cause and effect of product non-conformities, improve processes to ensure quality, products and services to adherence of quality standards. | 4/13/2018 |
| 1116 | GE West Melbourne, FL Integration Engineer BS/MS in Engineering field Exp: 1-5 yrs |
The integration engineer performs integration design for solution deployment on a given customer. | 4/13/2018 |
| 1117 | GE BARNSDALL, OK Quality Control Laboratory Technician (Chemicals) BS in Chemistry Exp: 1 yr |
ﾠThe Quality Control Laboratory Technician role is responsible for sample management, quality inspection and manufacturing support. | 4/13/2018 |
| 1118 | GE MINOT, ND HSE Specialist BS Exp: 0-3 yrs |
Perform all functions of the job with the highest level of compliance and integrity.Integrate the BHGE Safety Culture of HSE ownership throughout all areas of the facility. | 4/13/2018 |
| 1119 | GeneDx ELMWOOD PARK, NJ QC Coordinator, Microbiology BS in medical technology, Microbiology, chemistry, biology, or related life science Exp: 1-3 yrs |
Under the general supervision of the Microbiology Director, this management position requires the MT to write clearly, have a sense of urgency and strong organizational skills, pay attention to details, strictly adhere to protocols, maintain extensive and accurate documentation, and be able to think creatively to solve problems. The Microbiology Coordinator is expected to remain current with State, OSHA, CLIA, COLA, and CAP best practices. This position will also serve to cover the laboratory supervision in the absence of the Director or Supervisor. | 4/13/2018 |
| 1120 | GeneDx GAITHERSBURG, MD DNA Sequencing Technician BS in Biology, Biochemistry, or related-field Exp: 1-3 yrs |
A GeneDx DNA Sequencing Lab Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 4/13/2018 |
| 1121 | GeneDx GAITHERSBURG, MD DNA Extraction Lab Technician BS in Biology, Biochemistry, or related-field Exp: 0-1 yr |
ﾠA GeneDx DNA Extraction/CAND Lab Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner.ﾠ | 4/13/2018 |
| 1122 | GeneDx GAITHERSBURG, MD MicroArray Lab Technician? BS in Biology, Biochemistry, or related-field Exp: 0-1 yr |
A GeneDx MicroArray Lab Technician performs an entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 4/13/2018 |
| 1123 | GeneDx GAITHERSBURG, MD NextGen Lab Sequencing Technician BS in Biology, Biochemistry, or related-field Exp: 0-3 yrs |
A GeneDx NextGen Lab Sequencing Technician performs a higher than entry level role in the testing of clinical DNA specimens for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 4/13/2018 |
| 1124 | GeneDx GAITHERSBURG, MD Cytogenetics Lab Technician BS in Biology, Biochemistry, or related-field Exp: 0-2 yrs |
A GeneDx Cytogenetics Lab Technician performs a higher than entry level role in clinical cytogenetic analysis for the purpose of diagnosing genetic disease using manual and automated methods in a team environment, and following established policies and procedures in a professional manner. | 4/13/2018 |
| 1125 | Genentech South San Francisco, CA TECHNICAL DEVELOPMENT RESEARCH ASSISTANT, EARLY STAGE PHARM DEV BS/MS in Bio or Chemical engineering, analytical chemistry or closelyrelated scientific field Exp: 0-3 yrs |
The technical development research assistant will maintain and improve existing analyticalinstruments and explore opportunities to improve productivity and efficiency inthe Pharmaceutical Development function. In addition, s/he will interact withcore customers and serve as a single point of contact for liquidchromatographic instrumentation and methods supported by the core. | 4/13/2018 |
| 1126 | Generation Bio Cambridge, MA Research Associate/Sr Research Associate, Analytical Development MS in Analytical Chemistry, Biochemistry, or equivalent Exp: 1 yr |
The successful candidate will be part of the team designing and implementing bioanalytical and biophysical assays to characterize Generation Bioﾒs close-ended DNA genetic medicine products. This role will be reporting to the group leader for bioanalytical/biophysical assays and will further our understanding of this novel scientific modality.ﾠ | 4/13/2018 |
| 1127 | GENEWIZ South Plainfield, NJ Associate Scientist I, NGS BS in Biological Sciences Exp: 1 yr |
Prepare amplified template libraries for high-throughput sequencing | Carry out DNA |
| 1128 | GigaGen South San Francisco, CA Research Assistant BS Exp: 1-3 yrs |
This project involves high-throughput discovery and development of therapeutic antibody drug candidates from human and mouse immune repertoires. The work involves significant cell culture work, including a bioreactor and flow cytometry.ﾠ | 4/13/2018 |
| 1129 | Gilead Sciences Foster City, CA Packaging Engineer II MS in an engineering field Exp: 0 yr |
Works with staff from other functional areas to meet complex project deliverables such as new product launches or start-up of new manufacturing/packaging sites. | 4/13/2018 |
| 1130 | Gilead Sciences Foster City, CA Research Associate, Medicinal Chemistry BS/MS in Organic/Medicinal Chemistry Exp: 0 yr |
Under general supervision, performs experiments that support research activities in the Medicinal Chemistry job family. | 4/13/2018 |
| 1131 | Ginkgo Bioworks Boston, MA Media Prep Assistant BS in Biology or related Exp: 1 yr |
Glassware washing, storing, and ordering.Autoclaving glassware and prepping for sterile use.Autoclave validation testing. | 4/13/2018 |
| 1132 | Ginkgo Bioworks Boston, MA Research Associate, NGS BS/MS ?in biology, biochemistry, bioengineering, molecular biology, or related fields Exp: 1 yr |
You are more interested in operating the state of the art laboratory automation instruments to validate genetic modifications in many organisms than pipetting at the bench. You are also into tracking processes carefully and easily with custom software tools and recognize the importance of quality control and assurance. And you know that sometimes you just have to do things the "old-fashioned way" to make sure everything is working right. | 4/13/2018 |
| 1133 | GSK Upper Merion, PA Automation Specialist BS/MS in chemistry /engineering/biology or related scientific field Exp: 1 yr |
An exciting new opportunity exists to work in the US Product Design & Developability (PDD) Department within GSK R&D. As a member of PDD, the successful candidate will support the use of automation processes for evaluation of developmental candidates within Product Development. | 4/13/2018 |
| 1134 | GSK Upper Merion, PA Associate Scientist, Upstream Process Development BS/MS in Bioprocess/Biochemical/Chemical Engineering or related Biological Science Exp: 1 yr |
The candidate will be part of the Microbial and Cell Culture Department responsible for the upstream development of early and late phase processes for the production of therapeutic proteins. Work packages may include execution of small scale bioreactor studies for evaluation and/or optimization of processes for improved facility fit, small scale model qualification, evaluation and/or optimization of chemically defined media/feed platforms, and ATF/perfusion implementation. | 4/13/2018 |
| 1135 | GSK King of Prussia, PA Associate Scientist - Biopharma BS /MS degree in Pharmaceutics, Biology, Biochemistry, Chemistry, Chemical Engineering, or related scientific discipline? Exp: 0-5 yrs |
The successful candidate will join a Product Development Team within the Biopharmaceutical Product Sciences (BPS) department of the Biopharm Product Development & Supply (BPD&S) organization within GSK R&D and will work on developing drug product and delivery systems for protein & peptide-based therapeutics. Specific responsibilities will be focused around laboratory experimentation, analytical testing, and secondary manufacturing of putative formulations & drug delivery approaches for select protein therapeutics.ﾠ | 4/13/2018 |
| 1136 | GSK Upper Providence, PA Degradation Chemist MS in Organic or Analytical Chemistry Exp: 1 yr |
Design and execute full force degradation packages in support of method validation and regulatory submissions;Plan, design and execute work/experimental programmes to further the course of Discovery and Development Projects / programmes and enable key decisions, in the area of degradation chemistry. | 4/13/2018 |
| 1137 | GSK Hamilton, MT Validation Engineer BS Exp: 1 yr |
Validation Engineers directly implement, execute and support the validation strategy at use at the GSK Hamilton Site ensuring it is harmonized with local, regulatory, and GSK standards. | 4/13/2018 |
| 1138 | GSK Zebulon, NC Automation Engineer BS in a Science or Engineering related discipline Exp: 1-7 yrs |
You will implement and support projects and systems within the site Automation Strategy and provide Automation support (Pharmaceutical Fill/Finish/Packaging) to the Zebulon site within a multi-disciplinary and extended team of Automation, Instrumentation, IT, Control engineers, external contractors and consultants. ﾠﾠSuccessfully deliver compliant (financial, regulatory (e.g. cGMPs), GAMP) instrumentation, automation, business and control systems for new and existing pharmaceutical facilities, Building Management Systems and Environmental Monitoring Systems at Zebulon. | 4/13/2018 |
| 1139 | GSK Rockville, MD BPT Lab Associate Scientist Downstream BS in Life Sciences, bio-chemistry, Bio-engineering or equivalent technical discipline Exp: 1 yr |
The candidate will be involved in all aspects of the development of purification processes for therapeutic proteins including initial process screening, optimization and characterization, validation, scale-up and tech transfer to clinical manufacturing and/or commercial manufacturing partners. | 4/13/2018 |
| 1140 | Goodwin Biotechnology Inc. Plantation, FL Upstream Manufacturing Associate BS in?biological or physical science Exp: 1-2 yrs |
Assists in all Upstream Development/Manufacturing activities including; cell culture, cell banking, media optimization, seed train design, feed strategy, bioreactor parameter optimization, harvest clarification, and technology transfer to manufacturing. | 4/13/2018 |
| 1141 | GE Evendale, OH GE Aviation Casting Co-op/Intern BS/MS in Mechanical Engineering, Mechanical Engineering Technology or Chemical Engineering Exp: NA |
This rotational developmental program is focused on the students who want to gain deep knowledge and skills of turbine airfoils advanced technology through multiple co-op/intern rotations at our Dayton Cores and Casting Facility with the goal of a direct hire opportunity upon graduation to further develop domain expertise. | 4/13/2018 |
| 1142 | GE Mutiple, Mu GE Transportation Engineering Intern BS/MS in Electrical Engineering, Industrial Engineering, Computer Engineering, Software Engineering, Computer Science, Mechanical Engineering, Manufac Exp: NA |
Students in engineering & supply chain disciplines work on a wide variety of assignments with responsibilities and hands-on involvement in areas such as heat transfer, fluid mechanics, stress analysis, diesel engine engineering, software and systems engineering, reliability, supply chain, manufacturing, quality, and several other areas. Experienced GE managers mentor student contributions and support their technical and professional development during their GE intern assignments. In addition to valuable work experience, students have the opportunity to build leadership and functional skills through training workshops on Lean / Six Sigma methodologies, resume writing, presentation skills, communicating in the workplace, interviewing skills, finance for engineers, EHS and other selected topics. Some assignments may require moderate travel. | 4/13/2018 |
| 1143 | GE Niskayuna, NY Research Fellowship Interns MS in Physics, Material Science or Ceramic Engineering, Metallurgy or Chemistry, Electrical Engineering, Mechanical Engineering, Chemical Engineering, Exp: NA |
ﾠStudents will work side by side with experts in the field, completing challenging technical projects, applying their theoretical knowledge to real-life technical problems and developing skills in a cutting edge global environment. The program also includes seminars on cross-center technology and soft skills development. Opportunities for networking and showcasing project accomplishments are offered. | 4/13/2018 |
| 1144 | GE NA, NA Engineering Internship for Oil Field Services BS in an Engineering, Applied Science Exp: NA |
The Internship Program is a 12 weeks long, structured learning experience that offers practical work experience in the Oil and Gas Industry while undertaking one core and one complex project to generate value for BHGE and act as a vehicle for you to demonstrate your capability and commitment.ﾠ In addition to project execution you will have the opportunity to explore different aspects of the BHGE business which may open up potential opportunities for your ongoing employment.ﾠ Furthermore, you will build your network within the industry. | 4/13/2018 |
| 1145 | Fujifilm? NA, NA Internship BS in Life Science or Chemical/Mechanical/Electrical/Industrial Engineering disciplines Exp: NA |
Chemical/Mechanical/Electrical/Industrial Engineering disciplines, with positions open inﾠProcess Development, Quality Assurance, Environmental Health & Safety, Manufacturing Technology Support and Manufacturing. The successful candidates will have completed their sophomore or junior year or higher. We offer a supportive, collaborative teaching environment to develop our Internsﾒ skills and identify their career goals. This is a great opportunity to gain invaluable experience working for an industry-leading biopharmaceutical contract manufacturing organization. | 4/13/2018 |
| 1146 | job_pub_nr=890B8BBE-F1A9-4A11-B813-18A1F81C0559 p=homepage_de, Fr Carpinteria CA Exp: REGULATORY AFFAIRS SPECIALIST INTERN |
BS | NA |
| 1147 | FreeThink Technologies Branford, CT Summer Chemistry Intern BS in chemistry, chemical engineering, biochemistry, or related scientific field Exp: NA |
The intern will focus on an internal company research project exploring chemical or physical stability assessment.ﾠ The project will be chosen with the goal of publication in the peer-reviewed literature and will be able to be discussed externally.ﾠ | 4/13/2018 |
| 1148 | Ferring Pharmaceuticals San Diego, CA 2018 Summer Internship - Translational Research/Bioinformatics BS in computer science or bioinformatics Exp: NA |
The bioinformatics intern will be responsible for developing an interactive web-based omics data portal for FRI researchers. This tool will enable researchers to query genome-scale datasets in FRI therapeutic areas, select genes of interest, visualize their expression profiles and supporting gene-disease associations. | 4/13/2018 |
| 1149 | Ferring Pharmaceuticals San Diego, CA 2018 Summer Internship - Molecular Design BS in chemistry or related discipline Exp: NA |
The role of the summer intern is to assist medicinal chemistry efforts at FRI where there is a significant need for assistance in these associate-level laboratory duties. The intern will be assigned to a particular project and mentor in order to gain experience in the design and generation of peptides in a pharmaceutical setting. The mentor will work with the intern to develop their non-laboratory skills including scientific presentations, literature review and record keeping. | 4/13/2018 |
| 1150 | Five Prime Therapeutics South San Francisco, CA Summer Intern - Analytical Development (Assay Testing) BS in chemistry, biology, biochemistry, chemical engineering or a related area Exp: NA |
Reporting to a Senior Research Specialist in Analytical Development, this internship position will be responsible for a development project related to a Five Prime program. The position will also learn several different instruments, perform assay testing, and provide results that will be used to help drive decisions within the Manufacturing Sciences teams. The selected candidate will gain significant experience in analytical instrumentation and biophysical analytical assays in a fast-paced working environment. | 4/13/2018 |
| 1151 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC King of Prussia, PA Microbiologist II BS in Biology or Microbiology Exp: 1 yr |
Collection of samples from the facility water and clean steam systems; approx. 15 sites/day,ﾠﾠ M-F or as needed (ie. to fulfill needs of a validation protocol).ﾠ Samples need to be performed aseptically. | 4/7/2018 |
| 1152 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Rahway, Nk Oral Formulation Scientist BS in chemistry or related science Exp: 0-3 yrs |
Support of the design and development of solid oral dosage forms and associated manufacturing processes to enable the successful development of formulations | 4/7/2018 |
| 1153 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Kalamazoo, MI Parasitology Scientist BS in biology, chemistry, or other related degree concentration Exp: 1 yr |
Follow and comply with all Standard Operating Procedures (SOPs) associated with laboratory procedures and study protocols. Perform study related activities including record keeping, data acquisition and analysis, sample handling and preparation, clinical observations, dosing, animal handling and necropsy. | 4/7/2018 |
| 1154 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC South San Francisco, CA Pharmaceutical Research Associate BS/MS in biochemistry, chemistry, analytical chemistry, chemical engineering, or other related degree concentration Exp: 1-2 yrs |
Basic understanding of GMP and GLP procedures.Fundamental knowledge of proteins and antibodies; specific experience with protein formulation a plus.Data analysis (in Excel, Matlab, Jmp or other programs). | 4/7/2018 |
| 1155 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Andover, MA Quality Control Chemistry Analyst BS in biology, chemistry, or other related degree concentration Exp: 1-2 yrs |
Routine testing to support analytical laboratory; Using multiple analytical methods including HPLC, Spectrophotometer, analytics, pH, raw materials. | 4/7/2018 |
| 1156 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC East Hanover, NJ Quality Control Scientist BS in scientific discipline Exp: 0-2 yrs |
Responsible for performing routine QC Stability testing of all active substances, excipients, finished dosage forms and complaint samples. | 4/7/2018 |
| 1157 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Research Triangle Park, NC Sample Control Specialist BS Exp: 0-2 yrs |
Manufacturing sample pick-up 2-3 times daily or as required | QC Sample re |
| 1158 | Eurofins Lancaster Laboratories Inc. Portage, MI Chemist BS in biology, chemistry, or other related degree concentration Exp: 1 yr |
Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products | 4/7/2018 |
| 1159 | Evonik? Allentown, PA ADTS Chemist MS in Chemistry, Materials Science, Polymer Chemistry, or Chemical Engineering Exp: 1-2 yrs |
Responsibilities will include providing technical service and product introduction to new and existing customers, identifying new customer project opportunities and participation in Polyurethane industry activities to understand the insulation market segment trends and technology drivers. | 4/7/2018 |
| 1160 | Evonik? Birmingham, AL Associate Scientist BS/MS in Biochemistry, Biology, Chemistry, or Pharmaceutical Sciences Exp: 0-3 yrs |
This position is responsible for supporting the development of complex parenteral formulations and their associated manufacturing processes through the design and execution of research and development activities and analysis, interpretation, and communication of process, analytical, and/or pharmacokinetic data, results, and conclusions. | 4/7/2018 |
| 1161 | EXAGEN DIAGNOSTICS Vista, CA Medical Laboratory Technician BS in Medical Technology, Biology, Chemistry and related field Exp: 0-2 yrs |
The Medical Laboratory Technician (MLT) will work in Automated Chemistry area and performs moderate complexity testing. Performs and document quality control and preventive maintenance. Follow good laboratory practices and procedures for compliance. | 4/7/2018 |
| 1162 | EXAGEN DIAGNOSTICS Vista, CA Clinical Laboratory Scientist BS in Medical Technology, Biology, Chemistry and related field Exp: 0-2 yrs |
The Clinical Lab Scientist (CLS) will work in Flow Cytometry area and performs testing. Performs and document quality control and preventive maintenance. Follow good laboratory practices and procedures for compliance. | 4/7/2018 |
| 1163 | Exela Pharma Sciences, LLC. Lenoir, NC Compounding Chemist BS in Chemistry or related scientific discipline Exp: 1 yr |
The Compounding Chemist will be responsible for assisting with the compounding activities of manufacturing solutions and suspensions: weighing, adding and mixing raw materials, sterile filtration, steam sterilization, sanitization, and documentation activities associated with the production of drug products. This position supports the ongoing development, manufacture, and distribution of pharmaceutical products in compliance with local procedures, corporate policies, and the regulatory requirements of the U.S. Food and Drug Administration. | 4/7/2018 |
| 1164 | Exosome Diagnostics Waltham, MA Laboratory Technologist BS/MS in biological sciences or clinical laboratory sciences Exp: 0-2 yrs |
This position provides an opportunity to participate in an entrepreneurial company that is bringing its proprietary technology into clinical service. The ideal candidate will have a good understanding of CLIA requirements, will assist in the development and validation of Laboratory Developed Tests (LDTs) for diagnostic and clinical trials testing, and will be responsible for performing testing for a variety of biomarkers. | 4/7/2018 |
| 1165 | Finch Somerville, MA RESEARCH TECHNICIAN I BS in Biology, Microbiology, Molecular Biology, or a related field Exp: 1-2 yrs |
Research Technician I, with guidance from the Research Operations Core Manager, will perform Core Lab Methods to support data generation across all research programs. | 4/7/2018 |
| 1166 | Finch Somerville, MA RESEARCH ASSOCIATE - ANALYTICAL DEVELOPMENT BS in microbiology, chemistry or pharmaceutical Exp: 1-2 yrs |
Perform routine testing of in-process and finished products, develops test methods, qualification, transfer of methods to Quality and Manufacturing teams with some supervision and carry out special projects independently as required and assigned by Management. | 4/7/2018 |
| 1167 | FLUIDIGM Markham, CA Product Development Scientist MS in Analytical Chemistry or Biochemistry Exp: 1-2 yrs |
The Product Development Scientist will play an active role in interdisciplinary teams with an overall goal to provide high-quality mass cytometry reagents. The individual will support the execution of new product introduction and sustaining projects. Duties include tasks to support product scale-up, process optimization, technology transfer and process validation. | 4/7/2018 |
| 1168 | Foundation Medicine? Cambridge, MA Senior Research Associate BS in Bioinformatics, Computer Science, Biomedical Engineering or a related field Exp: 1 yr |
The candidate will be responsible for assisting the development of clinical diagnostic assays and biomarker signatures for pharmaceutical partners through research, genomic analysis, software implementation, and validation of advanced computational methods. The successful candidate will possess strong analytical skills, solid programming experience, a high level of professional maturity, ability to consistently meet deadlines under pressure, and ability to work independently. | 4/7/2018 |
| 1169 | Foundation Medicine? Cambridge, MA Laboratory Operations Assistant - 1st shift BS in a Biological or Life Science Exp: Entry levelﾠ |
Candidates should be highly motivated, confident with multi-tasking and attentive to details. This position will support laboratory technologists who perform patient sample testing. This position may include equipment maintenance and reagent preparation in addition to other tasks in a highly complex clinical diagnostic laboratory. | 4/7/2018 |
| 1170 | Foundation Medicine? Cambridge, MA Histotechnician BS in a Biological Science or life science? Exp: 0-2 yrs |
As a part of our lab team you will be integral to Foundation Medicinesﾒ culture and mission of transforming cancer care by allowing patients to make informed treatment decisions based on a deep understanding of the molecular changes that contribute to their disease. | 4/7/2018 |
| 1171 | Frontage Labs Exton, PA Associate Scientist, Analytical Services-CMC BS in Chemistry or related discipline Exp: 1-2 yrs |
Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines | 4/7/2018 |
| 1172 | Frontage Labs Exton, PA Senior Associate Scientist, Analytical Services-CMC MS in Chemistry Exp: 1-2 yrs |
This position will mainly focus on supporting drug development, analytical research and developing activities, as well as cGMP testing | 4/7/2018 |
| 1173 | Frontage Labs Exton, PA Scientist, Bioanalytical Services MS in Analytical Chemistry, Biochemistry, Pharmacology or related scientific discipline Exp: 1 yr |
Scientist / Bioanalytical Services Essential Functions Run sensitive, reliable and efficient LC-MS/MS bioanalytical assays for TK/PK assessment. | 4/7/2018 |
| 1174 | Freudenberg Medical Baldwin Park, CA ENGINEER I BS in Engineering or related field Exp: 0-2 yrs |
Work closely with project managersﾠ to gather/prepare all documentation relevant to a particular project. | 4/7/2018 |
| 1175 | Fresenius Kabi Wilson, NC MICROBIOLOGY ANALYST BS/BA in Science Exp: 1-2 yrs |
Responsibilities include routine testing to support product release, raw material release, and cleaning verification. The technician will rely on experience and judgment in order to plan and accomplish goals. | 4/7/2018 |
| 1176 | Fresenius Kabi Wilson, NC ENVIRONMENTAL MONITORING ANALYST? BS/BA in Science Exp: 1-2 yrs |
The Quality Control Environmental Monitoring Technician is responsible for day-to-day activities required to perform monitoring of aseptic areas and controlled environments. | 4/7/2018 |
| 1177 | Fresenius Kabi Grand Island, NY AQL SPECIALIST? BS in Life Sciences or related field Exp: 1-3 yrs |
Position is responsible for quality oversight and assistance with Inspection/Packaging processes at the FK Grand Island Manufacturing Facility. Position is also responsible for AQL sampling and AQL related product inspection. Position recommends corrective action in response to deviations noted and assures compliance to SOPs and cGMPs while following and reviewing Good Documentation Practices. | 4/7/2018 |
| 1178 | Fresenius Kabi Grand Island, NY QC TECHNICIAN II - Microbiology BS Exp: 0 yr |
This individual holding the position of QC Technician II shall be responsible for performing routine testing of in-process and finished product samples, raw material, stability, and utilities.ﾠ They shall be responsible for monitoring the environmental conditions in the laboratory and in manufacturing areas.ﾠ They shall support validation projects.ﾠ This position must be available to work overtime as assigned. | 4/7/2018 |
| 1179 | Fresenius Kabi Melrose Park, IL TECH TRANSFER SPECIALIST BS in physical science, engineering Exp: 1-3 yrs |
The individual is responsible for independently or as part of a project team, planning, designing, tracking and implementing effective project technical support systems as well as facilitating multiple technical transfer activities (e.g., protocols, batch records, operating procedures, training materials, etc.) to achieve a successful transfer of products. The position will support multiple sites within North America and Europe and reports into the Director of Production and Technology Transfers. | 4/7/2018 |
| 1180 | Fresenius Kabi Grand Island, NY QC TECHNICIAN II - Chemistry BS in Chemistry or related field Exp: 1-2 yrs |
Reports to QC Chemistry Supervisor | Individual mu |
| 1181 | Fresenius Kabi Melrose Park, IL STATISTICAL QUALITY ANALYST MS Exp: 1-3 yrs |
Position acts as the statistical subject matter expert for the facility.ﾠ Plans data collection, and analyzes and interprets numerical data from surveys, experiments, studies, and other sources and applies statistical methodology to provide information for scientific research and analysis.ﾠ Plans methods to collect information and develops questionnaire techniques according to survey design.ﾠ Conducts surveys, evaluates reliability of source information, adjusts and weighs raw data, analyzes and interprets statistics and organizes results.ﾠ The individual will prepare conclusions and predictions based on data summaries. | 4/7/2018 |
| 1182 | GE Aviation Hooksett, NH Manufacturing Production & Assembly BS Exp: 1 yr |
Setting-up and operating inspection and/or manufacturing tools/equipment such as conventional electrical discharge machines, grinders, precision assembly devices, peen, heat treat, plasma spray, etc.ﾕ Performing basic mathematical calculationsﾕUsing precision gages/fixtures and inspection measuring equipment and interpreting mechanical blueprints, sketches, engineering specifications and drawings, etc., to determine set-ups and operations necessary to complete job tasks. ﾕTraining duties.ﾕ Performing related environmental, health, safety, maintenance, quality, continuous improvement, and production-flow job duties to support plant machinery, equipment, and manufacturing-related initiatives and programs. ﾕMaintaining detailed job task documentation, reports, and records. | 4/7/2018 |
| 1183 | FUJIFILM? RESEARCH TRIANGLE PARK, NC Associate Scientist, Analytical & Formulation Development BS Exp: 1 yr |
The position will primarily provide support of product formulation and analytical development for biopharmaceuticals, including monoclonal antibodies and recombinant proteins; Responsible for sample preparation using automated systems, executing experimental studies and summarizing data, and producing high-quality documentation with supervision. | 4/7/2018 |
| 1184 | FUJIFILM? College Station, TX Downstream Manufacturing Technician III MS in Biology, Microbiology, Chemistry, Biochemistry, Engineering or other related field Exp: 1 yr |
The Downstream Manufacturing Technician III will work directly with a range of purification technologies including: filtration technologies (TFF and depth), chromatographic separations (Single Use GE AKTA systems), viral inactivation following aseptic techniques and procedures in a cGMP environment. | 4/7/2018 |
| 1185 | FUJIFILM? College Station, TX Upstream Manufacturing Technician III MS in Biology, Microbiology, Chemistry, Biochemistry, Engineering or other related field Exp: 1 yr |
The Upstream Manufacturing Technician III will work directly with a range of technologies following aseptic techniques and procedures in a cGMP environment. | 4/7/2018 |
| 1186 | Evonik? multiple, mu Summer Professional Enrichment (SPE) - Chemistry BS/MS Exp: NA |
Being an Evonik summer intern gives you an opportunity to apply for our International Professional Rotational Enrichment Program (IPREP) and go on international assignments to give your ideas a place to grow when you graduate. You can collaborate with dynamic colleagues who share your interest in creating solutions with a global reach. | 4/7/2018 |
| 1187 | CytomX Therapeutics South San Francisco, CA Translational Sciences Summer Intern BS/MS in biological sciences Exp: NA |
Reporting to a Senior Research Associate, Translational Sciences, over the 12-week assignment, the internﾠwill have the opportunity to gain skills in basic histological lab procedures, immunohistochemistry, immunofluorescence and biological sample preparation. The goal is for the intern to use these skills in developing an immunofluorescence assay to present to the Translational Sciences group at the end of the internship. | 4/7/2018 |
| 1188 | CytomX Therapeutics South San Francisco, CA Protein Engineering Summer Intern BS in Biology, Molecular Biology, Biochemistry, Protein Engineering, or similar Exp: NA |
Over the 12-week assignment, the intern willﾠlearn state-of-the-art molecular biology and protein engineering techniques in developing cancer therapies. One project aims at developing qPCR-based techniques to quantify gene copy number and a second projectﾠaims at interrogating variousﾠProbodyﾠarchitectures. | 4/7/2018 |
| 1189 | CytomX Therapeutics South San Francisco, CA Oncology Summer Intern BS/MS?in?Cell biology,?Immunology,?Biochemistry, Molecular Biology, or a related field? Exp: NA |
Reporting to a Senior Scientist, Oncology, over the 12-week assignment, the intern willﾠparticipate in target identification and validation in supporting the pre-clinical development of therapeutic antibodies.ﾠWe seek a highly motivated individual toﾠhelp tocharacterize novel oncology targets and evaluateﾠProbodyﾠdrug conjugates (PDCs) forﾠtreatment of cancers. | 4/7/2018 |
| 1190 | Emergent BioSolutions Gaithersburg, MD Intern (Post Bachelor's Degree) BS in life sciences Exp: 0-1 yr |
Review protocols and understands the study to be able to perform data analysis. Conduct research in area of anti-infectives (no laboratory work required).ﾠ Assist in program management activities including drafting, revising and organizing project reports. Follow good documentation practices. Maintain a database of reports. Build or populate a database of chemical structures and interact/work closely with the Medicinal Chemists. Maintain progress during the internship toward the specific goals outlined for the intern.ﾠ Adhere to Company safety guidelines. Complete all required training. | 4/7/2018 |
| 1191 | DNAnexus? Mountain View, CA Internships - Science and Engineering BS in computer science, bioinformatics, computational biology, genetics, or related discipline Exp: NA |
You will have the opportunity to be part of some pretty cool projects while learning how to use our platform and use the DNAnexus SDK. On a daily basis, you will be working hands-on with genomics sequence analysis, using popular tools such as NGS, BWA and GATK to translate data pipelines into the DNAnexus platform, use cloud resources to optimize and accelerate them, and confirm their scientific validity. Coding is a big part of the role so expect some of your time to be spent building core technologies for scaling up systems to thousands of servers for managing and analyzing petabytes of data.ﾠ | 4/7/2018 |
| 1192 | BARD? Salt Lake City, UT Internship - Quality Engineer BS Exp: NA |
Internships can be found in all departments working on a variety of projects ranging from product testing to post market launch.ﾠ Interns work under close supervision by the sponsoring function.ﾠ It is a mutually beneficial relationship as Bard creates a learning environment where the intern obtains industry hands-onﾠexperience.ﾠ | 4/7/2018 |
| 1193 | Daiichi Sankyo? Bernards, NJ Intern, Regional Quality Assurance The Americas?In?Bernards, NJ?At?DSI BS/MS Exp: NA |
Assist in Regional GMP Quality Assurance with audit proposals and tracking, preparing reports and presentations, applying Quality Audit metrics from the site data, preparing risk assessments and supporting Regional Quality Assurance meetings | 4/7/2018 |
| 1194 | Charles River Newark, DE Laboratory Intern BS in Biology, Microbiology or any related field Exp: NA |
While in a hands on educational setting and under the close supervision of a Manager or Lead Technologist you will provide daily support to ensure that all laboratory functions are carried out.ﾠ You will also learn how to carry out those functions within regulatory and GMP guidelines in accordance with 21 CFR parts 210 and 211. | 4/7/2018 |
| 1195 | Boehringer Ingelheim Ridgefield, CT Summer Intern - Manufacturing Purification BS/MS Exp: NA |
Management of GMP equipment Timelines | Maintaining |
| 1196 | Cytovance Biologics Oklahoma City, OK QA OPERATIONS ASSOCIATE BS Exp: 1-3 yrs |
Quality Assurance Associate I is a member of the Quality Assurance Operations team reporting directly to the Quality Assurance Operations Supervisor. They maintain quality oversight of operational areas by working closely with operationﾒs personnel and performing various checks during manufacturing processes. Maintain quality oversight and inspection of all raw materials and finished product. They also assess regulatory and quality risks in activities and processes according to regulatory agency rules and guidelines and Cytovance Standard Operating Procedures. | 3/30/2018 |
| 1197 | Cytovance Biologics Oklahoma City, OK QS&C SPECIALIST BS Exp: 1-3 yrs |
Takes an active role in assisting with the development, execution and management of the Quality Compliance Team.ﾠﾠA QS & C Specialist assists the Compliance Team in the identification and resolution of quality issues and regulatory concerns. | 3/30/2018 |
| 1198 | BARD Salt Lake City, UT Quality Engineer I - MDR MS Exp: 0 yr |
This position designs, develops and implements new products, processes, test methods and equipment. | 3/30/2018 |
| 1199 | BARD Covington, GA Quality Engineer I BS in Engineering, Engineering Technology, Science or equivalent Exp: 1 yr |
Represents the Corporation, Division and Quality Department in a professional manner;Participates on Project Team as Quality Representative. Ensures that principals of Design Control are applied to Product and Process Changes and New Product Development. | 3/30/2018 |
| 1200 | BARD Covington, GA Regulatory Affairs Specialist II BS Exp: 1-3 yrs |
The Regulatory Affairs Specialist is responsible for implementation of regulatory strategies including domestic and international submissions and other support of product project team. | 3/30/2018 |
| 1201 | BARD Warwick, RI Associate Regulatory Affairs International Specialist BS Exp: 0-3 yrs |
Provide international regulatory support through the product life cycle on product project teams (e.g., developing regulatory strategies, timeline development, change control and preparing submission related documents.). | 3/30/2018 |
| 1202 | DJO Global Austin, TX FEA & Testing Engineer BS in Mechanical Engineering or Equivalent Exp: 1 yr |
Under guidance and detailed instructions, plans, designs, tests, and develops mechanical systems, parts, equipments and packaging. Applies basic knowledge of engineering principles to design simple components and assemblies. Conducts engineering analysis and testing on designs using existing designs and tools. Participates in concept and design reviews and activities. Ensures design requirements and standards are met. Compiles mechanical design documentation and approvals. 90% of time is spent in a resource capacity. 10% of responsibilities are in leadership activities. | 3/30/2018 |
| 1203 | DJO Global Austin, TX Engineer-Specialty Instruments BS in Mechanical Engineering or Equivalent Exp: 1 yr |
Under guidance and detailed instructions, plans, designs, tests, and develops mechanical systems, parts and equipment. Applies basic knowledge of engineering principles to design simple components and assemblies. Conducts engineering analysis and testing as needed on designs using existing designs and tools. Participates in concept and design reviews and activities. Ensures design requirements and standards are met. Compiles mechanical design documentation and approvals. 100% of time is spent in a resource capacity. Works directly with Marketing, Sales Reps and Surgeon customersﾠin the design of specialty surgical instrumentation to meet the user needs of the requesting surgeon.ﾠ Coordinates manufacturing of specialty instruments with outside vendors and internal machine shop. | 3/30/2018 |
| 1204 | Deciphera Pharmaceuticals Lawrence, KS Scientist ? Biology MS in biochemistry, cell biology or related field Exp: 0 yr |
ﾠThe successful candidate will work as part of a team and apply their skills to identify kinase inhibitors that selectively block cancer or immune cell targets of interest. | 3/30/2018 |
| 1205 | Dr. Reddy?s Shreveport, LA Controlled Substance / Inventory Production Planning Associate BS Degree in Engineering or Sciences Exp: 1-2 yrs |
Conduct the controlled substance inventory audits for manufacturing, analytical, import & export registrations. | 3/30/2018 |
| 1206 | Dynavax Berkeley, CA Clinical Trial Assistant/Sr. CTA BS in life science Exp: 1-2 yrs |
Responsible for performing multiple tasks that support clinical trials, with duties that include assisting clinical operations staff with activities related to clinical trials, creating and maintaining documents and tracking systems, maintaining accurate files and filing systems, etc.ﾠ | 3/30/2018 |
| 1207 | Dynavax Berkeley, CA Research Associate I/II MS Exp: 1 yr |
The purpose of this position is to help advance Dynavaxﾒs immuno-oncology discovery research to inform clinical progression of our programs | 3/30/2018 |
| 1208 | DynoSenseTM Corp. San Jose, CA QA Engineer BS in Engineering Exp: 0-2 yrs |
Develop test plan, test cases, test scenarios based on Users Stories and productﾒs design description to meet business requirements and technical specifications | 3/30/2018 |
| 1209 | Editas Medicine Cambridge, MA Research Associate I/II - RNA Engineering BS/BA Exp: 1-2 yrs |
The successful candidate will contribute as part of a multidisciplinary team to improve gene-editing based therapeutics by developing techniques and researching new understandings in RNA folding and engineering. The successful candidate is expected to have proven practical experience in creating and analyzing next-generation sequencing data sets from mammalian cell culture experiments using cutting edge molecular biology techniques. RNA and cell culture experience in immortalized cell lines is expected. The candidate should be a scientifically motivated self-started, capable of independently conceiving, conducting, and critically analyzing his/her own innovative research with minimal supervision. Strong presentation skills, communication, and the ability to work in a fast-paced and team-oriented environment will also be vital. | 3/30/2018 |
| 1210 | Edwards Lifesciences Draper, UT Manufacturing Engineer I, EPC/MIS BS/MS Exp: 0 yr |
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution.ﾠ Please refer to the job description for additional details. | 3/30/2018 |
| 1211 | Edwards Lifesciences Draper, UT Engineer I, Quality--Product Verification Lab BS/MS Exp: 1 yr |
Applies knowledge of quality engineering principles and methods to ensure compliance with regulatory requirements and Edwards' systems/procedures to optimize product development, internal and external device manufacturing, and device distribution. Please refer to the job description for additional details. | 3/30/2018 |
| 1212 | Eli Lilly Terre Haute, IN Technician- QC Lab-FDE BS Exp: 1 yr |
The Quality Laboratory Technician performs accurate, precise, and timely testing of laboratory samples in accordance with approved methods in both the QC and culture laboratories. Expertise in lab operations, aseptic technique, attention-to-detail and thoroughness are critical components. The Lab Technician will participate in laboratory investigations, equipment qualification, and maintenance by executing well-defined protocols and procedures. Active in identifying, communicating, and participating in opportunities for improvement to lab operations. | 3/30/2018 |
| 1213 | Elstar Therapeutics Cambridge, MA RESEARCH ASSOCIATE, PROTEIN ENGINEERING, ANTIBODY DISCOVERY BS/MS in Biology or related field Exp: 1 yr |
Recombinant mammalian protein expression, including target design, transfection, HEK and CHO tissue culture, purification and characterization | 3/30/2018 |
| 1214 | Emergent BioSolutions Rockville, MD Manufacturing Associate I-TEMP BS/BA in Biology, Chemistry, or related discipline Exp: 0-2 yrs |
Recombinant mammalian protein expression, including target design, transfection, HEK and CHO tissue culture, purification and characterization | 3/30/2018 |
| 1215 | Emergent BioSolutions Lansing, MI Analyst I, QC Bioassay? BS/BA in Biology, Chemistry, or related discipline Exp: 0-2 yrs |
Author laboratory investigations using independent thought and collaboration and initiate Non-Conformance Events reports | Identifies an |
| 1216 | Emergent BioSolutions Baltimore, MD ANALYST II, QUALITY ASSURANCE PACKAGING? BS/BA Exp: 1 yr |
The QA Analyst II On the Floor is responsible for assuring the quality of products inspected and Packaged at the Emergent BioSolutions Baltimore Facility.ﾠﾠ The QA Analyst II on the Floor will perform Quality on the floor functions and support packaging activities.ﾠ Our QA Department provides expertise in problem solving and process improvements.ﾠ The QA Analyst II will interact with packaging personnel and the Quality Engineer to provide guidance necessary to maintain and improve CGMP compliance at the company. | 3/30/2018 |
| 1217 | Emergent BioSolutions Rockville, MD ANALYST II, QUALITY CONTROL MS? Exp: 0-2 yrs |
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.ﾠ The individual routinely conducts monitoring, testing, and SOP generation and revision. | 3/30/2018 |
| 1218 | Emergent BioSolutions Baltimore, MD Lead Technician, Cleanroom 3rd Shift BA/BS Exp: 0 yr |
The Manufacturing Technician, 2nd shift, is responsible for daily cleaning and sanitization activities throughout the production area and preparation of tubing, equipment, supplies, and other items associated with sterile filling processes. | 3/30/2018 |
| 1219 | Endotronix Lisle, IL R&D Engineer BS/MS in Biomedical Engineering Exp: 1-3 yrs |
Provide support in research and development efforts for novel analytical models combining multi-modal physiological data | 3/30/2018 |
| 1220 | QIAGEN Waltham, MA Research Associate BS/BA in Chemistry, Biochemistry, Molecular Biology or related fields Exp: 1-3 yrs |
The successful candidate will be an integral part of the sequencing development team and will be responsible for maintenance and operation of instruments, preparation of reagents according to SOPs as well as executing complex laboratory experiments.ﾠ | 3/30/2018 |
| 1221 | Epic Pharma Laurelton, NY QUALITY CONTROL CHEMIST BS in Chemistry, or a related science field Exp: 1-3 yrs |
Thorough understanding of cGMPs, specifically as they apply to a Pharmaceutical environment.Experience testing raw materials (API/Excipients), in-process, finished product and stability samples. | 3/30/2018 |
| 1222 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Durham, NC Biologist BsS in biology, biochemistry, cell biology, or other related degree Exp: 1 yr |
Perform aseptic tissue culture based virology assays on live viral vaccine products and process intermediates for the purpose of batch release | 3/30/2018 |
| 1223 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Indianapolis, IN Biochemist - Chromatography BsS in biology, biochemistry, cell biology, or other related degree Exp: 3 months |
Perform biochemical testing on proteins and antibodies including, but not limited to, CE, IC, HPLC, SEC, SDS-PAGE, UV, Protein A titer, ELISA and/or Bioassays | 3/30/2018 |
| 1224 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Malvern, PA Bioassay/Process Analytical Support Scientist BS/MS Exp: 1-3 yrs |
Perform method development, optimization, validation, and transfer of Bioassays;Immunoassays and PCR analysis. | 3/30/2018 |
| 1225 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Gaithersburg, MD Bioassay Scientist BsS in biology, biochemistry, cell biology, or other related degree Exp: 1 yr |
ﾠPerform bioanalytical cell based assay testing of recombinant protein therapeutics under cGMP. | 3/30/2018 |
| 1226 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Gaithersburg, MD Bioassay Development Scientist BsS in biology, biochemistry, cell biology, or other related degree Exp: 1-5 yrs |
Supporting cell-based bioassays and binding assays for biological characterization and testing of biopharmaceutical products | 3/30/2018 |
| 1227 | Eurofins Panlabs, Inc St Charles, MO Associate Scientist II MS/MA Exp: 1 yr |
The Associate Scientist II will support the Discovery Services and Products Team in contract research services. This role requires knowledge of scientific principles and experience in a general lab setting. | 3/30/2018 |
| 1228 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC South San Francisco, CA Associate Research Scientist BS/MS in biochemistry, chemistry, analytical chemistry, chemical engineering, or other related degree Exp: 1-2 yrs |
Basic understanding of GMP and GLP procedures;General chromatographic skills including protein characterization (SEC, IEC, RP) and wet chemistry skills including UV-visible spectroscopy and colorimetric assays . | 3/30/2018 |
| 1229 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Rahway, NJ Analytical Scientist - Preclinical Development BS/MS in Chemistry, Pharmaceutical Sciences, or related Sciences Exp: 1-3 yrs |
Help to troubleshoot the challenges associated with the development of solid and sterile drug products for small molecules, peptides and oligonucleotides through active collaboration with cross functional project teams | 3/30/2018 |
| 1230 | Eurofins Advantar Inc. San Diego, CA Analytical Chemist BS in Analytical Chemistry, Biochemistry, Pharmaceutical Science or related discipline Exp: 1-2 yrs |
Develop, qualify and validate analytical test methods for drug product, intermediates and excipients;Design and execute analytical development studies. | 3/30/2018 |
| 1231 | CSBio Menlo Park, CA Chemistry Intern (summer internship) BA/BS? Exp: NA |
Perform peptide synthesis or purification under close supervision; Assist in setting up and operating synthesis of purification systems;Perform HPLC, mass spectrometry, and other analytical techniques. | 3/30/2018 |
| 1232 | CryoLife Austin, TX Engineering Intern BS in Engineering Exp: NA |
Assist in the development and implementation of clear, complete and accurate working plans and detail drawings from rough or detailed sketches or notes for engineering or manufacturing purposes, according to specified dimensions using computer and specially designed software. | 3/30/2018 |
| 1233 | Boehringer Ingelheim? Ridgefield, CT Summer intern - Gas Chromatography MS Exp: NA |
Develop and validate chiral/achiral GC methods for the analysis of small molecule active pharmaceutical ingredients and intermediates. | 3/30/2018 |
| 1234 | CSL Behring L.L.C. Kankakee, IL Process Improvement Summer Intern BS/MS Exp: NA |
Under supervision, conduct entry-level process analysis, needs assessments and preliminary cost/benefit analysis in an effort to align operations, process, and technology with overall site process improvement initiatives. | 3/30/2018 |
| 1235 | Corning Kennebunk, ME Engr/Manuf Intern BS in Mechanical Engineering Exp: NA |
Intern will work as part of the Engineering Department.The intern will work on solo and team projects which can range from new materials, validations, experimentation/problem analysis, etc. | 3/30/2018 |
| 1236 | Corning Glendale, AZ Research and Development Intern BS Exp: NA |
Assist with experimental project development at direction of senior engineer | Assembly of p |
| 1237 | Corning Keller, TX PLM Engineering Manufacturing Intern BS/MS Exp: NA |
Lead a project related to product strategy development, product lifecycle management, or business process for the Product Management function of Corning Optical Communications | 3/30/2018 |
| 1238 | CytomX Therapeutics? South San Francisco, CA Clinical Development Summer Intern BS Exp: NA |
Reporting to the Head of Medical, the intern will have the opportunity to be a part of the development team at an early clinical development (phase I/II), and be exposed to the role of physicians in biotech.ﾠ | 3/30/2018 |
| 1239 | CytomX Therapeutics? South San Francisco, CA Cancer Immunology Summer Intern, Immuno-Oncology focused BS/MS in the biological sciences Exp: NA |
Reporting to an Associate Scientist, Cancer Immunology, over the 12-week assignment, the intern will learn to perform pre-clinical in vitro and cell-based functional assays to assess Probodies for immune oncology targets. We are seeking a highly motivated candidate with enthusiasm for learning. | 3/30/2018 |
| 1240 | CytomX Therapeutics? South San Francisco, CA Cancer Immunology Summer Intern, CAR focused BS/MS in the biological sciences Exp: NA |
Reporting to an AssociateﾠScientist, Cancer Immunology,ﾠover the 12-week assignment, the intern willﾠlearn to generate lentiviral particles, transduce primary T-cells, and characterize CAR-T effector function in cell-based assays. | 3/30/2018 |
| 1241 | Charles River Malvern, PA Technician I Microbiology 1 BS in biology or a related discipline Exp: 0-1 yr |
The responsibilities of this role as Microbiology Technician I will be specific to the Environmental Monitoring division of the Microbiology department.ﾠ | 3/23/2018 |
| 1242 | Corning Painted Post, NY Research Associate - Reliability MS in Material Science or Mechanical Engineering Exp: 0 yr |
This position of Research Scientist is in the Mechanics and Reliability department of the Science and Technology Division of Corning Incorporated. This department combines deep knowledge of the mechanics of materials with reliability science and practice to discover and explore failure modes in materials. The candidate should have a track record of combining experimental work with fundamental understanding to yield new insights into the mechanics of materials. Our projects are fast-paced, and we expect our scientists to produce an experimental and modeling strategy that produces knowledge from which program and product decisions can be made. | 3/23/2018 |
| 1243 | Corning Corning, NY Process Simulation Engineer MS in Mechanical Engineering, Civil, Materials, Physics or related discipline Exp: 1 yr |
Applying viscoelastic fundamental theories to understand the stress relaxation and structural relaxation material behavior during glass forming/reforming processes | 3/23/2018 |
| 1244 | Corning Corning, NY Process Engineer/Technologist BS in Ceramic Engineering, Glass Science, Materials Engineering or Chemical Engineering preferred Exp: 0-4 yrs |
Test proof of concept/feasibility for new manufacturing processes or significant capability improvement of existing manufacturing processes. | 3/23/2018 |
| 1245 | Corning Painted Post, NY Lab Systems Engineer BS in Engineering or related field Exp: 0-2 yrs |
The candidate will be responsible for delivering high impact in the organization by developing enabling software systems for the Research, Development, and Engineering divisions at Corning.ﾠ Delivering software solutions will be accomplished through the evolution of innovative concepts across early stage experimentation, proof-of-concept demonstrations, and prototypes.ﾠ The role requires a multidisciplinary approach including mechanical engineering, controls and software development, and scientific leadership. ﾠThe candidate should feel comfortable working within and communicating among a small team of individuals with diverse talents. | 3/23/2018 |
| 1246 | Cheminpharma LLC Branford, CT Associate scientist, Medicinal/Synthetic chemistry BS/MS in synthetic chemistry Exp: 0-5 yrs |
Major responsibilities will involve design, synthesis, purification and characterization of novel chemical entities and the management of general chemistry lab operations under the direction of senior scientific staff. The qualified individual is expected to contribute in process development and scale-up of key intermediates. | 3/23/2018 |
| 1247 | ChemPacific Corp Baltimore, MD Chemist MS in Chemistry or Organic Chemistry Exp: 1 yr |
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.ﾠ | 3/23/2018 |
| 1248 | Cibus San Diego, CA Research Associate/Senior Research Associate - Molecular Biology? BS/MS in biochemistry, molecular biology, or a related field Exp: 0-2 yrs |
The position will have a key role running, maintaining, and expanding an automated high-throughput molecular screening platform supporting Cibus' patented RTDS gene editing technology. The successful applicant will be expected to operate an automated liquid handling system for DNA extraction and genotyping and assist in all aspects of the screening workflow including developing robust molecular screening assays. Responsibilities will include sample preparation, reagent preparation, assay design and validation, conducting qPCR reactions and NGS library preparations, data analysis, tracking, and reporting, and training other team members. Depending on candidates experience level, supervision of a junior scientist may also be required. This position offers an excellent opportunity for a talented individual to learn and grow in a dynamic environment focused on cutting edge gene editing technology. | 3/23/2018 |
| 1249 | Clinilabs Inc. NY, NY Clinical Research Coordinator BS Exp: 1-2 yrs |
The Clinical Research Coordinator (CRC) is primarily responsible for coordinating the operational aspects of ongoing clinical projects to ensure that the clientsﾒ goals of time, cost, and quality are met. The CRC may serve as the primary contact with the client to ensure appropriate communications, project budget management, and meeting of timelines. The CRC may also serve as the project lead responsible for directing internal teams in the execution of the protocol and ensuring that all staff working on any given protocol have been properly delegated by the Principal Investigator and adequately trained on the protocol. | 3/23/2018 |
| 1250 | Takara Bio USA Ann Arbor, MI Production Associate I BS/BA Exp: 0-2 yrs |
Responsible for manufacturing assigned products/product lines by following established manufacturing procedures | 3/23/2018 |
| 1251 | Takara Bio USA Mountain View, CA Quality Control Associate ll-Temporary MS Exp: 0-2 yrs |
Responsible for testing assigned products/product lines | Responsible f |
| 1252 | Cogent Indianapolis, IN Analytical Chemist BS/MS in Analytical Chemistry or related scientific field Exp: 0-3 yrs |
Analyze research samples by LC/MS/MS and other instruments as needed | Determine and |
| 1253 | Complete Genomics? San Jose, CA Manufacturing Associate 2? BS Exp: 1-2 yrs |
The successful candidate will be responsible for manufacturing DNA Nanoballs as required by R&D, prepare libraries, formulate and assess a variety of reagents, run different biochemistry experiments, operate sequencing instruments, manage data, troubleshoot, and analyze data using various proprietary and nonproprietary tools.ﾠﾠﾠﾠﾠﾠ ﾠ ﾠ ﾠﾠﾠ ﾠ ﾠ ﾠ ﾠ ﾠ ﾠ ﾠ ﾠ ﾠ ﾠﾠ ﾠ ﾠ | 3/23/2018 |
| 1254 | Conagen Bedford, MA Research Associate - Microbial Synthetic Biology MS Exp: 1 yr |
This position will focus on microbial metabolic engineering and the candidate is expected to have a strong background in metabolic engineering, molecular biology, genetics, and ideally synthetic biology. Strong technical, organizational, and communication skills are essential. | 3/23/2018 |
| 1255 | Conagen Bedford, MA Research Associate - Automation BS in biology, biotechnology or related fields Exp: 1 yr |
The successful candidate will support and develop automation solutions related to the genetic engineering and screening of industrial microbes. | 3/23/2018 |
| 1256 | CONMED? Largo, FL Quality Engineer II - New Product Development BS/MS Exp: 0-3 yrs |
The Quality Engineer New Product Development (NPD) is responsible for supporting all quality engineering activities to support the new product life cycle, from concept through commercialization and sustaining changes, as part of a cross-functional development team.ﾠ Serves as the key resource for ensuring compliance to ISO, MDD and QSR requirements for Medical Devices. Takes the lead with quality initiatives with inter-organizational impact following QSR, ConMed Policies and standards. Works under direction from Quality Management. | 3/23/2018 |
| 1257 | CONMED? Denver, CO Quality Engineer - New Product Development BS/MS Exp: 0-3 yrs |
The Quality Engineer New Product Development (NPD) is responsible for supporting all quality engineering activities to support the new product life cycle, from concept through commercialization and sustaining changes, as part of a cross-functional development team.ﾠ Serves as the key resource for ensuring compliance to ISO, MDD and QSR requirements for Medical Devices. Takes the lead with quality initiatives with inter-organizational impact following QSR, ConMed Policies and standards. Works under direction from Quality Management. | 3/23/2018 |
| 1258 | CooperSurgical Houston, TX Laboratory Technician BS/MS in Biology or other related science Exp: 1 yr |
Performs complex molecular-based procedures on clinical samples. Analyzes clinical results and provides diagnoses.ﾠ Performs clinical tasks associated with clinical cases.ﾠ | 3/23/2018 |
| 1259 | CoreRx Clearwater, FL QUALITY CONTROL INSPECTOR BS/BA Exp: 1-2 yrs |
Adherence to all company procedures. Perform sampling of in-process and raw materials. Release of materials. Manage the retain program. Perform weekly cycle audits. Check in-process work. Oversight of environmental monitoring and water systems. Perform cleaning verifications. | 3/23/2018 |
| 1260 | Counsyl South San Francisco, CA Accessioning Intake Associate BS Exp: 0-2 yrs |
As an Intake Associate you will be a member of a team responsible for the timely and accurate data entry and management of our paper requisitions. You will be a significant contributor to our high-throughput workflow and an integral part of our busy CLIA lab. | 3/23/2018 |
| 1261 | Covance Madison, WI Research Tech BS Exp: 1 yr |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings | 3/23/2018 |
| 1262 | Covance Dallas, TX Research Technician BS Exp: 1-2 yrs |
Accurately perform blood pressure, pulse, weights, respiratory rate and temperature readings | 3/23/2018 |
| 1263 | Covance Madison, WI Research Assistant I BS/BA in chemistry or related field? Exp: 1-2 yrs |
Organizes and conducts routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. | 3/23/2018 |
| 1264 | Crown Bioscience? San Diego, CA Research Associate I - In Vitro BS Exp: 1-3 yrs |
Crown Bioscienceﾠ | 3/23/2018 |
| 1265 | Crown Bioscience? San Diego, CA Research Associate - In Vivo BS Exp: 1-2 yrs |
Crown Bioscience has an immediate opening for a full-time Research Associate in our In Vivo department. We are looking for individuals who are passionate about science, organized and detail oriented, want to work with a team of dedicated researchers, and are ready to significantly contribute to a mission and gain valuable career experience. If that sounds like you, then this is the opportunity for you! | 3/23/2018 |
| 1266 | CSBio? Menlo Park, CA Associate I? BA/BS in chemistry or related disciplines Exp: entry level |
Perform peptide synthesis or purification under close supervision | Assist in se |
| 1267 | CryoLife Kennesaw, GA Regulatory Affairs Specialist BS in Biology or related field Exp: 0-2 yrs |
The Regulatory Affairs Specialist works directly with the Regulatory Affairs Managers and/or Director to assist with regulatory submissions, primarily Tier II country submissions. In addition, the RA Specialist will provide support for country and state licensing activities and assist with responses to the FDA and other regulatory agencies as needed. | 3/23/2018 |
| 1268 | CSL Holly Springs, NC Specialist I/II, QA (Shop Floor) - Night BS Exp: 1 yr |
Perform real time documentation (batch record, logbook, etc.) review concurrent with manufacturing operations on the manufacturing floor. | 3/23/2018 |
| 1269 | CSL Kankakee, IL Quality Assurance Specialist BS/BA Exp: 0-2 yrs |
The primary work functions will be on the production floor, not in an office or laboratory setting. Responsibilities include assisting with investigating deviations relevant to area of responsibility. Responsible for driving continuous improvement on production floor to ensure compliance with cGMPs. Real time review of batch records, including critical processing steps with production floor presence.ﾠA very high level of attention to detail is required. | 3/23/2018 |
| 1270 | CSL Kankakee, IL Scientist I/II MS in chemistry, biochemistry, engineering or equivalent Exp: 0-3 yrs |
Responsible for performing research and laboratory tasks for projects and products in collaboration with internal, external, and global R and D peers. | 3/23/2018 |
| 1271 | CSL Holly Springs, NC Specialist I/II/III, QA (Shop Floor) BS Exp: 0-1 yr |
Perform real time documentation (batch record, logbook, etc.) review concurrent with manufacturing operations on the manufacturing floor. | 3/23/2018 |
| 1272 | CSL Holly Springs, NC Specialist I/II, Manufacturing Quality Systems BS Exp: 1 yr |
Performs deviation investigations for manufacturing using site procedures to ensure root cause is identified and appropriate corrective actions are put in place within 30 business days. | 3/23/2018 |
| 1273 | CSL Kankakee, IL Engineer Packaging BS in Packaging Engineering, Industrial Technology Exp: 1-2 yrs |
Researches, develops, tests, recommends and implements new or revised packaging components and initiates the corresponding component spec. | 3/23/2018 |
| 1274 | Cyprotex US, LLC? Watertown, MA Entry Level Scientist BS/MS Exp: Entry Levelﾠ |
The successful candidate will actively participate in experimental design, performing experiments, and troubleshooting, as well as performing data analysis and interpretation. The ideal candidate will be independent, self-motivated, collaborative and able to multitask effectively while frequently under pressure to meet tight deadlines.ﾠ | 3/23/2018 |
| 1275 | Cytovance? Oklahoma City, OK FACILITIES TECHNICIAN I BS Exp: 0-3 yrs |
Maintain and calibrate process, utility and other unit operations throughout the entire campus.ﾠﾠOperate utility systems throughout the entire campus.ﾠﾠThe Facilities Technician I position is quality-centered and follows company standard operating procedures (SOPs) geared toward FDA and other applicable regulations and in-line with current good manufacturing practices (cGMPs). | 3/23/2018 |
| 1276 | Boehringer Ingelheim Ridgefield, CT Summer Intern Biostatistics and Data Science MS in Bio/statistics Exp: NA |
Utilizes BI SOPs and guidelines, the trial protocol, annotated case report forms, trial and project data handling rules and standards and the Statistical Analyses Plan in preparation for the programming of the Medical Quality Review Plan (MQRP) and the safety tables, listings and graphs (TLG) required for the Clinical Trial Report (CTR).ﾠﾠ Gains specific knowledge about the clinical data collected for the trial. | 3/23/2018 |
| 1277 | Boehringer Ingelheim Fremont, CA Summer Intern - EHS BS/MS Exp: NA |
Provide support with Environmental, Health, Safety and Security programs to ensure regulatory compliance and continuously improve performance | 3/23/2018 |
| 1278 | Boehringer Ingelheim Ridgefield, CT Summer Intern Nonclinical Drug Safety BS/MS Exp: NA |
Mine open literature and other sources for key toxicology data on excipients and impurities | 3/23/2018 |
| 1279 | Corning Keller, TX Process Engineering Intern BS/MS in Mechanical, Electrical or Electromechanical Engineering Exp: NA |
Summer internship with the Corning Optical Connectivity Solutions Division Engineering organization supporting project work in the Regional Engineering group supporting project work within the Cable Assembly development group. The intern will gain experience in connector assembly processes and core processes related to Connectivity. | 3/23/2018 |
| 1280 | Corning Erwin, NY Measurements Engineering Intern BS in engineering or physical sciences Exp: 0-2 yrs |
Internship within a process and measurements engineering organization at a manufacturing site.ﾠ Intern will work with our team to plan, conduct and analyze process improvement and measurement system analysis activities.ﾠ The primary role includes data collection and analysis, as well as process and system improvement activities. | 3/23/2018 |
| 1281 | Corning Corning, NY Project Engineer Intern MS in technical disciplines Exp: NA |
This Intern position is designed to act as a project management and project engineering support in the Display Applications Lab to create compelling demonstrations of the value of Corning glass products for end-user applications in support of new business development and customer engagement. | 3/23/2018 |
| 1282 | Celerion Lincoln, NE Bioanalytical Intern - qPCR BS/MS in Biochemistry, Chemistry, Biology, or equivalent Exp: NA |
You will perform simple analysis of clinical samples from various biological matrices using molecular biology techniques.ﾠThe work in this role will result in an internal presentation / or report at the end of the summer which may be used in a Celerion presentation or publication. | 3/23/2018 |
| 1283 | CSI ?St. Paul, MN Design Assurance Intern BS/MS in Engineering Exp: NA |
TheﾠDesign AssuranceﾠIntern is one who possessesﾠgoodﾠcommunication skillsﾠandﾠdesire toﾠlearn newﾠmethods, tools and their use in a product development effort.ﾠﾠThe candidate will excel in a high energy, fluid environment, with multiple responsibilities.ﾠﾠGeneral knowledge ofﾠengineeringﾠdesign, materials and manufacturing methods as well as the ability to apply this knowledge will be required. | 3/23/2018 |
| 1284 | CSI ?St. Paul, MN Clinical Intern BS/MS Exp: NA |
The Clinical Research internship will provide a degree-seeking student in a Science/Health/Research related field with the opportunity to lead the planning, execution and launch of a Clinical Research project. The Intern will be assigned to a project focused on a Clinical process or system challenge. As part of the internship process, and in collaboration with their manager and mentor, the Intern is responsible for engaging with key stakeholders to understand the identified issue, desired outcome and develop a work plan with key milestones in order to successfully plan and execute the Clinical project. Additionally, during the 12-week internship, the Intern will participate in rotational educational sessions to build their understanding of the three functional areas of the Clinical Research department ﾖ Study Management, Clinical Operations and Scientific Affairs. | 3/23/2018 |
| 1285 | CSI ?St. Paul, MN Process Development Intern BS Exp: NA |
The position will perform process development engineering assignments under supervision of a Senior Engineer. | 3/23/2018 |
| 1286 | Boston Scientific Bloomington, IN Scientist I? BS in Science or Engineering Exp: 0-1 yr |
The Scientist I applies engineering/scientific skills and commitment to quality to execute experiments and complete data analysis in support of projects. This individual will gain knowledge in scientific/engineering concepts, business practices, and core business principles.ﾠ Work will be completed in office and Microbiology laboratory settings. | 3/18/2018 |
| 1287 | Bristol-Myers Squibb? Syracuse?, NY Manufacturing Technology Associate Engineer MS in Chemical, Mechanical or Biochemical Engineering or a related discipline? Exp: 1 yr |
The Manufacturing Technology Associate Engineer will champion process equipment within Manufacturing Operations (upstream and downstream processing, the cryogenics facility, as well as materials management) and will implement process improvements through equipment projects, equipment-related investigations and process equipment strategies to support robustness in manufacturing.ﾠ | 3/18/2018 |
| 1288 | BSN medical Cherokee, AL Process Engineer BS in Mechanical, Electrical, or Industrial Engineering, or other related engineering field Exp: 0-3 yrs |
The position serves as the day-to-day owner of the machine processes and process control systems for the plant. Own and manage the development of troubleshooting skills of the manufacturing professionals. Act as a subject matter expert for the machine processes. Participate and/or lead in Continuous Improvement projects. Help to identify and support projects that will improve productivity, waste, quality and safety performance on a long term basis. | 3/18/2018 |
| 1289 | C. R. Bard? Warwick, RI Associate Regulatory Affairs International Specialist BS Exp: 0-3 yrs |
This position is responsible for writing, supporting, and assisting in gaining approval of product registrations and other submissions to International Business Centers (IBCs). This position entails development of submissions in conjunction with other BDI Surgery departments, requiring working knowledge of products under review and of relevant regulations and guidance documents. | 3/18/2018 |
| 1290 | Caribou Biosciences? Berkeley, CA Animal Technician BS/MS in life sciences Exp: 0-3 yrs |
Caribou is seeking an experienced Animal Technician to join its R&D team at its facility in the Bay Area.ﾠﾠThe candidate must be motivated, enthusiastic, professional and committed to working as a team player.ﾠﾠThe ideal candidate enlists confidence, comfort and a working knowledge of laboratory animals, with a background in animal husbandry, restraint and handling.ﾠﾠIn addition, experience with injection and blood draw techniques, along with rodent surgery and anesthesia experience is desirable.ﾠﾠThe candidate must have the ability to effectively communicate with coworkers, take direction from supervisors, and be accountable for their actions.ﾠﾠThey must possess a strong attention to detail and always strive to perform quality work.ﾠﾠThis is an excellent opportunity to utilize and advance the ideal candidateﾒs laboratory animal skills in a progressive, state-of-the-art and diverse facility. | 3/18/2018 |
| 1291 | Cascadian Therapeutics Seattle, WA Clinical Trials Management Associate I/II/Senior BS Exp: 1-2 yrs |
The Clinical Trials Management Associate (CTMA) assists with overseeing operational aspects of clinical research studies, including vendor oversight, monitoring at select sites, and other logistical operations as required. | 3/18/2018 |
| 1292 | Cato Research Durham, NC Proposals Associate I BS Exp: 0-2 yrs |
Responsible for development of service contract bids and proposals including analyzing competitive and feasibility criteria, contract management from contract planning to award, and results and goal performance reporting to management in relation to corporate mission and goals.ﾠ | 3/18/2018 |
| 1293 | Celgene Warren, NJ Manufacturing Associate, CAR-T BS Exp: 0 yr |
Manufactures human blood derived components per Standard Operating Procedures (SOPs) in a controlled, cGMP cleanroom environment under the supervision of Manufacturing Management. Manufacturing Associates adhere to regulatory requirements while performing job functions. Job duties are performed within a team according to an assigned, production shift schedule. Communication of production deviations and assistance with quality investigations are required, as applicable. | 3/18/2018 |
| 1294 | Celgene Warren, NJ Coordinator, Training & Development CAR-T BS Exp: 1-3 yrs |
The Training & Development Coordinator is responsible for the successful implementation of the site Training Program.ﾠ This position ensures the successful coordination of training activities, including scheduling, ordering, ensuring space availability, etc.ﾠ This position also assists with the development of course content, and helps to facilitate the new hire onboarding program. | 3/18/2018 |
| 1295 | Cell Signaling Technology (CST) Danvers, MA Research Associate - Neuroscience BS/MS in a biological science Exp: 1 yr |
The Research Associate (RA) will support the Neuroscience team in driving product development, including development of both antibodies and other product types, such as kits.ﾠHe/she willﾠserve as a resource for the analysis of antibody specificity along the various stages of development, including assessment of antibody utility for immunoprecipitation and western blotting applications. In addition, team members are expected to continuously evaluate leading edge technologies and techniques, and to sponsor their implementation. | 3/18/2018 |
| 1296 | Cell Signaling Technology (CST) Danvers, MA Research Associate - Immunofluorescence BS in biology or a related discipline Exp: 1 yr |
The successful candidateﾒs primary role in this position will be to ensure batch-to-batch reproducibility between IF-approved materials originating from manufacturing. They will utilize tools such as confocal microscopy and high-throughput imaging to provide internal customers with detailed antibody performance reports. | 3/18/2018 |
| 1297 | Cell Signaling Technology (CST) Danvers, MA Research Associate - VSC BS in biology or a related discipline Exp: 1 yr |
The mission of the Validation Systems Coreﾠ(VSC)ﾠis to provide a single source of well-characterized, high quality cells and lysates to the Product Development organization to enable accelerated product development cycle times.ﾠAdditionally, theﾠVSCﾠserves as a center of innovation for the culture, treatment, lysis, and storage of cell lines. Team members are expected to continuously evaluate leading edge technologies and techniques, and to sponsor their implementationﾠin their work. | 3/18/2018 |
| 1298 | Cell Signaling Technology (CST) Danvers, MA Research Associate - Antibody Development BS/MS in a biological science Exp: 1 yr |
The Research Associate (RA) will support the Epigenetics team in driving product development, including development of both antibodies and other product types, such as kits.ﾠHe/she willﾠserve as a resource for the analysis of antibody specificity along the various stages of development, including assessment of antibody utility for immunoprecipitation and western blotting applications. In addition, team members are expected to continuously evaluate leading edge technologies and techniques, and to sponsor their implementation. | 3/18/2018 |
| 1299 | Cell Signaling Technology (CST) Danvers, MA Research Associate - Cell Biology BS in biology or a related discipline Exp: 1 yr |
We are seeking a highly self-motivated Research Associate to be part of our Antibody Discovery Team in Cell Biology.ﾠﾠThe mission of this dynamic team is to provide a resource for the validation of antibody specificity and sensitivity along the various stages of our development pipeline.ﾠ Responsibilities include the technical execution of SDS-PAGE, western analysis, immunoprecipitation, and dot blot. Applicants must be able to design moderately complex experiments with proper controls and are expected to independently interpret and report results. | 3/18/2018 |
| 1300 | Cell Design Labs (CDL) Emeryville , CA Research Associate, CAR T cell MS Exp: 0-2 yrs |
Contribute to the overall advancement and success of our THROTTLE SwitchTM CAR T research program. | 3/18/2018 |
| 1301 | Cellular Dynamics International (CDI) Madison, WI Formulation Specialist BS in Cell Biology, Molecular Biology, Biochemistry Exp: 1-2 yrs |
Restock and clean lab as needed.Understand basic laboratory concepts and be able to perform basic lab techniques, including routine and preventative maintenance.ﾠ | 3/18/2018 |
| 1302 | Cellular Dynamics International (CDI) Novato, CA Production Specialist? BS in Cell Biology, Molecular Biology, Biochemistry Exp: 1-2 yrs |
Understand basic laboratory concepts and be able to perform basic lab techniques, including aseptic technique for cell culture, medium preparation. | 3/18/2018 |
| 1303 | Corning Corning, NY Thermal Process Engineer BS/MS in chemical, materials, ceramic or mechanical engineering? Exp: 0-5 yrs |
Solve problems and improve processes based on fundamental understanding and structured problem solving methods such as KT, Designed Experimentation, or Six Sigma. | 3/18/2018 |
| 1304 | Corning Painted Post, NY Research Associate, Optical Physics MS in Physics, Chemistry, Material Science, Electrical Engineering Exp: 0 yr |
This position of Research Associate, Optical Physics is in the Micro and Nano Optics (MNO) department of the Science and Technology Division of Corning. MNO combines deep understanding of display and telecommunication systems with fundamental research in structured materials to develop new advantaged optical products. We seek out scientists with experience in optics and materials. The candidate should have a track record of combining experimental results and fundamental understanding to yield new insights about the interaction of optical fields with surface and volumetric structures within glass and ceramics. Our projects are fast-paced, and we expect our scientists to rapidly build up new experimental and modeling capabilities as the need arises. We constantly add to our experimental capabilities, which today include the full range of display system measurements, scattering measurements, waveguide measurements, and various linear and nonlinear spectroscopies. Our product design length scales go from tens of nanometers to tenths of millimeters --- requiring scientists knowledgeable in the variety of modeling techniques required to understand how features of these sizes impact material performance. | 3/18/2018 |
| 1305 | Corning Corning, NY Measurements Engineer BS in Engineering Exp: 1 yr |
Working with a global team of technical experts to develop new technologies for glass substrate manufacturing | develop and |
| 1306 | Corning Hickory, NC Controls Engineer BS in Engineering Exp: 1-3 yrs |
Controls Engineer will analyze user requirements, process design, and mechanical equipment design to create controls architecture for automated systems. | 3/18/2018 |
| 1307 | Corning Wilmington, NC Measurements Systems Engineer BS/MS in Mechanical, Electrical, Mechatronics Engineering, Physics, ECE, Optics Exp: 0-5 yrs |
Measurements Systems engineer is a technically diverse and challenging role that supports the glassmaking process for optical fiber manufacturing. The primary mission is to apply technical knowledge to advance manufacturing capabilities. Project assignments require a broad application of engineering skills with a specific focus on measurements and machine vision. Primary objectives include process improvement, cost reduction, process and raw material optimization, engineered safety improvements, and ensuring manufacturing readiness for new processes. Comprehensive process understanding is an expectation and requirement for success. | 3/18/2018 |
| 1308 | Corning Corning, NY Chemical Process Engineer BS/MS in chemical, materials, ceramic or mechanical engineering Exp: 0-5 yrs |
Improving processes and solving problems based on fundamental understanding gained through the use of the scientific method | 3/18/2018 |
| 1309 | Corning Newton, NC QA/QC Engineer II BS in Engineering Exp: 1-3 yrs |
Apply knowledge of engineering principles and practices to effectively accomplish technical assignments and projects. Make decisions independently based upon sound engineering and scientific methods. Strengthen the Product Quality Architecture within the plant by driving fundamental understanding and continual improvements that positively influence the Quality Management System. | 3/18/2018 |
| 1310 | Charles River? Ashland, OH DART Technical Trainer BS in animal or life sciences or related discipline Exp: 1-3 yrs |
Under general supervision, responsible for providing, coordinating, documenting and scheduling orientation and routine to moderately complex training activities. Also responsible for developing, revising, and implementing the use of training documents including SOPs and processes to support the overall training program. | 3/18/2018 |
| 1311 | Charles River? Skokie, IL Research Assistant I BS Exp: 0-2 yrs |
Responsible for performing basic to moderately complex laboratory work in collaboration with departmental staff. | 3/18/2018 |
| 1312 | Charles River? Reno, NV Research Assistant (Formulations) BS/BA in laboratory science or related discipline Exp: 0-2 yrs |
This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 3/18/2018 |
| 1313 | Charles River? Worcester, MA Associate Scientist BS Exp: 1-3 yrs |
This position will be involved in all aspects of studies supporting the bioanalysis of drug molecules in multiple matrices.ﾠ The position is hands-on, working in close cooperation with and under the guidance of more senior staff members in a fast-paced environment where a commitment to teamwork, quality data and speed is essential. | 3/18/2018 |
| 1314 | Charles River? Reno, NV Research Assistant I (Lab Sciences) BS/BA in laboratory science or related discipline Exp: 0-2 yrs |
This position will be responsible for handling and processing samples, and performing accurate data collection and reporting. Basic methods will be used to perform laboratory tasks with minimal supervision in the performance of studies. | 3/18/2018 |
| 1315 | Champion Oncology, Inc Baltimore, MD Research Technician I & II BS/MS in biology, pharmacology or related field? Exp: 1-3 yrs |
Perform basic laboratory tasks and banking in support of in vivo oncology studies in mice. Maintain and collect data using various systems. Manage studies and perform more advanced technical manipulations such as IV administration. Serve as a mentor for more junior staff. | 3/18/2018 |
| 1316 | Champion Oncology, Inc Rockville, MD Histology Laboratory Technician BS in biology, pharmacology or related field required Exp: 1 yr |
Assist with the Companyﾒs Research & Development program; Assist with the histology laboratory tasks, including the characterization of Tumorgrafts by tissue embedding, sectioning, H&E or IHC staining. | 3/18/2018 |
| 1317 | Champion Oncology, Inc Rockville, MD Vivarium Operations Technician BS degree in veterinary technology, animal sciences, biology, or related field Exp: 0-4 yrs |
Support research studies by providing the highest standard of humane treatment and care of all animals housed within our animal care and use program. | 3/18/2018 |
| 1318 | Ceva Lenexa, KS R&D Technician I BA/BS in Microbiology or Biology or equivalent? Exp: 0-3 yrs |
To assist in the development and licensure of viral, bacterial, recombinant and/or parasitic vaccines as well as new label claims or product improvement research of the licensed vaccines. | 3/18/2018 |
| 1319 | Ceva Lenexa, KS QC Lab Technician I BS in Biology Exp: 1 yr |
Perform titrations, inactivation and identity testing of viruses using embryonated chicken eggs or cell cultures. | 3/18/2018 |
| 1320 | Certara Atlanta, GA Regulatory Writer BS in Scientific discipline Exp: 1-3 yrs |
Participate on project teams that may be led by a Principal Regulatory Writer, Associate Principal Regulatory Writer, or Senior Regulatory Writer; Author documents per client specifications, templates, style guides, and other guidance documents. | 3/18/2018 |
| 1321 | Carl Zeiss Meditec Dublin, CA Intern - Advanced Technology and Concepts MS in Physics, Optics, Electrical Engineering, Mechanical Engineering or similar field Exp: NA |
Work and interact with Engineers and Scientists in Advanced Development and Concept Development | 3/18/2018 |
| 1322 | BTG Seattle, WA Pre-Clinical Student Summer Intern BSMS in bioengineering, biology, or biophysics curriculum or related field Exp: NA |
You will be able to assist in conducting in-vitro laboratory studies of bioefficacy, deliverability, optimization of acoustic protocols, and durability of EKOS products for the development of ultrasound enhanced thrombolysis. | 3/18/2018 |
| 1323 | BTG Seattle, WA Pre-Clinical Student Summer Intern (Matlab)? BS/MS Exp: NA |
You will be able to assist in conducting image processing and data analysis to optimize the performance of EKOS products and product concepts for the ultrasound enhancement of drug delivery in humans. | 3/18/2018 |
| 1324 | Brooks Automation Chelmsford, MA Quality Assurance Engineering Intern BS/MS in Computer Science, Engineering, Management Information Systems or Marketing Exp: NA |
Project #1: QMS Documentation Update | Project #2: L |
| 1325 | Brooks Automation Chelmsford, MA Materials Engineer Intern BS in Materials, Mechanical or Chemical engineering Exp: NA |
Primary intern project will include streamlining an existing tool for calculating gas composition, and make it easier to debug potential contamination issues in the field with cryopumps.ﾠ Tasks include verifying inputs, improving user interface and validating code results.ﾠﾠ | 3/18/2018 |
| 1326 | Takeda San Diego, CA 2018 Summer Internship - Protein Chemistry & Structural Biology? BS in Chemistry, Biochemistry or related field Exp: NA |
Conduct routine biochemical laboratory tasks including buffer and sample preparations | Perform rout |
| 1327 | BioMarin? SAN RAFAEL, CA INTERN, PROTEIN SCIENCES BS in Biochemistry, Structural Biology, Biophysics, Chemical Biology, Bioinformatics, or related discipline Exp: NA |
The candidate summer intern will work in a dynamic research driven environment, in support or early-stage and/or proof-of-concept research projects that hope to one day address serious unmet medical needs. ﾠProjects will be matched with the candidateﾒs skills and interests, but may include efforts centered on protein engineering, design, purification, characterization, and/or computational modelling. | 3/18/2018 |
| 1328 | BioMarin? SAN RAFAEL, CA INTERN, TRANSLATIONAL BIOLOGY BS/MS Exp: NA |
Research summer Intern will work on 1 major project over the 3-month internship. The successful candidate will partner closely with a team of scientists from translational biology, and other functional groups within the Research department at BioMarin. The Intern will primarily be responsible for the implementation and evaluation of disease associated tissue biomarkers by means of histological-based platforms such as immunohistochemistry and in situ hybridization. | 3/18/2018 |
| 1329 | BIOTRONIK Field Service?, Fi Field Clinical Specialist Internship BS in Biomedical Engineering or Biology. Exp: NA |
The FCS Intern acts as the technical support person for BIOTRONIK sales representatives and is responsible for covering all bradycardia and tachycardia product segments. The FCS Internﾠprofessionally represents BIOTRONIK and provides education, implantation services, follow-up services,ﾠin-service training, and other related services as necessary to physicians and patients in clinical settings, as well as to the sales force and other cardiac pacing-related professionals. | 3/18/2018 |
| 1330 | Bio-Techne Minneapolis, MN Cell Culture Media Internship BS Exp: NA |
The summer intern is expected to have a basic understanding of cell physiology and biology, media composition, cell culture processes and recombinant protein expression technology. She or he will conduct experiments under various cell culture conditions and perform various protein assays including western blot to evaluate various media components. The Summer Intern will be guided by a motivated team of scientists and research associates and responsible for analyzing data and providing both a written summary and a PowerPoint presentation after the summer project. | 3/18/2018 |
| 1331 | BioLegend San Diego, CA Quality Control Associate - Cell Separation BS in Immunology, Cell Biology, or a related Life Science area Exp: 1 yr |
BioLegend is seeking a highly motivated Quality Control Associate to join our Research and Product Development Team. This position will work under minimal guidance to perform quality control testing in a fast-paced, goal-orientated environment. The responsibilities include, but are not limited to, performing assays using a variety of approaches such as primary cell preparation, cell separation, immunofluorescent staining, and flow cytometry (FACS) data analysis, performing experiments (e.g. cell preparation, cell separation and flow cytometry testing), analysis and reporting of data, maintaining accurate documentation, using internal company databases for product filing and retrieval, and following company SOPs and ISO requirements. | 3/10/2018 |
| 1332 | BioLegend San Diego, CA Quality Control Associate (Cell Biology) MS in Biochemistry, Molecular Biology, or a related Biological Sciences area Exp: 0 yr |
The Quality Control Associate will function as an integral member of the Cell Biology-Quality Control group within the Molecular Immunology department. The primary job functions for this position include polyclonal and monoclonal antibodies and associate products, polyclonal antibody purification, affinity gel products manufacturing, and troubleshooting and communicating with supervisors regarding any quality control or manufacturing related problems, and keeping all documentations up to date. | 3/10/2018 |
| 1333 | BioLegend San Diego, CA Purification Associate BS in Biology, Biochemistry, Chemistry, or Science Exp: 1 yr |
This position is an individual contributor role within the Product Development team and will responsible for performing all essential functions related to antibody purification such as following procedures, optimizing processes, troubleshooting problematic results, performing buffer preparation, pre- and post-purification sample preparation, and database entry. This position is an individual contributor role within the Product Development team and will responsible for performing all essential functions related to antibody purification such as following procedures, optimizing processes, troubleshooting problematic results, performing buffer preparation, pre- and post-purification sample preparation, and database entry. This position is an individual contributor role within the Product Development team and will responsible for performing all essential functions related to antibody purification such as following procedures, optimizing processes, troubleshooting problematic results, performing buffer preparation, pre- and post-purification sample preparation, and database entry. | 3/10/2018 |
| 1334 | BioLegend San Diego, CA Research Associate-Cell Biology BS Exp: 1 yr |
The Research Associate position in Cell Biology group will support the development of new antibody and ancillary products. This position will play an integral role in antibody characterization for applications such as Western Blotting, immunofluorescence staining, immunoprecipitation, and Chromatin immunoprecipitation. | 3/10/2018 |
| 1335 | BioLegend Dedham, MA Regulatory Affairs Associate (Boston) BS Exp: 1 yr |
The Regulatory Affairs Associate will work with BioLegend's existing Quality Team to assist with meeting FDA requirements for class I medical devices, (IVD and ASR), and International In Vitro Diagnostic Medical Devices Directives. The RA Associate is also responsible for ensuring that products and their labeling meet all regulatory requirements (national and international). | 3/10/2018 |
| 1336 | BioLegend San Diego, CA Manufacturing Associate (Chemistry) BS in chemistry, biochemistry, material science or related field Exp: 1 yr |
This position will work in magnetic cell separation production team to manufacture magnetic nanoparticles and nanoparticle-biomolecule conjugates. Other duties will include maintenance of laboratory instruments, lab supplies, buffer preparations and cleaning glassware. | 3/10/2018 |
| 1337 | Bio-Techne Minneapolis, MN Research Associate 1 ?BS/MS in Biology, Biotechnology, Biochemistry? Exp: 0-2 yrs |
The primary responsibilities of this position are building custom Luminex kits to order for customers and preparing these kits for packaging. Perform additional duties as assigned. | 3/10/2018 |
| 1338 | Bio-Techne Minneapolis, MN Technical Service Associate BS in Biological Sciences, Biochemistry or equivalent Exp: 0-5 yrs |
The responsibilities of this position are to respond to incoming technical inquiries to provide first tier technical and sales assistance on all Bio-Techne reagent brands. Complete all customer requests including, e-mail responses and simple quotes. Maintain technical resources. Back up customer service department and keep up to date on technical information for old and new products. Perform additional duties as assigned. | 3/10/2018 |
| 1339 | BIOTRONIK US-Field Service, US Field Vascular Intervention Specialist 1 BS in health profession, science or engineering field preferred Exp: entry level |
The Field Vascular Intervention Specialist I is an entry level position that provides field support for the sales team and clinical studies for coronary products, including product-specific and clinical protocol training, data collection and device implant participation.ﾠ The ability to make recommendations necessary to promote medical acceptance of the vascular intervention products and to be the field technical expert on the devices are a required asset. | 3/10/2018 |
| 1340 | bluebird bio Cambridge, MA Associate Scientist, Genomics and Molecular Biology MS in molecular biology, cell biology, or related discipline Exp: 1 yr |
The new Sr. Associate Scientist will develop and support Next-Generation Sequencing-based assays to evaluate gene-editing based therapeutics for clinical applications. The new hire will also contribute to immunotherapy and hematopoietic stem cell (HSC) platforms. | 3/10/2018 |
| 1341 | bluebird bio Cambridge, MA Associate Scientist, Downstream Lentiviral Vector Process Development MS in Chemical Engineering, Biochemistry, Bioengineering, Molecular Biology, or related field preferred Exp: 0-2 yrs |
The candidate will have the opportunity participate in development, scale-up, and manufacturing. We seek candidates with proven ability to successfully work independently and collaboratively across functions to meet aggressive project timelines, with the ultimate goal to deliver therapies that transform the lives of patients. | 3/10/2018 |
| 1342 | bluebird bio Cambridge, MA Quality Control Specialist - Method Validation (Contract Role) BS,preferably in the biological sciences Exp: 0-2 yrs |
ﾠThe candidate will interface with the internal Quality Control GMP Testing Lab, Process and Analytical Development groups, and Supply Chain for the maintenance and shipping of critical reagents and critical test articles. A strong technical background in cell biology, biochemistry, and/or molecular biology will be utilized in the role. This position may require hands on laboratory. | 3/10/2018 |
| 1343 | bluebird bio Cambridge, MA Lab Technician, Upstream Process Development (Contractor) BS in (bio)chemical engineering or biological sciences Exp: 1-2 yrs |
Aid in performing general lab maintenance activities including material inventory management, tubing/labware preparation and autoclaving, as well as overall lab cleanliness. | 3/10/2018 |
| 1344 | Blueprint Medicines Cambridge, MA Scientist I, Computational Biology BS/MS Exp: 1 yr |
The ideal candidate will lead target identification effort using internal and external datasets, as well as support scientific computation and bioinformatics effort from early target discovery, optimization to late stage translational medicine investigation. This will be an exciting opportunity to be involved in various stages of the drug discovery process using your computational and analytical skills, and working in an innovative, motivating and collaborative environment. | 3/10/2018 |
| 1345 | Boehringer Ingelheim Fremont, CA MFG Associate, Upstream - Swing BS Exp: 1 yr |
Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures.ﾠﾠﾠﾠﾠ | 3/10/2018 |
| 1346 | Boehringer Ingelheim Fremont, CA MFG Associate, Downstream - Swing BS Exp: 1 yr |
Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures.ﾠﾠﾠﾠﾠ | 3/10/2018 |
| 1347 | Boehringer Ingelheim Fremont, CA MFG Associate, Downstream - Days BS Exp: 1 yr |
Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures.ﾠﾠﾠﾠﾠ | 3/10/2018 |
| 1348 | Boehringer Ingelheim Fremont, CA MFG Associate, Upstream - Days BS Exp: 1 yr |
Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures.ﾠﾠﾠﾠﾠ | 3/10/2018 |
| 1349 | Boehringer Ingelheim Fremont, CA Mfg Staging Technician - Downstream BS Exp: 1 yr |
Executes routine unit operations in Downstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures.ﾠﾠﾠﾠﾠ | 3/10/2018 |
| 1350 | Boehringer Ingelheim Fremont, CA Associate, Mfg Cell Culture BS in a science or engineering field Exp: 0 yr |
Executes routine unit operations in Cell Culture or Purification as assigned related to the manufacturing of bulk drug substance in a multi-product facility. This may include tank or bioreactor CIP/SIP, cell inoculation and transfer, harvest, chromatography, and tangential flow filtration. Performs duties under limited supervision and according to standard operating and manufacturing procedures. | 3/10/2018 |
| 1351 | Boston Analytical? Salem, NH QA Specialist BS Exp: 0-3 yrs |
The Quality Assurance Specialist supports the QA Lead and the companyﾒs quality program by auditing chemists analytical data, routine work, protocols and reports. | 3/10/2018 |
| 1352 | Boston Scientific Marlboro, MA Engineer II, R&D MS Exp: 0-3 yrs |
Consistently generates innovative and unique solutions to market needs and submits idea disclosures.ﾠ Work is expected to result in the development of new or refined products, processes or equipment. | 3/10/2018 |
| 1353 | Boston Scientific Maple Grove, MN Process Engineer II MS in Engineering. Exp: 0-2 yrs |
Boston Scientific is seeking a highly motivated and experienced engineer with expertise in new product development to lead the design and commercialization of new cutting edge technology.ﾠ | 3/10/2018 |
| 1354 | Boston Scientific Maple Grove, MN Process Engineer I? BS in Engineering (Chemical, Mechanical, Biomedical, Plastics, or equivalent) Exp: 0-2 yrs |
The polymers engineering position offers the opportunity to work on a wide variety of technically challenging projects that span across all of Boston Scientific, touching every franchise and site within the BSC network.ﾠ As an engineer within the team, you will be looked to as a key contributor in the exploratory development and ultimately the commercialization of various projects.ﾠ On top of the workhorse support, direct engagement in prototyping and exploratory efforts will allow you to take a concept and make it reality, with the support of a technically strong, experienced, and highly motived team. | 3/10/2018 |
| 1355 | Boston Scientific Maple Grove, MN Quality Engineer II? MS Exp: 0 yr |
Quality Engineer II who is responsible for the direct support of medical device manufacturing lines, specifically within the Core Tech Polymers production area at the Maple Grove site. This includes driving continuous improvement in product quality and compliance, managing the control of non-conformances, and being a key partner to the Production and Manufacturing Engineering teams. | 3/10/2018 |
| 1356 | Boston Scientific Maple Grove, MN Product Analyst I BS/MS Exp: 6 months |
Analyzes customer complaints to determine which are regulatory reportable and coordinates activities with internal, field, and end use customers.ﾠ Responsible for adherence to Good Manufacturing Practices (GMPs) and proper complaint handling per the Code of Federal Register (CFR) and other governmental regulations.ﾠ Communicates event investigation results via regulatory reports and written communications, as appropriate. | 3/10/2018 |
| 1357 | Boston Scientific Marlboro, MA R&D Engineer I BS in?Mechanical or Biomedical Engineering, or related technical field Exp: 0-1 yr |
The R&D Engineer I will developﾠproducts, materials, processes, or equipment for complex systems under limited supervision/guidance. You will compile, analyze, and report operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials. | 3/10/2018 |
| 1358 | Brammer Bio, LLC Alachua, FL Scientist - Upstream Process Development BS Exp: 1 yr |
The Biological Scientist will support the Upstream Process Development (PD) activities to ensure that Brammer Bioprovides clients with processes capable of manufacturing new investigational materials for clinical use. The incumbent will maintain various mammalian and insect cell lines for multiple projects and scale up culture, as needed, for recombinant vectors and protein production or for the production of non-GMP toxicological lots. The incumbent will be involved in the production and testing of research cell banks (RCB) and research viral banks (RVB) as well as the production of recombinant proteins and viral gene transfer vectors at large scale using bioreactors. Functions will also involve transfection of mammalian and insect cells; viral vector cloning and screening; single cell cloning and screening; media and cell line development. | 3/10/2018 |
| 1359 | Brammer Bio, LLC Alachua, FL EHS Specialist? BS in Environmental Engineering, Safety Science Exp: 1 yr |
Perform weekly site safety/environmental inspections noting potential deficiencies and areas for improvement. Then working with the appropriate parties to identify address the root cause and correct any areas of concern. | 3/10/2018 |
| 1360 | Brammer Bio, LLC Cambridge, MA Scientist Manufacturing Sciences MS in biochemical engineering, chemical engineering, biological sciences, , or biochemistry, manufacturing sciences Exp: 1-3 yrs |
The primary responsibility is to support technology transfer teams for the late stage and commercial manufacturing of viral vectors.ﾠ | 3/10/2018 |
| 1361 | Brammer Bio, LLC Cambridge, MA Technician II, Instrumentation & Controls BS Exp: 1 yr |
The Technician III, Instrumentation & Controls is responsible for supporting Brammer Bio facilities in Cambridge, MA with a scope encompassing building and utility systems for GMP manufacturing, process development, quality control, and warehouse operations. Will perform planned and unplanned calibrations and repairs of instrumentation and laboratory equipment. Will respond to instrumentation and equipment related issues that arise during facility operations. Will create and maintain relationships with other sites to develop and promote best practices. Will uphold, define, and police safety procedures and safe work practices. Will ensure work performed is in compliance with cGMP regulations and Brammer Bioﾒs SOPs. Will work closely with Manufacturing, Manufacturing Sciences, Quality Assurance, Quality Control, and other Engineering teams to complete all responsibilities. | 3/10/2018 |
| 1362 | Brammer Bio, LLC Cambridge, MA QA Associate 3 BS in biology, microbiology, chemistry, biotechnology Exp: 1-2 yrs |
Responsible for contributing to key functional, tactical, and operational aspects of Brammer Bio operations at the Cambridge site. This includes approval & oversight of MFG and QC activities associated with exceptions, CAPA, deviations, Analytical instrument validation, change control requests, and other documentation related to Mfg and QA operations. Responsible for evaluating impact, ensuring adherence to compliance standards, including technical ability to evaluate & approve these quality system elements, as delegated by management. Proficiency in project management, processes, improvement and ability to address through risk assessment. The able to work effectively, independently and within a team framework, across all business areas and levels of the organization is a requirement for this position. Excellent written & verbal communication skills. Mature leadership approach and understanding of their personal communication style and able to manage that effectively. | 3/10/2018 |
| 1363 | Brammer Bio, LLC Cambridge, MA Associate - Molecular, Quality Control BS in Life Sciences Exp: 1-3 yrs |
This position will work in the GMP compliant QC Laboratories to qualify, and conduct cell-based, nucleic acid-based, protein-based, and chemistry-based assays that support quality control of biopharmaceutical products being developed and manufactured. Will perform routine assays and testing including PCR, real time PCR, agarose gel electrophoresis, SDS-PAGE, immuno blotting, ELISAs, immunocytochemistry, and infectivity and reporter gene based cell assays using insect or mammalian cell lines. Functions also involve maintenance of cell lines used in the QC laboratories, maintenance (routine and preventive operation) of equipment, and preparation and purification of commonly used biological reagent and chemical supplies. The incumbent will be expected to technically interpret, write controlled documents and reports, and review data produced by self and participate in laboratory investigations. Will interact with other departments to ensure that sample flow, supply chain, and equipment disposition are correctly maintained. | 3/10/2018 |
| 1364 | Bristol-Myers Squibb? New Brunswick?, NJ Associate Biological Technician Level ? H24 BS Exp: 0-2 yrs |
This position in Toxicology Operations is crucial for the support of the portfolio by co-ordinating successful conduct of toxicology studies in DSE, NBR. The Biological Technician group is at a critical mass due to the departure of a Biotechnician and not filling this position will critically impact productivity, result in gaps in compliance and portfolio support. | 3/10/2018 |
| 1365 | Bristol-Myers Squibb? New Brunswick?, NJ R&D Associate Research Scientist MS in biological sciences or the equivalent Exp: 0-1 yr |
Perform necropsy on rodent and non-rodent animals.ﾠ Trim, fix, process, embed, microtome, and stain tissue specimens | 3/10/2018 |
| 1366 | BIOGEN Cambridge, MA Intern - Cell Culture BS in Biomolecular Engineering, Cell Biology, Biochemistry or a related field. Exp: NA |
We are seeking motivated and creative individuals to join our cell line technology team. As part of this team, the successful candidate will contribute to ongoing efforts to engineer mammalian cells using molecular biology for viral vector production. | 3/10/2018 |
| 1367 | Bio-Rad? Richmond, CA Intern - Chemical Engineer BS in Chemical Engineering Exp: NA |
Organize all plant P&IDﾒs. Conduct field inspections to compare field installation with drawings, red line the drawings and update electronic copies to reflect current installation. | 3/10/2018 |
| 1368 | Bio-Rad? Hercules, CA Intern - Chemist BS Exp: NA |
The intern will work on a short project aimed at solving problem relating to customer complaint. | 3/10/2018 |
| 1369 | BioMarin SAN RAFAEL, CA INTERN, MEDICAL AFFAIRS OPERATIONS BA/BS Exp: NA |
Medical Affairs Operations summer Intern will work on 1 major project and 1-2 minor projects over the 3-month internship.ﾠ Projects will be matched with the candidateﾒs skills and interests.ﾠ Projects may include developing data and reporting tools for selected Medical Affairs subject areas to support business process effectiveness and decision support.ﾠ For example:ﾠ KOL identification and management, Medical Affairs expenses and performance to budget, Medical Affairs department roster and territory management, and/or Medical Affairs systems and processes. | 3/10/2018 |
| 1370 | BioMarin SAN RAFAEL, CA INTERN, REGULATORY CMC BS Exp: NA |
The intern will work closely with a talented team ofﾠregulatory professionals,ﾠas well as cross-functional members, to understand the regulatory requirementsﾠnecessary to maintain commercially licensed enzyme replacement therapy products on a global scale.ﾠ The intern will gain valuable experience with international regulatory requirements and lifecycle management. | 3/10/2018 |
| 1371 | BioMarin SAN RAFAEL, CA INTERN, CELLULAR & MOLECULAR BIOLOGY BS/MS in Life Sciences, Biochemistry, Chemistry, Organic Chemistry Exp: NA |
Summer Research Internﾠwill work on 1 major projectﾠover the 3-month internship. This project will support a program within the research pipeline and involve LC/MS based assays, organic chemistry, biochemistry and data analysis | 3/10/2018 |
| 1372 | BD San Jose, CA Summer Intern - International Regulatory Affairs Specialist BS/MS in Biomedical, Biology, and Biochemistry. Exp: NA |
Interns will work with Regulatory team to prepare and document regulatory submissions for government agencies. Projects available span from registration in Greater Asia, Latin America & EMEA. Projects will span approximately three months depending candidate availability and responsibilities will be matched to the candidateﾒs experience and skill sets. | 3/10/2018 |
| 1373 | Bio-Techne Minneapolis, MN New Technologies Luminex Internship BS Exp: NA |
ﾠThe intern will perform cell culture to prepare relevant samples from established in vitro human cancer models and source cancer patient samples representing the same cancers. The intern will learn the Luminexﾮ multiplex assay technology by building their own assay as well as using existing products to test their samples. The intern will also learn to perform Western blotting and ELISA. | 3/10/2018 |
| 1374 | Bio-Techne Minneapolis, MN Protein Development Internship BS Exp: NA |
The intern will work with scientists in the Molecular Biology Department to develop new genetically altered cell lines to produce recombinant protein products. The intern will be exposed to gene cloning, cell culture techniques, plasmid transfections, transgenic cell line creation, fluorescence microscopy, and the design of novel cellular biological assays. | 3/10/2018 |
| 1375 | Bio-Techne Minneapolis, MN Stem Cell Internship BS Exp: NA |
Project Title: Culture Optimization of Adult Tissue-Specific Stem Cells | The intern fo |
| 1376 | Beckman Coulter Chaska, MN Technical Support Engineer I BS in electronics, bio-medical engineering, chemistry, medical technology Exp: 0-2 yrs |
The Technical Support Engineer I repairs and maintains internal Access 2 and DxI systems in Chaska. May also assist with the initiation, design, development and implementation of product improvements and changes. This position may also provide real time technical support to US field service engineers and Call Center personnel. | 3/2/2018 |
| 1377 | Beckman Coulter Hauppauge, NY Manufacturing Engineer BS in Chemical, Manufacturing, Mechanical, or Biomedical Engineering Exp: 0-6 months |
Supports the day to day manufacturing operations for Intercompany media, surface treatment processes or BioPharm in a Continuous Improvement environment. | 3/2/2018 |
| 1378 | Beckman Coulter Chaska, MN Manufacturing Engineer I BS in Mechanical, Industrial or Manufacturing Engineering Exp: 1 yr |
The Manufacturing Engineering position makes continuous improvements to manufacturing quality, cost and delivery for our customers in the Immunoassay diagnostic markets. This individual will be part of a highly engaged and capable manufacturing team focused on developing the best-in-class instrument manufacturing systems. The right candidate will be responsible for the following. | 3/2/2018 |
| 1379 | Baxter Marion, NC Quality Lab Assoc III-Chem MS in Chemistry or biological science Exp: 1-4 yrs |
Conduct biological, chemical and physical analyses on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at Baxter manufacturing facility. | 3/2/2018 |
| 1380 | Baxter Marion, NC Quality Lab Assoc. Micro-EM BS in Microbiology, or Biological Science Exp: 0-2 yrs |
Conduct microbiological analyses on raw materials, in-process and finished products. Collect samples related to Environmental Monitoring program at Baxter manufacturing area. | 3/2/2018 |
| 1381 | BioLegend San Diego, CA Production Associate - Recombinant Protein BS in Biochemistry, Molecular Biology or a related Biological Science area Exp: 6 months |
The Production Associate will an integral part of BioLegend's Recombinant Protein routing and will be responsible for performing routine cell culture, protein production, and raw material preparation in manufacturing scale and inventory maintenance. This position will also function as a member of the Molecular Cellular Immunology team to assist with intergroup tasks. | 3/2/2018 |
| 1382 | BioLegend San Diego, CA Manufacturing Assistant -Legendplex BS in Biology, Chemistry, or other relevant discipline Exp: 1 yr |
The Manufacturing Associate will be an important member of a fast growing team that will support kit production to ensure the success of the team. This is a great opportunity to enhance your knowledge and gain experience in a highly competitive biotechnology industry. | 3/2/2018 |
| 1383 | BioLegend Dedham, MA Regulatory Affairs Associate BS Exp: 1 yr |
The Regulatory Affairs Associate will work with BioLegend's existing Quality Team to assist with meeting FDA requirements for class I medical devices, (IVD and ASR), and International In Vitro Diagnostic Medical Devices Directives. The RA Associate is also responsible for ensuring that products and their labeling meet all regulatory requirements (national and international). | 3/2/2018 |
| 1384 | BioLegend San Diego, CA Research Associate (Chemistry) BS in Biochemistry, Bio-Organic Chemistry, Chemistry or Science Exp: 1 yr |
The Research Associate is part of the development team responsible for developing new immunology research reagents. The responsibilities for this position involve exploring new technology and developing new methods under the guidance of research scientists. The position will also support the antibody manufacturing teams by troubleshooting and optimizing processes for continuous improvement. | 3/2/2018 |
| 1385 | BioLegend San Diego, CA Manufacturing Associate (Finished Goods/Bulk Processing BA/BS in Biology, Biochemistry or related field Exp: 6 months |
The Manufacturing Associate will be an important member of our Finished Goods Inventory/Bulk Inventory team that supplies purified bulk antibodies for finished goods and custom bulk orders. This position will be responsible for performing all essential functions related to FGI and bulk antibody processing, including verifying specifications and sales order information, reviewing available inventory, adjusting concentration, performing buffer exchange if necessary and endotoxin assays. These materials will support customers in the areas of Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. This position will also interact with external groups including Planning, Bottling, Customer Service, Marketing and Internal Sales. This is a great opportunity to enhance your knowledge in the biotechnology industry. | 3/2/2018 |
| 1386 | BioLegend San Diego, CA Research Associate Cell Analysis BS in a Life Sciences related field Exp: 1 yr |
This position will actively participate in all stages of the development, optimization and validation of new products, including antibodies, proteins, and other probes for various research fields. The primary responsibilities include performing experiments (e.g. cell culture and flow cytometry), analyzing and reporting data, maintaining accurate documentations, etc. | 3/2/2018 |
| 1387 | BioLegend San Diego, CA Tissue Culture Associate BS in a Life Sciences related field Exp: 1 yr |
The Tissue Culture Associate position will be responsible for handling hybridoma lines in preparation for potential manufacturing activities. Functions will include culturing, subcloning, small-scale and large-scale production runs, banking, performing characterization assays, adaptations of cells to different media and/or conditions, and decontamination of cell lines as needed. All performed work will be documented in lab notebooks, controlled forms, and databases. This position is expected to work independently and in a team environment under established safety guidelines. Communication with various department representatives is expected with emails and meetings. | 3/2/2018 |
| 1388 | BiopharmX Menlo Park, CA RESEARCH ASSOCIATE BS/BA/MS in Cell Biology or related field Exp: 1-2 yrs |
The employee will be responsible for the scientific/technical aspects of assigned preclinical studies, including animal handling, cell culture, general biochemical techniques, such as western blotting and ELISA. The position's primary purpose is to assist the preclinical team with planning and execution of in vitro and in vivo experiments. | 3/2/2018 |
| 1389 | Bio-Rad Pleasanton, CA Research Assoc II (In Vitro Diagnostics Development) MS in molecular biology, biochemistry, cell biology or related life science field Exp: 0-2 yrs |
You will work in an assay development team on development of new in vitro diagnostic (IVD) tests for oncology using state-of-the-art droplet digital PCR (ddPCR) technology, in a multi-disciplinary department that includes assay research and development scientists, hardware engineers and software engineers. | 3/2/2018 |
| 1390 | Bio-Rad Pleasanton, CA Research Assoc I - Temp BS/MS in molecular biology, biochemistry or related fields. Exp: 1-2 yrs |
Verification and Validation of droplet digital biology products, including but not limited to assays, reagents, consumables, instruments and software. | 3/2/2018 |
| 1391 | Bio-Rad Hercules, CA Chemist II (Bio-Plex) BS in Life Sciences, Biology, Biochemistry or related field. Exp: 1-3 yrs |
Work in a team based environment to make in-process and final products as stated in the production documents. | 3/2/2018 |
| 1392 | Bio-Rad Pleasanton, CA Research Assoc II (In Vitro Diagnostics Development) MS in molecular biology, biochemistry, cell biology or related life science field Exp: 0-2 yrs |
You will work in an assay development team on development of new in vitro diagnostic (IVD) tests for oncology using state-of-the-art droplet digital PCR (ddPCR) technology, in a multi-disciplinary department that includes assay research and development scientists, hardware engineers and software engineers | 3/2/2018 |
| 1393 | Bio-Rad Hercules, CA Chemist I (Quality Control) BS/BA in Biology, Cell Biology, Micro Biology, Biochemistry Exp: 0-2 yrs |
Work in a team based environment to perform routine Precast QC assays on raw materials, in process and final products. | 3/2/2018 |
| 1394 | Bio-Rad Hercules, CA Chemist II (Quality Control) BS/BA in Biology, Cell Biology, Micro Biology, Biochemistry Exp: 0-2 yrs |
Work in a team based environment to perform routine Bio-Plex QC assays on raw materials, in process and final products. | 3/2/2018 |
| 1395 | Bio-Rad Richmond, CA Chemist II BS in an laboratory applicable field, preferably chemistry Exp: 1-2 yrs |
Perform Routine Quality Control Assays in accordance of approved Procedures; Compile data, analyze and summarize results; Troubleshoot assays, as required. | 3/2/2018 |
| 1396 | Biorasi Aventura, FL Clinical Trial Assistant BS in biomedical sciences or related scientific discipline Exp: 1-2 yrs |
Support Clinical Trial Manager (CTM) in preparing and/or reviewing study-related documents (e.g., Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, and CRF Completion Guidelines). | 3/2/2018 |
| 1397 | Bio-Techne Minneapolis, MN Manufacturing Associate BS in biochemistry, chemistry, biology, microbiology Exp: 0-2 yrs |
The responsibilities of this position are to process retail bottling of antibodies and proteins | capping and |
| 1398 | Bio-Techne Minneapolis, MN Research Associate 1 BS in Biology, Biochemistry, Cell Biology, Chemistry or related Biological Science Exp: 0-2 yrs |
The major responsibilities for this position involve generating correlative data for the ELISA assay by a variety of methods. Primary duties include running SDS-PAGE gels, electrophoretic transfer and performing Western blots. Additional duties may include mammalian cell culture, performing immunoprecipitations and running various kinds of assays. | 3/2/2018 |
| 1399 | Bio-Techne San Marcos, CA Manufacturing Chemist I BS in Chemistry, Biochemistry, Biological Science, or related field Exp: 0-2 yrs |
Responsible for processing and formulation of controls, calibrators, working solutions, and intermediates according to approved standard operating procedures. Responsible for manufacturing quality products on schedule. General knowledge and basic application of concepts, theories, terminology and practices that apply to manufacturing in a laboratory environment. | 3/2/2018 |
| 1400 | Bio-Techne Minneapolis, MN QC Laboratory Technician BS in Medical Technology or related Exp: 1 yr |
The responsibilities of this position are to test hematology products for homogeneity and fresh whole blood samples by following established methods. Set up, operate, calibrate, and maintain instruments. Monitor instrument performance and troubleshoot the instrument when necessary. QC the product on 50% of the lab instruments. Assist the QC Lab Manager with releasing products to bottle and ship, writing procedures, proofing labels, proofing assay sheets, and proofing instruction sheets. This position will include duties in the Assay Office interpreting data. This position will also attend scheduled meetings and adhere to safety regulations. Perform additional duties as assigned. | 3/2/2018 |
| 1401 | Bio-Techne Minneapolis, MN Antibody Development Internship BS Exp: NA |
The intern for this project will develop antibody-coated beads, prepare primary cells, activate cells in vitro, and analyze protein expression by flow cytometry. The major techniques used will include, but are not limited to, primary cell preparation, cell culture, and flow cytometry. This is an excellent opportunity for a student to gain exposure to both a scientific and industrial setting, and to provide beneficial technical support to the team in the laboratory. The intern will be expected to give a formal presentation on her or his work after the summer project. | 3/2/2018 |
| 1402 | Bio-Techne Minneapolis, MN Cell Culture Development Internship BS/MS Exp: NA |
This position is responsible for optimization of recombinant protein expression methods in the Cell Culture Development department. This will include either E. coli or insect cell/baculovirus-based expression systems. | 3/2/2018 |
| 1403 | Brooks Automation Chelmsford, MA Manufacturing Engineer Intern BS/MS Exp: NA |
Design, proto type, and procure production quantities of test fixtures, ProE; Complete new cart of Robots transfers for arm installed. | 3/2/2018 |
| 1404 | Brooks Automation Chelmsford, MA Quality Assurance Engineering Intern BS in Computer Science, Engineering, Management Information Systems or Marketing Exp: NA |
Project #1: QMS Documentation Update | Project #2: |
| 1405 | Brooks Automation Chelmsford, MA Materials Engineer Intern BS in Materials, Mechanical or Chemical engineering Exp: NA |
Primary intern project will include streamlining an existing tool for calculating gas composition, and make it easier to debug potential contamination issues in the field with cryopumps. Tasks include verifying inputs, improving user interface and validating code results. | 3/2/2018 |
| 1406 | Bio-Rad Hercules, CA Intern - Engineering BS in Engineering Exp: NA |
As part of this internship, you will be supporting our Manufacturing Engineering team by participating in the engineering design and execution of automated labeling and crimping devices to support our production needs. | 3/2/2018 |
| 1407 | Bio-Rad Irvine, CA R&D Intern BS/MS Exp: NA |
Assist in Hematology laboratory with formulation, running hematology instrumentation, inputting stability data | 3/2/2018 |
| 1408 | Bio-Rad Hercules, CA Intern - Supplier Quality Engineer BS in Engineering or related Science Exp: 1-3 yrs |
Collaborate with various stake-holders (Site Buyers and MFG Engineering, Global Commodity Management, R&D Engineering, and other peer stake-holders) to understand the suppliers, commodity, and other issues and concerns. | 3/2/2018 |
| 1409 | BioMarin SAN RAFAEL, CA INTERN, TRANSLATIONAL BIOLOGY BA/BS?MS in Biochemistry, Molecular Biology, or Genetics Exp: NA |
The successful candidate will partner closely with a team of scientists from translation biology, and other functional groups within BioMarin. He/She will primarily be responsible for executing in vitro, and ex vivo studies to assess pharmacokinetics, efficacy, biomarker, and mechanism of action of potential therapeutics to treat rare genetic diseases. | 3/2/2018 |
| 1410 | BioMarin SAN RAFAEL, CA INTERN, MEDICAL COMMUNICATIONS BS/MS Exp: NA |
The Medical Communications Summer Intern will assist in a number of projects focused on the dissemination of scientific and clinical data to healthcare providers at Scientific Congresses and Symposiums and in peer reviewed published journals. This position will assist the Global Medical Communication team in Medical Affairs within the Development Sciences group. Key functions include assistance with execution of publication development activities, conduction of systematic literature reviews, and development of key congress materials. Time management skills, attention to detail and learning to master complex software are skills acquired during this training. | 3/2/2018 |
| 1411 | BioMarin BRISBANE, CA INTERN, BIOMETRICS MS in Biostatistics, Computer Science, or Life Science Exp: NA |
BioMetrics (BMT) summer intern will work on 1 major project and/or 2 minor projects over the 3-month internship. All projects will involve graph generation, which may include (1) graph enhancement project; (2) data visualization project using R-Shiny; (3) dashboard generation project. | 3/2/2018 |
| 1412 | Takeda San Diego, CA Intern - CNS Biology BS Exp: NA |
The CNS intern will work under the guidance and mentorship of CNS biology experts to support the progression of early drug discovery targets and assist in validating the target for program readiness. | 3/2/2018 |
| 1413 | Takeda San Diego, CA Intern - BioTransformation (DMPK)- (San Diego, CA) BS in chemistry, medicinal chemistry, biochemistry or a related field Exp: NA |
Assists in the conduct of in vitro and in vivo drug metabolism studies designed to understand biotransformation pathways/routes of elimination of small molecules to guide synthetic efforts and to identify potentially active/reactive metabolites/fragments. | 3/2/2018 |
| 1414 | Takeda Cambridge, MA Summer 2018 Internship - Commercial Quality Assurance BS/MS Exp: NA |
Takeda's summer internship program blends real world experience with an extensive overview of the pharmaceutical industry. Knowledgeable mentors will provide guidance as you gain professional hands-on experience. The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 3/2/2018 |
| 1415 | BD Tempe, AZ Quality Intern BS/MS Exp: NA |
The incumbent is responsible for the development, implementation, and maintenance of information systems for Quality department. These activities include providing ongoing administration and maintenance of the company's systems for quality performance metrics and associated product technical files. | 3/2/2018 |
| 1416 | BD San Jose, CA Summer Intern - Research Associate in Reagents/Systems BS/MS in Chemistry, Biology, Immunology, Biomedical engineering and other Biological majors Exp: NA |
The summer intern will assist with innovation projects to preserve cells for a prolonged shelf life with superior performance for multiple biological applications. The intern will interact closely with the mentor in designing and executing experiments to develop preserving methods and monitor shelf life. The intern will also assist with evaluating functionality and efficacy of the matrix and analyzing experimental data. The potential applications of the preserved cells include flow cytometric analysis and genomic sequencing. At the conclusion of the internship the intern will present the scientific findings to BD leadership team. | 3/2/2018 |
| 1417 | BD Franklin Lakes, NJ R&D Summer Internship (BD Medical) BS/MS Exp: NA |
The summer internship program within the Medication and Procedural Solutions business unit of BD Medical provides the student with an opportunity to partner with peers, senior personnel, and supervisors who will provide informal mentoring and coaching towards success. Students will have the opportunity to be exposed to our process of designing and developing medical device products for different global markets. Selected students may work within cross-functional or interdisciplinary teams and may have multiple internal partners and customers. | 3/2/2018 |
| 1418 | Biogen Cambridge, MA Intern - Translational Cell Sciences MS in Biomedical/mechanical engineering, biophysics, (neuro)immunology Exp: NA |
Translational Cell Sciences is looking for a summer intern to help design and validate a microfluidic leukocyte adhesion assay. The intern will work with the Disease Model Engineering team to fabricate novel high throughput systems to enable the visualization and quantification of leukocyte capture on a functionalized surface. | 3/2/2018 |
| 1419 | Biogen Cambridge, MA Intern - Pharmacometrics MS Exp: NA |
The intern will be involved in development of the modeling framework, which can be used to predict efficacy or determining therapeutic window for the backup compounds, based upon the information or data (in-vitro and in-vivo) available for compound that are in the clinic and further ahead in the clinical development. | 3/2/2018 |
| 1420 | Biogen Cambridge, MA Intern - Biometrics MS Exp: NA |
The interns will work with one or multiple senior level statisticians on research projects that are closely related to clinical trials or non-clinical research. They will also have the opportunity to be exposed to the drug development process. The research work will be presented at the departmental seminar, and/or the company poster session, and may lead to an internal study report or a peer-reviewed publication. | 3/2/2018 |
| 1421 | Avitide Lebanon, NH Cleanroom Manufacturing Technician BS / MS in biological sciences, biochemistry, or biochemical / chemical engineering Exp: 1-3 yrs |
The successful candidate will join Avitide and undertake affinity resin manufacturing efforts as an integral role in the expanding manufacturing team. Responsibilities will center upon maintenance of the manufacturing clean room and process equipment used in performing resin activation and conjugation to ensure on-time delivery of our high quality affinity resin solutions. A key aspect of this is that manufacturing is undertaken in a quality environment to ISO9001:2015 standards with an emphasis on continual improvement of the process whilst maintaining consistency of the products. Avitide seeks candidates who are highly self-motivated to learn and can work in a collaborative fashion with other interdisciplinary team members in a fast-paced company that seeks to transform downstream bioprocessing. | 2/22/2018 |
| 1422 | Avomeen Ann Arbor, MI Analytical Chemist BS / MS in Chemistry Exp: 0-5 yrs |
Perform analysis to get approvals for innovative as well as generic pharmaceuticals | Perform test |
| 1423 | AXIO RESEARCH Seattle, WA BIOSTATISTICIAN MS in biostatistics Exp: 1 yr |
The Biostatistician may review protocols and case report forms, perform sample size calculations, write Statistical Analysis Plans, develop and produce interim and final reports. Additionally, this position will support Project Directors in the production and presentation of Data Monitoring Committee reports, analyzing data for regulatory submissions and publications, and communicating with clients and team members is desired. | 2/22/2018 |
| 1424 | Axsome Therapeutics New York City, NY Clinical Trials Assistant BS in biological or physical life science Exp: 1 yr |
The Clinical Trials Assistant is responsible for supporting the organization to successfully develop and implement clinical trials across its product portfolio and development pipeline. The Clinical Trial Assistant provides a key support function to the clinical operations team. Under general guidance from Clinical Operations, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with SOPs, FDA regulations, GCP and ICH guidelines. | 2/22/2018 |
| 1425 | Azzur Boston, MA Engineer II BS in Engineering Exp: 1-4 yrs |
We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever changing healthcare field while simultaneously and organically exuding Azzur's core values: | 2/22/2018 |
| 1426 | Azzur NA, MD Quality & Validation Specialist BA / BS Exp: 1 yr |
Completes Validation and document preparation for CTU manufacturing equipments.Maintains progress trackers for document preparation and execution activities.Attends meetings and handles assignments under direction of the area Lead. | 2/22/2018 |
| 1427 | Aziyo Biologics Richmond, CA Quality Assurance Associate BS in a life science Exp: 1 yr |
This position will perform donor and production record review efforts for all musculoskeletal products. This position will ensure all records are in compliance with appropriate systems, policies and procedures and perform final disposition of tissue products. This position will partner with operations to ensure compliance with applicable regulations and accomplish company goals of restoring health and mobility to the greatest number of patients possible. | 2/22/2018 |
| 1428 | Beckman Coulter Miami, FL Quality Assurance Scientist II - Complaint Handling MS in Science or Engineering discipline Exp: 1 yr |
The Quality Assurance Scientist II, on the Post Market team, will participate in complaint handling activities for the purpose of ensuring compliance with US and international regulatory compliance and medical device reporting requirements, as well as improving the customer experience. | 2/22/2018 |
| 1429 | Beckman Coulter Orange, CA Regulatory Affairs Specialist BA / BS Exp: 1-2 yrs |
This position is responsible for assisting in the preparation and submission of domestic and / or global product registrations. The candidate must have a basic working knowledge of domestic and / or international medical device regulations, including 510k and international registration dossier submissions. | 2/22/2018 |
| 1430 | Beckman Coulter Chaska, MN Supplier Quality Engineer I BS Exp: 0-2 yrs |
Plans and organizes routine tasks such as Supplier Selections, Supplier Change Notifications, Supplier Corrective Actions and Supplier Scorecards | 2/22/2018 |
| 1431 | Beckman Coulter Brea, CA Quality Assurance Analyst I BS in Technical Field (Science or Engineering) Exp: 0-2 yrs |
Review, evaluate and accept complaints to ensure the information is sufficient for a complete investigation. | 2/22/2018 |
| 1432 | Beckman Coulter Miami, FL Systems Engineer MS in Engineering Exp: 0-2 yrs |
Supports all engineering activities related to product and process development during project phases in accordance with design controls. | 2/22/2018 |
| 1433 | Beckman Coulter Houston, TX Process Engineer BS / MS in Chemical Engineering or Chemistry Exp: 1 yr |
To provide technical support for the use of Pall Energy products and technologies in the Americas region. To use this expertise to develop and support advantaged key / strategic customer processes and applications. | 2/22/2018 |
| 1434 | BD Franklin Lakes, NJ Engineer II - Materials MS in Materials Science & Engineering, Biomedical Engineering, or other related engineering field. MS in Materials Science & Engineering, Biomedical E Exp: 0-5 yrs |
Reporting to the Associate Director of Materials & Biological Science, the associate in this role will drive activities supporting the development and verification of technologies and products throughout the various portfolio stages including Technology Development, New Product Development, and Product Lifecycle Management. | 2/22/2018 |
| 1435 | BD Columbu, NE Quality Engineer BS in Science-related field, Quality Assurance, Engineering, Mathematics / Statistics Engineering degree preferred Exp: 1-3 yrs |
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 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. | 2/22/2018 |
| 1436 | BD San Diego , CA Manufacturing Engineer BS in Manufacturing or Industrial Engineering. Exp: 0-2 yrs |
This position reports to the Manufacturing Manager and will primary support manufacturing in the Infusion production lines. Responsible for the implementation of project and process support activities toward attainment of departmental and plant goals. Primary focus in areas of process, quality, waste and cost improvement programs. Required to handle multiple assignments of varying scope and complexity. | 2/22/2018 |
| 1437 | BD Baltimore, MD Laboratory Technologist BS in Chemistry, Biology, Microbiology or related discipline Exp: 1 yr |
Prepare reagents and solutions in accordance with production schedule following GMP and department procedure. Complete all required documentation neatly, accurately, and in accordance with FDA, GMP, and ISO. Maintain lab supplies and equipment to support production. Perform calculations and prepare solutions for use in the manufacture of complex panel formats. Handle materials per GMP, MSDS, and safety regulations. Effectively work in a team setting supporting team and business goals and objectives. Must be able to handle volumes in excess of 10 liters and lift up to 25 pounds. Must be able to work overtime when necessary to meet business requirements. Responsible for own work and accountable for decisions made. Responsible for follow through on responsibilities assigned. Able to function under minimal supervision. Able to successfully complete other tasks as assigned. | 2/22/2018 |
| 1438 | BD Salt Lake City, UT Engineer I, Quality MS in STEM Exp: 0 yr |
Develop sampling plans by applying attribute, variable, and sequential sampling methods. Develop local procedures, Test Methods, and standards. | 2/22/2018 |
| 1439 | BD Baltimore, MD QM Associate Scientist (Quality Control) BS in Biology, Microbiology or other related Life Science Exp: 1 yr |
The QM Associate Scientist is a laboratory Microbiologist who independently schedules and performs a wide variety of multiple, complex microbiological tests of complex biological raw materials and greater than 100 different complex products in response to customer demand. The QM Associate Scientist performs data analysis using visual, instrumented, graphical and calculative means based on the biochemical, selectivity and growth promoting properties of media, In addition, the QM Associate Scientist assures that documentation and procedures are followed, updated and maintained as required by internal Quality Policies and related FDA / GMP guidelines. The QM Associate Scientist performs non-routine detailed project support and investigational testing and is involved in resolution of technical issues related to microbiological processes. The QM Associate Scientist is subject to extended periods of sitting, and standing, frequent walking, and occasional lifting of materials weighing 25-50 pounds. The QM Associate Scientist must be able to use personal protective equipment (e.g. respirators, gloves, etc.). The QM Associate Scientist must be willing to Cross train in other sections of the Quality Laboratories for surge events and as needed. The QM Associate Scientist must be able to train other personnel on appropriate test methods and techniques thoroughly, as needed. The QM Associate Scientist must exhibit the Becton Dickinson Core Values to do what is right, take personal responsibility,anticipate and address the challenges of patients and customers globally, as well asinnovate and improve continuously, and respect, collaborate, challenge and care about each other. | 2/22/2018 |
| 1440 | Baxter Round Lake, IL Engineer II MS in Engineering Exp: 1-3 yrs |
Review individual complaints and associated service data to determine risk level and complete investigation into the "As Determined" problem and cause coding for each complaint. | 2/22/2018 |
| 1441 | Baxter Irvine, CA CAPA Engineer BS in Engineering Exp: 1-3 yrs |
Responsible for Corrective Action and Preventive Action (CAPA) implementation as well as Non-Conformance (NC) investigations and process activities. | 2/22/2018 |
| 1442 | Baxter Medina, NY Product Surv Quality Assoc I BS Exp: 0-3 yrs |
This position is responsible for Regulatory Reporting, including final reportability determination or reportability review and / or processing Medical Device Reports, FARs, or BPDRs. | 2/22/2018 |
| 1443 | Baxter Marion, NC Quality Engineer I BS in Engineering Exp: 0-2 yrs |
Display a solid technical understanding of engineering principles and procedures (e.g. CAD and its application or scheduling a series of technical tasks utilizing software-based tools. | 2/22/2018 |
| 1444 | Baxter Marion, NC Quality Lab Assoc. Chem. BS in Micro and Biology Exp: 0-2 yrs |
Conduct critical biological, chemical and physical analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Baxter manufacturing facilities. Work under minimum supervision. | 2/22/2018 |
| 1445 | Baxter Marion, NC Quality Lab Assoc II - Chem MS in Chemistry, or Biological Sciences Exp: 0-3 yrs |
Conduct critical biological, chemical and physical analyses on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at manufacturing facility.Work under minimum supervision. | 2/22/2018 |
| 1446 | Baxter Marion, NC Quality Engineer II BS in Engineering Exp: 1-3 yrs |
Responsible for designing, developing, implementing and evaluating optimal, cost-effective projects and technologies. In addition to providing technical support and service to these areas, the incumbent may also perform the following functions: supervising, requisitioning, defining, initiating, specifying, documenting and training. | 2/22/2018 |
| 1447 | BioAssay Systems Hayward, CA SCIENTIST - MANUFACTURING BS in chemistry, biochemistry or biology Exp: 1-2 yrs |
This position will entail preparing reagents for our assay kits, QCing and packaging the finished products. This candidate may also join part time in our R&D team. | 2/22/2018 |
| 1448 | Bioclinica Newark, CA Imaging Analysis Technician BS Exp: 0-1 yr |
Communicates with Clinical Project Managers, Clinical Operations Associates and / or Specialists regarding image quality, deliverables, and data discrepancies | 2/22/2018 |
| 1449 | Bioclinica Newark, CA Clinical Data Associate BS in Life Sciences or related field preferred Exp: 1 yr |
Reviewing documentation and requirements for new projects and anticipating impact to Data Management (DM) standards / processes | 2/22/2018 |
| 1450 | BioDuro, LLC. San Diego , CA Quality Assurance Specialist BS in science-related field Exp: 1-3 yrs |
The Quality Assurance Specialist facilitates and assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. | 2/22/2018 |
| 1451 | Biogen Cambridge, MA Associate Scientist I, Human ESC/iPSC Neuronal Cell Culture MS Exp: 1 yr |
Biogen is seeking a molecular and cellular biologist to join the Translational Cell Sciences Stem Cell & Genomic Editing group. The group develops cutting-edge human stem cell derived neuroscience models to enable drug discovery. | 2/22/2018 |
| 1452 | Biogen Cambridge, MA Associate III, Clinical Site Support BS / BA Exp: Entry Level |
The Associate III, Drug Supply Clinical Site Support, is responsible for drug supply management activities crossing global clinical operations and Clinical Drug Supply processes, including closely interacting with our partnership contract research organization (CRO). | 2/22/2018 |
| 1453 | Bioelectron Technology Corporation Mountain View, CA Lab Technician / Research Assistant - Bioanalytical BS in chemistry, biochemistry, or biomedical engineering preferred Exp: 1 yr |
We are seeking a highly organized and detail-oriented research assistant to support biomarker discovery and development efforts. This individual will be a key member of the bioanalytical group, supporting experiments conducted internally and with clinical collaborators. | 2/22/2018 |
| 1454 | BioDuro, LLC. San Diego , CA Formulation Intern BS in chemistry or related field Exp: 1 yr |
The Formulation Intern assists in the design and development of drug delivery systems and dosage forms. | 2/22/2018 |
| 1455 | Baxter Mountain Home, AR Operations Development Program Intern BS / MS in operations, supply chain, engineering, or quality-related field or Hard Sciences (BioChemistry, Chemistry, Microbiology) required Exp: NA |
The Operations Development Program (ODP) Intern will work in multi-discipline teams focused on providing a strong foundation in Baxter plant operations, manufacturing processes and systems. | 2/22/2018 |
| 1456 | BD Salt Lake City, UT Internship - Quality Engineer BS / MS Exp: NA |
Internships can be found in all departments working on a variety of projects ranging from product testing to post market launch. Interns work under close supervision by the sponsoring function. It is a mutually beneficial relationship as Bard creates a learning environment where the intern obtains industry hands-on experience. | 2/22/2018 |
| 1457 | BD Broken Bow, NE Microbiology Intern BS / MS Exp: NA |
The Microbiology Intern will work in the quality assurance Microbiology Lab in Broken Bow, NE and will assist with the plant sterilization assurance program. They will assist in various projects that may involve culturing microorganisms, bioburden testing, supporting contamination investigations, and supporting validation activities. | 2/22/2018 |
| 1458 | BD San Diego , CA Systems Engineering Intern BS Exp: NA |
The intern will be assigned an ongoing project and will have the opportunity to work closely with system engineers to develop novel medical device features. | 2/22/2018 |
| 1459 | Takeda Cambridge, MA Summer 2018 Internship - Oncology Sales Training BS / MS Exp: NA |
Takeda's summer internship program blends real world experience with an extensive overview of the pharmaceutical industry. Knowledgeable mentors will provide guidance as you gain professional hands-on experience. The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 2/22/2018 |
| 1460 | Takeda Cambridge, MA Summer 2018 Internship - Oncology Global Medical Affairs BS / MS Exp: NA |
This summer intern will take a holistic view of the investment that Takeda medical affairs makes in independent research studies and create a roadmap tying this investment to strategic brand imperatives. | 2/22/2018 |
| 1461 | Takeda Cambridge, MA Summer 2018 Internship - Quality Control (Vaccines Business Unit) BS / MS Exp: NA |
The QC intern will assist the QC team in areas of product stability, testing, and program management. The QC intern will have the ability to learn and gain hands-on experience with data trending and applicable statistical principals, method development and data review, and contract lab management. | 2/22/2018 |
| 1462 | Asuragen Austin, TX Summer Intern, Development BS / MS Exp: NA |
Asuragen internships offer exposure to cutting-edge, applied product development, but they also provide unique experiences that come from working in a scientific business. Projects will advance molecular assays that can help diagnose disease and / or inform patient treatments, and focus on interrogating biomarkers involved in neurodegenerative diseases and cancer therapy. Each intern is assigned a specific project and an Asuragen scientific mentor; projects are scoped to produce defined outcomes within the internship period. | 2/22/2018 |
| 1463 | ARTHREX Ave Maria, FL VALIDATION INTERN BS / MS in an Engineering Exp: NA |
To assist teams with administrative office support and help out on project work. | 2/22/2018 |
| 1464 | ARTHREX Ave Maria, FL QUALITY CONTROL INTERN BS / MS Exp: NA |
To assist teams with administrative office support and help out on project work. | 2/22/2018 |
| 1465 | ARTHREX Ave Maria, FL VALIDATION ENGINEERING INTERN BS / MS in an Engineering Exp: NA |
To assist teams with administrative office support and help out on project work. | 2/22/2018 |
| 1466 | ALBANY MOLECULAR RESEARCH, INC Rensselaer, NY RESEARCH SCIENTIST I/II - MEDICINAL CHEMISTRY BS / MS in chemistry or equivalent Exp: 0-5 yrs |
The Research Scientist I / II is expected to demonstrate expertise in both the theoretical and practical aspects of organic chemistry. Principal responsibility is the synthesis, purification, and identification of chemical intermediates and target compounds. A major component in the scientist's performance rating will be based on productivity. | 2/18/2018 |
| 1467 | ALBANY MOLECULAR RESEARCH, INC Rensselaer, NY RESEARCH SCIENTIST I/II - DMPK BS / MS Exp: 0-5 yrs |
The Research Scientist I / II is expected to assist in a variety of laboratory procedures in the area of DMPK. The scientist is expected to have an understanding of both the theoretical and practical aspects of biology, biochemistry, and chemistry as well as demonstrate independence on performance of routine tasks. The scientist is expected to demonstrate aptitude in a wide range of in vitro biochemical assays, sample processing, and analytical tools. | 2/18/2018 |
| 1468 | ALBANY MOLECULAR RESEARCH, INC Springfield, MO ANALYTICAL CHEMIST MS in analytical chemistry or related field Exp: 1-5 yrs |
To provide technical leadership to local Global API Analytical Technical Support team and to ensure the timely execution of analytical method transfers, method development and validations, and initial qualification and retesting of analytical reference standards. | 2/18/2018 |
| 1469 | EAG Easton, MD Assistant Scientist, Plant & Invertebrate BS / BA in biology Exp: 0-2 yrs |
The applicants will work with other staff biologists while conducting testing. In addition, the applicants will collect and analyze biological data. The individual may assist in the production of technical reports intended for review and evaluation by sponsoring clients and government agencies under the supervision of more senior biologists or scientists. | 2/18/2018 |
| 1470 | EAG Easton, MD Assistant Scientist, Avian BS / BA in biology Exp: 0-2 yrs |
The applicant will feed, water, and examine animals for signs of illness, disease, or injury sustained in the laboratory. The avian biologist must also be comfortable with handling live birds and assisting with blood collections and / or necropsies. In addition, the applicant will collect and analyze biological data in addition to providing guidance to technicians on the proper conduct of study assignments. The individual may produce technical reports intended for review and evaluation by sponsoring clients and government agencies under the supervision of more senior biologists or scientists. | 2/18/2018 |
| 1471 | ANI Pharmaceuticals Baudette, MN QC Analyst BS in Chemistry, Pharmacy or closely related field Exp: entry level |
This position is responsible for independently performing laboratory testing, as defined by governing test methods and standard operating procedures. This is an entry level professional position in the Quality Control Laboratory. | 2/18/2018 |
| 1472 | Antech Diagnostics Southfield, MI Laboratory Generalist - MI BS in Medical Technology Exp: 1 yr |
The Ideal Candidate will have prior experience as a Medical Technician that involved performing some clinical diagnostic testing & using testing equipment. In this integral role you will perform tests in all areas of the laboratory such as: Chemistry, Hematology, Coagulation, and Urinalysis. | 2/18/2018 |
| 1473 | Antech Diagnostics Lake Success, NY Laboratory Quality Assurance Technician BS in Medical Technology Exp: 1-2yrs |
This position will be responsible for the production and administration of our internal proficiency testing program for more than sixty veterinary diagnostic laboratories. | 2/18/2018 |
| 1474 | Antech Diagnostics Overland Park, KS Laboratory Generalist BS in Science related field Exp: 1 yr |
As a Laboratory Generalist you will perform laboratory testing that helps veterinarians diagnose and treat pets across the United States. You will join a fast-paced work environment that encourages teamwork and quality, and offers opportunities for personal growth. | 2/18/2018 |
| 1475 | Allergan Irvine, CA Associate Investigator, Operations Compliance BS in Industrial Engineering / Operations Management, the Sciences or related field. Exp: 1 yr |
Serves as an investigator and technical writer with responsibilities in Facilities, specifically with maintenance & calibration related issues and their impact to operations, production, process, and equipment at the BLI facility. | 2/18/2018 |
| 1476 | ArcherDX Boulder, CO Document Control Technician BS in molecular biology, biochemistry, chemistry or related field Exp: 1 yr |
Document Control assists in creating documents and preparing final document for approval according to ISO 13485 and 21 CFR 820 Quality System requirements. Document Control will be responsible for maintainings a comprehensive electronic and hard copy filing system and computer database for all documents. | 2/18/2018 |
| 1477 | ARTHREX Naples, FL Associate Clinical Specialist - Hand, Wrist and Elbow BS in bio-medical sciences or related field Exp: 1-2yrs |
Provide technical support for the training curriculum that addresses the changing needs of Arthrex sales force, in-house personnel and surgeon customers. Assist in the organization and conduct surgeon motor skills labs and training sessions offered by Arthrex. Resource for the product management, engineering, sales management, web master and regulatory affairs. | 2/18/2018 |
| 1478 | Assurex Mason, OH Lab Technician I BS in medical technology, clinical laboratory science, chemistry or chemical engineering, biological or other physical science Exp: 1 yr |
At Assurex The Laboratory Technologist I is responsible for specimen processing, test performance and reporting of test results according to laboratory procedures. This position reports to the Laboratory Manager. | 2/18/2018 |
| 1479 | Astex Pharmaceuticals Pleasanton, CA Drug Safety Intake Coordinator Contractor BA / BS Exp: 1 yr |
The Drug Safety Intake Coordinator Contractor will be responsible for providing tactical support to drug safety operations related to processing and reporting of serious adverse events (SAEs) from clinical trials managed in a paperless system, ensuring compliance with all applicable laws, regulations and professionals and partners. | 2/18/2018 |
| 1480 | Astex Pharmaceuticals Pleasanton, CA Clinical Trial Drug Supply Contractor BA / BS Exp: 1 yr |
The Clinical Trial Drug Supply Contractor will support the Clinical Supplies team's activities related to Clinical Trial Drug otherwise known as Investigational Medicinal Product (IMP) for Phase 1-4 clinical studies, cooperate with internal and external customers and partners in compliance with multinational regulations as well as internal procedures and GxP requirements. This position requires a very high degree of attention to detail. Responsibilities include supporting complex clinical studies requiring Clinical Supplies project management, packaging / labeling, IXRS support, Global distribution and IMP forecasting. This position will interface with Clinical, Project Management, QA, and CMC teams. | 2/18/2018 |
| 1481 | AstraZeneca Gaithersburg, MD Quality Assurance Analyst, Access Services BA / BS Exp: 1-2yrs |
The Quality Assurance Analyst (QAA), Access Services will be responsible for monitoring and documenting program performance quality in support of departmental goals and initiatives. As the QAA you will work directly with Access 360 Operations Leadership to design quality monitoring formats, quality standards, and execute on the overall QA strategy. You will fairly and consistently evaluate Access 360 program processes, performance, and team interactions with both internal and external parties. You will work collaboratively with the Access 360 Training and Operations teams to develop, monitor, and coach new hires. In addition you will also work with Access 360 Quality Assurance, Training, and Operations Leadership to ensure all aspects of program quality are addressed and that the program exhibits superior Customer experience and quality to patients, healthcare providers, and other stakeholders. You will develop, analyze, and provide regular reports on program performance, calibration deviations, trend data, and other actionable insights to the Access 360 QA, Training, and Operations Leadership teams. | 2/18/2018 |
| 1482 | Aucta North Brunswick, NJ Senior Scientist, formulation BS / MS Exp: 1-3 yrs |
Develop and scale up formulations and manufacturing processes for oral solid dosage forms with minimal guidance, including preformulation, formulation and process development | 2/18/2018 |
| 1483 | Aucta North Brunswick, NJ Senior Scientist, analytical BS / MS Exp: 1-3 yrs |
Quality control for API and drug product, including analytical method development and validation, stability study, etc. | 2/18/2018 |
| 1484 | Aucta North Brunswick, NJ Quality control for API and drug product, including analytical method development and validation, stability study, etc. BS Exp: 1-3 yrs |
Develop and scale up formulations and manufacturing processes for oral solid dosage forms under guidance, including preformulation, formulation and process development | 2/18/2018 |
| 1485 | aTyr Pharma San Diego, CA RESEARCH ASSOCIATE, UPSTREAM MS Exp: 1 yr |
In this role, the successful candidate will support upstream development activities, including execution of mammalian cell culture and microbial fermentation processes, support laboratory management and drive data management initiatives. | 2/18/2018 |
| 1486 | Aura Biosciences Cambridge, MA Assay Development Scientist, ELISA/Immunoassay BS / MS Exp: 1 yr |
Reporting to the Senior Scientist, the Assay Development Scientist, ELISA / Immunoassay will in a timely manner develop immunoassay (ELISA) methods to support DMPK study. | 2/18/2018 |
| 1487 | AustarPharma LLC Edison, NJ Regulatory Affairs Specialist MS in Pharmaceutics , Pharmaceutical Chemistry or closely related fields Exp: 1 yr |
Collecting and reviewing technical CMC documents, reviewing clinical study protocols and reports, and providing guidance to ANDA R&D departments for FDA and cGMP compliance. | 2/18/2018 |
| 1488 | Avitide Lebanon, NH Associate Scientist - Bioanalytical BS / MS Exp: 1 yr |
Qualified candidates will generate key analytic data for diverse biopharmaceuticals and enable results that allow rapid iterative product optimization in real time. This position will also be exposed to multiple opportunities for cross training in purification process development. Avitide seeks candidates who are highly self-motivated and can work in a collaborative fashion with other interdisciplinary team members in a fast-paced company that seeks to transform the downstream bioprocessing industry. | 2/18/2018 |
| 1489 | Averica Discovery Services Inc Marlborough, MA Analytical Chemistry Summer Intern BS / MS Exp: NA |
Support the routine day-to-day laboratory operation including glass washing and solution and sample preparation. | 2/18/2018 |
| 1490 | Asuragen Austin, TX Summer Intern, Bioinformatics BS / MS Exp: NA |
These internship positions offer exposure to cutting-edge, applied scientific research and provide unique experiences that come from working in a scientific business. Projects will advance computational methods that can help diagnose disease and / or inform the treatment of disorders ranging from autism to cancer. Each intern will have a specific project and an Asuragen scientific mentor; projects are scoped to produce defined outcomes within the internship period. Potential internship opportunities span the diagnostic product development spectrum, from conception and feasibility through late-stage development. | 2/18/2018 |
| 1491 | Asuragen Austin, TX Summer Intern, Research BS / MS Exp: NA |
Asuragen internships offer exposure to cutting-edge, applied scientific research, but they also provide unique experiences that come from working in a scientific business. Projects will advance molecular assays that can help diagnose disease and / or inform patient treatments, and focus on interrogating biomarkers with precision medicine applications. Each intern is assigned a specific project and an Asuragen scientific mentor; projects are scoped to produce defined outcomes within the internship period. | 2/18/2018 |
| 1492 | ARTHREX Ave Maria, FL QUALITY ASSURANCE - VALIDATION INTERN BS / MS in Biomedical Engineering, Chemical Engineering or Industrial Technology Exp: NA |
Assist in ongoing Cleaning validations to validate systems / processes used for cleaning of implants and instruments. | 2/18/2018 |
| 1493 | ARTHREX Ave Maria, FL QA VALIDATION INTERN BS / MS in Mechanical or Biomedical Engineering Exp: NA |
To assist teams with administrative office support and help out on project work. | 2/18/2018 |
| 1494 | ARTHREX Naples, FL PRODUCT SURVEILLANCE INTERN BS / MS Exp: NA |
To assist teams with administrative office support and help out on project work. | 2/18/2018 |
| 1495 | AngioDynamics Marlborough, MA INTERN, R&D - VASCULAR ACCESS IN BS / MS Exp: NA |
Work with the Vascular Access R&D engineering team on daily task on high priority projects. These tasks include but are not limited to hands-on testing of medical devices, develop test methods, test fixtures, product specifications, and technical reports. The candidate will attend project meetings and work with cross functional teams to gain experience in the development process of medical devices. | 2/18/2018 |
| 1496 | Alcon Laboratories Fort Worth, TX Summer 2018 Internship - Independent Medical Education BS / MS Exp: NA |
Interns are expected to work 40 hours per week during the length of their internship, unless otherwise specified by their manager. In addition to work assignments and projects, Alcon also provides the students the opportunity to socialize and network career development and networking opportunities throughout the duration of the summer internship program. | 2/18/2018 |
| 1497 | Alcon Laboratories Fort Worth, TX Summer 2018 Internship - Materials Science/Engineering - R&D BS / MS Exp: NA |
Summer 2018 Internship - Materials Science / Engineering-R&D | 2/18/2018 |
| 1498 | Takeda Pharmaceuticals U.S.A. Cambridge, MA Summer 2018 Internship - Regulatory Affairs CMC BS / MS in a healthcare, pharmacy or life science Exp: NA |
The interns under the supervision of the Regulatory Affairs Chemistry, Manufacturing and Controls (RA CMC) team will work with cross functional colleagues in gathering information. However, interns will work with various team members in the RA-CMC Cambridge MA team to support regulatory filings in the United States for commercial and clinical applications | 2/18/2018 |
| 1499 | Takeda Pharmaceuticals U.S.A. San Diego, CA 2018 Summer Internship - CNS Chemistry BS / MS in chemistry Exp: NA |
The intern will conduct medicinal chemistry to advance drug discovery research in the Central Nervous System (CNS) Drug Discovery Unit. | 2/18/2018 |
| 1500 | Takeda Pharmaceuticals U.S.A. Cambridge, MA Summer 2018 Internship - Bioinformatics BS / MS Exp: NA |
Organizing experimental data files , identify key elements of sample quality and genomic data to be parsed and uploaded to central SQL database for searching and analysis. | 2/18/2018 |
| 1501 | Adimab Lebanon, NH Research Associate BS in molecular biology, chemical engineering, or biochemistry Exp: 1 yr |
We are seeking a skilled molecular biologist to join our Antibody Discovery team. The Research Associate will work in a small team setting to support Adimab's novel antibody discovery, maturation, and production platform. This role will closely interface with the Protein Analytics, High Throughput Expression, Molecular Sciences, and Computational Biology teams. | 2/11/2018 |
| 1502 | Aldevron Fargo, ND In - Process Quality Assurance Specialist BS in a Life Sciences Exp: 1-2 yrs |
We are seeking Quality Assurance Specialists to join our team and support our quality system processes by acting as the primary contact for quality on the production floor. As an In-Process Quality Assurance (IPQA) Specialist, you have excellent communication, interpersonal, and organizational skills. You are analytically sharp and possess problem solving techniques. You are able to work with minimal supervision. You demonstrate high ethical standards and trustworthiness. | 2/11/2018 |
| 1503 | Aldevron Fargo, ND GMP/GMP - Source Lab Technician II BS Exp: 1-2 yrs |
We are seeking qualified Lab Technicians to support our GMP and GMP-Source teams. The Lab Technician will work daily within Aldevron's labs performing tasks associated with Aldevron's GMP and GMP-Source services. The Lab Technician is expected to become familiar with all of Aldevron's products and to be able to perform most tasks associated with the purification of plasmid DNA | 2/11/2018 |
| 1504 | Alere San Diego, CA Research Associate II BA / BS in biology, chemistry, physics or related field Exp: 1-3 yrs |
Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner.Conduct moderately complex experimentation including data collection, summary and analysis, in support of department research projects and guidelines. | 2/11/2018 |
| 1505 | Alere San Diego, CA Document Specialist, R&D BS in a biological science or engineering discipline Exp: 1-2 yrs |
Aid in writing, formatting and subsequent processing of documents (SOPs, MPs, RMS, Labeling) relating to the implementation of new products that are under design control. | 2/11/2018 |
| 1506 | AllCells, LLC Alameda, CA Quality Assurance/Quality Control Associate BS in a life science discipline Exp: 1 yr |
Reporting to the Associate Director of Quality Management, the main responsibility of the QA / QC Associate is to perform document control on all quality system documents, format SOPs, assist with the maintenance of the variance program (e.g. deviations, OOSs, CAPA, etc.), maintain training records, and assist with finished product release. | 2/11/2018 |
| 1507 | ATEC Spine Carlsbad, CA Design Engineer BS in mechanical or biomedical engineering Exp: 1-4 yrs |
Designs and develops implants and instruments utilizing SolidWorks.Assists in the development of new products and manufacturing processes and / or serves as a member of a development team. | 2/11/2018 |
| 1508 | Ajinomoto Althea San Diego, CA DRUG PRODUCT MANUFACTURING ASSISTANT BS in a Life Sciences discipline or equivalent Exp: 0-2 yrs |
The Drug Product Manufacturing Assistant is responsible for implementation of routine production and manufacturing procedures to optimize processes and regulatory requirements. | 2/11/2018 |
| 1509 | Ajinomoto Althea San Diego, CA ANALYTICAL TECH TRANSFER ASSOCIATE II BS in a Life Sciences discipline or equivalent Exp: 1-3 yrs |
Althea is currently seeking an Analytical Tech Transfer Associate II to transfer, qualify, and validate analytical methods and maintain analytical instrumentation. This position regularly exercises technical discretion in design, execution, and interpretation of experiments. | 2/11/2018 |
| 1510 | Ambrx San Diego, CA Research Associate (or SRA), Mammalian Cell Culture Process Development BS / MS in Chemical Engineering, Bioengineering, Biochemistry, or related scientific field Exp: 1 yr |
This position will be responsible for cell culture process development and material production to support R&D, pre-clinical, and clinical activities. In this role, the candidate will work closely with team members in the Process Development group as welland purification groups to evaluate new clones, develop new processes, and generate material. | 2/11/2018 |
| 1511 | Avantor Spring House, PA Laboratory Team Lead/Coordinator BS Exp: 1-4 yrs |
Conform to all customer requirements for background checks, health and safety issues, security.Knowledge of Information Access and ERP Systems; intermediate Microsoft Office Knowledge with proficiency in Microsoft Word, Excel, PowerPoint and basic understanding of Microsoft Access.Conform to all customer requirements for background checks, health and safety issues, security.Knowledge of Information Access and ERP Systems; intermediate Microsoft Office Knowledge with proficiency in Microsoft Word, Excel, PowerPoint and basic understanding of Microsoft Access.Conform to all customer requirements for background checks, health and safety issues, security.Knowledge of Information Access and ERP Systems; intermediate Microsoft Office Knowledge with proficiency in Microsoft Word, Excel, PowerPoint and basic understanding of Microsoft Access. | 2/11/2018 |
| 1512 | Avantor Boston, MA Team Lead BS Exp: 1-4 yrs |
The Team Lead is responsible to lead the day-to-day operation of the onsite SOW related to customer requirements for smaller customer locations. The Team Lead supports and leads a small team of VWR on-site personnel acting as a single point of contact for the customer. The Team Lead is typically dedicated to one customer, one site location, and reports to a manager. Much of the time is spent performing the work of those supervised. | 2/11/2018 |
| 1513 | Avantor Malvern, PA Laboratory Team Lead BS Exp: 1-4 yrs |
The Team Lead is responsible to lead the day-to-day operation of the onsite SOW related to customer requirements for smaller customer locations. The Team Lead supports and leads a small team of VWR on-site personnel acting as a single point of contact for the customer and is responsible for the accurate execution of laboratory protocols and procedures by the team (e.g. Media / Buffer Technicians). The Team Lead is typically dedicated to one customer, one site location, and reports to a manager. Much of the time is spent performing the work of those supervised. | 2/11/2018 |
| 1514 | Avantor Malvern, PA Sample Management Team Lead BS Exp: 1-4 yrs |
The Team Lead is responsible to lead the day-to-day operation of the onsite SOW related to customer requirements for smaller customer locations. The Team Lead supports and leads a small team of VWR on-site personnel acting as a single point of contact for the customer. The Team Lead is typically dedicated to one customer, one site location, and reports to a manager. Much of the time is spent performing the work of those supervised. | 2/11/2018 |
| 1515 | Amneal Pharmaceuticals LLC. Piscataway, NJ Scientist I, Quality Control BS in Chemistry or related Science discipline Exp: 1 yr |
The Scientist 1 - QC is an entry level role responsible to perform 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. | 2/11/2018 |
| 1516 | Amneal Pharmaceuticals LLC. Piscataway, NJ Validation Engineer BS / MS in Pharmaceutical or Biomedical Engineering Exp: 1 yr |
The validation engineer is responsible to perform validation and conducting development studies. This role is also responsible for monitoring, and analyzing to assist in improvising pharmaceutical systems and processes. | 2/11/2018 |
| 1517 | Amneal Pharmaceuticals LLC. Piscataway, NJ Scientist II MS in Chemistry or related Exp: 1 yr |
The Scientist-2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications / validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains / qualifies analytical equipment. | 2/11/2018 |
| 1518 | Amneal Pharmaceuticals LLC. Piscataway, NJ QA Inspector III BA / BS Exp: Entry Level |
To monitor and ensure all incoming raw materials, packaging components and returned goods are sampled, inspected and tested (where applicable) for the purpose of determining compliance with established specifications. To monitor and ensure all phases of drug manufacturing are in compliance with established specifications. To receive, inspect, release and control of labels and outserts. To ensure quality compliance before, during and after each packaging run. | 2/11/2018 |
| 1519 | Amgen Cambridge, MA Associate Pilot Plant BS in Biology, Chemistry, Biochemistry, Chemical / Biological Engineering, or related field Exp: 0 yr |
The Associate Pilot Plant will directly support the Amgen Massachusetts, Cambridge pilot plant, which provides a collaborative environment to develop and test new technologies and applications. The pilot plant also provides critical technical support for technology transfers, process development, and scale-up / scale-down activities. The pilot plant delivers data and material to support process development of early and late stage clinical biologic molecules. In addition, the pilot plant prototypes and develops new technologies to support advancement of Amgen's equipment and operations for current and future biologic facilities. | 2/11/2018 |
| 1520 | Amgen Thousand Oaks, CA Device Engineer MS Exp: 0 yr |
The engineer will be responsible for electro-mechanical delivery devices, such as; fluid transfer devices, automatic pen injectors, and micro-infuser delivery pump systems. The engineer will be part of a sustaining engineering team that ensures successful device design transfer of these mechanical and electro-mechanical delivery devices. The position will focus on design / development engineering assignments focused on commercial mechanical, electro-mechanical systems, and fluid-mechanical systems. | 2/11/2018 |
| 1521 | ALBANY MOLECULAR RESEARCH, INC Lebanon, NJ SENIOR CHEMISTRY ANALYST, CONTAINER TESTING MS Exp: 0-2 yrs |
Working under moderate supervision, performs simple and complex testing related to compendial general chapters with a high level of proficiency. leveraging relevant technical standards, principles, theories, concepts, and techniques. | 2/11/2018 |
| 1522 | ALBANY MOLECULAR RESEARCH, INC Albuquerque, NM MICROBIOLOGIST I BS in life science or related field Exp: 0-2 yrs |
Prepare, collect, and test plant purified water, manufacturing raw materials, product in-process, and finished product, and perform environmental monitoring. With limited supervision, learn and perform critical laboratory techniques and complete original work. Author problem reports and participate in investigations. This description is inclusive of EM and testing duties: actual percentages of time spent on each duty may vary based on business needs. | 2/11/2018 |
| 1523 | ALBANY MOLECULAR RESEARCH, INC West Lafayette, IN MICROSPECTROSCOPIST MS in Chemistry or related science Exp: 0-5 yrs |
We are currently seeking a Microspectroscopist for our Analytical Technology group in West Lafayette, IN. A successful candidate will be a highly motivated scientist who can perform instrumental analyses in support of solid state research and / or crystallization projects as well as oversee the maintenance of analytical instrumentation in a contract GMP pharmaceutical laboratory. | 2/11/2018 |
| 1524 | ALBANY MOLECULAR RESEARCH, INC Lebanon, NJ PRINCIPAL ANALYTICAL CHEMIST MS in analytical chemistry or related field Exp: 1-5 yrs |
To provide technical leadership to local Global API Analytical Technical Support team and to ensure the timely execution of analytical method transfers, method development and validations, and initial qualification and retesting of analytical reference standards. | 2/11/2018 |
| 1525 | Amgen Cambridge, MA Undergrad Intern - R&D (Associate Regulatory Writing) BS Exp: NA |
The intern will work under the direction of the Clinical Transparency & Disclosure staff and in collaboration with staff members from other functions within Research and Development | 2/11/2018 |
| 1526 | Amgen Cambridge, MA Undergrad Intern - R&D (Neuroscience) BS / MS in Biology, Biochemistry, Neuroscience or related discipline Exp: NA |
This internship provides the opportunity for executive and social networking events and to participate in community volunteer projects while providing a competitive compensation. | 2/11/2018 |
| 1527 | ATEC Spine Carlsbad, CA Summer Internship BS Exp: NA |
We are looking for enthusiastic, advanced communicators, creative thinkers and positive attitudes. Our interns will provide support on various tasks and projects | 2/11/2018 |
| 1528 | Allvivo Vascular Lake Forest, CA Scientific Intern BS in chemistry, engineering, biology, microbiology, pre-medicine or other related discipline Exp: NA |
The intern will support Allvivo's formulation group in the development of antimicrobial technologies for medical devices and combination products. In this position, they will learn techniques in medical device coating and drug delivery as well as some microbiology test methods. | 2/11/2018 |
| 1529 | Align Technology San Jose, CA Research Engineer Intern BS in engineering Exp: NA |
The Research Engineer Intern position is responsible for assisting the Research Engineer(s) in the R&D Product Innovation department. The Research Engineer Intern will work closely on individual research projects while assisting ongoing development and research projects. Projects focus on biomechanics, design, material characterization and process improvements. | 2/11/2018 |
| 1530 | Alcon Laboratories Johns Creek, GA Summer 2018 Internship - Chemistry - R&D BS / MS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern - assigned project(s) will align to one of our two business groups - Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 2/11/2018 |
| 1531 | Alcon Laboratories Fort Worth, TX Summer 2018 Internship - Regulatory Affairs - R&D BS / MS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern - assigned project(s) will align to one of our two business groups - Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 2/11/2018 |
| 1532 | Alcon Laboratories Johns Creek, GA Summer 2018 Internship - Biomedical Engineering - R&D BS / MS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern - assigned project(s) will align to one of our two business groups - Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 2/11/2018 |
| 1533 | Takeda Deerfield, IL 2018 Summer Internship - Quality, TPUSA BS Exp: NA |
The Quality Intern will work within the External Supply US Quality organization, and gain exposure to several lanes of the Quality business, including: Quality Management Systems, Packaging and Manufacturing Quality, Quality Compliance, and Continuous Improvement, as well as cross-functionally with Operations and Supply Chain. The intern will have the opportunity to obtain knowledge and experience the multidisciplinary teams to support the commercial product life cycle. | 2/11/2018 |
| 1534 | Takeda San Diego, CA 2018 Summer Internship - GI Chemistry (San Diego, CA) BS in chemistry Exp: NA |
Takeda California's internship program blends real world experience with an extensive overview of the pharmaceutical industry. Knowledgeable mentors will provide guidance as you gain professional hands-on experience. The internship will be ten to twelve weeks in duration for the summer of 2018 with flexible start dates. Student interns must be able to work full time. Interviews will take place in Fall / Winter for selected students. | 2/11/2018 |
| 1535 | Takeda Cambridge, MA Summer 2018 Internship - Quality Documentation and Training (Oncology & Biologics) BS / MS Exp: NA |
The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 2/11/2018 |
| 1536 | Danaher Chaska, MN Biologics Supplier Quality Engineer II MS Exp: 0-2 yrs |
Plans and organizes routine tasks such as Supplier Selections, Supplier Change Notifications, Supplier Corrective Actions and Supplier Scorecards | 2/4/2018 |
| 1537 | Danaher Timonium, MD Manufacturing Engineer BS in Manufacturing or Mechanical Engineering Exp: 1-3 yrs |
Control manufacturing and engineering specifications for the plant | Implement IC |
| 1538 | Danaher Sunnyvale, CA Biostatistician II MS Exp: 1 yr |
The position will support clinical trials by developing statistical analysis plans for clinical trials and author the final statistical report. This position will be point of contact for FDA questions pertaining to analysis. The position will also assist in any supporting analysis such as precision and reproducibility studies, interfering substances, limit of detection (LOD), exclusivity and inclusivity studies, method comparisons, accuracy, and linearity study carried out by development or the clinical trial group. | 2/4/2018 |
| 1539 | Achaogen South San Francisco, CA Research Associate I/II - Molecular Biology BS / MS Exp: 1 yr |
This role will be responsible for high throughput RT-PCR utilizing liquid handling robotics, cDNA sequencing and vector construction, amongst other activities. | 2/4/2018 |
| 1540 | Achaogen South San Francisco, CA Research Associate I/IIProtein Chemistry / Biochemistry BS / MS Exp: 0-5 yrs |
This role will be responsible for enabling drug discovery projects through the expression, purification and characterization of high quality recombinant proteins and antibodies. | 2/4/2018 |
| 1541 | ACORDA Chelsea, MA Quality Control Analyst BS in Physical or Chemical Sciences (life sciences) Exp: 1-2 yrs |
The Quality Control Analyst is responsible for executing QC testing and related analytical activities supporting product development, release and stability. This individual conducts routine and non-routine chemical and physical analyses of raw materials, in-process materials and drug products according to standard operating procedures. The Quality Control Analyst compiles data for documentation of test procedures that may include stability program testing and formulation studies, participates in the preparation of investigations, summaries and reports, and reviews data obtained for compliance to specifications and reports out-of-trend and / or out-of-specification results. The Quality Control Analyst revises and updates standard operating procedures as needed. | 2/4/2018 |
| 1542 | Precision Medicine Group Huntersville, NC Associate Research Scientist - HEOR Strategy MS / MA Exp: 1 yr |
As an Associate Research Scientist you will collaborate across a broad portfolio of sophisticated health economic and health policy research projects in a project team structure. You will also have the opportunity to collaborate regularly with nationally recognized health economists, policy experts, and clinicians. | 2/4/2018 |
| 1543 | Precision Medicine Group Boston, MA Associate Research Scientist - Health Economics and Outcomes Research MS Exp: 1 yr |
Associate Research Scientists are responsible for collaborating across a broad portfolio of sophisticated health economic and health policy research projects. | 2/4/2018 |
| 1544 | Precision Medicine Group Oakland, CA Associate Research Scientist - Evidence Synthesis MS Exp: 1 yr |
As an Associate Research Scientist in our Evidence Synthesis and Decision Modeling practice, you will be collaborating across a broad portfolio of sophisticated health economic and health policy research projects. | 2/4/2018 |
| 1545 | Precision Medicine Group Frederick, MD Molecular Laboratory Technician II BS in Biology, Chemistry or Life Sciences Exp: 1-2 yrs |
When bio-specimens are returned to our facility or requested for further testing, you will process biological samples to include isolating DNA, RNA and miRNA from clinical samples, quantifying, normalizing and aliqutoting nucleic acids for downstream assays. Evaluating and implementing new molecular extraction protocols. You will also be running technology platforms such as Nanostring and qPCR. | 2/4/2018 |
| 1546 | Adimab Lebanon, NH Research Associate BS in molecular biology, chemical engineering, or biochemistry Exp: 1 yr |
The Research Associate will work in a small team setting to support Adimab's novel antibody discovery, maturation, and production platform. This role will closely interface with the Protein Analytics, High Throughput Expression, Molecular Sciences, and Computational Biology teams. | 2/4/2018 |
| 1547 | ADMA Biologics Boca Raton, FL Chemist I BS in Chemistry, Biochemisty, Molecular Biology or related science discipline. Exp: 1-2 yrs |
Perform quality control testing of raw materials, in-process and final products; following general instructions on routine work and detailed instructions on new assignments. | 2/4/2018 |
| 1548 | ADMA Biologics Boca Raton, FL QC Lab Associate l BS in Biology, Chemistry, Medical Technology, or related scientific field. Exp: 1-3 yrs |
Performs quality control processing for Stability Products and Reserve Samples and performs appearance inspections.Completes processing documentation and data entry as required for procedures performed and tests performed at contract laboratories. | 2/4/2018 |
| 1549 | Advanced Cell Diagnostics Newark, CA Research Associate/ Sr. Research Associate BS in molecular biology, biochemistry, cell biology or related field Exp: 1 yr |
Perform RNAscope-based assays to support new product development and optimization, clinical assay development and validation, and provide customer service. You must be willing to learn new techniques quickly and adapt to shifting priorities in a fast-paced growing environment. | 2/4/2018 |
| 1550 | Aerie Irvine, CA Regulatory Affairs Specialist - CMC BS in a scientific field Exp: 0-3 yrs |
The Regulatory Affairs Specialist, CMC is responsible for participating in the processes and the preparation of documents required for meeting requirements established by U.S. and international governmental agencies in introducing and maintaining new products in the marketplace. | 2/4/2018 |
| 1551 | Agilent Frederick, CO Manufacturing Associate BS in chemistry, biology, biochemistry, science Exp: 1 yr |
Actively involved in the manufacturing of oligonucleotide APIs in a GMP environment.Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing. | 2/4/2018 |
| 1552 | Agios Cambridge, MA Senior Research Associate - Biology MS Exp: 1-3 yrs |
The successful candidate will utilize a variety of molecular and cell biology techniques to drive forward a translational research program evaluating data coming back from the clinic in real time and additionally driving novel science to help enhance success in the clinical setting. | 2/4/2018 |
| 1553 | Agios Cambridge, MA Research Associate/Senior Research Associate, Metabolic Immuno Oncology MS Exp: 1 yr |
The RA / SRA will utilize a variety of molecular and immunology techniques to support and drive forward a program of research evaluating and drugging novel immune targets. She / he will have the unique opportunity to work on target validation while getting exposure to the clinical candidate development process. She / he will interact and collaborate cross-functionally with a variety of scientists including biologists, biochemists, chemists, and pharmacologists. | 2/4/2018 |
| 1554 | AIT Bioscience Indianapolis, IN Laboratory Scientist - Ligand Binding Assay (LBA) BS in a life science Exp: 1-5 yrs |
The Laboratory Scientist performs and manages tasks that result in accurate and timely method development, validation and sample analysis of chemical and biological entities in biological matrix in a regulated environment utilizing various analytical technologies in a ligand binding assay laboratory. Displays versatility and accuracy in performing laboratory duties. | 2/4/2018 |
| 1555 | AIT Bioscience Indianapolis, IN Laboratory Scientist - LC - MS/MS BS in a chemical or life science Exp: 1-5 yrs |
The Laboratory Scientist performs and manages tasks that result in accurate and timely method development, validation and sample analysis of chemical and biological entities in biological matrix in a regulated environment utilizing various analytical technologies including mass spectroscopy. Displays versatility and accuracy in performing laboratory duties. | 2/4/2018 |
| 1556 | Alan Laboratories San Diego, CA Chemistry Lab Technician BS Exp: 0 yr |
To conduct formulation preparation or analytical test in direct support of the drug development team, including writing documents and reports. Responsible for the maintenance of lab instrumentation and general lab duties. | 2/4/2018 |
| 1557 | ALCON Johns Creek, GA QA Associate Quality Engineer BS Exp: 0 yr |
The Assoc Quality Engineer - Operations will lead activities involving product impact assessments, product quarantine, non-conformance reporting / issue resolution, auditing of production areas, and procedural updates to ensure the process and documentation is compliant to 21CFR820, ISO and internal requirements. | 2/4/2018 |
| 1558 | ALCON Lake Forest, CA Engineer (Research) BA / BS in Engineering Exp: 0 yr |
Execute Global Medical Affairs vitreoretinal strategic tactics (lab studies part of the Phase IIIB / IV study plan). Generates high quality scientific evidence to ensure effective support of the Vitreoretinal brand. | 2/4/2018 |
| 1559 | ALCON Houston, TX Operations Quality Engineer I BS in Engineering or Physical Sciences (e.g. Chemistry, Physics) Exp: 0-2 yrs |
The Operations Quality Engineer will lead activities involving assigned routine product inspections, product impact assessments for events, product quarantine activities, non-conformance reporting / issue resolution, auditing of production areas, and procedural updates to ensure the process and documentation is compliance with 21CFR820, ISO, and other regulatory requirements as well as internal requirements. | 2/4/2018 |
| 1560 | ALCON Fort Worth, TX Labeling Specialist II BS Exp: 0 yr |
Collaborate with R & D, Regulatory and Global Graphics Designers to create labeling for medical products. Ensure that labeling, art, film and proofs meet all medical, legal and regulatory requirements. Monitor changes in labeling requirements in the US and abroad. Review promotional labeling and ensure that it applies with approved labeling. May monitor, evaluate and recommend improvements to labeling process, quality, systems tools and / or policies. Develop solutions to a variety of problems of moderate scope and complexity. Refers to policies and procedures for guidance. Errors in judgment or failure to achieve results would normally require a moderate expenditure of resources to rectify. | 2/4/2018 |
| 1561 | ALCON Fort Worth, TX Summer 2018 Internship - Package Engineering BS in Package Engineering, Materials or Supply Chain function Exp: NA |
This internship will involve working with departmental Package Engineers and Product Lifecycle coordinators to identify all approved primary, secondary and tertiary components and how they are assembled into finished products so that an approved component catalog can be created and placed within a shared communication site with Alcon Fort Worth Manufacturing. Work will also involve reviewing secondary and tertiary components for development and execution of a harmonized approach to functional and material designs. | 2/4/2018 |
| 1562 | ALCON Fort Worth, TX Summer 2018 Internship - Biomedical Engineering - R&D BS / MS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern - assigned project(s) will align to one of our two business groups - Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 2/4/2018 |
| 1563 | ALCON Fort Worth, TX Summer 2018 Internship - Chemical Engineering - R&D BS / MS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern - assigned project(s) will align to one of our two business groups - Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 2/4/2018 |
| 1564 | Agilent Wilmington, DE Application Specialist, Intern BS in Chemistry or a related science Exp: NA |
Test analytical gas chromatograph performance.Design and validate applications on leading-edge GC instrumentation, including sample prep, instrument maintenance, and general lab work. | 2/4/2018 |
| 1565 | Takeda Cambridge, MA Summer 2018 Internship - CNS Therapeutic Area MS Exp: NA |
The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 2/4/2018 |
| 1566 | Takeda San Diego, CA 2018 Summer Internship - CNS In Vitro Pharmacology BS in Biology, Chemistry, Biochemistry or related Exp: NA |
The internship involves working in laboratory that evaluates novel chemical compounds against their enzyme / protein / receptor targets toward the furtherance of drug discovery. The intern will assist biologists in conducting biochemical assays, cell-based screening assays and solubility assays. The intern will work closely with a biochemist in a pharmaceutical research lab learning and applying practical aspects of biochemistry and cell-based assay. This individual will interact closely with other biologists and biochemists in the team. Responsibilities will also include maintaining a safe organized lab bench and become proficient with appropriate software necessary to execute the duties and keep an accurate and comprehensive notebook. | 2/4/2018 |
| 1567 | Takeda Deerfield, IL 2018 Summer Internship - Clinical Science USMO BS / MS Exp: NA |
Different aspects of phase 4 study activities and strategy of a product in IBD.Will interact with the study team and sites to ensure all data and information needed aligns with study milestones and timelines. | 2/4/2018 |
| 1568 | 3M Maplewood, MN Internship - R&D Graduate Intern MS in a Science or Engineering Exp: NA |
Individuals hired as a Graduate Summer Intern in 3M Research and Development will work with senior scientists and laboratory management to develop advanced technologies and products in one of 3M's Corporate Research Labs or Business Group Labs. At 3M, our researchers leverage our 46 technology platforms and capabilities to develop new technologies and products that solve customer problems across many businesses and markets. 3M offers over 55,000 products that are helping customers are used in consumer electronics, hospitals and clinics, industrial manufacturing, and safety products. 3M core technologies are highly varied that include material technologies such adhesives, nanotechnology, and biomaterials and process technologies such as precision coating, radiation processing, and polymer extrusions. | 2/4/2018 |
| 1569 | 3M Cynthiana, KY Internship - Corporate Engineering - Project Engineering Intern BS / MS in Engineering Exp: NA |
A Resident Project Engineering Intern uses engineering knowledge and skills as a leader of a cross functional teams to define the scope, cost and schedule for capital investment projects which support 3M's global manufacturing and research efforts. A project engineer also participates in cost reduction, quality improvements, new process and technology development programs, Lean Six Sigma and safety related activities. | 2/4/2018 |
| 1570 | 3M Wallingford, CT 3M HIS Quality Assurance Intern BS / MS Exp: NA |
Developing automation tools for testing linked HTML pages and their content;Developing automation tools for testing linked HTML pages and their content Develop a framework for testing web based applications and services using Amazon Web Services (AWS). | 2/4/2018 |
| 1571 | HD Biosciences San Diego, CA Research Associate I BS / MS Exp: 1 yr |
Work as a team to perform complex in vivo experiments utilizing tumor models (syngeneic, xenograft tumor models and humanized mouse models) in both immunocompetent and immunocompromised mice. | 1/22/2018 |
| 1572 | HD Biosciences San Diego, CA Research Associate II BS / MS Exp: 1 yr |
Conducting in vivo pharmacology experiments for preclinical CRO | Performing PK |
| 1573 | 23andMe Mountain View, CA Lab Operations Associate BS Exp: 1 yr |
Monitor 23andMe's contracted laboratories for both commercial testing and research projects | Follow up on |
| 1574 | 4D Molecular Therapeutics Emeryville, CA Research Associate, Analytical Development BS in Biochemistry, Chemistry, or Related Discipline Exp: 0-3 yrs |
The Research Associate will be responsible for the execution of routine testing in support of process development and routine manufacturing, and will contribute to the development of analytical assays for characterization of therapeutic products. The successful incumbent will need to make experimental observations, review and analyze data for presentations and reports, and will share maintenance responsibilities such as reagent preparation, material ordering, and general lab upkeep. | 1/22/2018 |
| 1575 | 3M New Ulm, MN Manufacturing Engineer - Electrical Markets Group BS in Mechanical or Manufacturing Engineering or Technology Exp: 1 yr |
The person hired for the position of Manufacturing Engineer will provide technical leadership and manufacturing support within the Plastic Molding and Assembly Plant. This position will be supporting development and deploying of new or improved process technology, new product development, cost reduction and quality improvements. In this position, the person is responsible for driving operational excellence within the areas of support and is expected to initiate and conduct broadly defined technical tasks within the process technology platforms. They are also responsible for advising, consulting and troubleshooting area processes within the plant. | 1/22/2018 |
| 1576 | 3M Decatur, AL Analytical Chemist BS / MS in Chemistry, Material Science or Chemical Engineering Exp: 1 yr |
The person hired for the position of Analytical Chemist / Materials Engineer will develop and apply specialty analytical measurements to solve polymer and film manufacturing problems. This position should appeal to an analytically-minded person with scientific curiosity and problem solving skills. This position provides abundant opportunity for technical growth for a self-motivated person. | 1/22/2018 |
| 1577 | 3M Menomonie, WI Manufacturing Engineer - Personal Care Division BS / MS in Chemical Engineering, Industrial Engineering, Manufacturing Engineering or Mechanical Engineering Exp: 1 yr |
The person hired for the position of Manufacturing Engineer will support the Personal Care Division in the IATD business as a part of the Film Manufacturing & Supply Chain Organization (FMSCO) from within the 3M Menomonie Facility. The person will be part of a team supporting the personal care business in producing hook products for multiple customers throughout the world. | 1/22/2018 |
| 1578 | 3M Maplewood, MN Sr. Synthetic Chemist MS in Chemistry Exp: 1 yr |
The person hired for the position of Sr. Synthetic Chemist will primarily be responsible for synthesis of new fluorinated materials supporting 3M Novec Engineered Fluids. This is an exciting position working in an attractive technical environment. This position requires an individual with strong leadership skills, who is a good decision maker with ability to collect facts and separate symptoms from problems. Typical development activities will take place in the lab, working directly with application development engineers. | 1/22/2018 |
| 1579 | 3M Maplewood, MN Quality Engineer/Technologist BS / MS in Mechanical Engineering, Chemical Engineering, Statistics, Chemistry, Microbiology or related discipline Exp: 1 yr |
The person hired for the position of Quality Engineer / Technologist will work and interact with other cross functional team members (lab, plant manufacturing, manufacturing technology, regulatory, quality systems, etc.) on quality assurance of our test systems. This position can provide a great opportunity to learn, grow, and develop as an employee. | 1/22/2018 |
| 1580 | 3M Brookings, SD Product Assurance Engineer BS / MS in a science or engineering discipline Exp: 1 yr |
The person hired for the position of Product Assurance Engineer will own commercialized biological indicators product lines within the manufacturing plant and manage change control and quality improvements in our Device Reprocessing business. This individual will lead and support projects that appreciably impact quality, performance, service, and cost, and will collaborate cross-functionally to include manufacturing, regulatory, lab, business, and plant personnel. | 1/22/2018 |
| 1581 | Abbiotec San Diego, CA Research Associate, Monoclonal Antibody Production BS in Cell Biology Exp: 0-5 yrs |
The position requires being technically competent in the field of monoclonal antibody production. The individual will carry out monoclonal antibody production by hybridoma technology for our contract research projects and in-house development projects. | 1/22/2018 |
| 1582 | Danaher Miami, FL Systems Engineer MS in Engineering Exp: 0-2 yrs |
Supports all engineering activities related to product and process development during project phases in accordance with design controls. | 1/22/2018 |
| 1583 | Danaher Sunnyvale, CA Optical Engineer I BS in Physics, Optical or Electrical Engineering or a related technical discipline Exp: 1-2 yrs |
The Optical Engineer I is responsible for the design, test, validation and transfer to production of high-sensitivity, multi-color, fluorimetric optical device modules that are key components of molecular diagnostic instruments. The Optical Engineer is also responsible to work routinely with a broad range of optics-related issues, from internal optical technical support of Cepheid instruments and fluorescence-based assays to development, test and validation of custom optical systems used in Manufacturing. | 1/22/2018 |
| 1584 | Danaher Chaska, MN Quality Assurance Engineer I - HW/SW Medical Device BS / MS in Engineering Exp: 0-2 yrs |
Collaborate with the QA functional group during the development and review of product design requirements, specification, protocols and reports for the characterization, verification and validation activities | 1/22/2018 |
| 1585 | Danaher Brea, CA Systems Engineer II MS in Electrical, Mechanical, Biomedical, Reliability, or Systems Engineering Exp: 1 yr |
Collect appropriate data to define, identify, analyze, correct and prevent potential system failures; Develop test plans and conduct bench and system level testing that cover the expected customer use environment and operation conditions. | 1/22/2018 |
| 1586 | Danaher Houston, TX Process Engineer BS / MS in Chemical Engineering or Chemistry Exp: 1 yr |
To provide technical support for the use of Pall Energy products and technologies in the Americas region. To use this expertise to develop and support advantaged key / strategic customer processes and applications. | 1/22/2018 |
| 1587 | Danaher Hauppauge, NY Manufacturing Engineer BS in Chemical, Manufacturing, Mechanical, or Biomedical Engineering Exp: 0-6 months |
Supports the day to day manufacturing operations for Intercompany media, surface treatment processes or BioPharm in a Continuous Improvement environment. | 1/22/2018 |
| 1588 | Abaxis UNION CITY, CA Manufacturing Engineer BS in Engineering or Industrial Technology Exp: 1-3 yrs |
Monitor, maintain and provide metrics for current MFG processes; Lead and coordinate the implementation of new processes to support the manufacturing line and personnel. | 1/22/2018 |
| 1589 | Abaxis UNION CITY, CA Document Control Specialist BS Exp: 1 yr |
Process Document Change Orders (DCOs) according to procedure(s), ensuring appropriate formatting, document classification, cross references, approvals, and proper record keeping in DCO forms. Be alert to obvious typographical errors and inconsistencies in documents. Monitor and facilitate timeliness of DCO approval in accordance with the Signature Authority Matrix. | 1/22/2018 |
| 1590 | Abaxis UNION CITY, CA Chemist 2 MS Exp: 1-2 yrs |
Participate in the development, maintenance and improvement of high sensitivity immunoassays using LSPR and / or magnetic bead and chip-based technology | 1/22/2018 |
| 1591 | Abaxis UNION CITY, CA Chemist 1 BS Exp: 0-1 yr |
Participate in the research and development of immunoassays; Validation of immunoassays in clinical samples; Ensure immunoassay compliance with regulatory standards in areas of sensitivity, specificity, reproducibility, and robustness through definition of test parameters and quality standards. | 1/22/2018 |
| 1592 | Abbott Plymouth, MN Engineer - Scientist I BS in engineering, biological science, animal science, or nursing Exp: 1-5 yrs |
We are seeking a high caliber Scientist-Engineer I to execute and administer pre-clinical studies to support Product Development efforts, clinical translation research, and regulatory submissions (FDA [510(K), IDE, PMA] and Foreign Notified Body [Design Dossier, CE Mark filings]). This includes procedural management of electrophysiology and cardiovascular laboratory equipment (such as the EnSite Velocity System, WorkMate Recording System, RF ablation generators, ViewMate Ultrasound System, etc.) and disposable products such as introducers, sheaths, guidewires, trans septal needles, and diagnostic and ablation catheters. It also includes oversight / supervision in anatomical analyses such as necropsy. | 1/22/2018 |
| 1593 | Abbott Temecula, CA Associate Quality Engineer BS in Mechanical, BioMed, Chemical, Manufacturing Exp: 0-2 yrs |
Primary Job Function Provide Process / Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process / Quality Engineering support to product development teams, helping to ensure development of highest quality new products. | 1/22/2018 |
| 1594 | Danaher New Port Richey, FL Intern - Research and Development (Year Round) BS in engineering or science Exp: NA |
This full-year intern will support ongoing R&D projects. He / she will primarily work in our labs under the direction of our R&D staff. | 1/22/2018 |
| 1595 | Danaher New Port Richey, FL Intern - Engineering (Throughout the Year) BS Exp: NA |
The Engineering Interns assist engineers in the design of products to conform to customer specifications and requirements. Perform Customer Specification and Source Control Drawing reviews against PAC Designs. Use engineering tools including CATIA 3-D solid modeling software, and basic finite element analysis tools. Perform dimensional tolerance analysis, fluid flow calculations, and basic stress calculations. Creation of manufacturing drawings and engineering documentation for the production of new products. | 1/22/2018 |
| 1596 | 3M MURRAY,, UT 3M HIS Health Systems Researcher Intern BS / MS Exp: NA |
Work with data specialists to create a useful health plan claims data set for research | Analyze claim |
| 1597 | 3M SILVER SPRING, MD 3M HIS NLP Intern BS / MS Exp: NA |
As an intern, you can grow through challenging work, get involved in meaningful projects and receive great coaching from our leaders. Here, you can apply your talent in bold ways that matter. | 1/22/2018 |
| 1598 | 3M Menomonie, WI Internship - Film Manufacturing Technology Process Engineering Intern BS / MS Exp: NA |
The person hired for the position of Manufacturing Technology Process Engineering Intern will provide technical and project leadership for FMSCO Coating Operations. They would lead process and operational improvement projects using Six Sigma and Lean Manufacturing Tools. The projects would impact new product development, cost reduction and quality improvement. This person will interact in various cross-functional teams. They would also be responsible for providing engineering support for experiments within a Pilot Plant, or in a larger scale manufacturing setting. | 1/22/2018 |
| 1599 | West Pharmaceutical Services Scottsdale, AZ Internship - Quality & Engineering BS Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience | 1/22/2018 |
| 1600 | West Pharmaceutical Services Scottsdale, AZ Internship - Research & Development BS Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience | 1/22/2018 |
| 1601 | West Pharmaceutical Services Scottsdale, AZ Internship - Engineering BS Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience | 1/22/2018 |
| 1602 | Stryker Tempe, AZ 2018 Summer Internship - Regulatory BS Exp: NA |
Work cross functionally with different departments including R&D Engineering, Supplier Quality, Marketing, and Clinical Affairs to assist in regulatory decision-making and develop a broad understanding of the medical device industry. | 1/22/2018 |
| 1603 | Takeda Cambridge, CA Summer 2018 Internship - Drug Product Development (Vaccines Business Unit) BS / MS Exp: NA |
The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 1/22/2018 |
| 1604 | Takeda Cambridge, CA Summer 2018 Internship - Technical Operations BS / MS Exp: NA |
The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 1/22/2018 |
| 1605 | Takeda Cambridge, CA Summer 2018 Internship - Operational Data & Analytics BS / MS Exp: NA |
Knowledgeable mentors will provide guidance as you gain professional hands-on experience. The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 1/22/2018 |
| 1606 | HD Biosciences San Diego, CA Research Associate I BS / MS Exp: 1 yr |
Work as a team to perform complex in vivo experiments utilizing tumor models (syngeneic, xenograft tumor models and humanized mouse models) in both immunocompetent and immunocompromised mice. | 1/22/2018 |
| 1607 | HD Biosciences San Diego, CA Research Associate II BS / MS Exp: 1 yr |
Conducting in vivo pharmacology experiments for preclinical CRO | Performing PK |
| 1608 | 23andMe Mountain View, CA Lab Operations Associate BS Exp: 1 yr |
Monitor 23andMe's contracted laboratories for both commercial testing and research projects | Follow up on |
| 1609 | 4D Molecular Therapeutics Emeryville, CA Research Associate, Analytical Development BS in Biochemistry, Chemistry, or Related Discipline Exp: 0-3 yrs |
The Research Associate will be responsible for the execution of routine testing in support of process development and routine manufacturing, and will contribute to the development of analytical assays for characterization of therapeutic products. The successful incumbent will need to make experimental observations, review and analyze data for presentations and reports, and will share maintenance responsibilities such as reagent preparation, material ordering, and general lab upkeep. | 1/22/2018 |
| 1610 | 3M New Ulm, MN Manufacturing Engineer - Electrical Markets Group BS in Mechanical or Manufacturing Engineering or Technology Exp: 1 yr |
The person hired for the position of Manufacturing Engineer will provide technical leadership and manufacturing support within the Plastic Molding and Assembly Plant. This position will be supporting development and deploying of new or improved process technology, new product development, cost reduction and quality improvements. In this position, the person is responsible for driving operational excellence within the areas of support and is expected to initiate and conduct broadly defined technical tasks within the process technology platforms. They are also responsible for advising, consulting and troubleshooting area processes within the plant. | 1/22/2018 |
| 1611 | 3M Decatur, AL Analytical Chemist BS / MS in Chemistry, Material Science or Chemical Engineering Exp: 1 yr |
The person hired for the position of Analytical Chemist / Materials Engineer will develop and apply specialty analytical measurements to solve polymer and film manufacturing problems. This position should appeal to an analytically-minded person with scientific curiosity and problem solving skills. This position provides abundant opportunity for technical growth for a self-motivated person. | 1/22/2018 |
| 1612 | 3M Menomonie, WI Manufacturing Engineer - Personal Care Division BS / MS in Chemical Engineering, Industrial Engineering, Manufacturing Engineering or Mechanical Engineering Exp: 1 yr |
The person hired for the position of Manufacturing Engineer will support the Personal Care Division in the IATD business as a part of the Film Manufacturing & Supply Chain Organization (FMSCO) from within the 3M Menomonie Facility. The person will be part of a team supporting the personal care business in producing hook products for multiple customers throughout the world. | 1/22/2018 |
| 1613 | 3M Maplewood, MN Sr. Synthetic Chemist MS in Chemistry Exp: 1 yr |
The person hired for the position of Sr. Synthetic Chemist will primarily be responsible for synthesis of new fluorinated materials supporting 3M Novec Engineered Fluids. This is an exciting position working in an attractive technical environment. This position requires an individual with strong leadership skills, who is a good decision maker with ability to collect facts and separate symptoms from problems. Typical development activities will take place in the lab, working directly with application development engineers. | 1/22/2018 |
| 1614 | 3M Maplewood, MN Quality Engineer/Technologist BS / MS in Mechanical Engineering, Chemical Engineering, Statistics, Chemistry, Microbiology or related discipline Exp: 1 yr |
The person hired for the position of Quality Engineer / Technologist will work and interact with other cross functional team members (lab, plant manufacturing, manufacturing technology, regulatory, quality systems, etc.) on quality assurance of our test systems. This position can provide a great opportunity to learn, grow, and develop as an employee. | 1/22/2018 |
| 1615 | 3M Brookings, SD Product Assurance Engineer BS / MS in a science or engineering discipline Exp: 1 yr |
The person hired for the position of Product Assurance Engineer will own commercialized biological indicators product lines within the manufacturing plant and manage change control and quality improvements in our Device Reprocessing business. This individual will lead and support projects that appreciably impact quality, performance, service, and cost, and will collaborate cross-functionally to include manufacturing, regulatory, lab, business, and plant personnel. | 1/22/2018 |
| 1616 | Abbiotec San Diego, CA Research Associate, Monoclonal Antibody Production BS in Cell Biology Exp: 0-5 yrs |
The position requires being technically competent in the field of monoclonal antibody production. The individual will carry out monoclonal antibody production by hybridoma technology for our contract research projects and in-house development projects. | 1/22/2018 |
| 1617 | Danaher Miami, FL Systems Engineer MS in Engineering Exp: 0-2 yrs |
Supports all engineering activities related to product and process development during project phases in accordance with design controls. | 1/22/2018 |
| 1618 | Danaher Sunnyvale, CA Optical Engineer I BS in Physics, Optical or Electrical Engineering or a related technical discipline Exp: 1-2 yrs |
The Optical Engineer I is responsible for the design, test, validation and transfer to production of high-sensitivity, multi-color, fluorimetric optical device modules that are key components of molecular diagnostic instruments. The Optical Engineer is also responsible to work routinely with a broad range of optics-related issues, from internal optical technical support of Cepheid instruments and fluorescence-based assays to development, test and validation of custom optical systems used in Manufacturing. | 1/22/2018 |
| 1619 | Danaher Chaska, MN Quality Assurance Engineer I - HW/SW Medical Device BS / MS in Engineering Exp: 0-2 yrs |
Collaborate with the QA functional group during the development and review of product design requirements, specification, protocols and reports for the characterization, verification and validation activities | 1/22/2018 |
| 1620 | Danaher Brea, CA Systems Engineer II MS in Electrical, Mechanical, Biomedical, Reliability, or Systems Engineering Exp: 1 yr |
Collect appropriate data to define, identify, analyze, correct and prevent potential system failures; Develop test plans and conduct bench and system level testing that cover the expected customer use environment and operation conditions. | 1/22/2018 |
| 1621 | Danaher Houston, TX Process Engineer BS / MS in Chemical Engineering or Chemistry Exp: 1 yr |
To provide technical support for the use of Pall Energy products and technologies in the Americas region. To use this expertise to develop and support advantaged key / strategic customer processes and applications. | 1/22/2018 |
| 1622 | Danaher Hauppauge, NY Manufacturing Engineer BS in Chemical, Manufacturing, Mechanical, or Biomedical Engineering Exp: 0-6 months |
Supports the day to day manufacturing operations for Intercompany media, surface treatment processes or BioPharm in a Continuous Improvement environment. | 1/22/2018 |
| 1623 | Abaxis UNION CITY, CA Manufacturing Engineer BS in Engineering or Industrial Technology Exp: 1-3 yrs |
Monitor, maintain and provide metrics for current MFG processes; Lead and coordinate the implementation of new processes to support the manufacturing line and personnel. | 1/22/2018 |
| 1624 | Abaxis UNION CITY, CA Document Control Specialist BS Exp: 1 yr |
Process Document Change Orders (DCOs) according to procedure(s), ensuring appropriate formatting, document classification, cross references, approvals, and proper record keeping in DCO forms. Be alert to obvious typographical errors and inconsistencies in documents. Monitor and facilitate timeliness of DCO approval in accordance with the Signature Authority Matrix. | 1/22/2018 |
| 1625 | Abaxis UNION CITY, CA Chemist 2 MS Exp: 1-2 yrs |
Participate in the development, maintenance and improvement of high sensitivity immunoassays using LSPR and / or magnetic bead and chip-based technology | 1/22/2018 |
| 1626 | Abaxis UNION CITY, CA Chemist 1 BS Exp: 0-1 yr |
Participate in the research and development of immunoassays; Validation of immunoassays in clinical samples; Ensure immunoassay compliance with regulatory standards in areas of sensitivity, specificity, reproducibility, and robustness through definition of test parameters and quality standards. | 1/22/2018 |
| 1627 | Abbott Plymouth, MN Engineer - Scientist I BS in engineering, biological science, animal science, or nursing Exp: 1-5 yrs |
We are seeking a high caliber Scientist-Engineer I to execute and administer pre-clinical studies to support Product Development efforts, clinical translation research, and regulatory submissions (FDA [510(K), IDE, PMA] and Foreign Notified Body [Design Dossier, CE Mark filings]). This includes procedural management of electrophysiology and cardiovascular laboratory equipment (such as the EnSite Velocity System, WorkMate Recording System, RF ablation generators, ViewMate Ultrasound System, etc.) and disposable products such as introducers, sheaths, guidewires, trans septal needles, and diagnostic and ablation catheters. It also includes oversight / supervision in anatomical analyses such as necropsy. | 1/22/2018 |
| 1628 | Abbott Temecula, CA Associate Quality Engineer BS in Mechanical, BioMed, Chemical, Manufacturing Exp: 0-2 yrs |
Primary Job Function Provide Process / Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process / Quality Engineering support to product development teams, helping to ensure development of highest quality new products. | 1/22/2018 |
| 1629 | Danaher New Port Richey, FL Intern - Research and Development (Year Round) BS in engineering or science Exp: NA |
This full-year intern will support ongoing R&D projects. He / she will primarily work in our labs under the direction of our R&D staff. | 1/22/2018 |
| 1630 | Danaher New Port Richey, FL Intern - Engineering (Throughout the Year) BS Exp: NA |
The Engineering Interns assist engineers in the design of products to conform to customer specifications and requirements. Perform Customer Specification and Source Control Drawing reviews against PAC Designs. Use engineering tools including CATIA 3-D solid modeling software, and basic finite element analysis tools. Perform dimensional tolerance analysis, fluid flow calculations, and basic stress calculations. Creation of manufacturing drawings and engineering documentation for the production of new products. | 1/22/2018 |
| 1631 | 3M MURRAY,, UT 3M HIS Health Systems Researcher Intern BS / MS Exp: NA |
Work with data specialists to create a useful health plan claims data set for research | Analyze claim |
| 1632 | 3M SILVER SPRING, MD 3M HIS NLP Intern BS / MS Exp: NA |
As an intern, you can grow through challenging work, get involved in meaningful projects and receive great coaching from our leaders. Here, you can apply your talent in bold ways that matter. | 1/22/2018 |
| 1633 | 3M Menomonie, WI Internship - Film Manufacturing Technology Process Engineering Intern BS / MS Exp: NA |
The person hired for the position of Manufacturing Technology Process Engineering Intern will provide technical and project leadership for FMSCO Coating Operations. They would lead process and operational improvement projects using Six Sigma and Lean Manufacturing Tools. The projects would impact new product development, cost reduction and quality improvement. This person will interact in various cross-functional teams. They would also be responsible for providing engineering support for experiments within a Pilot Plant, or in a larger scale manufacturing setting. | 1/22/2018 |
| 1634 | West Pharmaceutical Services Scottsdale, AZ Internship - Quality & Engineering BS Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience | 1/22/2018 |
| 1635 | West Pharmaceutical Services Scottsdale, AZ Internship - Research & Development BS Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience | 1/22/2018 |
| 1636 | West Pharmaceutical Services Scottsdale, AZ Internship - Engineering BS Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience | 1/22/2018 |
| 1637 | Stryker Tempe, AZ 2018 Summer Internship - Regulatory BS Exp: NA |
Work cross functionally with different departments including R&D Engineering, Supplier Quality, Marketing, and Clinical Affairs to assist in regulatory decision-making and develop a broad understanding of the medical device industry. | 1/22/2018 |
| 1638 | Takeda Cambridge, CA Summer 2018 Internship - Drug Product Development (Vaccines Business Unit) BS / MS Exp: NA |
The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 1/22/2018 |
| 1639 | Takeda Cambridge, CA Summer 2018 Internship - Technical Operations BS / MS Exp: NA |
The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 1/22/2018 |
| 1640 | Takeda Cambridge, CA Summer 2018 Internship - Operational Data & Analytics BS / MS Exp: NA |
Knowledgeable mentors will provide guidance as you gain professional hands-on experience. The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 1/22/2018 |
| 1641 | BioPharmGuy Anytown, US Contract Research Assistant Some college Exp: 0 |
Looking for someone to confirm employee numbers for companies we list. Must be able to accept payment via PayPal. | 01/17/18 |
| 1642 | Takeda Cambridge, MA Metrology Lab Instrumentation Specialist BS in chemistry, biology, pharmacy, engineering or related pharmaceutical science Exp: 0 yr |
Coordinate and assist in performance of installation, calibration, maintenance, and IQ / OQ / PQ activities for GxP and non-GxP analytical equipment. | 1/14/2018 |
| 1643 | LabCentral Cambridge, MA Lab Purchasing Assistant BS in life sciences Exp: 1-3 yrs |
Engage with current / future vendors and residents to enhance our mission | Employ your |
| 1644 | Barry-Wehmiller Philadelphia, PA Entry Level Project Engineer BS in Mechanical Engineering, Electrical Engineering, or equivalent technical degree Exp: 1-5 yrs |
Accountability for all aspects of project execution including line layout engineering, mechanical design, vendor / contractor management, equipment procurement, schedule management, project finances, site management and installation support. | 1/14/2018 |
| 1645 | Veracyte South San Francisco, CA Lab Assistant BS in the life sciences Exp: 1 yr |
The Lab Assistant will perform routine specimen accessioning, test analysis and recording of testing process in accordance with established protocols. The position will process specimens upon receipt in the lab and assist in molecular genetic testing on clinical specimens which includes expression array analysis. Additional responsibilities include all related clerical functions, lab maintenance and regulatory compliance tasks. You'll work alongside a highly engaged team of Lab Assistants and Clinical Lab Scientists and will collaborate with other groups across Veracyte. | 1/14/2018 |
| 1646 | Eurofins Viracor Lee's Summit, MO Clinical Laboratory Scientist or Laboratory Technician BS / BA in biological, physical, chemical or clinical laboratory science Exp: 1 yr |
The Laboratory Technician is primarily responsible for performing laboratory tests and analyses under the direction of a lab supervisor or scientist including specimen management, specimen pipetting, instrument operation / maintenance, data entry and specimen storage with a high degree of proficiency. Follow Standard Operating Procedures (SOPs). Ensure all laboratory equipment and work areas are clean, sterile, and in proper working order. May be responsible for calibration of instruments. Conducts routine tasks as directed. Closely supervised with little latitude for independent judgment. | 1/14/2018 |
| 1647 | Eurofins Viracor Lee's Summit, MO Clinical Laboratory Scientist I, II or III BS / BA in biological, physical, chemical or clinical laboratory science Exp: 1 yr |
The Clinical Laboratory Scientist (CLS) performs laboratory testing, preventive maintenance, troubleshooting, calibration of equipment, quality control procedures and is responsible for the validity of test results. | 1/14/2018 |
| 1648 | Waisman Biomanufacturing Madison, WI Quality Assurance Document Control Specialist BS in Biochemistry, Chemistry, Biology, Bacteriology, Virology or a related field Exp: 1-2 yrs |
The Document Control Specialist's primary responsibilities will include QA documentation and record keeping, QA raw material control, quality systems (documentation control, failure investigation, deviation reporting, etc.) and training documentation. They will also provide backup support for external audits. | 1/14/2018 |
| 1649 | Voyager Therapeutics Cambridge, MA Research Associate, Process Development (Downstream/Formulation Focus) BS in chemical engineering, biology, biochemistry, chemistry, biotechnology, or related fields Exp: 1 yr |
The qualified candidate will assist with and / or individually carry out chromatographic purifications, various filtration operations, formulation studies for Voyager s various rAAV products, and conduct stability studies. Work activities will also include following / preparing protocols, SOPs and final study reports, and general lab operations. | 1/14/2018 |
| 1650 | Voyager Therapeutics Cambridge, MA Research Associate Process Analytics BS in Biochemistry / Biology / Chemistry / Virology or a related field Exp: 1-3 yrs |
The qualified candidate will maintain adherent cell culture and plate cells for bioassays using aseptic conditions. The candidate will also perform analysis of process development and pre-clinical grade materials. After product testing, the candidate will be responsible for data analysis as well as reporting of data. | 1/14/2018 |
| 1651 | TA Instruments New Castle, DE Manufacturing Engineer BS Exp: 1-3 yrs |
Responsible for maintaining the design of released products with the goal of continuously improving quality, customer satisfaction, efficiency of production and cost effectiveness | 1/14/2018 |
| 1652 | Xenobiotic Laboratories Plainsboro, NJ Quality Control Associate I BS in chemistry, biology, or a related discipline Exp: 0-2 yrs |
Performs various mathematical calculations including subtraction, addition, multiplication, division, and statistical analysis including means, standard deviations, coefficient of variation (% std dev), percent change, percent difference, etc. | 1/14/2018 |
| 1653 | HD Biosciences San Diego, CA Research Associate I BS / MS Exp: 1 yr |
Work as a team to perform complex in vivo experiments utilizing tumor models (syngeneic, xenograft tumor models and humanized mouse models) in both immunocompetent and immunocompromised mice. | 1/14/2018 |
| 1654 | HD Biosciences San Diego, CA Research Associate II BS / MS Exp: 1 yr |
The design, optimization and execution of pharmacology experiments for compound screening, compound mode of action and efficacy in mechanistic and disease models, e.g. acute and chronic autoimmune / inflammatory conditions, and analyses and reporting of experiments. | 1/14/2018 |
| 1655 | WuXi AppTec Marietta, GA Laboratory Technician BS in Chemistry or equivalent experience Exp: 1 yr |
This position is responsible for processing samples for assigned tests in compliance with GLP, GMP and ISO standards. | 1/14/2018 |
| 1656 | WuXi AppTec Plainsboro, NJ Associate Scientist MS Exp: 0 yr |
Self- motivated, requiring some daily supervision to participate in the processes of in vitro assay screening and high throughput screening (HTS) of a wide array of protocols for a diverse client base that includes pharmaceutical and biotechnology companies. | 1/14/2018 |
| 1657 | Xenobiotic Laboratories Plainsboro, NJ Assistant Quality Assurance Specialist BS in biology, chemistry, or related field Exp: 1-4 yrs |
Maintains a current awareness of EPA, FDA, and OECD Good Laboratory Practice (GLP) regulations and any other related Regulations which may apply to XBL activities. | 1/14/2018 |
| 1658 | WuXi AppTec Plainsboro, NJ Laboratory Technician II, Genetic Stability, Sunday - Thursday BS in Biological Sciences or science related major Exp: 1 yr |
Performs 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). 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. Performs daily work activities with minimal supervision. | 1/14/2018 |
| 1659 | WuXiNextCODE Cambridge, MA CLINICAL GENOMICS SCIENTIST MS in human genetics, molecular genetics or related field Exp: 1 yr |
Analyzing and interpreting genetic testing results generated from clinical diagnostic sequencing | Working in co |
| 1660 | X-Chem Waltham, MA Research Associate High - Throughput Chemistry BS / MS in Chemistry or a related subject Exp: 1-4 yrs |
A track record of success in organic synthesis, particularly in the areas of reaction optimization or library synthesis. | 1/14/2018 |
| 1661 | Sekisui XenoTech Kansas City, KS Research Assistant BS in biological or chemical sciences Exp: 1 yr |
The Research Assistant assists with routine laboratory functions including: maintaining primary and immortalized cell lines, adherence to aseptic technique, diluting, labeling and dispensing of biological samples, reagent solution preparation, equipment repair, laboratory upkeep, maintaining an inventory of supplies, and various other responsibilities. | 1/14/2018 |
| 1662 | Zoetis Charles City, IA Associate Regulatory Compliance Specialist BA / BS Exp: 0-2 yrs |
Manage international regulatory compliance activities for Charles City Operations with emphasis on providing documentation to support new registrations, renewals and process changes of veterinary biological products produced in Charles City | 1/14/2018 |
| 1663 | Zoetis Charles City, IA Associate Process Specialist MS Exp: 0-2 yrs |
Provide the first line of response to address technical / process issues within Manufacturing, coordinating the engagement of the Global Manufacturing Technology (GMT) organization as needed. Identify and drive continuous process improvements. Take manufacturing lead in introduction of new / modified processes and product transfers as well as provide technical support in conducting investigations and preparation of QARs. Conducts all activities and makes decisions that are in accordance with Company policies & SOPs, Zoetis Values, & global regulatory guidelines (including cGMP / cGLP / cGCP), environmental guidelines, as appropriate, etc. | 1/14/2018 |
| 1664 | Zymergen Emeryville, CA RESEARCH ASSOCIATE I/II, STRAIN BANKING BS in Microbiology, Biology, or similar field Exp: 1-2 yrs |
This group will eventually be responsible for cell banking / QC of all banks made at Zymergen. This means this person will work with a wide variety of microbes used for screening at Zymergen in addition to commercial scale production at client sites | 1/14/2018 |
| 1665 | 10x Genomics Pleasanton, CA Research Associate Product Development BS in molecular biology, biochemistry, chemistry or related fields Exp: 1 yr |
The candidate will further the development of 10x Single Cell product portfolios using novel approaches in molecular biology, chemistry and microfluidics. This individual will execute and troubleshoot experiments that include cell handling, sample preparation, PCR, library preparation for sequencing, and other related techniques. S / he will also analyze and interpret data and assist in the preparation and delivery of presentations and documentations. | 1/14/2018 |
| 1666 | 10x Genomics Pleasanton, CA Production Associate I/II BS / MS in Molecular Biology, Analytical Chemistry, Chemical Engineering, or equivalent Exp: 0-5 yrs |
This is an entry to junior level non-exempt position in 10x reagent manufacturing team. Individuals applying to this position should have a basic understanding of industry manufacturing workflow and ERP system. This individual must be a self-starter, quick learner and detail oriented, work well in a team atmosphere, have good communication skills, ability to adapt and thrive in working at a fast-paced environment. | 1/14/2018 |
| 1667 | West Pharmaceutical Services Exton, PA Internship - Product Engineering - New Product Introduction BS in Biomedical, Mechanical, Chemical or Electrical Engineering discipline Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience. | 1/14/2018 |
| 1668 | West Pharmaceutical Services Exton, PA Internship - Regulatory Affairs BS in Pharmacy, Pharmaceutical Sciences, Pharmaceutical Chemistry, Biochemistry, biotechnology, Medicine, Veterinary Medicine, Bioengineering, Biology Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience. | 1/14/2018 |
| 1669 | West Pharmaceutical Services Exton, PA Internship - Pharmaceutical Processing BS in Chemistry, Engineering (Chemical, Mechanical, Electrical, or Bio Engineering), Physics or Materials Science Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience. | 1/14/2018 |
| 1670 | Syngenta Greensboro, NC Process Engineering Intern BS in Chemical Engineering or closely related discipline Exp: NA |
Provides process engineering capability for development projects in Production and Processing Technology, with appropriate guidance | 1/14/2018 |
| 1671 | Stryker San Jose, CA 2018 Summer Internship - Regulatory - California BS Exp: NA |
Work cross functionally with different departments including R&D Engineering, Supplier Quality, Marketing, and Clinical Affairs to assist in regulatory decision-making and develop a broad understanding of the medical device industry. | 1/14/2018 |
| 1672 | Stryker Mahwah, NJ 2018 Summer Internship - Regulatory - New Jersey - 24078BR BS Exp: NA |
Work cross functionally with different departments including R&D Engineering, Supplier Quality, Marketing, and Clinical Affairs to assist in regulatory decision-making and develop a broad understanding of the medical device industry. | 1/14/2018 |
| 1673 | Stryker Kalamazoo, MI 2018 Summer Internship - Regulatory - Michigan BS Exp: NA |
Work cross functionally with different departments including R&D Engineering, Supplier Quality, Marketing, and Clinical Affairs to assist in regulatory decision-making and develop a broad understanding of the medical device industry. | 1/14/2018 |
| 1674 | Takeda Cambridge, MA Summer 2018 Internship - Translational Research and Early Clinical (TREC) Imaging BS / MS Exp: NA |
Potential projects could include developing novel imaging methods to image animal models of disease or new clinical imaging biomarkers, or developing advanced image analysis methods for preclinical or clinical image data sets, or designing new approaches for modeling or machine learning of imaging data | 1/14/2018 |
| 1675 | Takeda Cambridge, MA Summer 2018 Internship - Quantitative Clinical Pharmacology/Quantitative Solutions BS / MS Exp: NA |
The intern will be given a real-world translational (oncology) modeling problem to tackle with close guidance of Takeda modelers, clinical pharmacologists, biologists, and clinicians. Example problems include: what does our study drug (or combination of study drugs) do to the trajectories of tumor burden in human subjects | 1/14/2018 |
| 1676 | Takeda Cambridge, MA Summer 2018 Internship - Cell - based Group, Lead Discovery BS / MS Exp: NA |
Takeda's summer internship program blends real world experience with an extensive overview of the pharmaceutical industry. Knowledgeable mentors will provide guidance as you gain professional hands-on experience. The summer internship program is 12 weeks in length and offers a unique perspective into a world-class pharmaceutical company. Compensation is competitive, and financed temporary housing is available to those who qualify. Our internship program also provides you the opportunity to network with people at Takeda through various planned events and activities. | 1/14/2018 |
| 1677 | Shire Los Angeles, CA Engineer II BS / MS in Engineering Exp: 0-3 yrs |
The primary responsibilities of this role are the execution of equipment and process improvement projects, to contribute to the design, development or enhancement of new and existing products and processes and being a system owner for manufacturing equipment and processes. Enhancing process knowledge and technical problem solving are major elements of this position. This positon will provide technical support to the manufacturing and maintenance functions for the operation of equipment and processes. | 1/7/2018 |
| 1678 | Synthetic Genomics La Jolla, CA Research Associate/ Research Associate II, Viral Systems BS in Molecular Biology, Cell Biology, Immunology, Virology or related field Exp: 1-3 yrs |
The successful candidate will support the overall program goals and strategy of the group which will include significant laboratory activities such as synthesis and assembly of target genes, development of novel vaccine platform technologies, characterization of RNA and protein expression in vitro. The candidate will have broad molecular and cellular biology experience. Previous experience with virology and viral vector construction will be considered a plus. Excellent verbal, presentation, and written communication skills are essential and the capability to effectively work in a team environment is required. | 1/7/2018 |
| 1679 | Synthetic Genomics La Jolla, CA Temporary Research Associate, Molecular Biology BS in Molecular Biology, Biochemistry, Microbiology, Cell Biology, Genetics, or related discipline Exp: 6 months |
Successful candidates for the position will work under the direction of R&D scientists on the Synthetic Systems and DNA Technologies team, and will support innovative experimental research aiming to advance the development and commercialization of novel microbial production platforms. | 1/7/2018 |
| 1680 | T2 Biosystems Lexington, MA Instrument Engineer BS in Biomechanical Engineering Exp: 1 yr |
We are seeking a talented and highly motivated individual to join our team as an Instrument Engineer. This position will report directly to the Manager of System Testing and Validation. | 1/7/2018 |
| 1681 | Takeda Brooklyn Park, MN Manufacturing Associate II BS in a scientific or engineering discipline Exp: 1-2 yr |
The Manufacturing Associate II performs and documents cGMP activities to support upstream and downstream production areas and operations. This involves operation of process equipment, execution of validation protocols, completion of cGMP documents, creating / revising cGMP documents and other assignments as directed. | 1/7/2018 |
| 1682 | Takeda Cambridge, MA Specialist, Pharmaceutical Sciences Strategic Sourcing & Vendor Management BS / BA Exp: 1-3 yrs |
The Specialist position supports the global Strategic Sourcing and Vendor Management function of Pharmaceutical Sciences through timely preparation, negotiation and execution of various contracts and other outsourcing-related documents. | 1/7/2018 |
| 1683 | Takeda Cambridge, MA Senior Research Associate, In Process Analytics MS in chemistry, biology, pharmacy, engineering or related pharmaceutical science Exp: 1 yr |
In this role, you will be empowered to execute method development for complex molecules, evaluate and implement new analytical assays besides routine assay support. You will participate in planning unit operations / experiments under supervision to ensure timely project support and drafting support documentation. | 1/7/2018 |
| 1684 | Takeda Cambridge, MA Research Associate - Analytical Development BS in chemistry, biology, pharmacy, engineering or related pharmaceutical science Exp: 0 yr |
Responsible for executing basic / routine experiments under supervision. This position also assists in the planning of basic experiments and experiments and performs specialized / complex experiments with assistance from supervisor as appropriate | 1/7/2018 |
| 1685 | Takeda Cambridge, MA Cell Culture Process Development Engineer III MS in chemistry, biology, pharmacy, engineering or related pharmaceutical science Exp: 0 yr |
The Engineer III will work primarily with scientists / senior research associates or engineers in the Cell Culture Process Development team to design and optimize consistent cell culture processes that produce quality recombinant proteins through laboratory studies. Additionally, as a fundamental component related to cell culture process design, the cell culture group will also ensure that these processes are predicable, scalable, and controlled. | 1/7/2018 |
| 1686 | Takeda Cambridge, MA Senior Research Associate, Formulations MS in chemistry, biology, pharmacy, engineering or related pharmaceutical science Exp: 0 yr |
In this role you will be developing pharmaceutical formulation of solid orals and / or parenterals. You will be developing and evaluating dosage forms such as powder flow, granulation, compaction, disintegration, dissolution and stability. | 1/7/2018 |
| 1687 | Weinberg Group Washington, DC Regulatory Specialists & Project Managers BS / MS Exp: 1-5 yrs |
Working with clients to develop regulatory strategies and plans for FDA;Crafting, writing, and editing regulatory submissions;Working with an internal project team and client to meet regulatory deadlines, respond to FDA issues and assure integrity of submissions. | 1/7/2018 |
| 1688 | Theravance Biopharma South San Francisco, CA Research Associate I/II BS / MS Exp: 1-2 yr |
This individual will play a key role in developing, optimizing, and automating new assays, conducting compound screening for SAR support, performing data analysis, and contributing to compound mechanism of action studies. As part of a multidisciplinary team, this individual will participate in drug discovery projects in several therapeutic areas and across multiple target classes. | 1/7/2018 |
| 1689 | Theravance Biopharma South San Francisco, CA Research Assistant/Research Associate I BA / BS Exp: 1 yr |
The successful candidate will have the opportunity to work closely with discovery program teams and scientists across functional areas and to present his or her work at group, department, and project team meetings. The candidate will be presented with opportunities for training on new techniques, cross-training between teams, and will be actively mentored. | 1/7/2018 |
| 1690 | Tocagen San Diego, CA Facility Lab Technician, Procurement Specialist BA / BS Exp: 1-3 yrs |
The Facility Lab Technician, Procurement Specialist will be responsible for the overall support of the facility operational needs including laboratory management, facility & laboratory equipment maintenance, facility & laboratory procurement of supplies, and companywide shipping & receiving. The position will require that you are self-motivated, able to work in a fast-paced environment on multiple tasks, quickly learn new techniques, organize tasks efficiently, communicate and collaborate well, and maintain current accurate records at all times. | 1/7/2018 |
| 1691 | Toxikon Corporation Bedford, MA Quality Assurance Associate BS in a life science Exp: 1 yr |
In this quality assurance role, the appropriate candidate will be responsible for the implementation, functioning, and monitoring of quality assurance activities. This includes monitoring biological and chemical studies, and creating reports in conformance with GLP practices. Candidates will review GMP, GLP and non-GLP reports for accuracy with reference to protocols, Quality Assurance Standards, Standard Operational Procedures, laboratory precision and accuracy limits, as well as reviewing all protocols for compliance and accuracy. Other quality assurance responsibilities include maintaining equipment performance, calibration records and preventative maintenance logs. Included duties are performing system and phase audits according to GLP and ISO guidelines, as well as all other activities required from quality assurance. | 1/7/2018 |
| 1692 | Adello Biologics Chicago, IL Assistant I , Manufacturing BS in a Biotechnology, Biology or Chemistry Exp: 0-2 yrs |
The Assistant I, Manufacturing is a regular employee in a full-time non-exempt position at Adello Biologics, LLC, in Chicago, IL, this employee will be responsible for the manufacturing of Biotechnology products for clinical and commercial human use. Employee employs aseptic techniques while working in controlled and classified environments, some of which require complete aseptic gowning. Must comply with Adello policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and any other government requirement. | 1/7/2018 |
| 1693 | Triclinic Labs West Lafayette , IN Analytical Scientist MS in Analytical Chemistry, or other relevant area Exp: 1-3 yrs |
The Analytical Scientist will perform activities related to analytical support for development of pharmaceuticals and fine chemicals. This position requires 1-3 years of relevant industry experience with focus on analytical development and analysis support for pharmaceutical small molecules and drug products. | 1/7/2018 |
| 1694 | Triphase San Diego, CA Clinical Research Associate (CRA) BS in a health-related science or equivalent Exp: 1-3 yrs |
The CRA will report to the Associate Director of Clinical and Regulatory Operations and is responsible for assisting with the design, administration, and monitoring of clinical trials; monitoring and managing clinical data from collection through locked database; and ensuring compliance with clinical protocols, their objectives, and ICH and GCP guidelines. | 1/7/2018 |
| 1695 | Tris Pharma Monmouth Junction, NJ Quality Control Chemist BS in Chemistry or related scientific discipline Exp: 1 yr |
QC Chemists perform analytical testing of raw materials, packaging component, in-process, finished product, stability samples, cleaning verification / validation, and process validation samples following Analytical Methods, Protocols, Procedures (SOP s) and company policies. He / she follows and maintains adherence to current industry standards (cGMP s, GLP s, etc.) to meet production and customer demand. Qualified candidates will be expected to work either independently or as a team to achieve company goals and initiatives. | 1/7/2018 |
| 1696 | Tris Pharma Monmouth Junction, NJ Scientist I Analytical R&D MS Exp: 0-2 yrs |
Under moderate supervision, performs laboratory analyses in the testing of raw materials, in process (IP), finished products (FP) and stability (ST) samples. Performs maintenance and calibration of analytical instruments, and prepares standard and sample solutions. Carries out laboratory work to support product development and method development. | 1/7/2018 |
| 1697 | Ultragenyx Novato, CA Research Associate MS in Molecular Biology, Cell Biology and / or related discipline Exp: 1 yr |
The candidate will work with nucleic acids, proteins, and mammalian cells to contribute to the development of biochemical and cell-based assays for target validation and advancement of biologics and small molecule therapeutics. Responsibilities include independent planning and execution of experimental work, data analysis and presentation of material at project team meetings. The candidate will be expected to collaborate and work dynamically on diverse projects, communicate effectively on scientific concepts and interact with colleagues in other functional areas. | 1/7/2018 |
| 1698 | uniQure Lexington, MA Validation Engineer BS in Life Sciences or Engineering Exp: 0-2 yrs |
The incumbent is responsible for assisting the Validation Manager in completion of all project milestones. This includes installation, operational and performance qualification of equipment and utilities, environmental qualification, process validation, and preparation of all relevant documentation to meet regulatory requirements for new and existing products (includes standard operating procedures, technical reports and risk assessments). | 1/7/2018 |
| 1699 | West Pharmaceutical Services Clearwater , FL Internship - Engineering BS in Mechanical Engineering or Industrial Engineering Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience. | 1/7/2018 |
| 1700 | West Pharmaceutical Services Exton , PA Internship - Analytical Lab Services BS in Chemistry, Engineering, Physics or Materials Science Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, well-rounded and marketable skills and experience. | 1/7/2018 |
| 1701 | West Pharmaceutical Services Exton , PA Internship - Scientific Communications BS in Chemistry or Chemical Engineering discipline Exp: NA |
At West, interns are key contributors to the company. During your 10 week, competitively paid internship program, you will gain significant, marketable skills and experience. | 1/7/2018 |
| 1702 | Takeda Cambridge, MA Summer 2018 Internship - Lead Discovery BS / MS in a engineering field Exp: NA |
We are seeking a student intern to join the Automation and Engineering Group. She or he would engage in a range of activities to support our lab automation efforts and support the high throughput screening activities within Lead Discovery. Projects might include developing a liquid handler QC process, electronics assembly (PCB assembly, soldering, etc.), and light programming / scripting. Additionally, she or he will have the opportunity to learn how to design objects in SolidWorks and subsequently fabricate them through 3D printing. She or he will be expected to document her / his projects and to present on them at the end of the internship. | 1/7/2018 |
| 1703 | Takeda San Diego, CA Intern - Bioanalytical Chemistry BS in chemistry, biochemistry or chemical engineering Exp: NA |
The intern will gain insight in how drug discovery works, within Takeda s DMPK Department. The focus of the internship will be centered around bioanalysis of drugs in various matrixes, operating and troubleshooting instruments, and presenting your work to a scientific group. | 1/7/2018 |
| 1704 | Takeda San Diego, CA Intern - GI Medicinal Chemistry BS in chemistry or biochemistry Exp: NA |
Preparation of solvents and solvent fills on Medicinal Chemistry analytical instruments | Preparation o |
| 1705 | Synthetic Genomics La Jolla, CA Intern - Molecular Biology BS / MS in Molecular Biology, Biochemistry, Microbiology, Cell Biology, Genetics, or related discipline Exp: NA |
The selected candidate for this unique industrial internship will work under the direction of R&D scientists on the Synthetic Systems and DNA Technologies team, and will support innovative experimental research aiming to advance the design and construction of microbes with synthetic genomes. | 1/7/2018 |
| 1706 | Syngenta Berthoud, CO Cereal Field Production Intern BS / MS Exp: NA |
To introduce the intern to the seed production operation, gaining experience by taking responsibility for selected field production operations in support of the production of a reliable supply of high quality seed. Position will take on several roles based upon field production practices, plant processing requirements and distribution needs. Perform a project to study a potential production improvement. | 1/7/2018 |
| 1707 | Syngenta Pasco, WA Field Production - Seeded Vegetables Intern BS in Agricultural Discipline Exp: NA |
As an intern at Syngenta, you have the opportunity to work alongside some of the brightest minds in the industry, and work on real projects finding real solutions. | 1/7/2018 |
| 1708 | Syngenta Greensboro, NC Regulatory and Stewardship Intern BS / MS in chemistry, environmental science or other science discipline Exp: NA |
Assist in the preparation of data summaries and reports that will be used in submissions to EPA and the State authorities for product registration, research historical records to support registration of products using departmental data management and document systems. Interact and network with the broader Syngenta R&D community to obtain supporting information for projects. The selected candidate will assist a senior Regulatory Manager in preparation of data summaries, position papers and basic product registration submissions or technical responses to address product registration issues. | 1/7/2018 |
| 1709 | Stryker Redmond, WA 2018 Summer Internship - Biomedical Engineering - Washington BS Exp: NA |
Impact the development and manufacturing of cutting edge products; Gain experience within a fast paced and growing industry; Apply classroom knowledge in a fast-paced and growing industry setting; Implement new ideas, be constantly challenged, and develop your skills | 1/7/2018 |
| 1710 | Stryker Fort Lauderdale, FL 2018 Summer Internship Biomedical Engineering Florida BS Exp: NA |
Impact the development and manufacturing of cutting edge products; Gain experience within a fast paced and growing industry; Apply classroom knowledge in a fast-paced and growing industry setting; Implement new ideas, be constantly challenged, and develop your skills | 1/7/2018 |
| 1711 | Stryker Mahwah, NJ 2018 Summer Internship Biomedical Engineering New Jersey BS Exp: NA |
Impact the development and manufacturing of cutting edge products; Gain experience within a fast paced and growing industry; Apply classroom knowledge in a fast-paced and growing industry setting; Implement new ideas, be constantly challenged, and develop your skills | 1/7/2018 |
| 1712 | Shire Lexington, MA Development Specialist MS Exp: 1-2 yrs |
As a member of Analytical Development Method Development team, he / she will work on method development, qualification and characterization of drug substance, drug product and reference standards for biological programs. Responsibilities include designing experiments per ICH guidelines, flawless execution of experimental studies, documenting results accurately in the laboratory notebooks, writing and reviewing technical reports, generating test methods to support high throughput and QC testing groups, participate in analytical, process development and QC meetings and discussions, etc. | 12/5/2017 |
| 1713 | Shire Lexington, MA Engineer II MS in Chemical & Biomolecular Engineering or related field Exp: 1 yr |
Seeking an Engineer II with the following duties: Act as key member of the Massachusetts process lab, part of the PDTS (Process Development and Technical Services) organization; execute product lifecycle and manufacturing support for global biologics network; emphasize hands-on, lab-based activities to design and execute studies to support late phase clinical and commercial manufacturing; | 12/5/2017 |
| 1714 | Shire Lexington, MA Downstream Development Engineer I BS in Chemical / Biochemical Engineering, Biochemistry or related discipline Exp: 0-2 yrs |
The individual will be a member within a group responsible for performing purification process development, including timely completion of small-scale experiments and process scale-up for programs that bring new biopharmaceutical products to pre-clinical, clinical and process validation manufacturing phases. The individual applies basic knowledge form various technical areas, industry practices and standards under close supervision. Provides quality and productive output that is consistently timely, reliable and reproducible. The candidate must be customer focused, results oriented, science driven and embrace Shire s values. | 12/5/2017 |
| 1715 | Shire Milford, MA Manufacturing Associate 1 BS Exp: 1 yr |
This position is focused on the downstream (purification) portion of the biologicsmanufacturing of Obizur, an FDA-approved treatment for Acquired Hemophilia A. Cross-training in the upstream aspect of the manufacturing process is alsopart of the job but primary responsibility is for executing all purificationproduction process steps while strictly adhering to cGMP, environmental healthand safety guidelines and any other related regulations which apply. | 12/5/2017 |
| 1716 | Shire Milford, MA Manufacturing Associate II BS Exp: 1-3 yrs |
This position is focused on the downstream portion of the biologicsmanufacturing of Obizur, an FDA-approved treatment for Acquired Hemophilia A. Cross-training in the upstream (cell culture) aspect of the manufacturing process is also part of the job but primary responsibility is for executing all purification steps in production process while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations which apply. | 12/5/2017 |
| 1717 | Shire Los Angeles, CA Automation Engineer I BS in Engineering (preferably in Chemical. BioChemical, Biomedical, or Mechanical) Exp: 0-1 yr |
Works as part of the team to partner with manufacturing in troubleshooting the automated control processes. Contributes to the successful implementation of system improvement projects and drives improvements around manufacturing KFA (key focus areas) goals including but not limited to people / safety, quality / regulatory / compliance, customer, financials, and operational excellence | 12/5/2017 |
| 1718 | Smithers Avanza Gaithersburg, MD Laboratory Suppoert Technician BS in biological sciences Exp: 1 yr |
Reviews laboratory workload and prepares schedules in conjunction with laboratory manager. | 12/5/2017 |
| 1719 | Smithers Avanza Gaithersburg, MD Animal Study Tech 1 BS in Biology, Life sciences, Chemistry or Science field Exp: 1 yr |
Learns how to review study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. | 12/5/2017 |
| 1720 | Smithers Avanza Gaithersburg, MD In Life Study Technician I BS in Biology, Life sciences, Chemistry or Science field Exp: 1 yr |
Learns how to review study protocol and ensure study tasks and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. | 12/5/2017 |
| 1721 | Smithers Avanza Gaithersburg, MD Research Scientist II MS in Molecular Sciences and Nanotechnology Exp: 1 yr |
Conduct Ligand-binding assays (e.g. ELISA / MSD) applicable to Pharmacokinetic, Biomarker and Immunogenicity studies. Conduct in-depth analysis including method transfer, development, validation and sample testing in support of GLP studies. Statistical and analytical data processing using Watson LIMS, Excel. Evaluate and interpret obtained data, translate and transfer data for further evaluation and provide data summaries for studies. Design studies to assure that their activities meet the regulatory, GLP, protocol, and SOP requirements. Maintain the experimental records and raw data in a secure way to protect data integrity. Review and check data generated by other staff. | 12/5/2017 |
| 1722 | Smithers Avanza Gaithersburg, MD Scientist 1 MS in Biological or Physical Sciences Exp: 1-2 yrs |
Perform analysis including method transfer, development, validation and sample testing in support of GLP studies.Responsible for data interpretation and provide data summaries for studies. | 12/5/2017 |
| 1723 | Spherotech Lake Forest, IL Quality Control Associate BS in Chemistry or related field Exp: 1 yr |
Duties include final product inspection, documentation, Quality Control testing etc | 12/5/2017 |
| 1724 | Spectrum Pharmaceuticals Irvine, CA Clinical Trials Assistant BS in life science Exp: 1-2 yrs |
Provide support to the Clinical Trial Managers and Clinical Research Associates in Clinical Trial conduct via preparation, distribution, and tracking of study supplies, mass mailings, copying, data entry, etc. | 12/5/2017 |
| 1725 | Q-State Biosciences Cambridge, MA Research Associate, Tissue Culture BS in biology, chemistry, or a related field Exp: 1 yr |
Q-State Biosciences is seeking a highly motivated Research Associate to support and execute its cutting edge discovery and screening efforts. The Research Associate will work closely with Q-State s scientific and management teams to perform studies in a high quality and scientifically rigorous fashion. | 12/5/2017 |
| 1726 | Ultivue Cambridge, MA Laboratory Technician BS in biology, chemistry, biochemistry, or a related field Exp: 1-2 yrs |
Ultivue is looking for a highly motivated and detail oriented Laboratory Technician to join our team. This versatile role will support the day-to-day laboratory operations that are the key to successful research and manufacturing processes. The applicant will be advised by and work directly with Ultivue s Research and Development team | 12/5/2017 |
| 1727 | Beryllium Discovery Corp. Bedford, MA Research Associate, Protein Purification BA / BS Exp: 1-2 yrs |
The successful candidate will be able to perform duties with some supervision and will collaborate within the group and across other core lab functions. Communication skills are essential. The successful candidate will be energetic, efficient and thrive in a fast-paced environment. | 12/5/2017 |
| 1728 | Confer Health Charlestown, MA Associate Scientist BA / BS Exp: 1-2 yrs |
Work in a fast-paced lab environment. We are constantly optimizing our lab to help push science forward at unprecedented rates. | 12/5/2017 |
| 1729 | Bluefin BioMedicine Cambridge, MA Research Associate, Molecular Biology BS in Molecular Biology, Biochemistry, or equivalent Exp: 1 yr |
The individual will report to the Director of Antibody Discovery and Upstream Process Development, joining a team of dedicated scientists engaged in developing therapeutic antibodies to novel cancer antigens. The successful candidate will contribute their molecular biology knowledge and cloning and expression of recombinant proteins experience to further our pre-clinical product development efforts. | 12/5/2017 |
| 1730 | Berg Health Framingham, MA Laboratory Operations Specialist I - CLIA Laboratory BS Exp: 0-2 yrs |
Accession clinical samples in the Laboratory Information Management System (LIMS) following laboratory s standard operating procedures (SOPs) for downstream processes | 12/5/2017 |
| 1731 | Merrimack College Cambridge, MA Adjunct Lecturer in Biology MS in biology Exp: 0-1 yr |
The instructor will consult with the lead instructor for the course and follow syllabus and the case-based format. They will be responsible for writing and grading exams and other assignments. Three hours lecturing plus 2 office hours per week. | 12/5/2017 |
| 1732 | Jounce Therapeutics NA, MA Senior Research Associate, Protein Production BS / MS in biochemistry or a related discipline Exp: 1-3 yrs |
He / she will be will be responsible for the production of antibodies and proteins for use in R&D that will enable the development of groundbreaking therapies. He / she will be expected to participate in experimental design, conduct experiments, optimize throughput, maintain detailed records, and generate standard operating procedures. This is an exciting opportunity to be part of a fast-paced, start-up environment in the dynamic field of immuno-oncology. | 12/11/2017 |
| 1733 | Platelet Biogenesis Boston, MA Bioreactor - Characterization Joint Research Associate BS / MS in biological sciences or related field Exp: 1-2 yrs |
This person will work directly with the two teams to advance the millifluidic bioreactor and characterize the product. The candidate will plan and execute experiments utilizing human and mouse cells to optimize the production of platelets. | 12/11/2017 |
| 1734 | CONTINUUS Pharmaceuticals Woburn, MA Analytical Chemist BS / MS in analytical chemistry / chemistry Exp: 1-3 yrs |
The candidate is expected to work on analytical method development, qualification, and implementation across CONTINUUS s different projects. | 12/11/2017 |
| 1735 | Instrumentation Laboratory Bedford, MA Scientist I BS Exp: 1 yr |
Performs entry level professional laboratory work of a routine nature requiring application of general and specialized methods, techniques, and instruments. | 12/11/2017 |
| 1736 | H3 Biomedicine Cambridge, MA Clinical Trial Associate BS Exp: 1-2 yrs |
This position provides support to the Clinical Operations team and will report to a clinical operations director This person will provides routine clerical support / administrative functions for staff members within the Clinical Operations Department. As well as providing technical and administrative services for the collection, review, maintenance, and tracking of regulatory documents for clinical study centers. Supports staff members in planning / coordination efforts. Work is performed under general supervision and guidance | 12/11/2017 |
| 1737 | Aerotek Boston, MA Medical Technologist BS Exp: 0-1 yr |
Employee will train one bench at a time until they are able to work on the bench without supervision | Employee will |
| 1738 | Stratacuity Boston, MA Research Associate, Cellular/Molecular Biology BS / MS Exp: 1-6 yrs |
Our exclusive client is starting something completely novel and so simple it may change the game. Funding, people, culture, seasoned and humble leadership...all there. If you can thrive in a startup and are seasoned in genetic screening, genome engineering, and in vitro biochemistry then please apply. | 12/11/2017 |
| 1739 | Commonwealth Sciences Boston, MA Associate Scientist - NGS BS / MS in Molecular Biology or equivalent Exp: 1-2 yrs |
Support research projects across diverse areas using next generation sequencing (NGS) technologies | Run several p |
| 1740 | Commonwealth Sciences Boston, MA Scientist - Formulation BS / MS Exp: 0-1 yr |
Work independently in supporting senior group scientists on their projects.Design, plan, and perform experiments in order to test hypotheses and advance understanding of fundamental scientific principles. | 12/11/2017 |
| 1741 | uniQure Lexington, MA Validation ENgineer BS in Life Sciences or Engineering Exp: 0-2 yrs |
The incumbent is responsible for assisting the Validation Manager in completion of all project milestones. This includes installation, operational and performance qualification of equipment and utilities, environmental qualification, process validation, and preparation of all relevant documentation to meet regulatory requirements for new and existing products (includes standard operating procedures, technical reports and risk assessments). | 12/11/2017 |
| 1742 | Whitehead Institute Cambridge, MA Technical Assistant I - GEM BS in biology or a field directly related to the work Exp: 1-2 yrs |
Designs and performs bench level experiments and small independent research projects to support scientific research objectives of a lab or group. Analyzes experimental data, addresses methodological problems in experimental protocols and results, and reports data to supervisor. Uses discretion in prioritizing and organizing workflow and in optimizing methodologies and results. | 12/11/2017 |
| 1743 | Roche Tucson, AZ Summer Intern - Biostatistics MS in biostatistics, statistics, epidemiology or relevant fields Exp: NA |
The candidate will help to perform a research project on clinical equivalence based on external concordance study for a follow-on CDx. | 12/11/2017 |
| 1744 | Roche Tucson, AZ Summer Intern - Analytical Methods MS with a chemical or bioscience degree Exp: NA |
The intern is requested to build a database of data on antibodies and proteins. This is a continuation of an intern project from 2017. The project will show the potential of analytical methods to offer an internal quality check for antibodies / formulations quickly and inexpensively, while minimizing risk. If implemented in upstream processes, the outcome will result avoiding intense trouble shooting / complex investigations. | 12/5/2017 |
| 1745 | Roche Tucson, AZ Summer Intern - Product Support Engineer BS / MS Exp: NA |
The intern in Global Technical Support team will assist in reducing complexity and also providing tools and procedures to the Field-based personnel. | 12/5/2017 |
| 1746 | West-Ward Pharmaceuticals Cherry Hill, NJ Manufacturing Specialist BS in techincal discipline Exp: 0-3 yrs |
Assist the shift lead in a hands-on approach to overseeing production activities including, filling, sterilization, component and equipment prep, and compounding. Completes quality systems activities including commitments, deviations, DCEs, and SOP revisions as necessary. Responsible for meeting budget, quality, and production goals, setting standards, and making employment and staffing recommendations. Interprets manufacturing policies, procedures, and programs | 12/2/2017 |
| 1747 | Regeneron Tarrytown, NY Research Associate II or Higher, Protein Biochemistry MS in Biochemistry, or related field Exp: 1-3 yrs |
We are seeking a talented and motivated Research Associate to join the Protein Biochemistry group. The qualified individual will be responsible for performing a variety biochemical and biophysical assays to characterize protein biologics to support late-stage development and commercialization efforts. The ideal candidate will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment. | 12/2/2017 |
| 1748 | Regeneron Tarrytown, NY Process Development Associate/ Engineer I BS / MS in Chemical Engineering, Biochemical Engineering, or Biochemistry Exp: 0-2 yrs |
The qualified individual will be responsible for purification process development and support purification of various non-clinical biological molecules to support reagent needs for Regeneron s research and discovery groups. The ideal candidate will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, as well as in a team environment. | 12/2/2017 |
| 1749 | Regeneron Tarrytown, NY Temp Research Associate, CRISPR Therapeutics BS Exp: 1-2 yrs |
The responsibilities for this position would include working with on-going in vivo rodent experiments (blood collection, animal handling, animal injections, necropsies). The applicant will also be to have basic understanding of molecular biology, cell biology, biochemistry, and genetics and be able to perform Westerns, ELISAs, and IHCs. The candidate must be able to correctly document the results, analyze the data and communicate the results clearly and concisely. | 12/2/2017 |
| 1750 | Regeneron Tarrytown, NY Temp - Clinical Trial Operations Associate, Clinical Trial Management MS Exp: 1-2 yrs |
Under general supervision, the CTOA II supports, coordinates, and implements clinical research projects. Assists and works with the study team in the initiation, maintenance and closeout of clinical projects according to GCP, ICH, CFR and Regeneron SOPs / WPDs. The CTOA II executes assignments with general instruction; more instruction may be required for new projects. Travel to study sites may be required to assist with monitoring clinical studies. The CRA II may have site responsibility. | 12/2/2017 |
| 1751 | Regeneron Rensselaer,, NY QA Validation Specialist BS / BA in Engineering, Chemistry, or Life Sciences Exp: 1 yr |
Validate / qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures. | 12/2/2017 |
| 1752 | Safis Solutions Indianapolis, IN Validation Analyst BS Exp: entry-level |
The Validation Analyst will be familiar with IT Software Validation regulatory expectations. Attention to detail is expected to ensure high quality documentation. | 12/2/2017 |
| 1753 | Samumed San Diego, CA Research Associate, Biology BS / MS in Biological Sciences Exp: 1-3 yrs |
Samumed is seeking a responsible, dynamic, creative and highly motivated individual to join its oncology team in the R&D division to contribute to preclinical research programs aimed at the development of treatments for cancer. | 12/2/2017 |
| 1754 | Valeant Pharmaceuticals International Ballwin, MO Engineer II, Manufacturing BS in an engineering discipline Exp: 1 yr |
This position provides manufacturing engineering support to a manufacturing operation. This may include designing and implementing new manufacturing processes, designing manufacturing tooling, improving existing manufacturing processes, repairing and coordinating the repair of production machinery, and providing technical guidance to manufacturing personnel. | 12/2/2017 |
| 1755 | Sanaria Rockville, MD Regulatory Affairs Specialist BS / MS Exp: 1-4 yrs |
Support regulatory submissions (INDs, Master Files, CTAs, IMPDs, BLA, etc) for product development process;Responsible for preparation and submission of standard regulatory documentation to support regulatory filings including, but not limited to, CMC and clinical amendments, IND annual reports, Investigator's Brochure (IB), safety reports, clinical trial progress reports, | 12/2/2017 |
| 1756 | Sanofi Swiftwater, PA ASSOCIATE QUALITY TECHNICIAN BA / BS in life sciences Exp: 1-3 yrs |
This Associate Quality Technician will perform quality inspections on incoming quality managed materials, documentation verification, statistical sample removal, and identity labeling of materials by strictly adhering to Sanofi Pasteur policies and procedures and cGMP. The position will also be required to perform cleaning of work areas, equipment, and any other jobs as required, ensure all duties are completed on time, and complete required Safety and Compliance training and associated training modules as assigned. | 12/2/2017 |
| 1757 | Sanofi Allston, MA AUTOMATION ENGINEER I MS in Engineering Exp: 0-2 yrs |
The Automation Engineer I assist more senior members to ensure reliable operation and implementation of all automation systems for a 24x7 commercial manufacturing facility. The work performed by this position typically follows standard practices and / or procedures, and is closely supervised, reviewed, and prioritized by supervisor or more senior engineers. | 12/2/2017 |
| 1758 | Sanofi Swiftwater, PA PRODUCTION TECHNICIAN BS Exp: 0 yr |
Performs production activities in accordance with volume fluctuation, business need, and effective procedures. Works to support production units by consistently providing required materials in a timely manner. Ensures all materials required for production are available prior to need. Identifies production issues and relays them to the leadership team. Ensures all required paperwork is complete, accurate and done in a timely manner to ensure accurate inventory. Completes tasks and corresponding documentation as required by cGMP. Works to prepare assigned areas for the oncoming shifts. | 12/2/2017 |
| 1759 | Sanofi Framingham, MA RESEARCH ASSOCIATE, BIOANALYTICS - CHARACTERIZATION MS in Biochemistry Exp: 0-2 yrs |
The primary responsibilities of this position will be to perform detailed analyses of protein structure, functional attributes, post-translational modifications and biophysical properties. | 12/2/2017 |
| 1760 | Sanofi Framingham, MA ASSOCIATE PROCESS ENGINEER MS in life sciences, engineering or equivalent Exp: 0-2 yrs |
The Associate Process Engineer position is part of Process Science in Global Manufacturing Science & Technology (MSAT) within Specialty Care Industrial Operations (SCIO). | 12/2/2017 |
| 1761 | Sanofi Genzyme Swiftwater, PA Scientist Engineer Manufacturing Technology - VIE Contract (W/M) MS in a scientific / engineering discipline Exp: 1-3 yrs |
This position of VIE scientist / Engineer, in the Manufacturing Technology (Mtech) function of Vaccine Industrial Affairs, participates in the execution of technical studies to industrialize upstream and downstream processes for Phase 3 and licensed production of biological drug substance. The mission of MTech is to deliver robust and efficient process & testing with associated know-how transfer to Manufacturing & Quality Control (QC). Mtech s function also provides daily support, for manufacturing and QC, toward industrial performance excellence. | 12/2/2017 |
| 1762 | Sanofi Genzyme Bridgewater, NJ Regulatory Affairs CMC Biologics Associate/Senior Associate MS Exp: 1 yr |
This position is responsible for providing regulatory Chemistry, Manufacturing and Controls (CMC) for licensed and clinical biological products. | 12/2/2017 |
| 1763 | Seattle Genetics Bothell, WA Medical Writer BS in a life sciences discipline Exp: 0-2 yrs |
We are currently seeking a Medical Writer to write and revise clinical documents for submission to the FDA and other regulatory agencies, and to support other clinical communication efforts including abstracts and presentations for medical congress meetings and manuscripts for peer-reviewed journals. | 12/2/2017 |
| 1764 | Seattle Genetics Bothell, WA Clinical Trial Transparency Associate BA / BS Exp: 0-2 yrs |
This position will be responsible for providing operational support for maintaining compliance with clinical trial transparency and data disclosure requirements and regulations. Key responsibilities include managing timely, accurate, consistent, and appropriate disclosure of clinical trial information globally, specifically with regard to established and emerging US and EU clinical trial transparency requirements. | 12/2/2017 |
| 1765 | Semma Therapeutics Cambridge, MA RA, Sr RA, Cell Biology BS / MS in biology, cell biology, tissue engineering or related discipline Exp: 1-3 yrs |
The full-time role will focus on cell and tissue culture, as well as cell biology experiments (differentiation of human embryonic stem cells into insulin producing pancreatic cells, and related assays). Under the supervision of Senior Scientists, the research associate will be responsible for the production and characterization of consistently high quality differentiated cells using standard operating protocols and development of a cell therapy product. | 12/2/2017 |
| 1766 | Semma Therapeutics Cambridge, Lab Manager BS Exp: 1-3 yrs |
The full -time role will focus on promoting efficient and organized laboratory operations. The lab manager will work closely with our science team to support the general operations and organization of the laboratory. | 12/2/2017 |
| 1767 | Santa Cruz Biotechnology Santa Cruz , CA Laboratory Assistant BS / BA in Biology, Molecular Biology or related field Exp: entry level |
This position will perform routine tasks in support of analytical and preparative procedures required for the purification, analysis of antibodies and associated reagents used in the scientific community. | 12/2/2017 |
| 1768 | SeraCare Gaithersburg, MD Quality Control Analyst II MS Exp: 1-3 yrs |
To ensure departmental adherence to Standard Operating Procedures, regulations and customer requirements. Perform ELISA, Western Blot, and related immunoassays, as well as bioburden and simple clinical and molecular analyses on both infectious and non-infectious raw material samples and finished products. Support Manufacturing and the Quality Management System through product testing and release, environmental monitoring, internal audits, and facility calibration programs. | 12/2/2017 |
| 1769 | Synthetic Genomics La Jolla, CA Research Associate/ Research Associate II, Viral Systems BS in Molecular Biology, Cell Biology, Immunology, Virology or related field Exp: 1-3 yrs |
The successful candidate will support the overall program goals and strategy of the group which will include significant laboratory activities such as synthesis and assembly of target genes, development of novel vaccine platform technologies, characterization of RNA and protein expression in vitro. The candidate will have broad molecular and cellular biology experience. Previous experience with virology and viral vector construction will be considered a plus. Excellent verbal, presentation, and written communication skills are essential and the capability to effectively work in a team environment is required. | 12/2/2017 |
| 1770 | Shire Round Lake, IL Quality Associate I BS Exp: 1-3 yrs |
Perform in-depth internal assessments and evaluations by collecting and analyzing accurate, objective evidence regarding risks and their magnitude. Assessments and information gathering may be through in-depth employee interviews, flow charting and other informational gathering techniques. Determine the logic, adequacy and effectiveness of processes, systems and related requirements. Develop plans to correct identified risks including areas of non-conformance, inform management and implement approved corrective action plans. | 12/2/2017 |
| 1771 | Shire Lexington, MA QC Investigator, EM/Microbiology BS Exp: 0-2 yrs |
Primary duties of the position are focused around non-laboratory support of the QC functions. Primary activities would generally include but not limited to investigation activity, data analysis, data trending, cross functional team support, document revisions, initiating / completing quality systems, identifying CAPA for system improvements, change control ownership, and other activities. | 12/2/2017 |
| 1772 | Shire Lexington, MA QC Analyst BS Exp: 0-2 yrs |
Primary Duties of this position will focus on the daily lab operations and execution of testing to support manufacturing operations / validation / or development studies. Testing may include but not limited to samples from drug substance and drug product manufacturing, stability, raw materials and various protocol studies using test methods derived from the various compendia and non-compendial sources. May assist in sampling activities. This position is expected to maintain operational and GMP readiness of the QC areas. In addition, the individual may participate in more complex projects, operational excellence initiatives, and various quality systems with supervision | 12/2/2017 |
| 1773 | Shire Lexington, MA QC EM/Micro Analyst I BS Exp: 0-2 yrs |
Primary Duties of this position will focus on the daily QC EM / Microbiology lab operations and execution of testing to support manufacturing operations / validation / or development studies. Testing may include but not limited to samples from drug substance and drug product manufacturing, stability, raw materials and various protocol studies using test methods derived from the various compendia and non-compendial sources. May assist in sampling activities. This position is expected to maintain operational and GMP readiness of the QC areas. In addition, the individual may participate in more complex projects, operational excellence initiatives, and various quality systems with supervision. | 12/2/2017 |
| 1774 | Shire Lexington, MA Downstream Development Engineer MS in Chemical / Biochemical Engineering or related discipline Exp: 0-2 yrs |
The individual will be a member within a group responsible for performing purification process development, including timely completion of small-scale experiments, scale-up, technology transfer and GMP floor support for programs that bring new biopharmaceutical products to pre-clinical, clinical and process validation manufacturing phases. The individual applies basic knowledge from various technical areas, industry standards and practices. Provides quality and productive output that is consistently timely, reliable and reproducible. The candidate must be customer focused, results oriented, science driven and embrace Shire s values. | 12/2/2017 |
| 1775 | Shire Los Angeles, CA Manufacturing Scientist BS Exp: 0-2 yrs |
Executing process development projects, process improvement projects, contract manufacturing, technology transfer projects, and support daily operations in the B5 fractionation facility. | 12/2/2017 |
| 1776 | Shire Cambridge, MA Validation Engineer I BS Exp: 0-3 yrs |
This position will be responsible for executing equipment, utilities, automation, and cleaning validation activities and projects for Shire. Technical duties include writing and executing validation documents, reviewing and analyzing data, adhering to domestic and international GMP regulations, incorporating continuous improvements into validation activities and policies, and participating in regulatory inspections. | 12/2/2017 |
| 1777 | Sanofi Genzyme Swiftwater, PA 2018 Vaccine Industrial Affairs Summer Internship Program BS Exp: NA |
Support the engineering team with daily activities and develop a spreadsheet that will be used to support regulatory agency audits | 12/2/2017 |
| 1778 | Roche Tucson, AZ Summer Intern - Research, Companion Diagnostics BS / MS Exp: NA |
The CDx Pharma service group at Ventana Medical Systems, a member of the Roche group, seeks an intern to conduct research in analytical methods for antibody and tissue characterization. The qualified candidate must major in biology, chemistry or life science. Prior lab experience with biomedical research or pathology is preferred but not required. We seek highly motivated individual who can adapt quickly to changing demands and priorities and be able to contribute in a team-oriented environment. | 12/2/2017 |
| 1779 | Roche Tucson, AZ Summer Intern - Development, CDx Antibodies MS Exp: NA |
Independently plans and executes assigned projects | utilizes tho |
| 1780 | Roche South San Francisco, CA Intern - Pharma Technical Operation - Facilities & Engineering BS / MS Exp: NA |
In this position, you will support engineering and project management related tasks. You will provide engineering, scientific and technical judgment as part of a team responsible for delivering high quality bio-pharmaceutical products to patients. Integrity, accountability, and strong dedication to the patients we serve are critical to this role. | 12/2/2017 |
| 1781 | PSC Irvine, CA Documentation Specialist BS Exp: 1 yr |
The person should have some familiarity with pharma construction documents.Experienced with basic documentation, filing, and validation binder assembly.Good organizational time management, sense of urgency, and ability to multitask. | 11/20/2017 |
| 1782 | Pulmatrix Lexington, MA Engineering Associate // Senior Engineering Associate BS / MS in Chemical Engineering, Biomedical Engineering, or related field Exp: 1-5 yrs |
We are seeking a highly motivated engineer to join the Pharmaceutical Development group supporting process development for respiratory drug products. | 11/20/2017 |
| 1783 | Pyramid Laboratories Costa Mesa, CA Environmental Monitoring Technician BS in chemistry, microbiology or related technical discipline Exp: 1-3 yrs |
Under general supervision, perform various microbiological related activities for a cGMP compliant Fill / Finish operation. Ability to apply standard practices, techniques, procedures and criteria, is necessary. Must be able to summarize findings and prepare or assist in the preparation of reports, documents, records, etc., for assigned tasks. | 11/20/2017 |
| 1784 | QIAGEN Waltham, MA Research Associate BS in Chemistry, Biochemistry, Molecular Biology or related fields Exp: 1-3 yrs |
QIAGEN is seeking candidates who will assist in the development, implementation and optimization of sequencing protocols on the GeneReader sequencer, QIAGEN s next generation massively parallel DNA sequencing platform. The successful candidate will be an integral part of the sequencing development team and will be responsible for maintenance and operation of instruments, preparation of reagents according to SOPs as well as executing complex laboratory experiments. | 11/20/2017 |
| 1785 | QIAGEN Frederick , MD Production Associate Scientist BS in Molecular Biology, Biochemistry, chemistry or related Life Sciences field Exp: 1-3 yrs |
Responsible for manual / automated production / assembly in compliance with relevant regulations and Standard Operating Procedures. | 11/20/2017 |
| 1786 | QPS, LLC Newark, DE Associate Scientist - BA BS Exp: 0-2 yrs |
Under general supervision, this position is responsible for conducting sample preparation for bioanalytical samples in an analytical chemistry lab, and recording study results and observations. | 11/20/2017 |
| 1787 | Par Pharmaceutical Companies, Inc Chestnut Ridge, NY Associate, Regulatory Affairs Operations BS Exp: 1-3 yrs |
The Associate, Regulatory Affairs Operations is responsible for the preparation and publishing of electronic regulatory documents and submissions and for ensuring these deliverables are compliant with health authority guidelines. This position is also responsible for the archiving of regulatory correspondence, the preparation and submission of Periodic Adverse Events Reports (PADERS), PADER Waivers, and maintenance of databases within the Regulatory Affairs department. Additionally, and as assigned, the incumbent will perform the essential duties and responsibilities related to pre- and post-approval submissions. | 11/20/2017 |
| 1788 | Quanterix Corporation Lexington, MA Quality Control Analyst I/II BS in Life Sciences Exp: 1-3 yrs |
Testing: Product Transfers, In-Process, and Product Release.Provide technical support to manufacturing department for process / product improvement. Peer Review of generated data | 11/20/2017 |
| 1789 | Quanterix Corporation Lexington, MA Research Associate - Assay Development BS / MS in Chemistry, Biochemistry, or Life Sciences. Exp: 1-3 yrs |
Responsibilities will broadly include developing and validating immunoassays to expand Quanterix's assay menu. You will apply laboratory skills and experience to develop new reagents, prototyping and optimizing immunoassay conditions. Generate high quality data in support of verification and validation. You will also be helping develop documentation and procedures for validation, testing, and transfer to manufacturing toward commercialization. | 11/20/2017 |
| 1790 | Synexus Glendale, AZ Clinical Research Coordinator BA / BS in a health sciences or related field Exp: 6 months |
Maintain a high level of knowledge and understanding of assigned protocols, including all protocol requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information, and drug accountability requirements. | 11/20/2017 |
| 1791 | Reckitt Benckiser Parsippany, NJ Regulatory Specialist, Compliance BA / BS in the natural or Life Sciences Exp: 1-2 yrs |
This role is responsible in providing regulatory support in regards to several internal and external processes for the regulatory compliance of RB s final products including: ingredient disclosure & compliance, Safety Data Sheets, WERCSmart, DOT hazardous materials shipping, US Customs & partner government agencies, and the management of DEA controlled substances | 11/20/2017 |
| 1792 | Regeneron Tarrytown, NY Research Associate I - II BS / MS Exp: 1-2 yrs |
The successful candidate is responsible for developing and performing binding assays, kinetic profiling assays, competition / blocking assays, and epitope binning of early therapeutic candidates, using a wide range of biophysical and biochemical methods such as Biacore, MASS-2, Octet, ITC, KinExA, etc. The candidate is expected to be self-motivated, resourceful, and proactive, in addition to possessing excellent organizational and interpersonal skills, and strong problem solving skills. | 11/20/2017 |
| 1793 | Regeneron Tarrytown, NY Research Associate I - II, Immunology & Infl BS / MS Exp: 1-4 yrs |
The preferred candidate will have training in the proper handling and care of mice, general surgical techniques, and the collection of blood and tissue samples. Experience in tissue culture (maintenance of transformed and primary cells), cell-based assays, ELISA, and MSD are highly desirable. The ideal candidate will be able to analyze data and interpret results of experiments within the context of research project goals, and work closely with supervisor to prepare and deliver effective oral presentations and papers in the area of expertise during internal and external meetings. Other expectations include maintenance of state-of-the-art laboratory equipment, and accurate and complete records. | 11/20/2017 |
| 1794 | Regeneron Tarrytown, NY Research Associate BS Exp: 1-3 yrs |
Duties are protein purification and characterization using liquid chromatography such as affinity, IEX, and SEC. Characterization of reagents, which will include western blotting, SDS PAGE electrophoresis, SEC chromatography, and concentration by UV. Protein conjugation of reagents with biotin, Alexa488, and PE, and other tags. Interpretation of results, notebook on LIMS, and power point presentation slides for characterization and documentation of reagents and antibodies purified. | 11/20/2017 |
| 1795 | Regeneron Rensselaer, NY QC Virology Analyst BS / BA in Cell Biology, Microbiology, Biochemistry, or related Science Exp: 1-3 yrs |
Perform routine and non-routine virus and mycoplasma testing (cell-based and molecular biology assays) of manufactured in-process commercial and clinical products according to cGMP and associated standard operating procedures. | 11/20/2017 |
| 1796 | Regeneron Tarrytown, NY Process Development Analytics I/II MS Exp: 0-4 yrs |
A laboratory scientist or engineer with a sound understanding of the principles and techniques used in modern analytical sciences. The ideal candidate is motivated by a dynamic, fast paced environment and a collegial team-oriented approach. He / she will execute analytical experiments independently with minimal guidance, in support of process characterization efforts within the department. He / she also takes the initiative to design and implement improvements that further the capabilities of the analytics team. | 11/20/2017 |
| 1797 | Regeneron Tarrytown, NY Temp - Clinical Compliance Associate BS Exp: 1 yr |
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, atopic dermatitis and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including rheumatoid arthritis, asthma, pain, cancer and infectious diseases. | 11/20/2017 |
| 1798 | Regeneron Tarrytown, NY Research Associate II or Higher, Protein Biochemistry MS in Biochemistry or related field Exp: 1-3 yrs |
We are seeking a talented and motivated Research Associate to join the Protein Biochemistry group. The qualified individual will be responsible for performing a variety biochemical and biophysical assays to characterize protein biologics to support late-stage development and commercialization efforts. The ideal candidate will be hardworking, efficient, flexible, and able to perform key responsibilities in a fast-paced, team environment. | 11/20/2017 |
| 1799 | ResMed San Diego, CA Product Specialist, Healthcare Informatics BS / MS Exp: 1-3 yrs |
The Product Specialist will seek to improve the efficiency of response to our field sales teams and internal questions from Technical Services, Customer Service, as well as working with these teams to ensure consistency of responses and shared knowledge. The position will be a one-stop-shop for product know how, presentations, marketing materials and other common inbound requests. The product specialist will work with product managers to develop additional support tools and processes to keep the latest information at the fingertips of our field teams. The product specialist may (as a more advanced function of the role) work closely with the product management team to suggest future product requirements based on their in depth understanding of the needs of the sales team and market. | 11/20/2017 |
| 1800 | Philips Pittsburgh, PA Procurement Engineer BS in Mechanical, Industrial, or Plastics Engineering Exp: 1-5 yrs |
You will have a comprehensive understanding of the product context End-to-End and will be responsible for delivering on the Business Procurement strategies, including the utilization of DFX. | 11/20/2017 |
| 1801 | Revance Newark, CA Manufacturing Documentation Specialist BS in Biological Sciences, Chemistry or related discipline Exp: 1-2 yrs |
The successful candidate will be responsible for the coordination and management of GMP documentation activities supporting Revance s manufacturing operations. This position requires close collaboration with the Process Sciences, Quality Control (QC), and Quality Assurance (QA) groups to ensure that all documentation activities are completed within the required timelines. A successful applicant in this position should have flexibility, good organization, excellent time and project management skills, good interpersonal skills and work with minimal supervision. | 11/20/2017 |
| 1802 | Revance Newark, CA Manufacturing Associate I - Drug Substance BS degree in biological sciences, chemical engineering or related discipline Exp: 0-3 yrs |
The incumbent will be a part of the manufacturing organization and provide hands-on execution of tasks related to the GMP manufacture of biopharmaceuticals working in fermentation, purification and / or fill-finish. | 11/20/2017 |
| 1803 | Roche South San Francisco, CA Manufacturing Technician - BioProcess BS in Life Sciences or engineering Exp: 1 yr |
Responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. Operates production equipment for cell culture or purification that may include culture growth, process monitoring, sampling, harvesting, purification, formulation, freeze thaw and transfer. Performs media / buffer solution preparation operations. Maintains records and clean room environment to comply with regulatory requirements utilizing current Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOP). | 11/20/2017 |
| 1804 | Roche Branchburg, NJ Lab Tech Ops BS Exp: 0-2 yrs |
Perform incoming inspection testing for raw materials, packaging materials, consumables, intermediates and finished kits as required to meet Operations goals and objectives with direction as appropriate. | 11/20/2017 |
| 1805 | Roche San Jose, CA Scientist I, Sequencing Operations Reagent Manufacturing BS in Biochemistry, Molecular Biology, Biological / Life Sciences or related field Exp: 0-3 yrs |
Responsible for producing innovative NIPT (Non Invasive Prenatal Testing) sequencing solutions with direct responsibility for reagent preparation, in-process testing, and dispensing activities. The individual will assist in the development of reagent manufacturing standards, SOPs systems and controls in cGMP manufacturing environment, and maintain areas in high state of inspection preparedness. | 11/20/2017 |
| 1806 | Roche Tucson, AZ Process Engineer, Associate BS Exp: Entry level |
The Associate Process Engineer will work on improving existing operations, incorporating new methods and processes and updating and developing standard work documents. This engineer will be involved in the resolution of daily production issues related to manufacturing operations and investigating problems affecting daily production. The engineer will work in a team environment with other engineers in the operations group and possess the ability to communicate effectively between all levels of employees and across technical disciplines. | 11/26/2017 |
| 1807 | West-Ward Pharmaceuticals Columbus, OH Engineer II, Validation BS in engineering or related scientific discipline Exp: 1-3 yrs |
Provides project leadership and guidance on validation / qualification initiatives to internal project teams and ensure project schedules are met. Ensures that West-Ward Pharmaceuticals systems, both computer and equipment, are in compliance with regulatory requirements through maintaining change control process and conducting periodic reviews. | 11/26/2017 |
| 1808 | Roche South San Francisco, CA Intern - Product Development - Therapeutic Area Business Operations BS in mathematics, statistics, computer science, or other quantitative field Exp: NA |
The position of Therapeutic Area Business Operations Intern will support data driven decision making across all therapeutic areas within Clinical Development Operations. The position will assess and analyze relevant data sources and identify trends, signals and bottlenecks in therapeutic area segments, countries and sites. The basic mission of the position is to identify areas of improvement, elucidate the root cause, and propose improvement plans all by using available data and multivariable analyses. | 11/20/2017 |
| 1809 | Roche Tucson, AZ Q&R Intern BS / MS Exp: NA |
Intern will be placed in Quality, Regulatory or a combination of both business functions. Previous projects have included regulatory submissions to Global Agencies, and process improvements within Global Quality Management Systems. | 11/20/2017 |
| 1810 | Roche Indianapolis, IN 2018 Summer Internship: STEM (Science, Technology, Engineering and Mathematics) BS / MS Exp: NA |
You re someone who wants to influence your own development. You re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point. | 11/20/2017 |
| 1811 | Regulus Therapeutics Inc. San Diego, CA Intern, Drug Metabolism and Pharmacokinetics BS in chemistry, pharmaceutical sciences, chemical engineering, bioengineering Exp: NA |
He / she will have the opportunity to learn bioanalytical techniques, starting from basic fundamentals such as preparing buffers for HPLS / MS and HPLC / FL systems and progressing to learning extraction procedures. In addition, the intern will be involved in lab equipment maintenance, cleaning the lab, and inventory management. | 11/20/2017 |
| 1812 | Regeneron Tarrytown, NY Purification Development Intern, Summer 2018 BS / MS Exp: NA |
This person will be working in Purification Development within Pre-Clinical Manufacturing and Process Development Department in Tarrytown, NY. The internship is intended to provide an overview and instruction of the downstream purification process with a focus on polishing chromatography and membrane unit operations. The bulk of the internship will focus on a designed research project, culminating in a presentation of the completed project to the purification group. The currently planned project is to evaluate mixed mode chromatography and its implementation into a monoclonal antibody platform. Loading capacity, flow properties, and column packing will be areas of interest. Additional projects, such as transition analysis to assess column integrity and performance, may be introduced depending on time constraints, performance of the studies and needs of the group. | 11/20/2017 |
| 1813 | Regeneron Rensselaer, NY Intern - Process Sciences MS in Engineering Exp: NA |
Discoverant team within Process sciences builds data models for Discoverant Software by collecting and designing scientific requirements. Discoverant is a data aggregation and analysis software that is used by several groups at IOPS in their routine trending and / or investigation purposes. Currently, we use an excel spreadsheet to collect requirements to build scientific solutions in Discoverant. This manual data gathering and verification process is very time consuming. The goal is to automate this process by creating a database / tool that improves the quality of the design and saves time. The intern will have an opportunity to not only learn about data analysis and aggregation software but also gain exposure to various source systems such as LIMS, QJMAS, Oracle etc. Our Data design is focused on the entire biologics manufacturing process, hence this will also give an intern an opportunity to learn our biologics process from Vial thaw operation to Drug product manufacturing. | 11/20/2017 |
| 1814 | Regeneron Rensselaer, NY Intern - QC Analytical Sciences BS / MS in Chemical Engineering, Materials Sciences, Chemistry, or applicable Life Sciences curriculum Exp: NA |
An intern will perform biochemical and chemical assays to evaluate the attributes of product and raw materials to evaluate the effect of Time out of Refrigeration (ToR). This project would partner with manufacturing and Process Sciences groups to identify any potential relationships associated with the time materials spend outside of controlled cold rooms. | 11/20/2017 |
| 1815 | PerkinElmer Springfield, IL Engineering Intern BS / MS Exp: NA |
DA lamp burn-in fixture: test 3 lamps daily by plugging into a DA and recording integration time. Probably a couple hours work every morning for 15 days. We will use this info to estimate the optimum burnin time for lamps. We have enough power supplies and cables to burn-in up to 10 at a time. | 11/20/2017 |
| 1816 | Par Pharmaceutical Chestnut Ridge, NY Associate, Regulatory Affairs Operations BS Exp: 1-3 yrs |
The Associate, Regulatory Affairs Operations is responsible for the preparation and publishing of electronic regulatory documents and submissions and for ensuring these deliverables are compliant with health authority guidelines. This position is also responsible for the archiving of regulatory correspondence, the preparation and submission of Periodic Adverse Events Reports (PADERS), PADER Waivers, and maintenance of databases within the Regulatory Affairs department. Additionally, and as assigned, the incumbent will perform the essential duties and responsibilities related to pre- and post-approval submissions | 11/18/2017 |
| 1817 | PAREXEL Home Based, Ho CLINICAL RESEARCH ASSOCIATE II, EARLY PHASE - ONCOLOGY BS in biological science, pharmacy or other health related discipline Exp: 1 yr |
Perform all clinical monitoring / site management activities for assigned projects in accordance with PAREXEL's standard operating procedures | 11/18/2017 |
| 1818 | PBL Assay Science Piscataway, NJ Product Application Scientist BS in the life sciences Exp: 1 yr |
The Product Application Scientist is responsible for designing and executing experiments to generate technical and application data on new and existing ELISAs, cytokine proteins, and antibody product lines to support both Product Development and Marketing initiatives. This position requires technical proficiency in cell-based assays, ELISA execution and development, and characterizing protein and antibody reagents. | 11/18/2017 |
| 1819 | PBL Assay Science Piscataway, NJ Assay Services Scientist BS in the life sciences Exp: 1 yr |
The Assay Services Scientist works primarily with bioassays, executing antiviral bioassays, other bioassays and ELISAs for characterizing proteins and reagents; performing cell culture; and developing new and custom assays to support the growth of the Assay Services Group. | 11/18/2017 |
| 1820 | Patheon Cincinnati, OH Scientist 1 - Microbiologist BS in Microbiology or related science Exp: 1-2 yrs |
This is a multi-functional position requiring flexibility and a broad understanding of pharmaceutical microbiology, and a willingness to learn. The successful candidate must be trained in aseptic technique and will be qualified as the primary back-up for raw materials testing, finished product testing, environmental monitoring, and utility support testing. The candidate should be familiar with compendial (USP <61>, USP <62>, and USP <51> or equivalent) testing, will be the primary person to complete compressed gas testing, will coordinate laboratory support functions such as isolate identifications for cryopreservation, media qualification, and growth promotion. Also oversees instrument audits, instrument maintenance-repair and will assist with client or regulatory audits as requested. | 11/18/2017 |
| 1821 | PerkinElmer Shelton, CT Associate Test Engineer BS Exp: 1-5 yrs |
Calibrate highly complex equipment and see that test records are properly maintained.Troubleshoot and resolve highly complex electro-mechanical assembly and optical quality / production issues. Perform troubleshooting and repair of microprocessors based electronics. | 11/18/2017 |
| 1822 | Personalis, Inc Menlo Park, CA Laboratory Assistant BS in Molecular Biology or related field Exp: 0-2 yrs |
Within a dynamic startup environment, the successful candidate, under direction of the Laboratory management, will help grow the sequencing services laboratory. You will participate in the daily activities of the laboratory in order to effectively maximize turnaround time, equipment, and material utilization while adhering to quality technical standards. | 11/18/2017 |
| 1823 | Personalis, Inc Menlo Park, CA Clinical Laboratory Scientist BS Exp: 1 yr |
The Experienced Clinical Laboratory Scientist is responsible for testing and reporting clinical laboratory results. | 11/18/2017 |
| 1824 | Perrigo Company plc Minneapolis, MN ARD Scientist/Sr. Scientist MS in Chemistry or Pharmaceutical Sciences Exp: 0-2 yrs |
This position provides technical support to assigned projects, using robust scientific methods which comply with standard operating procedures and scientific standards. As appropriate, may serve as a project leader to manage analytical support for projects with minimal supervision. Prepare documents for regulatory filings (ANDA, NDA, ANDS). Design experiments and provide data to support responses for FDA minor deficiency letters. Perform physical and chemical testing on raw material, in-process, finished product and stability samples. This includes documentation and review. Successfully investigate and resolve analytical problems, project issues and deviations. Accurately maintain all related documentation in compliance with SOPs. The ARD Scientist will research, prepare and review technical documents, including but not limited to SOPs, drug master files, technical packages, vendor qualification, raw material and release and stability specifications, stability summaries, test methods, and certificates of analysis which conform to company standards. Attend and present data at project-related meetings, interact with other departments and outside testing laboratories to ensure proper analytical testing. Participate in cross-functional project teams, and exercise and build basic team effectiveness skills. Utilize skills, established procedures, new methodologies, and experience to complete tasks; and provide formal and informal mentoring to junior team members. Develop, validate and transfer non-complex to complex analytical methods. | 11/18/2017 |
| 1825 | Pharmacyclics LLC Sunnyvale, CA Clinical Research Associate I BA / BS Exp: 1 yr |
Under direct supervision, the CRA I position begins gaining experience in clinical trial management procedures by assisting in the planning, designing, implementation of Pharmacyclics clinical trial protocols. Will interface with internal and external stakeholders, eg., study coordinators and investigators working with confidential patient and company data and may be directly involved in onsite monitoring, based on business need. In collaboration with senior level staff, participates in data quality review. Develops a basic understanding of the disease, molecule, and indication specific to the clinical trial. Maintains high level of professionalism within Pharmacyclics and external stakeholders. | 11/18/2017 |
| 1826 | PharmaForce New Albany, OH R&D Formulation Scientist MS in Pharmaceutical Science, Chemistry and Chemical Engineering or equivalent Exp: 1 yr |
Responsible for formulation and process development activities associated with parenteral drug product development following Quality by Design (QbD) principal. Participates in manufacturing process scale-up and technology transfer. Supports trouble shooting of manufacturing issues, ANDA submission and regulatory response to FDA deficiency. Responsible for training of laboratory personnel in areas of expertise. | 11/18/2017 |
| 1827 | PharmaForce New Albany, OH R&D Product Launch Coordinator MS Exp: 1-3 yrs |
The R&D product Launch Coordinator will be responsible for the effective coordination of R&D projects, maintaining and monitoring launch timelines, and facilitating Regulatory Filings. The project coordinator will assist in planning and organizing of assigned project(s) to meet or exceed company s safety, quality, cost, and scheduled expectations. | 11/18/2017 |
| 1828 | Portola Pharmaceuticals San Francisco, CA Manufacturing Sciences and Technology (MSAT) Associate BS in Chemical Engineering, Biochemical Engineering, Biology, or Biochemistry Exp: 0-2 yrs |
The Manufacturing Sciences and Technology Associate will primarily perform data analyses from clinical and commercial drug substance manufacturing campaigns for Portola's lead recombinant protein produced in Chinese hamster ovary (CHO) cells at Contract Manufacturing Organization (CMOs). The data analyses will be applied towards applications including process improvement, root cause analysis, trend analysis and continuous process verification. This position reports to the Associate Director, Manufacturing Sciences and Technology. | 11/18/2017 |
| 1829 | Poseida Therapeutics San Diego, CA Process Development Associate MS Exp: 1 yr |
This is a lab-based position that will involve hands-on development of clinical manufacturing processes for selecting, gene-modifying and growing T cell subsets. This position will interface with our Research and Development team as well as with outside Contract Manufacturing Organizations. The ideal candidate will be skilled in T cell culture techniques, flow cytometry and have experience working in or supporting cGMP manufacturing projects. The candidate will have good oral and written communication skills, and will work with minimal supervision to design experiments, manage projects, collect data, and prepare reports. | 11/18/2017 |
| 1830 | Precision Gladstone, NJ Medical Writer - Medical Communications Agency BS Exp: 1 yr |
As a Medical Writer at Precision for Value, you will research, write, and develop medical content for a variety of promotional resources in our payer marketing agency. This position is also responsible for evaluating and identifying supporting documentation, organizing and annotating references. | 11/18/2017 |
| 1831 | Precision Oakland, CA Associate Research Scientist MS Exp: 1 yr |
The Associate Research Scientist will have a basic familiarity with the application of research methods (e.g. literature review, modeling, observational research, statistical programming). This position will perform a wide range of activities including: project management; literature review; analysis; preparing reports, slide decks and meeting notes; quality assurance / review; and other activities, under the direction and supervision of a project leader. | 11/18/2017 |
| 1832 | Premier Research Research Triangle Park, NC Document Specialist BS Exp: 0-1 yr |
The Document Management team is responsible for the oversight and management of the Trial Master File (TMF) to ensure that documents are being processed and filed accurately and according to Premier Research Standard Operating Procedures, Sponsor, and ICH / GCP requirements. In addition, the team is responsible for ensuring security and controlled access to the Secure File Room as well as completing visual quality checks to ensure document completeness and legibility. | 11/18/2017 |
| 1833 | Progyny New York, NY Call Center Quality Assurance Analyst BS Exp: 1-3 yrs |
The Quality Assurance Analyst will be responsible for reviewing and auditing incidents, email and telephone interactions along with reviewing and investigating customer survey responses for the Call Center. The QA will also be responsible for facilitating calibration / group sessions regarding our quality program. You will own identifying areas of service improvements and developing programs that improve the overall quality of the customer s experience when interacting with the Call Center. The Quality Assurance Analyst is responsible for the overall quality of the customer interactions, making improvement recommendations to the team Manager and monitoring the result of stated recommendations. | 11/19/2017 |
| 1834 | Promega Madison, WI Formulations Scientist 1, Operations BS in biological science or chemistry Exp: 1-2 yrs |
Manufacture materials according to approved protocols and standard operating procedures. This includes materials such as buffers, reagents, solutions, dialysis tubing and buffered phenol. The scale of manufacturing can range from 10ml to 2000 liters. | 11/19/2017 |
| 1835 | Prometheus Laboratories Inc. San Diego, CA Clinical Laboratory Scientist I BS Exp: 0-4 yrs |
Performs pre-analytical and analytical testing, interprets and reports patient results to ordering physicians. | 11/19/2017 |
| 1836 | ProteinSimple SAN JOSE, CA MANUFACTURING ASSOCIATE BS Exp: 1-2 yrs |
This individual will work with other members of the production team as well as a multidisciplinary team of engineers and scientists to support our consumables production demand. | 11/19/2017 |
| 1837 | ProteinSimple SAN JOSE, CA MANUFACTURING ASSOCIATE CHIP FABRICATION BS in science or engineering Exp: 1-3 yrs |
The successful applicant will work with other members of the consumable production team as well as a multidisciplinary team of engineers and scientists to support a microfluidic chip production process. | 11/19/2017 |
| 1838 | ProteinSimple SAN JOSE, CA MANUFACTURING LABORATORY TECHNICIAN I BS in biotech, chemistry, Biology, or engineering related field Exp: 0-3 yrs |
The successful applicant will work with other members of the consumable production team as well as a multidisciplinary team of engineers and scientists to support routine production activities of the consumables manufacturing team. | 11/19/2017 |
| 1839 | ProteinSimple SAN JOSE, CA MANUFACTURING VALIDATION ASSOCIATE BS in Biology, Chemistry, Biochemistry or related engineering discipline preferred Exp: 1-5 yrs |
Protein Simple is looking for a manufacturing associate for production qualification testing on our Simple Western and Ice lines of protein analysis instruments. | 11/19/2017 |
| 1840 | PRC Clinical Burlingame, CA CLINICAL PROJECT INTERNSHIP BS Exp: NA |
You will gain valuable experience from the CRO to Sponsor perspective. Some of the job duties include: making client regulatory and SOP binders, participating in meetings and teleconference, administrative support, updating spreadsheets, and communication with investigator sites as well as pharmaceutical and biotech sponsors. | 11/18/2017 |
| 1841 | PerkinElmer Hopkinton, MA Microfluids Applications Intern BS / MS Exp: NA |
Candidate will be responsible for assisting our Application Scientists with investigations centered around our LabChip microfluidic technology, with the goal of developing the background knowledge necessary to design and execute experiments with minimal supervision. These experiments may be part of an independent project run by the candidate or may contribute to an ongoing project run by the Applications Group. | 11/18/2017 |
| 1842 | PerkinElmer Hopkinton, MA Diagnostics R&D Intern Exp: NA |
Candidate will be responsible for assisting our hardware engineering team with product development, engineering analyses, and component creation, with the goal of developing the background knowledge necessary to design and execute small projects with minimal supervision. These projects may be independently run by the candidate or may contribute to an ongoing project run by the broader R&D organization Group. | 11/18/2017 |
| 1843 | PerkinElmer Waltham, MA Intern - Core Chemistry BS / MS in Chemistry, Organic Chemistry, Physical Chemistry, Biochemistry or equivalent Exp: Entry Level |
The goal of the internship is to improve the accuracy and scope of the Structure to Name and Name to Structure functions in ChemDraw. The result will be in next release of ChemDraw product distributing worldwide | 11/18/2017 |
| 1844 | Patheon Cincinnati, OH Chemist Internship BS IN CHEMISTRY Exp: NA |
The Patheon Chemist Intern Program provides college students with the opportunity to gain hands-on work at Patheon while continuing their studies at their universities. The program usually begins in the student s junior year or senior year. The work assignments are at our Cincinnati, Ohio facility in the Quality Control Laboratories. Internships may commence at any time during the school year and summer. | 11/18/2017 |
| 1845 | Thermo Fisher Scientific Bedford, MA Intern, Manufacturing Science & Engineering BS Exp: NA |
The Summer Internship position at Thermo Fisher Scientific (Bedford) is responsible for Support of Raw material risk mitigation projects along with process improvement and troubleshooting projects (business and / or technical processes) in the area of POROS chromatography resins, Chemilluminessence and POP polymers. | 11/18/2017 |
| 1846 | Thermo Fisher Scientific South San Francisco, CA Intern, Genetic Analysis Product Management BS Exp: NA |
Perform, collect and organize market research to validate business assumptions on market trends | 11/18/2017 |
| 1847 | Thermo Fisher Scientific Asheville, NC Manufacturing Engineering Intern BS / MS in an engineering Exp: NA |
Work to establish new manufacturing processes and continuously improve existing processes to improve product quality, delivery and overall customer satisfaction. | 11/18/2017 |
| 1848 | Merck & Co. Boston, MA 2018 MRL ONCOLOGY DISCOVERY INTERN BS / BA degree in biology, biochemistry, molecular or cell biology, biomedical engineering, or a related field Exp: NA |
The successful candidate will serve as an integral member of a multidisciplinary drug discovery project team developing novel modalities for Immuno-Oncology. The candidate will work with a scientific mentor to develop and carry out biochemical, and / or cell-based assays to characterize potential therapeutic molecules. | 11/18/2017 |
| 1849 | Merck & Co. Cambridge, MA 2018 MRL BIOCONJUGATION & MEDICINAL CHEMISTRY INTERN BS / MS in chemical biology, chemistry, or a related field Exp: NA |
The intern will perform basic techniques in support of bioconjugation and chemical biology research, including preparation of buffers and reagents. The student will meticulously apply pre-defined procedures to execute experiments, observe all details and record results in a highly organized manner. The successful candidate will effectively communicate results in both written and oral form, contributing to a diverse team while asking questions. | 11/18/2017 |
| 1850 | Merck & Co. Rahway, NJ 2018 MRL REGULATORY EDUCATION AND LEARNING INTERNSHIP BS Exp: NA |
This position will support the Health Registration Management (HRM) team with developing and implement strategies to for education, training and change management. | 11/19/2017 |
| 1851 | MPI Research Mattawan, MI Research Associate - LBA Development MS / BS / BA Exp: 0-2 yrs |
This position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and / or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. | 11/11/2017 |
| 1852 | MPI Research Mattawan, MI Research Associate 1 - Clinical Pathology BS Exp: 0-2 yrs |
This position is responsible for providing humane care to all laboratory animals and to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. | 11/11/2017 |
| 1853 | Novavax Gaithersburg, MD Senior Research Associate MS in biological science, molecular biology, immunology Exp: 1-3 yrs |
This individual will play an important role testing clinical samples as well as in assay development and validation. Qualified individuals are expected to generate and qualify cell banks & virus banks & to perform ELISAs & cell-based assays for clinical testing, in addition to training new technicians and leading a group of technicians in high throughput clinical testing. | 11/11/2017 |
| 1854 | Novavax Gaithersburg, MD Manufacturing Specialist I MS Exp: 0 yr |
This position will have a wide range of responsibilities to support GMP manufacturing. In addition to a strong technical background, the ideal candidate will have significant experience with continuous improvement initiatives, problem solving, and project management. | 11/11/2017 |
| 1855 | Novavax Gaithersburg, MD Associate / Senior Associate, Analytical Development, Critical Reagents (Contractor) MS in biological science or biochemistry Exp: 0 yr |
The candidate is responsible for coordination and hands-on execution of development, optimization, and qualification of Reference Standard and Critical Reagents that will be used for vaccine products. The qualified individual should have general knowledge and experience on analytical techniques commonly used in biotechnology industry such as immunoassays, chromatographic and electrophoretic methods and maintaining database using Excel. | 11/11/2017 |
| 1856 | Nurix Inc San Francisco, CA Research Associate/Senior Research Associate BS in immunology, cancer biology or related field Exp: 1-2 yrs |
This individual will work closely with our drug discovery project scientists on late-stage lead optimization of novel compounds to support dose and schedule optimization, execution of pharmacodynamic biomarker assays, in vivo efficacy, and characterization of ex vivo immune cell function. The candidate must be self-driven, organized, able to work well with project scientists, and able to thrive in an exciting environment in a rapidly-growing company. | 11/11/2017 |
| 1857 | Ocular Therapeutix Bedford, MA Engineer/Scientist I, R&D BS / MS in Chemistry, Bio-Medical Engineering, Material Science or related field Exp: 0-2 yrs |
Execute research and development activities as assigned by management, including routine prototype product and processes and documentation. Work with management and project team members to design and implement research or product development program plans. | 11/11/2017 |
| 1858 | Omeros Seattle, WA Temporary Clinical Data Associate BS Exp: 1 yr |
In this role, you will be responsible for supporting the data management study team leads in data cleaning and database testing activities on studies, assisting in ensuring complete, accurate and consistent clinical data output. | 11/11/2017 |
| 1859 | Omeros Seattle, WA Clinical Data Associate BS Exp: 1 yr |
In this role, you will be responsible for supporting the data management study team leads in data cleaning and database testing activities on studies, assisting in ensuring complete, accurate and consistent clinical data output. | 11/11/2017 |
| 1860 | Omeros Seattle, WA Regulatory Affairs Specialist/Sr. Specialist BS Exp: 1-5 yrs |
Supporting preparation of program annual reports as well as CMC, nonclinical, pharmacovigilance, and clinical regulatory filings | 11/11/2017 |
| 1861 | Thermo Fisher Scientific South San Francisco, CA Scientist I, Molecular Biology BS in Biochemistry, Molecular Biology or equivalent discipline Exp: 1 yr |
The successful candidate will optimize, integrate and validate reagents, protocols, sequencing chips and instruments to support Ion Torrent product development with the objective of meeting customers requirements for the genetic testing assays. | 11/11/2017 |
| 1862 | Thermo Fisher Scientific South San Francisco, CA Bioinformatics and Database Specialist BS in computer science, bioinformatics, genetics, or a related field Exp: 1-3 yrs |
The Bioinformatics R&D Group in the Microarray business unit of Thermo Fisher Scientific seeks a talented individual with extensive experience with relational databases and excellent bioinformatics domain knowledge. The successful candidate will curate data in a large, relational database for genomic research and will drive the acquisition of information from both internal and public sources. Additional duties include the analysis of microarray and genomic data and performing PostgreSQL database administration. You will work in an interdisciplinary, dynamic team of scientists and engineers to develop and support a broad array of products for genomic research. | 11/11/2017 |
| 1863 | Thermo Fisher Scientific Millersburg, PA Quality Assurance Engineer BS in engineering or science related field Exp: 1 yr |
Collect, analyze and present quality data.Establish and optimize test methods and product specifications.Write and conduct validations (IQ / OQ / PQ) for manufacturing processess and equipment. | 11/11/2017 |
| 1864 | Ora Andover, MA Site Operations Associate BS in Life Sciences Exp: 1 yr |
Assists in organizing research information for clinical projects and ensures compliance with protocol and overall clinical objectives while working under the direction and supervision of the Principal Investigator to assist the Principal Investigator in performing the administrative aspects of a clinical trial. As a member of the clinical team, relies on instructions and pre-established guidelines to participate in clinical research activities involving human research subjects while working under immediate supervision of a supervisor or manager to collect basic indications of a subject s health status. | 11/11/2017 |
| 1865 | Ora Andover, MA Site Operations Associate - Per Diem BS in Life Sciences Exp: 1 yr |
The Site Operations Associate - Per Diem is called upon to augment existing staff by assisting in organizing research information for clinical projects, performing administrative aspects of a clinical trial, and ensuring compliance with protocol and overall clinical objectives under the direction and supervision of the Principal Investigator. Demonstrated patient facing skills are required. As a member of the clinical team, relies on instructions and pre-established guidelines to participate in clinical research activities involving human research subjects while working under immediate supervision of a supervisor or manager to collect basic indications of a subject s health status. | 11/11/2017 |
| 1866 | Osiris Therapeutics Columbia, MD Document Control Specialist - Biotech/Biopharmaceuticals BA in Biology or related field Exp: 1-2 yrs |
The primary purpose of this position is to work within the Quality Assurance department in several key roles relating to document control functions. This position is critical in ensuring compliance with 21 CFR 210, 211, and 1271. | 11/11/2017 |
| 1867 | Oxford Immunotec Memphis, TN Quality Assurance Specialist I BS in a life science Exp: 1-5 yrs |
Under some supervision and with a good understanding of science and technology, monitors operations and participates in quality improvement initiatives to ensure that systems are safe, effective, appropriate, compliant, current, and adhered to by staff for the company s North American operations. | 11/11/2017 |
| 1868 | Pace Analytical Life Sciences Oakdale, MN Quality Assurance Data Reviewer BS in Chemistry Exp: 6months-1 yr |
The ideal candidate is one who thrives working in a highly dynamic, team- oriented environment sharing the common goal of providing our clients with the information they need to improve the safety and effectiveness of materials produced and used in pharmaceutical and medical device products. | 11/12/2017 |
| 1869 | Pace Analytical Life Sciences Maplewood, MN Document Assistant BS Exp: 0-1 yr |
Seeking an entry-level candidate for a lab support position performing data and document updates. Must have strong computer skills, attention to detail, and an interest to be outside of the lab. | 11/12/2017 |
| 1870 | Pace Analytical Life Sciences Maplewood, MN Entry - Level Lab Analyst BS in Chemistry or related science field Exp: 0-1 yr |
This candidate will perform routine laboratory experiments, stability and release testing in a high throughput laboratory as part of a quality group involved in infection prevention. | 11/12/2017 |
| 1871 | Pace Analytical Life Sciences Maplewood, MN Lab Analyst - Cell Culture BS in biomedical sciences Exp: 1 yr |
This candidate will be responsible for maintaining cell lines, performing experiments, and analyzing results. A variety of analytical methods will be used including advanced microscopy techniques. | 11/12/2017 |
| 1872 | Pace Analytical Life Sciences Maplewood, MN Chemist - HPLC BS in Chemistry or related science Exp: 1-2 yrs |
Candidate will perform analytical testing to support product development on an inhalation device. Analytical lab experience is necessary, specifically with HPLC. | 11/12/2017 |
| 1873 | Pace Analytical Life Sciences Maplewood, MN Regulatory Coordinator BS in Chemistry, Biochemistry, Biology or related science (toxicology, industrial hygiene, environmental science) Exp: 1 yr |
Candidate will analyze customer products in regards to toxicology and human health effects and product compliance, and make recommendations for environmental health and safety in this entry-level scientific, non-laboratory position. We are looking for a team player who is self-motivated and able to manager multiple projects. | 11/12/2017 |
| 1874 | Pace Analytical Life Sciences Fort Dodge, IA Microbiology Lab Analyst BS in Microbiology or a related science Exp: 0-2 yrs |
This candidate will perform testing using traditional microbiological techniques for proteins and enzymes. They will be supporting product development and continued product improvement. Experience with cell culture, bacteriology, and virology in the industry or through research is expected. | 11/12/2017 |
| 1875 | PacBio Menlo Park, CA Scientist (Sequencing) MS in Biology Exp: 6 months |
Provide support aimed at development of new technologies for SMRT sequencing. Work will involve hands-on laboratory work in preparing templates for in-house experimentation, monitoring these experiments and making observations and working to improve existing sequencing applications and develop new ones. Will perform development and optimization of protocols for full-length cDNA sequencing. Assist with, and conduct, hands-on laboratory work including preparing samples and provide analysis based upon observations as well as interpretation, troubleshooting, and verbal and written reporting of experimental results. | 11/12/2017 |
| 1876 | Thermo Fisher Scientific Bedford, MA Engineering Intern II BS / MS Exp: NA |
The manufacturing team at Thermo Fisher Scientific (Bedford) is responsible for manufacturing and testing chromatography media (large and small scale), disposable columns, and Performance Optimized Polymers and Chemiluminescence synthesis / formulations. We are seeking an energetic individual with strong communication, leadership, technical and operational skills to join our dynamic and fast paced team. The candidate will follow SOPs and work in compliance with safety, regulatory and quality guidelines. This position will provide direct labor within multiple work centers and will provide indirect support for projects / troubleshooting, maintenance, engineering and / or training initiatives. | 11/11/2017 |
| 1877 | Thermo Fisher Scientific Sugarland, TX R&D Intern BS Exp: NA |
This position is to work with engineering team regarding new product test, existing product improvement and sustaining task including part substitution, Engineering Change Order ECO implementation, product certification supporting task. | 11/11/2017 |
| 1878 | Thermo Fisher Scientific Madison, WI Chemical Applications Intern BS in life sciences, physical science, chemistry, or engineering discipline Exp: NA |
The Applications Scientist Intern will be responsible for testing various samples and competitive products associated with our Core UV product line. This position requires a scientist with knowledge and experience in laboratory instrumentation and software. He / she must be capable of both doing laboratory work and critically analyzing experimental results. Applications Scientists also participate in new product development and R&D activities. | 11/11/2017 |
| 1879 | Novartis Fort Worth, TX Summer 2018 Internship Chemistry R&D BS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern assigned project(s) will align to one of our two business groups Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 11/11/2017 |
| 1880 | Novartis Johns Creek, GA Summer 2018 Internship Materials Science/Engineering R&D BS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern assigned project(s) will align to one of our two business groups Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 11/11/2017 |
| 1881 | Novartis Johns Creek, GA Summer 2018 Internship Biomedical Engineering R&D BS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern assigned project(s) will align to one of our two business groups Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 11/11/2017 |
| 1882 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Large Animal Toxicology BS Exp: 0-2 yrs |
This position is responsible for providing humane care to all laboratory animals and to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. | 11/11/2017 |
| 1883 | Merck Kenilworth, NJ 2018 MRL BIOLOGICS ANALYTICAL SCIENCES & PROCESS DEVELOPMENT INTERN BS / BA in Chemical / Bio Engineering, Biology, Biochemistry, Chemistry, or relevant discipline. Exp: NA |
Advance research towards the development of novel Biotherapeutics with a vision towards Clinical Development and Commercialization. | 11/11/2017 |
| 1884 | Merck Kenilworth, NJ 2018 MRL SCIENTIFIC ENGINEERING AND DESIGN INTERN BS in Electrical, Computer / Software, Mechanical or Biomedical Engineering or a related field. Exp: NA |
The group is offering a summer internship opportunity for an undergraduate student to learn how to design custom instruments that impact the drug discovery process in the "Big Pharma" setting. | 11/11/2017 |
| 1885 | Merck Cambridge, MA 2018 MRL BIOCONJUGATION & MEDICINAL CHEMISTRY INTERN BS / MS in chemical biology, chemistry, or a related field Exp: NA |
The intern will perform basic techniques in support of bioconjugation and chemical biology research, including preparation of buffers and reagents. The student will meticulously apply pre-defined procedures to execute experiments, observe all details and record results in a highly organized manner. | 11/11/2017 |
| 1886 | MPI Research Mattawan, MI QC Associate - Laboratory Sciences QC MS / BS / BA Exp: 0-2 yrs |
This position is responsible for verification and archival of study data and departmental records according to established Standard Operating Procedures (SOPs), protocols, methods, and processes. This individual contributes to the department by working independently, completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. | 11/4/2017 |
| 1887 | MPI Research Mattawan, MI Report Coordinator Associate/Senior Report Coordinator - Report Services MS / BS / BA Exp: 0-2 yrs |
A Report Coordinator Associate is responsible for: coordinating the reporting processes to produce quality, on-time reports; providing support for assigned Study Director(s); and prioritizing his / her workload. Good communication skills and the ability to adhere to deadlines are necessary for success. | 11/4/2017 |
| 1888 | MPI Research Mattawan, MI Research Assistant 1/Research Associate 1 - Clinical Pathology BS Exp: 0-2 yrs |
This position is responsible for performing assigned basic support functions in the Clinical Pathology Laboratory setting. Functions include Set-up, Processing, Sample Management, and / or administrative Laboratory setting. Functions include Set-up, Processing, Sample Management, and / or administrative. | 11/4/2017 |
| 1889 | MPI Research Mattawan, MI Research Assistant 1/Research Associate 1 - Histology - Laboratory Operations Support BS Exp: 0-2 yrs |
This position is responsible for performing assigned basic support functions in the Histology Laboratory setting. Functions include set-up, sample management, and / or administrative functions as outlined in a protocol or appropriate Standard Operating Procedures (SOPs). | 11/4/2017 |
| 1890 | MPI Research Mattawan, MI Research Assistant/Research Associate 1 - Pathology Services - Tissue Trimming BS Exp: 0-2 yrs |
This position is responsible for performing the technical functions in tissue trimming including soft tissue, bones, and measuring fixed organ weights, as well as for performing technical support functions, as necessary. It is expected to perform assigned technical and administrative functions within the guidelines necessary. It is expected to perform assigned technical and administrative functions within the guidelines reliable data from which to evaluate the efficacy. toxicity of a test compound. Other functions may be | 11/4/2017 |
| 1891 | MPI Research Mattawan, MI Research Associate - LBA Development MS / BS / BA Exp: 0-2 yrs |
This position is responsible for following established methods to quantify chemical entities according to This position is responsible for following established methods to quantify chemical entities according toThis position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and / or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. applicable Standard Operating Procedures (SOPs) and / or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others. This position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and / or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others.This position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and / or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned projects on time, participating in process improvement initiatives, and communicating effectively with others.This position is responsible for following established methods to quantify chemical entities according to This position is responsible for following established methods to quantify chemical entities according toThis position is responsible for following established methods to quantify chemical entities according to applicable Standard Operating Procedures (SOPs) and / or GxP regulations. This individual demonstrates proficiency in the use of instrumentation and laboratory techniques. This individual contributes to the department by completing assigned project | 11/4/2017 |
| 1892 | Medtronic Danvers, MA Sourcing Continuity Engineer MS in Chemical Engineering, Polymer Engineering or Materials Engineering Exp: 0-2 yrs |
This role will be responsible for engineering work with all suppliers who provide products and services for the Danvers Shared Technology Center | 11/4/2017 |
| 1893 | Medtronic Danvers, MA Assoc Materials Engineer BS in Engineering Exp: 0-1 yr |
Conducts prototype development and clinical phases of new product introduction. | provides Adv |
| 1894 | Medtronic Mounds View, MN Associate Regulatory Opererations Specialist BS Exp: 1 yr |
This primary focus for this position will be to assume the responsibilities of a submission Publisher including assembling, publishing and filing of electronic submissions and associated regulatory correspondence. | 11/4/2017 |
| 1895 | Medtronic Mansfield, MA International Regulatory Affairs Specialist BS Exp: 1 yr |
The International Regulatory Affairs Specialist is responsible for the creation and maintenance of International registrations. | 11/4/2017 |
| 1896 | Nanosyn Santa Clara, CA Research Associate, Synthetic Organic or Medicinal Chemis MS / BS in organic chemistry or related field Exp: 0-5 yrs |
Develop and implement synthetic routes for production of arrays of synthetic compounds;Perform laboratory synthesis of organic molecules and prepare the intermediates for the synthesis of these molecules;Apply modern techniques of organic synthesis including a variety of organic reactions at several scales, microwave chemistry, inert atmosphere techniques, LC-MS, HPLC, MS, flash chromatography, recrystallization, and distillation. | 11/4/2017 |
| 1897 | NanoString Seattle, WA Manufacturing Research Associate I BS in a scientific discipline Exp: 0-2 yrs |
The Manufacturing Research Associate I is responsible for supporting the production of reagents used in nCounter Analysis Systems. The role requires learning and performing both manual and automated production processes for the manufacture of raw, intermediate, and final reagents needed for the multiplexed detection and quantification of many different types of target molecules from biological samples. This individual learns to use professional concepts and apply company policies and procedures to resolve routine issues, in addition to acquiring the skills to use equipment, perform SOPs, use Document Control systems, ERP systems, etc. | 11/4/2017 |
| 1898 | NantKwest La Jolla, CA Research Associate (Process Development) MS in biological sciences Exp: 1 yr |
Support the scientific operation of the laboratory by maintaining mammalian cells in cultures and supporting process development team in upstream and downstream processes | 11/4/2017 |
| 1899 | Natera San Carlos, CA Laboratory Technician (Temporary) BS / BA in a biological science Exp: 0-1 yr |
You will work primarily with R&D Scientific Operations providing biosamples to Associates / Scientists for use in clinical and research efforts. | 11/4/2017 |
| 1900 | Natera San Carlos, CA Quality Assurance Specialist BS in Life Sciences, Engineering Exp: 1 yr |
This is an entry-level position to assist the Quality Department in continuous compliance and improvement. | 11/4/2017 |
| 1901 | Natera San Carlos, CA Clinical Laboratory Scientist I BS / BA in Medical Technology, Biological Sciences, or related field Exp: 1-4 yrs |
Natera is currently seeking an experienced, licensed Clinical Laboratory Scientist I to analyze clinical laboratory specimens following the standard methods and procedures. Maintain equipment and instruments in good operating condition, recognize any malfunctions and troubleshoot as needed. | 11/4/2017 |
| 1902 | Nelson Laboratories Salt Lake City, UT Lab Analyst BS Exp: 6 months-1 yr |
Laboratory Analysts conduct testing in accordance with established procedures using Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and under the supervision of the Study Director. Additionally, Laboratory Analysts record data concurrently, maintain traceability of samples throughout testing and notify the Study Director of any unforeseen circumstances that occur during testing. | 11/4/2017 |
| 1903 | Nephron Pharmaceuticals West Columbia, SC Microbiologist I BS in Biology, Microbiology or Life Science Degree Exp: 1 yr |
Perform microbiology department related tests according to USP methods and established procedures that follow cGMP guidelines and demonstrate outstanding aseptic techniques. | 11/4/2017 |
| 1904 | Neurona Therapeutics South San Francisco, CA Research Associate (Discovery Biology) BS in cell / molecular biology or related field Exp: 1 yr |
Maintain human pluripotent stem cells and differentiated cells.Perform stem cell differentiation and characterize differentiated cultures.Conduct fluorescence-activated cell sorting, as well as magnetic sorting, experiments.Execute immune-cyto-chemistry experiments to analyze gene expression. | 11/4/2017 |
| 1905 | NGM Biopharmaceuticals South San Francisco, CA Contract Research Associate/Senior Research Associate In vivo Pharmacology BS in Biological Science Exp: 1 yr |
Proficiency with in vivo techniques, e.g. p.o, s.c, i.v, i.p. injections and organ harvesting in cancer immunology;Sample processing, homogenization, or generation of single-cell suspensions for ex vivo analysis;Proficiency in in vitro cell culture, cell culture scale-up for implantation. | 11/4/2017 |
| 1906 | NGM Biopharmaceuticals South San Francisco, CA Research Associate/Senior Research Associate - Antibody Engineering MS in biology / biotechnology-related discipline Exp: 1-2 yrs |
The person will mainly involve in the work of selecting and characterizing therapeutic antibodies from both na ve and immune sources, hybridoma sequencing, lead antibody humanization, developing cutting-age technologies for antibody discovery and optimization. The candidate is expected to work in a highly collaborative environment and to be able to work on multiple tasks simultaneously. | 11/4/2017 |
| 1907 | Novan, Inc Durham, NC Associate Scientist BS / MS in chemistry, chemical engineering, or related discipline. Exp: 0-5 yrs |
The Associate Scientist will be responsible for conducting performance testing on raw materials, drug substance intermediates, active pharmaceutical ingredients (API), and finished dosage forms (FDF). Additional responsibilities will include the creation of standard operating procedures for new or existing analytical equipment, performing preventative maintenance and calibration of analytical laboratory equipment, and assisting with method development and interpretation of data when appropriate. This position shall adhere to the Company's quality system including but not limited to the applicable standards, policies and procedures in the areas of responsibility defined in this job description. | 11/4/2017 |
| 1908 | Navigate BioPharma Svcs. Carlsbad, CA Lab Assistant BS in technology science or health-related field Exp: 1 yr |
Entry level laboratory position providing support to the Accessioning and Specimen Archiving departments. Primary responsibilities include checking patient specimens into the archival storage system, organization and maintenance of slide storage room, archive records maintenance, and fulfilling specimen returns and check-out requests. | 11/4/2017 |
| 1909 | Alcon Laboratories Fort Worth, TX Labeling Specialist I BS Exp: 0 yr |
Collaborate with R & D, Regulatory and Global Graphics Designers to create labeling for medical products. Ensure that labeling, art, film and proofs meet all medical, legal and regulatory requirements. Monitor changes in labeling requirements in the US and abroad. Review promotional labeling and ensure that it applies with approved labeling. May monitor, evaluate and recommend improvements to labeling process, quality, systems tools and / or policies. Solve routine problems of limited scope and complexity following established policies and procedures. Errors do not typically have a major effect on the organization. | 11/4/2017 |
| 1910 | Alcon Laboratories Lake Forest, CA Summer 2018 Internship Optical / Visualization Engineering R&D BS / MS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern assigned project(s) will align to one of our two business groups Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 11/4/2017 |
| 1911 | Alcon Laboratories Johns Creek, GA Summer 2018 Internship Chemistry R&D BS / MS Exp: NA |
As an R&D Intern, you will have the opportunity to be working side-by-side with over 1,800 highly skilled individuals dedicated to innovate and find solutions for current and future unmet needs in eye care. These unmet medical needs include glaucoma, cataract & refractive error, retina and external disease. As an R&D Intern assigned project(s) will align to one of our two business groups Surgical or Vision Care where opportunities to learn more about the discovery and identification of new eye care solutions and treatments are in the future. | 11/4/2017 |
| 1912 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Animal Services BS Exp: 0-2 yrs |
This position is responsible for providing humane care to all laboratory animals and to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. Additional expectations may be denoted in the core skills list or as outlined below. | 11/4/2017 |
| 1913 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Large Animal Toxicology BS Exp: 0-2 yrs |
This position is responsible for providing humane care to all laboratory animals and to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. Additional expectations may be denoted in the core skills list or as outlined below. | 11/4/2017 |
| 1914 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Reproductive Toxicology DART BS Exp: 0-2 yrs |
This position is responsible for providing humane care to all laboratory animals and to perform assigned technical and administrative functions within the guidelines / requirements outlined in a protocol or Standard Operating Procedure (SOP), thus producing sound, reliable data from which to evaluate the efficacy or toxicity of a test compound. Additional expectations may be denoted in the core skills list or as outlined below. | 11/4/2017 |
| 1915 | Merck Rahway, NJ 2018 MRL DISCOVERY SAMPLE MANAGEMENT ANALYTICAL CHEMISTRY INTERN BS in chemistry, biochemistry, chemical engineering, material science or pharmaceutical science or a related field Exp: NA |
The summer intern will be exposed to core instrumentation critical to modern pharmaceutical analysis, process characterization, and drug substance physical attributes determination. Additionally, interns will learn the fundamentals of sound analytical and physical chemistry method development necessary to problem solve as a member of an integrated team in support of the Merck small and large molecule pipeline. The Discovery Sample Management Department will expose the intern to various expert groups in the area of sample management, high-throughput analysis, molecular and materials characterization including high end mass spectrometry techniques to further broaden the experience | 11/4/2017 |
| 1916 | Merck West Point, PA 2018 MRL SALAR TOXICOLOGY DART INTERN BS / MS in Bioinformatics, Developmental Biology, Chemical / Bio Engineering, Biology, Chemistry, Toxicology, Pharmacology, Pharmacy, or relevant disc Exp: NA |
The Summer Intern in the Investigative Developmental and Reproductive Toxicology (iDART) group would have an opportunity to understand current regulatory guidance for testing novel chemical entities; importantly, the intern will further explore various emerging novel innovative assays to predict DART risk including genomic-based approaches to explore transcriptional changes underlying normal human development and the effects of drug exposure. The intern will learn techniques to identify novel molecular biomarkers relevant to developmental toxicity | 11/4/2017 |
| 1917 | Merck Cambridge, MA 2018 MRL BIOCONJUGATION & MEDICINAL CHEMISTRY INTERN BS / MS in chemical biology, chemistry, or a related field Exp: NA |
The intern will perform basic techniques in support of bioconjugation and chemical biology research, including preparation of buffers and reagents. The student will meticulously apply pre-defined procedures to execute experiments, observe all details and record results in a highly organized manner. | 11/4/2017 |
| 1918 | Thermo Fisher Scientific Sunnyvale, CA Engineering Intern BS / MS in an Engineering discipline (Chemistry preferred) Exp: NA |
Develop / evaluate / improve column packing and testing processes through accurate and complete documentation of all appli | 11/4/2017 |
| 1919 | Thermo Fisher Scientific Asheville, NC Intern II BS / MS in an engineering Exp: NA |
Summer internship to assist Senior Packaging Engineer in support of Manufacturing Engineering and Product Optimization Engineering projects. | 11/4/2017 |
| 1920 | Thermo Fisher Scientific Asheville, NC Manufacturing Engineering Intern BS / MS in an engineering Exp: NA |
Work to establish new manufacturing processes and continuously improve existing processes to improve product quality, delivery and overall customer satisfaction. | 11/4/2017 |
| 1921 | MedImmune Gaithersburg, MD Research Animal Technician I/II BA / BS Exp: 0-1 yr |
Day to day responsibilities would be observing appropriate |