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4624 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 | |
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| 2 | KBI Biopharma, Inc. 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 |
| 3 | KBI Biopharma, Inc. 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’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 |
| 4 | KBI Biopharma, Inc. Durham, NC Manufacturing Associate I/II-Downstream BS Exp: 0 yr |
Coordinate and perform cGMP manufacturing operations for manufactured biopharmaceutical products. | 4/29/2018 |
| 5 | KBI Biopharma, Inc. 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 |
| 6 | KSQ Therapeutics, Inc. 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. | 4/29/2018 |
| 7 | 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 |
| 8 | 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. 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 |
| 9 | 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 |
| 10 | 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 |
| 11 | 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 |
| 12 | 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. | 4/13/2018 |
| 13 | 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 |
| 14 | 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 |
| 15 | 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, M-F or as needed (ie. to fulfill needs of a validation protocol). Samples need to be performed aseptically. | 4/7/2018 |
| 16 | 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 |
| 17 | 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 |
| 18 | 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 |
| 19 | Foundation Medicine Cambridge, MA Laboratory Operations Assistant - 1st shift BS in a Biological or Life Science Exp: Entry level |
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 |
| 20 | 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’ 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 |
| 21 | Freudenberg Medical Baldwin Park, CA ENGINEER I BS in Engineering or related field Exp: 0-2 yrs |
Work closely with project managers to gather/prepare all documentation relevant to a particular project. | 4/7/2018 |
| 22 | 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’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 |
| 23 | 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. A QS & C Specialist assists the Compliance Team in the identification and resolution of quality issues and regulatory concerns. | 3/30/2018 |
| 24 | 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 |
| 25 | 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 |
| 26 | 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 |
| 27 | 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 |
| 28 | Crown Bioscience San Diego, CA Research Associate I - In Vitro BS Exp: 1-3 yrs |
Crown Bioscience | 3/23/2018 |
| 29 | 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 |
| 30 | 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. Operate utility systems throughout the entire campus. The 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 |
| 31 | 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 |
| 32 | 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. | 3/18/2018 |
| 33 | 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 |
| 34 | 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 |
| 35 | 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 |
| 36 | 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 |
| 37 | 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 |
| 38 | 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 |
| 39 | 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 |
| 40 | 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 |
| 41 | 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 |
| 42 | 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 |
| 43 | 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 |
| 44 | 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 |
| 45 | 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 |
| 46 | 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 |
| 47 | 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 |
| 48 | 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 |
| 49 | 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 |
| 50 | 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 |
| 51 | 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 |
| 52 | 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 |
| 53 | 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 |
| 54 | 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 |
| 55 | 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 |
| 56 | 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 |
| 57 | 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 |
| 58 | 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 |
| 59 | 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 |
| 60 | 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 |
| 61 | 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 |
| 62 | 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 |
| 63 | 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 |
| 64 | 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 |
| 65 | 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 |
| 66 | 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 |
| 67 | Ajinomoto Althea, Inc. 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 |
| 68 | Ajinomoto Althea, Inc. 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 |
| 69 | 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 |
| 70 | 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 |
| 71 | 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 |
| 72 | 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 |
| 73 | 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 |
| 74 | 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 |
| 75 | 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 |
| 76 | 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 |
| 77 | 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 |
| 78 | 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 |
| 79 | 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 |
| 80 | Danaher Timonium, MD Manufacturing Engineer BS in Manufacturing or Mechanical Engineering Exp: 1-3 yrs |
Control manufacturing and engineering specifications for the plant; Implement ICR's / ECR's;Maintain plant ISO procedures. | 2/4/2018 |
| 81 | 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 |
| 82 | 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 |
| 83 | 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 |
| 84 | 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 |
| 85 | 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 |
| 86 | 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 |
| 87 | Advanced Cell Diagnostics, Inc. 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 |
| 88 | 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 |
| 89 | 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 |
| 90 | 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 |
| 91 | 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 |
| 92 | 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 |
| 93 | 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 |
| 94 | 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 |
| 95 | 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 |
| 96 | 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 |
| 97 | 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 |
| 98 | 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 |
| 99 | 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 |
| 100 | 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 |
| 101 | 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 |
| 102 | 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 |
| 103 | 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 |
| 104 | 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 |
| 105 | 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 |
| 106 | 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 |
| 107 | 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 |
| 108 | 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 |
| 109 | West Pharmaceutical Services, Inc. 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 |
| 110 | West Pharmaceutical Services, Inc. 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 |
| 111 | West Pharmaceutical Services, Inc. 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 |
| 112 | 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 |
| 113 | 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 |
| 114 | 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 |
| 115 | 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 |
| 116 | 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 |
| 117 | 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 |
| 118 | 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 |
| 119 | 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 |
| 120 | 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 |
| 121 | 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 |
| 122 | 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 |
| 123 | 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 |
| 124 | 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 |
| 125 | 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 |
| 126 | Veracyte, Inc. 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 |
| 127 | Eurofins Viracor, Inc. 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 |
| 128 | Eurofins Viracor, Inc. 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 |
| 129 | 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 |
| 130 | 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 |
| 131 | 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 |
| 132 | 10x Genomics, Inc. 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 |
| 133 | Synthetic Genomics, Inc. 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 |
| 134 | Synthetic Genomics, Inc. 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 |
| 135 | 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 |
| 136 | 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 |
| 137 | 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 |
| 138 | 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 |
| 139 | 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 |
| 140 | Tris Pharma, Inc. 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 |
| 141 | Tris Pharma, Inc. 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 |
| 142 | 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 |
| 143 | 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 |
| 144 | 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 |
| 145 | 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 |
| 146 | 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 |
| 147 | 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 |
| 148 | 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 |
| 149 | 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 |
| 150 | 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 |
| 151 | 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 |
| 152 | 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 |
| 153 | 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 |
| 154 | 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 | 12/5/2017 |
| 155 | Spectrum Pharmaceuticals, Inc. 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 |
| 156 | Q-State Biosciences, Inc. 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 |
| 157 | Ultivue, Inc. 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 |
| 158 | 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 |
| 159 | Confer Health, Inc. 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 |
| 160 | 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 |
| 161 | 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 |
| 162 | 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 |
| 163 | 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 |
| 164 | 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 |
| 165 | CONTINUUS Pharmaceuticals, Inc. 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 |
| 166 | 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 |
| 167 | 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 |
| 168 | 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 be working with a lead or senior tech to learn and will watch and then perform benchwork with that lead;Employee will be working with a lead or senior tech to learn and will watch and then perform benchwork with that lead. | 12/11/2017 |
| 169 | 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 |
| 170 | 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 projects simultaneously with minimal manager supervision;Build standard sequencing libraries using commercial reagents. | 12/11/2017 |
| 171 | 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 |
| 172 | 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 |
| 173 | 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 |
| 174 | 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 |
| 175 | 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 |
| 176 | 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 |
| 177 | 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 |
| 178 | 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 |
| 179 | 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 |
| 180 | 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 |
| 181 | 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 |
| 182 | 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 |
| 183 | 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 |
| 184 | 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 |
| 185 | Valeant Pharmaceuticals International, Inc. 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 |
| 186 | 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 |
| 187 | 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 |
| 188 | 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 |
| 189 | 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 |
| 190 | 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 |
| 191 | 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 |
| 192 | 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 |
| 193 | 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 |
| 194 | Seattle Genetics, Inc. 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 |
| 195 | Seattle Genetics, Inc. 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 |
| 196 | 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 |
| 197 | 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 |
| 198 | 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 |
| 199 | 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 |
| 200 | Synthetic Genomics, Inc. 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 |
| 201 | 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 |
| 202 | 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 |
| 203 | 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 |
| 204 | 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 |
| 205 | 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 |
| 206 | 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 |
| 207 | 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 |
| 208 | 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 |
| 209 | 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 |
| 210 | Roche Tucson, AZ Summer Intern - Development, CDx Antibodies MS Exp: NA |
Independently plans and executes assigned projects; utilizes thorough technical and theoretical understanding of numerous analytical techniques. | 12/2/2017 |
| 211 | 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 |
| 212 | 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 |
| 213 | 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 |
| 214 | 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. | 11/20/2017 |
| 215 | 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 |
| 216 | 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 |
| 217 | 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 |
| 218 | 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 |
| 219 | 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 |
| 220 | 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 |
| 221 | 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 |
| 222 | 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 |
| 223 | 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 |
| 224 | 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 |
| 225 | 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 |
| 226 | 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 |
| 227 | 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 |
| 228 | 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 |
| 229 | 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 |
| 230 | 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 |
| 231 | 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 |
| 232 | 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 |
| 233 | 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 |
| 234 | 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 |
| 235 | 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 |
| 236 | 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 |
| 237 | 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 |
| 238 | 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 |
| 239 | 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 |
| 240 | 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 |
| 241 | 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 |
| 242 | 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 |
| 243 | 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 |
| 244 | 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 |
| 245 | 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 |
| 246 | 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 |
| 247 | 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 |
| 248 | 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 |
| 249 | 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 |
| 250 | 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 |
| 251 | 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 |
| 252 | 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 |
| 253 | 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 |
| 254 | 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 |
| 255 | 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 |
| 256 | 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 |
| 257 | PharmaForce, Inc. 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 |
| 258 | PharmaForce, Inc. 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 |
| 259 | Portola Pharmaceuticals, Inc. 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 |
| 260 | Poseida Therapeutics, Inc. 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 |
| 261 | 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 |
| 262 | 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 |
| 263 | 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 |
| 264 | 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 |
| 265 | 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 |
| 266 | 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 |
| 267 | 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 |
| 268 | 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 |
| 269 | 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 |
| 270 | 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 |
| 271 | 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 |
| 272 | 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 |
| 273 | 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 |
| 274 | 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 |
| 275 | 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 |
| 276 | 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 |
| 277 | 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 |
| 278 | 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 |
| 279 | Merck & Co., Inc. 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 |
| 280 | Merck & Co., Inc. 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 |
| 281 | Merck & Co., Inc. 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 |
| 282 | 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 |
| 283 | 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 |
| 284 | Novavax, Inc. 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 |
| 285 | Novavax, Inc. 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 |
| 286 | Novavax, Inc. 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 |
| 287 | 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 |
| 288 | Ocular Therapeutix, Inc. 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 |
| 289 | 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 |
| 290 | 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 |
| 291 | 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 |
| 292 | 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 |
| 293 | 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 |
| 294 | 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 |
| 295 | 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 |
| 296 | 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 |
| 297 | Osiris Therapeutics, Inc. 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 |
| 298 | Oxford Immunotec, Inc. 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 |
| 299 | 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 |
| 300 | 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 |
| 301 | 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 |
| 302 | 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 |
| 303 | 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 |
| 304 | 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 |
| 305 | 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 |
| 306 | 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 |
| 307 | 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 |
| 308 | 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 |
| 309 | 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 |
| 310 | 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 |
| 311 | 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 |
| 312 | 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 |
| 313 | 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 |
| 314 | 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 |
| 315 | 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 |
| 316 | 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 |
| 317 | 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 |
| 318 | 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 |
| 319 | 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 |
| 320 | 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 |
| 321 | 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 |
| 322 | 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 |
| 323 | 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 |
| 324 | Medtronic Danvers, MA Assoc Materials Engineer BS in Engineering Exp: 0-1 yr |
Conducts prototype development and clinical phases of new product introduction.; provides Advanced Manufacturing Engineering support in the commercialization phase of major new product introductions. | 11/4/2017 |
| 325 | 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 |
| 326 | 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 |
| 327 | 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 |
| 328 | 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 |
| 329 | 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 |
| 330 | Natera, Inc. 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 |
| 331 | Natera, Inc. 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 |
| 332 | Natera, Inc. 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 |
| 333 | 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 |
| 334 | 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 |
| 335 | 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 |
| 336 | NGM Biopharmaceuticals, Inc. 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 |
| 337 | NGM Biopharmaceuticals, Inc. 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 |
| 338 | 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 |
| 339 | Navigate BioPharma Svcs., Inc. 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 |
| 340 | Alcon Laboratories, Inc. 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 |
| 341 | Alcon Laboratories, Inc. 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 |
| 342 | Alcon Laboratories, Inc. 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 |
| 343 | 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 |
| 344 | 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 |
| 345 | 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 |
| 346 | 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 |
| 347 | 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 |
| 348 | 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 |
| 349 | 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 |
| 350 | 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 |
| 351 | 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 |
| 352 | MedImmune Gaithersburg, MD Research Animal Technician I/II BA / BS Exp: 0-1 yr |
Day to day responsibilities would be observing appropriate safety and study requirements by reading, understanding and following Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations and study protocols. Observing appropriate safety and health practices including personal protective equipment and barrier requirements. | 10/28/2017 |
| 353 | MedImmune Gaithersburg, MD Associate Scientist I/II MS in Mechanical / Biomedical / Electrical / Materials / Chemical Engineering or related field Exp: 0-3 yrs |
The candidate will be a part of Medimmune Drug Delivery and Device Development group working on combination device characterization and functionality, development of novel technologies, and transforming scientific knowledge / analysis into practical implementations. | 10/28/2017 |
| 354 | MedImmune Gaithersburg, MD R&D Associate II - Pharmacology & DMPK BS in Life Sciences Exp: 0-2 yrs |
Laboratory-based position for performing ligand binding immunoassay methods on routine basis according to SOPs with minimal supervision and relatively high throughput, supporting non-clinical and clinical PK and ADA. | 10/28/2017 |
| 355 | Medtronic Jacksonville, FL Regulatory Affairs Specialist MS Exp: 0 yr |
As a Regulatory Affairs Specialist you will be responsible for activities that lead and maintain regulatory approval / clearance of these devices; assesses the regulatory implications of changes to these devices. | 10/28/2017 |
| 356 | Medtronic Mounds View, MN Clinical Research Specialist MS Exp: 1 yr |
Coronary Structural Heart Clinical is looking for an enthusiastic, motivated candidate to be a Clinical Research Specialist in our dynamic environment. The incumbent has responsibility for meeting the milestones of a clinical study in compliance with applicable clinical and regulatory standards and in alignment with the Study Manager as well as business needs. Work is completed under general direction. | 10/28/2017 |
| 357 | Medtronic Northridge, CA Associate Quality Systems Specialist BS / MS Exp: 3 months-1 yr |
The primary responsibility of this position is to facilitate the creation and maintenance of high quality master data related to Medtronic Diabetes finished goods as an individual contributor in the Quality Systems department. This position will interact with Regulatory, Finance, and Supply Chain departments to ensure Material Data Management (MDM) is maintained correctly. By implementing, improving and executing policies and procedures at the local level to ensure master data meets global standards, the IT Bus Systems Analyst in Configuration Management plays an important role in protecting a key Medtronic asset: the master data that enables the company to share information, process transactions and plan and execute business operations globally. | 10/28/2017 |
| 358 | Medtronic Mounds View, MN (RF) Regulatory Affairs Specialist MS Exp: 1 yr |
The Telecom Regulatory Affairs Specialist is responsible for coordinating, facilitating and supporting all global submission for radio / telecom certification compliance, in order to enable marketing, sales, distribution, and operation of current and upcoming Medtronic CRHF products with radio / telecom features. | 10/28/2017 |
| 359 | Medtronic Northridge, CA Labeling Quality Systems Specialist MS Exp: 1 yr |
Ensure high quality of user documentation for patients and healthcare professionals around the world. Use your knowledge and expertise to ensure that released documentation meet all quality and compliance requirements. Perform timely reviews, investigate labeling quality issues, analyze labeling-related processes with an eye for continuous improvements, own and participate in CAPA activities related to labeling, and support labeling-related audits. | 10/28/2017 |
| 360 | Medtronic Santa Rosa, CA Assoc R&D Engineer BS Exp: 0 yr |
The Associate R / D Engineer will apply advanced technical principles, theories, and concepts in working on complex technical problems, and will provide technical leadership of projects from concept generation through early phase development. This position will work under general direction with latitude to determine technical objectives of assignments | 10/28/2017 |
| 361 | Medtronic Mounds View, MN International Clinical Evidence Specialist MS Exp: 0 yr |
The Clinical Evidence Specialist plans and develops clinical evaluation reports (CERs) and related evidence deliverables in compliance with applicable clinical and regulatory standards and in alignment with Medtronic business needs. This specialist collaborates with cross-functional teams on in-depth device and clinical data descriptions and analyses. This individual also manages project schedules for each document to ensure timely execution. | 10/28/2017 |
| 362 | Merck West Point, PA ASSOCIATE SCIENTIST - VACCINE PROCESS DEVELOPMENT BS in Chemical Engineering or Biological Sciences Exp: 1 yr |
The primary job responsibility will be to deliver on specific assigned objectives related to development of robust and scalable processes for the manufacture of clinical supplies and subsequent technical transfer of such processes to GMP operations or manufacturing division. Candidate will, under the close supervision of a more senior scientist, hold responsibility for a range of specific activities including, but not limited to: (1) evaluating downstream process unit operations, (2) chromatography screening and development, (3) membrane filtration, (4) analytical process monitoring, (5) high throughput microscale process development, (6) electronic notebook recording and maintenance, and (7) training for support of GMP operations. | 10/28/2017 |
| 363 | Merck Elkton, VA ASSOCIATE SPECIALIST, ENGINEERING BS / MS in biology, biochemistry, biochemical engineering, biological systems engineering, biomedical engineering, chemical engineering Exp: 0-3 yrs |
The successful candidate will have the opportunity to apply their enthusiasm and technical skills as a member of a multidisciplinary team supporting the operation of pharmaceutical, biopharmaceutical, vaccine product manufacturing facilities. | 10/28/2017 |
| 364 | Mersana Cambridge, MA Associate Scientist, Analytical Chemistry - CMC BS / MS in chemistry or a related discipline Exp: 1-2 yrs |
Under guidance from the senior scientists perform RP / IEX / SEC HPLC, LC / MS, CE / cIEF and spectrophotometry based testing of research materials including small molecules, polymers and biologics. | 10/28/2017 |
| 365 | Merz Franksville, WI Quality Metrics Engineer BS in Engineering Exp: 0-2 yrs |
The Quality Metrics Engineer will provide metrics and statistical sampling support to the Quality Department. Coordinate and execute product data and metrics reviews as appropriate to the Technical Operations Site. Evaluate the operation of Manufacturing and Quality activities in relation to compliance to Quality Standards and Regulations and recommend where corrections or improvements are indicated. Provide direct support to Quality Management / Quality Assurance personnel regarding operation of the department and Quality System. Provide support to other departmental activities as directed. | 10/28/2017 |
| 366 | MESO SCALE DIAGNOSTICS, LLC. Rockville, MD Quality Technician BS in Biochemistry, Microbiology, or Chemistry or related field Exp: Entry-level |
Entry-level position in Quality Assurance (QA), for the purpose of performing quarantine, hold tag removal, scrap materials, temp chart management, incoming raw material receipt and other functions as required. | 10/28/2017 |
| 367 | Mayne Pharma Greenville, NC Analytical Chemist I BS in Chemistry or Biology Exp: 0-1 yr |
This position is primarily responsible for performing routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. | 10/28/2017 |
| 368 | Micropoint Bioscience, Inc. Santa Clara, CA Quality Control Associates MS in chemistry, biology, or related scientific field Exp: 0 yr |
We are looking for highly motivated QC Associates (two openings) to join our quality team. 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. | 10/28/2017 |
| 369 | Miltenyi Biotec, Inc. Cambridge, MA Regulatory Affairs Associate BS in life sciences or chemistry Exp: 1 yr |
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. | 10/28/2017 |
| 370 | Miltenyi Biotec, Inc. Sunnyvale, CA QC Assay Development Associate MS in biological science or related discipline Exp: 1-3 yrs |
As a member of the Miltenyi Biotec Quality team, you will have the opportunity to participate in the daily Quality Control activities associated with biological and molecular assay development processes, transfers, and qualifications. Additionally you will be involved with QC release testing and environmental monitoring to support the GMP manufacturing of T Cells and CAR T Cells. The unique duties of this position will consist of supporting the QC assay development process including the design, execution, and analysis of development studies and reports, the execution of QC release, in-process and stability testing of raw materials, intermediates and cell based final products. Furthermore, you will be responsible for writing, reviewing, and revising test methods, assay qualification protocols, SOPs, and other controlled documents. Overall, your technical nature will champion the continued development of Miltenyi Biotec products and growing success. | 10/28/2017 |
| 371 | Miltenyi Biotec, Inc. 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. Overall, your keen ability to carry out key cell processing and manufacturing procedures will champion the continued development of Miltenyi Biotec products and growing success. | 10/28/2017 |
| 372 | MPI Research Mattawan, MI Research Technician 1/Research Specialist 1 - Reproductive 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. | 10/28/2017 |
| 373 | MPI Research Mattawan, MI Research Technician 1/Research Associate 2 - Second Shift Operations 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 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. | 10/28/2017 |
| 374 | MPI Research Mattawan, MI Research Technician 1/2 - Surgery In - Life - Primates 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 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. | 10/28/2017 |
| 375 | MPI Research Mattawan, MI Research Technician 1 - Animal Services - Colony Management 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 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. | 10/28/2017 |
| 376 | MPI Research Mattawan, MI Research Technician 1 - 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 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. | 10/28/2017 |
| 377 | MPI Research Mattawan, MI Research Technician 1 - ADME 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 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. | 10/28/2017 |
| 378 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Small 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 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. | 10/28/2017 |
| 379 | Myriad Genetics Inc Salt Lake City, UT Process Technician - Temporary MS in a chemical, physical, biological or clinical laboratory / medical technology science Exp: 6 months |
A major part of the position will be participating in continuous improvement projects in conjunction with staff and Technical Development, and participating on cross-functional teams to help execute the Automation Software Development Life Cycle (ASDLC) for new protocols. This position will work with Automation Development, Technical Development, and other PEG-Auto members. As directed by management, this role may also support other needs in the PEG-Auto group as they arise. | 10/28/2017 |
| 380 | Novartis Fort Worth, TX Summer 2018 Internship Materials Science/Engineering R&D BS / MS Exp: NA |
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. | 10/28/2017 |
| 381 | Novartis Fort Worth, TX Summer 2018 Internship Chemical Engineering R&D BS / MS Exp: NA |
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. | 10/28/2017 |
| 382 | Thermo Fisher Scientific Rockford, IL R&D Intern, Antibodies BS in biological science or related discipline Exp: NA |
Work closely with our scientific staff on a specific project that would lead to the development of a poster and oral presentation to be presented during the Summer Science Forum. | 10/28/2017 |
| 383 | Thermo Fisher Scientific Madison, WI R&D Scientist Intern BS Exp: NA |
A scientist intern is responsible for performing experiments independently, reporting those results to business leadership, and utilizing those results to drive meaningful changes in the company s processes and products | 10/28/2017 |
| 384 | Merck Boston, MA 2018 MRL DISCOVERY CHEMISTRY INTERN BS in Chemistry, Chemical Biology or a related field Exp: NA |
The interns will also attend departmental and team meetings to provide a wider perspective on the drug development process in the pharmaceutical industry. The intern is responsible for accurate electronic notebook recording, reaction set-up techniques, use of vacuum evaporation devices, thin-layer chromatography, flash chromatography, basic workup procedures, basic NMR interpretation, basic MS interpretation, and safe lab practices. Intern will have the opportunity to gain further knowledge and skill sets via refinement of organic chemistry skills, introduction to new spectroscopic and purification techniques, exposure to problems in process research, and perspective on the practical aspects of drug development. | 10/28/2017 |
| 385 | Merck Kenilworth, NJ 2018 MRL DISCOVERY PHARMACEUTICAL SCIENCES INTERN BS / MS in Pharmaceutics, Pharmaceutical Sciences, Chemical Engineering, Materials Science and Engineering, Analytical Chemistry, and other relevant d Exp: NA |
Utilization of a variety of physical and chemical characterization techniques to develop an understanding of the physicochemical characteristics of drugs and associated formulations | 10/28/2017 |
| 386 | Merck Boston, MA 2018 MRL DISCOVERY PROCESS CHEMISTRY INTERN BS in Chemistry or Chemical Biology Exp: NA |
The interns will also attend departmental and team meetings to provide a wider perspective on the drug development process in the pharmaceutical industry. The intern is responsible for accurate electronic notebook recording, reaction set-up techniques, use of vacuum evaporation devices, thin-layer chromatography, flash chromatography, basic workup procedures, basic NMR interpretation, basic MS interpretation, and safe lab practices. Intern will have the opportunity to gain further knowledge and skill sets via refinement of organic chemistry skills, introduction to new spectroscopic and purification techniques, exposure to problems in process research, and perspective on the practical aspects of drug development. | 10/28/2017 |
| 387 | Laboratory Corporation of America Phoenix, AZ Molecular Technologist BS / MS in Biology, Chemistry or related scientific discipline Exp: 0-1 yr |
The Integrated Oncology Division of LabCorp is seeking a Molecular Technologist to join their Molecular Oncology team! The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Oncology-Phoenix site processes DNA and RNA from a wide variety of oncology specimens, such as blood, bone marrow and paraffin-embedded tissues. A variety of molecular genetics techniques are used to analyze these specimens, such as real time PCR, Sanger Sequencing and fragment analysis | 10/15/2017 |
| 388 | Laboratory Corporation of America South San Francisco, CA QA Coordinator - Documentation (Monogram Biosciences) BS / BA Exp: 1-2 yrs |
Overall management of Monogram's Controlled Documentation Systems including its electronic documentation system (MasterControl), Controlled Document Master Files, Controlled Document Manuals (SOP Binders) and associated processes (e.g. Training, Annual Review) required for the effective maintenance and continued improvement of the document control system. | 10/15/2017 |
| 389 | Laboratory Corporation of America Phoenix, AZ Lab Technician BS in Biology or related life sciences Exp: 0 yr |
The lab technician is responsible for supporting the workflow in the Cytogenetics / FISH department while maintaining quality control in completing assigned tasks. | 10/15/2017 |
| 390 | Laboratory Corporation of America Englewood, CO Medical Laboratory Tech/ QA Analyst BA / BS Degree 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. | 10/15/2017 |
| 391 | Laboratory Corporation of America Lincoln, NE Medical Technologist/Quality Analyst BA / BS Degree 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. | 10/15/2017 |
| 392 | Laboratory Corporation of America Burlington, NC Pathology Assistant BA / BS in Biology Exp: 1-3 yrs |
Performs postmortem examinations and dissections on received tissue specimens within the histology laboratory. Performs gross dissection on more complex surgical specimens. | 10/15/2017 |
| 393 | Eurofins Viracor, Inc. Lee's Summit, MO Reagent Scientist I or II BS / BA in biological, physical, chemical, clinical laboratory science Exp: 1-2 yrs |
The Reagent Scientist is primarily responsible for manufacturing laboratory reagents for use by internal and external customers.. | 10/15/2017 |
| 394 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC West Greenwich, RI Quality Control Raw Materials Scientist - Compendial BS / MS in chemistry, biochemistry, life sciences or other related degree concentration Exp: 1-2 yrs |
Perform testing and data review for compendial, non-compendial methods, and routine laboratory procedures (experience with USP / EP is preferred) | 10/15/2017 |
| 395 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Andover, MA QC Instrumentation Analyst BS in biology, chemistry, or other related degree concentration Exp: 1-2 yrs |
Instrument qualification, validation support and documentation support;Supporting data integrity initiative for analytical instruments. | 10/15/2017 |
| 396 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Andover, MA QC Chemistry Analyst BS in biology, chemistry, or other related degree concentration Exp: 1-2 yrs |
Routine testing to support analytical laboratory;Routine testing to support analytical laboratory Using multiple analytical methods including HPLC, Spectrophotometer, analytics, pH, raw materials.Routine testing to support analytical laboratory;Routine testing to support analytical laboratory Using multiple analytical methods including HPLC, Spectrophotometer, analytics, pH, raw materials.Routine testing to support analytical laboratory;Routine testing to support analytical laboratory Using multiple analytical methods including HPLC, Spectrophotometer, analytics, pH, raw materials. | 10/15/2017 |
| 397 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Indianapolis, IN Particulates Biochemist BS in chemistry Exp: 3 months |
Performing analytical testing using instrumentation including, but not limited to, HIAC, Micro-flow imaging, osmolality, and turbidity | 10/15/2017 |
| 398 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Groton, CT Organic Chemist: Process Chemistry BS Exp: 1 yr |
Apply a strong technical / scientific foundation to deliver high quality scientific results in a laboratory environment in a safe and effective manner. | 10/15/2017 |
| 399 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC West Point, PA Microbiologist BS in Chemistry, biology, or related science Exp: 6 months |
Execution of studies for evaluation / implementation of Rapid Microbiology Technology | 10/15/2017 |
| 400 | 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. | 10/15/2017 |
| 401 | Eurofins Lancaster Laboratories Inc. Lancaster, PA Associate Chemist BS in chemistry, biology, biochemistry, or other related degree concentration Exp: 1 yr |
Perform physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, aerosols, liquids, creams, and gels) | 10/15/2017 |
| 402 | Eurofins Lancaster Laboratories Inc. Lancaster, PA Associate Chemist/Chemist BS in chemistry or other related degree concentration Exp: 1 yr |
Perform HPLC, IC, UV, KF, Dissolution, and physical testing on pharmaceutical products according to client / compendial procedures and departmental SOPs | 10/15/2017 |
| 403 | Eurofins Lancaster Laboratories Inc. Lancaster, PA Associate Scientist/Associate Technical Data Evaluator BS in chemistry or other related degree concentration Exp: 1 yr |
Ensure that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and / or GLP regulations | 10/15/2017 |
| 404 | Eurofins Lancaster Laboratories Inc. Lancaster, PA Associate Scientist/Scientist BS in chemistry or other related degree concentration Exp: 1 yr |
Perform HPLC, IC, UV, KF, Dissolution, and physical testing on pharmaceutical products according to client / compendial procedures and departmental SOPs | 10/15/2017 |
| 405 | Eurofins Genomics, LLC Louisville, KY DNA Sequencing Technician I BS in biology, chemistry, or other related degree concentration Exp: 12-18 months |
Carry out all laboratory activities related to the process of Sanger DNA Sequencing;Receive and prioritize packages arriving daily. | 10/15/2017 |
| 406 | Lannett Company, Inc. Carmel, NY Regulatory Affairs Associate BS in Science, preferably in Chemistry or Pharmacy Exp: 1-2 yrs |
We are seeking a detail oriented person that is ready to assist Regulatory Affairs Management in the preparation, review and submission of applications to the Food and Drug Administration (FDA), as well as have responsibility over the review and approval of GMP documents. | 10/15/2017 |
| 407 | Latitude Pharma San Diego , CA Research Associate BS in Chemistry, Pharmaceutical Sciences or Biochemistry Exp: 1-5 yrs |
LATITUDE is seeking a 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 other formulation 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. | 10/15/2017 |
| 408 | Leidos JACKSON, MI Associate Distribution Engineer BS Exp: entry level |
This Associate Distribution Engineer will perform field inspections, develop project design drawings, material lists, and cost estimates for electrical power delivery ranging from 4.8kV to 14.4kV. | 10/15/2017 |
| 409 | Leidos OAK RIDGE, TN Jr. Scientist/Engineer BS in Geology or related Science, or Engineering Exp: 0-2 yrs |
Candidates will work under supervision of Senior Staff to assist on environmental projects, including investigations, remediation, and monitoring at government and commercial sites within the CONUS. Anticipated task activities will include, but are not limited to: site surveys and inspections, soil sampling, surface water and sediment sampling, groundwater sampling, groundwater monitoring well installation / abandonment, and assisting with remediation system design / construction / maintenance. Candidates will also aid in the preparation of technical work plans, reports, and permits. Candidates will conduct scientific analyses of environmental data resulting from field operations, including development of maps, figures, tables, and written materials describing investigation data and results of data analyses. Candidates will assist with coordinating technical documents through various stages of generation and production, communicating and working effectively with diverse project teams and project management, and working within designated schedules and budgets. | 10/15/2017 |
| 410 | Leidos PEORIA, IL Energy Program Engineer BS Exp: 0-2 yrs |
The position will be responsible for reviewing technical energy efficiency applications for incentives and rebates for Ameren Illinois electric and natural gas customers. The position will help provide technical review of gas and electric utility demand-side management (DSM) projects around the state of Illinois. | 10/15/2017 |
| 411 | Leidos VIENNA, VA Project Support Specialist (Entry Level) BS Exp: 0-2 yrs |
The Project Support Specialist will assist with tasking related to several areas within the Software Development Life Cycle (SDLC). The ideal candidate will be a motivated, self-starter who performs well under general direction and supervision. He / she should be a team player with a commitment to quality and a drive to be a problem-solver. The Project Support Specialist will be responsible for preparing, reviewing, revising, and maintaining technical / user documentation and will assist with general software testing. | 10/15/2017 |
| 412 | Leidos ROCKVILLE, MD Project Control P1 BS Exp: Entry level |
Will assist in tracking cost, managing multiple subcontractors, invoicing, maintaining financial systems and financial reporting. The position supports the functional team by providing data analysis and ad hoc reporting, while also looking for areas to improve process flows, cost controls and efficiency. | 10/15/2017 |
| 413 | Leidos SAN DIEGO, CA Jr Signal Processing Engineer BS Exp: 1 yr |
Junior signal processing analyst with a mathematical background in linear algebra, probability, stochastic processes, spectral estimation, signal detection and estimation, and signal processing will focus on developing and evaluating the performance of mathematical and signal processing techniques / algorithms for radars and infrared sensors operating in challenging sensing environments. | 10/15/2017 |
| 414 | Lifecore Biomedical, LLC Chaska, MN Stability Chemist I BS in Chemistry Exp: 0-2 yrs |
This individual will ensure accurate, reproducible, and timely analytical testing in support of stability studies on an as-needed basis and participate in methods improvements in the laboratory. They will perform testing of stability samples, communicating results through appropriate documentation. They will also support the stability program by participating in study initiation; retrieving samples for routine testing; performing general lab upkeep; participating in laboratory investigation; and meeting tight timelines for stability requirements. | 10/15/2017 |
| 415 | Lifecore Biomedical, LLC Chaska, MN QC Microbiologist I BS in Microbiology Exp: 0-2 yrs |
This individual will ensure accurate, reproducible, and timely QC testing in support of manufacturing; support development, validation and stability studies on an as-needed basis; participate in methods improvements within the laboratory. They will perform testing on in-process product, final product, and raw materials for routine testing, validation testing, and stability testing; communicate results through appropriate documentation and batch records, statistical analysis and trending; acquire and maintain cleanroom and gowning qualification; participate in rotation to provide weekend and holiday coverage; perform instrument maintenance; identify and report equipment and method failures; identify areas for continuous improvement. | 10/15/2017 |
| 416 | LinaTech Sunnyvale, CA Field Service Engineer BS in an Engineering Exp: entry level |
The Field Service Engineer position's primary role includes providing functional and technical support for all our Radiation Oncology Products. | 10/15/2017 |
| 417 | Leidos WALLED LAKE, MI Controls Intern BS Exp: 1 yr |
Their role would be working mainly with the teams who develop building management software for large scale industrial clients. Initial jobs would involve software screen layouts and configuration. As the technical skillset of the candidate grew they would be moved into more programing oriented tasks. | 10/15/2017 |
| 418 | Intuitive Surgical, Inc. Sunnyvale, CA Industrial Design Intern BS / MS in ndustrial Design Exp: NA |
The Industrial Design intern will help drive and craft new product platforms, helping to shape the future of surgery through the lens of a world-class user experience. A natural collaborator, with experience in creative processes, the Industrial Designer will assist engineering and user facing teams on the framing, and definition of future product opportunities; leading to creation and presentation of concepts that stretch the mind and illustrate possibilities. Focusing on physical aspects of the product, he / she employs comprehensive understanding of aesthetics and form to address these opportunities and transform complex mechanical designs into elegant forms that are usable, beautiful and manufacturable. | 10/15/2017 |
| 419 | Reynolds American WInston-Salem, NC 2018 SUMMER INTERN (UNDERGRADUATE) - OPERATIONS (ENGINEERING) BS degree in the scientific or engineering Exp: NA |
This role is highly visible and is an integral part of the RJRT Manufacturing team with tremendous learning opportunities. The intern in this position will be provide decision and analytical support to critical cross-functional areas and the manufacturing management team. | 10/15/2017 |
| 420 | Reynolds American WInston-Salem, NC 2018 SUMMER INTERN (UNDERGRADUATE) - RESEARCH & DEVELOPMENT BS degree in the scientific or engineering Exp: NA |
During the summer of 2018, the Research and Development function will be offering several internship opportunities to assist the function in developing new products consistent with our Growth, Innovation and Harm Reduction Platforms. Summer interns will have Winston-Salem based assignments and conduct research to support established research programs and projects in collaboration with other researchers and scientists. | 10/15/2017 |
| 421 | Reynolds American WInston-Salem, NC 2018 SUMMER INTERN (GRADUATE) - RESEARCH & DEVELOPMENT MS in analytical or organic chemistry, biology, microbiology, biostatistics, bioinformatics, agronomy, statistics, mathematics, engineering or any oth Exp: NA |
During the summer of 2018, the Research and Development function will be offering several internship opportunities to assist the function in developing new products consistent with our Growth, Innovation and Harm Reduction Platforms. Summer interns will have Winston-Salem based assignments and conduct research to support established research programs and projects in collaboration with other researchers and scientists. | 10/15/2017 |
| 422 | Kashiv Pharma, LLC. Bridgewater, NJ CMC Technical Writer MS in Pharmaceutics Exp: 0-2 yrs |
Create, Compile, and Review CMC regulatory documents and sections for ANDA submissions as well as other technical reports. Demonstrate solid teamwork with Analytical R&D, PD, RA, and other R&D team members to meet aggressive deadlines to ensure timely delivery of documents to meet Company s goals and objectives. | 10/5/2017 |
| 423 | KBI Biopharma, Inc. Durham, NC PD Associate/Senior PD Associate - Upstream MS in biotechnology or related area Exp: 0 yr |
Shake flask study set-up using design provided by a scientist. Bioreactor preparation, autoclaving, media hold, inoculation. Media, feed, buffer preparation and filtering. | 10/5/2017 |
| 424 | KBI Biopharma, Inc. Boulder, CO Microbiology - Environmental Services Associate BS Exp: 1-2 yrs |
Performs microbiological in-process and release testing in support of GMP manufacturing. Tests include, but are not limited to, bioburden, microbial purity and endotoxin. | 10/5/2017 |
| 425 | KBI Biopharma, Inc. Durham, NC Research Associate/Sr. Research Associate - Analytical Dev BS Exp: 0-2 yrs |
Perform contract development services, including, analytical development programs for monoclonal antibodies, recombinant proteins and peptides. | 10/5/2017 |
| 426 | KBI Biopharma, Inc. The Woodlands, TX Process Development Associate MS in the Life Sciences (biology, immunology, medical technology) Exp: 1 yr |
This individual will conduct a variety of cell culture and analytical assays in support of product characterization and potency assessment. The position will also participate in process development, optimization, validation, and tech transfer to GMP. | 10/5/2017 |
| 427 | Pfizer Rocky Mount , NC Quality Engineer Ops Investigator BS Exp: 0-2 yrs |
The Quality Engineer- Investigations is responsible for completing investigations providing documented evidence of root cause and Corrective and Preventative Actions for plant quality issues. This individual will work closely with employees at multiple levels within the organization in order to achieve timely completion of investigations. | 10/5/2017 |
| 428 | Pfizer Kalamazoo, MI Automation Engineer BS in a technical field Electrical, Mechanical, Chemical, or Computer Engineering, Computer Science Exp: 1 yr |
Provide highly effective automation to Active Pharmaceutical Ingredient (API) Control systems. This includes following the software lifecycle (requirements, design, implementation and testing) for many different platforms, which include Allen Bradley PLCs, Wonderware HMIs, Siemens PLCs, Foxboro, Honeywell, and DeltaV. Also, provide information collection and reporting, and manufacturing workflow solutions for the Pfizer Global Supply (PGS) Kalamazoo facility. Participate in the design, development, deployment, integration and maintenance of control systems. | 10/5/2017 |
| 429 | Pfizer Lake Forest, IL CQ Lab Analyst BS in science discipline (preferably chemistry, biochemistry or biology) Exp: 0-1 yr |
The primary responsibility of this role includes using Functional / Technical skills to perform analytical testing and data processing in accordance with procedure, regulatory guidelines (FDA, MHRA, TGA, ICH, and DEA). | 10/5/2017 |
| 430 | Pfizer Kalamazoo, MI QO Technical Associate III BS / MS in Chemistry, Biochemistry, or related science Exp: 1-3 yrs |
This position is in the Kalamazoo QO Rapid Turn Laboratory working on first shift. Opportunity for schedule flexibility exists as the Laboratory supports business and customer needs on weekends and holidays. Technologies employed in the Rapid Turn Laboratory include HPLC, GC, titrations, Karl Fisher, UV, and general analytical procedures. | 10/5/2017 |
| 431 | Pfizer Cambridge, MA Technical Associate, Animal Care 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, bleeds) 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. | 10/5/2017 |
| 432 | Pfizer Kalamazoo, MI API Manufacturing Specialist BS Exp: 1 yr |
The successful candidate will assume professional responsibilities within the API (Active Pharmaceutical Ingredient) compliance group. Primary responsibilities include managing all cleaning and process validation activities for their assigned manufacturing areas. In addition, the candidate must interface regularly with customer and regulatory auditors and take a lead role in evolving compliance programs with the API area. | 10/5/2017 |
| 433 | Pfizer Kalamazoo, MI QO Technical Associate BS in Microbiology, Bacteriology, Immunology, Molecular Biology, Cell Biology or related specialized biological sciences preferred Exp: 1-3 yrs |
Using standardized testing procedures, the candidate will conduct a variety of microbiological and / or immunological analyses on finished products and / or raw materials. The tests and assays are performed as a function of a high output microbiological / immunological testing laboratory. In addition to performance of routine testing, the candidate will assist in the overall operation of the laboratory including: development of standard operating procedures, stocking and ordering of laboratory supplies, routine maintenance of equipment and overall lab upkeep. Testing of blood / blood products may also be performed periodically. | 10/5/2017 |
| 434 | SeraCare Milford, MA Manufacturing Associate I BS in Biology, Chemistry or related science Exp: 0.5 yr |
The Manufacturing Associate / Technician provides direct labor for the manufacturing of high quality diagnostic products using manual and semi-automated equipment and prepares / completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 10/5/2017 |
| 435 | Lab Pros Cambridge, MA Senior Research Associates - Metabolic MS in biochemistry, bioengineering, microbiology, molecular biology, or equivalent Exp: 1 yr |
Perform biochemical techniques including protein expression, purification and analysis and enzymatic activity assays in support of research projects. | 10/5/2017 |
| 436 | Laboratory Corporation of America Englewood, CO Lab Assistant/Technician BS in a life science field of study such as chemistry, biochemistry or biology Exp: 1-2 yrs |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in a designated technical department. Interprets results, subject to verification by Technologist / Supervisor, and providing allowance by State regulations. This position will focus on ELISA assays. | 10/5/2017 |
| 437 | Laboratory Corporation of America Brentwood , TN Laboratory Assistant BS Exp: 1-2 yrs |
Perform all paperwork, technical, and non-technical procedures required to process and submit specimens. | 10/5/2017 |
| 438 | Laboratory Corporation of America Austin, TX Cytogenetic Technologist BS in chemical, physical, biological or clinical laboratory science Exp: 1 yr |
Integrated Oncology is seeking a Cytogenetics Technologist to join its team in Austin, TX! The Cytogenetics Technologist is responsible for performing all routine and special Cytogenetics procedures, microscopic / virtual analysis, and maintaining quality control. With minimum supervision, this position will participate in trouble shooting, and training of other employees as necessary. | 10/5/2017 |
| 439 | Laboratory Corporation of America Seattle, WA Certified Histotechnician/Histotechnologist BS Exp: 1-3 yrs |
Performs technical duties related to production of histolopathological slides. Researches, troubleshoots, and resolves histology related inquiries and problems within the laboratory and for LabCorp's clients. | 10/5/2017 |
| 440 | Laboratory Corporation of America San Antonio, TX Cytotechnologist, CT (ASCP) BS in Biological Science Exp: 1-3 yrs |
Screens and evaluates any gynecologic and non-gynecologic specimen sent to the laboratory for the determination of possible malignant or related abnormal conditions. | 10/5/2017 |
| 441 | Laboratory Corporation of America Seattle, WA Technician/Medical Technologist BS Exp: 1-3 yrs |
Performs tests and analyses according to established procedures in the Chemistry Department. | 10/5/2017 |
| 442 | Laboratory Corporation of America Phoenix, AZ Quality Analyst BS 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. Duties include, but are not limited to: Document control, competency assessment paperwork, initiate PT failure reports, internal auditor responsibilities, conducting monthly audits, calibration checks, responsible for new hire quality orientation / training, track standardization notices, technical bulletins and recalls, PT reagent lot change roll over tasks, and continuing education assigning and tracking (i.e. CAP courses). | 10/5/2017 |
| 443 | LakePharma, Inc. Hayward, CA Associate Scientist/Scientist Protein Chemistry (Cloning/DNA Production) MS in biology or related field Exp: 1 yr |
This candidate will be primarily responsible for, but not limited to, conducting many different steps of molecular cloning, including DNA purification, PCR, gene synthesis, site-mutagenesis, agarose gel electrophoresis, and DNA sequencing analysis. | 10/5/2017 |
| 444 | LakePharma, Inc. Hayward, CA Associate Scientist/Scientist - Analytical and Formulation Science BS / MS in Biochemistry, Biology, Chemistry, Biotechnology or related discipline Exp: 1 yr |
The candidate will be primarily responsible for conducting various bioanalytical assays, including capillary electrophoresis (CE), HPLC / UPLC, charge variation analysis by cIEF and IEX-HPLC, SDS Page, Mass Spec, and other assays. The ideal candidate would have experience with some to all of these assays and should be able to prepare project study reports. | 10/5/2017 |
| 445 | Lampire Biological Labs, Inc. 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. | 10/5/2017 |
| 446 | Eurofins Lancaster Laboratories West Greenwich, RI Scientist Analytical Chemist BS / MS in Analytical Chemistry, Biology, Molecular Biology, Immunology, or related field Exp: 0-2 yrs |
Perform testing and data review for HPLC / UPLC (high and ultra-high liquid chromatography), titre, ATOL purification using TECAN and plate reader, CE (capillary electrophoresis), CEX (cation exchange), HILIC (hydrophilic interaction), TOC (total organic carbon), LAL (endotoxin testing), ELISA, and DNA testing | 10/5/2017 |
| 447 | Eurofins Lancaster Laboratories Lancaster, PA Scientific Data Review Specialist BS in biochemistry, chemistry, or other related Exp: 1 yr |
Ensure that the client receives quality reports that meet their expectations by reviewing laboratory data for accuracy, clarity, consistency, and adherence to client requirements | 10/5/2017 |
| 448 | Eurofins Lancaster Laboratories 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 receipt and GMP documentation of sample moves. | 10/5/2017 |
| 449 | Eurofins Lancaster Laboratories Andover, MA Research Associate, Nanomedicine Development and Manufacturing BS in biochemistry, chemistry, or other related Exp: 0-2 yrs |
Supporting the development, evaluation and manufacturing of polymer nanoparticle drug delivery formultations for the controlled release of small molecules, peptides, proteins and alternative modalities as needed | 10/5/2017 |
| 450 | LAM Therapeutics Guilford, CT Research Internship BS / MS Exp: NA |
This position will be responsible for performing research in the context of drug activity assays, molecular and cell biology experiments that are relevant to our clinical programs. | 10/5/2017 |
| 451 | Reynolds American Inc. Winston-Salem, NC 2018 SUMMER INTERN (UNDERGRADUATE) - OPERATIONS (ENGINEERING) BS in Engineering Exp: NA |
You will be assigned a challenging research project with a focus on process controls engineering, requiring creative thinking, problem solving, and teamwork as you interact with other personnel throughout our winning organization. | 10/5/2017 |
| 452 | Reynolds American Inc. Winston-Salem, NC 2018 SUMMER INTERN (UNDERGRADUATE) - RESEARCH & DEVELOPMENT BS in the scientific or engineering field Exp: NA |
During the summer of 2018, the Research and Development function will be offering several internship opportunities to assist the function in developing new products consistent with our Growth, Innovation and Harm Reduction Platforms. Summer interns will have Winston-Salem based assignments and conduct research to support established research programs and projects in collaboration with other researchers and scientists. | 10/5/2017 |
| 453 | Reynolds American Inc. Winston-Salem, NC R&D APPIAN INTERN BS / MS Exp: NA |
If you are a real go getter and are excited about gaining real work experience, The S&RA function at RAI is offering an internship opportunity to assist in providing could completing a sprint of Agile development for an Appian report and see it though testing and implementation. Other project options Appian E-signature or an R&D workflow on IM s backlog. You will exercise initiative, creative problem solving skills, teamwork and leadership as you interact with other personnel throughout our winning organization. | 10/5/2017 |
| 454 | Intuitive Surgical, Inc. Sunnyvale, CA Supplier Engineering Intern BS / MS in Engineering Exp: NA |
The mission of Supplier Engineering is to ensure high quality and stable delivery of purchased production supplies from suppliers operating under robust quality systems to maximize Patient Value. Supplier Engineer is responsible for ensuring their Suppliers meet ISI requirements for product safety, quality, cost, delivery, and service. | 10/5/2017 |
| 455 | Intuitive Surgical, Inc. Sunnyvale, CA Validation Engineering Intern BS in Biomedical Engineering, Mechanical Engineering, or related fields Exp: NA |
The primary function of the position is to automate the completion of datasheets that are used in the Cleaning and Sterilization lab. | 10/5/2017 |
| 456 | Intuitive Surgical, Inc. Sunnyvale, CA Manufacturing Engineering Intern BS Exp: NA |
Contributes to the successful manufacture of complex surgical devices used in computer-enhanced surgical applications | 10/5/2017 |
| 457 | BioPharmGuy Anytown, US Contract Research Assistant Some college Exp: 0 |
Looking for someone to confirm mailing addresses and phone numbers for companies we list. Must be able to accept payment via PayPal. Will be a few hours per week most likely. | 10/04/17 |
| 458 | GSK Various US cities, Va GMS Engineering Associate - Future Leaders Program - US - 2018 BS in Engineering Exp: 0-1 yr |
Working in conjunction with other parts of the business, we ensure the smooth and rapid transition of newly developed products into full-scale manufacture. By using a variety of processes and the latest efficient technology, our global network is able to deliver to patients and customers four billion packs of medicines and healthcare products every single year. Working in conjunction with other parts of the business, we ensure the smooth and rapid transition of newly developed products into full-scale manufacture. By using a variety of processes and the latest efficient technology, our global network is able to deliver to patients and customers four billion packs of medicines and healthcare products every single year. Working in conjunction with other parts of the business, we ensure the smooth and rapid transition of newly developed products into full-scale manufacture. By using a variety of processes and the latest efficient technology, our global network is able to deliver to patients and customers four billion packs of medicines and healthcare products every single year. | 9/29/2017 |
| 459 | GSK Rockville, MD Associate Biochemist BS in Chemistry, Biochemistry, Immunology, Molecular Biology or other science field Exp: 0-1 yr |
Conducts a wide range of quality control tests and analyses on products to uncover defects. Reports to management who make the decision to allow or deny the release. Testing for process monitoring. Testing of Raw Materials | 9/29/2017 |
| 460 | Immunomedics, Inc. Morris Plains, NJ QA Associate, Raw Material Release and Clinical Shipments BS in biology, chemistry, or related field Exp: 1-3 yrs |
We are seeking a Quality Assurance Associate to be responsible for all QA-related aspects of material handling, storage, shipping and control, and associated documentation. This position may also be cross-trained on product disposition and regulated document / training functions. | 9/29/2017 |
| 461 | Immunomedics, Inc. Morris Plains, NJ Bioreactor Technologist BS in biotechnology, biology, or related discipline Exp: 0-2 yrs |
We are seeking a Bioreactor Technologist to be responsible for the operation of mammalian cell culture production processes in compliance with cGMP regulations. | 9/29/2017 |
| 462 | IMPAX Hayward, CA Reviewer I, QC Document BS in Chemistry Exp: 1-3 yrs |
Review laboratory documents to ensure that they are accurate and complete, and that the work performed is in compliance with applicable procedures, and analytical methods. | 9/29/2017 |
| 463 | 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. | 9/29/2017 |
| 464 | Inovio Pharmaceuticals, Inc. Plymouth Meeting, PA Clinical Trial Associate BS / MS Biology, Immunology, Bioengineering, Cell or Molecular Biology Exp: 0-1 yr |
Set-up and maintain Trial Master File (TMF) including project documentation files, investigator files, study books, and project databases on more complex projects. | 9/29/2017 |
| 465 | Inovio Pharmaceuticals, Inc. Plymouth Meeting, PA Associate/Sr Associate, ImmunoInformatics BS / MS in computational biology or biotechnology Exp: 1-4 yrs |
This is a position at the interface of research, engineering, product development and clinical development groups. Working together with the Clinical and Product Development groups, the candidate will be responsible for data analysis of cellular (e.g., flow cytometric and ELISpot) and humoral (e.g., ELISA) immune assays as well as data generated from biomarker platforms including microRNA, DNA methylation and gene arrays. The candidate will also be responsible for managing data sent to the company from clinical trial sites, including working internally in collaboration with the Product Development, Engineering and Clinical teams in order to analyze clinical trial data. Strong organizational skills are imperative. A robust understanding of immunology and / or biomarker platforms listed above is preferred. | 9/29/2017 |
| 466 | Inovio Pharmaceuticals, Inc. San Diego, CA Manufacturing Engineer II BS / MS Exp: 1-3 yrs |
The Manufacturing Engineer II assists in developing and improving manufacturing processes, techniques and procedures associated with building and maintaining medical devices (electromechanical and sterile disposable) used in ongoing clinical trials. The tasks are completed by the Manufacturing Engineer with a steady focus on continuous improvement of product quality through leaner concepts and activities. | 9/29/2017 |
| 467 | Integral Molecular Philadelphia, PA Research Associate I BS in biology, bioengineering, or a related field Exp: 1-2 yrs |
This position will involve conducting laboratory research and supporting general R&D operations at Integral Molecular. The position will involve both research and production of biomedical research products. You will be working with a dedicated group of scientists on the development and commercialization of biomedical technologies. Projects may involve cell culture, virology, DNA preparation, liquid handling automation, and cell-based assays (western blot, ELISA, immunofluorescence, flow cytometry). | 9/29/2017 |
| 468 | Integrated DNA Technologies Coralville, IA Research Scientist II MS in Biology, Genetics, Chemistry or a related life sciences field Exp: 1 yr |
The Research Scientist II, under minimal supervision, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with development and characterization of new IDT genomics products in the CRISPR domain. A background in bacterial genetics and / or protein engineering is highly preferred. This position is responsible for planning and executing experiments, analyzing data and reporting / presenting findings as well as supporting IDT customers. This position is equivalent to a Research Assistant II position at an academic institution. | 9/29/2017 |
| 469 | Joining Intuitive Surgical, Inc. Sunnyvale, CA RMA Line Engineer RMA Line Engineer RMA Line Engineer BS in an Engineering discipline Exp: 1-2 yrs |
Line Engineer is responsible for supporting production released robotic systems. Deliver improvements in reliability, serviceability, manufacturability, capacity, and cost. Provide mechanical support for cross-functional team including electrical and software disciplines. | 9/29/2017 |
| 470 | Intrexon Germantown, MD Research Associates BS / MS in Biology, Molecular Biology, Immunology, Biochemistry, Synthetic Biology, life sciences or related field Exp: 1 yr |
Intrexon is seeking highly motivated and creative Research Associates with experience in molecular biology, immunology, biochemistry and / or assay development to support efforts within our Human Therapeutics and Immunology teams. We are seeking candidates looking for a fast paced, exciting working environment utilizing state of the art technology. Level will be determined based on candidate experience. | 9/29/2017 |
| 471 | Intrexon South San Francisco, CA Research Associate I/II BS / MS in microbiology, genetics, molecular biology, or a related field Exp: 1 yr |
The Research Associate I / II (level determined by candidate experience), DNA Construction will be responsible for molecular biology operations as part of Intrexon s Industrial Product Division (IPD) high-throughput DNA construction team. The candidate will work closely with other group members in a fast-paced, dynamic team environment to enable heterologous product generation through metabolic and strain engineering. | 9/29/2017 |
| 472 | inVentiv Health, Inc. Miami, FL Clinical Study Manager Associate BS Exp: 1-3 yrs |
The clinical study manager associate is responsible for supporting project management within the clinical division by ensuring that protocols, procedures, client requests, timelines and subject safety are all adhered to. | 9/29/2017 |
| 473 | Thermo Fisher Scientific Rockville, MD Engineer I, Validation BS Exp: 1-2 yrs |
Work with the Validation Team in developing and implementing equipment and process validation protocols to ensure compliance to applicable regulatory requirements, internal company standards and industry practices. | 9/29/2017 |
| 474 | Thermo Fisher Scientific Remote / Field, CA IOMS Service Engineer BS Exp: 1-3 yrs |
Ensures customer satisfaction through excellence in repair and support of customers products. Maintains communication with customer to ensure understanding of status, cost, and scheduling of all aspects of the service event. | 9/29/2017 |
| 475 | Thermo Fisher Scientific Pleasanton, CA Scientist 1 BS / MS in life science Exp: 1-2 yrs |
The candidate may be required to manufacture Oligonucleotides from start to finish, including but not limited to synthesis, formulation, purification, QC and analysis as per Standard Operating Procedures in the Custom Manufacturing lab. This position exercises judgment within defined procedures and practices to determine appropriate action. The Scientist I normally receives general instruction on routine work, detailed instruction on new assignments. The job encounters recurring work situations with occasional variations from the norm, involving a moderate degree of complexity. Employee will work on problems where analysis of situation or data requires a review of identifiable factors. Accuracy is required in performing all functions of this position. Mistakes in work could cause substantial interpretive errors. The Scientist I complies with all company safety regulations and procedures. | 9/29/2017 |
| 476 | Invivoscribe San Diego, CA Manufacturing Associate II BS Exp: 1 yr |
The Manufacturing Associate II will assist with all aspects of production, including the production of master mixes, controls and assay kits. | 9/29/2017 |
| 477 | Invivoscribe San Diego, CA Clinical Laboratory Scientist BS in Clinical Laboratory Science (or equivalent) Exp: 0-3 yrs |
A Clinical Laboratory Scientist (CLS) is responsible for receiving samples and performing data entry for specimens received. This position will provide professional customer service to our clients. Clinical Laboratory Scientist will respond effectively to changes in the workflow. | 9/29/2017 |
| 478 | Jounce Therapeutics, Inc. Cambridge, MA Clinical Trial Associate BS / BA Exp: 1 yr |
The successful candidate for this CTA position 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 FDA regulations, Good Clinical Practice (GCP), and company standard operating policies and procedures. | 9/29/2017 |
| 479 | JUNO THERAPEUTICS, INC. Seattle, WA Research Associate, Assay Support Group (Analytical Development) MS Exp: 1 yr |
In this individual contributor, lab-based role, the Research Associate will work in a collaborative environment to perform process analytics testing to support Juno s development programs. This position will report to the Manager of the Analytical Core Group. The incumbent will join an analytical testing group that values data quality, high productivity and teamwork. Key responsibilities include: | 9/29/2017 |
| 480 | JUNO THERAPEUTICS, INC. Seattle, WA Research Associate MS Exp: 1 yr |
In this individual contributor, lab-based role, the Research Associate will work in a collaborative environment to perform Analytical testing to support Juno s development programs. This position will report to the Manager of Analytical Core (AC). The incumbent will join an analytical testing group that values data quality, high productivity and teamwork. The key deliverables for this role are precise, accurate, and high quality date. This position will require thorough documentation of all experimental steps and final data readout. | 9/29/2017 |
| 481 | JUNO THERAPEUTICS, INC. Bothell, WA Quality Control Associate I/II, Cell Biology BS Exp: 1 yr |
The primary focus of the QC Associate I / II in Flow Cytometry will be to perform GMP testing to support product lot release and in-process testing. | 9/29/2017 |
| 482 | JUNO THERAPEUTICS, INC. Seattle, WA Pharmacovigilance Associate BS Exp: 2 yr |
The Pharmacovigilance (PV) Associate responsibilities include, but are not limited to, performing the intake of safety information received by Juno PV, reviewing and processing the safety information in accordance with department procedures, and distribution of Individual Case Safety Reports (ICSRs) to appropriate destinations. The PV Associate will support other case management and clinical trial activities as needed. | 9/29/2017 |
| 483 | JBS United Sheridan, IN Swine Research Project Intern BS / MS Exp: NA |
If you are selected, you will learn about foundational experimental design and the importance of research detail conducted on livestock farms and in a research-focused laboratory. You will work within a confined hog operation, exposed to poultry batteries, and a nutritional laboratory all while maintaining stringent biosecurity procedures established by JBS United. Knowledge gained by conducting research in swine production facilities will be valuable upon graduation. | 9/29/2017 |
| 484 | Thermo Fisher Scientific Madison, WI R&D Scientist Intern BS / MS Exp: NA |
A scientist intern is responsible for performing experiments independently, reporting those results to business leadership, and utilizing those results to drive meaningful changes in the company s processes and products | 9/29/2017 |
| 485 | Thermo Fisher Scientific Madison, WI Manufacturing Engineering Intern BS in an engineering Exp: NA |
The Manufacturing Engineering Intern position provides an opportunity for Industrial, Mechanical, or Electrical Engineering students to gain real world manufacturing experience and will focus on process optimization, lean methodologies, and emerging technologies. This intern will assist with projects designed to hit key productivity and savings goals, maximize quality, and accelerate products through the development phase. | 9/29/2017 |
| 486 | Thermo Fisher Scientific Madison, WI Marketing - Chemical Applications Intern BS / MS in natural science degree Exp: NA |
The Marketing Chemical Applications Intern will support the Product Management and R&D teams in developing and testing new hardware and software tools used in Fourier Transform Infrared (FTIR) spectroscopy. This position will involve working in a cross-functional team that includes key stakeholders in engineering, software development, and marketing to evaluate FTIR methods, workflows, results, and software interfaces. This individual will also work with the Product Management and Marketing Communication groups to design and deliver customer facing marketing material for new product launches. | 9/29/2017 |
| 487 | Joining Intuitive Surgical, Inc. Sunnyvale, CA Procedure Development Intern BS / MS in a pre-medical program Exp: NA |
Conducts and presents clinical-technical analysis assessing key metrics to facilitate procedure prioritization | 9/29/2017 |
| 488 | Joining Intuitive Surgical, Inc. Sunnyvale, CA Operations Analyst Intern BS / MS Exp: NA |
Intern will work with Manufacturing, Supply chain, Marketing and Engineering teams to fully understand demand and supply needs. The intern will be exposed to top level master scheduling process and how Master Production Scheduling is created as well as how production and capacity planning is developed. | 9/29/2017 |
| 489 | Joining Intuitive Surgical, Inc. Sunnyvale, CA Clinical Affairs Intern BS / MS in a bioengineering or life-sciences degree Exp: NA |
This position reports to a manager of Clinical Affairs with oversight from a Senior Director. The purpose of this job function is to work with Clinical Project Managers on the development and implementation of clinical study design and strategy with an emphasis on understanding patient reported outcomes. This role may also drive their own project, contributing their own analysis on big data sets for surgical procedures across multiple modalities. The job function may also be responsible for interpreting data and results collected through a clinical study and reviewing literature to identify the clinical relevance of the data. | 9/29/2017 |
| 490 | Ginkgo BOSTON, MA Automation Padawan (1 year paid internship) BS / MS Exp: NA |
Our foundry encompasses high throughput genetic engineering of microbes as well as high resolution analytics to assess cell performance; you will be responsible for helping to transition and adapt protocols and new unit operations to run on Ginkgo's automated platforms. | 9/29/2017 |
| 491 | Ginkgo BOSTON, MA Fermentation Padawan (1 year paid internship) BS / MS in chemical engineering, microbiology, or related field Exp: 1yr |
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. | 9/29/2017 |
| 492 | Ginkgo BOSTON, MA Organism Engineering Padawan (1 year paid internship) BS / MS in biochemistry, metabolic engineering, molecular biology, or related fields Exp: 1yr |
We are looking for highly talented and motivated students to join our development processes, including strain design, DNA / strain construction, evaluation of strain performance, pathway optimization and troubleshooting. | 9/29/2017 |
| 493 | PSC Biotech N/A, CA Entry Level CSV Engineer BS chemical, mechanical, or electrical engineering Exp: 0 yrs |
PSC Biotech is one of the world's largest biotechnology consulting firms in the pharmaceutical and biotechnology industry. Presently we are recruiting for (1) Entry Level Engineer to train in Computer Software Validation for one of our clients in Northern CA. | 9/28/2017 |
| 494 | Biotechne Minneapolis, MN Research Associate I BS / BA biochemistry, chemistry, biology, or realted Exp: 0-2 yrs |
Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, and endotoxin assay. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis and communication of results within the Department and across different groups. Other duties include instrument maintenance, record keeping and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity and team building across the QC Department or the entire company. Perform additional duties as assigned. | 9/28/2017 |
| 495 | Biotechne Minneapolis, MN Research/Manufacturing Associate AS / BS biology, biotechnology, biochemsitry, or related Exp: 0-2 yrs |
The responsibilities of this position are manufacturing standards for the Quantikine, DuoSet, and DuoSet IC product lines. Primary responsibilities will include manufacturing standards for different kits and running assays to insure quality. Perform additional duties as assigned. | 9/28/2017 |
| 496 | Reata Pharmaceuticals Irving , TX Biopharmaceutical Leadership Development Program BS / MS biotechnology, cellular and molecular biology, or related Exp: 0 yrs |
Reata is currently recruiting for its 2017 class of the Biopharmaceutical Leadership Development Program (BLDP) at the company s headquarters in Irving, near the center of the Dallas-Fort Worth Metroplex. This program attracts top talent and is designed to provide high-potential future leaders with a unique opportunity to gain in-depth exposure to core functions that are critical to the development and commercialization of Reata s products and long-term success of the organization. The multi-disciplinary rotational assignments are tailored to each individual for growth and development of technical and leadership skills. Throughout the course of the program, BLDP analysts will regularly interact with members of the senior management team, as well as be provided with training, networking, and mentoring opportunities. | 9/28/2017 |
| 497 | RB Parsippany, NJ Regulatory and Government Affairs Internship BS scientific discipline Exp: 2 yrs coursework |
The Regulatory Intern will work with the Regional Regulatory Teams and on special research projects, as needed. He / she will also interface cross functionally with marketing, supply and R&D scientific staff. | 9/28/2017 |
| 498 | RB Parsippany, NJ Information Services Graduate Development Program BS computer engineering, information technology, or related Exp: 0 yrs |
This three year rotational program will take you through three analyst-level roles, exploring the core businesses that IS supports at RB. | 9/28/2017 |
| 499 | RB Parsippany, NJ Information Services Internship BS computer engineering, information technology, or related Exp: 2 yrs coursework |
We are looking for current juniors to join RB as an Information Services Intern for summer 2017. | 9/28/2017 |
| 500 | RB Parsippany, NJ Regulatory Specialist, Compliance BS 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. | 9/28/2017 |
| 501 | RB Parsippany, NJ Regulatory Specialist BS natural sciences Exp: 0-5 yrs |
Implement New Regulations and Guidances: Keep current with all relevant guidances and regulations. Work with stakeholders to implement requirements of new regulations and guidances within specified timelines. Assess and communicate all requirements to stakeholders in order to maintain compliance without delay to business due to regulatory issues. Adjust and monitor timelines to support the business. Support Infrastructure and Systems Integration: Contribute to supporting a high quality and effective infrastructure to meet the regulatory requirements which support the launch of associated products within RB NA. Execute systems integration for optimal functionality and use. Contribution to infrastructure (processes, procedures, systems etc.) to be made within agreed upon timelines. Deliver project and brand specific activities assuring they are correct, complete and on-time, including registration submissions, labeling, etc. Gain Understanding of Legislative and Regulatory Climate: Understand how the government operates and key touch points RB can access to influence policy development. Monitor and gain an understanding of new policies and objectives involving federal and local government affairs. Review trade association materials (newsletters, meeting minutes, agenda items) to gain an understanding of where influencing opportunities exist. | 9/28/2017 |
| 502 | RB Montvale, NJ Research & Development Future Leadership Program BS scientific discipline Exp: 0 yrs |
Our Future Leadership Program is an exclusive program for exceptional students from the best universities in the world. Only 16 individuals selected every year to start in our different centers of excellence based in UK, USA, India and more who will be prepared for truly dynamic careers. It s a fast-track program for RB s leaders of the future! | 9/28/2017 |
| 503 | Recro Gainesville, GA QC Analyst I - 2nd Shift BS chemistry or related Exp: 1 yr |
The QC Analyst I position is an entry level analyst position. The QC Analyst I is required to complete the most comprehensive in-house training program for all laboratory activities. Documented proficiency is required before the QC Analyst I can perform tasks independently. Because of the level of experience required for this position, the scope of work is generally limited to routine testing explicitly following written test protocols, however, upon the discretion of QC supervisory staff the QC Analyst I may be called upon to execute non-routine testing to support method validation, and method transfer. In addition, the QC Analyst I may be called upon to write or revise SOPs, analytical procedures, and analysis reports, or qualify as trainers on specific procedures. | 9/28/2017 |
| 504 | Recro Gainesville, GA Scientist I BS chemistry or related Exp: 6 months |
The primary objective of the Scientist I position is to support early stage product development through commercialization efforts. The Scientist I will be expected to perform duties including, but not limited to, routine analytical testing, method development and validation, method transfer, and equipment purchase and qualifications. The Scientist I will work under the guidance of more senior staff to develop the ability to work independently. The Scientist I may be required to write or revise SOPs, analytical procedures, analysis reports, validation documents, etc. | 9/28/2017 |
| 505 | Regeneron Rensselaer, NY QA Associate/QA Specialist BS / BA scientific discipline Exp: 0-2 yrs |
Performs activities in support of dispositioning product and / or raw materials while ensuring compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents. | 9/28/2017 |
| 506 | Regeneron Rensselaer, NY Intern - Quality Control (Technical Resources) BS biomedical engineering, biology, biochemistry, chemical engineering, or related Exp: 3 yrs coursework |
This internship will provide the intern with the opportunity to learn the principles behind assay validation. The scope of this internship is to evaluate critical parameters involved in a method validation and obtain hands-on experience in the lab through execution of validation studies. During this internship, the intern will be able to determine the critical parameters for the testing method and improve the method based on the outcome of the study. In addition, the intern will gain knowledge of ICH (International Conference on Harmonisation) and USP (United States Pharmacopeia) guidelines on assay validation, detailed design and construction of validation protocol and protocol execution. This internship will also provide exposure to statistical analysis and report writing. At the end of the internship, the intern will also have the opportunity to present their work as a whole to a broad audience. | 9/28/2017 |
| 507 | Regeneron Rensselaer, NY Intern - Process Sciences BS chemical engineering, biochemistry, biomedical engineering Exp: 3 yrs coursework |
A number of process related impurities, such as cell culture additives, are introduced into the monoclonal antibody manufacturing processes. Elimination of these impurities is demonstrated for each molecule during process performance qualification and worst-case exposure scenarios are presented in regulatory filings. Throughout this project, the intern would generate experimental data which supports the removal of antifoam, insulin, and potentially other impurities at levels greater than what is observed in the manufacturing process through the use of existing laboratory scale models. These experiments would be designed and conducted over the diafiltration step of the UFDF unit operation such that the results would be generally applicable for multiple existing product programs and also apply for future molecules which utilize the same processes. | 9/28/2017 |
| 508 | Regeneron Rensselaer, NY Intern - Drug Product, Combination Products BS biomedical engineering, electrical engineering, physics Exp: 2 yrs coursework |
As medical devices are becoming smarter and thus more dependent on electrical functionality, one area which needs specific development is the ability to determine when drug has been fully expelled from the primary container within a medical device. The intern will investigate previous methods used, propose alternate methods to detect the end of injection, and perform comparative testing to evaluate these methods. Possible methods may involve optical, mechanical, or firmware-based technologies and their interplay with the electrical systems in the device. | 9/28/2017 |
| 509 | Regeneron Rensselaer, NY Biotech Production Dispensing Technician I - III AS scientific discipline Exp: 0-2 yrs |
Performs all tasks necessary for the manufacturing dispensing operations. | 9/28/2017 |
| 510 | Regeneron Rensselaer, NY Quality Control Analyst BS / BA biology or related Exp: 0 yrs |
Performs a variety of biochemical analyses on raw materials, products, in-process materials, or stability samples in support of the company s quality program. | 9/28/2017 |
| 511 | Regeneron Rensselaer, NY Process Sciences Associate I - IV BS / MS chemical or biomedical engineering or related Exp: 0-2 yrs |
Supports the Manufacturing and Process Sciences Departments through small scale laboratory experiments, as well as analysis, troubleshooting, and validation of manufacturing bioprocesses. | 9/28/2017 |
| 512 | Relypsa Redwood City, CA Research Associate (Product/Drug Analysis) MS chemistry or biochemistry Exp: 1 yr |
Involved in development of novel drugs incl. analytical method development and qualification and improvement for methods to analyze small molecule compounds, in line with appropriate safety and regulatory requirements. | 9/28/2017 |
| 513 | Repligen Waltham, MA Document Control Specialist BS technical discipline Exp: 1-2 yrs |
The successful candidate will be responsible for assisting the QA Document Control department revise / create, file, organize, and review production documents. The candidate will work closely with the Manufacturing team and Document Control department to ensure the changes are accurate and are made effective in a timely manner. | 9/28/2017 |
| 514 | Philps Bothell, WA Co - op Electrical Engineering BS / MS Electrical engineering or related Exp: 3 yrs coursework |
Are you interested in a CO-OP Intern opportunity with Philips We welcome currently enrolled undergraduate (BS) and graduate (MS) level students to participate in 6 month paid CO-OP opportunities at our sites across the US. Through these roles you will gain meaningful, hands-on experience in engineering for a HealthTech company. | 9/28/2017 |
| 515 | Philips Murrysville, PA Manufacturing Quality Engineer BS electrical or mechanical engineering or related Exp: 1 yr |
Understand and apply FDA CFR 820, ISO 13485, ISO 14971, Canadian, Japanese, Brazilian and European medical device regulations. Provide quality engineer support to ensure that products are manufactured with a high level of quality, while being in compliance with standards and regulations governing medical device manufacturing. Administer and manage delivery holds and reconciliations for assigned product lines. Provide support for field actions as needed. Develop, review and approve procedures, technical / validation reports, change notices, risk assessments, and other related quality system documentation. Lead, support, or facilitate investigations, CAPAs, process changes, quality plans and other Quality activities. Lead or support internal and external quality system audits. Drive resolution of nonconformities. Manage quality engineering aspects of the transfer of new or existing products into the manufacturing facility. Drive continuous improvement of products and processes to reduce the cost of non-quality (out-of-box failures, line yield, nonconforming material, and other available data). Be team-oriented, communicate suggestions and concerns, generate solutions, be flexible, and provide positive interaction and feedback with peers and internal departments. Occasional travel may be required. | 9/28/2017 |
| 516 | Philips Nashville, TN Complaint Specialist BS technical discipline Exp: 0 yrs |
The Complaint Specialist is an entry level position into Quality Compliance within Medical Devices. You will be trained to effectively act as a member of the Quality & Regulatory team and be responsible for ensuring quality records, identifying potential FDA reportable events and / or Business Unit follow up and escalations. This role is also responsible for corresponding with the Customer Care Solutions Center and Field Service Organization to ensure a complete and quality record. Within this team you will gain knowledge and acumen on Medical devices, Regulations as well as be a part of a team with room for career advancement. | 9/29/2017 |
| 517 | Philips Monroeville, PA Co - op Research Engineering BS mechanical, biomedical, or electrical engineering Exp: 2 yrs coursework |
The Research Engineer will be working with a team of engineers that have complementary skills, in mechanical, biomedical, electrical engineering (algorithms / software), as well as medicine and clinical research. Projects tend to be small bedside devices, or devices that can be worn. They span diagnostics and therapy for sleep disordered breathing, as well as other sleep and related disorders. | 9/29/2017 |
| 518 | Philips Andover, MA Regulatory Affairs Specialist BS technical discipline Exp: 1 yr |
Andover is in need of an RA specialist to support the expanding portfolio of products. There are currently 35 projects in the business unit with several new NPI projects to start in 2017. Further assistance is necessary to maintain appropriate regulatory support and compliance. The business unit is in need of strategy planning for 510k submissions and future country registrations. | 9/29/2017 |
| 519 | Philips Bothell, WA Co - op - Hardware Engineering BS / MS Electrical engineering or related Exp: 2 yrs coursework |
We welcome you to join Philips as a Hardware Development Engineer Intern in our Bothell, WA location for a 6+ month long coop. We are seeking a graduate student with a passion for technology to work with the R&D electronics design team for an exciting internship opportunity that will provide an invaluable development experience. Find out why Philips is a best place to work as you work with a top notch design team and make a meaningful contribution to next generation ultrasound. | 9/29/2017 |
| 520 | Philips Andover, MA Co - op Test Engineering BS / MS biomedical, electrical, or computer engineering Exp: 3 yrs coursework |
Gain meaningful, hands-on experience in engineering for a HealthTech company. Philips Ultrasound Supply Chain Test Engineering develops and deploys manufacturing test equipment to verify the performance and safety requirements of ultrasound transducers that are currently changing the way that doctors practice medicine. | 9/29/2017 |
| 521 | RetroViro San Diego, CA Medicinal Chemistry and Database Support BS chemistry or related Exp: 0 yrs |
The company is seeking a part-time intern to support the medicinal chemistry efforts for the Company s internal discovery programs funded by the National Institutes of Health (NIAID). Hundreds of experimental molecules are synthesized at RetroVirox to determine their antiviral and immunomodulatory activities. These small-molecules are recorded in a chemistry database and their activity and structure relationships used to guide future medicinal chemistry efforts. We are seeking highly proactive candidates able to handle the chemistry database of the company and input their information on a customized database. This is a paid position. | 9/29/2017 |
| 522 | Revolve Biotechnologies Baltimore , MD Robotics Technician BS biomolecular / medical engineering or related Exp: 0 yrs |
Revolve is seeking a highly motivated, organized, and proficient Robotics Technician to take ownership of all things related to our laboratory liquid handling robot. This includes running, servicing, and developing software to increase functionality and improve throughput. The ideal candidate will have significant programming experience and be able to work a minimum of 10-15 hours per week. The candidate must work well independently and in a small team setting. Flexibility to take on a range of varied responsibilities as required in the startup environment is critical. Compensation commiserate with experience | 9/29/2017 |
| 523 | Catalent Madison, WI Associate, Quality Control - Raw Materials BS / BA in Biotechnology Exp: 0-2 yrs |
This position will perform a variety of laboratory procedures to support Quality Control. The position will perform daily work assignments accurately and in a timely and safe manner. | 9/23/2017 |
| 524 | Catalent Madison, WI Sample Coordinator, Quality Control BS / MS in Biotechnology, or related field Exp: 0-3 yrs |
This position requires experience in a Quality Control setting with an emphasis in sample coordination, as well as to perform a variety of skills necessary for biotech company operations. The position is expected to follow procedures with periodic direct supervision. The position is responsible for accurately performing and documenting established procedures. | 9/23/2017 |
| 525 | Catalent Madison, WI Associate Scientist, Cell Line Development MS in Biotechnology, or related field Exp: 1 yr |
The Associate Scientist, Cell Line Development will perform daily work assignments accurately and in a timely and safe manner. This position will independently evaluate, select and apply standardized scientific and techniques to assignments of moderate complexity, involving potentially conflicting design requirements, unavailability of materials or processes, etc. This position seeks continual improvement of work practices from experience with moderate-sized projects; develops extensions to existing methods and protocols. | 9/23/2017 |
| 526 | Catalent Madison, WI Sr. Associate, Analytical MS / MA in Biotechnology, or related field Exp: 0 yr |
This positon requires a variety of skills necessary for biotech company operations. Perform routine testing of process samples, raw materials, finished products and stability samples, while adhering to SOPs and working in a cGMP compliant environment. Position will Analyze and interpret results in written and oral format. Additionally, this position will support Preventative Maintenance and basic Laboratory maintenance activities while maintaining a GMP quality system. Other duties will include data review / archiving, database entry / review and contributions to process improvement initiatives. | 9/23/2017 |
| 527 | Catalent Madison, WI Sr. Associate, Sample Coordinator MS / MA in Biotechnology, or related field Exp: 0 yr |
This positon requires a variety of skills necessary for biotech company operations. Perform sample coordination for the laboratory, routine testing of process samples, raw materials, finished products and stability samples, as necessary, while adhering to SOPs and working in a cGMP compliant environment. Position will analyze and interpret results in written and oral format. Additionally, this position will support Preventative Maintenance and basic Laboratory maintenance activities while maintaining a GMP quality system. Other duties will include data review / archiving, database entry / review and contributions to process improvement initiatives. | 9/23/2017 |
| 528 | Catalent Madison, WI cGMP Manufacturing Associate Scientist MS in a scientific discipline or related field Exp: 1 yr |
The position is responsible for performing manufacturing operations according to standard operating procedures and batch instructions under limited supervision. Responsible for performing solution preparation, cell culture and\or purification operations. | 9/23/2017 |
| 529 | Ginkgo BOSTON, MA Automation Engineer BS / MS in engineering or equivalent Exp: 1 yr |
Developing automated experimental workflows genetic engineering processes, strain cultivation, sample preparation, and NGS / mass spec analysis. | 9/23/2017 |
| 530 | GSK Marietta, PA Manufacturing Operator BS Exp: 1 yr |
The operator will use proper aseptic technique while performing tasks in the Grade A / B areas to include: bulk formulation, vial filling, routine and non-routine aseptic interventions; operating filling and auto loading equipment using automated control systems, unloading of autoclaves and management of sterilized components. | 9/23/2017 |
| 531 | GSK East Durham, NY Associate Process Engineer BS / MS in Chemical Engineering or related Engineering discipline Exp: 0-1 yr |
Drive Process Understanding, Capability and Control improvement projects to support the site strategy, delivering safe, compliant and robust operations from a Process Engineering perspective. Involved in new product introductions, technology transfers, process design and generating innovative engineering solutions to drive continuous improvement. | 9/23/2017 |
| 532 | GSK Memphis, TN Operations Support Specialist BA / BS Exp: 1-2 yrs |
Daily oversight of scheduling and planning of on the floor activities and resources;Manufacturing / packaging system knowledge. | 9/23/2017 |
| 533 | GSK Rockville, MD Associate Biochemist BS Exp: 1-2 yrs |
The Associate Biochemist I performs quality sampling, testing, and data review for in process and bulk biopharmaceutical ingredients, finished biopharmaceutical products. | 9/23/2017 |
| 534 | GSK Zebulon, NC Automation Engineer (Junior Level) BS in a Science or Engineering related discipline Exp: 1 yr |
To 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. To successfully 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. | 9/23/2017 |
| 535 | GSK Zebulon/Rockville, NC GMS Pharmaceutical Sciences Associate - Future Leaders Program - US - 2018 BS in Pharmaceutical Sciences, Pharmaceutics, Drug Design / Development or related degree Exp: 0-1 yr |
By joining the three-year rotational GMS Technical Development Program, you will have the opportunity to make a significant difference to lives around the world, whilst enjoying some of the healthiest career prospects in the industry. | 9/23/2017 |
| 536 | GSK Zebulon/Research Triangel Park, NC GMS Quality Associate - Future Leaders Program - US - 2018 BS in Chemistry, Chemistry-related science, Analytical Sciences, Microbiology, Biomedical Sciences Exp: 0-1 yr |
Our Global Manufacturing and Supply organization (GMS) leads the rapid commercialization and distribution of GSK products, allowing team members to take a proactive, hands-on approach to shaping the world around them. Working in conjunction with other parts of the business, we ensure the smooth and rapid transition of newly developed products into full-scale manufacture. By using a variety of processes and the latest efficient technology, our global network is able to deliver to patients and customers four billion packs of medicines and healthcare products every single year. | 9/23/2017 |
| 537 | 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. | 9/23/2017 |
| 538 | Greatbatch Brimfield, MA Quality Engineer BS Exp: 0-2 yrs |
Identifies and evaluates procedures to ensure the production of quality product. Develops new and unique approaches to complex problems and can advance technology beyond previous achieved levels. Applies engineering concepts to resolve acute or chronic problems. Conducts studies to understand capability for process and / or measurement systems. Provides management with technical guidance as required. Identifies and develops appropriate documentation for process improvement and project implementation. Maintains liaison with individuals and units within or outside the organization with responsibility for acting independently on technical matters pertaining to their filed. | 9/23/2017 |
| 539 | Greatbatch Alden, NY Manufacturing Engineer I BS Exp: 0-2 yrs |
The primary purpose of this position is to evaluate, select and apply standard engineering practices, techniques and procedures while using sound judgment when making adaptations and / or modifications to machinery, test and measurement equipment and / or systems. Ensures Integer internal and external customer expectations are met or exceeded. | 9/23/2017 |
| 540 | Greatbatch Alden, NY Chemical Engineer I BS Exp: 0-2 yrs |
Apply principals of chemistry and engineering to perform experiments. Designs chemical equipment and devises processes for manufacturing chemicals and products. Control movement, storing, and packaging of solids, liquids and gases. Prepares written and oral reports and provides recommendations to others. Provides support in areas where needed. May troubleshoot problems with chemical manufacturing processes. | 9/23/2017 |
| 541 | GreenLight Biosciences Medford, MA Research Associate/Sr. Research Associate BS / MS IN CHEMICAL ENGINEERING OR EQUIVALENT Exp: 1-3 yrs |
The successful candidate will define and develop scalable recovery processes at the benchtop scale by applying state-of-the-art DSP techniques in the context of milestone-driven projects. The candidate will scale those processes from benchtop- to pilot- to industrial-scale. Strong technical, organizational, and communication skills are essential as well as the ability to develop creative solutions to challenging problems. | 9/23/2017 |
| 542 | Grifols Clayton, NC Senior Associate Process Development Engineer I MS in Biology, Physics, Chemistry, Biochemistry, or Engineering Exp: 1 yr |
Provide technical support through process development, process transfer, and technical support of production processes for plasma derived proteins. | 9/23/2017 |
| 543 | Grifols Clayton, NC Assistant Chemist BS / BA in chemistry 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. This position will support Chemistry testing for final container release , intermediates, stability, in-process samples and raw materials. | 9/23/2017 |
| 544 | Grifols Clayton, NC Assistant Biologist BS in biology, chemistry or related field Exp: 6-12 months |
This position is responsible for performing bioburden and endotoxin testing of in-process product samples and raw materials to support plasma production processes, including process and equipment activities. Environmental Assurance department must maintain adequate staffing to support all production operations 24 hours per day, 7 days a week. In addition to in-process product monitoring, this position may also assist with environmental monitoring of production and testing areas. This position is part of the budgeted staff necessary to complete this sampling and testing and to ensure that Clayton site production processes and production areas remain in a state of control. | 9/23/2017 |
| 545 | Grifols Emeryville, CA Manufacturing Assoc I BS in one of the biological or physical sciences Exp: 1-3 yrs |
This manufacturing associate position is responsible for the production of recombinant antigens, peptides and or buffers. Refer to the associated department-specific Task List for additional requirements. | 9/23/2017 |
| 546 | Hovione East Windsor, NJ Process Technician - Drug Product Continuous Manufacturing BS in 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. | 9/23/2017 |
| 547 | ICON US, US CRA I BS in medicine, science or related discipline Exp: 1 yr |
Identify, select, initiate, and close-out appropriate investigational sites for clinical studies. Monitor those sites in order to ensure that studies are carried out according to the study protocol, ICON SOPs / WPs, applicable regulations and the principles of ICH-GCP. Depending upon experience, become involved, when required, in other areas of study management and staff training and contribute to the review of ICON systems and procedures as appropriate. Provide a benchmark of monitoring competence to inexperienced / less experienced colleagues. | 9/23/2017 |
| 548 | ICON San Antonio, TX Data Coordinator BS Exp: 1 yr |
Oversee CRA monitoring visit and complete queries generated from visit. Perform additional quality control checks prior to case report form completion. | 9/23/2017 |
| 549 | ICON Farmingdale, NY Configuration & QC Specialist (Study Start - Up Specialist) BS Exp: 1 yr |
The Study Start-Up Specialist will be support the Project Management Team (PM) in configuring and QC ing new clinical studies in all ILS systems according to the specifications of the Client Laboratory Worksheet (CLW). You will create supporting documents for the site to facilitate proper specimen collection, coordinate packaging and shipping including visit requisitions, reference range tables, and study specific Lab Manuals and collection guides. Ensure information is clear and accurate and seek guidance on any parameters that need clarification. | 9/23/2017 |
| 550 | Ignyta San Diego, CA Research Associate / Sr. Research Associate, PK MS Exp: 0 yr |
The position will provide the support for pharmacokinetic(PK) / pharmacodynamics and toxicokinetic (TK) components for clinical / preclinical development programs. | 9/23/2017 |
| 551 | Horizon Pharma plc Lake Forest, IL UIC Students - Internship Program Application BS / MS Exp: NA |
Cross-functional engagement with multiple business units.Complete and present a milestone project that addresses current topics in the industry. | 9/23/2017 |
| 552 | Ginkgo BOSTON, MA Process Engineering Padawan (1 year paid 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 process leveraging Ginkgo's engineered organisms. | 9/23/2017 |
| 553 | 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. | 9/23/2017 |
| 554 | 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. | 9/23/2017 |
| 555 | GE NA, OH Field Engineer Intern BS / MS Electronics, Biomedical Engineering, Medical Imaging Technology or Mechanical Principles degree program Exp: NA |
Intern will observe and perform various equipment service processes and procedures to drive customer satisfaction and ensure proper functionality | 9/23/2017 |
| 556 | GE United States, Un GE Healthcare Quality Regulatory Leadership Program Intern MS in engineering, science, biology, clinical research, health policy, health product regulation, public health, quality assurance or related field Exp: NA |
The Quality Regulatory Leadership Program Intern is the premier development program for high potential individuals seeking a career at GE Healthcare in Quality Assurance and Regulatory Affairs. The internship consists of working experience in one or more of the following areas: Quality Assurance, Regulatory Affairs, Complaint Handling, Corrective & Preventative Action, QMS Compliance, Medical & Clinical Affairs, Global Audit and much more. | 9/23/2017 |
| 557 | GE Brunswick, GA Biomedical Technician Intern BS / MS Electronics, Biomedical Engineering, Medical Imaging Technology or Mechanical Principles degree program Exp: NA |
In this role, the Biomedical Technician Intern will respond to service calls to evaluate, diagnose, perform repair and planned maintenance (PM) on basic biomedical equipment and drive customer satisfaction through Service Excellence. | 9/23/2017 |
| 558 | EMD Billerica, MA Associate Scientist Downstream Process Development MS in biotechnology, biochemistry or engineering field Exp: 1 yr |
Candidates will be primarily responsible for DSP production of GLP Tox drug substance but also for developing purification processes for a variety of therapeutic candidate proteins including monoclonal antibodies and Fc fusion proteins. Scope of work will include, but are not limited to, protein purification, biochemical and biophysical characterization of proteins, novel purification technologies, purification process development, data analysis and project reporting. Candidates should have experience in writing technical documents for process transfer to manufacturing. The candidate is expected to have excellent time management skills, with the ability to adapt to rapid changes in projects priorities and meeting aggressive timelines. | 9/16/2017 |
| 559 | Fresenius Kabi Boston, MA ASSOCIATE SCIENTIST BS in biological sciences Exp: 1-2 yrs |
Responsible for performing routine testing of in-process and finished product samples. Monitors environmental conditions in the production and lab areas. Summarizes environmental monitoring and product test results. Provides project support to Scientist and Lead Scientist. Prepares media and reagents and equipment. | 9/16/2017 |
| 560 | Fresenius Kabi Skokie, IL SCIENTIST/ASSOCIATE SCIENTIST BS / MS in Chemistry Exp: 0-3 yrs |
We currently have an opportunity for an Associate Scientist or Scientist who will be responsible for conducting product stability testing, reviewing data, and organizing test results in a scientific manner. | 9/16/2017 |
| 561 | Fresenius Kabi Boston, MA CHEMIST, METHOD DEVELOPMENT MS in Chemistry Exp: 1-3 yrs |
The Chemist, Method Development has broad expertise in routine as well as complex chemical methods of analysis. The incumbent conducts all aspects of Quality Control testing including method development, method validation, experimentation, routine and non-routine quality control testing, and record keeping. The incumbent must be able to develop, validate, and implement methods that meet project needs. The incumbent is typically assigned the more complex test methods due to their advanced training in specialized methods of analysis. The position is responsible for conducting studies with increasing complexity in nature and solving problems to ensure a robust method can be performed in the laboratory. | 9/16/2017 |
| 562 | Fresenius Kabi Melrose Park, IL VALIDATION ENGINEER BS in a Science or Engineering field Exp: 1-3 yrs |
Responsible for providing technical support to operations in terms of equipment / system / process initial validation and equipment / system / process requalifications. Will participate in process and equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. Individual must also perform HEPA filter integrity / velocity testing and critical area (class 100) airflow pattern testing. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (class 100, 10,000 and 100,000). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 9/16/2017 |
| 563 | Fresenius Kabi Melrose Park, IL TECH TRANSFER SPECIALIST BS in physical science, engineering Exp: 1-3 yrs |
The Technology Transfer Specialist is responsible for assisting with and / or coordinating the transfer and implementation of products and technology to the plant manufacturing site. The position is also responsible for designing manufacturing procedures for new or modified products with the support of the manager. The incumbent is responsible for planning, coordination, and oversight of the product life cycle which includes development, stability, process performance qualification and cleaning validation / verification. This position provides technical support to manufacturing operations as assigned by management. | 9/16/2017 |
| 564 | Frontage Laboratories, Inc Exton, PA Safety Specialist BS Exp: 1-2 yrs |
The mission of the Safety Specialist is to provide expertise in safety and develop comprehensive safety services. The purpose of this role is to promote an overall safe workplace, and to create safety awareness throughout the organization. | 9/16/2017 |
| 565 | Frontage Laboratories, Inc 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. | 9/16/2017 |
| 566 | Frontage Laboratories, Inc 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 | 9/16/2017 |
| 567 | FUJIFILM Diosynth Biotechnologies 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. | 9/16/2017 |
| 568 | FUJIFILM Diosynth Biotechnologies 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. | 9/16/2017 |
| 569 | FUJIFILM Diosynth Biotechnologies COLLEGE STATION, TX Quality Control Chemist II MS in Chemistry or Biochemistry Exp: 1 yr |
The Quality Control Chemist II will be responsible for participating in the Technology Transfer of established methods into the FujiFilm Biotechnologies Diosynth Texas (FDBT) Quality Control Laboratory. Following Tech-Transfer Activities, the candidate will be responsible for performing release and stability testing using the established analytical methods. | 9/16/2017 |
| 570 | FUJIFILM Diosynth Biotechnologies COLLEGE STATION, TX Process Development Technician III MS Exp: 1 yr |
The Process Development Technician III is responsible for laboratory testing for the product monitoring process, in-process analytical testing, equipment performance and maintenance, assisting in process verification / validation and executing development initiatives using laboratory and processing equipment in lab production scale-up environments for the Upstream, Downstream, or Virology groups. | 9/16/2017 |
| 571 | FUJIFILM Diosynth Biotechnologies COLLEGE STATION, TX Methods Development Tech II MS in Biology, Biotechnology, Biochemistry, Analytical Chemistry or other related field Exp: 1 yr |
The Methods Development Tech II will assist in the transfer and development of analytical methods for in-process, and finished product including release testing and testing of critical reagents. This individual will also be involved in assisting with the performance of methods for quantifying virus samples. | 9/16/2017 |
| 572 | FUJIFILM Diosynth Biotechnologies COLLEGE STATION, TX Biotechnology Process Engineer/Scientist MS in Chemistry, Biology, Life Sciences or related field Exp: 1 yr |
The Biotechnology Process Engineer / Scientist, functions within a team based organization to actively address complex cGMP manufacturing issues. The individual is responsible for analyzing process technologies in support of new project proposals and assist in the technical transfer into the manufacturing group. This individual must work in a collaborative manner coordinating the transfer of biological drug processes from process development (internal or client) groups in a CMO environment. | 9/16/2017 |
| 573 | Catalent Winchester, KY QC Analyst BS in Chemistry, Biology, Chemical Engineering or Life Sciences (Preferred in Chemistry or Biology). Exp: 0-5 yrs |
Perform efficient / reliable / high quality analytical testing in accordance with USP / NF / EP / JP / FCC / etc. or customer supplied guidelines. Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc. | 9/16/2017 |
| 574 | 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. | 9/16/2017 |
| 575 | Catalent Kansas City, MO Associate Scientist, Microbiology BS Exp: 1-3 yrs |
Under general supervision, the Associate Scientist performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. This will include but not limited to, microbial limits testing, sterility testing, preparation of media, sample tracking and lab supply inventory. Some evaluation, originality or ingenuity is required. The Associate Scientist follows established protocols and work plans, may assist scientists in projects, and will comply with divisional and site Environmental Health and Safety requirements. | 9/16/2017 |
| 576 | Catalent Madison, WI Associate, cGMP Biomanufacturing Operations BS in Biotechnology, or related field Exp: 0 yr |
This is an entry level position and is the starting point to acquire skills and training required for a cGMP Biomanufacturing environment. The position is expected to follow detailed instructions and established procedures with frequent supervision. | 9/16/2017 |
| 577 | Catalent Winchester, KY Quality Control Analyst BS in Chemistry, Biology, Chemical Engineering or Life Sciences (Preferred in Chemistry or Biology). Exp: 0-5 yrs |
Catalent s QC Analytical Chemist is an entry level position for individuals who use their understanding of science to perform the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. Their work is hands on in an analytical lab and requires analytical testing, computer operating, record keeping, and report writing abilities. This position performs the quality testing needed for raw material, in-process, finished goods, stability, and cleaning validation analysis. | 9/16/2017 |
| 578 | Catalent Madison, WI Sr. Associate, Upstream Manufacturing BS Exp: 0 yr |
Catalent Pharma is growing! Our Madison, WI site is looking to hire a Senior Associate in Upstream Biomanufacturing Operations. The position is expected to follow detailed instructions and established procedures with frequent supervision. The shift for this role will be a 4 / 10 schedule of 7 AM - 5 PM, Sunday through Wednesday. | 9/16/2017 |
| 579 | Catalent Emeryville, CA Research Associate/Sr. Research Associate, Bioanalytical Chemistry MS in biology, biotechnology or related field Exp: 0 yr |
The Senior Research Associate will be responsible for the research, development and implementation of extended characterization assays for biologics, including: payload-linkers, antibodies and antibody-drug conjugates. | 9/16/2017 |
| 580 | Catalent Madison, WI Associate, cGMP Biomanufacturing BS in Biotechnology, or related field Exp: 0 yr |
Performs aseptic techniques within in a clean room environment. Executes and properly documents cGMP Biomanufacturing activities. Operates cGMP Biomanufacturing equipment, including pH / conductivity meters, mixing tanks (SUMs), tubing fusers / sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). | 9/16/2017 |
| 581 | GENEWIZ South Plainfield, NJ Bioinformatics Scientist, Next Generation Sequencing MS in Bioinformatics Exp: 1-3 yrs |
Work collaboratively with bench scientists, comprehend project objectives, evaluate and provide informatics solutions | 9/16/2017 |
| 582 | GenMark Carlsbad, CA Formulations Specialist I - Temp BS in basic sciences or life sciences Exp: 6-12 months |
This position formulates reagents in a controlled manufacturing environment. This position also executes validation studies, executes test protocols, investigates Non-Conformances, evaluates processes & procedures, and inspects & tests equipment. May conduct training on reagent formulations, methods, and procedures. Interfaces with R&D, Manufacturing, Quality, and Supply Chain within the company and when appropriate with customers and suppliers on quality related issues. | 9/16/2017 |
| 583 | Genomatica San Diego, CA Research Associate I/II - Process Development BS in chemistry, chemical engineering, biochemistry or related field Exp: 1-3 yrs |
As a member of this team you are joining a creative, fun, challenging, and fast-paced work environment. This position will be responsible for executing lab and pilot-scale experiments that contribute to the development of novel processes for the production of chemicals via fermentation. Technical areas of responsibility include downstream separation and purification steps such as filtration, centrifugation, chromatography, extraction, and distillation as well as chemical reactions. He / she will assist in experimental planning, independently set-up, operate, clean and maintain equipment at the bench and pilot scale; collect experimental samples, perform sample assays, perform data analysis and reporting, and maintain / order lab supplies. | 9/16/2017 |
| 584 | Genomatica San Diego, CA Research Associate I/II, Strain Eng. BS in Life Sciences or related field Exp: 1-3 yrs |
Assists in conducting basic laboratory experiments, applying defined protocols and procedures; generates reproducible and reliable results. | 9/16/2017 |
| 585 | Genomic Health Redwood City, CA Laboratory Associate I BS in molecular biology, genetics, biochemistry or biology Exp: 0-2 yrs |
As the Laboratory Associate I, you will be responsible for providing technical support within a cross-functional team to research and develop novel NGS or PCR-based products and services in the area of cancer biology. | 9/16/2017 |
| 586 | Genoptix Carlsbad, CA Laboratory Assistant BS in technology science or health-related field Exp: 1 yr |
Provide laboratory support by assisting the technical staff and physicians. Open shipping packages containing human medical specimens; transcribe handwritten and printed documentation and patient and test information onto worksheets and into the laboratory information system. | 9/16/2017 |
| 587 | Gilead Sciences Inc. Foster City, CA Packaging Engineer I BS in packaging engineering, mechanical engineering, or a related scientific field Exp: Entry-level |
Represent the DDCPE functional area on multiple product development teams, delivering container closure solutions on schedule throughout development (e.g., Phase 1 through commercial transfer) | 9/16/2017 |
| 588 | Genentech South San Francisco, CA PROCESS DEVELOPMENT SPRING 6 - MONTH INTERNSHIP BS / MS Exp: NA |
As a Process Development Intern, you will be assigned a project in one of the following areas within USBTD | 9/16/2017 |
| 589 | Genentech South San Francisco, CA INTERN - PRODUCT DEVELOPMENT - CLINICAL OPERATIONS - RESOURCE MANAGEMENT BS Exp: NA |
Product Development - Clinical Operations is responsible for effectively managing and implementation of global clinical programs. The clinical operations teams evaluate the safety and efficacy of our molecules for numerous diseases including oncology, immunology, ophthalmology, respiratory, and psychiatric diseases. These programs meet scientific, medical, regulatory and patient demands for new and innovative medicines globally. The results of these studies form the basis of regulatory and commercial approval of medicines. | 9/16/2017 |
| 590 | GE United States, Un GE Healthcare Engineering Intern BS / MS Exp: NA |
GE Healthcare Technical Interns work on a variety of assignments with responsibilities and hands-on involvement in areas in design. There will be project-oriented assignments where a manager and mentor are assigned for support. The primary areas our Technical interns will work in are medical imaging, information technologies and patient monitoring. | 9/16/2017 |
| 591 | GE United States, Un GE Healthcare ARC V&V Engineering Co - op/Intern BS / MS in Computer Science, Biomedical, Electrical, Mechanical or Computer Engineering areas Exp: NA |
GE Healthcare V&V Engineering co-ops work on a variety of assignments with responsibilities and hands-on involvement in areas of system and software verification. There will be project-oriented assignments where a manager and mentor are assigned for support. These positions will work primarily with Anesthesia and Respiratory Care (ARC) products. | 9/16/2017 |
| 592 | GE Waukesha, WI GE Healthcare OMLP Intern BS Exp: NA |
Operations assignments vary on assigned department. A fulfillment assignment may include working on material shortage issues, and working on materials planning while a sourcing assignments will entail working closely with the engineering team and strategic suppliers to identify opportunities for productivity -reducing costs- and supplier consolidation. The primary areas our Operations interns will work in are medical imaging, information technologies and patient monitoring. Operations assignments could include core operations and fulfillment activities which may consist of Manufacturing, Lean Action Workouts, Accessory Planning, or Capital Equipment order fulfillment or sourcing activities such as working with the engineering department and outside vendors and suppliers on materials. There will be project-oriented assignments where a manager and mentor are assigned for support | 9/16/2017 |
| 593 | Stryker Allendale, NJ Laboratory Technician AS scientific discipline Exp: 0-3 yrs |
Through partnerships with other Engineers and Managers, the Laboratory Technician will learn to and thus be able to do the following: Maintain various inventories of research parts, supplies and associated hardware Maintains a library of operating manuals and other technical documentation for the research center (including industry standard testing practices) Assists in the organization and maintenance of the laboratory and associated tools and equipment Assists with facilities management in the planning, scheduling and monitoring of work for the equipment installation, use, maintenance, etc Maintains safety systems and related supplies and equipment Participate / support Project Teams as necessary | 9/18/2017 |
| 594 | Stryker Salt Lake City, UT 2018 Summer Internship - Biomedical Engineering BS engineering or related Exp: 1 yr coursework |
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 | 9/18/2017 |
| 595 | Stryker Flower Mound, TX 2018 Summer Internship - Biomedical Engineering BS engineering or related Exp: 1 yr coursework |
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 | 9/18/2017 |
| 596 | Stryker Flower Mound, TX 2018 Summer Internship - Mechanical Engineering BS mechanical engineering or related Exp: 1 yr coursework |
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 | 9/18/2017 |
| 597 | Stryker Tempe, AZ 2018 Summer Internship - Mechanical Engineering BS mechanical engineering or related Exp: 1 yr coursework |
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 | 9/18/2017 |
| 598 | Stryker San Jose , CA 2018 Summer Internship - Biomedical Engineering BS engineering or related Exp: 1 yr coursework |
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 | 9/18/2017 |
| 599 | Dr. Reddy's Middleburgh, NY Quality Associate BS biochemistry or related Exp: 0-3 yrs |
Responsible for supporting the Middleburgh site in Quality Assurance activities. | 9/18/2017 |
| 600 | Propharma St. Louis, MO Jr. Validation Engineer BS technical discipline Exp: 1 yr |
Preparing and executing validation documents. Project execution for multiple systems validation. Understanding the hours budgeted for completion of each task on a specific. Individuals must represent the company and division at client sites and interact confidently with clients, contractors, management and peers. Develop Installation, Operational and simple Performance qualification documents. | 9/18/2017 |
| 601 | ProteinSimple San Jose , CA Manufacturing Associate AS biotech, chemistry, biology, biochemistry, or related 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. | 9/18/2017 |
| 602 | Prozyme, Inc Hayward, CA Production Associate AS / BS scientific discipline Exp: 0-2 yrs |
The Production Associate is responsible for the efficient manufacture of products to inventory, safely, on time, within specifications and budget under the requirements of the Quality System. | 9/18/2017 |
| 603 | PSC Biotech San Francisco, CA IT/Automation Engineer BS computer science, engineering, or related Exp: 1-3 yrs |
The resource will be working with the IT Manufacturing Team. | 9/18/2017 |
| 604 | PSC Biotech Madison, WI Quality Control Intern BS / MS scientific, engineering, biotechnology, or related Exp: 1 yr coursework |
BioTechnique is currently recruiting for a Quality Control (QC) Intern to use and grow your understanding of science to support basic and critical experimental work of day-to-day analysis, including generation and analysis of data, to ensure cGMP compliance and provide support of the manufacturing and packaging of sterile injectable products. You will support the Quality Director and Quality Control Supervisor in the development and maintenance of Quality Systems including: deviations, investigations, change control, auditing programs, CAPA, review and approval of controlled documents, and training. The work is hands on in an analytical lab and requires analytical testing, computer operating, record keeping, and report writing abilities. You will perform the quality testing needed for raw material, in-process, finished goods, stability, and cleaning validation analysis. You will apply and learn biology / microbiology knowledge in a highly regarded pharmaceutical industry manufacturing environment. The QC Intern contributes to the pursuit, capture, management and execution of air and surface quality management and compliance. The QC Intern will collect and analyze aseptic environment samples in support of GMP facility qualification. The individual selected for this position will be gowning into an ISO 5 facility. The QC Intern will also be testing to support cleaning and product changeover in the facility. | 9/18/2017 |
| 605 | PSC Biotech Madison, WI Validation Intern BS engineering or biotechnology Exp: 1 yr coursework |
We are currently seeking to bring on a current student to locally support our CMO Facility. This will offer a start-up environment, with hands-on opportunities to develop your analytical, technical and problem solving abilities. Validation Engineer Intern wanted to train on GMP facilities and cGMP requirements. Intern will learn equipment validation, computerized systems validation, Quality Systems in an FDA-regulated environment. Intern will also learn the business aspects of operating a small business. Intern will be exposed to a wide variety of business situations that will better prepare them for a full time job. | 9/18/2017 |
| 606 | PSC Biotech Madison, WI Manufacturing Intern BS / MS scientific discipline, engineering, biotechnology, or related Exp: 1 yr coursework |
The Manufacturing Intern works with and supports the manufacturing team to manufacture and package high quality pharmaceutical products in an efficient, safety compliant, and cost effective manner in accordance to cGMP and SOPs. The position requires a hands-on approach with the ability to work in a team environment and establish good working relationships with other employees. | 9/18/2017 |
| 607 | PSC Biotech Many, CA Entry Level Validation Engineer BS engineering or technical degree Exp: 0 yrs |
Entry Level Validation Engineer wanted to train on GMP facilities and cGMP requirements. In addition, applicant will be trained on writing technical reports, and Validator Software. Applicant will be working in a biotech / pharmaceutical environment as a consultant / contractor for various clients. He / she will be working closely with client's employees on various projects and various GMP facilities to help client with validation issues. Applicant must be willing to learn new ideas, techniques and systems. Applicant must be willing to commute to clients' manufacturing sites. | 9/18/2017 |
| 608 | PSC Biotech Many, OK QC CSV Laboratory Validation Engineer MS analytical chemistry Exp: 1-2 yrs |
Our client has an immediate opening for a QC CSV Laboratory Validation Engineer to help run the QC Lab Metrology Program in Oklahoma. Applicant will help lead implementation for the Water's Empower Software. | 9/18/2017 |
| 609 | PSC Biotech San Diego, CA Jr. CSV/Lab Qualification Engineer BS computer science, biomedical, pharmaceutical, chemical engineering, or related Exp: 1-3 yrs |
PSC Biotech is a leading life sciences consulting firm currently seeking a Jr. Level CSV / Lab Qualification Engineer to support one of our clients in San Diego, CA. | 9/18/2017 |
| 610 | Pyramid Laboratories, Inc Costa Mesa, CA Environmental Monitoring Technician BS chemistry, microbiology, or related 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. | 9/18/2017 |
| 611 | Qiagen Germantown, MD Technical Associate - Kit Assembly AA / AS technical discipline Exp: 1-3 yrs |
The Technical Associate in Kit Assembly comprehends and performs assigned manual production tasks according to established standard operating procedures. | 9/18/2017 |
| 612 | Qiagen Frederick , MD Production Associate Scientist BS molecular biology, biochemistry, chemistry, life sciences, or related Exp: 1-3 yrs |
Responsible for manual / automated production / assembly in compliance with relevant regulations and Standard Operating Procedures. Monitor and maintain the proper operation of general lab environment and instrumentation. Independently conduct bench testing and research studies following sufficient guidance from senior level manager. Maintain good written records of laboratory procedures, results and conclusions. Perform and report interim analysis of accumulated data to monitor work process. Concludes results from raw data to meaningful terms, e.g., numbers, graphs or simple forms. Contribute to and support department / corporate goals. Other duties as assigned. This job has no supervisory responsibilities. | 9/18/2017 |
| 613 | Qpharma Morristown, NJ Junior Validation Engineer/Scientist/Specialist BS science, engineering, or related Exp: 6 months - 2 yrs |
Our Professional Services team is looking for new Validation resources that we can train and mentor for internal and external projects. The specific duties for this position will be to develop validation documentation with input and direction for senior team members. | 9/18/2017 |
| 614 | QPS, LLC Newark, DE Associate Scientist - Bioanalytical BS analytical chemistry, biochemistry, pharmacology, or related Exp: 1 yr |
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. | 9/18/2017 |
| 615 | QPS, LLC Newark, DE Associate Scientist, IBA BS biochemistry, immunology, pharmacology, medical technology, biology, or related Exp: 0-2 yrs |
This is a laboratory role focused on the analysis of drug or other targets in complex biologic matrices using immunologic methods. Responsibilities include laboratory stewardship, wet-lab operations as well as data reduction and documentation. The work is done in a regulated environment controlled by company SOPS, analytical procedures and department policies and governed by the Good Laboratory Practices (GLPs), Good Clinical Practices (GCPs) and Good Documentation Practices (GDPs). Much of the work is independent and comprehensive from frozen sample to data point - not piecemeal, though each staff member is also a part of team. Team-members cooperatively support one-another's timelines, quality and high performance. Each team is self- and externally-supported by process and technical experts. There are multiple daily interactions with teammates and staff from other units within TLM, other support groups within QPS as well as Clients and regulators. The ability to effectively communicate scientific concepts and explain laboratory events to clients is vital. | 9/18/2017 |
| 616 | Quintiles Overland Park, KS PRN Clinical Research Technician - Phase I Research BS life sciences or related Exp: 0 yrs |
Perform a variety of clinical procedures to collect data on volunteers enrolled and / or seeking enrollment in clinical studies. Ensure data is collected and processed according to standard operating procedures (SOPs). | 9/18/2017 |
| 617 | Biotechne San Jose , CA Manufacturing Laboratory Technician I AS / BS 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. | 9/18/2017 |
| 618 | Biotechne Minneapolis, MN Technical Service Associate 1 or 2 BS biological sciences, biochemistry, or related 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. | 9/18/2017 |
| 619 | Biotechne Minneapolis, MN Research Associate I BS biology, biochemistry, cell biology, chemistry, or related biological science Exp: 0-2 yrs |
The responsibilities of this position include assaying specimens on a variety of platforms for client or evaluation studies following applicable GLP, ISO 9001:2008, and ISO 13485:2003 requirements; documenting and recording data, and summarizing assay and / or evaluation results into final spreadsheets and reports. This requires being familiar with guidelines specific to each study and ensuring they are being followed throughout testing. Secondary responsibilities would include assisting with receiving shipments of specimens, assigning accession numbers, and labeling and verifying specimens. Other responsibilities would include assisting with writing, reviewing, and updating standard operating procedures (SOP s), assisting with Installation, Operation, & Performance Qualifications (IQ / OQ / PQs), and assisting with sample type, assay, or equipment evaluation and validation studies. As the workload of the BTS lab is variable and dependent upon customer demand, all members of the BTS Lab are also expected to assist with work in other departments as time allows. Perform additional duties as assigned. | 9/18/2017 |
| 620 | Biotechne Minneapolis, MN Lab Assistant AS / BS technical discipline Exp: 0-2 yrs |
Primary duties include assisting with component inventory, eBook entry, aliquoting and labeling components for custom kits as well as miscellaneous laboratory tasks. | 9/18/2017 |
| 621 | Biotechne Minneapolis, MN Research Associate 2 or 3 MS biology or related Exp: 0-3 yrs |
The responsibilities of this position are to purify proteins to restock the supply of existing products and modify existing protocols for larger scale production of proteins. This position receives no instructions on routine work and brief support on new assignments. Perform additional duties as assigned. | 9/18/2017 |
| 622 | Biotechne Minneapolis, MN Research Associate 1 BS biology, biochemistry, cell biology, chemistry, or related biological science Exp: 0-2 yrs |
The responsibilities of this position are to assist team members with feasibility and product development of Simple Plex immunoassays. Assist with the optimization of components, develop manufacturing procedures, and perform necessary troubleshooting. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained. | 9/18/2017 |
| 623 | DXC Technology Little Rock, AR Editor I BS Exp: 0-1 yr |
Responsible for editing, rewriting, and authenticating technical user manuals, application papers, product description, data sheets, and specification books. | 9/10/2017 |
| 624 | DXC Technology Tallahassee, FL Documentation Specialist BS Exp: 0-1 yr |
Responsible for editing, rewriting, and authenticating technical user manuals, application papers, product description, data sheets, and specification books. | 9/10/2017 |
| 625 | Edwards Lifesciences Irvine, CA Quality Engineer II - Critical Care MS Exp: 1 yr |
Seeking a high caliber Engineer to support the Quality Assurance and Engineering teams. This position will partner with Quality, Regulatory, Manufacturing / Operations, and R&D to investigate field failures, analyze product performance, and report to Management. This position will also prepare for new product launches and assist with development of post market surveillance plans. This person must be comfortable in a regulated environment, possess excellent teamwork and communication skills, and be able to apply an analytical mindset that leverages data to better improve the customer experience. | 9/10/2017 |
| 626 | Edwards Lifesciences Irvine, CA Associate Specialist, Clinical Research - Transcatheter Mitral & Tricuspid Therapies BS Exp: 1 yr |
The Associate Specialist, Clinical Research will ensure trial patients safety by assuring trials are conducted ethically and within regulatory compliance, data accuracy, and protocol adherence. | 9/10/2017 |
| 627 | Edwards Lifesciences Irvine, CA Manufacturing Engineer I - Transcathether Heart Valve BS in a related engineering field Exp: 0-2 yrs |
The Manufacturing Engineer I will provide manufacturing engineering support in the design and development of implantable devices and delivery systems used to treat cardiovascular disease. As part of this innovative team, you will be responsible for conducting engineering activities from early product development through product launch. | 9/10/2017 |
| 628 | Elite Pharmaceuticals Northvale , NJ Process Development Engineer / Technical Services Specialist BS in a technical field Exp: 1-2 yrs |
Responsible for collecting, coordinating, organizing, summarizing and entering all new product development and characterization data. This will include individual sample tracking and the graphing of all data needed to assess a formulation or process. This database must be kept current to allow effective decision making and planning. Report to Manager R&D. | 9/10/2017 |
| 629 | Moderna therapeutics Cambridge, MA Manufacturing Associate BS 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. He / she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in the Pilot Plant, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. | 9/10/2017 |
| 630 | Moderna therapeutics Cambridge, MA Research Associate, Delivery Innovation MS Exp: 1-2 yrs |
This Contract Research Associate will be responsible for preparation and characterization of mRNA containing nanoparticles within a dynamic and highly interdisciplinary environment. He / she will be responsible for executing lab experiments, reporting results and maintaining a high-quality lab notebook. The successful candidate will work well within a larger team of chemists, engineers, formulation scientists and associates while mentoring and training junior members of the Delivery Innovation team. Experience with polymeric nanoparticle preparation techniques, biophysical / chemical characterization, and surface modification are preferred. | 9/10/2017 |
| 631 | Moderna therapeutics Cambridge, MA Research Associate, In Vivo Pharmacology, Onkaido MS 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. Applicants should be both great team members and have a track record of independent research accomplishments. The ability to effectively communicate with internal team members is required. | 9/10/2017 |
| 632 | EMD Serono Billerica, MA Associate Scientist, Exploratory Immunology MS in immunology, biology, biochemistry or related discipline Exp: 1-2 yrs |
The successful candidate will participate in new target discovery and validation, using a variety of cell based and biochemical assays and tools to characterize the function of new genes in human immune pathologies. In addition to broad expertise in immunology and cellular biology the candidate will be required to exhibit open-minded and innovative approaches and an ability to learn and acquire new techniques and methodologies in often uncharted biological systems. The successful candidate will have excellent oral and written communication skills, work well independently and as part of a team, and be able to work on multiple projects simultaneously. The position is a hands-on, laboratory based role. The candidate is expected to be able to plan, design, develop methodologies, analyze, record and report data and execute projects according to plans and protocols with appropriate supervision. | 9/10/2017 |
| 633 | EMD Serono Kankakee, IL Quality Control Scientist BS in Biology, Chemistry, or other health-related field Exp: 1-3 yrs |
Understands and works within a broad range of guidelines, standard operating procedures and / or technical methods that involve a variety of routine work procedures with a moderate degree of supervision | 9/10/2017 |
| 634 | EMD Serono St. Louis, MO Bio - Chemist/Bio - Conjugation Scientist MS in biochemistry, biology, chemistry or related field Exp: 0-1 yr |
Leverage experience in protein biochemistry and / or conjugation chemistry to on-board / develop, optimize and scale up bio-conjugation process chemistry unit operations. | 9/10/2017 |
| 635 | EMD Serono St. Louis, MO ELISA Scientist - Quality BS / BA in chemistry, biochemistry, biology, or related life science Exp: 1 yr |
Cherokee Quality Control in St. Louis, MO, supports manufacturing of custom products including active pharmaceutical ingredients, excipients, and raw materials used within the health care industry. | 9/10/2017 |
| 636 | EMD Serono Billerica, MA Associate Scientist II, Biomarkers, Immuno - Oncology BS in molecular biology, biochemistry, or related fields Exp: 1 yr |
Build tissue profiling capabilities for preclinical biomarker profiling using in situ and in vitro biochemical, molecular, and cellular assays. | 9/10/2017 |
| 637 | EMD Serono Rockville, MD Associate Scientist II BS / MS in scientific discipline Exp: 0-1 yr |
The Associate Scientist II (AS II) will perform a wide variety of assays or tests required to characterize product or material safety. He / she will make scientific observations, maintain detailed workbooks / documentation and ensure all documentation fulfills generally accepted professional / industry standards. He / she will maintain an understanding of technological principles and applications of the organization s services. Demonstrate ability to use and maintain laboratory equipment including but not limited to: centrifuges, incubators, biosafety cabinets, Vi-CELL XR Cell Viability Analyzer, Coulter Counter Z1, and various types of micropipettes. Demonstrate ability to maintain adherent and suspension cell cultures by following aseptic techniques. Perform NGLP Screening Ames assays (plate incorporation method, pre-incubation method, spot test method, and Ames II method). Perform portions of Comet Single Cell Gel Electrophoresis assay (preparation of slides, processing of organs, electrophoresis of slides, scoring of slides, and analysis of data). Perform portions of the Unscheduled DNA Synthesis (UDS) assay (animal handling, perfusion of animals, cell counting, cell seeding, handling of radioactive reagents, termination of assay, and scoring of slides). Perform In Vitro Cytogenetic Micronucleus assays in CHO and HPBL cells (seeding of cells, dosing of cells, washing of cells, harvesting / termination of cells and scoring of cell cycle kinetics). Neutral Red Uptake Assay in HPBL and CHO cells (seeding of cells, dosing of cells, washing of cells, harvesting / termination and scoring). Receive training in conduct of Bhas 42 Cell Transformation assay (maintenance of cell cultures, plating the assay, scoring the assays by spectrophotometer or microscope). | 9/10/2017 |
| 638 | EMD Serono Billerica, MA Associate Scientist Upstream Process Development MS in biotechnology, biochemistry or engineering field Exp: 1 yr |
The Protein Science / Late Stage Upstream Processing (USP) group, a core function that develops upstream processes for new biologics moving into the clinic, is seeking a motivated associate scientist to join our antibody discovery program at EMD Serono. Candidates will be primarily responsible for mammalian USP production of GLP Tox drug substance but will also develop processes at bench scale and later scale up to 200L bioreactors for a variety of therapeutic candidate proteins including monoclonal antibodies and Fc fusion proteins. Scope of work will include, but are not limited to, protein production for pre-clinical studies, UPS process development developing novel USP processes, data analysis and project reporting. Candidates should have experience in writing technical documents for process transfer to manufacturing. The candidate is expected to have excellent time management skills, with the ability to adapt to rapid changes in projects priorities and meeting aggressive timelines. These individuals should enjoy working in a team setting and can work well with research scientists, the manufacturing group as well as external collaborators. | 9/10/2017 |
| 639 | Endo International plc Malvern, PA 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. | 9/10/2017 |
| 640 | Envigo Princeton, NJ QC Specialist BS Exp: 0-2 yrs |
The Quality Control Specialist is responsible for the review of validation and sample analysis study data / reports in support of regulated non-clinical and clinical bioanalytical studies. | 9/10/2017 |
| 641 | 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. | 9/10/2017 |
| 642 | QIAGEN Beverly, MA Production Planning Specialist BS / MS in Life Science or Chemical Engineering discipline Exp: 1-2 yrs |
The Production Planning Specialist will assist in managing the transactional and configuration aspects of reagent products; ensuring that the content and composition of these products meet the internal and customer-specified quality standards and are delivered in a timely manner. The Production Planning Specialist will work cross-functionally with internal departments (Manufacturing, Quality Assurance, Quality Control, Sales / Marketing, Shipping etc.) to ensure internal and external deadlines are met. | 9/10/2017 |
| 643 | Evonik Corporation Mapleton, IL ASSOCIATE MAINTENANCE ENGINEER BS in engineering Exp: 0-2 yrs |
Assume Leadership of Emergency Equipment Failures. Coordinate needed resources to minimize the process downtime, allowing the planning process to remain on schedule. | 9/10/2017 |
| 644 | Evonik Corporation Richmond, VA CHEMIST II MS in chemistry or scientific discipline Exp: 1 yr |
Provision of technical service in support of Coating Additives products. Planning, execution and reporting of laboratory projects as assigned by the Technical Service Manager. Assistance in product recommendations and delivery of presentations and training to customers and distributors. Communication with Essen laboratories on project and other technical matters. | 9/10/2017 |
| 645 | 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. | 9/10/2017 |
| 646 | 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. | 9/10/2017 |
| 647 | Exactech Gainesville, FL TEST DESIGN ENGINEER BS Exp: 1 yr |
Provide design, engineering, testing and analysis support to other engineers and designers in the development and maintenance of orthopedic implants and instruments. | 9/10/2017 |
| 648 | Exelixis, Inc. South San Francisco, CA Assistant Research Scientist II MS / MA Exp: 0-2 yrs |
The successful candidate will be joining the Biology team to evaluate the activity of small molecule inhibitors and drive lead optimization in our oncology and immune-oncology drug discovery programs. The candidate will be a key contributor in developing, optimizing, and automating cell-based and biochemical assays, conducting compound screening for SAR support, and performing data analysis. This position will require the candidate to have excellent organization, communication, and teamwork skills, as well as flexibility and versatility to meet tight deadlines in a dynamic, fast-moving environment. | 9/10/2017 |
| 649 | Exosome Diagnostics Cambridge, CA 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. | 9/10/2017 |
| 650 | Ferring Pharmaceuticals Parsippany, NJ Technician, QC Microbiology BS Exp: 1-5 yrs |
Work in a cGMP-compliant manner in support of production, facilities, clean utilities and general microbial testing on second shift. Participate in assay transfer processes and qualification of equipment. Create / Revise equipment qualification protocols, test methods, and procedures as required. Work independently with minimal supervisory guidance. Apply aseptic clean room practices during execution of all work tasks. Must have prior clean room aseptic sampling experience in water and environmental monitoring. | 9/10/2017 |
| 651 | Five Prime Therapeutics, Inc. South San Francisco, CA Research Associate I - II, Analytical Development BS / MS in biochemistry, chemistry, chemical engineering, or a related discipline Exp: 0-5 yrs |
This position will be responsible for the development of a wide range of analytical assays for a number of pre-clinical and clinical programs. The research associate will also support process development and formulation studies within the Manufacturing Sciences department and other research groups. The motivated research associate will also contribute to protein characterization studies within Analytical Development and be a key contributor to the team. This position reports to Scientist lll, Analytical Development. | 9/10/2017 |
| 652 | Five Prime Therapeutics, Inc. South San Francisco, CA Research Associate I - II, Molecular Biology BS in Molecular or Cell Biology Exp: 0-4 yrs |
The successful candidate will be responsible for learning and implementing recombinant DNA approaches to support research team needs which include plasmid and minicircle DNA production and QC, recombinant DNA cloning, Sanger sequence data analysis, and tracking the DNA preparations in databases and Excel spreadsheets. The candidate must be self-motivated, detail oriented and thorough, and be capable of working both independently and in a team environment. | 9/10/2017 |
| 653 | Fluidigm South San Francisco, CA Temporary Research Associate MS in molecular biology, biochemistry or related field Exp: 1 yr |
We are looking for a highly motivated individual to support product sustaining activities using Fluidigm s microfluidic platforms. The candidate will be working in the R&D department, together with an interdisciplinary team, to manage multiple product sustaining and improvement activities for sample preparation, gene expression, genotyping, and NGS applications. | 9/10/2017 |
| 654 | Fortive Everett, WA Test Engineer I BS Exp: 1-2 yrs |
As a Test Engineer I on our Fluke biomedical operations engineering team you will be asked to become an expert on the functionality and tests required to produce top of the line Biomedical test equipment. This candidate will work with products like infusion device analyzers, defibrillator analyzers, electrical safety analyzer, X- ray analyzers, and electrical surgical unit analyzers | 9/10/2017 |
| 655 | Foundation Medicine Cambridge, MA Associate, BioPharma Operations BS Exp: 1-2 yrs |
Foundation Medicine is actively seeking an Associate, Biopharma Operations to provide comprehensive operational and tactical support for the company s pharmaceutical alliances. The Associate, Biopharma Operations will be responsible for implementing and monitoring the execution plans for each of our pharmaceutical collaborations, including day-to-day project management, specimen tracking and resource management. In this role, he / she will work collaboratively with internal and external teams across a number of functions to manage timelines, resource plans, and critical path activities, directly impacting the successful implementation and on-going execution of our Biopharma partnerships. | 9/10/2017 |
| 656 | Fresenius Kabi Melrose Park, IL TECH TRANSFER SPECIALIST BS in physical science, engineering or equivalent experience Exp: 1-3 yrs |
The Technology Transfer Specialist is responsible for assisting with and / or coordinating the transfer and implementation of products and technology to the plant manufacturing site. The position is also responsible for designing manufacturing procedures for new or modified products with the support of the manager. The incumbent is responsible for planning, coordination, and oversight of the product life cycle which includes development, stability, process performance qualification and cleaning validation / verification. This position provides technical support to manufacturing operations as assigned by management. | 9/10/2017 |
| 657 | Fresenius Kabi Grand Island, NY QC TECHNICIAN II - Chemistry BS in Chemistry or related field Exp: 1-2 yrs |
Individual must use judgment to determine when independent action is appropriate or to contact supervisor for direction. | 9/10/2017 |
| 658 | Personalis Menlo Park, CA Clinical Laboratory Scientist BS scientific discipline Exp: 0-2 yrs |
The Clinical Laboratory Scientist is responsible for testing and reporting clinical laboratory results. | 9/11/2017 |
| 659 | Pharmacyclics Sunnyvale, CA Clinical Research Associate I BS scientific discipline 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. | 9/11/2017 |
| 660 | Pharmacyclics Sunnyvale, CA Scientist I, Pharmacokinetics MS pharmaceutical sciences Exp: 0-3 yrs |
Provide pharmacokinetic support to preclinical and clinical pharmacokinetic studies to advance the area of oncologic therapies. The candidate will also work closely with Bioanalytical and Drug Metabolism scientists to integrate PK, PKPD, and DM data to support preclinical development of drug candidates and Clinical Operations, Biometrics, and Regulatory to support clinical trials and regulatory submissions. | 9/11/2017 |
| 661 | Luitpold Pharmaceuticals, Inc Shirley, NY MV Scientist II MS chemistry or related Exp: 1 yr |
Method Validation applies to analytical procedures used to determine chemical identity, potency and purity of pharmaceutical products manufactured at Luitpold Pharmaceuticals, Inc. in Shirley, New York, and does not apply to microbial or environmental testing. The MV Scientist, Level II, will perform analytical validations according to current guidance and established procedures for analysis of raw materials, bulk, finished product, stability samples, process cleaning and process validation samples in the Quality Control Laboratories. | 9/11/2017 |
| 662 | Pharmatech Denver, CO IT Developer BS technical discipline Exp: 0-1 yrs |
We are seeking an entry level developer for contract-to-hire position. The developer will work on designing and building new applications for a mid-size CRO company. Other main responsibilities will be supporting help desk needs, including hardware and software support for employees. This will be an exciting opportunity to work in a small team responsible for every aspect of the application including application design, development, testing, and deployment. | 9/11/2017 |
| 663 | Catalent Madison, WI Associate, cGMP Biomanufacturing BS / BA biotechnology or related Exp: 0 yrs |
Performs aseptic techniques within in a clean room environment. Executes and properly documents cGMP Biomanufacturing activities. Operates cGMP Biomanufacturing equipment, including pH / conductivity meters, mixing tanks (SUMs), tubing fusers / sealers, filter integrity testers, peristaltic pumps, balances and Biosafety Cabinets (BSC) or Laminar Flow Hoods (LFH). Maintains effectiveness of Quality system. Stages raw materials / components for use within cGMP Biomanufacturing. Performs general cleanroom housekeeping, including room and equipment cleaning(s), disposal of trash and recyclables, and adherence to 5S standards. Accurately completes routine and preventive maintenance on designated equipment. Supports Biomanufacturing staff with proper completion of Standard Operating Procedures (SOP), Batch Production Records (BPR) and Job Aid (JA) revisions, deviation investigations, and change control / protocol execution, by established due dates. Actively participates in team meetings and / or training sessions. Performs media / solution preparation. Works scheduled shift and other off-shift coverage as required | 9/11/2017 |
| 664 | Catalent Madison, WI Associate, Quality Control - Raw Materials BS / BA biotechnology or related Exp: 0 yrs |
This position will perform a variety of laboratory procedures to support Quality Control. The position will perform daily work assignments accurately and in a timely and safe manner. | 9/11/2017 |
| 665 | Catalent Kansas City, MO Operations Technician III AS technical discipline Exp: 1-3 yrs |
At the direction of the Senior Operator, the Operations Tech III with is responsible for the set up / tear down, manufacture and cleaning of all equipment and processes associated with manufacturing operations including, but not limited to Blending, Roller Compaction and Encapsulation. | 9/11/2017 |
| 666 | Catalent Winchester, KY Quality Control Analyst - Weekend Shift BS chemistry, biology, chemical engineering, or life sciences Exp: 0-5 yrs |
Catalent s QC Analytical Chemist is an entry level position for individuals who use their understanding of science to perform the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. Their work is hands on in an analytical lab and requires analytical testing, computer operating, record keeping, and report writing abilities. This position performs the quality testing needed for raw material, in-process, finished goods, stability, and cleaning validation analysis. | 9/11/2017 |
| 667 | Catalent Woodstock, IL Chemist BS chemistry or related Exp: 0-5 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. | 9/11/2017 |
| 668 | Catalent Madison, WI Laboratory Associate, Analytical Development BS / BS biotechnology or related Exp: 0-2 yrs |
The Analytical Development team is responsible for developing analytical methods to support cell. line, upstream, and downstream development, qualifying the methods, and transferring them to the QC department. The team is also responsible for characterizing primary and high order structures of proteins / mAbs manufactured. This is an entry level position and is the starting point to acquire skills and training required for a biotech lab setting. The position is expected to follow detailed instructions and established procedures with frequent supervision. | 9/11/2017 |
| 669 | Catalent Emeryville, CA Research Associate/Sr. Research Associate, Bioanalytical Chemistry MS biology, biotechnology, or related Exp: 0 yrs |
Catalent is seeking a responsive and self-motivated individual with a strong desire to work with a team of passionate and motivated scientists on cutting edge technologies and novel biotherapeutic drug development. The Senior Research Associate will be responsible for the research, development and implementation of extended characterization assays for biologics, including: payload-linkers, antibodies and antibody-drug conjugates. This position may be filled at a lower level (Research Associate) commensurate with education and years of experience. | 9/11/2017 |
| 670 | Stryker Kalamazoo, MI Engineer - Process Development, Advanced Operations BS mechanical engineering or related Exp: 0-2 yrs |
Basic FunctionSupports the execution of assigned project elements with an emphasis on the manufacturing process, technology and procedures required for the manufacture of new products. | 9/11/2017 |
| 671 | Stryker Ft. Lauderdale, FL 2018 Summer Internship - Mechanical Engineering BS mechanical engineering or related Exp: 1 yr coursework |
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 | 9/11/2017 |
| 672 | Stryker Mahwah, NJ 2018 Summer Internship - Mechanical Engineering BS mechanical engineering or related Exp: 1 yr coursework |
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 | 9/11/2017 |
| 673 | Stryker Ft. Lauderdale, FL 2018 Summer Internship - Biomedical Engineering BS biomedical engineering or related Exp: 1 yr coursework |
Interns collaborate with cross-functional teams to support product sustainment. When non-conforming issues arise in production, it is our responsibility to perform robust root cause analysis and implement effective corrective actions. Do you enjoy deep dive investigations and driving collaboration and communication to achieve issue resolution If so, you may be a great fit for this team! PQE interns are focused on quality, compliance and continuous improvement. They use their education to work with a variety of tools including CAD for fixture design, root cause analysis methods, LabView, and validation activities to optimize production, inspection, and quality system processes. | 9/11/2017 |
| 674 | Stryker Mahwah, NJ 2018 Summer Internship - Biomedical Engineering BS biomedical engineering or related Exp: 1 yr coursework |
Interns collaborate with cross-functional teams to support product sustainment. When non-conforming issues arise in production, it is our responsibility to perform robust root cause analysis and implement effective corrective actions. Do you enjoy deep dive investigations and driving collaboration and communication to achieve issue resolution If so, you may be a great fit for this team! PQE interns are focused on quality, compliance and continuous improvement. They use their education to work with a variety of tools including CAD for fixture design, root cause analysis methods, LabView, and validation activities to optimize production, inspection, and quality system processes. | 9/11/2017 |
| 675 | Stryker San Jose, CA Quality Engineer - Process BS engineering or related Exp: 0-2 yrs |
Responsible for the analysis and resolution of production issues through collaboration with engineering and material procurement teams. Perform monitoring of process data and analysis of trends, financial results and customer feedback. Exhibit a commitment to quality, compliance and continuous improvement through the implementation of projects which optimize production, inspection, and quality system processes. | 9/11/2017 |
| 676 | Stryker Lakeland, FL Engineer, Manufacturing BS engineering (mechanical, electrical, biomedical, chemical, or industrial) Exp: 0 yrs |
Support and improve existing processes using Statistical, Lean, Good Manufacturing Practice (GMP) and Six Sigma methodologies Effectively transfer new products, design changes or line extended devices onto the production floor Foster an environment of continuous improvement and provide support to customers in all functional areas Discuss progress and interim findings at periodic design / project review meetings Perform Failure Analyses (FAs) and improve Functionality / Performance of medical devices Implement process improvements and machining improvements on production lines Reduce Reject Rates(scrap)and optimize manufacturing processes Implement safety improvements on production lines Assist in the development and execution of technical protocols and, generation of reports Implement operating procedures, standard work, visual work instructions, and visual work references Assist with training to Production for all new product launches and design changes to existing products or processes Expectation of acquired knowledge of FDA / ISO requirements associated with the development of medical devices including Design Control Perform other duties as directed or assigned by Manager | 9/11/2017 |
| 677 | Plexxikon Berkeley, CA Research Associate 2, DMPK and Assay Screening MS biological sciences, chemistry, or related Exp: 1 yr |
We are seeking a Research Associate 2 with a joint appointment in the Drug Metabolism and Pharmacokinetic (DMPK) and Assay & Screening departments. The qualified candidate will be a critical member of both groups and work closely with our established team performing various in vitro metabolism assays, metabolite identification studies, bioanalytical work, and biochemical / functional assays to screen chemical entities for new drug candidates. This is an exceptional opportunity to work with two core discovery groups within a successful biopharmaceutical company and bring drugs from ideas to the clinic. | 9/11/2017 |
| 678 | Portola Pharmaceuticals San Francisco, CA College Internship BS technical discipline Exp: 1 yr coursework |
An internship with Portola Pharmaceuticals provides an opportunity to be part of an organization helping patients through the innovative field of biotechnology. Whether your passion is science and research or business, an internship at Portola is more than just a summer job. Portola offers the chance to develop your skill sets by working with accomplished professionals and the opportunity to learn what it takes to keep our organization thriving | 9/11/2017 |
| 679 | Poseida Therapeutics San Diego, CA Process Development Associate MS immunology, molecular biology, or related Exp: 1 yrs |
The Development Associate will be a key member of a dynamic team that develops and implements characterization strategies to support and enable process and clinical development of gene-engineered cell products. 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. | 9/11/2017 |
| 680 | Preclinical San Bruno, CA Clinical Project Internship BS clinical trials program or related Exp: 1 yr coursework |
Get the experience necessary to enter the pharmaceutical and biotech clinical research industry. 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. | 9/11/2017 |
| 681 | Precision Medicine Group Oakland , CA Research Assistant BS scientific discipline Exp: 1 yr |
Research Assistants support teams in our Policy practice with a wide variety of project activities including coordination of client meetings; project documentation; copyediting; preparation of presentations; review and abstraction of literature; and general administrative project support tasks. This opportunity is being offered out of Oakland, CA. | 9/11/2017 |
| 682 | Progenra Malvern, PA Research Associate BS / MS life sciences 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. | 9/11/2017 |
| 683 | Promega Madison, WI Scientific Training Instructional Designer MS biological sciences or related Exp: 1 yr |
Scientific Training is responsible for the design and development of effective and engaging learning interventions for global Sales, Technical Services Scientists, and Distributors. Our Training Programs are conducted remotely and in-person at our three training centers located in Madison, France and Singapore. | 9/11/2017 |
| 684 | Promega Madison, WI Process Engineer Co - op BS chemical, bioprocess engineering, or related Exp: 3 yrs coursework |
Apply engineering principles and methods to tasks which support the ongoing projects and responsibilities of the Promega Engineering department. | 9/11/2017 |
| 685 | Promega Madison, WI Production Scientist 1 - Project Position BS scientific discipline Exp: 0-3 yrs |
Manufacture products and perform quality control tests. | 9/11/2017 |
| 686 | Prometheus San Diego, CA Clinical Lab Scientist I BS scientific discipline Exp: 0-4 yrs |
Performs pre-analytical and analytical testing, interprets and reports patient results to ordering physicians. | 9/11/2017 |
| 687 | ProMetic BioTherapeutics, Inc. Rockville, MD Research Associate I - Process Development BS scientific discipline or related Exp: 0-2 yrs |
Our Process Development Department currently has an open vacancy for a Research Associate (Level I) at our Rockville, Maryland location. The candidate will be responsible for leaning basic purification techniques, buffer preparation, column packing, data entry, and performs routine laboratory maintenance under direct supervision of their designated Scientist. | 9/11/2017 |
| 688 | GE US, US Biomedical Engineer Apprentice BS / MS in Electronics, Biomedical Engineering, Medical Imaging Technology or Mechanical Principles degree program Exp: 0 yr |
In this role, the Biomedical Technician Apprentice will respond to service calls to evaluate, diagnose, perform repair and planned maintenance (PM) on basic biomedical equipment and drive customer satisfaction through Service Excellence. | 8/27/2017 |
| 689 | Claritas Genomics Cambridge, MA Variant Scientist - Genomics MS in human genetics, or molecular biology Exp: 1-3 yrs |
Apply expertise towards genomic variant curation, classification and interpretation; put into the context of relevance to human genetic disorders | 8/27/2017 |
| 690 | Clinilabs Inc. New York, NY Sleep Technicians BS / BA Exp: 6 months |
The Sleep Technician is responsible for performing all neurophysiologic studies performed in the scope of laboratory services. This includes the preparation of laboratory facilities and equipment, preparation of patients for recording data acquisition, and all clinical and research tests performed in the laboratory (these tests include the NPSG, CPAP Titration, MSLT, MWT and other montages). The Sleep Technician is responsible for the accuracy and integrity of data collected in the laboratory. | 8/27/2017 |
| 691 | Clinilabs Inc. New York, NY Regulatory Affairs Specialist BS Exp: 1-3 yrs |
The Regulatory Affairs Specialist (RAS) performs tasks related to study related regulatory documents, IRB submissions, and other site documentation, including quality control of study documentation. The RAS is responsible for developing and maintaining positive relationships with sponsors as well as internal study teams through oral and written communications regarding submission requirements, clarification and follow-up of submissions under review | 8/27/2017 |
| 692 | CMC Biologics Bothell, WA Development Associate I BS in Biochemistry, Analytical Chemistry, or related field Exp: 0-2 yrs |
We are seeking an energetic and highly motivated associate with a strong background in protein analytical development to join the Analytical and Formulation Development group. This position provides the opportunity to contribute to a diverse set of contract manufacturing projects in a fast-paced, collaborative team environment. | 8/27/2017 |
| 693 | CMC Biologics Bothell, WA Development Associate BS in Biochemistry, Analytical Chemistry, or related field Exp: 0-5 yrs |
Providing mass spectrometry support to clinical and commercial projects by developing methods, delivering results on tight timelines, and training / mentoring others. | 8/27/2017 |
| 694 | 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 | 8/27/2017 |
| 695 | CombiMatrix Irvine, CA Clinical Lab Scientist I/II/ III BS / BA in biological, physical, chemical or clinical laboratory science Exp: 1-2 yrs |
The ideal candidate will be responsible for performing all aspects of genetic testing including microarray, SNP and NGS according to established policies and procedures. | 8/27/2017 |
| 696 | Commonwealth Cambridge, MA Research Associate - in Vivo BS in Biology Exp: 1 yr |
Responsible for mouse handling, injections, blood samples, and collection tissues. | 8/27/2017 |
| 697 | Commonwealth Waltham, MA BSL2 Lab Technician BS Exp: 1 yr |
Provide administrative support and manage shipments of dangerous goods | 8/27/2017 |
| 698 | Commonwealth Cambridge, MA Associate Scientist - Process Development BS in ChemE or rleated area Exp: 1 yr |
Support the development of next-generation scalable lentiviral vector manufacturing process. | 8/27/2017 |
| 699 | ConforMIS Billerica, MA MANUFACTURING ENGINEER I BS / MS in Engineering Exp: 0-3 yrs |
The Manufacturing Engineer I will be responsible for the selection, development, qualification, and scale-up of production processes and equipment in the Selective Laser Sintering department. Process objectives are the high quality, high volume production of patient-tailored implants and associated instruments. | 8/27/2017 |
| 700 | Corbus Pharmaceuticals, Inc. Norwood, MA Clinical Research Associate BS / BA Exp: 1-2 yrs |
The primary point of contact for investigator sites, the CRA ensures the clinical trial is being conducted according to CFR, ICH guidelines and in accordance with GCP. The successful candidate will efficiently execute monitoring and other clinical trial management activities, including tracking the progress of assigned studies / projects and proactively identifying potential challenges. You will develop appropriate actions to resolve issues and achieve target objectives, performing investigator site pre-study site qualification visits including collection of site regulatory documents. | 8/27/2017 |
| 701 | Cook Myosite Inc. Pittsburgh, PA Associate Systems Analyst BS Exp: 0-4 yrs |
In a highly regulated environment, the Associate System Analyst at Cook Myosite Inc. provides technical subject matter expertise and system operational support of a business or manufacturing system (i.e. CRM, ERP, Lab, eQMS, RAM, HRIS, or BMS). This can include new application installations or support of existing application installations. | 8/27/2017 |
| 702 | CoreRx Clearwater, FL ANALYTICAL CHEMIST BS in Chemistry or related discipline Exp: 1-3 yrs |
Independently perform routine testing of process validation samples, raw materials, finished products, and stability samples, while adhering to SOPs and GLPs, and working in a cGMP compliant environment. Analyze and interpret results in written and oral format. Assist Manager in conducting investigations as needed. | 8/27/2017 |
| 703 | 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. | 8/27/2017 |
| 704 | Counsyl SOUTH SAN FRANCISCO, CA Intake Associate BS / BA 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. | 8/27/2017 |
| 705 | Counsyl SOUTH SAN FRANCISCO, CA Clinical Laboratory Assistant, Accessioning BS in Biological Sciences Exp: 0-2 yrs |
As a Clinical Laboratory Assistant in our Accessioning department you would be responsible for the beginning stages of sample preparation for our high-throughput operation. This is a crucial role as your job duties set the stage for the rest of our dynamic workflow. | 8/27/2017 |
| 706 | Covance Madison, WI Lab Technician I (BioA) BS / BS in chemistry or related scientific field Exp: 0 yr |
Determine the concentration of Active Pharmaceutical Ingredients within a variety of matrices via LC-MS in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. | 8/27/2017 |
| 707 | Covance Salt Lake City, UT QC Reviewer II BS / BA Exp: 1 yr |
Assists co-workers and internal customers with interpretation and understanding of regulatory requirements (e.g., GLPs), SOP requirements, and other guidance documents, as applicable. | 8/27/2017 |
| 708 | Covance Daytona Beach, FL Clinical Research Coordinator BS / BA in life science, pharmacy or related subject preferred Exp: 1-2 yrs |
Provides consolidated comments from the clinical site on the draft study protocol to the PM, taking into account operational and subject safety issues | 8/27/2017 |
| 709 | Covance Madison, Wi Associate Analytical Chemist BS Exp: 0 yr |
Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. | 8/27/2017 |
| 710 | Covance Madison, Wi Assoc Analytical Chemist I BS Exp: 0 yr |
Learns to conduct routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines. | 8/27/2017 |
| 711 | Covance Los Angeles, CA Histotechnologist BS Exp: 1 yr |
Utilize knowledge and experience with histology samples to maintain proper storage conditions and facilitate accessioning of blocks and slides (stained and unstained). | 8/27/2017 |
| 712 | Covance Madison, Wi Study Technician - Dose Formulation Entry Level BS in chemistry or related scientific field Exp: 6 months |
As a Study Technician in Dose Formulations you will learn how to review and interpret study protocol for test material formulation procedures and to ensure that a study tasks are conducted according with protocol, SOPs, and GLPs | 8/27/2017 |
| 713 | Crescendo Bioscience South San Francisco, CA Research Associate I BS in molecular biology, genetics, biochemistry Exp: 1-3 yrs |
As a Research Associate, your duties will be to provide support for our Research, Development, and Clinical Laboratories at Crescendo Bioscience, a wholly-owned subsidiary of Myriad Genetics. You will be working cooperatively in a busy laboratory environment, responding to change with flexibility and adapting quickly to evolving circumstances. This is an excellent opportunity for a team player to participate in the growth of a fast-paced, pioneering company that is developing systematic approaches to applying molecular diagnostics to health, disease, and medical practice. | 8/27/2017 |
| 714 | CSBio Menlo Park, CA Chemist, GMP Quality Control BS / MS in Chemistry, Biochemistry or a related field Exp: 0-2 yrs |
As a quality control team member, you will be responsible for conducting QC testing for release, stability, and raw materials as well as executing experiments in support of routine QC testing utilizing various analytical techniques. You will play a critical role in the production of life-changing and cutting edge medicine! | 8/27/2017 |
| 715 | CSL Kankakee, IL Quality Assurance Specialist BS / BA in chemistry, biology, physics, engineering, computer science, technical writing Exp: 0-2 yrs |
Responsible for assisting with investigating deviations, relevant to area of responsibility. Responsible for driving continuous improvement on production floor to ensure compliance to cGMPs. Real time review of batch records, including critical processing steps with production floor presence. | 8/27/2017 |
| 716 | CTI Remote, Re Clinical Research Associate BS / MS in allied health fields Exp: 1-2 yrs |
Manages investigative site activity for multiple protocols / indications and provides ongoing updates of site status to study manager / sponsor | 8/27/2017 |
| 717 | CTK Biotech San Diego , CA Research Associate/ Associate Scientist MS in Cell Biology, Immunology or related discipline Exp: 1-2 yrs |
The candidate will function as an integral member of the Antibody Discovery team to support antibody development and production. Primary responsibilities include but are not limited to antibody development using cell fusion technology, hybridoma screening via ELISA and WB, mammalian cell culture, antibody purification and characterization. | 8/27/2017 |
| 718 | CTK Biotech San Diego , CA Research/Production Assistant BS Exp: 1-2 yrs |
Test and manufacture ELISA kits and intermediate components | 8/27/2017 |
| 719 | Crinetics Pharmaceuticals San Diego , CA Undergraduate Research Assistant/Intern (Biology) BS in Biochemistry, Biology, or related field Exp: NA |
You will help support our team in many different aspects of our efforts to discover new drugs. | 8/27/2017 |
| 720 | GE US, US GE Aviation UDC Student Engineer - Spring BS / MS Exp: NA |
This role will work with full-time engineers in the area of FlightManagement Systems requirement validation, software development,and software verification responsibilities. In this role, you will follow anindividual work plan and meet day-to-day short-term objectives whileresolving issues. | 8/27/2017 |
| 721 | GE US, US 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. | 8/27/2017 |
| 722 | GE US, US Summer 2018 Engineering Intern BS / MS Exp: NA |
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. | 8/27/2017 |
| 723 | Novum Pittsburgh , PA Clinic Quality Control Associate BS technical discipline Exp: 1 yr |
The Clinic Quality Control Associate is responsible for performing day-to-day quality control activities to ensure study compliance meets company, client, and regulatory agency requirements. These activities include transcription and proofreading, identifying errors, developing correction actions and tracking / trending processes for improvement under management direction. Will also observe and audit study activities to ensure compliance with Standard Operating Procedures and study protocols and report / present findings to study management. At the discretion of management, will recall and audit past study files for quality assessment | 8/31/2017 |
| 724 | Biotechne Minneapolis, MN Research Associate I BS / BA biochemistry, chemistry, biology, or related Exp: 0-2 yrs |
Perform routine quality control testing of protein, peptide or antibody products using standard operating procedures to determine lot status, product release and product stability. Tests include: concentration determination, SDS-PAGE with densitometry, and endotoxin assay. Participation in the validation of new and existing laboratory methods is also expected. The position requires routine documentation, analysis and communication of results within the Department and across different groups. Other duties include instrument maintenance, record keeping and lab support. Within this job function, the Research Associate must also pursue annual goals that aim to facilitate innovation, efficiency, productivity and team building across the QC Department or the entire company. Perform additional duties as assigned. | 8/31/2017 |
| 725 | Biotechne Minneapolis, MN Research Associate 1 or 2 BS biochemistry, cell biology, chemistry Exp: 0-5 yrs |
The responsibilities of this position are to characterize monoclonal and polyclonal antibodies on natural samples using Immunocytochemistry and Immunohistochemistry. Screen multiple sera or hybridoma culture supernates to select potential products. Validate purified antibodies using natural samples. This is an entry level position. The person will develop problem solving and decision making skills, while maintaining appropriate contact and communication with the supervisor. Maintain and treat cell lines to induce protein expression. Refer to pertinent literature, databases and competitor product information on specific antibody targets. Maintain clear notebook enter data in PDPT and perform calculations. Apply company policies and resolve routine issues under guidance. Perform additional duties as assigned. | 8/31/2017 |
| 726 | Biotechne Minneapolis, MN Research/Manufacturing Associate AS / BS biology, biotechnology, biochemistry, or related Exp: 0-2 yrs |
The responsibilities of this position are manufacturing standards for the Quantikine, DuoSet, and DuoSet IC product lines. Primary responsibilities will include manufacturing standards for different kits and running assays to insure quality. Perform additional duties as assigned. | 8/31/2017 |
| 727 | Biotechne San Marcos, CA Intern BS technical discipline Exp: 1 yr coursework |
Primary area of work will be assisting in the preparation of our products using approved procedures in a GMP environment. | 8/31/2017 |
| 728 | NuVasive San Diego, CA Associate Software Engineer BS software or computer engineering or related Exp: 1 yr |
You will tap into your software development expertise as you tackle complex issues utilizing multi-threaded components to problem solve taking design, requirements and standards into account. You are a full lifecycle developer who loves the challenges of software development as you design, code and unit test your code. Because you take pride in your work, you understand the importance of code standards as you develop quality, sustainable code with a solid design. Hitting milestones and deadlines is part of your nature so you enjoy partnering with team members to ensure on-time delivery. With an eye on continual improvement, you possess a great can-do attitude and openly share ideas to help the Dev Team improve the software development process and overall development environment. | 8/31/2017 |
| 729 | NuVasive San Diego, CA Associate Test Engineer BS software engineering or related Exp: 1 yr |
As a talented Software Test Engineer, you will be a part of a SCRUM team responsible for testing current mobile (iOS and Android) software and web applications. You are part of an equally talented team of testers and developers who take pride in the work you do and the quality code you produce. As a test professional, you relish the opportunity to be involved in every aspect of the SDLC and creating automated test cases. With an eye on detail, you verify and recreate defects submitted by clients, other testers, and the development team, view error logs and troubleshoot to isolate system issues and develop tools and scripts to automate performance and load testing. You thoroughly enjoy trying to reveal the defects and fix them at their root cause! | 8/31/2017 |
| 730 | NuVasive Memphis, TN Field Inventory Specialist AS technical discipline Exp: 1-3 yrs |
The Field Inventory Specialist will work to reconcile materials used in each surgery event by reviewing all materials requested for each surgery, reviewing items billed, the return of materials and then will work with the Sales Force to resolve any missing material issues. This will be accomplished by issuing an RMA (Return of Material Authorization) for return of the missing inventory, having the Sales Representative submit a corrected chargesheet order to include the missing inventory or (future) charging the applicable cost center for the missing inventory. | 8/31/2017 |
| 731 | NuVasive Dayton, OH Manufacturing Engineer BS technical engineering discipline Exp: 1 yr |
As a Manufacturing Process Engineer at NuVasive Manufacturing, each day will offer new challenges as you tackle a variety of responsibilities | 8/31/2017 |
| 732 | Ocean Ridge Biosciences Deerfield Beech, FL Technical Sales Associate BS molecular biology, chemistry, or other life sciences discipline Exp: 0 yrs |
The Technical Sales Associate will be responsible for understanding ORB's services in the Basic Research, Drug Discovery & Drug Development market sectors and for contributing to the maintenance of a focused database of scientists conducting innovative research throughout the United States who could benefit from ORB services. This individual will be responsible for the development of a pipeline of appointments with Biotech Executives and Scientists via efficient e-mail and telephone marketing campaigns as well as in-person cold calls . The Technical Sales Associate will also manage to effectively communicate the benefits of ORB services to potential customers at Academic Institutes and Biotechnology Companies in on-site meetings, and maintain relationships with potential and current customers in order to close sales in an expeditious manner. Additional duty will involve representing ORB at Scientific Meetings, Symposia, and Industry Trade Shows. | 8/31/2017 |
| 733 | Ocular Therapeutix Bedford, MA Engineer/Scientist I, R&D BS / MS chemistry, biomedical engineering, material science or related 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. | 8/31/2017 |
| 734 | Olympus Waltham, MA Intern, Mechanical Engineering (ID: 2753BR) BS mechanical engineering or related Exp: 2 yrs coursework |
Olympus America is seeking interns to participate in a 10 week program designed to expose university-enrolled students to a holistic real-world, work experience through the completion of company learning sessions and finite, interest-based tasks and projects. An intern will experience specific assignments based on his or her field of study in connection with one of four program tracks: Communications / Corporate Services,Compliance, Legal & Corporate Governance, Finance / Operations and Life Science / Technology. This position will be based in Waltham, MA. Relocation assistance and the opportunity to work remotely are not available for this position. This is a short-term position that will run for approximately 10 weeks. | 8/31/2017 |
| 735 | Olympus Bartlett, TN Design Assurance Engineer I (ID: 2747BR) BS engineering Exp: 0-2 yrs |
The Design Assurance Engineer I is responsible for contributing to the design, development and management of projects for legacy products and support of new products under development. The Design Assurance Engineer provides organizational support with a focus on Design Quality activities. Works with internal / external manufacturers providing finished products, services, components, and sub-assemblies to ensure compliance with company policies and procedures and medical device regulations. The Design Assurance Engineer will partner with Operations, R&D, Supply Chain and other departments to continuously improve products and processes that meet all internal and external requirements and regulations. | 8/31/2017 |
| 736 | Olympus Bartlett, TN Machine Maintenance Technician (ID: 2116BR) AS industrial maintenance technology or related Exp: 1 yr |
The Machine Maintenance Technician will be primarily responsible for repairs and scheduled maintenance of production machines and equipment. The incumbent will also responsible for fabrication of needed parts and modifications to existing machines and equipment. EOE M / F / D / V | 8/31/2017 |
| 737 | Olympus Redmond, WA Product Development/Nitinol Engineer I (ID: 2676BR) BS / MS mechanical engineering, material science, or related Exp: 1 yr |
The Product Development Engineer I will apply learned scientific principles and expertise in the highly specialized field of application of Nitinol material, to advance and develop technology in medical devices. The incumbent will work directly with, and provide guidance to, internal and external engineering and technical professionals. | 8/31/2017 |
| 738 | Olympus Littleton, MA System Designer (ID: 2671BR) BS technical discipline Exp: 1 yr |
The System Designer applies reference system designs to meet specific customer requirements. The incumbent documents all facets of system integration including comprehensive drawing sets, parts lists, cable schedules and system configuration details | 8/31/2017 |
| 739 | Thermo Fisher Scientific Fremont, CA Electrical Engineer I MS electrical engineering Exp: 0-5 yrs |
The Electrical Design Engineer is responsible for the design and integration of control electronics for focused ion and semiconductor diagnostic systems. These products are complex electro-mechanical systems that employ charged particle optics, gas chemistries, lasers and other technologies for sub-micron structural modifications, imaging and device characterization. The system elements under electronic control include: charged particle beam focusing and deflection elements; electron detection, pre-amplifiers and signal processing; process gas delivery; laser scanning microscopes; IR imaging; and precision mechanical positioning systems. | 8/31/2017 |
| 740 | Thermo Fisher Scientific Waltham, MA Information Technology Leadership Development Program MS / BS computer science, biotechnology innovation &computation, or related Exp: 0 yrs |
The program prepares participants for roles of increasing responsibility through a combination of rotational assignments, structured learning, formalized feedback, and mentoring. Program participants will have the opportunity to interact with senior IT leaders and participate in various key IT initiatives. | 8/31/2017 |
| 741 | Thermo Fisher Scientific Carlsbad, CA Operations Rotation Program BS technical discipline Exp: 0 yrs |
As part of early talent development, the Operations Rotation Program is designed to attract and build future supply chain leaders. The program offers talented individuals the opportunity to build broad business knowledge over 2 years. The program consists of four (4) six-month rotations that will build the employee s technical and leadership skills. Possible rotational assignments include Manufacturing, Quality, Supply Planning, Logistics and Project Management. The specific rotations will be determined based on the employee s interest & background, and the business needs & opportunities. This program is a tremendous opportunity to work side by side with supply chain leaders at one of the most respected global biotechnology companies in the world. Upon completion of the rotations, the employee will have accelerated their professional growth and developed a very strong foundation and network across the company. | 8/31/2017 |
| 742 | Ora Andover, MA Clincal Trial Associate BS scientific discipline 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. Placement at the CTA I, CTA II or Sr. CTA level will be determined based on the candidate s qualifications. | 8/31/2017 |
| 743 | Ora Andover, MA Clincial Trial Documents Associate BS life sciences or related Exp: 1 yr |
The Clinical Trial Documents Associate will be responsible for supporting clinical operations on the conduct of clinical trials within the department. This position is focused on TMF maintenance / review and processing of Investigator and vendor payments. Excellent understanding of clinical trial documents (e.g. protocols, ICFs, CVs, 1572s) and TMF filing structures are mandatory. | 8/31/2017 |
| 744 | Ora Andover, MA Site Operations Associate BS life sciences or related 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. | 8/31/2017 |
| 745 | Organogenesis Canton, MA Validation Engineer I AS / BS technical discipline Exp: 1-3 yrs |
The Validation engineer I will be responsible for performing validation studies and testing of equipment and processes to ensure the highest quality products are created. The engineer will work with existing validation standards, create testing protocols using existing templates, prepare test equipment, execute protocols, document test results, and create reports from existing templates. | 8/31/2017 |
| 746 | Organogenesis Canton, MA Clinical Research Associate I BS life sciences or related Exp: 1-3 yrs |
The CRA I will assist clinical affairs in creating, reviewing and preparing documents, maintaining the Trial Master File for each study and preparing any documentation needed for regulatory filings and / or IRB submissions. S / he will have a proven ability to independently prioritize and manage multiple tasks and projects with competing priorities and deadlines, screen and prioritize communications and opportunities from external sources. The ideal candidate will be dynamic, articulate, high-energy, organized, and able to support cross-functional coordination in a fast paced environment. | 8/31/2017 |
| 747 | Organogenesis La Jolla, CA Manufacturing Technician I, DG Growth Systems AS / BS biotechnology Exp: 0-1 yrs |
Manufacturing Technician I is responsible for completing and assisting with daily tasks associated with cell-related functions, including producing cells, intermediate product, and manufacturing final product for commercial distribution. Additionally, the Technician I will be responsible for following SOPs, performing daily tasks in a clean room / cGMP environment per the current QSRs. The Manufacturing Technician I may also be responsible for the troubleshooting of manufacturing challenges. Follows established company rules, regulations and safety precautions, and maintains quality standards. | 8/31/2017 |
| 748 | Organogenesis La Jolla, CA Manufacturing Technician I, Support Services AS / BS biotechnology, pharmaceutical science or related Exp: 0-1 yrs |
The Manufacturing Technician I is responsible for completing and assisting with daily tasks associated with support related functions including assembly and sterilization of sub-assembly items, material management and manufacturing final product for commercial distribution. Responsible for following SOPs, performing daily tasks in a clean room / cGMP environment per the current QSRs. May also be responsible for troubleshooting manufacturing product challenges. Follows established company rules, regulations and safety precautions, and maintains quality standards | 8/31/2017 |
| 749 | Organovo San Diego, CA Lab Technician AS / BS biology, physiology, moleculare and cellular biology, or related Exp: 6 months |
Under the direction of senior staff, the Lab Tech performs duties related to cell and tissue culture and analysis per established protocols. | 8/31/2017 |
| 750 | Osiris Therapeutics, Inc. Columbia , MD Manufacturing Operator - Biosurgery AS scientific discipline Exp: 1-2 yrs |
Responsible for hands-on execution of activities surrounding final packaging of product units outside the cleanroom; label acceptance, usage, reconciliation, and storage; equipment preparation; and inventory and material stocking in the Biosurgery manufacturing area. All duties performed in compliance with GMP / GTP, American Association of Tissue Banks Standards, and Osiris Standard Operating Procedures (SOPs). The candidate should have a commitment to high standards of quality. | 8/31/2017 |
| 751 | Osiris Therapeutics, Inc. Columbia , MD Biotechnology Manufacturing Associate BS scientific discipline Exp: 1-2 yrs |
Responsible for hands-on execution of all activities in the Biosurgery manufacturing area, which encompasses the processing and packaging of tissue products for transplantation and for use in surgical procedures. All duties are performed in compliance with GMP / GTP, American Association of Tissue Banks Standards, and Osiris Standard Operating Procedures (SOPs). The candidate should have a commitment to high standards of quality. | 8/31/2017 |
| 752 | Albany Molecular Research, Inc. Grafton, WI Quality Control Analyst BS scientific discipline Exp: 1-2 yrs |
Conducts testing using approved analytical methods. Applies established laboratory methods or techniques to analysis, develops solutions to problems. Contributes to technical reports by providing detailed experimental write-ups. Clearly documents research and results in laboratory notebooks so that others can readily reproduce work. Maintains up-to-date laboratory records in accordance with company guidelines. Provides interpretation of data and possible solutions to unexpected results. Conducts testing of raw materials, intermediates, final products, or stability samples. Determines if products meet specifications for release. Performs wet chemical analysis from USP or approved procedures. Participates as member of safety committees as assigned. | 8/31/2017 |
| 753 | Viracor Eurofins Lee's Summit, MO Reagent Scientist I or II BS / BA in biological, physical, chemical, clinical laboratory science Exp: 1-2 yrs |
The Reagent Scientist is primarily responsible for manufacturing laboratory reagents for use by internal and external customers.. | 9/3/2017 |
| 754 | Cynosure Westford, MA Quality Assurance Specialist BS Exp: 0-2 yrs |
The QA Specialist performs quality activities in support of new and existing products. The position has a great deal of interaction with many internal departments, including Engineering, Manufacturing, Materials, Quality Control, and Customer / Field Service. The position may also have interactions with external entities including contractors, suppliers, and customers. The QA Specialist performs a wide variety of activities to ensure compliance with applicable regulatory requirements; such as documentation reviews; conducting quality audits; assisting with employee training; quality database maintenance; and data analysis. | 9/3/2017 |
| 755 | Dart NeuroScience LLC San Diego, CA Research Associate I/II, Analytical Chemistry BS in Chemistry, Pharmaceutical Sciences or related fields Exp: 0-2 yrs |
The Product Development group at Dart Neuroscience (DNS) is seeking a Research Associate to join the analytical chemistry team. The position will perform assigned laboratory duties to support analytical activities of DNS small molecule drug substances (NCE), drug products, and will work closely with process chemistry, formulations development, and external contract manufacturing and testing organizations. Interaction with external contract manufacturing and testing organizations may be required. | 9/3/2017 |
| 756 | Dart NeuroScience LLC San Diego, CA Clinical Trial Associate, Clinical Operations BS Exp: 1-2 yrs |
Provide support to the Clinical Operations functional line in project-specific tasks, tracking and the overall management of clinical trials. | 9/3/2017 |
| 757 | Deciphera Pharmaceuticals, LLC Waltham, MA Junior Medical Writer BS Exp: 1 yr |
The Junior Medical Writer researches, writes, and edits clinical regulatory documents that may be submitted to Investigational sites, as well as the Food and Drug Administration and other global health authorities for submission and publication. | 9/3/2017 |
| 758 | Dexcom, Inc. San Diego, CA Engineer I - UI Human Factors BA / BS in Human Factors, Cognitive / Experimental Psychology, Industrial Design, Engineering Psychology or equivalent technical degree Exp: 1 yr |
Working under the direction of a Senior Human Factors Engineer, this individual will prepare study materials for usability tests, conduct formative and summative usability tests for medical devices and mobile device applications, analyze data, and compile results and findings for multidisciplinary teams of engineers, developers, clinicians, and executives. | 9/3/2017 |
| 759 | Dexcom, Inc. San Diego, CA Research Associate 1 BA / BS Exp: 1-2 yrs |
Incumbent provides technical support for material and process development related to DexCom s Fusion Transmitter technology platforms. | 9/3/2017 |
| 760 | Dexcom, Inc. San Diego, CA Engineer I - Manufacturing Process Development BS / MS in Chemistry, Physics, Chemical Engineering, Bioengineering, Mechanical Engineering or related field required Exp: 1 yr |
Supports development of new manufacturing processes. Assist lead engineers in defining processing or handling equipment requirements and specifications, and reviews processing techniques for manufacture of new products and to decrease cost, improve throughput, and improve overall quality for commercial product lines. Support transfer and scale up new products from R&D. Provide manufacturing support to identify and resolve technical issues through product life cycle. | 9/3/2017 |
| 761 | Dexcom, Inc. San Diego, CA Engineer 2 - Manufacturing Process Development MS in Chemistry, Physics, Chemical Engineering, Bioengineering, Mechanical Engineering or related field required Exp: 0 yr |
Supports development of new and modified sensor manufacturing processes including related sterilization process effects. Assist lead engineers in defining processing or handling equipment requirements and specifications, and reviews processing techniques for manufacture of new products and to decrease cost, improve throughput, and improve overall quality for commercial product lines. Support transfer and work on process development / scale up or new products from R&D. Manufacturing support to identify and resolve technical issues. Involvement may begin from feasibility at vendors to full scale manufacturing. | 9/3/2017 |
| 762 | Dexcom, Inc. San Diego, CA Engineer 2 - Process Development MS in Mechanical Engineering, Bioengineering or equivalent Exp: 0 yr |
It takes drive, innovation and hard work to design leading edge medical products that transform the medical industry. Dexcom is leading the way in the mobile health revolution with its body worn Continuous Glucose Monitor (CGM), empowering patients to take control of their diabetes and change the way healthcare is managed. Our world class research and development team is looking for a driven Engineer to help us advance diabetes treatment and improve the lives of millions of people. | 9/3/2017 |
| 763 | Dexcom, Inc. San Diego, CA Biocompatibility and Sterilization Quality Engineer II MS Exp: 0 yr |
Position may be responsible for various aspects of Quality Engineering, including administration of specific aspects of the quality system. Job tasks require interfacing with all functions (Operations, Quality Assurance, Engineering, Regulatory Affairs, Clinical Affairs, Biometrics, Marketing, Legal, Finance, Sales, Customer Operations, Human Resources and upper levels of management). Personnel in this role must be systematic, highly organized and articulate and work in a team environment. A positive attitude is important while working in a fast-paced environment and dealing with shifting priorities. | 9/3/2017 |
| 764 | Dexcom, Inc. San Diego, CA Quality Support III BS in science, engineering, quality or other technical field Exp: 1-2 yrs |
Assist with the day-to-day operations associated with Control of Nonconforming Material, Corrective and Preventive Action (CAPA), and Internal Audits. Assist management to ensure that products, procedures, processes, contracts and services comply with applicable federal and state rules and regulations; as well as internal standards. | 9/3/2017 |
| 765 | Quidel Corporation Athens, OH Manufacturing Associate I (BioReagents Antibody) BS in a life science field or equivalent Exp: 1-2 yrs |
The Manufacturing Associate I is responsible for the production of monoclonal antibodies, production of hybridoma medium and / or other reagents required in monoclonal growth, fluorescent labeling process and production of the associated bulk reagent preparations made from these reagents. The position is also responsible for production of sera controls and reagents used in Thyretain product lines. | 9/3/2017 |
| 766 | Quidel Corporation Athens, OH Manufacturing Associate (Temporary) BS / BA Exp: 1-2 yrs |
The Manufacturing Associate in Cell Culture Operations will participate in the production of cell culture products by preparing in-process and finished goods materials. | 9/3/2017 |
| 767 | Quidel Corporation Athens, OH Manufacturing Associate BS / BA Exp: 1-2 yrs |
The Manufacturing Associate in Cell Culture Operations participates in the production of cell culture products by preparing in-process and finished goods materials. | 9/3/2017 |
| 768 | DPT Laboratories, Ltd San Antonio, TX Associate Scientist BS Exp: 0-2 yrs |
Performs a wide variety of laboratory analyses to support the manufacturing and releasing of a chemical or product. | 9/3/2017 |
| 769 | DPT Laboratories, Ltd San Antonio, TX QC Temporary Associate Scientist BA in a Physical or Life Science Exp: 0-2 yrs |
Performs review of Empower error messages and compare to raw analytical data. Perform review of laboratory investigations and categorize deviation conlcusions. | 9/3/2017 |
| 770 | DuPont Johnston, IA Research Associate BS Exp: Entry Level |
This employee will ensure our global customers have the inventory needed to deliver genotypic data to our customers. The position will perform end to end processing of inventory utilizing a variety of procedures and equipment in a high through put lab environment. | 9/3/2017 |
| 771 | DuPont Palo Alto, CA Formulations Research Assistant BS / MS Exp: Entry Level |
Responsibilities will include contributing to the development of liquid and solid enzyme formulations through preparation, characterization, and testing of a wide variety of prototype enzyme compositions. Activities will include producing test samples and characterizing them using a broad range of analytical and application assays. The successful candidate will develop and troubleshoot methods aimed at measuring the chemical, physical, and microbiological characteristics of protein formulations. | 9/3/2017 |
| 772 | DuPont Cedar Rapids, IA Application Scientist I Fermentation MS in microbiology, bioprocess / chemical engineering, yeast physiology, or related field Exp: 1-5 yrs |
Investigation and characterization of yeast physiology and response during fermentation of grains | 9/3/2017 |
| 773 | DuPont Pryor, OK Maintenance Reliability Engineer BS in Engineering Exp: 1-3 yrs |
Employees in positions allocated to this series use their knowledge of engineering, chemistry, equipment design, predictive and preventive maintenance practices, planning, and project execution to drive equipment reliability, maintainability, and availability. The objective is to support site goals by the development, execution, and analysis of maintenance plans for site equipment and facilities. Some engineers engage in reliability improvement efforts (such as Physical Failure Analysis, Root Cause Failure Analysis, Reliability Centered Maintenance analysis, and Weibull analysis). Others coordinate maintenance activities (such as Daily Planning and Scheduling, Shutdown planning and coordination, personnel skills assessments, and the identification and implementation of precision maintenance procedures). Others use predictive tools to evaluate equipment and facility condition (such as vibration analysis, infra red analysis, oil analysis, and process monitoring). Others identify and manage reliability focused equipment and facility capital improvements. Differences in levels relate principally to greater depth and breadth of knowledge and experience in maintenance policies, practices, and techniques and the ability to apply various combinations of these to cost effectively maintain plant equipment availability and output goals. | 9/3/2017 |
| 774 | DuPont Parlin, NJ Reliability & Equipment Engineer BS in Engineering Exp: 1-3 yrs |
Establish ownership and update Process Technology Package for Utilities Areas including; Boilerhouse, Refrigeration, Domestic Water System, and Site Sewers and Outfalls | 9/3/2017 |
| 775 | DuPont Palo Alto, CA Research Assistant, Applications Research BS / MS in Biology, Biotechnology, Biochemistry, Biochemical Engineering Exp: 0-2 yrs |
Use their Biology / Biochemistry / Biotechnology expertise to investigate the effects of enzymes in industrial biotech applications, focusing on the Household and Personal Care industry. | 9/3/2017 |
| 776 | DuPont Johnston, IA Research Associate, Soybean Transformation BS in plant science, biological science or related field Exp: 1-3 yrs |
The transformation Research Associate (RA) may take direction from a Technology Leader, Research Scientist, or other management team members. A RA will conduct transformation experiments for soybean according to established protocols, document experimental data accurately into database system(s), and produce adequate numbers of transgenic events to support trait development efforts. In addition, he / she will participate in implementation, development and improvement of established methods to increase the efficiency of transformation pipelines. | 9/3/2017 |
| 777 | Dynavax Berkeley, CA Research Associate I/II BS / MS in life science either in immunology, biochemistry, analytical chemistry and / or other related discipline Exp: 1 yr |
This individual s responsibilities will include, but are not limited to, execution of immune cell-based assays and various biochemical assays. These assays include primary immune cell bioactivity assays, cytokine / chemokine ELISAs, Taqman quantitative PCR, and flow cytometry, as well as (bio)analytical methods such as tissue processing / organic extraction and reverse phase HPLC. In addition, responsibilities will include test article preparation and sample management. | 9/3/2017 |
| 778 | Dynavax Berkeley, CA Research Associate I BS in Biological Science or Immunology Exp: 1 yr |
This position s primary responsibilities will be focused on supporting studies exploring the activity and mechanism of action of Dynavax s immunomodulatory compounds for cancer immunotherapy. The area of responsibility will include but not be limited to the execution of in vivo and in vitro experiments with a focus on immune cell functions, and the set-up and performance of experiments using tumor tissue. | 9/3/2017 |
| 779 | DuPont Nationwide, Na 2018 Summer Intern/Co - op: Chemical Engineering Student BS / MS in Chemical Engineering Exp: NA |
The assignments provide students with opportunities to develop by integrating classroom theory with practical work and to demonstrate their skills for future career opportunities at DuPont. | 9/3/2017 |
| 780 | 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. | 9/3/2017 |
| 781 | Dextera Surgical Inc. Redwood City, CA ENGINEERING INTERN/ENGINEERING CO - OP BS / MS in Engineering Exp: NA |
Assist the engineering team with design, development, and testing of new technology and products | 9/3/2017 |
| 782 | Merit Medical South Jordan, UT 2017 Sensors Internship (Sensors Engineering) BS / MS Exp: NA |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts, and may service or repair simple instruments or equipment. Will compile and review equipment documentation packages and process them for change control. May edit and generate equipment detail drawings and schematics. Will also support Sensors by performing product testing. | 9/3/2017 |
| 783 | Merit Medical South Jordan, UT 2017 R&D Material Science Internship BS / MS in Material Science, Biomedical Engineering, and / or Engineering. Exp: NA |
Specification documentation;Validation Protocol documentation;Test execution. | 9/3/2017 |
| 784 | Merit Medical South Jordan, UT 2017 Molding Engineering Internship (Full - time temporary) BS / MS Exp: NA |
Interns will be called upon to support a variety of analytical based activities in a fast paced, medical device engineering environment | 9/3/2017 |
| 785 | GE United States, Un GE Renewable Energy Technical EID (Intern/Co - Op) BS / MS in an engineering Exp: NA |
GE Renewable Energy includes Onshore Wind, Offshore Wind, Hydro Solutions. GE Renewable Energy EID positions in the US are primarily Onshore Wind focused. We are solving some the most complex challenges across the globe. | 9/3/2017 |
| 786 | GE Portland, ME Intern/Apprentice BS / MS in Electronics, Biomedical Engineering, Medical Imaging Technology or Mechanical Principles degree program Exp: NA |
In this role, the Client Service Technician Intern will observe and perform various equipment service processes and procedures to drive customer satisfaction and ensure proper functionality of less complex customer diagnostic imaging equipment. | 9/3/2017 |
| 787 | GE United States, Un GE Healthcare Quality Regulatory Leadership Program Intern MS in engineering, science, biology, clinical research, health policy, health product regulation, public health, quality assurance or related field Exp: NA |
The Quality Regulatory Leadership Program Intern is the premier development program for high potential individuals seeking a career at GE Healthcare in Quality Assurance and Regulatory Affairs. The internship consists of working experience in one or more of the following areas: Quality Assurance, Regulatory Affairs, Complaint Handling, Corrective & Preventative Action, QMS Compliance, Medical & Clinical Affairs, Global Audit and much more. | 9/3/2017 |
| 788 | BioPhase Solutions Inc Los Angeles County, CA Chemist I BS / BA in Life Sciences (Chemistry, Biology, Biochemistry) Exp: 1 yr |
The level I Chemist will perform standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. | 8/12/2017 |
| 789 | BioPhase Solutions Inc San Diego, CA Manufacturing Associate BA / BS in a chemistry, biology, chemical engineering or related field Exp: 1-3 yrs |
Duties involve use with chromatography, ultrafiltration, normal flow filtration, and single-use technologies. | 8/12/2017 |
| 790 | BioPhase Solutions Inc San Diego, CA Development Associate MS in the field of immunology, molecular biology, or related field Exp: 1 yr |
This position will interface with the R&D team as well as with outside CMOs. The ideal candidate will be skilled in 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. | 8/12/2017 |
| 791 | BioPhase Solutions Inc San Diego, CA Production Chemist (1st shift) BS in chemistry, or relevant discipline Exp: 1-3 yrs |
Responsible for the synthesis and purification of peptides under Good Manufacturing Practices (cGMP). | 8/12/2017 |
| 792 | BioPhase Solutions Inc San Diego, CA Research Associate MS in Cell Biology, Stem Cell science, Molecular Biology or related fields Exp: 0-2 yrs |
Be a key member of the division that will support the execution of primary cell isolation and propagation and / or stem cell line derivation and differentiation. | 8/12/2017 |
| 793 | BioPhase Solutions Inc San Diego, CA Clinical Lab Scientist BS in Medical Technology, Biology, Chemistry or related field Exp: 1-3 yrs |
Under general supervision, the CLS will work in all areas of the laboratory to include chemistry, hematology, immunoassay testing and routine laboratory testing. Perform and document quality control and preventative maintenance. Follow good laboratory practices and procedures for compliance. | 8/12/2017 |
| 794 | BioPhase Solutions Inc San Diego, CA Production Associate BS Exp: 1 yr |
Inventory lab supplies, consumables, chemicals, reagents;Receive stock items and replenish to proper stocking areas;Stock laboratories from common stock area. | 8/12/2017 |
| 795 | 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). | 8/12/2017 |
| 796 | BioReliance Rockville, MD Quality Specialist BS Exp: 0-1 yr |
Review assay data, protocols, reports, technical specifications, certificates of analysis, RIRs, Cell banking Production Records for compliance requirements. | 8/12/2017 |
| 797 | BioReliance Rockville, MD Molecular Biologist - Associate Scientist BS / MS Exp: 1 yr |
As an associate scientist / Moleuclar Biologist within our Next Generation Sequencing (NGS) group in our Rockville facility, your activities will support the development and implementation of NGS to the field of biosafety testing and contribute to the advancement of the global commercial NGS offerings of the company. | 8/12/2017 |
| 798 | BioReliance Rockville, MD Associate Scientist II BS / MS Exp: 0-1 yr |
He / she will maintain an understanding of technological principles and applications of the organization s services. Demonstrate ability to use and maintain laboratory equipment including but not limited to: centrifuges, incubators, biosafety cabinets, Vi-CELL XR Cell Viability Analyzer, Coulter Counter Z1, and various types of micropipettes. | 8/12/2017 |
| 799 | Bio-Technical Resources Manitowoc , WI Assistant Research Scientist, Fermentation Technician/Operator BS in chemical / biochemical engineering, microbiology, or microbial physiology Exp: 6 months |
Bio-Technical Resources is seeking an Assistant Research Scientist to work with supervision as a fermentation technician / operator as part of a team developing fermentation and biotransformation processes for the production of antibiotics, enzymes, metabolites, and proteins. | 8/12/2017 |
| 800 | STERIS Mentor, OH Associate Scientist I BS in Biology, Microbiology, Molecular Biology, Biochemistry, or Chemistry is preferred Exp: 0-5 yrs |
Culture, characterize, and evaluate various microorganisms and their resistance to various modes of sterilization and disinfection. | 8/12/2017 |
| 801 | Bluebird bio Cambridge, MA Associate Scientist II, Downstream Lentiviral Vector Process Development MS in Chemical Engineering, Biochemistry, Bioengineering, Molecular Biology, or related field preferred Exp: 0-2 yrs |
Execution of viral vector purification development activities encompassing early and late stage development. | 8/12/2017 |
| 802 | Boston Analytical Salem, NH QC Chemists BS in Chemistry or a related science discipline Exp: 0-3 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. | 8/12/2017 |
| 803 | Boston Heart Diagnostics Framingham, MA Laboratory Technologist BS in life or laboratory science Exp: 1-3 yrs |
Responsible for all aspects of the HDL Map and CoQ10 assays | 8/12/2017 |
| 804 | Boston Scientific Valencia, CA Regulatory Affairs Specialist II MS in Scientific discipline / engineering required Exp: 0-2 yrs |
Support the regulatory submission activities to obtain and maintain approvals for conducting clinical investigations and for commercially distributing products worldwide. Participate in activities to ensure compliance with worldwide regulatory requirements. | 8/12/2017 |
| 805 | Brammer Bio, LLC Cambridge, MA Manufacturing Associate 3 BS in Life Sciences Exp: 0-3 yrs |
Responsibilities include performing basic to moderately complex activities related to operating bioprocess manufacturing equipment, completing the associated documentation of those activities, monitoring assigned processes using automated production systems and controls. | 8/12/2017 |
| 806 | Brammer Bio, LLC Cambridge, MA Associate Raw Material Handling, Quality Control BS in Biological Science or related technical field Exp: 1-3 yrs |
Responsible for conducting analyses of raw materials, manufacturing environment, in-process & finished formulations according to SOPs. | 8/12/2017 |
| 807 | 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. | 8/12/2017 |
| 808 | Bristol-Myers Squibb Syracuse, NY Associate Quality Analyst I BS in science, engineering, biochemistry or related discipline Exp: 1-3 yrs |
The Associate Quality Analyst I is responsible for supporting the site supplier quality and material disposition system. | 8/12/2017 |
| 809 | Bristol-Myers Squibb Syracuse, NY Manufacturing Technology Engineer MS in Chemical, Mechanical or Biochemical Engineering or a related discipline Exp: 1 yr |
The Manufacturing Technology 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. | 8/12/2017 |
| 810 | Bristol-Myers Squibb Syracuse, NY Associate Scientist I - Validation BS / MS in Biology, Chemistry or Chemical / Biochemical Engineering Exp: 0-3 yrs |
The Site Validation Services Group is responsible for Installation, Operational and Performance Qualification (IQ / OQ / PQ) of process equipment, in-process analytical equipment, validation of SIP processes and validation of critical process utility systems. | 8/12/2017 |
| 811 | Bristol-Myers Squibb Devens, MA Associate Engineer MS in the biological sciences or chemical / biochemical engineering Exp: 0-2 yrs |
The successful candidate will be a key contributor in a dynamic and highly collaborative team environment. The candidate will set appropriate objectives and priorities, overcome obstacles; and deliver results within project timelines. | 8/12/2017 |
| 812 | Bristol-Myers Squibb Devens, MA Assistant Automation Engineer BS in Chemical Engineering, Electrical Engineering Exp: 0-2 yrs |
Participate in Run the Business initiatives such as change implementation, investigations, corrective actions, and manufacturing support. | 8/12/2017 |
| 813 | Bryllan Brighton, MI Pharmaceutical Production Technician Bs in Life Sciences or Engineering Exp: 0-2 yrs |
Dispensing,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). | 8/12/2017 |
| 814 | C. R. Bard, Inc. Covington, GA Regulatory Affairs Specialist I BS Exp: 1-3 yrs |
The Temporary Regulatory Affairs Specialist is responsible for implementation of regulatory strategies including domestic and international submissions and other support of product project team. | 8/12/2017 |
| 815 | Cancer Genetics Los Angeles, CA Clinical Laboratory Scientist BS in Medical Technology, Biology, Microbiology, or other related science Exp: 1 yr |
Under the general supervision of the Medical Director, the Clinical Laboratory Scientist (CLS) is responsible for performing pre-analytical, analytical, and post-analytical molecular procedures within the clinical laboratory. | 8/12/2017 |
| 816 | CapsoVision, Inc. Saratoga, CA Regulatory Affairs Specialist BS in Life Sciences or Engineering Exp: 1-5 yrs |
Prepare documentation in support of regulatory filings and monitor and access changes in regulatory requirements impacting CapsoVision s products | 8/12/2017 |
| 817 | CardioDx Redwood City, CA Quality Assurance Associate BS in a scientific discipline Exp: 1-3 yrs |
This position will represent Quality Assurance on cross-functional teams to complete projects and ensure compliance with CLIA, CAP, QSR, and other applicable regulations. The candidate will be expected to work with minimal supervision and to react quickly and professionally to changes in business priorities. They should be detail oriented, dependable, and focused to ensure completion of tasks in a timely and accurate manner. | 8/12/2017 |
| 818 | CardioDx Redwood City, CA Laboratory Assistant BS Exp: 1 yr |
Responsible for specimen processing including opening specimen boxes and organizing samples for testing and stocking, putting away laboratory supplies, and maintaining the work area. Works under the supervision of a Laboratory Supervisor and, in the absence of a supervisor, takes direction from a licensed Clinical Laboratory Scientist. | 8/12/2017 |
| 819 | 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. | 8/12/2017 |
| 820 | Cayman Chemical Company Ann Arbor, MI Synthetic Chemist BS in Chemistry Exp: 1-3 yrs |
Conducts product synthesis, purification and analysis, and process transfer. Working knowledge with liquid chromatography, mass spectroscopy, and NMR spectrometry. | 8/12/2017 |
| 821 | Cayman Chemical Company Ann Arbor, MI QC Chemist I - Chemistry BS in Chemistry Exp: 1-3 yrs |
Conducts method development, material and final product qualifications ; working with moderate independence | 8/12/2017 |
| 822 | C. R. Bard, Inc. Tempe, AZ Regulatory Affairs Intern BS / MS Exp: NA |
This position is responsible for assisting in the development and implementation of CE Marking for International documentation such as Design Dossiers and Technical Files. The candidate will be expected to review and summarize published literature as it relates to the CE Marked product. This position will also assist in the coordination of global product registrations by supporting requests from C. R. Bard, Inc. International Business Centers. | 8/12/2017 |
| 823 | BioPhase Solutions Inc San Diego, CA Clinical Laboratory Scientist BS in medical technology or biological sciences Exp: 1 yr |
The Clinical Laboratory Scientist (CLS) will perform laboratory tests according to approved policies and procedures for all phases of testing; pre-analytic, analytic, and post-analytic, as well as general laboratory systems. | 8/16/2017 |
| 824 | BioPhase Solutions Inc San Diego, CA In Vivo Research Associate BS in a scientific discipline Exp: 0-3 yrs |
Accurately perform in vivo studies that include the following laboratory procedures in mice | 8/16/2017 |
| 825 | BioPhase Solutions Inc San Diego, CA Manufacturing Technician BS in a biology, chemistry or related field Exp: 0-5 yrs |
Carry out laboratory activities in support of production schedules and objectives as directed by senior staff. | 8/16/2017 |
| 826 | BioPhase Solutions Inc San Diego, CA Research Associate, In Vivo BS in life sciences related field Exp: 1-8 yrs |
Interacts with the Bioengineering and In Vivo Groups within the Discovery Research Department to facilitate the development of novel, and improvement, of existing methods of in vivo gene electrotransfer (GET). Responsible for conducting a variety of experimental procedures using research animals, including syngeneic mouse tumor models. Coordinates longitudinal studies and In Vivo groups, and cross-over studies, as needed. Assists with maintenance of GEM (genetically engineered models) rodent colonies. | 8/16/2017 |
| 827 | Cyprotex US, LLC Watertown, MA Associate Scientist, Bioanalytical BS Exp: 1 yr |
The successful candidate will actively participate in experimental design, performing experiments, and troubleshooting, as well as performing data analysis and interpretation. | 8/16/2017 |
| 828 | Celgene Corporation Warren, NJ Associate Bioengineer I BS / MS in Biology or related discipline Exp: 0-3 yrs |
Design, perform, and interpret experiments, with minimal supervision, to support analytical development objectives. Ensure smooth day-to-day operation of the analytical laboratory. Advance assays to Quality Operations. | 8/16/2017 |
| 829 | Celgene Corporation Warren, NJ Associate Bioengineer II MS in Biochemical, Chemical, or Biomedical Engineering or Cell Biology / Immunology related discipline Exp: 0-3 yrs |
Design, perform, and interpret experiments, with little supervision, focused on appropriate goals, participate in process transfers, troubleshoot issues, and support GMP manufacturing activities. Ensure smooth day-to-day operation of the cell culture laboratory and communicate with collaborators. Participate in process characterization and validation activities. | 8/16/2017 |
| 830 | Celgene Corporation Summit, NJ Analyst, Commercial Analytics BS / MS Exp: 1 yr |
The Senior Analyst is responsible for conducting and overseeing the day-to-day variable Incentive Compensation operations. They will ensure the steady and accurate flow of communications and instructions between IC Leadership and the offshore processing team, as well as conduct QCs and validate the accuracy of reports and scorecards. Additionally, they will field requests and inquiries both from IC Leadership and Sales Leadership regarding compensation matters, and provide support to the Regional Directors and Regional Business Managers in areas of analytics and field reporting. | 8/16/2017 |
| 831 | Cell Signaling Technology, Inc. Danvers, MA Research Associate - VSC BS / MS in a biological science (e.g. molecular biology, cell biology, biochemistry or biotechnology) 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 seek, champion and evaluate techniques and technological opportunities that will improve quality, efficiency or scalability of cell culture, lysate preparation and generation of knock-out cell lines. | 8/16/2017 |
| 832 | Cell Signaling Technology, Inc. Danvers, MA Research Associate - Monoclonal Antibody Development BS in Cell Biology or Immunology Exp: 1 yr |
The Research Associate is responsible for working independently with supervision in the Monoclonal Development team in support of the Antibody Development Core initiatives at CST. The successful candidate is expected to assist with the preparation of rabbit and mouse monoclonal antibodies to transfer potential product clones to downstream pipelines for final product release. | 8/16/2017 |
| 833 | Cellular Dynamics 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. | 8/16/2017 |
| 834 | Cellular Dynamics Madison, WI Formulation Specialist BS in Cell Biology, Molecular Biology, Biochemistry Exp: 1-2 yrs |
The position of Formulation Specialist is to manufacture media and maintain laboratory supplies in clean, ready and working order. | 8/16/2017 |
| 835 | Corning Painted Post, NY Process Engineer - Firing BS / MS in an engineering discipline (ceramic, chemical or materials preferred) Exp: 1 yr |
To provide engineering expertise and leadership for equipment and process technologies within the Environmental Technologies Division Engineering Firing Technology group. Lead firing technology and engineering project sub-teams. | 8/16/2017 |
| 836 | Corning Erwin, NY Process Engineer, Dry Blend BS / MS in Chemical, Electrical, Mechanical, or Ceramic / Materials Engineering Exp: 1-3 yrs |
Support all Plant Safety programs and continually provide a safe working environment. Serve as a resource for troubleshooting of production equipment / processes in the Batching facility. | 8/16/2017 |
| 837 | Corning Painted Post, NY Development Engineer - EIG BS in Materials Science, Physical Chemistry, Chemical Engineering, Physics or equivalent Exp: 0-5 yrs |
The successful candidate will be an individual contributor and innovation project leader or team member who performs cutting edge materials process and product development, contributing to critical new business projects ranging from novel finishing and planar processing of glass, fluid / surface interactions and processing methods, functional coatings for product performance, and innovative continuous glass / ceramic process development. These activities will serve to generate new business for Corning that address significant market challenges for products such as optics, mobile devices, sensors, energy storage, communications, and life sciences. | 8/16/2017 |
| 838 | Corning Erwin, NY Environmental Health and Safety Engineer BS in Health and Safety, Industrial Hygiene, or related subject Exp: 0-5 yrs |
This position is responsible for promoting a safe and healthy work environment for all plant employees. The Environmental, Health & Safety (EHS) Engineer will help drive continuous improvement in overall environmental, health and safety performance while promoting an interdependent organizational culture. | 8/16/2017 |
| 839 | Cellular Technology Limited (CTL) Cleveland, OH Laboratory Assistant (Contract Research Laboratory) BS Exp: 1 yr |
We are seeking a Laboratory Assistant for our Contract Research Laboratory who will perform immunology testing of client specimens collected from both pre-clinical and clinical studies using the following test methods: ELISPOT, ELISA, flow cytometry, etc. You will help support our quality improvement projects in conjunction with QA, support our quality system by data quality control, communicate with fellow laboratory personnel, maintain laboratory equipment, write reports, etc. All work is performed according to general laboratory safety standards, internal standard operating procedures (SOPs), client protocols, and applicable international, federal and state regulations. | 8/16/2017 |
| 840 | Certara NA, PA Technical Support Analyst BS Exp: 1-2 yrs |
The only artificial intelligence assisted medical writing service in the pharmaceutical industry. This transformative technology helps clients to better meet global transparency and disclosure requirements. | 8/16/2017 |
| 841 | Certara All Locations, Al Regulatory Writer BS 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 | 8/16/2017 |
| 842 | Champion Oncology, Inc. Rockville, MD Husbandry Technician BS 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. | 8/16/2017 |
| 843 | Champion Oncology, Inc. Rockville, MD Formulation Technician BS Exp: 0-2 yrs |
Provide all chemistry and formulation support for in vivo research. Develop preparation methods if not provided. Document all work for a regulatory environment. | 8/16/2017 |
| 844 | Champion Oncology, Inc. Rockville, MD Histology Laboratory Technician BS in biology, pharmacology or related field Exp: 6 MONTHS-1 yr |
Perform histology tasks in support of R&D studies. Maintain and collect data using various systems. | 8/16/2017 |
| 845 | 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. | 8/16/2017 |
| 846 | Chempacific 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. Equipments and tolls used included NMR, UV, MS and IR, Reactor (from 50ml to 221 to 10000l), vacuum pump, water aspirator, condenser, rotavap, voltage transformer, chromatography columns, TLC monitor, lyophilizer, separation funnel and addition funnel. | 8/16/2017 |
| 847 | Chiltern International Ltd. All Locations, Al Pharmacovigilance Officer BS Exp: 0-2 yrs |
Attend project and departmental meetings, as required.When appropriate, in conjunction with the sponsors and senior team members, review pharmacovigilance aspects of a given study. | 8/16/2017 |
| 848 | Chromocell Corporation North Brunswick, NJ SENIOR LABORATORY ASSISTANT BS / MS in food chemistry, chemistry, biology, or a related discipline Exp: 0-2 yrs |
The natural products analytical chemistry department is responsible for a variety of activities including but not limited to extracting plant samples, fractionating its chemical components for screening of taste modulators and quantitative and qualitative analysis using modern analytical instruments. We are seeking a motivated laboratory assistant that will provide support to the group in their daily experiments. | 8/16/2017 |
| 849 | Chromocell Corporation North Brunswick, NJ R&D Lab Assistant - Robotics, Cell Culture and Biology BS in biology, genetics, chemistry Exp: 0-2 yrs |
The positions will involve implementation of cell biology techniques and routine laboratory tasks as detailed below. | 8/16/2017 |
| 850 | Chromocell Corporation North Brunswick, NJ Laboratory Assistant, Research & Development Night - Time Crew BS in life sciences, chemistry, or engineering programs Exp: 0 yr |
The position will consist of supporting company projects with routine laboratory tasks. More specifically the lab assistant will assist with cell culture, operate state of the art liquid handling machinery, biological assays, wet chemistry, and lab maintenance. Full training will be provided. | 8/16/2017 |
| 851 | GE US, US Spring 2018 Engineering Co - op/Intern BS / MS Exp: NA |
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. | 8/16/2017 |
| 852 | GE US, US GE Healthcare Nuclear Pharmacy Intern BS in Pharmacy Exp: NA |
A nuclear pharmacist is responsible for following good sterile compounding practices in preparation and dispensing of radiopharmaceuticals. Acts as the shift supervisor in line with pharmacy policy & procedures during their respective shift. | 8/16/2017 |
| 853 | GE US, US Environmental, Health, & Safety Intern - GE Aviation - Fall BS in Environmental Health & Safety Engineering 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 s reputation and distinguishes us as a socially responsible company. | 8/16/2017 |
| 854 | GE US, US Environmental, Health, & Safety Intern - GE Aviation - Spring BS in Environmental Health & Safety Engineering 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 s reputation and distinguishes us as a socially responsible company. | 8/16/2017 |
| 855 | GE US, US Environmental, Health, & Safety Intern - GE Aviation - Summer BS in Environmental Health & Safety Engineering 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 s reputation and distinguishes us as a socially responsible company. | 8/16/2017 |
| 856 | Circuit Therapeutics Menlo Park, CA Intern - Drug Discovery BS in biology, neuroscience, or related fields Exp: NA |
Designing and executing rodent behavioral assays; Rodent handling and drug dosing; Assisting in rodent surgeries, anatomical mapping studies, immunohistochemistry and microscopy. | 8/16/2017 |
| 857 | Corning Oneonta, NY Manufacturing Intern BS / MS in Technical Manufacturing degree Exp: NA |
Provide support as team member of a major development project. Create or provide input to project plans, establish project plan and milestones scope, schedule, cost estimate, strategy Provide regular updates on project status, including design reviews. Conduct or contribute to a project critique at completion and share key learning(s). | 8/16/2017 |
| 858 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Small Animal Toxicology BS technicial discipline 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. | 8/6/2017 |
| 859 | MPI Research Mattawan, MI Research Technician 1/Research Associate 1 - Safety Pharmacology BS technical discipline 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. | 8/6/2017 |
| 860 | MPI Research Mattawan, MI Research Technician 2 BS technicial discipline Exp: 1-2 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 | 8/6/2017 |
| 861 | MPI Research Mattawan, MI Training Associate - Corporate Training and Development BS technical discipline Exp: 1-3 yrs |
A Training Associates is responsible for the instruction of technical skills for staff. This includes providing and / or coordinating technical training, conducting skill proficiency assessments, maintaining training documentation, and providing feedback to corporate training program governance representative(s) and managers of the trainees. | 8/6/2017 |
| 862 | NantKwest La Jolla, CA Research Associate (Process Development) MS biological sciences Exp: 1 yr |
The successful candidate will work as part of the Process and Analytical team at NantKwest Inc., to support adoptive cell therapy projects based on our Natural Killer (NK) cell platform. We are a growing company that offers competitive salaries and benefits. We are seeking a motivated Research Associate to assist in developing and transfer of robust and scalable upstream processes for cell therapy projects. The applicant will have previous experience of working in an Immunology laboratory (preferably working with primary cells and cell lines) and will be responsible for supporting the efficient operation of the laboratory and performing scientific studies to support cell therapy projects. | 8/6/2017 |
| 863 | NantKwest Culver City , CA Document Control Specialist BS life sciences Exp: 1-3 yrs |
NantKwest is seeking a Document Control Specialist who is proud of their quality focus. This individual will ensure NantKwest documentation and record keeping processes conform to cGMP and regulatory requirements as well as approved procedures | 8/6/2017 |
| 864 | NantKwest Culver City , CA Regulatory Submissions Coordinator BS pharmaceutical or biopharmaceutical sciences Exp: 1-4 yrs |
Under the supervision of the Regulatory Operations Associate Director, this position is responsible for providing support for all submission-related activities including, submission project management, production of submission-ready documents, performing quality and technical submission reviews, and maintaining an electronic archive for regulatory documents. This position will also assist the Regulatory Affairs team with any special projects as assigned. | 8/6/2017 |
| 865 | Natera Austin, TX Quality Assurance Specialist BS 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. | 8/6/2017 |
| 866 | Natera San Carlos, CA Clinical Laboratory Scientist I BS / BA medical technology, biological sciences, or related Exp: 1-2 yrs |
Natera is currently seeking a 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. | 8/6/2017 |
| 867 | Natera San Carlos, CA QC Reagent Associate I BS biology, chemistry, or related Exp: 0-1 yrs |
Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. | 8/6/2017 |
| 868 | Natera San Carlos, CA Clinical Sample Associate I BS / BA scientific discipline or related Exp: 1 yr |
Work primarily with R&D Scientific Operations providing biosamples to Associates / Scientists for use in clinical and research efforts. Maintain the sample bank inventory and fulfill interdepartmental sample requests. | 8/6/2017 |
| 869 | Natera Austin, TX Junior Inside Sales Specialist BS biology, life sciences, or equivalent Exp: 0 yrs |
The Junior Inside Sales Specialist (Jr. ISS) is made up of inbound / outbound calls managing a pipeline and opportunities while walking the patient through the entire process from initial call through submission. | 8/6/2017 |
| 870 | Natus Seattle, WA Manufacturing Technician AA / AS technical discipline Exp: 6 months - 1 yr |
Work closely with Electronic and Electro / Mechanical Assembly and Factory Service departments to improve processes, on tooling and fixturing requirements, and troubleshooting and solving problems, Assist the Manufacturing Engineering group in maintaining a quality manufacturing documentation control system in compliance with Good Manufacturing Practices (GMP). | 8/6/2017 |
| 871 | Natus Middleton, WI Quality Assurance Engineer BS science, engineering, or related Exp: 1-4 yrs |
The QA Engineer will Participate in the maintenance of quality system requirements, including: audits, CAPA, data analysis, design, production, and post production activitiesThe QA Engineer will Participate in the maintenance of quality system requirements, including: audits, CAPA, data analysis, design, production, and post production activities | 8/6/2017 |
| 872 | Natus Middleton, WI Repair Techician I AA / AS technical discipline Exp: 6 months - 1 yr |
Stay up-to-date and follow all Quality System procedures related to this job, which can affect the quality of products or services provided to our customers. Test and calibrate assemblies to meet quality standards Trouble shoots assemblies independently with exceptional computer skills Maintain a less than 2% failure rate on repairs Maintain a 10 business day repair turnaround time on customer owned properties Maintain minimum stock with refurbished parts to assure same day order fulfillment to assure best in class customer satisfaction Needs to communicate with internal customers and some external customers Remanufacture systems up to the latest revocation. Perform transactions on corporate computer inventory control system and customer relations database based on requirements of the position Provide data for managerial reports Prepare tested assemblies for customer Perform electronic calibration and verify fixture Working knowledge of Corporate and Customer Care Department Procedures and policies Monitor processes and recommend improvements Develop / Design test processes / procedures based on product specifications Provide / show elite technical skills with the ability to train and work with any department on technical issues Technical input prior to new product releases Exceptional organizational skills Perform as a product technical resource for department Lead role in the test and calibration of new products Test fixture maintenance including logging information to guarantee compliance with our quality system Design and develop new test fixtures based on product specifications Design / redesign circuitry for product maintenance Proactively problem solves departmental related issues independently and mentors other technicians in this process Responsible for developing queries Responsible for inventory transactions Responsible for maintaining ESD data Responsible for inventory in technicians own locations Other duties as assigned | 8/6/2017 |
| 873 | Nelson Laboratories Salt Lake City, UT Laboratory Analyst - Healthcare Reprocessing BS microbiology, or biological sciences Exp: 1 yr |
The Laboratory Analyst conducts GLP and non-GLP studies following established approved procedures and under the supervision of the Study Director. Additionally, the Laboratory Analyst records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. | 8/6/2017 |
| 874 | Nelson Laboratories Salt Lake City, UT Laboratory Analyst - Microbiology AS / BS microbiology or biological sciences Exp: 1 yr |
The Laboratory Analyst conducts GLP and non-GLP studies following established approved procedures and under the supervision of the Study Director. Additionally, the Laboratory Analyst records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. | 8/6/2017 |
| 875 | Nelson Laboratories Salt Lake City, UT Lab Analyst - Packaging AS / BS microbiology or biological sciences Exp: 1 yr |
The Laboratory Analyst conducts GLP and non-GLP studies following established approved procedures and under the supervision of the Study Director. Additionally, the Laboratory Analyst records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. | 8/6/2017 |
| 876 | Neogen Lincoln, NE Lab Technician I - Vet DX AS / BS science discipline Exp: 1-2 yrs |
This person will join us in a small veterinary diagnostic lab setting with a fun, fast-paced, and positive environment, with strong emphasis on quality and accuracy, committed to same day results. Good communication skills and the desire and ability to work in a team are a must, previous experience in microbiology or veterinary science setting and experience with real time PCR and / or ELISA are beneficial. The individual will have strong attention to detail, be self-motivated and can thrive in a high throughput environment, working as a team but also alone. | 8/6/2017 |
| 877 | Neogen Lincoln, NE Laboratory Tech I - Processing BA / BS scientific discipline Exp: 1-2 yrs |
Preference for those with affinity toward attention to details, ability to complete tasks in an efficient and accurate manner, can read and follow SOPs precisely, but also innovate ideas for process improvements. The individual should understand not just the what but the why and how processes work. Good communication skills and Microsoft Office experience are a plus. Within Processing Lab will have routine exposure to robotics, low and high volume amplification reactions, and hood work utilizing single and multichannel pipettes. Must contribute to an established processing workflow with welcomed ideas for process improvements. | 8/6/2017 |
| 878 | Neogen Lincoln, NE Laboratory Technician I, DNA BA / BS scientific discipline Exp: 1-2 yrs |
DNA Extraction department is seeking an energetic, group-oriented, and organized individual, who thrives in high throughput positive environment. The ideal candidate has strong attention to detail, strong work ethic, and good time management skills. Flexibility with schedule, good communication skills, and key emphasis on quality are required. Strong preference towards individuals with Microsoft Office experience, lab experience, and the ability to multi-task. Within the lab, the responsibilities include quality control for sample tracking, extracting DNA from multiple sample types from a variety of species, and performing final quantification to ensure proper yield has been achieved. Contribute to established protocols with suggestions to improve. | 8/6/2017 |
| 879 | Neogen Lansing, MI Lateral Flow Chemist - Reveal Diagnostics Manufacturing BS protein chemistry, chemistry, biochemistry, or related Exp: 1 yr |
The Food Safety Division is currently seeking a candidate for a Lateral Flow Chemist position. The selected candidate would be responsible for formulating reagents and preparation of some components used in the assembly of Diagnostics, Accupoint, and Dairy Antibiotics products. Others duties would include testing and documenting results following ISO and GMP procedures. The candidate will also be involved in the transfer of new products from R&D to the Manufacturing group. The ideal candidate should have the ability to perform basic mathematical operations, follow and document all manufacturing procedures, be capable of identifying and resolving problems in a timely manner and be able to work both independently, as well in a group setting. | 8/6/2017 |
| 880 | Neogen Lansing, MI Production Chemist - ELISA Manufacturing BS biology, immunology, protein chemistry, food science, or related Exp: 1-3 yrs |
The Food Safety Division is currently seeking a candidate for a Production Chemist position. The ideal candidate should have the ability to perform basic mathematical operations, follow and document all manufacturing procedures, be capable of identifying and resolving problems in a timely manner and be able to work both independently, as well in a group setting. The selected candidate would be responsible for formulating reagents used in the manufacturing of ELISA products. Others duties would include testing and documenting results following ISO and GMP procedures. The candidate will also be involved in the transfer of new products from R&D to the Manufacturing group. | 8/6/2017 |
| 881 | Neogen Lexington, KY QA/QC Technician Level II BS technicial discipline Exp: 1 yr |
Neogen s Animal Safety Division is seeking a QA / QC Technician Level II for its Diagnostic Operations group. 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 s ELISA Drug Detection and Life Science test kits and verifying conformity to specifications for release. | 8/6/2017 |
| 882 | Nephron Pharmaceuticals Corporation West Columbia, SC Microbiologist I BS 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. Demonstrate high proficiency level on tests performed. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 8/6/2017 |
| 883 | Neurovigil San Diego, CA Internship BS computational neuroscience, neuroengineering, or related Exp: 1 yr coursework |
we are always interested in exceptional students looking for internship opportunities in the fields of Computational Neuroscience (NASA) or Neuroengineering (San Diego). | 8/6/2017 |
| 884 | New England BioLabs Inc Cambridge, MA Part - Time Sales Associate BS core life science discipline Exp: 1 yr |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the New England Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Boston or Cambridge area. | 8/6/2017 |
| 885 | New England BioLabs Inc Ipswich, MA Postbaccalaureate Fellowship - RNA Biology Division BS scientific discipline Exp: 0 yrs |
The fellow will work with NEB scientists, and projects will be a part of a research program on different aspects of RNA biology. Research will be undertaken in a highly collaborative and academic environment and will offer motivated and talented students an opportunity to confirm their interest in basic and applied research. | 8/6/2017 |
| 886 | Neurona Therapeutics San Francisco, CA Lab Assistant AS / BS biology, biotechnology, or related Exp: 0 yrs |
The Laboratory Assistant will perform operations that will aid in maximizing the research productivity of the laboratory staff. Day-to-day functions include reagent preparation, cleaning and autoclaving of equipment and materials, solid and liquid waste disposal, inventory management and other duties to support daily operations of the R&D teams. Neurona Therapeutics is an early stage biotechnology company based in South San Francisco focused on the development of neuronal stem cell-based therapies for neurological disease. This is a fantastic opportunity to join a small team and take part in building an exciting, science-driven company. | 8/6/2017 |
| 887 | Nexgen Research Triangle Park, NC Prenatal Genomic Screening Technologist BS biology or related Exp: 1 yr |
The Integrated Genetics Division is seeking a Genomics Sequencing Technologist to join their Prenatal Genomic Screening team! The team performs non-invasive prenatal screening testing utilizing NexGen sequencing (NGS | 8/6/2017 |
| 888 | NGMBio San Francisco, CA Research Associate/Senior Research Associate - Antibody Engineering MS biology / biotechnology - related discipline Exp: 1-2 yrs |
We are currently looking for a highly motivated research associate / senior research associate to join our antibody engineering team that focuses on therapeutic antibody discovery and optimization using various molecular biology and protein engineering approaches. 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. | 8/20/2017 |
| 889 | NGMBio San Francisco, CA Contract Research Associate/Senior Research Associate - In vivo Pharmacology BS 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 Experience performing immunology-related biological assays, flow cytometry and analysis is a plus. | 8/20/2017 |
| 890 | NGMBio San Francisco, CA Research Associate - Molecular Bilogy/Protein Engineering BS / MS molecular biology, cell biology, or related Exp: 1 yr |
We are currently looking for a creative, highly motivated and experienced individual to join the Cloning and Expression Group within the Biologics function. The successful candidate will play an integral role as a key team member of a group focused supporting our therapeutic candidate discovery efforts. | 8/20/2017 |
| 891 | Nordson Amherst, OH Mechanical Engineer - Product Development BS mechanical engineering Exp: 1 yr |
The Product Development Engineer is responsible for supporting new and existing products for the Industrial Coating Systems organization for worldwide markets. | 8/20/2017 |
| 892 | Nordson Amherst, OH Designer BS mechanical engineering Exp: 1 yr |
The Designer will be responsible for supporting Industrial Coating Systems lines of business. This individual must be able to support Engineers and provide system and component detail drawings in an autonomous environment. | 8/20/2017 |
| 893 | Nordson Austintown, OH Laser Clad Technician AS technical discipline Exp: 1-3 yrs |
The Cladding cell operator will receive a barrel and then clad the barrel to drawing requirements. The Operator will be also responsible for grinding of that barrel, performing routine preventive maintenance on equipment and maintaining proper inventory on barrels and consumables. Flexibility to work different shifts to accommodate training and process improvements. | 8/20/2017 |
| 894 | Insperity Mankato, MN Quality Technician AA technical discipline Exp: 6 months - 1 yr |
This position is responsible for coordinating the development and implementation of the quality system and to research, develop and implement process improvements necessary to eliminate waste and reduce inventory. This position is responsible for the development of the performance metric system used to report on continuous process improvements. | 8/20/2017 |
| 895 | Insperity Merrifield, MN Engineering Technician AS technical discipline Exp: 1-2 yrs |
We will rely on your experience and dedication to assist our Engineering department. In this position you will primarily assist the New Product Introduction and Production departments with various tasks | 8/20/2017 |
| 896 | Insperity Mankato, MN Manufacturing Engineer BS mechanical engineering, manufacturing, or electrical engineering Exp: 0 yrs |
The Manufacturing Engineer will be developing manufacturing methods, systems and processes; providing product support to engineering and manufacturing teams; resolving engineering problems; evaluating manufacturing systems applications and equipment; confirming systems and components capabilities; developing manufacturing processes and standards; assuring product quality & preparing technical product reports. | 8/20/2017 |
| 897 | Alvogen Norwich, NY Research Assistant - Analytical Chemist II BS chemistry or related Exp: 1-2 yrs |
The Method Development and Analytical Services (MDAS) Research Assistant is a technical resource in performing the analytical testing necessary to support development and commercialization of new pharmaceutical products. The MDAS Research Assistant is responsible for performing the bench chemistry testing for release, stability and product characterization. The MDAS Research Assistant will work under the supervision of more experienced technical staff. | 8/20/2017 |
| 898 | Nova Biomedical Waltham, MA Quality Assurance Associate BS technical discipline Exp: 1-2 yrs |
In this role you will be part of the team that works to ensure the company is compliant with ISO 13485, ISO 9001 and FDA QSR. This role reports to Quality Assurance Manager. | 8/20/2017 |
| 899 | Nova Biomedical Waltham, MA Regulatory Affairs Specialist BS / MS life sciences Exp: 0-3 yrs |
In this role, you will focus on supporting new product introductions with US 510k, Health Canada Licensing, International Device Submissions, and global licensing and registration requirements,. We work closely with the Quality function to assure compliance to ISO / FDA QSR, IVDD, ISO 13485, and look to the future with MDSAP and IVDR. | 8/20/2017 |
| 900 | Alcon Research Ltd. Irvine, CA Quality Engineer III, Product Line MS engineering or physical / biological sciences Exp: 1 yr |
Alcon is currently seeking an Engineer III Quality Product Line for the Manufacturing Technical Operations division located in Irvine CA. The Engineer III Quality Product Line Develops, modifies, applies and maintains quality standards and protocol for processing materials into partially finished or finished materials product. Collaborates with engineering and manufacturing functions to ensure quality standards are in place. | 8/20/2017 |
| 901 | Novartis Emeryville, CA Scientist Medicinal Chemistry (ID: 221054BR) BS / MS chemistry Exp: 0-4 yrs |
The successful candidate will help perform innovative research in the preparation of novel organic molecules to aid in the discovery and development of new therapeutically relevant compounds. | 8/20/2017 |
| 902 | Novartis Morris Plains, NJ Associate Scientist Bioanalytics (ID: 214358BR) BS.MS biology, chemistry, biochemistry, microbiolgy, or related Exp: 0-5 yrs |
Perform Bio-Analytical testing such as Flow, ELISA, cell count, cell viability, residual bead assessment, qPCR. Follows quality policies. Work on shifts covering daytime / evening and one or both weekend days. Execute method qualification / optimization of methods as per appropriate protocols. Contribute to OOS / OOE investigations and deviation investigations. Interface with regulatory agencies during audits. Contribute to assigned projects. Knowledge of LabWare LIMS and / or other QC data systems. Maintain GMP / GLP quality systems. Monthly review of laboratory logbooks and monthly laboratory cleaning. Performing daily equipment startup and PQ Assure stock of reagents and materials Performs other job duties as assigned. | 8/20/2017 |
| 903 | Novartis Morris Plains, NJ Scientist (Bioanalytics) (ID: 210124BR) MS biology, chemistry, biochemistry, microbiology, or related Exp: 1-3 yrs |
This role will be focused on work in the QC molecular biology lab. Perform qPCR assays (SYBR Green & Taqman), DNA / RNA extraction and nucleic acid quantification. Development and optimization of qPCR methodologies. Operation of equipment such as Quantstudio, Tecan M200, QIAgility, and QIAcube. Candidate will also be involved in Bio-Analytical testing such as flow cytometry, ELISA, cell count, cell viability. | 8/20/2017 |
| 904 | Novartis Johns Creek, GA Associate Scientist (ID: 220676BR) MS scientific discipline Exp: 0-2 yrs |
To support the research and development of superior surface coatings for new Alcon contact lenses and other relevant research projects, through efficient, effective and innovative science and solutions. Assist in the design, development, testing and implementation of science processes (such as surface chemistry and process) to meet the needs of new and existing products, including from conception research to commercialization Apply basic principles of scientific analysis to provide solutions to rudimentary problems arising within the department. Design appropriate experiments and execute them with hands-on work in research lab and / or pilot lab Identify and perform testing funnels to evaluate surface properties and other lens properties for contact lenses Document experimental results in appropriate formats (laboratory notebook, memo and / or report) and perform statistical analysis of data as needed, communicate idea and data effectively to supervisors Support cross functional, as appropriate, in execution of project plans prepared in cooperation with project team leadership | 8/20/2017 |
| 905 | Novartis Fort Worth, TX Regulatory Affairs Analyst (ID: 220127BR) BS science related discipline Exp: 1 yr |
The Regulatory Affairs Analyst will provide worldwide regulatory affairs support for Class I, II, and Class III medical devices. The Regulatory Affairs Analyst is responsible for activities that lead to, and maintain regulatory approval for these medical devices. | 8/20/2017 |
| 906 | Novartis Fort Worth, TX Fall Intership - IT Collaboration and Communications (ID: 220757BR) MS technology discipline Exp: 1 yr coursework |
Thank you for your interest in Alcon s Internship and Co-Op Program. These programs are jointly managed by Alcon and PRO Unlimited. This partnership continues our long standing collaboration providing Alcon s Interns and Co-Op Students real-world experience by discovering new ways to enhance sight and improve people s lives. As an Alcon Intern or Co-Op you will be employed by PRO Unlimited. | 8/20/2017 |
| 907 | Novavax Gaithersburg, MD Clinical Research Associate BS / BA life sciences Exp: 1-5 yrs |
The Clinical Research Associate (CRA), will provide support to the Clinical Project Manager in the execution of one or more phase 1-4 clinical trials from protocol through clinical study report finalization for regulatory submission. Ensure compliance with ICH-GCP, FDA / EMA, other regulations and SOPs, as applicable. Ensure all operational trial deliverables are met according to timelines, budget, operational procedures and quality standards. Responsible for the management of CROs and ensure adherence to scope of work within timelines and budget. | 8/20/2017 |
| 908 | Novavax Gaithersburg, MD Formulation Development Associate I/II BS pharmaceuticals, chemistry, biology, or related Exp: 0-2 yrs |
Development of liquid formulations for protein nanoparticle based vaccines through logical screening of excipients Analytical testing of formulation excipients, bulk formulations and final product Following SOPs and performing routine stability indicating assays (SDS-PAGE, Western Blot, Chromatography HPLC / GC, Particle sizing, ELISA, Protein assays, UV Spectroscopy, etc.) Assisting in the writing, reviewing, and editing of reports Maintenance of accurate records of analysis of samples from formulation development Assisting in the maintenance of department records and raw material / finished product inventories Assisting in the preparation and tracking of reagents for pre-clinical testing of research / discovery, process development and formulation samples Aseptic filling of vials and pre-filled syringes Knowledge of accelerated stability testing as per ICH guidelines. Knowledge of protein stability, degradation and aggregation testing | 8/20/2017 |
| 909 | Novavax Gaithersburg, MD Research Associate I BS biological science, molecular biology, immunology, or related Exp: 0-2 yrs |
We are seeking a Research Associate I to join our Clinical Immunology team. This is a great opportunity to broaden your skills with a talented team. The qualified individual should have a bachelor's degree and be familiar with aseptic technique and working in a laboratory setting. | 8/20/2017 |
| 910 | NovelMed Cleveland, OH Research Intern BS / MS scientific discipline Exp: 1 yr coursework |
A team of excellent scientists supports the research & development efforts at NovelMed. Working together, we ve become one of the world s leading research-focused biotechnology companies. Our success is built on continuous innovation and unsurpassed curiosity and we are at the forefront of the biotechnology industry. We use human genetic information to develop antibody based drugs for orphan and non-orphan diseases. NovelMed has multiple therapies under development from acute to chronic clinical conditions.We believe that our employees are our most important asset and they drive our development to commercialization process. We are currently recruiting for internship positions. | 8/20/2017 |
| 911 | Noven Miami, FL Value Stream Engineer BS mechanical, industrial, electrical or related engineering discipline Exp: 1-5 yrs |
Responsible for the support of manufacturing processes, instrumentation and equipment from manufacturing values steam. Integral part of the value stream team accountable for delivery of improvements in the areas of safety, quality, service and cost per the team goals and metrics. Provides expertise engineering, design and process and / or scale-up. Assists manufacturing operation in problem solving with regards to materials, components, equipment and systems. Develops and recommends new process solutions and technologies to achieve cost effectiveness and improved product quality. Recommends process improvements for the production of therapeutic products using tankage, piping, coating / oven systems, laminating dies, pouching machines, printing, bar code, vision and packaging systems. | 8/20/2017 |
| 912 | Novo Nordisk Clayton, NC Manufacturing Process Technician I AA / AS biology or related Exp: 1 yr |
Operate manufacturing equipment to achieve production goals. | 8/20/2017 |
| 913 | Novo Nordisk Many, Ma Pharma Field Sales - Diabetes Care Specialist BS scientific discipline Exp: 1 yr |
This position represents Novo Nordisk within an assigned territory with the goal of maximizing sales and positioning Novo Nordisk as the leading company in diabetes care. The DCS must assume responsibility for achieving sales goals by implementing marketing and sales strategies aimed at effectively selling and promoting Novo Nordisk s portfolio of diabetes products to physicians, pharmacists, nurses, and other paramedical customers and current co-promotion partners who make or are involved in purchasing and prescribing decisions. This position also determines and recommends the most appropriate Novo Nordisk product and approved usage for the needs of the customers. | 8/20/2017 |
| 914 | Novo Nordisk Clayton, NC QC Chemist I BS chemistry or related Exp: 1 yr |
Perform and review analysis of in process and filled product in accordance with cGMP, site and corporate procedures and policies. | 8/20/2017 |
| 915 | Novo Nordisk Lebanon, NH QC Analyst MS scientific discipline Exp: 1-5 yrs |
The QC Analyst, Analytical position conducts routine testing using analytical techniques. He / she exercises judgment and maintains a high level of compliance with cGMP s. | 8/20/2017 |
| 916 | Novo Nordisk Lebanon, NH Manufacturing Technician BS scientific discipline Exp: 0 yrs |
This position has primary responsibility to support the manufacturing processes for Purification. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 8/20/2017 |
| 917 | Novozymes Blair, NE QC Analyst, Glbal Quality Control BS chemistry or related Exp: 0 yrs |
As our QC Analyst, you will perform operations required in the chemical laboratory by following written directions and procedures, while maintaining accurate up-to-date records of all work performed. As a QC Analyst, you will be challenged to work closely with other analysts under the direction of the QC Team Leader in our new state of the art facility. You will perform assays with accuracy and precision then calculate and record data in form / records, LIMS and SAP databases. You will also provide reports of analytical data, ensure compliance to method controls and conduct tests to effectively support OPS. You will perform basic troubleshooting techniques as outlined in SOPs and perform routine instrument maintenance and calibration. | 8/20/2017 |
| 918 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Small Animal Toxicology BS technicial discipline 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. | 8/6/2017 |
| 919 | MPI Research Mattawan, MI Research Technician 1/Research Associate 1 - Safety Pharmacology BS technical discipline 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. | 8/6/2017 |
| 920 | MPI Research Mattawan, MI Research Technician 2 BS technicial discipline Exp: 1-2 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 | 8/6/2017 |
| 921 | MPI Research Mattawan, MI Training Associate - Corporate Training and Development BS technical discipline Exp: 1-3 yrs |
A Training Associates is responsible for the instruction of technical skills for staff. This includes providing and / or coordinating technical training, conducting skill proficiency assessments, maintaining training documentation, and providing feedback to corporate training program governance representative(s) and managers of the trainees. | 8/6/2017 |
| 922 | NantKwest La Jolla, CA Research Associate (Process Development) MS biological sciences Exp: 1 yr |
The successful candidate will work as part of the Process and Analytical team at NantKwest Inc., to support adoptive cell therapy projects based on our Natural Killer (NK) cell platform. We are a growing company that offers competitive salaries and benefits. We are seeking a motivated Research Associate to assist in developing and transfer of robust and scalable upstream processes for cell therapy projects. The applicant will have previous experience of working in an Immunology laboratory (preferably working with primary cells and cell lines) and will be responsible for supporting the efficient operation of the laboratory and performing scientific studies to support cell therapy projects. | 8/6/2017 |
| 923 | NantKwest Culver City , CA Document Control Specialist BS life sciences Exp: 1-3 yrs |
NantKwest is seeking a Document Control Specialist who is proud of their quality focus. This individual will ensure NantKwest documentation and record keeping processes conform to cGMP and regulatory requirements as well as approved procedures | 8/6/2017 |
| 924 | NantKwest Culver City , CA Regulatory Submissions Coordinator BS pharmaceutical or biopharmaceutical sciences Exp: 1-4 yrs |
Under the supervision of the Regulatory Operations Associate Director, this position is responsible for providing support for all submission-related activities including, submission project management, production of submission-ready documents, performing quality and technical submission reviews, and maintaining an electronic archive for regulatory documents. This position will also assist the Regulatory Affairs team with any special projects as assigned. | 8/6/2017 |
| 925 | Natera Austin, TX Quality Assurance Specialist BS 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. | 8/6/2017 |
| 926 | Natera San Carlos, CA Clinical Laboratory Scientist I BS / BA medical technology, biological sciences, or related Exp: 1-2 yrs |
Natera is currently seeking a 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. | 8/6/2017 |
| 927 | Natera San Carlos, CA QC Reagent Associate I BS biology, chemistry, or related Exp: 0-1 yrs |
Executes the preparation and qualification of molecular diagnostic reagents. Performs Quality Control tests on new incoming shipments of raw materials and small scale manufacturing procedures (formulations and dispensing) reagent. Reviews data obtained for compliance to specifications and reports abnormalities. Maintains and improves QC documentation pertaining to raw material specification, reagent qualification, and QC testing. | 8/6/2017 |
| 928 | Natera San Carlos, CA Clinical Sample Associate I BS / BA scientific discipline or related Exp: 1 yr |
Work primarily with R&D Scientific Operations providing biosamples to Associates / Scientists for use in clinical and research efforts. Maintain the sample bank inventory and fulfill interdepartmental sample requests. | 8/6/2017 |
| 929 | Natera Austin, TX Junior Inside Sales Specialist BS biology, life sciences, or equivalent Exp: 0 yrs |
The Junior Inside Sales Specialist (Jr. ISS) is made up of inbound / outbound calls managing a pipeline and opportunities while walking the patient through the entire process from initial call through submission. | 8/6/2017 |
| 930 | Natus Seattle, WA Manufacturing Technician AA / AS technical discipline Exp: 6 months - 1 yr |
Work closely with Electronic and Electro / Mechanical Assembly and Factory Service departments to improve processes, on tooling and fixturing requirements, and troubleshooting and solving problems, Assist the Manufacturing Engineering group in maintaining a quality manufacturing documentation control system in compliance with Good Manufacturing Practices (GMP). | 8/6/2017 |
| 931 | Natus Middleton, WI Quality Assurance Engineer BS science, engineering, or related Exp: 1-4 yrs |
The QA Engineer will Participate in the maintenance of quality system requirements, including: audits, CAPA, data analysis, design, production, and post production activitiesThe QA Engineer will Participate in the maintenance of quality system requirements, including: audits, CAPA, data analysis, design, production, and post production activities | 8/6/2017 |
| 932 | Natus Middleton, WI Repair Techician I AA / AS technical discipline Exp: 6 months - 1 yr |
Stay up-to-date and follow all Quality System procedures related to this job, which can affect the quality of products or services provided to our customers. Test and calibrate assemblies to meet quality standards Trouble shoots assemblies independently with exceptional computer skills Maintain a less than 2% failure rate on repairs Maintain a 10 business day repair turnaround time on customer owned properties Maintain minimum stock with refurbished parts to assure same day order fulfillment to assure best in class customer satisfaction Needs to communicate with internal customers and some external customers Remanufacture systems up to the latest revocation. Perform transactions on corporate computer inventory control system and customer relations database based on requirements of the position Provide data for managerial reports Prepare tested assemblies for customer Perform electronic calibration and verify fixture Working knowledge of Corporate and Customer Care Department Procedures and policies Monitor processes and recommend improvements Develop / Design test processes / procedures based on product specifications Provide / show elite technical skills with the ability to train and work with any department on technical issues Technical input prior to new product releases Exceptional organizational skills Perform as a product technical resource for department Lead role in the test and calibration of new products Test fixture maintenance including logging information to guarantee compliance with our quality system Design and develop new test fixtures based on product specifications Design / redesign circuitry for product maintenance Proactively problem solves departmental related issues independently and mentors other technicians in this process Responsible for developing queries Responsible for inventory transactions Responsible for maintaining ESD data Responsible for inventory in technicians own locations Other duties as assigned | 8/6/2017 |
| 933 | Nelson Laboratories Salt Lake City, UT Laboratory Analyst - Healthcare Reprocessing BS microbiology, or biological sciences Exp: 1 yr |
The Laboratory Analyst conducts GLP and non-GLP studies following established approved procedures and under the supervision of the Study Director. Additionally, the Laboratory Analyst records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. | 8/6/2017 |
| 934 | Nelson Laboratories Salt Lake City, UT Laboratory Analyst - Microbiology AS / BS microbiology or biological sciences Exp: 1 yr |
The Laboratory Analyst conducts GLP and non-GLP studies following established approved procedures and under the supervision of the Study Director. Additionally, the Laboratory Analyst records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. | 8/6/2017 |
| 935 | Nelson Laboratories Salt Lake City, UT Lab Analyst - Packaging AS / BS microbiology or biological sciences Exp: 1 yr |
The Laboratory Analyst conducts GLP and non-GLP studies following established approved procedures and under the supervision of the Study Director. Additionally, the Laboratory Analyst records data concurrently, maintains traceability of samples throughout testing and notifies the Study Director of any unforeseen circumstances or events that occur during testing. | 8/6/2017 |
| 936 | Neogen Lincoln, NE Lab Technician I - Vet DX AS / BS science discipline Exp: 1-2 yrs |
This person will join us in a small veterinary diagnostic lab setting with a fun, fast-paced, and positive environment, with strong emphasis on quality and accuracy, committed to same day results. Good communication skills and the desire and ability to work in a team are a must, previous experience in microbiology or veterinary science setting and experience with real time PCR and / or ELISA are beneficial. The individual will have strong attention to detail, be self-motivated and can thrive in a high throughput environment, working as a team but also alone. | 8/6/2017 |
| 937 | Neogen Lincoln, NE Laboratory Tech I - Processing BA / BS scientific discipline Exp: 1-2 yrs |
Preference for those with affinity toward attention to details, ability to complete tasks in an efficient and accurate manner, can read and follow SOPs precisely, but also innovate ideas for process improvements. The individual should understand not just the what but the why and how processes work. Good communication skills and Microsoft Office experience are a plus. Within Processing Lab will have routine exposure to robotics, low and high volume amplification reactions, and hood work utilizing single and multichannel pipettes. Must contribute to an established processing workflow with welcomed ideas for process improvements. | 8/6/2017 |
| 938 | Neogen Lincoln, NE Laboratory Technician I, DNA BA / BS scientific discipline Exp: 1-2 yrs |
DNA Extraction department is seeking an energetic, group-oriented, and organized individual, who thrives in high throughput positive environment. The ideal candidate has strong attention to detail, strong work ethic, and good time management skills. Flexibility with schedule, good communication skills, and key emphasis on quality are required. Strong preference towards individuals with Microsoft Office experience, lab experience, and the ability to multi-task. Within the lab, the responsibilities include quality control for sample tracking, extracting DNA from multiple sample types from a variety of species, and performing final quantification to ensure proper yield has been achieved. Contribute to established protocols with suggestions to improve. | 8/6/2017 |
| 939 | Neogen Lansing, MI Lateral Flow Chemist - Reveal Diagnostics Manufacturing BS protein chemistry, chemistry, biochemistry, or related Exp: 1 yr |
The Food Safety Division is currently seeking a candidate for a Lateral Flow Chemist position. The selected candidate would be responsible for formulating reagents and preparation of some components used in the assembly of Diagnostics, Accupoint, and Dairy Antibiotics products. Others duties would include testing and documenting results following ISO and GMP procedures. The candidate will also be involved in the transfer of new products from R&D to the Manufacturing group. The ideal candidate should have the ability to perform basic mathematical operations, follow and document all manufacturing procedures, be capable of identifying and resolving problems in a timely manner and be able to work both independently, as well in a group setting. | 8/6/2017 |
| 940 | Neogen Lansing, MI Production Chemist - ELISA Manufacturing BS biology, immunology, protein chemistry, food science, or related Exp: 1-3 yrs |
The Food Safety Division is currently seeking a candidate for a Production Chemist position. The ideal candidate should have the ability to perform basic mathematical operations, follow and document all manufacturing procedures, be capable of identifying and resolving problems in a timely manner and be able to work both independently, as well in a group setting. The selected candidate would be responsible for formulating reagents used in the manufacturing of ELISA products. Others duties would include testing and documenting results following ISO and GMP procedures. The candidate will also be involved in the transfer of new products from R&D to the Manufacturing group. | 8/6/2017 |
| 941 | Neogen Lexington, KY QA/QC Technician Level II BS technicial discipline Exp: 1 yr |
Neogen s Animal Safety Division is seeking a QA / QC Technician Level II for its Diagnostic Operations group. 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 s ELISA Drug Detection and Life Science test kits and verifying conformity to specifications for release. | 8/6/2017 |
| 942 | Nephron Pharmaceuticals Corporation West Columbia, SC Microbiologist I BS 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. Demonstrate high proficiency level on tests performed. Additional work duties or responsibilities as evident or required. Performs other duties as assigned or apparent. | 8/6/2017 |
| 943 | Neurovigil San Diego, CA Internship BS computational neuroscience, neuroengineering, or related Exp: 1 yr coursework |
we are always interested in exceptional students looking for internship opportunities in the fields of Computational Neuroscience (NASA) or Neuroengineering (San Diego). | 8/6/2017 |
| 944 | New England BioLabs Inc Cambridge, MA Part - Time Sales Associate BS core life science discipline Exp: 1 yr |
New England Biolabs (NEB) is seeking a Part-Time Sales Associate to assist the New England Field Account Manager with prospecting, generating and closing sales leads in the territory. With guidance from the Account Manager, a goal for the Part-Time Sales Associate will be to eventually work independently on assigned accounts. This is a 20 hour a week position. The ideal candidate will live in the Boston or Cambridge area. | 8/6/2017 |
| 945 | New England BioLabs Inc Ipswich, MA Postbaccalaureate Fellowship - RNA Biology Division BS scientific discipline Exp: 0 yrs |
The fellow will work with NEB scientists, and projects will be a part of a research program on different aspects of RNA biology. Research will be undertaken in a highly collaborative and academic environment and will offer motivated and talented students an opportunity to confirm their interest in basic and applied research. | 8/6/2017 |
| 946 | Neurona Therapeutics San Francisco, CA Lab Assistant AS / BS biology, biotechnology, or related Exp: 0 yrs |
The Laboratory Assistant will perform operations that will aid in maximizing the research productivity of the laboratory staff. Day-to-day functions include reagent preparation, cleaning and autoclaving of equipment and materials, solid and liquid waste disposal, inventory management and other duties to support daily operations of the R&D teams. Neurona Therapeutics is an early stage biotechnology company based in South San Francisco focused on the development of neuronal stem cell-based therapies for neurological disease. This is a fantastic opportunity to join a small team and take part in building an exciting, science-driven company. | 8/6/2017 |
| 947 | Nexgen Research Triangle Park, NC Prenatal Genomic Screening Technologist BS biology or related Exp: 1 yr |
The Integrated Genetics Division is seeking a Genomics Sequencing Technologist to join their Prenatal Genomic Screening team! The team performs non-invasive prenatal screening testing utilizing NexGen sequencing (NGS | 8/6/2017 |
| 948 | 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. | 8/2/2017 |
| 949 | Baxter Irvine, CA Engineer II - Quality (CAPA) BS in Engineering Exp: 1-3 yrs |
Lead product and process improvement CAPA projects with minimal supervision, managing cross-functional teams to timely and effective closure. | 8/2/2017 |
| 950 | Baxter Marion, NC Reliability Engineer I BS in Engineering Exp: 0-1 yr |
Works as part of a team performing standard engineering work requiring application of standard engineering techniques, procedures and criteria. Work is closely supervised.Works as part of a team performing standard engineering work requiring application of standard engineering techniques, procedures and criteria. Work is closely supervised.Works as part of a team performing standard engineering work requiring application of standard engineering techniques, procedures and criteria. Work is closely supervised. | 8/2/2017 |
| 951 | BERG Framingham, MA Research Associate I BS in chemistry, biochemistry, or related discipline Exp: 1-3 yrs |
The successful candidate will join a team responsible for biomarker discovery / validation in multiple disease areas, including neurodegenerative diseases, diabetes, obesities, and cancer, using state-of-the-art quantitative proteomics platforms. The successful candidate will gain valuable hands-on experience operating and troubleshooting chromatography and mass spectrometry instruments and confidence in laboratory methodology. | 8/2/2017 |
| 952 | BERG Framingham, MA Laboratory Operations Specialist I BS Exp: 0-2 yrs |
Reporting to the Chief Precision Medicine Officer, the entry level Laboratory Operations Specialist will process laboratory specimens (aliquoting and accessioning) for the OMICS division. | 8/2/2017 |
| 953 | BioAssay Systems Hayward, CA Scientist BS in biochemistry, chemistry, biology or related field Exp: 1 yr |
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. | 8/2/2017 |
| 954 | BioClinica Orlando, FL Clinical Research Coordinator - Outpatient Neurology BS in a health-related field Exp: |
The Clinical Research Coordinator (CRC) is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials is congruent with the philosophy and mission of the company. The CRC plans, coordinates, evaluates, and manages the care of both the participants and the data for their assigned research projects. The CRC follows study-specific protocol guidelines and communicates and interacts with Investigators, clinic staff, sponsoring agencies, and others to effectively perform clinical research and to coordinate research activities. All duties carried out by the CRC are done so in accordance with company policies and SOPs, as well as all applicable local, state, and federal regulations. Professionals in this role actively participate in outstanding customer service and accept responsibility for developing and maintaining mutually respectful relationships. | 8/2/2017 |
| 955 | BioClinica Orlando, FL Prescreen Coordinator BS Exp: 1-2 yrs |
The Prescreen Coordinator assists the CRC with patient care and data management for the enrollment and maintenance of subjects in clinical trials. | 8/2/2017 |
| 956 | Bioduro San Diego, CA Assistant Scientist/Associate Scientist, Quality Control BS in Chemistry or a related scientific discipline Exp: 1-2 yrs |
The Quality Control Assistant Scientist facilitates and assists in execution of systems to assure cGMP compliance for all relevant operations carried out within and for BioDuro, LLC. Responsible for performing advanced experiments and general laboratory duties. | 8/2/2017 |
| 957 | Biogen Research Triangle Park, NC Associate I/II, QC Bioassay BS / MS Exp: 0-5 yrs |
The QC Bioassay group in RTP, NC has an opportunity for an Associate I / II. QC Bioassay supports Quality Control testing of GMP samples using biological analytical methods, as well as reagent qualification testing, validation / transfer of analytical methods, and technical support of QC investigations. | 8/2/2017 |
| 958 | Biogen Cambridge, MA Associate I, Media Development BS in Engineering, Biology or Chemistry Exp: 0-2 yrs |
The ideal candidate will be responsible for providing a variety of non-GMP services to internal Biogen customers within the research and technical development departments. These services include preparation of complex biological solutions, microbiological growth media, and cell culture media. This candidate will be instrumental in the development of formulations and provide technical expertise on preparation procedures. | 8/2/2017 |
| 959 | Biogen Cambridge, MA Associate Scientist II, In Vitro Neuropharmacology MS Exp: 1 yr |
The successful candidate will be responsible for developing in vitro assays to perform compound screening, target validation and mechanism of action studies, in support of programs within the neuropharmacology therapeutic area. | 8/2/2017 |
| 960 | Biogen Biogen, MA Associate Sci II/Eng 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 from laboratory studies is a requirement of the position. Laboratory support of department innovation initiatives is also an expectation of the position. | 8/2/2017 |
| 961 | Biogen Biogen, MA Pharmacovigilance Specialist BS / MS in biologic or natural science Exp: 6 months-1 yr |
Pharmacovigilance Specialist supports the PV Scientist group by participating in signaling activities (managing documentation, supporting meeting logistics, etc.), supporting aggregate reporting (PSUR calendar, tracking global requirements (PSUR, RMP or REMS) / submissions, archiving documentation), supporting ad hoc regulatory responses (QC, archiving documents, logistical support), participating in QC of documents and other tasks as assigned. Supports review of literature through documentation archiving and maintenance. Assists with inspection readiness by ensuring documentation is complete and archived, maintaining archive sites, and conducting other activities as assigned. | 8/2/2017 |
| 962 | Quidel San Diego, CA Technical Support Specialist BS / BA in Life Sciences Exp: 1 yr |
Provides technical support to medical professionals, sales representatives and laypersons primarily via the telephone. Demonstrates medical knowledge and communication skills while providing excellent customer service to facilitate resolution of customer problems. Works closely with domestic Sales, Marketing, Customer Service, QA, QC, Research and Development to address customer concerns, determine corrective action and customer follow-up. | 8/2/2017 |
| 963 | Quidel Athens, OH Manufacturing Associate BS / BA Exp: 1-2 yrs |
The Manufacturing Associate in Harvesting will participate in the production of cell culture products by preparing in-process and finished goods materials. | 8/2/2017 |
| 964 | BioLegend San Diego, CA Manufacturing Associate - Immunoassay BS / BA in Biology or related Life Sciences area Exp: 1 yr |
The Manufacturing Associate will be responsible for making immunoassay components and kits, including planning, formulating, testing, and analyzing data. | 8/2/2017 |
| 965 | BioLegend San Diego, CA Scientist (Biomarker and Immunoassay) MS in Biology, Immunology, Biotechnology, Analytical Chemistry, or other relevant discipline Exp: 0-2 yrs |
Under the general supervision of the head of the biomarker business, the scientist performs scientific and laboratory work to develop and commercialize immunoassays and other new bioanalytical products. This position is also responsible for supporting the Manufacturing and Marketing departments and overall business and customer needs. | 8/2/2017 |
| 966 | BioLegend San Diego, CA Manufacturing Associate - Tissue Culture 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 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. | 8/2/2017 |
| 967 | BioLegend San Diego, CA Research Associate (ELISA) BS in Biochemistry, Molecular Biology, or a related Biological Science area Exp: 1 yr |
In this role, you will work closely with a Senior Scientist and develop immunoassay products including ELISA, multiplex, and additional reagents for assay development. In addition to playing an active role in the product development process, you will have opportunity to interact with a variety of teams, such as manufacturing and QC, and to expand your skill sets in a rapidly growing company. | 8/2/2017 |
| 968 | BioLegend San Diego, CA Manufacturing Associate (Purification) BS in Biochemistry, Biology, Chemistry, or a related field Exp: 1-5 yrs |
The Manufacturing Associate is an important member of the team that manufactures and provides antibodies and reagents to a diverse set of research areas, including Immunology, Neuroscience, Cancer, Stem cells, and Cell Biology. This is a great opportunity to enhance your knowledge in a highly competitive biotechnology industry. BioLegend is a fast growing company and an industry leader who is committed the effort to provide top line quality products to our customers and the best tools for scientific community. | 8/2/2017 |
| 969 | BIOMARIN SAN RAFAEL, CA RESEARCH ASSOCIATE II (TEMPORARY) MS Exp: 1-2 yrs |
Assist in the pharmacology / toxicology evaluation and support of early to late stage drug candidates as well as marketed products. | 8/2/2017 |
| 970 | BIOMARIN NOVATO, CA RESEARCH ASSOCIATE I MS Exp: 0-2 yrs |
This position will include working with new technologies such as gene therapy as well as protein therapeutics. The individual will be focusing on small-scale cell culture activities in the laboratory, developing processes in bench-top bioreactors as well as larger scale activities that may involve the transfer of processes to either Clinical of Commercial Manufacturing Facilities. | 8/2/2017 |
| 971 | BIOMARIN NOVATO, CA FORMULATIONS ASSOCIATE (ASSOCIATE, FORMULATIONS) (TEMPORARY) BS / BA Exp: 0-2 yrs |
Assist in preformulation characterization and formulation development studies including routine and semi-routine laboratory activities under direct supervision. | 8/2/2017 |
| 972 | BIOMARIN NOVATO, CA ANALYST, QC RAW MATERIALS BS / BA Exp: 0-1 yr |
The Quality Control Raw Materials Analyst, under direct supervision, is responsible for performing biochemical and chemical evaluations of all raw materials. | 8/2/2017 |
| 973 | BIOMARIN NOVATO, CA ANALYST, QC I (TEMPORARY) BS in a Biological or Biochemical Science Exp: 0-2 yrs |
The Quality Control Analyst s main job responsibility is to manage the Quality Control In-Process department documents to ensure their accuracy, quality and integrity. The candidate will organize, maintain, track and archive department documents and records while adhering to the BioMarin's document lifecycle procedures and in accordance with the records retention schedule. The QC Analyst may be required to develop new processes and improve upon the current system to allow retrieval of data records more effectively. Periodically, the QC analyst may be responsible for training employees on records management procedures and policies, which include documentation, retention, retrieval, destruction and disaster recovery. The candidate may also assist with audits of data record systems and perform administrative tasks as needed. | 8/2/2017 |
| 974 | BioPhase Solutions Inc Sacramento, CA Associate Chemist, Quality Control BS / MS in Chemistry or closely related field Exp: 1-3 yrs |
Performing routine analysis of bulk and pharmaceutical chemicals where procedures are well established and guidance is readily available. | 8/2/2017 |
| 975 | BioPhase Solutions Inc San Francisco, CA Associate Automation Engineer BS / MS Exp: 1 yr |
Support the transition of manually intensive and error prone processes onto automated equipment. | 8/2/2017 |
| 976 | BioPhase Solutions Inc San Francisco, CA Quality Assurance / Quality Control Lab Technician (Food Manufacturing) BS Exp: 1-2 yrs |
Perform sensory, physical, chemical, and / or instrumental evaluation of raw material, in process, or finished products following SOP and specifications. | 8/2/2017 |
| 977 | BioPhase Solutions Inc San Francisco, CA Research Associate, Molecular Biology BS / MS in molecular biology, microbiology, bioengineering, or related discipline Exp: 1 yr |
The Research Associate will be focused on molecular biology in support of high throughput workflows. | |
| 978 | BioPhase Solutions Inc Orange County, CA QA Document Control Specialist BS in the Physical Sciences or related scientific area Exp: 1 yr |
Requesting raw material and finished good specifications and other required documentation from contract manufacturers and raw material suppliers | |
| 979 | BioPhase Solutions Inc San Francisco, CA Regulatory Affairs Coordinator - Cosmetic BS / BA in Chemistry or related field Exp: 1 yr |
Review raw material and ingredient compositions for regulatory conformity based on industry guidelines / international restrictions. | |
| 980 | BioPhase Solutions Inc Los Angeles County, CA Sr. Research Associate, Flow Cytometry MS in the life sciences Exp: 1 yr |
Developing, qualifying, and executing flow cytometry methods for production of T-cell therapy products within the Product Sciences department | |
| 981 | Bio-Rad Irvine, CA Technical Associate III BS / BA in Life Science or related discipline Exp: 0-2 yrs |
Perform quality inspection & testing of raw materials according to specified procedures and verifying specifications. | |
| 982 | Bioduro San Diego, CA Lab Assistant Intern BS in Chemistry or a related scientific discipline Exp: 1 yr |
The Laboratory Assistant will be providing support to the Analytical Chemistry and Formulation Development departments. | |
| 983 | Merck Rockville, MD Quality Specialist BS science or technical degree Exp: 0-1 yrs |
Review assay data, protocols, reports, technical specifications, certificates of analysis, RIRs, Cell banking Production Records for compliance requirements. Review lab records, batch records, SOPs and other documents for auditing requirements. Audit routine assays. Conduct Systems Inspections. Interact with other departments to ensure compliance with internal procedures and FDA regulations Demonstrate verifiable turnaround times. Participate in projects, as assigned | 7/31/2017 |
| 984 | Merck Billerica , MA Research Associate I (Buffer/Media Prep and QC) BS technical discipline Exp: 1-5 yrs |
Scope of work include but not limited to, media / buffer preparation, equipment maintenance and calibration, data analysis, electronic lab notebook and batch record documentation. The candidate should have relevant industrial experience, aseptic skills, excellent communication skills and enjoys working in a fast paced environment. Collaboration with other PCS scientists and process development colleagues will be critical to this position. Responsible for media and buffer preparation to meet GLP tox protein production and reference run schedules, which includes raw material and chemical procurement and inventory control. The candidate will be responsible for documenting in batch records, electronic lab notebook, and revise ROPs related to GLP tox protein production. Ensure operations and documentation conform to ROPs and batch records are maintained to reflect current manufacturing methods. The candidate will also perform analyses including SDS-PAGE, SE-HPLC, LAL, HCP, HC-DNA and res-Protein A. In addition, the candidate will coordinate and execute equipment maintenance and calibration, and provide reports and prepare scientific presentations as needed. | 7/31/2017 |
| 985 | Merck Rockville, MD Associate Scientist I, Clearance Services BS scientific discipline Exp: 0-3 yrs |
The Associate 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. | 7/31/2017 |
| 986 | Merck Rockville, MD Virology Services - Associate Scientist I BS scientific discipline Exp: 0-3 yrs |
The Associate I (ASI) will perform safety testing required to manufacture clinical and commercial products. The ASI 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. | 7/31/2017 |
| 987 | Merck Billerica , MA Associate Scientist Upstream Process Development BS / MS biotechnology, biochemistry, or engineering Exp: 1-5 yrs |
The Protein Science / Late Stage Upstream Processing (USP) group, a core function that develops upstream processes for new biologics moving into the clinic, is seeking a motivated associate scientist to join our antibody discovery program at EMD Serono. Candidates will be primarily responsible for mammalian USP production of GLP Tox drug substance but will also develop processes at bench scale and later scale up to 200L bioreactors for a variety of therapeutic candidate proteins including monoclonal antibodies and Fc fusion proteins. Scope of work will include, but are not limited to, protein production for pre-clinical studies, UPS process development developing novel USP processes, data analysis and project reporting. Candidates should have experience in writing technical documents for process transfer to manufacturing. The candidate is expected to have excellent time management skills, with the ability to adapt to rapid changes in projects priorities and meeting aggressive timelines. These individuals should enjoy working in a team setting and can work well with research scientists, the manufacturing group as well as external collaborators. | 7/31/2017 |
| 988 | Mission Pharmacal Manhattan, NY Pharmaceutical Sales Rep - WH BS life science Exp: 1-2 yrs |
This position will report directly to the District Manager and must consistently meet or exceed all sales budgets / goals on all products assigned. Territory Sales Managers are expected to possess a high level knowledge of their product, customer and territory. An average of 10 sales calls / presentations per day to prescribers as well as triage nurses plus Pharmacy sales presentations as needed. All calls must be entered into the company assigned system along with notable post call notes, sample activity, etc. Territory Sales Managers are also expected to attend all company, regional and divisional meetings. Various administrative duties such as expense reporting are also required. Must also complete all fleet safety training and must maintain an acceptable driving record regarding accidents and incidents. | 7/31/2017 |
| 989 | Moderna Cambridge, MA Assoicate Engineer/Engineer, Process Development MS chemical engineering, chemistry, biochemical engineering, biochemistry, biophysics, or related Exp: 1 yr |
Moderna is seeking a highly skilled and motivated Associate Engineer / Engineer to join our Personalized Vaccines Unit. In this role, you will have the opportunity to contribute to the development of mRNA and LNP production processes for our Personalized Cancer Vaccine program, as well as separations of plasmid DNA template material. The incumbent is expected to participate in development of new unit operations, process scale-down, optimization, and the evaluation / acquisition of new process technologies. The applicant will work closely with the PVU team, as well as Moderna s core platform process development, analytical development and automation engineering departments to adapt existing technologies or develop new technologies for application in personalized medicine manufacturing. May collaborate with the PVU external manufacturing team for technical transfer to the manufacturing facility for GMP production. | 7/31/2017 |
| 990 | Moderna Cambridge, MA (Contract) Research Associate, In Vivo Pharmacology, Onkaido MS 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. Applicants should be both great team members and have a track record of independent research accomplishments. The ability to effectively communicate with internal team members is required. | 7/31/2017 |
| 991 | Moderna Cambridge, MA Manufacturing Associate BS technical discipline 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. He / she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in the Pilot Plant, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. | 7/31/2017 |
| 992 | Moderna Cambridge, MA (Contract) Research Associate, Delivery Innovation MS chemistry, biochemistry, biology, chemical engineering, or related Exp: 1-2 yrs |
This Contract Research Associate will be responsible for preparation and characterization of mRNA containing nanoparticles within a dynamic and highly interdisciplinary environment. He / she will be responsible for executing lab experiments, reporting results and maintaining a high-quality lab notebook. The successful candidate will work well within a larger team of chemists, engineers, formulation scientists and associates while mentoring and training junior members of the Delivery Innovation team. Experience with polymeric nanoparticle preparation techniques, biophysical / chemical characterization, and surface modification are preferred. The successful candidate must have a foundation in chemical, biological, or biochemical sciences or materials engineering with experience in the drug delivery field. | 7/31/2017 |
| 993 | Miltenyi Biotec Cambridge, MA Regulatory & Compliance Associate BS life sciences, chemistry, or related Exp: 1-3 yrs |
As a member of the Miltenyi Biotec Regulatory Affairs Team, you will be responsible to support company regulatory objectives in the maintenance of change control documentation, ensuring the utmost quality and accuracy at all times. You will use your excellent organization skills and attention to detail to support regulatory projects by assisting and maintaining change control systems. Overall, you will be a key contributor to the continued success of all submissions to North American regulatory agencies. | 7/31/2017 |
| 994 | Molecular Diagnostic Services San Diego, CA Molecular Biologist Technologist BS molecular biology or related Exp: 0 yrs |
Molecular Diagnostic Services, Inc (MDS) is currently seeking experienced Cellular / Molecular Biologist to join our talented team of scientists . Opportunities exist for eligible senior or graduate students seeking Molecular or related Biology degree | 7/31/2017 |
| 995 | Molecular Stethscope San Diego, CA Associate Bioinformatics Scientist MS bioinformatics or computer science Exp: 0 yrs |
We are looking for an associate bioinformatics scientist with strong programming skills and good understanding of molecular biology. He / she will work closely with the assay team both to provide bioinformatics support and develop novel analysis algorithms. Additional duties will include mining and analyzing publically available molecular and clinical databases. The successful candidate is expected to conduct his / her job responsibilities with a high degree of urgency, accuracy and professionalism. | 7/31/2017 |
| 996 | MolecularMD Portland , OR Clinical Medical Technologist II MS biology, medical technology, molecular biology, or related Exp: 0 yrs |
The CMT II will competently perform molecular procedures, including nucleic acid isolation, polymerase chain reaction; process clinical specimens using the appropriate equipment, instruments, or techniques to assure optimum patient specimen integrity and positive identification throughout the test process; perform and evaluate quality control procedures to assure that test execution, test methodologies, and equipment performance are all within the clinical protocol specifications; provide collaborative assistance to colleagues as requested; release findings per laboratory procedures using the Laboratory Information System; complete testing and assigned projects in a timely manner consistent with expected deliverables; assist with implementation of testing protocols; actively participate in development of guidelines, procedures, and operating instructions for assays / instruments as directed; participate in proficiency testing, maintain competency, and execute other projects and duties as assigned. This is a Mon-Fri position, including occasional weekends and holidays as required. | 7/31/2017 |
| 997 | MolecularMD Portland , OR Clinical Medical Technlogist I BS biology, medical technology, molecular biology, or related Exp: 0 yrs |
The CMT I will competently perform molecular procedures, including nucleic acid isolation, polymerase chain reaction; process clinical specimens using the appropriate equipment, instruments, or techniques to assure optimum patient specimen integrity and positive identification throughout the test process; perform and evaluate quality control procedures to assure that test execution, test methodologies, and equipment performance are all within the clinical protocol specifications; provide collaborative assistance to colleagues as requested; release findings per laboratory procedures using the Laboratory Information System; complete testing and assigned projects in a timely manner consistent with expected deliverables; assist with implementation of testing protocols; actively participate in development of guidelines, procedures, and operating instructions for assays / instruments as directed; participate in proficiency testing, maintain competency, and execute other projects and duties as assigned. | 7/31/2017 |
| 998 | Momenta Cambridge, MA Process Engineer I MS biochemistry, chemical / bichemical engineering, or related Exp: 0-3 yrs |
The individual will play a key role in developing purification process for biosimilars and innovative biologics to have desirable product quality attributes as well as supporting GMP manufacturing. Candidates must have a strong background in biologics process development (chromatography and filtration) and statistical data analysis. In addition, the responsibilities will include working with both internal collaborators and external CMOs to meet group objectives. | 7/31/2017 |
| 999 | Momenta Cambridge, MA Quality Control Associate BS / MS scientific discipline Exp: 1-3 yrs |
The QC Associate contractor will provide support for activities related to, installation / operation / performance qualification (IQ / OQ / PQ) scheduling and review. Equipment troubleshooting / maintenance, QC sample receipt, sample handling and record review related to data integrity. The QC Associate contractor will generate and / or maintain records or documents in a detailed and consistent manner in accordance with acceptable laboratory practices and regulatory criteria. | 7/31/2017 |
| 1000 | MPI Research Mattawan, MI Equipment Technician - Animal Services BS scientific discipline Exp: 1-3 yrs |
An Equipment Technician is part of a multi-faceted team that is responsible for providing compliant caging and support equipment for all laboratory animals and for performing assigned technical and administrative functions within the guidelines / requirements outlined in Standard Operating Procedures (SOPs) that are essential for producing sound, reliable data. The individual in this role may need to handle animals of multiple species | 7/31/2017 |
| 1001 | MPI Research Mattawan, MI QC Associate - Laboratory Sciences QC BS / MS scientific discipline 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. | 7/31/2017 |
| 1002 | MPI Research Mattawan, MI Research Assistant 1/Research Associate 1 - Pathlogy Services Histology AS technical discipline 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). | 7/31/2017 |
| 1003 | MPI Research Mattawan, MI Research Associate - LBA Development BS / MS technical discipline 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. | 7/31/2017 |
| 1004 | MPI Research Mattawan, MI Research Technician (Intern) - Animal Services BS technical discipline 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. | 7/31/2017 |
| 1005 | MPI Research Mattawan, MI Research Technician (Intern) - Large Animal Toxicology BS technical discipline 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. | 7/31/2017 |
| 1006 | MPI Research Mattawan, MI Research Technician (Intern) - Reproductive Toxicology DART BS technical discipline 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 | 7/31/2017 |
| 1007 | Assurex Mason, OH Lab Technician BS medical technology, clinical laboratory science, chemistry, chemical engineering, or related Exp: 1 yr |
At Assurex The Laboratory Technologist is responsible for specimen processing, test performance and reporting of test results according to laboratory procedures. This position reports to the Laboratory Manager. | 7/31/2017 |
| 1008 | Assurex Mason, OH Biostatician MS biostatistics Exp: 1 yr |
At Assurex the Biostatistician will provide statistical leadership in design, analysis, interpretation, and reporting of clinical trials and predictive modeling of pharmacogenomics data that help build the business. This position is in the Medical Affairs and Clinical Development and reports to the Senior Director of Biostatistics or his designee. | 7/31/2017 |
| 1009 | NAMSA Northwood, OH Metrologist BS engineering or scientific discipline Exp: 1-2 yrs |
Performs metrology assignments involving laboratory equipment. Maintains data in Equipment Management systems. Performs routine instrument calibrations. Generates appropriate documentation regarding calibrations, nonconformances, deviations, etc. Coordinates metrology assignments performed by outside vendors (including, but not limited to scheduling metrology events with approved vendors, providing vendors with correct standards to be followed, routing paperwork for approvals, reviewing vendor reports or compiling failure investigations when items are returned, etc.) Assists Engineers as needed with equipment qualifications / requalifications and other Engineering Projects. Other duties as assigned by the Engineering Manager. | 7/31/2017 |
| 1010 | nanoString Seattle, WA Manufacturing Research Associate I BS scientific discipline Exp: 0-2 yrs |
This position is responsible for supporting the production of Consumables 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. | 7/31/2017 |
| 1011 | Nanosyn Santa Clara, CA Research Associate, Synthetic Organic or Medicinal Chemist BS / MS organic chemistry or related Exp: 0-5 yrs |
The successful candidate must have the ability to work on multiple projects and adapt rapidly to new projects, must be a highly motivated, independent, and productive team player. Candidates with a demonstrated record of expertise in modern synthetic organic chemistry methods or medicinal chemistry are preferred. | 7/31/2017 |
| 1012 | NantKwest Inc. La Jolla, CA Research Associate (Analytical Development) MS biological science Exp: 1 yr |
The successful candidate will work as part of the Analytical team at NantKwest Inc., to support adoptive cell therapy projects based on our Natural Killer (NK) cell platform. We are a growing company that offers competitive salaries and benefits. We are seeking a motivated Senior Research Associate to assist in developing, optimizing and validating bioassays to support cell therapy projects. The applicant will have previous experience of working in an immunology laboratory (preferably working with primary cells and cell lines) and will be responsible for supporting the efficient operation of the laboratory and performing scientific studies to support cell therapy projects. | 7/31/2017 |
| 1013 | Assurex Mason, OH Quality Assurance Specialist III BS / BA Exp: 1-2 yrs |
The QA Specialist works closely with the Clinical Development team to provide support and strategic planning for the QA oversight of Clinical Development activities, including but not limited to regulatory authority GCP inspections, clinical sites preparation, SOP creation and implementation, and all other associated study documentation. This full-time position reports to the Associate Director of Clinical Development. | 7/24/2017 |
| 1014 | Assurex Mason, OH Lab Technician I BS / MS in medical technology, clinical laboratory science, chemistry or chemical engineering, biological or other physical science Exp: 1 yr |
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. | 7/24/2017 |
| 1015 | AstraZeneca Gaithersburg, MD R&D Associate II MS in Life Sciences Exp: 0-2 yrs |
Laboratory-based position for performing ligand binding immunoassay methods on routine basis according to SOPs with minimal supervision and relatively high throughput, supporting non-clinical and clinical PK and ADA. | 7/24/2017 |
| 1016 | AstraZeneca Gaithersburg, MD Operations Global Graduate Associate - US BS Exp: NA |
Your programme will provide an invaluable blend of on-the-job experience and coaching. There will be a huge support network behind you, including a highly credible and experienced mentor and programme manager. | 7/24/2017 |
| 1017 | AstraZeneca Gaithersburg, MD Research Associate II/Associate Scientist I MS in Biology, Bioengineering, or Molecular Biology Exp: 0-5 yrs |
The successful candidate will be responsible for a broad range of bioassay (binding and cell-based) development in the areas of cell biology and molecular biology. This individual focuses principally on developing immune- and cell-based assays, and carrying out biological characterization and testing of biopharmaceutical products, such as therapeutic monoclonal antibodies and recombinant proteins. | 7/24/2017 |
| 1018 | AstraZeneca Wilmington, DE Patient Safety Associate BS in biosciences Exp: 1-2 yrs |
The Patient Safety Associate conducts a wide range of pharmacovigilance activities of minimal to sometimes moderate scope and complexity on an individual basis working within established timeframes ensuring compliance with global and local procedures, policies, and processes. | 7/24/2017 |
| 1019 | AstraZeneca Gaithersburg, MD Research Associate I/II BS in chemistry, biochemistry or other related fields Exp: 1 yr |
The successful candidate will develop and utilize chromatographic, electrophoresis and spectroscopic methods to support the development of biopharmaceutical products. | 7/24/2017 |
| 1020 | Shanghai Aucta Pharmaceuticals Co., LTD 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 | 7/24/2017 |
| 1021 | Shanghai Aucta Pharmaceuticals Co., LTD 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. | 7/24/2017 |
| 1022 | Shanghai Aucta Pharmaceuticals Co., LTD North Brunswick, NJ Scientist, formulation 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 | 7/24/2017 |
| 1023 | Aura Biosciences Cambridge, MA Research Associate Cell Culture MS in biology or related field Exp: 1 yr |
Responsibilities include the cultivation of mammalian cells, transient transfection and harvest of culture biomass for the isolation of recombinantly produced prototocapsids. | 7/24/2017 |
| 1024 | 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. | 7/24/2017 |
| 1025 | 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. | 7/24/2017 |
| 1026 | Axsome Therapeutics New York, NY Clinical Trials Assistant BS in a 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. | 7/24/2017 |
| 1027 | Bausch + Lomb Tampa, FL Microbiology Technician III BS in Microbiology, Biology, or related science Exp: 1-2 yrs |
Perform routine testing for release of raw materials, finished products, stability samples and R&D products. Perform Environmental and Utility Monitoring in aseptic areas. | 7/24/2017 |
| 1028 | Bausch + Lomb Union City, GA Contract Quality Control Associate - Microbiology BS Exp: 1 yr |
The successful candidate will assist with product testing, environmental monitoring, raw material testing and general laboratory maintenance. The ability to function in a fast-paced, highly technical environment, and communicate effectively is essential to success. | 7/24/2017 |
| 1029 | Bausch + Lomb Union City, GA Quality Control Specialist BS Exp: 1 yr |
Performs routine and non-routine analysis of environmental monitoring program, as well as raw materials, in-process and finished products during release or stability testing. | 7/24/2017 |
| 1030 | Bausch + Lomb Rochester, NY Engineer 1, Process Development BS / MS in Chemical Engineering Exp: 0-3 yrs |
Performs and coordinates associated new product development action items. Provides support for compounding, filling, packaging and labeling of sterile lens care solution products in Pilot Facility for development, stability and clinical study supplies to support new product development and product lifecycle management activities. Performs statistical data analysis. | 7/24/2017 |
| 1031 | Bausch + Lomb Union City, GA Contract Quality Control Associate - Bioassay BS Exp: 1 yr |
The successful candidates will assist with product testing, raw material testing and general laboratory maintenance. The ability to function in a fast-paced, highly technical environment, and communicate effectively, is essential to success. | 7/24/2017 |
| 1032 | Bausch + Lomb Union City, GA QC Specialist - Lab Services BS Exp: 1-3 yrs |
This is an exciting position accountable for laboratory support of Dendreon s products and in accordance with appropriate regulatory, corporate and scientific guidelines. The ability to function in a fast-paced, highly technical environment, and communicate effectively is essential to success. | 7/24/2017 |
| 1033 | Baxter Mountain Home, AK Engineer I BS in Engineering Exp: 0-1 yr |
Document development work including writing specifications for manufacturing or scientific test results. | 7/24/2017 |
| 1034 | Baxter Cleveland, MS Quality Lab Assoc I BS in Chemistry, or Biological Science Exp: 0-2 yrs |
Perform chemical and physical analysis on medical products through all stages of the manufacturing process from incoming raw materials through to product release. Areas include raw materials, initial, in-process and finished products, stability program, protocol support, instrumental analysis and instrument calibration / qualifications. | 7/24/2017 |
| 1035 | Baxter Round Lake, IL Engineer II BS in Engineering Exp: 1-3 yrs |
Supports IV Administration Disposable sets. Displays standard engineering principles to resolve difficult problems, from conception to final design with supervision from senior level engineering individuals. Plans, schedules and leads project assignments (Change Control) on low-to-mid level complexity projects in the evaluation, selection and adaptation of various engineering techniques, procedures and criteria with minimal guidance. | 7/24/2017 |
| 1036 | Baxter Medina, NY Quality Engineer II, Mfg Sup BS in Engineering Exp: 1-3 yrs |
The Quality Engineer II position has primary responsibility for driving overall quality performance, improvement, and compliance throughout the organization. | 7/24/2017 |
| 1037 | Baxter Round Lake, IL Quality Engineer II BS in Engineering Exp: 1-3 yrs |
The Quality Engineer II is responsible to review and analyze quality data, identify emerging issues, and drive improvements. The Quality Engineer II is responsible for his / her own individual efforts to achieve quality and business objectives. | 7/24/2017 |
| 1038 | Baxter Marion, NC Quality Lab Assoc III 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. | 7/24/2017 |
| 1039 | Baxter Marion, NC Quality Lab Assoc I - Chemist BS in Chemistry, or Biological Science 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. | 7/24/2017 |
| 1040 | BD Columbus, NE Process Engineer BS Exp: 0 yr |
This position is responsible for supporting the manufacturing operation. This individual will develop and implement improved methods of manufacturing, procedures, and processes that result in improved efficiencies, yields, machine operations, and quality. Provides technical support to the development group for the implementation of new products or processes. | 7/24/2017 |
| 1041 | BD Baltimore, MD Scientist I - Cell Culture BS Exp: 0-2 yrs |
The Scientist I - Cell Culture focuses on lab management and maintenance to support the design and development of cell culture media and supplement formulations. The Scientist I will also participate on R&D teams to support studies in the areas of new product development and existing product support | 7/24/2017 |
| 1042 | BD Franklin Lakes, NJ R&D Engineer I MS in Mechanical, Materials Science, or Biomedical Engineering Exp: 0-2 yrs |
Actively participate in aspects of design and development activities for a variety of drug delivery products in a design control environment | 7/24/2017 |
| 1043 | BD Mannford, OK Quality Engineer I BS Exp: 1 yr |
As directed by the Quality Manager, the Quality Engineer I is accountable for supporting new product development and product maintenance through the application of Quality engineering skills for medical devices. This person will handle projects and tasks, from product inception through product launch and maintenance and play an active role in the processes to ensure products meet quality standards consistent with both Corporate and unit policies, while meeting all design control and other regulatory requirements. | 7/24/2017 |
| 1044 | BD Broken Bow, NE Quality Engineering Assistant BS Exp: 1 yr |
The Quality Engineering Assistant tests product and / or components for function; Collects and analyzes data; Plans and coordinates special project activities / Factory Work Orders; Administers product testing procedures; Executes and / or supports plant studies and validations; Writes and / or Revises all types of documents, forms and policy procedures; Writes / Originates ECR / O s; Serves as backup for incoming inspection. | 7/24/2017 |
| 1045 | Averica Discovery Services Inc Marlborough, MA Analytical Chemistry Summer Intern BS in Chemistry or related Exp: NA |
Support the routine day-to-day laboratory operation including glass washing and solution and sample preparation. | 7/24/2017 |
| 1046 | aTyr Pharma San Diego, CA SCIENTIFIC INTERN BS in a life sciences Exp: NA |
Tasks will include assisting scientific staff with a number of different types of assays such as ELISA and other immunological assay techniques, as well as maintaining cell lines in culture and performing in vitro cell based experiments including the use of flow cytometry. | 7/24/2017 |
| 1047 | Arthrex, Inc. Naples, FL Pre - Production Intern BS Exp: NA |
The goal of this internship is to provide a candidate with experience in data management within a structured project. The intern will contribute by sorting data tables by relevant criteria necessary for input into risk assessments. | 7/24/2017 |
| 1048 | Medtronic Brooklyn Center, MN Technician I AS applied science or related Exp: 0-2 yrs |
In addition to performing electrical and mechanical testing to support data analysis, the selected candidate will also provide logical troubleshooting of electronic circuits. Other tasks that may occur are on a daily basis are: Setting up experiments using oscilloscopes, power supplies, and multimeters. Building and assembling test boards for batteries and capacitors. Developing and following procedures to test electrical components. | 7/24/2017 |
| 1049 | Merz Mesa, AZ Engineering Technician AS scientific discipline Exp: 1 yr |
Work from drawings, written and oral instructions, or defined plans to fulfill process and product development project requirements. Assignments / Requirements include documentation of assembly procedures, test methods, qualifications, specifications and drawings of parts, fixtures and molds | 7/24/2017 |
| 1050 | MSD Gaithersburg, MD Research Associate I BS life sciences, cellular and molecular biology, protein sciences, or related 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. | 7/24/2017 |
| 1051 | Metabolon Research Triangle Park, NC Assistant Scientist, Data Curration BS physical or mathematical science Exp: 0 yrs |
This is an entry-level position and will be responsible for checking software matches to chemical spectra from biological samples to a library of biochemicals. The successful candidate will have experience in basic chemistry or strong mathematical skills. This is a 6 month temporary position. | 7/24/2017 |
| 1052 | Mayne Pharma Group Greenville, NC Analytical Calibration Technician AS applied science or related Exp: 1 yr |
This position is an intermediate level metrology technician position. | 7/24/2017 |
| 1053 | Mayne Pharma Group Greenville, NC Analytical Chemist I BS / BA chemistry, pharmaceutical sciences, biology, or related Exp: 0-1 yrs |
This position is primarily responsible for performing routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. | 7/24/2017 |
| 1054 | Idex Corporation Bristol, CT All Level Machining AS / BS technicial discipline Exp: 1 yr |
Operates numerical control machines to perform various machine functions such as cutting, drilling, milling, reaming and boring by performing the following duties. | 7/24/2017 |
| 1055 | Idex Corporation Albuquerque, NM Applications Engineer BS physics, engineering, or related Exp: 1-3 yrs |
Generates new and maintains present business with existing and new customers within the Defense, Sensing, and Security (DSS) and Industrial (IND) market segments; assists in identifying new product improvement and development opportunities; assists in identifying and assessing competitors within the DSS and IND segments; handles the technical portion of trade compliance paperwork, including import and export related documentation. Assists in developing and maintain processes for trade compliance for sales and operations. Stays current with optical industry trends and technology in addition to trade compliance changes and updates. Provides technical assistance as needed to sales team. | 7/24/2017 |
| 1056 | Idex Corporation Rochester, NY Optical Manufacturing Engineer BS / MS engineering Exp: 1-5 yrs |
Apply experience with opto-mechanicalassemblies and laser alignment to develop and implement equipment & procedures necessary to assemble, test, and contribute to the manufacture of high performance imaging systems Review customer / design engineering specifications, drawings and other supporting documents. Investigate and initiate corrective action to manufacturing problems arising in the manufacture of one or more of the following: optical components, parts and materials, assembly of optical, mechanical, electrical, electronic or electromechanical units, assemblies, subsystems and systems or manufacturing problems associated with the inspection and / or testing of organization produced products. Review, evaluate, propose and make drawing changes on production released material and coordinates these changes with manufacturing and support groups Act as technical liaison between production planning and engineering personnel. Use tools, such as interferometers, laser alignment stations, power meters and distortion test equipment Apply experience with manufacturing processes including Six Sigma, lean manufacturing, and statistical process control (SPC) Lead the transitions of projects from design to production | 7/24/2017 |
| 1057 | Micropoint Santa Clara, CA Quality Control Associate MS chemistry, biology, or related Exp: 0 yrs |
We are looking for highly motivated QC Associates (two openings) to join our quality team. 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. | 7/24/2017 |
| 1058 | MicroVention Terumo Tustin, CA Engineer I, Manufacturing Process (ID: 4009BR) BS engineering Exp: 0-3 yrs |
The Manufacturing Process Engineer I supports manufacturing process development and the manufacturing of products for medical devices including writing or verifying specifications, maintaining product process, designing fixtures, test processes, equipment and raw materials to ensure the concepts, subassemblies, finished products, and / or prototypes meet requirements. The successful candidate will also work closely with R&D, Quality, and Regulatory in supporting the development of new products and manufacturing processes to achieve a smooth, successful transfer to Manufacturing Engineering and Production for launch. | 7/24/2017 |
| 1059 | MRIGlobal Charlottesville, VA Microbial Scientist BS / BA biology, molecular biology, microbiology, biochemistry, or related Exp: 0 yrs |
Our laboratory located in Charlottesville, Virginia is looking for an entry level scientist to work in a microbial forensics laboratory. This staff member will become an integral part of our team receiving vital experience with research, sample preparation and analysis, while gaining a thorough understanding of relevant federal regulations, QA / Safety / SOPs, and instrumentation. | 7/24/2017 |
| 1060 | MRIGlobal Kansas City, MO Electrical Engineer BS electrical engineering Exp: 0 yrs |
MRIGlobal has an exciting opportunity for an entry level Electrical Engineer in our Intelligence, Surveillance, and Reconnaissance Division located in Kansas City, MO. In this unique opportunity, the selected candidate will work with other engineering and technical disciplines in the design, prototyping, and testing of custom systems to meet customer requirements. | 7/24/2017 |
| 1061 | Takeda San Diego, CA Intern - Structural Biology and Biophysics BS / MS healthcare, pharmacy, or life science Exp: 2 yrs coursework |
Takeda'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. | 7/24/2017 |
| 1062 | Takeda San Diego, CA Intern - Analytical Development BS / MS healthcare, pharmacy, or life science Exp: 2 yrs coursework |
The internship is a laboratory position that involves sample preparation and analysis in a pharmaceutical research lab . The intern will work closely with analytical / formulation scientists in the lab and learn techniques in characterizing small molecule drug candidates. | 7/24/2017 |
| 1063 | Takeda San Diego, CA Intern - Intellectual Property BS / MS healthcare, pharmacy, or life science Exp: 2 yrs coursework |
The purpose of this position is to continuously provide support to the IP Department in the areas of sorting, scanning, and saving IP documents as well as other admin duties. | 7/24/2017 |
| 1064 | Takeda Brooklyn Park, MN Quality Control Analyst I - BioAssay BS / MS life science 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. Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS). Follow SOPs to perform methods requiring precise analytical skills and understanding of biology and chemistry principles. | 7/24/2017 |
| 1065 | Takeda Brooklyn Park, MN Automation Engineer BS chemical engineering or related Exp: 0-5 yrs |
Act as technical owner for Process and Utility Systems, with respect to automated process. Assist Process Engineering personnel with equipment qualification, support of ongoing operations, deviation resolution, maintenance, and decommissioning | 7/24/2017 |
| 1066 | Takeda Brooklyn Park, MN Quality Systems Specialist II MS life science Exp: 0-2 yrs |
This individual will serve as the primary Business Administrator and lead subject matter expert (SME) for Takeda's Electronic Quality Management System (EQMS) and other applications, as they arise. This person supports and delivers training on quality management procedures and workflows (e.g., deviation, OOS, CAPA). This position is responsible for routine monitoring, reporting and escalation of quality performance metrics according to established controlled procedures. | 7/24/2017 |
| 1067 | Takeda Brooklyn Park, MN Quality Control Laboratory Technician BS life science or related Exp: 0-3 yrs |
Perform supportive activities for general lab readiness including laboratory media and solution preparation, maintenance of equipment and glassware. Perform laboratory sample receipt, preparation, coordination, and maintenance of laboratory sample and supply inventories. Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS). Follow SOPs to perform activities and test methods requiring an understanding of biology and chemistry principles, as well as cGMP laboratory | 7/24/2017 |
| 1068 | Merck Carlsbad, CA Environmental Monitoring Technician AS scientific discipline Exp: 1 yr |
The Technician will support or perform environmental monitoring and a wide variety of testing required to support process development and manufacturing under supervision. Perform a wide variety of laboratory testing activities such as media growth promotion bioburden testing, endotoxin testing, execution of protocols, qualification and testing of biological indicators, identify and assess isolated colonies and ensure that SOPs are followed and data generated are accurate | 7/24/2017 |
| 1069 | Merck Haverhill, MA QC Technician BS chemistry Exp: 1 yr |
This position is responsible for the quality test and release of all materials received and produced at our Haverhill, MA facility. Standard tests include Karl Fischer titration, NMR spectroscopic analysis, ICPOES, ICPMS and HPLC analyses. This position will also be responsible for the quality release of goods in our SAP QM system as well as product CoA creation. | 7/24/2017 |
| 1070 | Merck Rockville, MD Scientific Associate I BS scientific discipline Exp: 0-3 yrs |
The Associate I (ASI) will perform safety testing required to manufacture clinical and commercial products. The ASI 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. | 7/24/2017 |
| 1071 | Merck Sheboygan Falls, WI Associate Production Scientist BS chemistry, biochemistry, biology, chemical engineering, or related 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. | 7/24/2017 |
| 1072 | Merck Jaffrey, NH Automation & Robotics Technician AS technical discipline Exp: 1-2 yrs |
The role of Automation Technician IV in the Production Maintenance Department reporting to the Maintenance Supervisor. This position will focus on the daily maintenance and continuous improvement of automated production equipment. This position will also provide technical support for the engineering department with the execution of change controls, OQ / IQ protocols and other related actions. This position will also provide guidance and support to more junior level technical maintenance personnel. | 7/24/2017 |
| 1073 | Merck Billerica, MA Associate Scientist Upstream Process Development BS / MS biotechnology, biochemistry, engineering, or related Exp: 1-5 yrs |
The Protein Science / Late Stage Upstream Processing (USP) group, a core function that develops upstream processes for new biologics moving into the clinic, is seeking a motivated associate scientist to join our antibody discovery program at EMD Serono. Candidates will be primarily responsible for mammalian USP production of GLP Tox drug substance but will also develop processes at bench scale and later scale up to 200L bioreactors for a variety of therapeutic candidate proteins including monoclonal antibodies and Fc fusion proteins. Scope of work will include, but are not limited to, protein production for pre-clinical studies, UPS process development developing novel USP processes, data analysis and project reporting. Candidates should have experience in writing technical documents for process transfer to manufacturing. The candidate is expected to have excellent time management skills, with the ability to adapt to rapid changes in projects priorities and meeting aggressive timelines. These individuals should enjoy working in a team setting and can work well with research scientists, the manufacturing group as well as external collaborators. | 7/24/2017 |
| 1074 | Merck Billerica, MA Associate Scientist Downstream Process Development BS / MS biotechnology, biochemistry, engineering, or related Exp: 1-5 yrs |
The Protein Science / Late Stage Downstream Processing (DSP) group, a core function that develops purification processes for late stage and produces drug substance for pre-clinical GLP Tox studies, is seeking motivated and experienced scientists to join our antibody discovery program at EMD Serono. Candidates will be primarily responsible for DSP production of GLP Tox drug substance but also for developing purification processes for a variety of therapeutic candidate proteins including monoclonal antibodies and Fc fusion proteins. Scope of work will include, but are not limited to, protein purification, biochemical and biophysical characterization of proteins, novel purification technologies, purification process development, data analysis and project reporting. Candidates should have experience in writing technical documents for process transfer to manufacturing. The candidate is expected to have excellent time management skills, with the ability to adapt to rapid changes in projects priorities and meeting aggressive timelines. These individuals should enjoy working in a team setting and be able to work well with research scientists, the manufacturing group as well as external collaborators. | 7/24/2017 |
| 1075 | Miltenyi Biotec Sunnyvale, CA Manufacturing & PD Intern BS life sciences, immunology, and / or cell biology Exp: 1 yr coursework |
As an intern with the Miltenyi Biotec Sunnyvale Team, you will have the exciting opportunity to assist in both the process development and manufacturing of cell therapy products within a regulated environment. | 7/24/2017 |
| 1076 | Miltenyi Biotec Santa Barbara, CA Owl - Production Intern BS mechanical engineering or related Exp: 1 yr coursework |
This will be a paid part-time internship for an undergraduate in the Engineering field. The ideal candidate will have the strong ability to troubleshoot problems and provide solutions using critical thinking, engineering fundamentals, and rapid prototyping. The intern will assist the Operations team with incoming and outgoing inspections as well as assist with the fabrication and development of tools and fixtures used during production to improve manufacturing quality and efficiency. | 7/24/2017 |
| 1077 | Miltenyi Biotec Cambridge, MA Regulatory Affairs Associate BS 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. | 7/24/2017 |
| 1078 | Alkermes Waltham, MA In - Vitro Pharmacology, Contractor BS / MS Exp: 0-3 yrs |
Alkermes is searching for a contract research associate to help with general routine lab work, including cell culture, protein / plasmid DNA purification and quantitation, and compound preparation, and management for assay-ready plates (96 and 384-well format). | 7/18/2017 |
| 1079 | Ajinomoto Althea, Inc. San Diego, CA QC Raw Materials BS in a Life Sciences discipline Exp: 0-2 yrs |
The QC Assistant, Raw Materials will conduct routine analysis, inspect, test and release raw materials and Active Pharmaceutical Ingredients (APIs) under supervision. The QC Assistant may focus in a specialized area and provide a supporting role in any of the following areas: incoming material inspection and sampling, inspection of vials and stoppers for defects, test method qualification, material qualification, dimensional analysis of components, chemical identification or other lab tests, inspection of commercial packaging materials, lab cleaning and maintenance, maintenance of QC files and paperwork. | 7/18/2017 |
| 1080 | Ajinomoto Althea, Inc. San Diego, CA QC Micro BS in a Life Sciences discipline Exp: 0-2 yrs |
The QC Assistant Micro is responsible for performing environmental monitoring and testing of the utilities using microbiological methods and other means. The QC Assistant Micro may also perform routine analysis and testing according to standard operating procedures in a GMP environment. | 7/18/2017 |
| 1081 | Ajinomoto Althea, Inc. San Diego, CA LIMS ANALYST BS in Chemistry, Chemical Engineering Exp: 0-2 yrs |
The LIMS Analyst supports the development, validation, and maintenance of the SampleManager Laboratory Information Management System (LIMS) and related technologies within Ajinomoto Althea s GMP facilities. In this role you will collaborate with the LIMS Administrator, internal Quality groups and Manufacturing, as well as IT to develop and maintain solutions that provide a more efficient and compliant work environment. | 7/18/2017 |
| 1082 | AMAG Pharmaceuticals, Inc. Tucson, AZ Quality Control Technician BS Exp: 1 yr |
As a member of the Quality team, this role is responsible for providing our internal customers with technical expertise while maintaining the highest quality services possible. | 7/18/2017 |
| 1083 | AMAG Pharmaceuticals, Inc. Waltham, MA QA Specialist - Product Complaint BS in science, engineering Exp: 1 yr |
The QA Specialist - Product Complaint is responsible for overseeing the Product Quality Complaint (PQC) process as well as participating in additional aspects of the post-market surveillance program at AMAG. This role will initiate incoming Product Complaints, lead and / or facilitate investigations both at AMAG and at CMOs, and will interface with end users and call centers to obtain Product Complaint information. This role will interface with key members of Quality, Technical Operations, and Pharmacovigilance to perform the previously described functions. | 7/18/2017 |
| 1084 | Amgen Cambridge, MA Associate Rapid Analytics BS in Analytical Chemistry, Physical, Life Sciences or related technical discipline Exp: 1-3 yrs |
The Associate responsibilities include, but are not limited to, the following:Obtain assignment and follow scientific direction of Rapid Analytics managers, flag issues and seek guidance appropriately. | 7/18/2017 |
| 1085 | Amgen South San Francisco, CA Senior Associate MS Exp: 1 yr |
Position to work as Senior Associate in the anatomic pathology laboratory. Validate and execute specialized tissue-based assays that are geared to support specific portfolio related questions on target expression. Use your extensive repertoire of pathology expertise to manage / troubleshoot projects independently | 7/18/2017 |
| 1086 | Amneal Pharmaceuticals Piscataway, NJ Regulatory Affairs Associate I eCTD publisher BS Exp: 1-2 yrs |
The RA Associate I eCDT Publishing, performing the routine submission publishing activities associated with electronic submission of ANDA / IND / NDA using ISIWriter , ISIToolBox and eCTDXpress with thorough knowledge of FDA s guidance such as PDF specifications, Content and Format of ANDA, Providing Regulatory Submissions in Electronic Format as well as ICH M2 and M4 guidance. | 7/18/2017 |
| 1087 | Amneal Pharmaceuticals Brookhaven, NY Jr. Validation Engineer BS Exp: 0-1 yr |
This position provides support to perform equipment, facility and utility qualification activity and requalification activity to ensure compliance to cGMP and Amneal quality requirement. | 7/18/2017 |
| 1088 | Amneal Pharmaceuticals Brookhaven, NY Project Management Coordinator BS in Regulatory Affairs, Pharmacy, Pharmaceutical Chemistry or related fieled Exp: 1 yr |
The Project Management Coordinator will handle the complete portfolio on Excipients for all R&D and filed projects of Amneal US starting from project initiation till products gets commercialized. | 7/18/2017 |
| 1089 | Amneal Pharmaceuticals Piscataway, NJ Scientist I - ArD BS in Chemistry or related Science discipline Exp: 0-1 yr |
The Scientist-I position is an entry level, and it contributes to tasks associated to pharmaceutical analysis intended for drug product development. The preliminary activity includes following schedules, direction of compendia standards and in-house standard operating procedures to analyze pharmaceutical drug substance, excipients, drug product testing for release and stability samples. | 7/18/2017 |
| 1090 | Amneal Pharmaceuticals Piscataway, NJ Scientist I - AR&D BS in Chemistry or related Science discipline Exp: 0-1 yr |
The Scientist-I position is an entry level, and it contributes to tasks associated to pharmaceutical analysis intended for drug product development. The preliminary activity includes following schedules, direction of compendia standards and in-house standard operating procedures to analyze pharmaceutical drug substance, excipients, drug product testing for release and stability samples. Perform quantitative analysis for pharmaceutical drug-substances, excipients and drug products using USP / NF, EP, in-house test methods and standard protocols, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs. Utilize techniques of Spectrophotometry, HPLC, GC, dissolution, and wet chemistry tests in accordance with the USP. Interpret and communicate analytical results. Contribute to technical problem solving and troubleshooting as needed. | 7/18/2017 |
| 1091 | Albany Molecular Research, Inc. GRAFTON, WI QUALITY CONTROL ANALYST BS Exp: 1-2 yrs |
Conducts testing using approved analytical methods. Applies established laboratory methods or techniques to analysis, develops solutions to problems. | 7/18/2017 |
| 1092 | Albany Molecular Research, Inc. Albany, NY Research Scientist I - Analytical Technologies BS / MS in Natural Science or Pharmacy Exp: 0-2 yrs |
The principal responsibility of the Research Scientist I is the analysis by multiple procedures of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the chemist's performance rating will be based on productivity. | 7/18/2017 |
| 1093 | Albany Molecular Research, Inc. Lebanon, NJ Analytical Chemist (Temporary) BS in Chemical Engineering, Chemistry or related science Exp: 1-5 yrs |
Assist laboratory manager in the performance of raw materials testing according to USP, EP, JP, FCC, ASTM, AOCS, and / or methods provided by clients. | 7/18/2017 |
| 1094 | Albany Molecular Research, Inc. Springfield, MO Analytical Chemist MS in analytical chemistry or related field (forensic chemistry, material sciences, organic chemistry) 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. | 7/18/2017 |
| 1095 | Albany Molecular Research, Inc. Rensselaer, NY Research Scientist I/II - Analytical BS / MS in Chemistry, Pharmaceutical Science or related science Exp: 0-5 yrs |
The principal responsibility of the Research Scientist I / II is the analysis of intermediates and target compounds by multiple procedures. The Research Scientist I / II is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist's performance rating will be based on productivity. | 7/18/2017 |
| 1096 | Albany Molecular Research, Inc. Burlington, MA QUALITY ASSURANCE INCOMING MATERIAL TECHNICIAN BS in chemistry or microbiology Exp: 1-3 yrs |
The Quality Assurance (QA) incoming Material Technician will be responsible for the receipt, inspection, sampling, and release of incoming materials and components. | 7/18/2017 |
| 1097 | Albany Molecular Research, Inc. Lebanon, NJ QUALITY ASSURANCE DOCUMENTATION SPECIALIST BS Exp: 1-2 yrs |
Ensure integrity of Quality Assurance Documents and assist Quality Assurance Unit in maintaining Quality Systems in accordance with FDA regulations. | 7/18/2017 |
| 1098 | EAG Laboratories St. Louis, MO Scientist MS in Chemistry Exp: 0-2 yrs |
At EAG, you will be part of a diverse team of research chemists and scientists responsible for chemical analysis and formulation support. Our chemical testing lab offers formulation (reverse engineering) contaminant identification, custom synthesis, product development, litigation support and expert witness services. | 7/18/2017 |
| 1099 | EAG Laboratories Easton, MD Quality Assurance Representative BS in biology, Chemistry or any other related scientific field Exp: 0-2 yrs |
The ideal candidate will have Quality Assurance responsibilities for toxicology programs. | 7/18/2017 |
| 1100 | EAG Laboratories Gainesville, FL Biologist 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. | 7/18/2017 |
| 1101 | EAG Laboratories Easton, MD Chemist, Analytical Chemistry BS / BA in Chemistry Exp: 0-4 yrs |
This individual is responsible for performing all assigned related tasks in accordance with relevant regulatory requirements to include Good Laboratory Practice (GLP) The ideal individual will be responsible for the conduct of analytical procedures used to assess the concentration and degradation of chemicals (pesticides, industrial chemicals, and pharmaceutical products) in a variety of matrices. | 7/18/2017 |
| 1102 | Antech Diagnostics Richmond, VA Laboratory Generalist I BS Exp: 0-1 yr |
As a Laboratory Generalist I you will work with the Lead Laboratory Technician to ensure the lab is running efficiently to meet and / or exceed goals. The ideal candidate will have prior experience performing some clinical diagnostic testing. | 7/18/2017 |
| 1103 | Antech Diagnostics Richmond, VA Laboratory Generalist - Float Tech BS in Medical Technology Exp: 1 yr |
As a Laboratory Generalist - Float Tech you will work closely with the management team to ensure the department is running efficiently to meet and / or exceed departmental goals. The ideal candidate will have prior experience performing some clinical diagnostic testing. | 7/18/2017 |
| 1104 | Applied Medical Rancho Santa Margarita, CA Product Quality Engineer BS in Mechanical Engineering, Biomedical Engineering, or similar engineering discipline Exp: 1 yr |
Evaluate product performance upon return from the customer;Perform device analysis in accordance with model-specific procedures and protocols. | 7/18/2017 |
| 1105 | Applied Medical Rancho Santa Margarita, CA Process Engineer II BS in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 yrs |
As a Process Engineer II, you will use skills related to sustaining and improving production manufacturing processes as part of a cross-functional team. | 7/18/2017 |
| 1106 | Applied Medical Rancho Santa Margarita, CA Regulatory Affairs Analyst, Post Market BS Exp: 1 yr |
Track the status of complaints throughout the entire complaint handling process;Facilitate the effective and efficient management of this process to enable timely closure of complaints. | 7/18/2017 |
| 1107 | Applied Medical Rancho Santa Margarita, CA Quality Engineer II BS in an Engineering or STEM field Exp: 1-2 yrs |
As a Quality Engineer II, you will use your skills to support medical device quality through design controls, process validations and documentation as part of a cross-functional team. | 7/18/2017 |
| 1108 | Applied Medical Rancho Santa Margarita, CA Quality Assurance Specialist BS in Engineering, Physical or Biological Sciences, other technical disciplines or equivalent Exp: 1-5 yrs |
Provide Quality Management System input and support to teams in an effort to implement improvements to Applied Medical's product design and manufacturing processes | 7/18/2017 |
| 1109 | Applied Medical Rancho Santa Margarita, CA Associate Engineer BS in Engineering, Science Exp: 1 yr |
Develop and update engineering documents such as manufacturing instructions, drawings and test procedures | 7/23/2017 |
| 1110 | Applied Medical Rancho Santa Margarita, CA Design Engineer II BS in Mechanical, Biomedical, Industrial, or Manufacturing Engineering Exp: 1-2 yrs |
As a Design Engineer II, you will use skills related to design and development of medical device components and fixtures as part of a cross-functional team. | 7/23/2017 |
| 1111 | Array BioPharma Boulder/Cambridge/Morrisville, CO GCP/Sr. GCP QA Specialist BA / BS Exp: 1-2 yrs |
This position is responsible for evaluating the compliance of clinical studies to FDA and International regulations and guidelines, as well as corporate policies and standard operating procedures | 7/24/2017 |
| 1112 | 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. | 7/18/2017 |
| 1113 | MedPace Many, Ma University of Kentucky - Clinical Trial Recruitment Intern BS scientific discipline Exp: 1 yr coursework at University of Kentucky |
Medpace is looking for a qualified Clinical Trial Recruitment Intern! As a paid, part-time clinical trial recruiter you will have the opportunity to work externally as a representative of Medpace s Clinical Pharmacology Unit on your college campus for the 2017-2018 academic year. | 7/18/2017 |
| 1114 | MedPace Dallas , TX Clinical Research Associate - Dallas Entry Level BS health science or related Exp: 1 yr |
The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and / or health / life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!. The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and / or health / life science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!. | 7/18/2017 |
| 1115 | LabCorp Durham, NC Cytogenetic Technologist Trainee BS biology, cytogenetics, clinical lab sciences, or related Exp: 0 yrs |
FISH technologists independently perform laboratory tasks designed to diagnose chromosomal abnormalities from patient specimens | 7/18/2017 |
| 1116 | LabCorp San Antonio, TX Technician AS medical laboratory technology or related Exp: 1-3 yrs |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in a designated technical department. Interprets results, subject to verification by Technologist / Supervisor, and providing allowance by State regulations. | 7/18/2017 |
| 1117 | LabCorp Phoenix, AZ Technologist - Chemistry AS / BS medical technology or related Exp: 1-3 yrs |
Under general supervision, the Medical Technologist performs a variety of routine and complex clinical laboratory tests on body fluids and substances requiring independent judgment, speed and accuracy and with the highest standard of professional performance. Manage problems that affect test performance or reporting of test results. Adhere to quality control procedures including documentation, instrument and procedural calibrations and instrument maintenance. Perform all job duties in accordance with established standards and quality control to ensure high quality patient care. Other duties as assigned. | 7/18/2017 |
| 1118 | LabCorp Durham, NC Molecular Oncology Technologist BA / BS biology or related Exp: 1 yr |
The Integrated Oncology division of LabCorp is seeking a Technologist to join their Molecular Oncology team! Assays performed in the Molecular Oncology Department utilize a variety of scientific techniques, including PCR, fragment analysis, sequence analysis, and gel electrophoresis. | 7/18/2017 |
| 1119 | LabCorp Quantico, VA Biologist BS biology, chemistry, or related Exp: 1 yr |
The Biologist will be responsible for assisting the Forensic Examiners in DNA disciplines (nuclear and mitochondrial) with processing and examining a wide range of evidence and forensic materials associated with IED-s.The Biologist will also be also responsible for interacting and collaborating with other group and / or team members and other forensic staff to ensure a high quality and accurate product. | 7/18/2017 |
| 1120 | LabCorp Tampa, FL Medical Technician AS medical laboratory technology or related Exp: 1-3 yrs |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in a designated technical department. Interprets results, subject to verification by Technologist / Supervisor, and providing allowance by State regulations. | 7/18/2017 |
| 1121 | LabCorp Westborough, MA Molecular Technologist BS / MS biology, chemistry, or related Exp: 0-1 yrs |
The Integrated Genetics Division of LabCorp is seeking a Molecular Technologist to join their Molecular Diagnostics team! The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing 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 | 7/18/2017 |
| 1122 | Medtronic Portsmouth, NH Quality Engineer MS electrical engineering or related Exp: 0 yrs |
This position has the responsibility and authority to perform Quality Engineering functions including inspection and testing, calibration, procedure writing, and statistical analysis of quality data. The Quality Engineer must be able to prioritize activities and allocate resources for greatest effectiveness. The Quality Engineer must deal with both concrete and abstract problems on a daily basis. | 7/18/2017 |
| 1123 | Medtronic Mounds View , MN Associate Hardware Engineer BS electrical engineer r related Exp: 0-1 yrs |
As an Associate Hardware Engineer, you will design and develop verification environments, test benches, tools, and methodologies used to evaluate a medical device based on an embedded architecture. This job requires the development and operation of tools in a UNIX / LINUX operating system. This job requires knowledge of embedded device verification, which requires formal documentation, technical reviews, and demonstrating compliance to regulations. This job requires knowledge of an embedded device consisting of a microprocessor and embedded firmware. | 7/18/2017 |
| 1124 | Medtronic Fridley, MN System Analyst MS computer science or related Exp: 0-3 yrs |
As a Systems Analyst, you will be responsible for developing and implementing integrated process and business system initiatives related to AirWatch Mobile Device Management. You will communicate with functional areas and define business requirements related to technology and provide technical assistance in identifying, evaluating, and developing systems and procedures, which are cost effective and meet user requirements. | 7/18/2017 |
| 1125 | Medtronic Louisville, CO Product Quality Advocate MS scientific discipline Exp: 0 yrs |
This position has the responsibility and authority to handle product complaints to ensure compliance with US and International regulatory agencies. Under the direction of the Product Quality Experience Manager, the Product Quality Advocate performs complaint handling and associated activities pertaining to product complaint investigation for Medtronic Neurosurgery. This includes, but is not limited to: receiving and investigating reports of worldwide complaints / events on a variety of products; entering information into the complaint database; providing guidance to less experienced employees within the department, helping to gather information to allow for the filing of appropriate medical devices reports with various regulatory agencies; participating in and sharing complaint information with various cross-functional teams (e.g. Regulatory, Quality Engineering). Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are engaged by a work culture that is team-oriented, fast paced and progressive. | 7/18/2017 |
| 1126 | Medtronic Louisville, CO Associate Product Quality Advocate BS technical discipline Exp: 1 yr |
This position has the responsibility and authority to handle product complaints to ensure compliance with US and International regulatory agencies. Under the direction of the Product Quality Experience Manager, the Associate Product Quality Advocate performs complaint handling and associated activities pertaining to product complaint investigation for Medtronic Neurosurgery. This includes, but is not limited to: receiving and investigating reports of worldwide complaints / events on a variety of products; entering information into the complaint database; with some guidance, helping to gather information to allow for the filing of appropriate medical devices reports with various regulatory agencies; participating in and sharing complaint information with various cross-functional teams (e.g. Regulatory, Quality Engineering). Employees act on their strong desire to make a difference, partner with others and put ideas into action. Employees are engaged by a work culture that is team-oriented, fast paced and progressive. | 7/18/2017 |
| 1127 | Medtronic Mounds View , MN Regulatory Affairs Specialist MS technical discipline Exp: 0-2 yrs |
The Regulatory Affairs Specialist is responsible for coordinating and preparing submissions related to our medical devices including clinical applications, initial product approval, changes to products and product renewals which may require direct interaction with regulatory agencies. | 7/18/2017 |
| 1128 | Medtronic Santa Rosa, CA R/D Engineer MS engineering (chemical, materials, mechanical, or biomedical) or chemistry Exp: 0 yrs |
The main purpose of this job is to support development of current and next generation drug-coated balloon (DCB) projects to treat peripheral vascular disease. These combination products integrate biotechnology, polymer science, and pharmaceutical molecules onto balloon platforms. As the Medtronic DCB portfolio has grown, additional resources are needed to support combined research and development (R&D) and design assurance engineering (DAE) activities. The employee will be a member of multiple projects through different stages of the product development cycle, bringing products to commercialization. | 7/18/2017 |
| 1129 | Merck West Point, PA Associate Specialist, Engineering BS mechanical, chemical, or biological engineering or chemistry Exp: 6 months |
West Point Technical Operations Pneumo / Pedvax Integrated Product Team (IPT) is seeking highly motivated individuals to join a technical support team for a multi-product vaccine manufacturing facility. This role will partner with Operations and Quality to meet the targeted manufacturing and compliance initiatives for the Pneumo / Pedvax IPT. The subject position will be responsible for the following: | 7/18/2017 |
| 1130 | Merck Boston, MA 2017 MRL Bioanalytics Scientist Co - Op BS / MS life sciences Exp: 1 yr coursework |
MRL Boston Bioanalytics is currently recruiting for a Co-Op position. This position involves working with therapeutic modalities that are under investigation for neurological disorders with high unmet medical need. The position is a full-time, paid, (4) to (6) month co-op assignment. A housing subsidy is not available as part of this program. The selected candidate will have the opportunity to learn and apply technologies that allow her / him to contribute to the overall bioanalytical strategy at MRL Boston within the framework of project specific objectives. | 7/18/2017 |
| 1131 | Merck San Francisco, CA Research Associate II - Cardio - Renal and Metabolic Diseases MS pharmacology, physiology, pathology, or related Exp: 0 yrs |
The Cardiometabolic Disease therapeutic area within Discovery Research at Merck is seeking to recruit Scientists that are highly motivated to applying their skills towards the identification and development of novel targets to treat a broad array of cardio-renal and metabolic diseases. However, the most important singular quality we are looking for is a drug hunter that seeks to put patients first as the front and central goal of their research. The location will be the preclinical research laboratories at our new state of the art facility in the South San Francisco Bay Area where you will be able to participate in a vibrant culture connecting leading academic and biotech research centers | 7/18/2017 |
| 1132 | Merck West Point, PA Maintenance Engineer BS engineering Exp: 1-3 yrs |
Under the supervision of a Senior Engineer or Manager, is responsible to provide day-to-day equipment and facility engineering support for assigned areas including vaccine bulk manufacturing, and / or associated facility / utilities mechanical support. Assigned tasks include support and monitoring of equipment performance and maintenance, propose & develop equipment and facility improvements and troubleshoot process equipment to ensure reliable, compliant and efficient operations. Actively ensures compliance to current Good Manufacturing Practices, Safety, and Environmental regulations while achieving operating cost goals. | 7/18/2017 |
| 1133 | Merck Boston, MA Scientist Neuroscience MS biological sciences Exp: 0 yrs |
The Merck Early Discovery Neuroscience team is seeking a talented and motivated scientist with a strong background in Neuroscience to join our Boston-based team to support the identification and validation of novel targets to treat CNS diseases including neurodegenerative disease such as Alzheimer s disease and Parkinson s disease. Candidates should be able to work independently, but will be expected to collaborate proactively and effectively with colleagues across disciplines. Primary responsibilities include design and execution of in vitro experiments including cell culture and development of immunoassays. Ideal candidate will be able to bridge between in vitro and in vivo techniques. The successful candidate will have demonstrated effective teamwork and communication skills. Merck offers a competitive compensation package commensurate with experience. | 7/18/2017 |
| 1134 | Merck Durham, NC VBF Technician (Process Support B Shift Days) BS life sciences or engineering Exp: 1 yr |
An 02 Technician will support the manufacturing process through the hands on activities in Process Support. Key responsibilities for the Technician include aseptic practice and GMP (Good Manufacturing Practices) adherence, working in a team environment to accomplish departmental goals, as well as the ability to direct your own work through the assembly process and in unclassified areas. | 7/18/2017 |
| 1135 | Merck Rahway, NJ Scientist, Analytical Chemistry MS analytical chemistry or related Exp: 0 yrs |
The Analytical Research & Development department of Merck Research Laboratories is seeking applicants for an analytical chemist at the Scientist level. The position is available at Merck s Rahway, New Jersey research facility. The position is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of chemistry and engineering disciplines to enable development of active pharmaceutical ingredients (APIs). The successful candidate must function well and be able to collaborate in a fast-paced, integrated, multidisciplinary team environment. | 7/18/2017 |
| 1136 | Meridian Bioscience, Inc, Cincinnati, OH Engineer, R&D Instrumentation BS engineering, computer science, or other technical degree Exp: 1-5 yrs |
The candidate will be responsible for coordinating firmware and software development with outside vendors (both foreign and domestic) for new medical diagnostic instrumentation, working in a cross-functional team up and down the management structure. | 7/18/2017 |
| 1137 | Merit Medical South Jordan, UT Molding Engineer Internship (ID: 400 - 12804) BS engineering Exp: 2 yrs coursework |
Interns will be called upon to support a variety of analytical based activities in a fast paced, medical device engineering environment | 7/18/2017 |
| 1138 | Merit Medical South Jordan, UT Summer Internship (Sensors Engineering) (ID: 210 - 12563) BS mechanical, chemical, or electrical engineering Exp: 2 yrs coursework |
Performs routine technical tasks including assembling or constructing simple or standard equipment or parts, and may service or repair simple instruments or equipment. Will compile and review equipment documentation packages and process them for change control. May edit and generate equipment detail drawings and schematics. Will also support Sensors by performing product testing. | 7/18/2017 |
| 1139 | Merit Medical South Jordan, UT Manufacturing Engineer II (ID: 210 - 12846) MS engineering , science, or related technical degree Exp: 1 yr |
Performs routine and complex technical work such as the design, manufacture and operation of structures, machines and systems under broad supervision and guidelines. | 7/18/2017 |
| 1140 | Merit Medical South Jordan, UT Summer Internship (Regulatory Affairs) (ID: 571 - 12568) BS technical discipline Exp: 2 yrs coursework |
Performs routine tasks involved in a Regulatory Affairs environment. | 7/18/2017 |
| 1141 | Mersana Therapeutics Cambridge, MA Associate Scientist, Analytical Chemistry BS / MS chemistry, biochemistry, or related Exp: 1-2 yrs |
Under guidance from the senior scientists perform RP / IEX / SEC HPLC, LC / MS, CE / cIEF and spectrophotometry based testing of research materials including small molecules, polymers and biologics Perform HPLC and LC / MS analyses and routine maintenance on analytical instrumentation Participate in the development / evaluation of new analytical methods to support our growing drug pipeline and assist our synthetic chemistry group with their sample preparation and analysis Prepare calibration standards, buffer solutions, schedule and perform routine maintenance on analytical instrumentation Schedule, implement method development and research activities; maintain accurate laboratory records and notebooks; follow analytical procedures and validation protocols in compliance with regulatory requirements and industry standards; write analytical reports and SOPs Maintain laboratory supplies and perform laboratory housekeeping tasks Under guidance from the senior scientists develop and validate new analytical / bioanalytical methods for research materials evaluation | 7/18/2017 |
| 1142 | Merz Raleigh, NC Lead Clinical Research Associate BS scientific discipline Exp: 1 yr |
The Lead Clinical Research Associate (LCRA) is responsible for managing the development, coordination and implementation of site management and clinical monitoring responsibilities for assigned protocols with guidance from the clinical study manager (CSM) or the Clinical Project Director. | 7/18/2017 |
| 1143 | Abaxis UNION CITY, CA Manufacturing Engineer BS Engineering 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; Participate as team member for new product introduction and implementation to manufacturing;Participate and or lead validation activities and line studies. | 7/15/2017 |
| 1144 | Abbiotec, Inc. 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. | 7/15/2017 |
| 1145 | Abcam plc. Eugene, OR Quality Control Associate BS in Biology or closely related discipline Exp: 1 yr |
The core responsibility will be to provide support to the quality control team by testing our catalog of products after they have completed the manufacturing process. These products include sandwich ELISA kits, Western blot antibodies and cocktails, immunocytochemistry antibodies, and flow cytometry kits. | 7/15/2017 |
| 1146 | Abcam plc. Eugene, OR Research Associate - Simple Step ELISA BS in Biology, immunology or closely-related degree Exp: 1 yr |
The core responsibility will be to provide support to the immunoassay development team through formulation, validation and testing of antibody pairs in standard and proprietary sandwich ELISA formats. Additional use of antibody-based laboratory techniques such as direct ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis may be required. | 7/15/2017 |
| 1147 | Abcam plc. Cambridge, MA Senior Research Associate - Services BS in Biology or closely related discipline Exp: 1 yr |
The successful candidate will participate in every aspect of the Service Lab, from sample receiving through running the assays, data analysis, report generation and supporting the customers as they interpret the results. | 7/15/2017 |
| 1148 | Abcam plc. Eugene, OR Manufacturing Associate BS in Life Sciences or Chemistry Exp: 1 yr |
This role will also provide support to the development team by manufacturing intermediates used in the development of new kits. | 7/15/2017 |
| 1149 | Abcam plc. Eugene, OR Research Associate - Multiplex Immunoassays BS in Biology or closely related discipline Exp: 1 yr |
The core responsibility will be to provide support to the immunoassay development team through the use of antibody-based laboratory techniques such as sandwich ELISA, Western blot, immunocytochemistry, and flow cytometry as well as the generation of biological materials for analysis. | 7/15/2017 |
| 1150 | Absorption Systems Exton, PA Associate Scientist Bioanalysis BS / MS in chemistry, biochemistry or related discipline Exp: 1-3 yrs |
Absorption Systems is seeking a motivated individual with a strong science background (biology or chemistry) to join a team involved in the bioanalysis of preclinical in-vitro and in-vivo ADME (Absorption, Distribution, Metabolism, and Excretion) and pharmacokinetic studies. 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. | 7/15/2017 |
| 1151 | Acceleron Pharma Inc. Cambridge, MA Analyst, Quality Control - Raw Materials and Microbiology BS in a Biology / Microbiology / Chemistry / Biochemistry or related field Exp: 1-3 yrs |
Support Acceleron s Environmental Monitoring (EM) program through sampling, data review / trending and resolving microbiological issues through the Alert / Action system that arise within the Clinical Manufacturing Facility (CMF) | 7/15/2017 |
| 1152 | DePuy Synthes, Inc West Chester, PA Associate R&D Engineer - DePuy Synthes Trauma/CMF BS / MS in Mechanical Engineering, Biomedical Engineering or other technical discipline Exp: 1 yr |
The Associate R&D Engineer assists in the design and development of new implants and instrumentation and / or support in-market products through their product life-cycle within a multi-functional project team. This includes communication with surgeons and sales consultants, understanding of clinical issues, defining the design parameters, and ensuring the correct product is provided to the custome | 7/15/2017 |
| 1153 | Acumed Hillsboro, OR Clinical Research Specialist BS / BA in Quality Assurance, Regulatory Affairs, Clinical Research or related field required Exp: 1-3 yrs |
The Clinical Research Specialist (CRS) is responsible for the facilitating assigned research studies in accordance with established procedures and regulations. The CRS executes strategies for pre- and post-market clinical studies and facilitates operational and logistical tasks to ensure efficient clinical trials. Collaborates with VP, Quality, Regulatory, Compliance, to ensure study activities occur in compliance with the appropriate regulations, including Food and Drug Administration (FDA) regulations, Investigational Device Exemption (IDE), 510 (k) guidelines, etc. The CRS coordinates resources for patient recruitment, trial site selection, and execution of trials with a focus on quality. | 7/15/2017 |
| 1154 | Acumed Hillsboro, OR Process Engineer 1 BS in Engineering (Mechanical, Manufacturing, Industrial) or equivalent Exp: 1-2 yrs |
The Process Engineer (PE) supports production cells and new product development teams to meet operational objectives by developing, integrating, and improving production processes and systems. The Process Engineer also ensures compliance to Acumed, FDA, and ISO regulations. | 7/15/2017 |
| 1155 | Adaptive Biotechnologies Seattle, WA Production Associate BS in Biology, Molecular Biology, Immunology or Medical Technologist Exp: 1 yr |
The Production Associate position is responsible for processing client samples using high throughput DNA sequencing technology. The successful candidate will work within a team of other Laboratory Scientists in a fast-paced, high production setting to process clinical and research samples. | 7/15/2017 |
| 1156 | Advanced BioScience Laboratories, Inc Rockville, MD LABORATORY RESEARCH SPECIALIST: CELL BIOLOGY BS Exp: 0-2 yrs |
The primary role of the Research Specialist is to provide technical support to the department of Cell Biology to meet laboratory and contractual research objectives. The Research Specialist will also provide the necessary technical and laboratory support to develop novel approaches for analyzing immune and virological outcomes from preclinical research studies that are necessary to meet current obligations of government contracts and for attracting new funding for contractual work. | 7/15/2017 |
| 1157 | Aegerion Pharmaceuticals Cambridge , MA Clinical Project Coordinator BS Exp: 1 yr |
The Clinical Project Assistant will work internally with clinical development and clinical operations and may also directly interact with outside Clinical Research Organizations and vendors. This position will include both administrative and clinical department tasks. | 7/15/2017 |
| 1158 | Agena Bioscience, Inc. San Diego, CA Quality Assurance Analyst BS in Life Science or Engineering Exp: 1-2 yrs |
The Quality Assurance Analyst will be responsible for supporting a variety of activities within the Quality Department including the Quality Management System (QMS) and maintenance of active and inactive documents pertaining to the QMS and the production and testing of all Agena products. In the QMS support area these activities include reviewing Device History Records (DHR) / Production Batch Records (PBR), QA release of product to inventory, and documenting non-conformances and deviations as they pertain to materials and production processes. In the document support area these activities include ensuring the timely and accurate processing of Change Orders (COs) and new documentation under the guidance of a Document Control Specialist. | 7/15/2017 |
| 1159 | Agilent Technologies, Inc. Carpinteria, CA Research Assistant - R&D BS / MS in biological sciences Exp: 0-2 yrs |
Perform experiments under guidance to validate prototype immunohistochemical (IHC) assays in the Companion Diagnostics business area. A general understanding of cell and molecular biology, histology and cancer pathology is essential. Participate in project teams with technical input. Assist in facilitating transfer of completed development projects into commercial products. Assist in writing and reviewing study protocols, technical reports, and product packaging materials. Maintain a laboratory notebook and provide impeccable documentation to support quality control, regulatory affairs and clinical affairs. Experience with Microsoft Office and Outlook is required. Must work well in a dynamic team environment. | 7/15/2017 |
| 1160 | Agilent Technologies, Inc. Carpinteria, CA Manufacturing Engineering - Quality Tech Support BS Exp: 0-2 yrs |
Performs technical work to ensure that equipment and machinery relating to manufacturing and quality activities are maintained at best working conditions with minimum down time. May perform calibration and maintenance, or work with third parties to ensure calibration and maintenance is performed per schedule and to specification. | 7/15/2017 |
| 1161 | Charles River Laboratories International, Inc. Charleston, SC Quality Assurance Auditor I BS / BA Exp: 1-2 yrs |
Perform audits of basic records and reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. | 7/15/2017 |
| 1162 | Charles River Laboratories International, Inc. Reno, NV Associate Quality Assurance Auditor BS / BA Exp: 0-1 yr |
With guidance and oversight by Quality Assurance (QA) auditors, perform audits of basic records and reports and inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures | 7/15/2017 |
| 1163 | Charles River Laboratories International, Inc. Skokie, IL Research Assistant I BS / BA Exp: 0-2 yrs |
Responsible for performing basic to moderately complex laboratory work in collaboration with departmental staff | 7/15/2017 |
| 1164 | Agios Pharmaceuticals Cambridge, MA Research Associate, Biology BS Exp: 0-4 yrs |
Perform cell-based assays to assess the impacts of small molecule inhibitors, shRNA, or CRISPR-mediated knockout on cancer cell proliferation as well as pathway-based biomarkers. | 7/15/2017 |
| 1165 | Applied Genetic Technologies Corporation Alachua , FL Research Associate I Downstream Exp: 1-3 yrs |
AGTC is seeking a highly motivated individual who will be responsible for providing support for downstream process development activities as needed, working independently when appropriate, and on a timely basis, in order to achieve department and company goals. | 7/15/2017 |
| 1166 | Alamo Houston, TX Oncology Supportive Care Specialist BS / BA in life science Exp: 1-2 yrs |
This position will report directly to the District Manager and must consistently meet or exceed all sales budgets / goals on all products assigned. Territory Sales Managers are expected to possess a high level knowledge of their product, customer and territory. An average of 10 sales calls / presentations per day to prescribers as well as triage nurses plus Pharmacy sales presentations as needed. All calls must be entered into the company assigned system along with notable post call notes, sample activity, etc. Territory Sales Managers are also expected to attend all company, regional and divisional meetings. Various administrative duties such as expense reporting are also required. Must also complete all fleet safety training and must maintain an acceptable driving record regarding accidents and incidents. | 7/15/2017 |
| 1167 | Alcami Corporation Germantown, WI REGULATORY COMPLIANCE SPECIALIST MS in Chemistry, Biology, or related scientific field Exp: 1 yr |
The Regulatory Compliance Specialist performs activities to ensure quality and compliance with applicable internal and regulatory requirements. These activities may include conducting internal audits, hosting customer audits and health authority inspections, and maintaining quality metrics as part of the Quality Management System. As a subject matter expert, the role holder will create (or assist with the creation of) the applicable Quality Management System documentation such as SOPs, training materials or investigation reports. Depending on experience, may serve as the lead auditor for external audits as well. | 7/15/2017 |
| 1168 | Alcami Corporation Germantown, WI CR & D CHEMIST I BS / MS in Chemistry Exp: 0-7 yrs |
Execute chemical reactions on a gram to multi-kilogram scale. Isolate and purify products and intermediates by using standard laboratory techniques. Perform routine analytical procedures to monitor reaction progress (i.e. TLC, GC, NMR, HPLC, KF). | 7/15/2017 |
| 1169 | Aldevron Fargo, ND Quality Control Analyst II BS Exp: 1 yr |
The Quality Control Analyst II supports the manufacturing, validation and process development and stability functions of Aldevron by analyzing GMP projects by through testing, sampling, and completing the applicable documentation. | 7/15/2017 |
| 1170 | Alkermes, Inc. Waltham, MA Sr Research Associate MS in biology, pharmacology, neuroscience or related fields Exp: 1-5 yrs |
The CNS Disease Biology group at Alkermes is seeking a highly motivated and experienced senior research associate to conduct rodent behavioral studies in support of in vivo research projects. | 7/15/2017 |
| 1171 | Alkermes, Inc. Wilmington, OH QC Analyst I BS in Chemistry Exp: 0-2 yrs |
The position requires the individual to perform routine / non-routine physical, chemical, and in-vitro assays of clinical, commercial, process and cleaning validation samples, and process development samples to support Manufacturing. Performs physical and / or chemical analyses of product to ensure stability. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance to specifications and reports abnormalities. Revises and updates standard operating procedures as needed. May perform special projects on analytical and instrument problem solving. Expected to adhere to cGMP s in all work practices, proactively assist other team members, and review peer's work as needed. | 7/15/2017 |
| 1172 | Alkermes, Inc. Wilmington, OH Process Engineer - Bulk BS in Engineering Exp: 1-2 yrs |
Support and assist in the manufacture of pharmaceutical products for commercial and clinical supplies. Scale-up and transfer formulations / processes to production facility, design and recommend equipment purchases, write and execute qualification / validation protocols. Troubleshoot automated equipment for pharmaceutical formulation and packaging. Identify and implement process / equipment improvements (utilizing Change Control system) to reduce waste and increase process reliability. | 7/15/2017 |
| 1173 | Alkermes, Inc. Wilmington, OH Manufacturing Associate - Filling BS in scientific discipline including Chemistry / Pharmaceutical Sciences or related field Exp: 1-2 yrs |
Production, filling and inspection of pharmaceutical formulations. | 7/15/2017 |
| 1174 | Alkermes, Inc. Waltham, MA Library Specialist (Contract) BS / MS in life sciences Exp: 0-3 yrs |
As Library Specialist in the Knowledge Management Services / Scientific Affairs group, the individual will play a key role in supporting in daily operations for the growing department. Some of those roles includes: supporting the Alkermes Global R & D organization with respect to peer reviewed publication requests, information and database searches and provide citation management services to support clinical development programs, product pipeline and marketed products. | 7/15/2017 |
| 1175 | Agilent Technologies, Inc. NA, NA Manufacturing Engineer, Intern, Microarray Fab BS / MS in a technical field Exp: 0-2 yrs |
Joining the Manufacturing Engineering team, you will follow established techniques to design, develop and improve the products, processes and components that make us world leaders, and be supported and encouraged to expand your skills and knowledge every step of the way. | 7/15/2017 |
| 1176 | Agilent Technologies, Inc. Wilmington, DE Gas Chromatography R&D Intern BS Exp: NA |
As an Intern in the GC R&D Department you will be involved in the development of products and tools in Agilent's portfolio of Gas Chromatograph, Automated Sample Handling and Automated Sample Preparation products. You will be part of a highly skilled, innovative and multidisciplinary team of Engineers and Scientists developing the next generation of products in Agilent's industry-leading Gas Phase Products Division. | 7/15/2017 |
| 1177 | Akina, Inc. West Lafayette, IN Laboratory Intern BS Exp: NA |
Looking for an intern to assist in research and development of medical products including but not limited to restiex expanders, biodegradable ureteral stents, and development of the polyvivo line of biodegradable polymer products. | 7/16/2017 |
| 1178 | Latitutde Pharmaceuticals Inc. San Diego, CA Research Associate BS chemistry, pharmaceutical sciences, or biochemistry Exp: 1-5 yrs |
Assist the supervising Formulation Scientist to complete individual formulation development projects. Assist in the design, execution and interpretation of formulation development based on the defined deliverables, as well as in the planning of activities to meet the project timelines. Prepare presentations of data and progress and assist in regular presentations to external clients during formulation development projects. Perform related duties as assigned by supervisor. Maintain and ensure safe laboratory environment and work practices. Maintain compliance with all company policies (employee- or laboratory-based) and procedures | 7/10/2017 |
| 1179 | Leidos Fort George G Meade, MD Data Scientist I BS computer science or mathematics Exp: 1 yr |
The Cyber & SIGINT Solutions Operation of Leidos is seeking Data Scientists for our customer site on Fort Meade, Maryland. Design and develop methods, processes, and systems to consolidate and analyze structured and unstructured, diverse sources including big data sources. Develop and use advanced software programs, algorithms, querying and automated processes to cleanse, integrate and evaluate datasets and models complex problems. Familiarity with disciplines such as machine learning, predictive modeling, statistical analysis and hypothesis testing. Identify meaningful insights and interpret and communicate findings and recommendations. May develop information tools, algorithms, dashboards, and queries to monitor and improve performance. | 7/10/2017 |
| 1180 | Leidos San Diego, CA Biomechanist MS kinesiology, biomechanics, or related Exp: 1 yr |
The mission of the Naval Medical Center San Diego (NMCSD) is to prepare to deploy in support of operational forces, to deliver quality health services, and to shape the future of military through education, training, and research. As a central component of the Clinical Investigations Department at NMCSD, their mission is to support the Command s mission of operational readiness, patient care, and medical education by facilitating scientifically-sound research and publications and by sponsoring training protocols that ensure skill acquisition, maintenance, and improvements in clinical practice. Clinical Investigations Department requires the services of a Clinical Research Pharmacist to support research investigators, other research assistants, or nurse researchers in the performance of moderately complex research and experimentation at NMCSD and Naval Hospital Camp Pendleton (NHCP). | 7/10/2017 |
| 1181 | Leidos San Diego, CA Research Assistant BS kinesiology, biomechanics, bioengineering, or related Exp: 1 yr |
The mission of the Naval Medical Center San Diego (NMCSD) is to prepare to deploy in support of operational forces, to deliver quality health services, and to shape the future of military through education, training, and research. As a central component of the Clinical Investigations Department at NMCSD, their mission is to support the Command s mission of operational readiness, patient care, and medical education by facilitating scientifically-sound research and publications and by sponsoring training protocols that ensure skill acquisition, maintenance, and improvements in clinical practice. Clinical Investigations Department requires the services of a Clinical Research Pharmacist to support research investigators, other research assistants, or nurse researchers in the performance of moderately complex research and experimentation at NMCSD and Naval Hospital Camp Pendleton (NHCP). | 7/10/2017 |
| 1182 | Leidos San Diego, CA Laboratory Technologist BS biology, biochemistry, genetics, or related Exp: 1 yr |
The mission of the Naval Medical Center San Diego (NMCSD) is to prepare to deploy in support of operational forces, to deliver quality health services, and to shape the future of military through education, training, and research. As a central component of the Clinical Investigations Department at NMCSD, their mission is to support the Command s mission of operational readiness, patient care, and medical education by facilitating scientifically-sound research and publications and by sponsoring training protocols that ensure skill acquisition, maintenance, and improvements in clinical practice. Clinical Investigations Department requires the services of a Clinical Research Pharmacist to support research investigators, other research assistants, or nurse researchers in the performance of moderately complex research and experimentation at NMCSD and Naval Hospital Camp Pendleton (NHCP). | 7/10/2017 |
| 1183 | Leidos Frederick, MD Biological Life Scientist MS scientific discipline Exp: 1 yr |
The candidate will apply scientific expertise and process management experience to support the various committees, teams, and task forces formed by the consortium to build out the Program s clinical platform. You will work closely with NIH staff including program officers and senior staff. The ability to work collegially and efficiently in teams is very important. | 7/10/2017 |
| 1184 | Leidos Frederick, MD Biomedical Life Scientist MS biomedical sciences Exp: 1-2 yrs |
Candidate will apply scientific expertise to several Congressionally-directed, medical (predominately cancer-related) research programs. The job entails, but is not limited to, the detailed analysis, integration, categorization, summarization, and application of a broad spectrum of biomedical and health-related information and data in response to a diversity of customer-generated requirements. Responsiveness, as well as open and frequent coordination and discussion with a multidisciplinary and goal-oriented group, are inherent elements of the day-to-day operations. Candidate must be capable of independent action and initiative. Candidate will use expertise in one or more of the following areas: biochemistry, immunology, cell biology, molecular biology, medicinal chemistry, clinical and experimental therapeutics, pharmacology, military operational medicine, etc. This position is located in Frederick, Maryland. Some travel required. | 7/10/2017 |
| 1185 | Leidos Groton, CT Audiology Research Assistant BS experimental sciences Exp: 0-2 yrs |
The Audiology Research Assistant will be responsible for assisting in developing, setting up, executing, and monitoring of hearing related experiments and testing for a variety of projects in the field of hearing conservation. | 7/10/2017 |
| 1186 | LifeSensors Malvern, PA Entry Level Scientist BS / MS biological science 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. 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 | 7/10/2017 |
| 1187 | Iovance Biotherapeutics San Carlos, CA Intern - IT SharePoint Development BS computer science or related Exp: 1 yr coursework |
SharePoint development leveraging templates and processes already developed. The intern would also work as a junior BA helping to gather requirements from the different business units. | 7/10/2017 |
| 1188 | Lonza Durham, NC Cell Culture Technician I - RTP NC BS / AS life sciences Exp: 0-3 yrs |
This position is based in our Morrisville, NC facility and is responsible for the manufacture of cell products used in primary research including isolation and culturing of primary cells derived from human or animal tissues and organs. Responsible for the operation of production equipment, maintaining records, and laboratory environment to comply with Good Manufacturing Practices, ISO 9000 regulations, and Standard Operating Procedures. May perform with in-process testing to assure batches meet specifications. | 7/10/2017 |
| 1189 | Lonza Portsmouth, NH MSAT Associate Scientist Intern AS / BS chemical engineering or biochemistry Exp: 1 yr coursework |
Role Purpose: This person is responsible for assisting in the execution of laboratory based studies or associated assay support. This person performs assigned duties according to specified procedures and receives detailed instructions. The individual is not expected to be a subject matter expert for any aspect of the role. | 7/10/2017 |
| 1190 | Lonza Portsmouth, NH Manufacturing Internship AS / BS scientific discipline Exp: 0-3 yrs |
The Manufacturing Internship position will provide the employee with an introduction into the manufacture of therapeutic proteins (API) under cGMP conditions. The intern will gain exposure through training in executing process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. | 7/10/2017 |
| 1191 | Lonza Portsmouth, NH Engineering Intership - Capital Project BS chemical or mechanical engineering Exp: 2-3 yrs coursework |
Lonza is currently executing a large scale capital project to build additional manufacturing capability at the Portsmouth, NH facility. This project is highlighted by a new 20,000 L mammalian bioreactor train and incorporation of state of the art disposable technology. The successful candidate will have the opportunity to support this project from design through to construction, commissioning, and qualification. | 7/10/2017 |
| 1192 | Luna Blacksburg, VA Student Intern - Lightware Division BS physics or engineering Exp: 1 yr coursework |
We seek an Intern to support the Lightwave Contract Research team whose primary role will be fabricating and testing composite systems and fabricating and testing sensors under development. | 7/10/2017 |
| 1193 | Lundbeck Deerfield, IL Associate, Case Processing GPV - US BS scientific discipline Exp: 1 yr |
The Associate, Case Processing GPV-US is responsible for the collection, assessment and processing of adverse events and product complaints for Pre- and Post-Marketed products to ensure compliance with worldwide reporting regulations. | 7/10/2017 |
| 1194 | Lygos Berkeley, CA DSP Research Associate I BS chemistry, chemical engineering, or related Exp: 0-3 yrs |
Lygos is seeking down stream processing (DSP) research associate candidates to maintain, set up, run our pilot plant. The successful candidates will have experience with operating large equipment, general lab procedures, data interpreting / reporting and be comfortable in a fast paced, multitasking environment. | 7/10/2017 |
| 1195 | LSNE Contract Manufacturing Manchester, NH Inside Sales Support Associate BS life science or related Exp: 1-5 yrs |
The Inside Sales Support Associate will work closely with the Sales Team to provide assistance to the team to reach quarterly goals. This position is responsible for sales administration and support to include complete market research to identify potential leads passing them on to the Sales Group. Other duties will include providing data and reports to help the sales team. | 7/10/2017 |
| 1196 | LSNE Contract Manufacturing Manchester, NH Manufacturing Technician I AS / BS biology, chemistry, biotechnology, or related Exp: 1-3 yrs |
This position is responsible for performing a variety of complex tasks under general guidance and in accordance with the manufacturing instruction set and current GMP / ISO requirement and standards. With general supervision, the individual will perform routine and critical manufacturing operations, including but not limited to work functions in equipment prep, dispensing, dissolution, formulation, purification, aseptic compounding, filling and packaging activities for biopharma and medical device products. Work with Master production records, standard operating procedures, and device records. | 7/10/2017 |
| 1197 | LSNE Contract Manufacturing Manchester, NH Quality Chemist II BS analytical chemistry, chemistry, or related 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. | 7/10/2017 |
| 1198 | MacroGenics Rockville, MD Quality Control Analyst I BS scientific discipline Exp: 0 yrs |
The QC Analyst I / II (EM) is responsible for conducting quality control testing primarily in the area of environmental monitoring and microbiological testing. This individual will be required to complete the testing in a timely manner while adhering to standard operating procedures and under GMPs. The role also requires timely and accurate documentation and reporting of results to ensure compliance. | 7/10/2017 |
| 1199 | Marin Biologic Laboratories Novato, CA Research Associate BS / MS cell biology, molecular biology, or related 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. | 7/10/2017 |
| 1200 | Masy Bioservices Hatfield, PA Validation Technician AS engineering or science Exp: 1-2 yrs |
Responsibilities for this position involve validation equipment preparation, protocol execution and final report generation. This position will support a wide range of validation activities focused on environmental chambers, including: cryo-freezers, cold rooms, refrigerators, incubators, sterilizers, depyrogenation ovens, stability chambers, warehouses, etc. Also Steam in Place (SIP) validation using biological indicators. | 7/10/2017 |
| 1201 | Maxim Biomedical, Inc. Rockville, MD Manufacturing Level 1 Technician BS / BA biosciences or related Exp: 0 yrs |
Operate automated EIA plate coating and heat sealing equipment. Print labels and label components by hand and by using an automated label machine. Assemble and inspect kits as schedule following SOPs. Clean, calibrate, and maintain laboratory equipment. Clean glassware, autoclave equipment and waste as necessary. Properly package and dispose of hazardous waste. Clean, calibrate, and maintain laboratory equipmentent. Maintain accurate production documents, lab records, and log books. Follow Good Manufacturing (GMP), Quality System Regulation (QSR), and safety regulations. Assist Product Technology with validations. Write and revise written procedures (Standard Operating Procedures (SOP), Manufacturing Procedures (MP)) as necessary. Support kit assembly and packaging operations, as well as Gel production, when required.Other duties as assigned | 7/10/2017 |
| 1202 | Maxim Biomedical, Inc. Rockville, MD Quality Control Level 1 Technician BS biological studies or related Exp: 0 yrs |
Follow Good Manufacturing Practice (GMP) / Good Laboratory Practice (GLP), Quality Systems Regulation (QSR), Environmental Protection Agency (EPA) and safety regulations in an FDA licensed facility. Maintain accurate laboratory logbooks and testing documentation, per established procedures. Assist in keeping procedures current to QSR guidelines as established by the FDA. Evaluate materials by way of Western Blot, Microbial / Sterility, Infectivity and general chemical analysis testing methods.Evaluate environmental conditions (Surface and Air) per USP and FDA guidelines. Assist in the generation and revision of Standard Operating Procedures (SOP). Assist in the generation and implementation of validation protocols. Conduct stability testing per established protocols, as well as assist in the generation of stability protocols. Conduct complaint investigation testing when requested by Supervisor. Work closely with all areas to ensure quality processes are maintained and supported. Perform incoming inspection and test and subsequent approval of received materials Review batch history records for accuracy and completeness. Assist in QC analyst training and other additional duties as assigned. | 7/10/2017 |
| 1203 | MDx Health Inc Irvine, CA Clinical Laboratory Scientist I/II BS / MS chemical, physical, or biological sciences 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. | 7/10/2017 |
| 1204 | Kimball Electronics Fabrications Indianapolis, IN Mechanical Engineer Intern BS mechanical engineering or related Exp: 1 yr coursework |
This internship is with the Kimball Electronics - Indianapolis (KEFAB). This position reports to Louie Kissee, Operations Manager. This position will have opportunities to interact and work with different areas within KEFAB including Quality Systems, Manufacturing Processes, and Engineering. | 7/10/2017 |
| 1205 | Pfizer Durham, NC Associate Scientist - Bioprocess R&D BS biological science or chemical / biochemical engineering Exp: 0-3 yrs |
This position will join a larger team of scientists across multiple sites focused on developing and optimizing cell culture processes for recombinant proteins, recombinant viral vectors and biological macromolecules for early- and late-phase clinical trials. The Associate Scientist will be responsible for working with fellow scientists to develop robust, efficient, scalable strategies for improving upstream process performance. The job function requires judgment and innovation to achieve a solution within standard practices and procedures. Responsibilities will include conducting experiments, tests, analyses as part of a variety of research and development activities, e.g., small-scale studies, pilot plant and manufacturing upstream studies. The Associate Scientist will be expected to summarize, evaluate the study results, develop and test new hypotheses to improve the fundamental understanding of upstream cell culture processes. This position will support process validation, quality by design, regulatory approaches, and innovative research. This position will be expected to prepare internally reviewed technical reports, and make oral presentations to scientists and management. The successful candidate must be able to endorse change to business infrastructure to ensure pipeline, legacy and technology success | 7/10/2017 |
| 1206 | Pfizer St Louis, MO Associate Scientist , QC BS chemistry, analytical chemistry, biochemistry, biology, or related Exp: 1-3 yrs |
The qualified candidate will join the Analytical R&D organization to enable development of biological therapeutics in Chesterfield, MO. The qualified candidate will be responsible for applying analytical methods in the assessment of product quality, biological activity, and detection of impurities. This group also supports transfers, verifications, qualifications and validations as well as method troubleshooting. | 7/10/2017 |
| 1207 | Pfizer Rocky Mount, NC Manufacturing Quality Engineer - R2 Night Shift BS scientific discipline Exp: 0-2 yrs |
The Manufacturing Quality Engineer provides oversight and guidance in R2 SVP manufacturing operations, ensuring continuous facility and GMP compliance. The MQ Quality Engineer will coach manufacturing personnel on proper GMP and SOP compliance and empower them to identify and escalate quality issues, to ensure quality product. | 7/10/2017 |
| 1208 | Ultragenyx Novato, CA Clinical Trial Specialist, Medical Affairs BS Exp: 1 yr |
The CTS will support the day-to-day management and coordination for one or more expanded access clinical trials, ISTs and Early Access programs across multiple therapeutic areas and products. The CTS works closely with the Program Leads and cross-functional team to ensure site start-up through closeout activities are conducted in accordance with Standard Operating Procedures (SOPs) and applicable regulations. The successful candidate will be a self-starter with excellent organizational skills, attention to detail and a proven track record for managing multiple projects. | 7/6/2017 |
| 1209 | Ultragenyx Novato, CA Clinical Trial Specialist BS Exp: 1 yr |
The Clinical Trial Specialist (CTS) is responsible for providing logistical support for one or more clinical trial programs. This position will work closely with cross-functional teams to ensure site start-up through close-out activities are conducted in accordance with Standard Operating Procedures (SOPs) and applicable regulations governing the conduct of clinical trials. | 7/6/2017 |
| 1210 | uniQure Lexington, MA Raw Materials Buyer/Planner II BS Exp: 1 yr |
Reporting to the Director of Supply Chain, the Raw Material Buyer / Planner is an integral member of the Operations department. The function requires strong interaction skills with the different disciplines within Operations: Manufacturing, Quality Assurance, Quality Control, Logistics, Technical Services, Facility Management and Suppliers. | 7/6/2017 |
| 1211 | LabCentral Cambridge, MA Lab Purchasing Assistant BS in a life sciences degree Exp: 1-3 yrs |
Engage with current / future vendors and residents to enhance our mission Employ your life sciences knowledge to assist residents with the ordering process Work with Purchasing Lead to provide ordering support across multiple sites | 7/6/2017 |
| 1212 | EnBiotix, Inc Cambridge, MA Associate Scientist MS in a field of biological science Exp: 1 yr |
Design and develop phage display libraries for screening and selection Design and develop robust screening and selection methods Develop and perform quantitative, validated assays for analysis of phage display and engineered phage characterization | 7/6/2017 |
| 1213 | Torus Therapeutics Cambridge, MA Research Associate BS in Biology, Biochemistry, Molecular Biology or related discipline Exp: 1-3 yrs |
The successful candidate would report directly to the Senior Scientist, Platform Development and will assist in the development of Torus s overall platform technology. | 7/6/2017 |
| 1214 | TridentUSA Newtown, PA Medical Technologist - Weekend Shift BS Exp: 1 yr |
The Medical Technologist (MT) performs routine and specialized clinical laboratory tests which include chemical, microscopic, immunologic, hematologic, immunohematologic. | 7/6/2017 |
| 1215 | Valeant Pharmaceuticals International, Inc. Rochester, NY Scientist, Microbiology MS Exp: 0-2 yrs |
Monitoring product quality by performing predetermined microbiology tests to support marketed and pre-marketed product formulations in accordance with SOPs and regulations. | 7/6/2017 |
| 1216 | Valeant Pharmaceuticals International, Inc. Union City, GA Quality Control Specialist BS in a scientific discipline or equivalent Exp: 1 yr |
Performs routine and non-routine analysis of environmental monitoring program, as well as raw materials, in-process and finished products during release or stability testing. | 7/6/2017 |
| 1217 | Valeant Pharmaceuticals International, Inc. Union City, GA QC Specialist - Lab Services BS in a scientific discipline or equivalent Exp: 1-3 yrs |
This is an exciting position accountable for laboratory support of Dendreon s products and in accordance with appropriate regulatory, corporate and scientific guidelines. The ability to function in a fast-paced, highly technical environment, and communicate effectively is essential to success. | 7/6/2017 |
| 1218 | Valeant Pharmaceuticals International, Inc. Union City, GA Contract Quality Control Associate - Bioassay BS in a scientific discipline or equivalent Exp: 1 yr |
This exciting position is accountable for testing of Dendreon s products in accordance with appropriate regulatory, corporate and scientific guidelines. The successful candidates will assist with product testing, raw material testing and general laboratory maintenance. The ability to function in a fast-paced, highly technical environment, and communicate effectively, is essential to success. | 7/6/2017 |
| 1219 | Vapotherm Exeter, NH R&D Technical Document Coordinator BS Exp: 1-5 yrs |
The position of R&D Technical Document Coordinator is responsible for maintaining and updating all hard copy and digital documents related to R&D projects in accordance with Standard Operating Procedures (SOPs) and FDA regulations. The R&D Technical Document Coordinator shall also maintain business systems impacted by engineering changes. | 7/6/2017 |
| 1220 | Vector Laboratories Burlingame, CA QC Technician BS in Life Science, Biochemistry or related field Exp: 1-3 yrs |
The Quality Control Technician is responsible for the analyses of in-process materials, raw materials, finished goods, and stability samples following established operating procedures. The individual may also be required to analyze samples from the Research and Development department using established testing procedures. S / he is also responsible for organizing and maintaining laboratory reagents / supplies and cell cultures. The individual must have sound judgment, be self-motivated, and possess the social skills necessary to work well with colleagues. | 7/6/2017 |
| 1221 | Charles River Laboratories International, Inc Worcester, MA Research Associate I BS Exp: 0-6 months |
The individual in this position will be involved in all aspects of studies supporting the in vivo services group. This position is hands-on with responsibilities including, but not limited to animal husbandry, animal handling and restraint, administration via various routes, clinical observations, sample collection and processing, and accurate data collection. | 7/6/2017 |
| 1222 | Charles River Laboratories International, Inc Newark, DE Molecular Technologist BS 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. | 7/6/2017 |
| 1223 | Charles River Laboratories International, Inc Charleston, SC Quality Control Assistant BS Exp: 1-2 yrs |
Ensure the quality and integrity of product by testing incoming materials, excipients and final product.Perform environmental monitoring of LAL (Limulus Amebocyte Lysate) and Crude Lysate production areas to ensure appropriate conditions are maintained.Perform Crude Lysate recovery procedures during the Bleeding Season. Attention to detail in all aspects of work is essential. | 7/6/2017 |
| 1224 | Charles River Laboratories International, Inc Worcester, MA Associate Scientist BS Exp: 0-6 months |
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. | 7/6/2017 |
| 1225 | Charles River Laboratories International, Inc Spencerville, OH Study Coordinator I BS Exp: 1 yr |
The Study Coordinator will perform collection, preparation, and distribution of information necessary for protocol development and study initiation for routine studies. During a typical day, you will also assist the Study Director during in- and post-life phases of studies by providing and coordinating scientific and administrative support, as well as assist in the production of high quality, accurate, and timely study reports. | 7/6/2017 |
| 1226 | Charles River Laboratories International, Inc Ashland, OH Technical Trainer I BS in animal or life sciences 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. | 7/6/2017 |
| 1227 | Charles River Laboratories International, Inc Reno, NV Research Assistant I (Lab Sciences) BS in laboratory science or related discipline Exp: 0-2 yrs |
Generate and record data with minimal supervision in the performance of studies. Responsible for handling and processing samples, and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. | 7/6/2017 |
| 1228 | West-Ward Pharmaceutical Corp. Columbus, OH Scientist I / II - QC Lifecycle BS in a scientific discipline Exp: 0-3 yrs |
To perform routine and non-routine, work-flow processes within the Quality Control Laboratory to meet regulatory (FDA & ICH), internal and external customer requirements by testing of starting materials, intermediates, non-commercial finished products, method development and validation while ensuring regulatory compliance standards are met by West-Ward Pharmaceuticals. | 7/6/2017 |
| 1229 | West-Ward Pharmaceutical Corp. Columbus, OH Scientist I, Quality Control BS in Chemistry or a science-related field Exp: 1 yr |
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. | 7/6/2017 |
| 1230 | West-Ward Pharmaceutical Corp. Eatontown, NJ Quality Assurance Inspector BS Exp: 1-3 yrs |
Under routine supervision, the Quality Assurance Inspector is responsible for conducting inspection, audit and sampling of manufacturing and packaging operations, as well as, providing general quality oversight of those operations to ensure current good manufacturing compliance and essential housekeeping practices to support company and customer expectations for drug product quality, safety, identity, purity and efficacy. | 7/6/2017 |
| 1231 | XenoBiotic Laboratories, Inc. Plainsboro, NJ Associate Scientist III BS in chemistry, biology, or a related discipline Exp: 1-3 yrs |
Perform routine procedures without supervision.Delivers accurate results on assigned task and expected results.May assume the duty of a trainer to new hires.Maintains research notebooks in a well-organized manner. All necessary documentation is recorded. | 7/6/2017 |
| 1232 | Xencor San Diego, CA Clinical Trial Administrator (CTA) BA / BS Exp: 1-2 yrs |
Schedule and coordinate key Department, Project Team and Ad-Hoc meetings;Assist Department and Project Teams with travel arrangements, expense reports, copying, mailing, and shipping needs. | 7/6/2017 |
| 1233 | Sekisui XenoTech, LLC Kansas City, KS QA Auditor I BS in a biological scientific discipline or equivalent Exp: 1 yr |
Audit of non-clinical laboratory studies for compliance with US, EU and Japanese GLP regulatory directives (FDA, OECD and MHLW) | 7/6/2017 |
| 1234 | Zimmer Inc. Warsaw, IN Packaging Engineer BS in Packaging Engineering or Engineering Exp: 0-3 yrs |
Responsible for the design, development, and processing of implant and instrument packaging under the direction of a project leader or manager. | 7/6/2017 |
| 1235 | Zimmer Inc. Warsaw, IN Quality Engineer BS in engineering Exp: 0-3 yrs |
Responsible for assuring products conform to established requirements and standards through appropriate audit, inspection, and test activities. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals. | 7/6/2017 |
| 1236 | Zymergen Emeryville, CA RESEARCH ASSOCIATE, MICROBIAL GENOME TECHNOLOGY DEVELOPMENT BS / MS Exp: 0-2 yrs |
he Research Associate will help create new technologies, bring in cutting edge protocols described in the literature, and improve existing Zymergen protocols to provide newer and better workflows to our microbe engineering Factory. | 7/6/2017 |
| 1237 | 3M Columbia, MO Quality Assurance Engineer BS / MS Exp: 1 yr |
The person hired for the position of Quality Assurance Engineer will work with multiple medical device products in Chronic and Critical Care Solutions including 3M Press-On Lenses, Micro card and Cavilon Barrier Films. | 7/6/2017 |
| 1238 | 3M Decatur, AL Sr. Analytical Chemist/Materials Engineer BS / MS in a science or engineering discipline Exp: 1 yr |
The person hired for the position of Sr. 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. | 7/6/2017 |
| 1239 | 3M Columbia, MO Quality Product Assurance Engineer BS / MS Exp: 1 yr |
Provide product assurance engineering support for commercialized healthcare products including specification and design control, design transfer, change and risk management, investigations, and continuous improvement. | 7/6/2017 |
| 1240 | Abaxis UNION CITY, CA Process Engineer 1 BS Engineering Exp: 0-3 yrs |
Conduct GMP-compliant machine and process validations on internally designed and constructed automated manufacturing equipment. This will include: leading machine design reviews, performing engineering studies and DOEs to identify critical-to-quality process parameters, conducting machine / process risk analyses, IQ / OQ / PQ, post-validation change control. Partnering effectively with internal automation engineering group will be key success factor. | 7/6/2017 |
| 1241 | Zimmer Inc. Warsaw, IN Research Intern, Fall 2017 BS in Materials Science and Engineering, Polymer Science and Engineering, or Biomedical Engineering with an emphasis on Biomaterials Exp: NA |
The co-op will be responsible for projects assigned by a Project Manager which may entail design, manufacturing / process development, and quality control of product / process. For each assigned project, the student may be responsible for researching background information on the project topic, developing an experimental protocol, and documenting experimental results in a final report format to be reviewed by pertinent departments including quality engineering, regulatory affairs, and manufacturing engineering. The co-op student will gain experience in various analytical methods for characterizing material properties as well as manufacturing methods for various orthopedic devices. The co-op student may also assist in other areas as needed. | 7/6/2017 |
| 1242 | Vedanta Biosciences Cambridge, MA INTERN/CO - OP, MOLECULAR BIOLOGY BS in molecular biology, biology, microbiology, biochemistry or related field Exp: NA |
The intern, or co-op, will conduct studies in the microbiology laboratory to bolster the research and development unit of Vedanta Biosciences. The principal activities of this role will be to aid in the characterization of organisms from the human microbiome through the execution of established molecular biology assays. General tasks will focus on PCR and product verification, sample organization, and coordination of tasks with the microbiology team. Additionally, the intern or co-op, will support the preparation of samples for off-site DNA sequencing. | 7/6/2017 |
| 1243 | Accriva Diagnostics San Diego, CA Chemist BS chemistry or related Exp: 1-2 yrs |
The Chemist is responsible for applying knowledge and skill in support of chemical formulation and analysis of production blends, and for testing incoming raw material component products. | 6/11/2017 |
| 1244 | Juno Therapeutics Bothell, WA Manufacturing Associate BS scientific discipline Exp: 0-2 yrs |
The primary focus of the Manufacturing Associate role will be cellular therapeutic manufacturing at JuMP during process transfers, routine production, and technology improvements. | 6/11/2017 |
| 1245 | Juno Therapeutics Bothell, WA QC Associate I/II Sample Management BS scientific discipline Exp: 1-4 yrs |
The primary focus of the QC Associate I / II is to provide support for sample management and routine laboratory operations. This role is responsible for performing and coordinating sample accessioning, testing, shipping and data handling. | 6/11/2017 |
| 1246 | Juno Therapeutics Seattle, WA Research Associate, Analytical Development - Cell Based Assays MS scientific discipline Exp: 1 yr |
The Research Associate will work in a collaborative environment to develop and qualify cell-based assays for QC release and stability testing. In addition, the Research Associate will develop and perform product functionality testing for Juno s cell therapy products. The position will report to the head of Cell-Based Assay Group, joining a subgroup within Analytical Development. | 6/11/2017 |
| 1247 | Kai Research Ann Arbor, MI Junior Software Developer BS / MS computer science or related Exp: 1 yr |
The software that you develop will help create a sustained, system-wide improvement in children s oral health, and ultimately improve the oral health of more than 1 million children across the state of Michigan. You ll report to a Center Director, and work in an Agile environment alongside a team of Software Developers, Business Analysts, and Public Health Analysts in our Ann Arbor office. During your career at Altarum, you will have the opportunity to make important software and web development contributions to multiple healthcare projects such as java based web applications for public health, clinical decision support tools, EHR integration, and mobile applications. | 6/11/2017 |
| 1248 | KBI Biopharma Durham, NC Research Associate/Sr. Research Associate BS technical discipline Exp: 0-2 yrs |
Responsible for the development of analytical test methods used for testing samples from the upstream and downstream development organization and performing elementary data analysis. Responsible for the development and execution of method qualification protocols of developed analytical test methods. | 6/27/2017 |
| 1249 | KBI Biopharma Woodlands, TX Process Development Associate MS life sciences Exp: 1 yr |
This individual will conduct a variety of cell culture and analytical assays in support of product characterization and potency assessment. The position will also participate in process development, optimization, validation, and tech transfer to GMP. | 6/27/2017 |
| 1250 | KBI Biopharma Woodlands, TX Microbiology - Environmental Services Associate BS scientific discipline Exp: 1 yr |
Perform daily environmental monitoring and assist in collection and transfer of samples for laboratory analysis and reporting of results | 6/27/2017 |
| 1251 | KBI Biopharma Houston, TX Cell Therapy Associate II BS scientific discipline Exp: 0-5 yrs |
Manufacture cell therapy products per manufacturing batch records and in compliance with current regulations and quality standards. The duties required include basic cell culture and specialized cell culture techniques including, but not limited to, cell selection, transduction, and purification protocols. Collaborate with Development to transfer new procedures into Manufacturing. Train junior associates on technical and facility cleaning procedures, analyze manufacturing data for trending, work with others to assist in transfer of new procedures into manufacturing. Perform operations in a cleanroom environment, applying controls to assure aseptic processing including gowning, cleaning, and isolation procedures. May provide direction to junior staff and act as lead when necessary. Document each task involving manufacturing procedures, line clearance, maintenance and cleaning procedures per Good Documentation Practices upon completion. Utilize and perform maintenance on equipment per standard operating procedures. Demonstrate proficiency in current Good Manufacturing Practices and how they apply to specific tasks and responsibilities. Prepare documentation of non-conformance, deviations, and CAPAs. | 6/27/2017 |
| 1252 | Pfizer Andover, MA Associate Scientist BS scientific discipline Exp: 1-2 yrs |
The incumbent candidate will be responsible for conducting experiments in support of developing, evaluating and characterizing novel delivery formulations / processes, components and supporting devices for diverse therapeutic modalities including (but not limited to) mammalian and microbial fermentation derived candidate molecules, vaccines, gene medicine and cell-based therapies, and targeted delivery strategies. This individual functions cooperatively with other members of the team to achieve the project goals. The incumbent displays technical awareness in various aspects of drug discovery and development, strong drive in learning new techniques and scientific commitment, and impactful scientific and technical contributions within Pharmaceutical Research &; Development team and the respective project teams. | 6/27/2017 |
| 1253 | Pfizer Pearl River, NY Associate Scientist, Analytical R&D BS / MS chemistry, biochemistry, or related Exp: 0-3 yrs |
The candidate will be responsible for performing various scientific tasks related to project deliverables with supervision. The candidate is responsible for generating high quality data in support of other business lines in ARD using core analytical methodologies (such as HPLC and CE) for biological molecules, reviewing others experiments and data, and documenting data / results according to applicable compliances including authoring documentation. Effective oral and written communication skills as well as the ability to work in a team-based, fast-pace environment are also required. | 6/27/2017 |
| 1254 | Pfizer Andover, MA 2nd Shift Automation Engineer BS chemical, mechanical, or electrical engineering Exp: 1 yr |
Provide engineering technical support related to the maintenance, installation, startup / commissioning, testing, and qualification of automation systems for process equipment and process related systems within a biopharmaceutical manufacturing facility. Also, provide some detailed engineering on change controls and limited functionality upgrades to existing systems. | 6/27/2017 |
| 1255 | Pfizer Andover, MA Associate Scientist, Assay Development MS scientific discipline Exp: 1 yr |
Work under supervision of Senior Scientist With limited degree of independence, responsible for development of robust and reliable ligand binding in biological matrix (plasma, serum) and / or cell-based assays suitable for characterizing the disposition and immunogenicity of biotherapeutics in various matrixes using a range of potential screening platforms and assay techniques. With limited degree of independence, responsible for the design, trouble shooting, validation and conduct of the assay to support biotherapeutic programs. Timely delivery of concentration and immunogenicity data to PDM BioTX principal investigators and other partners in compliance with local or global regulatory requirement. Responsible for following departmental SOPs Accurate execution and documentation of bioanalytical method in a regulatory compliant manner. Ensure GLP compliance is maintained in laboratory during study support Laboratory focused position | 6/27/2017 |
| 1256 | Knudra Transgenics Salt Lake City, UT Laboratory Technician BS scientific discipline Exp: 1 yr |
Responsibilities include PCR, Restriction enzyme digestion, Gel electrophoresis, DNA isolatin, Oligo design, Sequence interpretation, Laboratory maintenance (making solutions, ordering supplies, etc), Effective communication with teammates, Other assignments as directed | 6/27/2017 |
| 1257 | Knudra Transgenics Salt Lake City, UT C. elegans Technician 1 BS scientific discipline Exp: 1 yr |
Responsibilities include Perform basic C .elegans tasks (picking, strain maintenance, identifying phenotypes, lysis) Microinjections PCR Restriction enzyme digestion Gel electrophoresis Effective communication with teammates Other assignments as directed | 6/27/2017 |
| 1258 | SeraCare Milford, MA Manufacturing Associate I BS biology, chemistry, or related Exp: 0.5 yrs |
The Manufacturing Associate / Technician provides direct labor for the manufacturing of high quality diagnostic products using manual and semi-automated equipment and prepares / completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured | 6/27/2017 |
| 1259 | La Jolla Pharmaceutical San Diego, CA Research Associate, PD Synthesis BS chemistry or chemical engineering Exp: 0-3 yrs |
The Research Associate will support the research and development lab by carrying out chemical synthesis experiments, sampling, testing, measuring, recording, and analyzing the results as part of a scientific team. Research Associate will provide all the required technical support to enable the laboratory to function effectively while adhering to standard operating procedures and health and safety guidelines. Research Associate will also maintain good documentation practices while troubleshooting and resolving problems with management supervision. | 6/27/2017 |
| 1260 | LabCorp Westborough, MA Molecular Technologist BS / MS biology, chemistry, or related Exp: 0-1 yr |
The Integrated Genetics Division of LabCorp is seeking a Molecular Technologist to join their Molecular Diagnostics team! The Molecular Technologist will be responsible for performing complex molecular testing and results analysis according to established standard operating procedures. The Integrated Genetics-Westborough site processes extracted DNA from peripheral blood and prenatal samples (amniotic fluid and chorionic villi) for genetic testing. A variety of molecular genetics techniques are used to include Next Generation Sequencing, real time PCR, Sanger Sequencing 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. | 6/27/2017 |
| 1261 | LabCorp Birmingham, AL Medical Lab Technician AS medical laboratory technology or related Exp: 1 yr |
Performs a variety of laboratory tests and assays in accordance with established policies, procedures and regulations in Microibiology department. Interprets results, subject to verification by Technologist / Supervisor, and providing allowance by State regulations. | 6/27/2017 |
| 1262 | Lake Pharma Hayward, CA Associate Scientist/Scientist - Protein Chemistry (Cloning/DNA Production) BS / MS biology or related Exp: 1 yr |
This position provides a unique opportunity for a person with aspiration to join and contribute to a fast-paced team at a rapidly expanding company with a cutting-edge technology platform and ample opportunity to grow with the company. LakePharma offers a competitive compensation package and is an equal opportunity employer. | 6/27/2017 |
| 1263 | Lake Pharma San Francisco, CA Associate Scientist Protein Chemistry BS / MS biochemistry, biophysics, biotechnology Exp: 1 yr |
LakePharma is inviting applications for a full-time Associate Scientist / Scientist position in its Protein Chemistry unit. The candidate will be primarily responsible for protein purification and protein conjugation. | 6/27/2017 |
| 1264 | Eurofins Groton, CT Analytical Chemist - Product Development BS science or related Exp: 1 yr |
Ability to work in a GLP or GMP environment with appropriate documentation and safety practices. Support formulation development through hands-on generation of accurate and precise analytical chemistry data using routine laboratory techniques such as liquid chromatography (HPLC, UPLC), NMR (liquid), mass spectrometry, vibrational spectroscopy, USP / EP dissolution testing, Karl Fischer titration. Development of dissolution methodology that will provide some measure of an in vivo / in vitro relationship and serve as a quality control procedure. Development and execution of studies to ascertain degradation mechanisms in the solution and solid state. Assess stability risks by evaluating process changes and impact on degradation chemistry or dissolution profile. This would involve DoEs and accelerated stability studies. Development of assay / purity methods and assessment of method robustness / ruggedness. Development and execution of method validation protocols. Transfer of analytical methods to other laboratories and remote sites. Hands-on generation of data in support of accelerated and registration stability studies. | 6/27/2017 |
| 1265 | Eurofins La Jolla, CA Associate Formulations Scientist, Part - Time AS / BS chemistry or related Exp: 0-3 yrs |
Preparation of prototype formulations (solutions, suspensions, tablets, capsules, etc.) for exploratory studies in in-vitro and in-vivo models. This includes development of oral, topical and intravenous (sterile) dosage forms for feasibility studies and small scale manufacturing operations. Measurement of key active compound and formulation properties (such as solubility, pH, isotonicity, color, gelling tendency, etc.). Assessment of the chemical and physical stability of prototype formulations. Identifying potential stability and performance issues with prototype formulations. Development of protocols for preparation of formulations at preclinical study sites. Routine preparation of solution and suspension formulations for use in preclinical studies. | 6/27/2017 |
| 1266 | Eurofins Indianapolis, IN Biochemist - Chromatography BS biology, biochemistry, chemistry, or related 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. Enter data into LIMS. Participate in conducting investigations. Document test results in notebooks and reports | 6/27/2017 |
| 1267 | Eurofins West Point, PA Biologics Process Development Scientist BS chemical engineering, biomedical engineering, or biological sciences Exp: 6 months |
Perform tissue culture based experiments on live vaccine products, process intermediates, and related experimental samples. Prepare solutions and culture media. Maintain multiple cell lines. Perform lab-scale downstream processing and in-process assay support for vaccine products and intermediates using standard purification techniques (e.g. depth filtration, centrifugation, sonication, etc). Maintain records and test results following good manufacturing practices (GMP). Management of lab supplies and raw materials. Work independently and efficiently. Document work clearly and perform tests accurately. Communicate effectively with client staff members | 6/27/2017 |
| 1268 | Eurofins Lee's Summit, MO Clinical Laboratory Scientist BS 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. | 6/27/2017 |
| 1269 | Eurofins West Point, PA Downstream Scientist BS chemistry, biochemistry, biochemical engineering, or related Exp: 0-1 yr |
Setup process equipment for lab-scale experiments. Prepare laboratory reagents, solutions and culture media. Perform lab-scale downstream processing of vaccine process intermediates. Perform process monitoring assays. Analyze, collate, track, and report data back to client staff members. Maintain records and test results following good laboratory practices (GLP). Work independently and efficiently. Document work clearly and perform tests accurately. Communicate effectively with client staff members | 6/27/2017 |
| 1270 | Eurofins Lancaster, PA Laboratory Intern BS scientific discipline Exp: 1 yr coursework |
Understand and follow Quality System documents relevant to responsibilities, e.g., Quality Manual, SOPs, and Methods. Adhere to appropriate quality measures to meet or exceed the standards set by ISO / IEC 17025, government regulatory, and company requirements relevant to assigned duties. Adhere to all health, safety, and environmental regulations relative to assigned analytical work; maintain and assist others in maintaining a clean, safe work environment. Registration of incoming samples (as needed), maintaining a neat and accurate record system of work performed on a daily basis and as needed for quality control tests or regulatory purposes. Enter the sample data into Eurofins eLIMS sytem in a timely and accurate manner. Complete laboratory testing on all incoming samples in an accurate, efficient and timely manner; ensure sample turnaround time goals are met or exceeded. Verify results and submit results to the appropriate personnel for transmission, in a timely manner. Identify process difficulties and report these together with proposed solutions to supervisor. Maintain a perpetual state of readiness and willingness to respond to the queries and needs of clients, staff, and co-workers. Maintain cooperative working relationships with all company employees; communicate orally and in writing to co-workers; this includes "intra" and "inter" departmental employees. Promote the company image through the exercising of sound and ethical business practices as related to the public and our customers. Continually strive to improve the quality of work we provide to our clients through existing and new technologies. Identify non-confromances and out-of- specifications and investigate to determine the possible root causes. Perform other related duties as assigned | 6/27/2017 |
| 1271 | Lannett Philadelphia, PA AR&D Technician BS chemistry or related Exp: 0-2 yrs |
The ARD Technician is responsible for cleaning laboratory glassware and operating glassware washing machine, disposal of organic waste, calibrating balances on the day of use, pH meters and Karl Fischer water analyzer, if necessary. These duties must be performed following cGMP s / GLP s and OSHA standards. Perform other duties as assigned. Detailed description is below. | 6/27/2017 |
| 1272 | Lannett Seymour, IN Regulatory Affairs Labeling Associate BS technical discipline Exp: 1-2 yrs |
Prepare, compile, review and maintain pending and commercial product labeling components. | 6/27/2017 |
| 1273 | Shire Social Circle, GA Operations Analyst BS in Chemical Engineer, Biological / Biotech Engineer or Biotechnology Exp: 0-4 yrs |
The position will support the development of a new, state-of-the-art plasma fractionation facility that will bring Shire additional capacity for fractionating, purification, and fill and finish for its biologic medications. This position will play a key role in start-up operations supporting manufacturing in areas like documents authoring, deviations investigation and CAPA determination and change controls implementation | 6/19/2017 |
| 1274 | Shire Social Circle, GA Mfg Science Specialist BS Exp: 0-1 yr |
Play a role in support of laboratory operations or manufacturing sciences. Maintain and manage laboratory operations, instrument qualification and maintenance as needed. | 6/19/2017 |
| 1275 | Shire Los Angeles, CA Engineer BS in Engineering 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. | 6/19/2017 |
| 1276 | Shire Round Lake, IL Manufacturing/Reliablity Engineer II BS in Engineering Exp: 1-3 yrs |
Develop the maintenance strategy, plans, SOPs, parts lists, BOMs and frequencies for new and modified equipment. | 6/19/2017 |
| 1277 | Shire Social Circle, GA Production Engineer I BS in Engineering Exp: 0-3 yrs |
Accountable for all operational aspects for a given unit operation within the manufacturing area. Focused on ensuring operational readiness and successful startup of the facility. Support the design and qualification of the manufacturing facility and equipment, and specific technology transfer efforts for the process. | 6/19/2017 |
| 1278 | Shire Lexington, MA Environmental Specialist BS / BA in technical discipline Exp: 0-3 yrs |
The primary role of the Environmental Specialist is to support all environmental compliance activities across the Shire Lexington Massachusetts Site locations. This includes activities related to air, hazardous / regulated waste, wastewater, chemical inventory, and environmental release compliance initiatives. Maintaining environmental permits, performing required inspections, gathering data for reports, providing training, assembling metrics and supporting sustainability initiatives will be core responsibilities. | 6/19/2017 |
| 1279 | Takeda Brooklyn Park, MN Process Engineer BS / MS in Engineering Exp: 0-5 yrs |
Serve as the engineering lead for a specific process area (cell culture, harvest, purification, clean-in-place, or clean / facility utilities equipment) ensuring systems remain in a qualified state | 6/19/2017 |
| 1280 | Takeda Brooklyn Park, MN Manufacturing Associate II BS Exp: 1-2 yrs |
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. | 6/19/2017 |
| 1281 | 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. | 6/19/2017 |
| 1282 | Teleflex, Inc Mansfield, MA Associate Manufacturing Engineer BS Exp: 1 yr |
Responsible for supporting manufacturing, designing and developing processes, and sustaining existing products, including design calculations, creating solid models, and detailing prints with minimal supervision. This is a hands-on position which will provide key technical support throughout the manufacturing process. Under supervision, this role will take a role in manufacturing and engineering functions such as specifying and validating new equipment and materials, troubleshooting processes, identifying and implementing process / product improvements. Work with cross functional teams to monitor and improve yields, resolve material issues, customer complaints and review customer issues. Interface with customers, vendors, and internal departments to achieve our goal of high quality products and on-time delivery. | 6/19/2017 |
| 1283 | Teleflex, Inc Jaffrey, NH Associate Quality Engineer BS in engineering, chemistry, physical science or related field Exp: 1 yr |
The Associate Quality Engineer shall support the Jaffrey, NH facility, Value Stream teams and Quality Assurance department in the development, implementation, and maintenance of the quality system, in order to maintain compliance to FDA 21CFR Part 820, ISO 13485 and Teleflex Global and Local procedures. | 6/19/2017 |
| 1284 | Teleflex, Inc Mansfield, MA Regulatory Affairs Specialist BS in a technical discipline required Exp: 1 yr |
The Regulatory Affairs Specialist is responsible for managing all aspects of regulatory affairs associated with the OEM business unit, including but not limited to, technical file review, labeling review, and design control review. This position will complete Regulatory Strategy documents for US, Canadian, and EU submissions; will be responsible for supporting and participating in the management of interactions with the US FDA, Health Canada, Notified Bodies (ISO), and other global regulatory authorities; and will support and participate in interactions with OEM customers' Regulatory Affairs representatives to support global submissions and resolve issues. The Regulatory Affairs Specialist will also need to stay abreast of evolving global regulatory requirements | 6/19/2017 |
| 1285 | Teleflex, Inc Maple Grove, MN Regulatory Product Specialist BS Exp: 1 yr |
The Regulatory Product Specialist will serve as a core project team member in advancing our new mechanical products to market. With strong, continued investment in the internal development of new and increasingly complex mechanical and biological products, it s an exciting time to be a part of our RA group. If you are interested in being part of a fast-paced, technically challenging and rewarding RA environment, we would like to hear from you as we build this critical part of our organization. | 6/19/2017 |
| 1286 | Teleflex, Inc Morrisville, NC Supplier Quality Data Analyst BS in scientific / technical discipline Exp: 1-3 yrs |
The Supplier Quality Data Analyst develops, implements, and maintains supplier databases and collects and analyzes supplier quality data in preparation for generation of statistical and analytical reports. | 6/19/2017 |
| 1287 | TESARO, Inc. Waltham, MA CMC Operations Specialist BS in Life Sciences Exp: 1-2 yrs |
The CMC Operations Specialist, CMC PM will be responsible for managing the logistics of contract execution within Pharmaceutical Development. The candidate will assist with the coordination of the various financial deliverables for the Pharmaceutical Development portfolio. S / he will play an integral role in the planning of the Pharmaceutical Development Annual Operating Plan (AOP). The candidate will assist with the development and implementation of various processes and tools to increase efficiencies and reporting within the Pharmaceutical Development organization. | 6/19/2017 |
| 1288 | Teva Pharmaceuticals Salt Lake City, UT Chemist I BS in Chemistry or related science Exp: 0-1 yr |
Performs basic testing of finished products, maintenance and calibration of analytical instruments, prepares standard and sample solutions, and maintains appropriate records. | 6/19/2017 |
| 1289 | Teva Pharmaceuticals Salt Lake City, UT MS&T Specialist I BS Exp: 1-2 yrs |
Under general supervision, determines the critical aspects of manufacturing equipment with regard to product and process, and writes protocols and other records related test results. Prepares final reports that identify the results of protocol testing and the conditions of release. Assists in conducting efficiency studies and in the identification of process improvement opportunities. Participates in project coordination activities. | 6/19/2017 |
| 1290 | Teva Pharmaceuticals Elizabeth, NJ EHS Engineer BS in Engineering / Science preferably in Occupational Safety and / or Environmental Engineering or Science or other closely related field Exp: 1 yr |
Work in the EHS team towards ensuring the environmental & OSHA compliance and support health & safety programs. | 6/19/2017 |
| 1291 | Teva Pharmaceuticals Elizabeth, NJ QC Auditor I BS in Chemistry or related science Exp: 0-1 yr |
Performs peer review of chemist s work and assembles data packets; Performs LIMS entry, review and maintains database; Generates Test Reports, Certificate of Compliance, and other documents using Excel and Word. | 6/19/2017 |
| 1292 | Teva Pharmaceuticals Elizabeth, NJ EHS Engineer BS in Engineering / Science preferably in Occupational Safety and / or Environmental Engineering or Science or other closely related field Exp: 1 yr |
The incumbent is responsible for assisting with Environmental, safety and occupational health programs and projects by identifying and mitigating safety and health hazards impacting the work environment, and compliance with safety and environmental regulations & permits. The employee will provide support in assessing, monitoring and auditing operations to insure regulatory compliance with Environmental Protection Agency (EPA) and Occupational Health & Safety Agency (OSHA) regulations. | 6/19/2017 |
| 1293 | West Pharmaceutical Services, Inc Scottsdale, AZ Project Associate BS in Engineering Exp: 0-3 yrs |
Supports all quality system and functions. Assists in establishing systems to support the facility to drive continuous improvements and minimize the costs of non-conformance. Plans, schedules, executes and communicates all items regarding quality issues, complaints, validations and other projects to the QA Manager and / or other interested parties. Performs all duties associated with compliance-related items for ISO standards and cGMps. | 6/19/2017 |
| 1294 | West Pharmaceutical Services, Inc Kearney, NE Manufacturing Engineer BS Exp: 1-3 yrs |
Supports manufacturing through identification, design and implementation of process improvement projects; Ensures compliance with environmental regulations; | 6/19/2017 |
| 1295 | Theravance Biopharma South San Francisco, CA Research Associate I/II BS in a Biological Science o Exp: 1 yr |
The Drug Metabolism and Pharmacokinetics (DMPK) department at Theravance BioPharma is seeking an experienced, laboratory-based Research Associate to support in vivo small-molecule drug discovery and development. This individual will assume a hands-on role within the in vivo DMPK team and contribute to multiple research projects. The successful candidate will exhibit strong communication and interpersonal skills and desire to work in a fast-paced, flexible and dynamic environment. | 6/19/2017 |
| 1296 | Thermalin Diabetes, LLC Cleveland, OH Entry Level Protein Specialist BS in biochemistry or related science Exp: 1 yr |
Organize and purify a variety of insulin analogs and their precursors from microbial and synthetic sources | 6/19/2017 |
| 1297 | Tricida, Inc. South San Francisco, CA Research Associate, Analytical Development BS / MS in Analytical Chemistry or related disciplines Exp: 0-3 yrs |
The chemist will be responsible for performing analyses by following established methods as well as assisting with development of methods for impurities assessment and characterization. The successful candidate must possess a strong understanding of chromatographic techniques used in drug development. The position will collaborate closely with cross-functional team members, including quality control, quality assurance, process development (drug substance and drug product), regulatory and clinical operations. | 6/19/2017 |
| 1298 | TriLink BioTechnologies, LLC San Diego, CA GMP Assistant Chemist BS in Chemistry or Biology Exp: 1 yr |
This individual will be involved in the synthesis, processing and purification of synthetic DNA and RNA, mRNA compounds for research, diagnostic or therapeutic application. Techniques include oligonucleotide synthesis, HPLC analysis and purification, gel electrophoresis, gel filtration, conjugation chemistry and spectral analysis. | 6/19/2017 |
| 1299 | Triphase San Diego, CA Clinical Research Associate 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. | 6/19/2017 |
| 1300 | Tris Pharma, Inc. 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. | 6/19/2017 |
| 1301 | Tunnell Consulting Framingham, MA Automation Technician V MS in Engineering Exp: 1 yr |
The Automation Engineer assists more senior members to ensure reliable and smooth operation of all automation systems for a 24x7 commercial manufacturing facility. The AE works independently, under general supervision on projects that do not require significant independent decision making. The work performed is generally reviewed for soundness of judgment and overall adequacy and accuracy by manager or lead engineers. | 6/19/2017 |
| 1302 | Theravance Biopharma South San Francisco, CA Bioinformatics Biology Internship BS / MS in Bioinformatics, Biology, Genetics Exp: NA |
Engage biologists to fully understand biological questions and project objectives, typically gene expression and pathway analysis, GWAS, proteomics, or target identification | 6/19/2017 |
| 1303 | Theravance Biopharma South San Francisco, CA Biometrics Internship MS in biostatistics Exp: NA |
Theravance Biopharma, Inc. is seeking a Summer Intern in Biometrics biostatistics group. Reporting to the Associate Director of biostatistics, this position will support a statistical research project, and the analysis of clinical studies. | 6/19/2017 |
| 1304 | Tris Pharma, Inc. Monmouth Junction, NJ Scientist I - R&D Formulation/Product Development MS in Pharmaceutical Sciences / Pharmaceutics / Industrial Pharmacy Exp: 1 yr |
Prepares formulation batches for compatibility studies, stability studies, pilot batches and pivotal batches. | 6/19/2017 |
| 1305 | Takeda San Diego, CA Intern - Protein Chemistry BS Exp: NA |
Conduct routine biochemical laboratory tasks including buffer and sample preparations | 6/19/2017 |
| 1306 | Takeda San Diego, CA Intern - Systems Engineering BS in Mechanical / Electrical Engineering, Biology, Biochemistry Exp: NA |
Systems Engineering is responsible for the operations of both Takeda s High Throughput Crystallization Robotics and Compound Management. An intern has been utilized to perform critical tasks in advance of running automated instrumentation to ensure smooth operations and to allow core fulltime staff to focus on higher level tasks. The objective of the Systems Engineering Intern is to support protein crystallization efforts and compound management order fulfillment. The tasks performed by the intern are tailored to ensure maximum productivity for SE automated systems and on-time fulfillment of deliverables to stakeholders. | 6/19/2017 |
| 1307 | Takeda San Diego, CA Intern - Biophysical Chemistry/NMR BS / MS Exp: NA |
Conduct routine biochemical laboratory tasks which include manual pipetting, plate-based assays, and buffer and sample preparation. | 6/19/2017 |
| 1308 | Shire Cambridge, MA Regulatory Submission Specialist BS Exp: 0-4 yrs |
The PLS Submissions Specialist is responsible for the planning, publishing (paper, NeES, eCTD), review and dispatch of regulatory compliance submissions to global Health Authorities within required timeframes as well as maintenance of the global registration tracking tool. The primary accountability for this role is for the publishing of submissions. They also represent Global Regulatory Operations in special initiatives, process design and validation testing of new and upgraded software. | 6/12/2017 |
| 1309 | Shire Social Circle, GA Quality Control Analyst II MS in Chemistry, or Biological Sciences Exp: 0-3 yrs |
Execute activities as part of the Quality Control Investigation team to ensure the safety and reliability of Shire products are in compliance with quality and regulatory requirements. Complete robust investigations that determine accurate root causes and effective corrective and preventive actions that mistake proof against the root causes. Support Contamination Control Master Plan (CCMP) initiatives. Interface with Manufacturing, Quality Assurance, and Quality Systems to support product fulfillment and regulatory requirements. Continuously drive the application of Lean and Six Sigma principles to the floor level through activities such as Kaizen, Six Sigma projects and VIPs. | 6/12/2017 |
| 1310 | Shire Social Circle, GA Quality Control Analyst I BS in Chemistry, or Biological Science Exp: 0-2 yrs |
Assist in the development of lab test methods on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Shire manufacturing facilities. Work under minimum supervision. | 6/12/2017 |
| 1311 | Shire Social Circle, GA Quality Control Analyst BS in Biology, Microbiology, or Chemistry Exp: 0-2 yrs |
Conduct critical microbiological analyses on raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at Shire manufacturing facilities. Work under minimum supervision. | 6/12/2017 |
| 1312 | Shire Social Circle, GA Quality Control Associate MS in Chemistry, or Biological Sciences Exp: 0-3 yrs |
Conduct biological, chemical and physical analyses on pharmaceutical products and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs. | 6/12/2017 |
| 1313 | Shire Social Circle, GA Manufacturing Associate BS Exp: 0 yr |
Process understanding of primary work areas (e.g. Buffer preparation, fractionation, purification, fill, finish). | 6/12/2017 |
| 1314 | Shire Social Circle, GA Manufacturing Assoc 2 BS Exp: 0 yr |
The position will support the development of a new, state-of-the-art plasma processing facility that will bring Shire additional cGMP capacity for fractionation, purification, filling, and packaging for its biologic medications. | 6/12/2017 |
| 1315 | Smithers Avanza Gaithersburg, MD Animal 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. | 6/12/2017 |
| 1316 | Smithers Avanza Gaithersburg, MD Formulations Lab Tech 1 BS in Biology, Life sciences, Chemistry or Science field Exp: 1 yr |
Learns how to review study protocol and ensure study formulations and data for pre-clinical research studies are conducted in accordance with established protocols, SOPs, GLPs, and other pertinent regulatory requirements. | 6/12/2017 |
| 1317 | 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. | 6/12/2017 |
| 1318 | Smithers Avanza Gaithersburg, MD Research Scientist II MS in Molecular Sciences and Nanotechnology Exp: 1 yr |
Research Scientist II to work in Gaithersburg, MD: 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. | 6/12/2017 |
| 1319 | Smithers Avanza Gaithersburg, MD Scientist 1 MS in Biological or Physical Sciences Exp: 1-2 yrs |
Experience and knowledge of Ligand-binding assays (e.g. ELISA / MSD) applicable to Pharmacokinetic, Biomarker and Immunogenicity studies is required. | 6/12/2017 |
| 1320 | Sorrento Therapeutics Inc. San Diego, CA RESEARCH ASSOCIATE/SENIOR RESEARCH ASSOCIATE, ANALYTICAL DEVELOPMENT AND QUALITY CONTROL BS / MS in analytical chemistry, biochemistry, protein chemistry or related disciplines Exp: 0-5 yrs |
The qualified candidate will be responsible for the development, implementation and maintenance of a variety of analytical assays to support research and pre-clinical development of protein therapeutics. The successful candidate needs to have knowledge and hands on experience in spectroscopy (UV), chromatography (SEC, IEX, HIC, RP), electrophoresis (SDS-PAGE and CE), and other protein analysis techniques. | 6/12/2017 |
| 1321 | Spectranetics Maple Grove, MN Clinical Research Associate II MS in engineering biological sciences or related medical / scientific field Exp: 1-2 yrs |
You will work with our Clinical Project Manager to meet applicable regulatory standards and company requirements for Global Clinical Studies. You will support study management activities, general site management and oversight of CRO, and need to have expertise in GCP, EU regulatory environment as well as interfacing with multiple functional groups: Clinical Field Specialists, Marketing, Sales, Regulatory, Quality, Data Management, Finance / Accounts Payable. | 6/12/2017 |
| 1322 | 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. | 6/12/2017 |
| 1323 | Stratacuity Portsmouth, NH Associate Scientist - Bioanalytical Sciences BS / MS Exp: 1 yr |
Assist with LCMS-based bioanalysis for a gene therapy platform working on biological sample extraction and execution of established LCMS-based methods | 6/12/2017 |
| 1324 | Stratacuity Portsmouth, NH Clinical Trial Coordinator BS / MS Exp: 0-2 yrs |
Collaborate closely with Clinical Study Manager, study teams (internal / external) and CRO partners | 6/12/2017 |
| 1325 | Stratacuity Portsmouth, NH Microbiology Research Associate BS in biochemistry, microbiology, or related field Exp: 1-2 yrs |
Develop and perform SOP-driven assays for characterization of microorganisms; Analyze data rigorously and critically, and report it out in a timely fashion;Participate in developing core intellectual property. | 6/12/2017 |
| 1326 | Stratacuity Portsmouth, NH RNA Research Associate BS / MS Exp: 1-6 yrs |
Deep knowledge of RNA production, handling, and characterization;Additional skills in primary cell culture and related reporter assays will be viewed favorably; Ability to multitask and stay organized is a must - critical thinking is desired and welcome. | 6/12/2017 |
| 1327 | Stratacuity Portsmouth, NH Associate Scientist - Bioanalytical Sciences BS / MS Exp: 1 yr |
Assist with LCMS-based bioanalysis for a gene therapy platform working on biological sample extraction and execution of established LCMS-based methods | 6/12/2017 |
| 1328 | Stryker Portage, MI Regulatory Affairs Specialist BS in engineering, science, legal or regulatory degree preferred Exp: 0-2 yrs |
The Regulatory Affairs Specialist is involved with the regulatory practices associated with commercialization of medical devices. | 6/12/2017 |
| 1329 | Synthetic Genomics, Inc. La Jolla, CA Temporary Research Associate BS in microbiology, phycology, biology or related discipline Exp: 1-2 yrs |
Under supervision, the Research Associate will assist in performance of laboratory scale cultivation and productivity measurements of algae as a member of a focused strain development team working toward improved carotenoid yield from algae. | 6/12/2017 |
| 1330 | Synthetic Genomics, Inc. La Jolla, CA Temporary Research Associate BS in microbiology, phycology, biology or related discipline Exp: 1-2 yrs |
Under supervision, the Research Associate will assist in adaptive evolution of algal cultures and productivity measurements of algae as a member of the photosynthesis team working towards increasing the productivity of algae. | 6/12/2017 |
| 1331 | Supernus Pharmaceuticals Rockville, MD QC CHEMIST BS Exp: 0 yr |
To provide QC support for solid dosage pharmaceutical forms, primarily by using dissolution testing, spectroscopy, HPLC, wet chemistry, and by maintaining log books and performing data management / report writing as necessary. | 6/12/2017 |
| 1332 | Supernus Pharmaceuticals Rockville, MD Calibration Assistant I BS in Chemistry, Engineering Exp: 0 yr |
Responsible for the calibration and preventative maintenance of all laboratory instruments / equipment for the Analytical Sciences (AS) and Quality Control (QC) departments | 6/12/2017 |
| 1333 | Supernus Pharmaceuticals Rockville, MD QUALITY ASSURANCE ASSOCIATE I BS in a life sciences discipline Exp: 0 yr |
To support the Company s Quality Assurance and compliance programs by initiating & reviewing documentation, maintaining compliance systems, and performing inspections of GMP facilities, and mastering CFR and / or FDA guidance. | 6/12/2017 |
| 1334 | Sutro Biopharma, Inc. San Carlos, CA QC Microbiologist BS / BA Exp: 1 yr |
The QC Microbiologist coordinates and performs routine and non-routine GMP microbiological testing, including environmental monitoring (EM) of classified clean rooms and critical utilities, release of product, and testing for validation protocols. Performs organism identification. Reads and interprets microbiological cultures and other related tests including but not limited to environmental monitoring, bioburden tests, growth promotion, microbial limits tests, endotoxin (LAL), and TOC testing. | 6/13/2017 |
| 1335 | Sutro Biopharma, Inc. San Carlos, CA Manufacturing Associate / Sr. Manufacturing Associate (Contract) BS in a biological sciences discipline or equivalent Exp: 1 yr |
Perform various manufacturing tasks such as operating, troubleshooting, sterilizing, maintaining, preparing, and cleaning of various process equipment such as stirred-tank bioreactors, media / buffer solutions, disc stack centrifuges, homogenizer, pelletizer, dryer, TFF skid, chromatography systems, parts washers, and CIP systems, under the guidelines of established SOPs and cGMP regulations. | 6/13/2017 |
| 1336 | Sword Diagnostics Chicago, IL Research Associate I, Product Applications BS in Biology, Molecular Biology or related field Exp: 1-3 yrs |
Your main responsibilities will be to perform functions in support of Product Application Scientist(s) and other individuals as needed, perform common laboratory testing (including ELISA) using established protocols, prepare buffers and other chemical solutions as needed and use proper personal protective equipment (PPE) and good aseptic technique to handle biological (including human) samples. On a day-to-day basis, you will be expected to suggest, plan and carry out studies with guidance of supervisor, record data for evaluation, analyze results with guidance of supervisor and assist other lab personnel as needed, maintain organized records of studies performed, and other duties and responsibilities as assigned. | 6/13/2017 |
| 1337 | Syngenta NA, NA P&S Development Program Associate BS Exp: NA |
As a PSDP Associate, you will learn and acquire business knowledge, skills and attributes required for placement into future leadership or management positions within P&S at Syngenta | 6/13/2017 |
| 1338 | Takeda Brooklyn Park, MN Automation Engineer BS in Engineering Exp: 0-5 yrs |
Act as technical owner for Process and Utility Systems, with respect to automated process. | 6/18/2017 |
| 1339 | Takeda San Diego, CA Intern - Biophysical Chemistry BS / MS Exp: NA |
Conduct routine biochemical laboratory tasks which include manual pipetting, plate-based assays, and buffer and sample preparation. | 6/19/2017 |
| 1340 | Shire Social Circle, GA Intern Technical Services BS / MS in Chemical Engineering or Biochemistry Exp: NA |
Support development and troubleshooting of protein purification / isolation processes. | 6/12/2017 |
| 1341 | Singulex Alameda, CA Clinical Research Intern MS Exp: NA |
Interns will be involved in the clinical research activities at Singulex. The program is centered on external collaborations with academic sites globally, as well as internal research and development. In addition to gathering, organizing, and analyzing laboratory data, interns will help designing and developing an internal library for scientific literature. Interns will also have the opportunity to participate in clinical research meetings as well as contribute to communication initiatives. | 6/12/2017 |
| 1342 | Surmodics, Inc. Eden Prairie, MN Information Systems Intern BS in Engineering Exp: NA |
Preparing new computers (imaging) and decommissioning old computers (wiping). | 6/12/2017 |
| 1343 | Sera Prognostics, Inc. Salt Lake City, UT CLINICAL TRIAL ASSOCIATE BS / BA in scientific or healthcare discipline Exp: 1 yr |
seeking a highly successful clinical trial associate to support the clinical trial operations | 6/5/2017 |
| 1344 | Regeneron Rensselaer, NY QA Raw Material Specialist BS / BA Exp: 1 yr |
Determines disposition of raw materials and ensures compliance with Quality Assurance (QA) policies and procedures, cGMPs, SOPs, and Regeneron Standard Requirement Documents. | 6/5/2017 |
| 1345 | Regeneron Tarrytown, NY Research Associate I - II, Infectious Diseases BS / MS Exp: 0-8 yrs |
Incumbent will function as part of a larger team. The ultimate goal is to design, validate and develop immunotherapeutic reagents for the treatment and / or prevention of virus infections. | 6/5/2017 |
| 1346 | SeraCare Life Sciences, Inc. Milford, MA Manufacturing Associate II BS / BA Exp: 0.5 yr |
The Manufacturing Associate II provides direct labor for the manufacturing of high quality diagnostic products using manual and semi-automated equipment and prepares / completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 6/5/2017 |
| 1347 | SeraCare Life Sciences, Inc. Milford, MA Manufacturing Associate I BS / BA Exp: 0.5 yr |
The Manufacturing Associate / Technician provides direct labor for the manufacturing of high quality diagnostic products using manual and semi-automated equipment and prepares / completes required documentation on manufacturing procedures. This position is responsible for set-up, calibration, and operation of all manufacturing equipment in accordance with cGMP, POPs, SOPs, Safety, and departmental policies. This position utilizes good judgment and critical thinking skills to make operator level decisions regarding the quality of the products manufactured. | 6/5/2017 |
| 1348 | Relypsa Redwood City, CA Medical and Scientific Affairs Coordinator BA / BS Exp: 1 yr |
The Medical and Scientific Affairs Coordinator will be responsible for operational project coordination to support the broad functions of the Medical and Scientific Affairs (MSA) Department. The position will report to the Executive Director, Medical Affairs. | 6/5/2017 |
| 1349 | Revance Newark, CA Manufacturing Associate I, DP BS 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. | 6/5/2017 |
| 1350 | Rho, Inc Chapel Hill, NC Research Associate - Quality Assurance BS Exp: 1-2 yrs |
The Research Associate will assist the Quality Assurance team in day-to-day operations of Quality Assurance activities as it relates to Rho's audit, internal support and quality management system activities. This position will perform a variety of administrative duties in support of the QA efforts, including reviewing, maintaining and filing of documents, scheduling meetings, and working with project teams and databases. | 6/5/2017 |
| 1351 | Roche Pleasanton, CA Scientist I (Clinical Operations) BS in Biological / Life Sciences, Chemistry Exp: 1-3 yrs |
After introduction to work processes, begins to organize, conduct and monitor laboratory testing for Clinical Trials in accordance with study Protocol, Good Laboratory Practices, Good Laboratory | 6/5/2017 |
| 1352 | Roche Los Gatos, CA Scientist I BS in Biological / Life Sciences, Chemistry, Biochemistry or related field Exp: 0-3 yrs |
After introduction to work processes, begins to organize, conduct and monitor laboratory experiments utilizing established and published procedures, and technical and theoretical understanding. | 6/5/2017 |
| 1353 | Roche Santa Clara, CA Lab Tech III, Sequencing BS in Biology, Chemistry, Biochemistry, Molecular Biology or a related field Exp: 1-3 yrs |
The candidate will be doing repetitive tasks, such as raw material release based on CofA s, therefore should be detail oriented and has strong record keeping and communication skills. The candidate should also have excellent troubleshooting and problem solving skills, along with some experimental design experience. | 6/5/2017 |
| 1354 | West-Ward Pharmaceuticals Cherry Hill, NJ Manufacturing Specialist BS 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 | 6/5/2017 |
| 1355 | West-Ward Pharmaceuticals Columbus, OH Scientist I, Quality Control BS in Chemistry or a science-related field Exp: 1 yr |
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. | 6/5/2017 |
| 1356 | Safis Solutions Indianapolis, IN Validation Analyst BS / MS Exp: Entry-leve |
The Validation Analyst is responsible for understanding software validation in a government regulated environment with special attention to the Software Development Lifecycle (SDLC) validation processes which meet regulatory requirements. The Validation Analyst will provide support to Senior Validation Analysts and Advisors in all areas of IT Software Validation activities. They will work with internal staff in implementation of improved capabilities in the areas of documentation, coding and validation, will assist in performing analysis of current validation situations, review internal controls, create policies and procedures to ensure validation is in compliance with applicable State and Federal guidelines and policies, and will respond promptly to external and internal concerns; implementing corrective actions as appropriate | 6/5/2017 |
| 1357 | Sangamo Therapeutics, Inc. Richmond, CA Clinical Research Associate BA / BS in a life sciences or health-related discipline is required Exp: 1-3 yrs |
Assist in the implementation of clinical research projects in accordance with standard clinical practice and corporate policies and procedures | 6/5/2017 |
| 1358 | Sanofi Framingham, MA QC ANALYST I BS in Life Sciences discipline Exp: 1 yr |
Quality Control Chemistry is responsible for testing intermediate and final product samples to demonstrate that all products meet all standards required for cGMP operations. Various techniques are utilized in Quality Control including HPLC, GC, Gel Electrophoresis and multiple types of spectrophotometry. Additional functions include stability testing, assay transfers and the qualification of new instrumentation utilized in the Quality Control laboratory. | 6/5/2017 |
| 1359 | Sanofi Framingham, MA RESEARCH ASSOCIATE MS in the life sciences Exp: 0-2 yrs |
The primary responsibilities for this position focus on the expression, purification, and characterization of recombinant proteins from mammalian, baculovirus / insect cell, and E. coli expression systems. The successful candidate will present data in well-organized written and oral formats and to work effectively in a collaborative team environment. | 6/5/2017 |
| 1360 | Sanofi Framingham, MA QUALITY CONTROL ANAYST II MS in the life sciences Exp: 1 yr |
This position is responsible for performing routine and complex testing of in-process samples, stability samples and final products in accordance with SOPs for product release and validation. | 6/5/2017 |
| 1361 | Sanofi Westborough, MA PROCESS ENGINEER I MS in Chemical or Biochemical Engineering, or related engineering discipline Exp: 0-2 yrs |
The position will support manufacturing and other internal groups with development and implementation of new methodologies and technologies for improved process understanding and robust control strategies. The incumbent will ensure that the highest standards of safety and environmental compliance are maintained in the workplace; and operate under the regulatory requirements for product development and manufacturing. | 6/5/2017 |
| 1362 | Sanofi Framingham, MA PROCESS ENGINEER I BS / MS in Chemical Engineering / Biochemistry / Biotechnology / Biological Sciences Exp: 0-4 yrs |
The Process Engineer I works in the Manufacturing Science group to provide expert technical support to Commercial Operations at the Framingham Biologics site. This includes, but is not limited to, experimental support for deviations or manufacturing investigations; process troubleshooting, raw material evaluation, Planning and execution of validation programs, continuous process monitoring and improvement. This person is also responsible for analyzing and drawing accurate conclusions and recommendations from the process and experimental data. | 6/5/2017 |
| 1363 | Sanofi Framingham, MA LAB COORDINATOR BS Exp: 0-2 yrs |
The Lab Coordinator will support upstream cell culture, downstream purification, and analytical development in a newly established MSAT lab. This individual will have the opportunity to have early and significant impact in this growing group. | 6/5/2017 |
| 1364 | Sanofi Swiftwater, PA QUALITY TECHNICIAN ASSOCIATE BS in Life Sciences discipline Exp: 1 yr |
The Associate Quality Technician - Quality Control candidate filling this position will performs testing in the Quality Control Bioassay laboratory while strictly adhering to site work instructions, Federal Regulations, cGMP and Sanofi Pasteur policies and procedures. This position requires the individual to perform routine testing as scheduled to support production, method validation as well as the stability program and completing required documentation. They 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. Knowledge and experience of immunology based testing is preferred. Experience in immunodiffusion techniques is desired. | 6/5/2017 |
| 1365 | Santa Cruz Biotechnology Santa Cruz, CA Laboratory Assistant BS in Biology, Molecular Biology or related field Exp: 0 yr |
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. | 6/5/2017 |
| 1366 | Sanofi Genzyme Westborough, MA Process Engineer I MS in Chemical or Biochemical Engineering, or related engineering discipline Exp: 0-2 yrs |
The position will support manufacturing and other internal groups with development and implementation of new methodologies and technologies for improved process understanding and robust control strategies. The incumbent will ensure that the highest standards of safety and environmental compliance are maintained in the workplace; and operate under the regulatory requirements for product development and manufacturing. | 6/5/2017 |
| 1367 | Scanogen Baltimore, MD Research Technician BS / MS in molecular biology, biotechnology or related field Exp: 1 yr |
The main focus is to support the R&D team by preparing materials, testing assays and maintaining the laboratory inventory | 6/5/2017 |
| 1368 | Seattle Genetics Bothell, WA Research Associate I/II Antibody Discovery BS in biological sciences or related disciplines Exp: 3 months |
We are seeking someone to initially assist with cell culture to generate and screen said antibodies, but also someone who exhibits long-term growth potential. In addition to being responsible for maintaining cell lines and hybridomas and antibody quantification, the research associate will be responsible for generating antibodies and additional key deliverables for other groups. Thus, the successful applicant will not only be adept at experimentation, but also be an effective team player. | 6/5/2017 |
| 1369 | Seattle Genetics Bothell, WA Quality Control Analyst I/II BS Exp: 0-3 yrs |
This position is located within the Quality Control department and is responsible for performing potency / binding assays (cellular bioassays and ELISA) and other related Quality Control methods for release and stability testing. | 6/5/2017 |
| 1370 | Semma Therapeutics Cambridge, MA Research Associate / Senior Research Associate - Cell Biology BS / MS in biology, cell biology, tissue engineering or related discipline Exp: 1-3 yrs |
Seeking an outstanding research associate to join its growing team. 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. | 6/5/2017 |
| 1371 | 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. | 6/5/2017 |
| 1372 | Second Genome South San Francisco, CA Research Intern, Data Curation BS / MS in Molecular Biology or related discipline Exp: NA |
Responsibilities will include reviewing and curating existing metadata, searching, reading and analyzing scientific literature to identify relevant novel findings and working closely with the internal scientific group to integrate findings into our existing database. | 6/5/2017 |
| 1373 | RetroVirox San Diego, CA Medicinal Chemistry and Database Support BS in Chemistry or Biochemistry Exp: NA |
The company is seeking a part-time intern to support the medicinal chemistry efforts for the Company s internal discovery programs funded by the National Institutes of Health (NIAID). Hundreds of experimental molecules are synthesized at RetroVirox to determine their antiviral and immunomodulatory activities. These small-molecules are recorded in a chemistry database and their activity and structure relationships used to guide future medicinal chemistry efforts. We are seeking highly proactive candidates able to handle the chemistry database of the company and input their information on a customized database. | 6/5/2017 |
| 1374 | Roche South San Francisco, CA Intern (6 months) - Corporate Groups - Site Services: Plant Engineering and Reliability BS / MS Exp: NA |
Site Services is a multi-disciplinary group at Genentech that focuses on making great work possible. Departments include Security, Facilities, Environment, Health & Safety, Work Environments, as well as Design & Construction. | 6/5/2017 |
| 1375 | Roche South San Francisco, CA Intern - Early Clinical Development - Clinical Imaging MS in Engineering Exp: NA |
Group (CIG) Machine / Deep Learning pilot team is seeking a graduate student summer intern to join an ongoing effort to demonstrate the value of Machine / Deep Learning on clinical imaging to drug discovery and development. Responsibilities will include data preparation, model development, and evaluation. | 6/5/2017 |
| 1376 | Roche South San Francisco, CA Intern (6 - month) - Pharma Technical Operations - PTDMM Portfolio Reporting & Analytics Group (PRA) BS / MS Exp: NA |
Portfolio & Project Management (PTDM) is a global organization that facilitates the end-to-end Drug Development Process to deliver our clinical and commercial product pipeline from early development to product launch. PTDM generates and executes technical development strategies, plans, & risk assessments, and monitors the technical project budgets. | 6/5/2017 |
| 1377 | RTI Surgical, Inc Greenville, NC Operations Engineer Intern BS / MS in Engineering Exp: NA |
Support quality system for Statistical Process Monitoring and Control;Analyze data using statistical techniques;Perform research assistant activities such as literature searches, summaries, and reports. | 6/5/2017 |
| 1378 | Pfizer St. Louis, MO Inspector B 3rd Shift (ID: 1055310) AS science related discipline Exp: 1 yr |
Inspection of all syringes, cartridges, assemblies and components using manual or automated systems / procedures. | 6/6/2017 |
| 1379 | Pfizer Groton, CT Drug Safety R&D Pathology Technician (ID: 1055300) BS biology Exp: 0-2 yrs |
The Pathology Technician is responsible for performing accurate, high quality necropsy / histology study work for rodent and non-rodent safety studies in compliance with the study protocol, Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP) regulations, Environmental Health and Safety (EHS) standards, animal welfare regulations, and departmental policies / procedures. The pathology data collected and processed on these studies by the Pathology Technician enable candidate selection, first-in-human studies, 13-week studies and early research and target safety and investigative work. | 6/6/2017 |
| 1380 | Pfizer Andover, MA Associate Scientist, Formulation and Process Development (ID: 1055300) BS pharmaceutics, chemistry, biology, chemical, biochemical engineering, or related 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, cell-based therapies 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. | 6/6/2017 |
| 1381 | Inova Diagnostics San Diego, CA Chemist II BS biological sciences or related Exp: 1-2 yrs |
Development duties include the development of antigens and antibodies according to research procedures. Assists in coordination of production pilot schedules. Major development duties include participation in the purification of antigens for autoimmune diagnostic products and the development of antibodies and conjugation of antibodies. Assistance may be necessary on the manufacturing group when production demands are required. | 6/7/2017 |
| 1382 | Integral Molecular Philadelphia, PA Information Technology Specialist BS computer science or related Exp: 1 yr |
This full-time position will involve information technology support, such as maintenance of phone and server systems and website support, for a biotechnology company consisting of approximately 35 scientists. This involves routine maintenance, new PC installations, and upgrades including hardware / software troubleshooting for 50+ computers. The successful candidate will provide website support including updates, search engine optimization, and back-end support for e-commerce. The position will also involve some database design, user interface programming, and software troubleshooting multiple internal applications used to manage complex biological data. Qualifications include knowledge of programming using C#, VBA, database / SQL queries involving Access and VB6, HTML, and CSS are helpful. | 6/7/2017 |
| 1383 | Integrated DNA Technologies Coralville, IA EHS Intern - 2 AS / BS chemistry or science-related program Exp: 1 yr coursework |
The EHS Intern works directly with EHS staff to assist in populating a chemical data inventory and perform routine work orders. | 6/7/2017 |
| 1384 | Integrated DNA Technologies Coralville, IA EHS Intern - 3 AS / BS chemistry or science-related program Exp: 1 yr coursework |
The EHS Intern works directly with EHS staff to assist in populating a chemical data inventory and perform routine work orders. | 6/7/2017 |
| 1385 | Integrated DNA Technologies Coralville, IA Research Scientist Intern BS biology, genetics, chemistry, or related life science Exp: 1 yr coursework |
The Research Scientist Intern, under supervision of an experienced Scientist, conducts bench scientific experimentation that advances the basic science of nucleic acids and nucleic acid biochemistry and assists with development and characterization of new IDT genomics products in NGS, qPCR and / or functional genomics. Ultimately, the intern should be able to apply practical, real world knowledge gained through this program into a possible future career in Research. | 6/7/2017 |
| 1386 | Intrexon San Francisco, CA IT Applications Specislist BS biology, computer sciences, or related Exp: 0 yrs |
The IT Applications Specialist will work on all phases of laboratory and enterprise systems development life cycle. Responsibilities will include; working with scientists and other stakeholders to elicit user requirements and business processes, analyze requirements, troubleshoot and resolve issues, document and execute support procedures, administer applications and databases, create and deliver training material. This will be a versatile role with responsibilities including business analysis, business process improvements, system configuration, script development, reporting, and end-user training and support. The IT Applications Specialist will leverage enterprise software systems experience, and excellent interpersonal, communications, and team collaboration skills in delivering high quality solutions and service in a fast-paced environment. Open to location in Davis or South San Francisco, CA. | 6/7/2017 |
| 1387 | Intrexon Germantown, MD Research Associate BS / MS biology, molecular biology, immunology, or related Exp: 1 yr |
Intrexon is seeking highly motivated and creative Research Associates with experience in molecular biology, immunology, biochemistry and / or assay development to support efforts within our Human Therapeutics and Immunology teams. We are seeking candidates looking for a fast paced, exciting working environment utilizing state of the art technology. Level will be determined based on candidate experience. | 6/7/2017 |
| 1388 | Intuitive Surgical Raleigh, NC Software Engineering Co - op BS software engineering or related Exp: 1 yr coursework |
Intuitive Surgical s Co-Op Program is a paid, full-time, multi-semester partnership designed for students who wish to begin their professional careers before completing their degree program. An ideal candidate will spend multiple terms with Intuitive Surgical, alternating taking classes and working, before graduating. The Co-Op will work with a group of talented and dedicated employees to improve and extend Intuitive Surgical s robotic product lines and, during alternating terms, will be responsible for ensuring a smooth transition of their work to incoming Co-Op students. The Co-Op s efforts will contribute to a technology that has already helped save or improve the lives of millions of people. | 6/7/2017 |
| 1389 | Intuitive Surgical Raleigh, NC Mechanical Engineering Co - op BS mechanical engineering Exp: 2 yrs coursework |
We are seeking a mechanical engineering student interested in a multi-semester co-op partnership focused on mechanical design and manufacturing support of surgical robotic systems and instruments. | 6/7/2017 |
| 1390 | Intuitive Surgical Raleigh, NC System Test Engineering Co - op BS biomedical engineering or related Exp: 1 yr coursework |
The System Test function is responsible for Verification Testing of surgical robots. The primary function of this position is to design, develop, and execute test protocols for functional SW verification for intricate robotic surgical systems. | 6/7/2017 |
| 1391 | inVentiv Health Inc. Princeton, NJ Clinical Research Associate II BS science, biology, or related Exp: 1 yr |
Perform site qualification, site initiation, interim monitoring, and close-out visits ensuring regulatory and protocol compliance. Visits may be performed on-site or remotely. Review completion of proper informed consent procedures. Ensure accurate data reporting via review of site source documents and medical records. Interpret data to identify protocol deviations and risks to subject safety / data integrity. Generate queries and manage resolutions with site personnel. Perform investigational product accountability as per the protocol and Study Monitoring Plan. Evaluate execution of study protocol at the site level. Use judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicate / escalate serious issues to the project team. Obtain, review, and process essential regulatory and administrative documents. Conduct audits of essential regulatory documents to ensure completeness, accuracy, and regulatory compliance. Document activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required study documents as per SOPs and Study Monitoring Plan. Understand project scope, budgets, and timelines; manage site-level activities / communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt to changing variables to achieve goals / targets. Enter data into tracking systems as required. Act as primary liaison with study site personnel. Enter data into tracking systems as required. Participate in the identification and selection of investigators and clinical sites. Maintain a working knowledge of ICH / GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs / processes; complete assigned training as required. Provide clinical and technical support for project team as required. May interact with representatives of client affiliates as per project requirements. | 6/7/2017 |
| 1392 | inVentiv Health Inc. Princeton, NJ Lab Support Specialist AS / BS chemistry or related Exp: 0 yrs |
Prepare process and distribute regulatory and non-regulatory documents internally and / or externally while ensuring adherence to deadlines and procedures. Help with the blood donation procedure. Remove, store and prepare regulated wastes from the laboratories and maintain disposal records. Assist in the routine and non-routine maintenance of the facility. Prepare solutions and mobile phases in the laboratory. Provide operational support to the inventory control and purchasing functions. Coordinate vendor qualification activities. Perform shipping and receiving duties. Review laboratory data and associated documentation for accuracy and completeness. Review general use laboratory notebooks to ensure accuracy and completeness. Assist in general organization of file / document control systems. Assist in the routine and non-routine maintenance of the facility and associated laboratory equipment. Responsible for performing activities that are in compliance with applicable Corporate and Divisional Policies, Standard Operating Procedures and Operating Guidelines and performing other duties as assigned by management. | 6/7/2017 |
| 1393 | Invicro Boston, MA Associate Scientist, in vivo BS biomedical sciences or related Exp: 0 yrs |
The Associate Scientist, in vivo position s primary focus is that of an animal technician supporting all in vivo, small animal medical imaging studies. These studies include nuclear medicine (PET / SPECT), computed tomography (CT), and magnetic resonance imaging (MRI). The In Vivo Research Technician will maintain the animal facility and provide study support in mouse and rat disease models ranging from basic injections to training on surgical procedures. Selected candidate will receive a wide range of exposure and opportunity for growth with respect to scientific scope and overall laboratory capabilities. An ideal candidate meets the below qualifications, is enthusiastic about biomedical research, as well as able and willing to rapidly learn new skills and begin applying them immediately. | 6/7/2017 |
| 1394 | Invicro New Haven , CT Data Management Associate BS life sciences or related Exp: 1-2 yrs |
The Data Management Associate plays an essential role in the establishment and maintenance of database standards, the efficient design of sponsor databases, the integration and reporting of data from multiple sources, and the reporting and analysis of key study data metrics. The incumbent will recommend and drive solutions for efficient database design and data reporting. This role is critical for meeting sponsor study data specification requirements. | 6/7/2017 |
| 1395 | Invitae San Francisco, CA Operations Analyst Internship BS technical discipline Exp: 1 yr coursework |
This individual would support our data and analytics efforts such as developing visuals / dashboards with business intelligence software to improve operations. | 6/7/2017 |
| 1396 | Thermo Fisher Scientific Asheville, NC NPD and Automation Manufacturing Engineer BS mechanical engineering or related Exp: 1-3 yrs |
The New Product Development (NPD) Manufacturing Engineer is responsible for developing and continuously improving the processes which turn design-intent drawings into future products which meet our customer's requirements. | 6/7/2017 |
| 1397 | Thermo Fisher Scientific Fair Lawn, NJ Manufacturing Engineer BS chemical engineering or related Exp: 0-2 yrs |
The Manufacturing Engineer is a critical role in Laboraotry Chemicals. This position provides leadership and technical support to the value stream. With a focus on continuous improvement, this is a great opportunity to make an impact in a high profile segment of our growing business. | 6/7/2017 |
| 1398 | Thermo Fisher Scientific Many, CA Associate Lab Support Scientist BS chemistry or a bioscience equivalent Exp: 1 yr |
A dynamic and self-motivating individual is required to support state-of-the-art LCMS instrumentation as an AssociateDemonstration Chemist. As a member of the Thermo Fisher Scientific North America Demonstration and Applications Labs, the candidate will work within a multi-disciplinary matrix team that includes regional sales representatives, marketing and service professionals, product development scientists, and engineers. Primary responsibilities will be to aid and help senior personnel enact LCMS product demonstrations related to small molecule applications. | 6/7/2017 |
| 1399 | Thermo Fisher Scientific Grand Island, NY Packaging Engineer II BS engineering, material science, or related Exp: 1 yr |
As a member of the Custom Cell within Grand Island Operations, the successful applicant will be responsible for developing packaging designs to meet customer requirements. The packaging engineer will have frequent interactions with customers, sales representatives, product managers and business development professionals on current and new packaging opportunities. | 6/7/2017 |
| 1400 | Thermo Fisher Scientific San Jose, CA Supplier Quality Engineer BS engineering or related technical field Exp: 0-5 yrs |
Works with R&D in conjunction with supplier on New Product Introduction (NPI) projects. Leads supplier development activities by conducting reviews and visiting supplier sites focusing on developing and implementing improvements / modes of control within the supplier processes to minimize non-conformances. Establishes and reports on quality benchmarks and metrics for measuring efficiencies and effectiveness of all supplier performances that affect Thermo Fisher Scientific products and services. Develops initiatives and reviews metrics to identify cost of poor supplier quality. Using various data collection methodologies, will measure, analyze and improve Supplier performance and reduce supplier non-conformances. Ensure Quality Assurance for existing suppliers including source inspection, review of incoming raw materials (as required), and change control process management. Drive continuous improvement process (CIP) activities such as PPI, Kaizen, Lean Review supplier manufacturing process and collaborate with them on process improvement opportunities Perform and maintain product / process risk analysis and ensure mitigations are implemented and effective (Supplier Process FMEA) Execute Lead Auditor function for assigned suppliers based on ISO 9001, 13485 and 21CFR820 clauses Ownership / leadership mindset | 6/7/2017 |
| 1401 | Thermo Fisher Scientific San Jose, CA Intern Scientist MS chemistry, biochemistry, or related Exp: 1 yr coursework |
Develop methods for several clinical applications, such as therapeutic drug monitoring or drugs of abuse Develop simple sample preparation and / or extraction strategies for blood and urine samples Test different method configurations and define optimum parameters Transfer methods to different instrument types, such as ion traps, triple quadrupoles and Orbitraps Exchange information with external collaborators and implement feedback | 6/7/2017 |
| 1402 | Thermo Fisher Scientific Franklin, MA Depot Repair Tech II AS technical discipline Exp: 1-3 yrs |
Cleans, inspects, and documents pre-repair condition of Environmental and Process Monitoring Instrumentation. Performs troubleshooting including component and system failure analysis using standard diagnostic techniques. Replaces non-conforming and preventative maintenance parts as required. Performs full checkout, testing, and calibration of repaired instrumentation, providing appropriate test data / documentation. Generates, maintains, and provides record keeping functions for Return Authorizations, Service Quotes, and Service Orders. Ability to work in a busy multi-tasking service environment. Participate in lean practices and continuous improvement events | 6/7/2017 |
| 1403 | Invivoscribe San Diego, CA Manufacturing Associate II BS scientific discipline Exp: 1 yr |
Production of master mixes, controls and assay kits. Manufactures products adhering to existing Quality System Regulations accompanied by appropriate documentation. The Manufacturing Associate II will contribute to the drafting and review of new documents, including Standard Operating Procedures, Batch Records, Validation Protocols and Purchasing Specifications. | 6/7/2017 |
| 1404 | Ionis Pharmaceuticals San Diego, CA Research Associate MS biology or related Exp: 0-3 yrs |
The Antisense Drug Discovery department seeks a Research Associate (BS / MS) to join the lead identification team in the discovery of antisense inhibitors against novel gene targets. This will be a temporary-to-hire position. In this position, the successful candidate will evaluate the effect of antisense oligonucleotides on the expression of specific transcripts, characterize lead inhibitors as well as examine the cellular mechanisms that contribute to oligonucleotide activity in mammalian cells. Primary responsibilities include mammalian cell culture, oligonucleotide transfection, RNA isolation and quantitative RT-PCR. We are looking for motivated individuals with strong attention to detail, experience in cellular and molecular biology | 6/7/2017 |
| 1405 | Ionis Pharmaceuticals San Diego, CA Scientist MS neurobiology or related Exp: 0-3 yrs |
We currently have active projects in many neurodegenerative diseases with high unmet medical need. Successful candidates will contribute to initiating and executing neuroscience drug discovery projects at all stages, including new target identification, preclinical target validation, and drug lead identification for clinical development. The candidate will become an integral part of an interdisciplinary team of scientists in the Ionis neuroscience group. | 6/7/2017 |
| 1406 | Ironwood Pharmaceuticals Cambridge, MA Clinical Pharmacology Fall Intership MS pharmaceutical sciences Exp: 2 yrs coursework |
This student will conduct research in clinical pharmacology using innovative modeling approaches such as PK / PD, population PK, & physiological-based PK modeling. | 6/7/2017 |
| 1407 | Irvine Scientific Santa Ana, CA Research & Development Summer Intern BS biological scientific degree Exp: 3 yrs coursework |
Summer internships at the R&D department provide an opportunity to work closely with our senior scientists in an industrial environment devoted exclusively to cell culture media research and development. The intern is expected to gain knowledge and hands-on experience of how to develop cell culture media for desired applications such as supporting specific cell growth and productivity. In addition, the student would also gain experience in project design, data analysis and scientific presentation. Internships cover a minimum of eight weeks starting in May or June, 2017. The ideal candidate will be an ambitious, highly motivated undergraduate student with previous laboratory experience in biology and chemistry who wants apply techniques learned in an academic setting while obtaining new skills. | 6/7/2017 |
| 1408 | Prometheus San Diego , CA Clinical Lab Scientist I BS Exp: 0-4 yrs |
Performs pre-analytical and analytical testing, interprets and reports patient results to ordering physicians. | 6/4/2017 |
| 1409 | ProMetic BioTherapeutics Inc. Rockville , MD RESEARCH ASSOCIATE I PROCESS DEVELOPMENT BS Exp: 0-2 yrs |
The candidate will be responsible for leaning basic purification techniques, buffer preparation, column packing, data entry, and performs routine laboratory maintenance under direct supervision of their designated Scientist. | 6/4/2017 |
| 1410 | ProPharma Group St. Paul, MN Quality Control Coordinator BS Exp: 1-3 yrs |
The Quality Control Coordinator (QCC) is critical in evaluating and reviewing the adverse events and product complaints completed by the Contact Center Specialists before being sent to the designated clients. The QCC must ensure that all work is accurate and sent to the client within required timeframes. The QCC also prepares and reviews reconciliation reports to ensure that all cases have been sent to the clients. This position requires someone with an extreme technical ability for proofreading and keeping a variety of processes and timelines straight within a regulated environment. | 6/4/2017 |
| 1411 | ProZyme, Inc. Hayward, CA QC Associate BS / BA in Life Science Exp: 1-4 yrs |
Performs testing and lab maintenance, including product release testing, stability testing and other testing as requested. | 6/4/2017 |
| 1412 | PSC Biotech Corporation Madison, WI Validation Engineer BS / MS Exp: 1-3 yrs |
The validation engineer will perform consulting activities for clients in Life Science, Pharma and Biotech industries. This individual is responsible for performing validation protocols, including writing and execution; calibration, temperature mapping, data interpretation for equipment and writing of SOP s. Strong technical writing skills are required. | 6/4/2017 |
| 1413 | PSC Biotech Corporation Madison, WI Formulation Scientist - Entry Level MS in Biomedical Engineering, Chemical Engineering, Chemistry, or Biochemistry a plus Exp: Entry Level |
The Formulation Scientist is required to maintain currency with the latest operational information about the trends, improvement methods, and functions of currently used pharmaceutical drugs and will, at times, be expected to prepare projects demanded on special requests by BioTechnique or our customers. The Formulation Scientist will organize, design, and arrange the procedures of formal and informal constancy experimentation, chemical refining and deduction, scale up fabrication, and formulation evolution. The Formulation Scientist will also ensure proper packaging assessment processes, procedures related to the improvement of formulation calculus methodologies, and the examination and processing of modern drug commodities and materials. | 6/4/2017 |
| 1414 | PSC Biotech Corporation NA, So Entry Level Validation Engineer BS Exp: Entry Level |
Entry Level Validation Engineer wanted to train on GMP facilities and cGMP requirements. In addition, applicant will be trained on writing technical reports, and Validator Software. Applicant will be working in a biotech / pharmaceutical environment as a consultant / contractor for various clients. He / she will be working closely with client's employees on various projects and various GMP facilities to help client with validation issues. Applicant must be willing to learn new ideas, techniques and systems. Applicant must be willing to commute to clients' manufacturing sites. | 6/4/2017 |
| 1415 | PSC Biotech Corporation NA, OK QC CSV Laboratory Validation Engineer MS in analytical chemistry Exp: 1-2 yrs |
QA Documentation Validation Review; Computer systems validation experience with knowledge in Part 11 / Annex 11; Generate and execute computer systems instruments qualification / validation protocols; Perform a gap analysis of existing QC equipment (analytical equipment validation) ;Creation, modification, and execution of validations (IQ, OQ, PQ). | 6/4/2017 |
| 1416 | PSC Biotech Corporation San Diego, CA Jr. CSV/Lab Qual. Engineer BS in Biomedical, Pharmacuetical, Chemical or any other variety of engineering Exp: 1-3 yrs |
Execution of IQ, OQ and CSV for lab-scale equipment used in the production of medical device;Execution of qualifying cold storage units, thermal systems, and laboratory measurement devices (Preferably spectroscopy, chromatography, DNA / RNA quantitation, and / or DNA / RNA sequencing instrumentation) | 6/4/2017 |
| 1417 | PSC Biotech Corporation NA, No Entry Level CSV Engineer BS in Engineering Exp: Entry Level |
Will be responsible for generating and executing the following Computer System Validation (CSV) deliverables | 6/4/2017 |
| 1418 | Puma Biotechnology, Inc. South San Francisco, CA Clinical Trial Specialist BS Exp: 1 yr |
The Clinical Trial Specialist (CTS) is responsible for providing operational support for the day-to-day execution of clinical trials, following established SOPs, GCP and applicable regulatory requirements in the execution of all activities; proactively identifying and resolving operational project issues; and participating in process improvement initiatives as required. | 6/4/2017 |
| 1419 | QIAGEN Germantown, MD Scientist I MS Exp: 1-4 yrs |
The Scientist I, Production Molecular Biology must comprehend and perform scheduled routine and complex bulk formulation production tasks according to established procedures in accordance with applicable regulations; support general laboratory maintenance including material and instrument upkeep and work environment improvements. | 6/4/2017 |
| 1420 | QIAGEN Beverly, MA Protein Purification Technician I BS Exp: 1-2 yrs |
The Production Technician I performs assigned manufacturing and process development duties in a ISO 13485 environment. | 6/4/2017 |
| 1421 | QIAGEN Frederick, MD Production Associate Scientist BS in Molecular Biology, Biochemistry, Chemistry or related Life Sciences field. Exp: 1-5 yrs |
Responsible for manual / automated production / assembly jobs in compliance with relevant regulations and Standard Operating Procedures. | 6/4/2017 |
| 1422 | QPharma, Inc. Morristown, NJ Junior Validation Engineer/Scientist/Specialist BS Exp: 6 months- 2 yrs |
The specific duties for this position will be to develop validation documentation with input and direction for senior team members. | 6/4/2017 |
| 1423 | QPS, LLC Newark, DE Associate Scientist BS in Analytical Chemistry, Biochemistry, Pharmacology or related scientific discipline Exp: 0-2 yrs |
Under general supervision, this staff member is responsible for conducting assigned study duties according to SOPs and study protocols, and recording study results and observations. | 6/4/2017 |
| 1424 | Regeneron Tarrytown, NY Process Development Associate/Engineer BS / MS in Chemical Engineering or Bio-related Engineering Exp: 0-2 yrs |
He / she will perform studies at a benchtop scale to develop cell culture medium that improves cell growth, cell productivity, and / or product quality. In this role, the individual will perform cell culture experiments, small scale bioreactor development, and literature searches. The ability to design experiments, statistically interpret results, and communicate findings is required. | 6/4/2017 |
| 1425 | Regeneron Rensselaer, NY QA Validation Specialist BS / BA in Engineering, Chemistry, or Life Sciences Exp: 1 yr |
The QA Validation Specialist implements policies and procedures to validate / qualify equipment, systems, and processes in accordance with regulatory requirements and company manufacturing standards. | 6/4/2017 |
| 1426 | Radiant Research Evansville, IN Clinical Research Coordinator BA / BS in a health sciences Exp: 6 months |
Working under the supervision of the Principal Investigator and Site Director, this position will coordinate the conduct of clinical drug studies from pre-study planning through successful completion of all patient visits and documentation. | 6/4/2017 |
| 1427 | Regeneron Tarrytown, NY Temp Research Associate I BS / MS in biochemistry, biophysics or related life science Exp: 0-4 yrs |
This position will involve molecular and cellular based assays to prepare samples for Proteomics and mass spectrometry analysis. The individual should have excellent problem solving skills, oral and written communication skills as well as the ability to multi-task and pursue multiple projects on a daily basis. | 6/4/2017 |
| 1428 | Regeneron Tarrytown, NY Process Development Engineer I BS / MS in Chemical Engineering or Bio-related Exp: 0-2 yrs |
Job responsibilities will include cell line selection experiments, and process optimization and robustness in support of commercial manufacturing productions. | 6/4/2017 |
| 1429 | Regeneron Tarrytown, NY Research Associate I/II (Protein Development) BS Exp: 1-3 yrs |
Purification and biochemical characterization of protein reagents and antibodies in support of the company s VelocImmune fully human antibody pipeline and Immune Oncology programs. Experience in affinity, IEX, SEC chromatography, SDS PAGE electrophoresis, Western-blotting, and spectrophotometry. This position will be primarily focused on purification of therapeutic reagents and antibodies. Database entry and documentation of purified characterized reagents in LIMS is critical. | 6/4/2017 |
| 1430 | Regeneron Tarrytown, NY Process Development Associate BS in Chemical Engineering or Bio-related Engineering Exp: 0-2 yrs |
Job responsibilities will include cell line selection experiments, and process optimization and robustness in support of commercial manufacturing productions. | 6/4/2017 |
| 1431 | Regeneron Tarrytown, NY Research Associate II/III - Neurodegenerative Diseases BS / MS Exp: 0-4 yrs |
The goal will be to identify and validate novel therapeutic targets and mechanisms. Additionally, this position will support and expand the development of new technologies, to this same end. This candidate will work within a multi-disciplinary group; we are looking for a highly organized, flexible and motivated research associate. | 6/4/2017 |
| 1432 | Reata Pharmaceuticals, Inc. Irving, TX Unpaid Intern BS / MS Exp: NA |
As a member of the Strategy group, the Intern will garner invaluable experience on developing the direction of a promising, young biotech. The Intern is expected to actively contribute to team efforts and ongoing projects, working closely with upper level management, both internal and external to the group, to ensure seamless cross-functional coordination on alignment of objectives. The intern will support an extensive variety of tactically-minded projects based on the timely needs of the group and company. These could range from assessment of competitor product strengths and weaknesses, product market fit for Reata s internal pipeline, review of drug candidates for potential in-licensing, as well as research on drug and disease markets. | 6/4/2017 |
| 1433 | Horizon Pharma Lake Forest, IL Intern, Regulatory Affairs MS in regulatory science, molecular biology, biomedical sciences, engineering, or related field Exp: NA |
The Horizon Pharma Internship Program offers aspiring professionals an opportunity to build a strong foundation of business acumen, technical skills, and knowledge about the pharmaceutical industry. We are committed to providing program participants with experience-based learning, multidimensional assignments, targeted training, and continual coaching and development. | 6/4/2017 |
| 1434 | Horizon Pharma Lake Forest, IL Bioinformatics Services Core Intern, Summer 2017 BS / MS Exp: NA |
This person will be working in Technology and Discovery Centers in the Bioinformatics Services Core Department in Tarrytown, NY. The student will participate in a project that entails database ETL activities (Extract Transform Load) from open source databases and internally generated data. There will be learning opportunities in MySQL, Genome Browsers, R, and Shiny as well as REGENERON technologies. | 6/4/2017 |
| 1435 | Regeneron Tarrytown, NY Pre - Therapeutic Target Discovery Intern, SUmmer 2017 MS in Biochemistry, Cellular and Molecular Biology, Biomedical Engineering or Biology Exp: NA |
The student will validate an immunostaining protocol to visualize developing vasculature in whole-mount mouse embryos using 3D imaging. Immunostaining protocol validation will include testing antibodies on mouse embryo sections to compare and contrast extant of vascular staining, and testing a cocktail of antibodies to possibly improve quality of staining. 3D imaging modalities for which we are interested in validating immunostaining protocols for are: Optical Projection Tomography (OPT) and High Resolution Episcopic Microscopy (HREM). | 6/4/2017 |
| 1436 | Thermo Fisher Scientific South San Francisco, CA Chemical and Material Science Engineering Sr. Intern Exp: NA |
As a Sr. Intern at Thermo Fisher Ion torrent, you will be helping characterize the Ion torrent DNA sequencing S5 chip. You will be expected to help design experiments, collect and analyze data, and present your results. | 6/4/2017 |
| 1437 | Thermo Fisher Scientific Pleasanton, CA Intern II, Engineering BS Exp: NA |
Lead a process improvement project. Install and qualify equipment. Support process improvement projects with experiments, data analysis and recommendations. Help troubleshoot OpenArray equipment and processes. General laboratory operation and maintenance tasks. | 6/4/2017 |
| 1438 | Thermo Fisher Scientific Pleasanton, CA Intern II BS Exp: NA |
Plan, design and implement efficient business and systems solutions for optimization of process improvement database system | 6/4/2017 |
| 1439 | PerkinElmer Inc. Waltham, MA QA Intern BS in Engineering Exp: NA |
Assist in designing test plans, write, execute test cases for functional and / or automation testing within the domain assigned | 6/4/2017 |
| 1440 | PerkinElmer Inc. Hopkinton, MA Microfluidic 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. | 6/4/2017 |
| 1441 | PerkinElmer Inc. Hopkinton, MA Reagents & Applications Development Intern BS in Chemistry, Biology, Biochemistry, Biomedical Engineering, or related field Exp: NA |
Learn to independently run and analyze experiments on Alpha platform using a variety of biological, biochemical and protein-based techniques, including the use of automation. | 6/4/2017 |
| 1442 | PSC Biotech Corporation Madison, WI Validation Intern BS Exp: NA |
We are currently seeking to bring on a current student to locally support our CMO Facility. This will offer a start-up environment, with hands-on opportunities to develop your analytical, technical and problem solving abilities. Validation Engineer Intern wanted to train on GMP facilities and cGMP requirements. Intern will learn equipment validation, computerized systems validation, Quality Systems in an FDA-regulated environment. Intern will also learn the business aspects of operating a small business. Intern will be exposed to a wide variety of business situations that will better prepare them for a full time job. | 6/4/2017 |
| 1443 | Patheon St. Louis, MO Biopharmaceutical Production Technician BS / MS in Biology,Biochemistry, Chemistry,Chemical Engineering Exp: 1-3 yrs |
The candidate will be responsible for the performance of operations in support of the manufacture of Commercial and Clinical Biologics. He / She will be responsible for following Current Good Manufacturing Practices (cGMP) and carrying out a variety of functions related to Upstream (cell culture) and Downstream (purification) biopharmaceutical manufacturing. These functions may include but are not limited to activities such as propagation of mammalian cell culture, conducting aseptic cell culture operations, execution of large scare production bioreactors (50L - 2000L), conducting large scale chromatography, viral inactivation, viral filtration, ultrafiltration and diafiltration, as well as aseptic filling of bulk drug substance. | 5/27/2017 |
| 1444 | Pearl Therapeutics, Inc. Durham, NC Research Associate II, Analytical Sciences MS Exp: 0 yr |
Support Pearl MDI product development from product definition stages to product approval and launch by devising and conducting analytical experiments | 5/27/2017 |
| 1445 | Pearl Therapeutics, Inc. Redwood City, CA Research Associate I/II, Inhalation Product Development BS in Chemical Engineering, Chemistry, Pharmaceutics Exp: 0-3 yrs |
Responsibilities include design and execution of experiments, analysis and interpretation of data, as well as communicating results to management and team under general guidance. The successful candidate is expected to effectively work in a team environment with some degree of independence. The successful candidate will have experience with pharmaceutical processes and a wide variety of analytical techniques including aerosol, powder and solid state characterization. Hands on experience on processes to manufacture pharmaceutical aerosols, such as spray drying or jet milling, is desirable. | 5/27/2017 |
| 1446 | Pearl Therapeutics, Inc. Durham, NC Process Engineer BS in Chemical Engineering Exp: 1 yr |
Support Pearl MDI product development from product definition stages to product approval and launch conducting MDI manufacturing and process development. | 5/27/2017 |
| 1447 | PerkinElmer Inc. Hebron, KY Laboratory Technician I BS in Biology, Biochemistry, Medical Technology, or related science preferred Exp: Entry Level |
The Laboratory Technician I must possess the knowledge and ability to perform the necessary activities related to cord blood or tissue processing or testing, which includes ABO, Hematology and Flow Cytometry. These activities are performed in compliance with industry regulations, site operating procedures, quality and safety policies, cost and established time standards. | 5/27/2017 |
| 1448 | Personalis, Inc. Menlo Park, CA Laboratory Assistant BS in Science 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. | 5/27/2017 |
| 1449 | Personalis, Inc. Menlo Park, CA Clinical Laboratory Scientist BS Exp: 0-2 yrs |
The Clinical Laboratory Scientist is responsible for testing and reporting clinical laboratory results. | 5/27/2017 |
| 1450 | Perrigo Company Allegan, MI Associate Scientist / Scientist - Analytical R&D BS in Chemistry or Pharmaceutical Sciences Exp: 1-5 yrs |
The incumbent will work with minimal supervision and, as appropriate, may serve as a project leader to manage analytical support for projects with supervision. The incumbent will perform physical and chemical testing on raw material, in-process, finished product and stability samples, including documentation and review. The Associate Scientist will develop, validate and transfer non-complex analytical methods and assist in researching, preparing and reviewing 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. | 5/27/2017 |
| 1451 | Perrigo Company Charlottesville, VA Regulatory Affairs Associate BS Exp: 1-2 yrs |
Develop and maintain product labeling in compliance with laws and regulations. | 5/27/2017 |
| 1452 | Perrigo Company Bronx, NY Production Engineer I BS in an Engineering discipline Exp: 1 yr |
To provide production engineering support for day-to-day operations of a lean six sigma pharmaceutical manufacturing facility. Initiate and drive continuous improvement efforts in assigned process area. | 5/27/2017 |
| 1453 | Pharmacyclics Sunnyvale, CA Clinical Trial Assistant BA / BS Exp: 1-3 yrs |
The Clinical Trial Assistant (CTA) / Senior CTA provides support to the clinical study teams in the execution of clinical trials. Primary responsibilities include maintaining Trial Master File (TMF) and Clinical Trial Management System (CTMS) in an inspection-ready state, assisting with site management, initiating collection, reviewing and tracking of essential documents throughout the life of the trial. Contributes to the production and distribution of study materials and site / study communications. | 5/27/2017 |
| 1454 | Precision Medicine Costa Mesa, CA Medical Writer - Medical Communications Agency BA / BS in life sciences Exp: 1 yr |
We are recruiting for a Medical Writer to 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. | 5/28/2017 |
| 1455 | PharmaForce, Inc. New Albany, OH R&D Analytical Chemist BS in Chemistry Exp: 1-2 yrs |
This R&D position will be responsible for testing of raw materials, finished products, stability samples, using existing HPLC, GC, IC, UV analytical methods. | 5/27/2017 |
| 1456 | PharmaForce, Inc. New Albany, OH R&D Formulation Scientist MS in Pharmaceutical Science, Chemistry and Chemical Engineering or equivalent required 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. | 5/27/2017 |
| 1457 | Pace Analytical Services, LLC Northridge, CA Chemist - Entry Level (CA) BA / BS in a science related field Exp: entry level |
The person hired for the position of Quality Lab Technician will perform specialized tests and experiments of finished Inhalation products to ensure quality standards are met and maintained. Reports all results that are not within specification. Utilizes Lab computer systems to report results and document processes. Participates in efforts to improve cycle time, and lab safety. | 5/27/2017 |
| 1458 | Pace Analytical Services, LLC Decatur, AL Chemist / Lab Technician (AL) BS in Chemistry or related science Exp: 0 yr |
We are currently seeking a Chemist / Lab Technician to provide a variety of laboratory testing supporting a manufacturing line. Candidate will be testing films, adhesives and resins. | 5/27/2017 |
| 1459 | PBL Assay Science Piscataway, NJ Quality Control Scientist I BS in biological sciences Exp: 1-2 yrs |
To ensure the quality of PBL reagents the Quality Control (QC) Scientist I will perform release and stability bioassay testing of interferons and antibodies and release testing of manufactured ELISA kits. In addition, the QC Scientist I will perform bioassays to troubleshoot relevant customer issues and design and initiate experiments and projects to improve the quality of PBL products. The QC Scientist I may also serve as back up to the Manufacturing, Product Development, or Assay Services departments as needed: such additional duties may include running cell-based assays, designing and performing ELISA testing protocols, vialing finish products, and solution preparation. This individual will be involved with document control, SOP writing, and recordkeeping. | 5/27/2017 |
| 1460 | Catalent San Diego, Inc. San Diego, CA Quality Assurance Associate - Data Review BS / BA science degree (Chemistry or Biochemistry preferred) Exp: 1-2 yrs |
Quality Assurance Associates are responsible for supporting quality systems to advance the development and manufacture of drug candidates, including data and document review and approval, support of GMP manufacturing, and assistance with internal and external auditing. | 5/27/2017 |
| 1461 | Catalent San Diego, Inc. San Diego, CA Chemist/Analyst I BS in Chemistry or Biochemistry preferred Exp: 0-3 yrs |
Entry-level Chemists / Analysts perform various analytical techniques and conduct pharmaceutical chemistry related studies to advance the development of drug candidates including methods development and qualification, pre-formulation testing, and release and stability testing. As an entry level Chemist / Analyst you will have an opportunity to develop your skills in in a fast-paced, dynamic company environment. | 5/27/2017 |
| 1462 | PRA Lenexa, KS Safety Data Coordinator BS in life science Exp: 1-3 yrs |
Leads the development and implementation of medical coding in clinical data management systems; participates in management of individual case safety reports (SAEs, AEs of Special Interest, Adverse Drug Reactions), AE / SAE reconciliation and data retrievals from the clinical and / or safety databases; provides support for endpoint adjudication committees. | 5/27/2017 |
| 1463 | PRA Salt Lake City, UT Medical Research Associate BS in a clinical, health- related area Exp: 1 yr |
Perform study specific clinical procedures, collect and record study data on CRF / SDs and interact with subjects during confinement and outpatient periods of clinical studies. Maintain the safety of subjects and data integrity for all studies. | 5/27/2017 |
| 1464 | Promega Biosciences Madison, WI Production Scientist 1 BS Exp: 0-3 yrs |
Manufacture a variety of biologics and / or biochemical products so as to meet product specifications. Follow production schedules to assure on-time delivery of finished product. Understand basic laboratory concepts and perform basic lab techniques. | 5/28/2017 |
| 1465 | Promega Biosciences Madison, WI Production Scientist BS Exp: 0-3 yrs |
Manufacture a variety of biologics and / or biochemical products so as to meet product specifications. Follow production schedules to assure on-time delivery of finished product. Understand basic laboratory concepts and perform basic lab techniques. | 5/28/2017 |
| 1466 | Progenra Inc. Malvern, PA Research associates BS / MS in a life science Exp: 1- 10 yrs |
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. | 5/28/2017 |
| 1467 | Catalent San Diego, Inc. San Diego, CA Lab Assistant (Intern) BS in Chemistry, Biochemistry, or Biology Exp: NA |
Lab Assistants will have the opportunity to learn analytical chemistry techniques such as: volumetric analysis, spectroscopy, and liquid chromatography. | 5/27/2017 |
| 1468 | Pharmacyclics Sunnyvale, CA Intern - Clinical Operations BA / BS Exp: NA |
Provide temporary support to Clinical Operations teams to ensure that study documents are properly organized and filed, follow PCYC work instructions and SOPs, FDA and ICH-GCP guidelines | 5/27/2017 |
| 1469 | Promega Biosciences San Luis Obispo, CA R&D Intern BS Exp: NA |
This internship will be performing synthesis in an exciting arena with a strong interaction with an expert chemist. Under supervision, this intern will perform laboratory experiments, tasks, and associated paperwork as assigned. May present experimental results to individuals and groups. Generally assist in the operations and maintenance of the laboratory. | 5/28/2017 |
| 1470 | Pfenex San Diego, CA Intern Bioinformatics BS in biological science, computer science, or mathematics Exp: NA |
Under the guidance and mentorship of a Senior Scientist, the bioinformatics intern will assist in establishing a Next Gen RNA-Seq based characterization of Pfenex bacterial strains designed for therapeutic protein production. Project scope will include: designing experiments focused on analyzing global gene expression changes in bacterial cell populations in response to different growth conditions; analyzing and interpreting large differential gene expression datasets (as generated by an outsourced lab); cataloging the levels of transcripts identified and mapping gene expression results to metabolic pathways. The intern will summarize the work in a report and present significant findings to an internal scientific audience. | 5/27/2017 |
| 1471 | Thermo Fisher Scientific South San Francisco, CA Engineering Intern BS in Mechanical, Chemical or Bio Engineering Exp: NA |
Engineer will support new Capillary Electrophoresis consumables development. This individual will work with a multi-disciplinary team to develop new concepts, and / or modify and test editing concepts. Ideal candidate will have a design tool skills as well as analytical skills. | 5/27/2017 |
| 1472 | Thermo Fisher Scientific Ann Arbor, MI Intern - Oncology Informatics BS Exp: NA |
Develop a database to store and maintain information about genomic variants in the context of oncology sequencing panels, in order to facilitate queries about panel capabilities. | 5/28/2017 |
| 1473 | ProMed Molded Products, Inc. Plymouth, MN Quality Intern BS Exp: NA |
Maintain and work with ProMed Pharma Quality System to improve assisting with facilitating audits, writing test protocols, reviewing and approving quality and regulatory documents, supporting cGMP (current Good Manufacturing practices) and cGDP (current good documentation practices) practices in the company for new and existing product lines. | 5/28/2017 |
| 1474 | PRC Clinical San Bruno, 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. | 5/28/2017 |
| 1475 | PerkinElmer Inc. Hopkinton, MA Imaging Scientist Intern BS / MS in physics, biomedical engineering, electrical engineering, or a related field Exp: NA |
A TALENTED AND MOTIVED INTERN WHO WORKS WELL IN A CROSS-FUNCTIONAL TEAM ENVIRONMENT AND IS EXCITED TO LEARN ABOUT IMAGING INSTRUMENTATION AND GAIN SOME EXPERIENCE IN AN INDUSTRY ENVIRONMENT. ABLE TO INDEPENDENTLY DESIGN AND EXECUTE EXPERIMENTS, AND TO COMMUNICATE THE RESULTS TO A MULTI-DISCIPLINARY SCIENTIFIC AND ENGINEERING TEAM. | 5/28/2017 |
| 1476 | PerkinElmer Inc. Hopkinton, MA Engineering Intern - - Manufacturing Engineering BS in Engineering Exp: NA |
The candidate will perform basic engineering duties to support the goals of the microfluidic, automation, and imaging engineering team. Specific skills will include a strong background in mathematics, physics, and / or core engineering coursework. Candidate must have an interest in electromechanical fabrication and assembly. | 5/27/2017 |
| 1477 | Patheon Greenville, SC EH&S Intern BS in Life / Physical Science, Environmental Engineering, Safety, or Industrial Hygiene Exp: NA |
EHS Intern will be assist EH&S group by providing support to relevant stakeholders across all aspects of the site. - | 5/27/2017 |
| 1478 | HTG Molecular Tucson , AZ Software Test Engineer, Associate AS computer science or related Exp: 0-2 yrs |
Contributes to the timely achievement of overall project goals. Executes project related tasks. Develop high level and detailed Product Test Strategies and / or Plans from the Product Specifications and Design Documents and by working with the Development Engineers. Be aware of and incorporate the appropriate industry standards into the new product. Incorporate reuse as often as possible. Obtain, setup, and maintain all test equipment required for Product Testing. Assist in development of any required test software programs needed to perform the testing. Automate System Test activities when possible. Execute the system, acceptance or automated tests, document the results, and monitor the status of the system, acceptance or automated tests. This also includes creating scripts for automated tests, detecting defects, submitting defect reports, and verifying that the defects have been resolved. Maintain the highest standards and awareness of software quality. Develop test strategies and / or plans using applicable standards, tools and reporting methods. Independently executes tests and experiments. Interfaces with hardware, software, and systems engineers to evaluate test alternatives. Applies functional expertise routinely on the job. | 5/31/2017 |
| 1479 | Human Longevity, Inc. San Diego, CA Software Engineer BS computer engineering or related Exp: 1-5 yrs |
Human Longevity, Inc. is looking for a Software Engineer to perform the high quality transfer, management, and delivery of complex data (Big Data) derived from next generation DNA / Genome sequencing analysis efforts. | 5/31/2017 |
| 1480 | Human Longevity, Inc. San Diego, CA Clinical Lab Associate BS molecular biology, biochemistry, or related Exp: 1-2 yrs |
The successful candidate will have responsibilities including but not limited to accessioning, documentation of sample quality, sample storage and management. Additionally, this position will participate in manual and automated extraction procedures including quality assessment of nucleic acids (DNA & RNA) isolated from a diverse collection of human tissues and fluids. This position will work closely with the HLI Sequencing Operations leadership team to ensure the accurate, precise and timely processing of samples from receipt through evaluation and processes. This position will report directly to the Company s Lead Pre-Analytical Processes, and work directly with a team of Laboratory Scientists and Research Associates. | 5/31/2017 |
| 1481 | HumanZyme Chicago, IL Sales Representative BS molecular biology, biochemistry, or related Exp: 1 yr |
Our Regional Sales Managers will be responsible for the usual sales activities and duties: plans and strategies to expand the customer base in the territory, supports customers and monitors competitive activity and market trends, and develops sales strategy for the territory that ensures attainment of company sales goals. Also prepares action plans for effective development of sales leads, and prospects, initiates and coordinates development of action plans to penetrate new accounts. | 5/31/2017 |
| 1482 | Icon Whitesboro, NY Metrology Technician I AS scientific discipline Exp: 1 yr |
The Metrology Technician will calibrate and maintain assigned laboratory equipment in laboratories, update the calibration schedule and equipment lists as work is performed. Monitor, calibrate and maintain assigned equipment (e.g., freezers, refrigerators, pipettes, balances, water system, thermometers, weights, ovens, temperature and humidity monitors, REES Environmental system). You will act as an escort for the approved vendor performing required external calibration and review calibration notebooks per applicable SOPs / procedures. | 5/31/2017 |
| 1483 | Ignite Immunotherapy San Francisco, CA Research Associate MS microbiology, virology, molecuar biology, or engineering Exp: 1 yr |
We are hiring a passionate Research Associate to join our team of scientists to optimize our Directed Evolution platform. The Research Associate will work as part of a highly collaborative and interdisciplinary team, employing cutting-edge tools and techniques to develop more effective oncolytic viruses. At IGNITE, the Research Associate will be a critical member of the foundational technical team not only identifying improved viruses, but also actively engineering virus for improved cancer therapy. As a member of a small team, the Research Associate will have the opportunity to learn a wide-range of new skills and to shape R&D best practices in a highly collaborative and stimulating environment. | 5/31/2017 |
| 1484 | Illumina San Diego, CA Software Test Engineer I (ID: 7875BR) BS bioscience, computer science, or engineering Exp: 1-2 yrs |
This position will require the candidate to test Windows based software operating Illumina's sequencing instrumentation. The candidate will work with automated tests on a regular basis and will also utilize SQA skills to write and execute manual tests in accordance with the company's established SDLC methodology. The successful candidate will display a strong sense of ownership, motivation, and attention to detail | 5/31/2017 |
| 1485 | Illumina San Diego, CA Clinical Trials Assistant (ID: 7860BR) BS life sciences or related Exp: 1-2 yrs |
The Clinical Trials Assistant will provide support for diagnostic product development to achieve clearances and approvals in the US and internationally. The role will provide support for clinical development activities consistent with applicable regulations, guidelines and procedures and may be responsible for supporting multiple clinical studies. | 5/31/2017 |
| 1486 | Illumina San Diego, CA CLIA Lab Technician I (ID: 7850BR) BS molecular biology or related Exp: 0-2 yrs |
We are looking for a team-oriented Clinical Lab Technician 1 to join our team in the Fast Track Services group. The ideal individual must have the ability to think on his / her feet and troubleshoot issues in a fast-paced, high-throughput lab. | 5/31/2017 |
| 1487 | Illumina San Diego, CA Manufacturing Research Associate II, NPI (ID: 7768BR) MS molecular biology, biochemistry, chemistry Exp: 1 yr |
Highly motivated and team-oriented individual to provide technical support and project oversight to Manufacturing. | 5/31/2017 |
| 1488 | Illumina Redwood City, CA Clinical Lab Scientist I (2nd Shift) (ID: 7748BR) BS technical discipline Exp: 1 yr |
The Clinical Lab Scientist 1 is responsible for testing and reporting clinical laboratory results, as well as providing direct and constant supervision for the Clinical Laboratory Technicians (CLTs). Ability to work 2nd shift hours, 3pm-11:30pm, Monday-Friday with 1 in 3 Saturday rotation. | 5/31/2017 |
| 1489 | Immucor Norcross, GA RBC Processing Technician AS life science Exp: 1-3 yrs |
As a Red Cell Processing Technician, you will perform your production tasks in a clean-room environment. In addition, it will be your responsibility to ensure that your work is consistently in compliance with Good Manufacturing Practices and Good Documentation Practices. | 5/31/2017 |
| 1490 | Immucor Norcross, GA Intern - Systems Engineering BS bioengineering or mechanical engineering Exp: 1 yr coursework |
You will work with the systems engineering team in the development and testing of electro-mechanical systems designed to execute testing in support of blood and organ transfusion. You will have hands on experience in the laboratory working with the systems and elvaluating devices | 5/31/2017 |
| 1491 | Immucor Waukesha, WI Internship - Manufacturing BS sciences, biomedical engineering, or related Exp: 2 yrs coursework |
We are currently seeking college Sophomores, Juniors or Seniors for Internships in our Manufacturing team. You will be perfoming a variety of manufactuing tasks associated with the production of Immucor reagents. | 5/31/2017 |
| 1492 | Immune Technology Corp. Many, Ma Sales Representative BS life sciences or related Exp: 1 yr |
Full / part time position, responsible for ensuring customer retention through account management and increasing revenue through marketing activities and generation of sales leads. | 5/31/2017 |
| 1493 | Immunogen Waltham , MA Quality Assurance Specialist BA / BS chemistry, microbiology, biology, biochemistry, or related Exp: 1-2 yrs |
The position will work in close collaboration with the Non-clinical, Clinical, Regulatory and Pharmacovigilance departments to ensure compliance with Good Clinical Practice(s), Good Pharmacovigilance Practices (GVPs) and Good Clinical Laboratory Practices (GCLPs),. In this position, you will be responsible for supporting the Immunogen Quality system, including company oversight of vendors / CROs / clinical sites. | 5/31/2017 |
| 1494 | Impax Hayward , CA Chemist I/II, Quality Control MS chemistry Exp: 0 yrs |
QC Chemist II is primarily responsible for the testing of raw material or finished product for commercial purpose. | 5/31/2017 |
| 1495 | Impax Hayward , CA Reviewer I, QC Document (Temp) BS chemistry or related Exp: 1-3 yrs |
Support the culture of Quality with the comprehensive review of documentation, analytical data, protocols and reports generated within the QC laboratory and related third party documents to verify and ensure that the laboratory records are in compliance with all established and approved procedures. | 5/31/2017 |
| 1496 | Impel Neuropharma Seattle , WA Research Associate BS chemistry, biochemistry, biology, or related Exp: 0-2 yrs |
The Research Associate will provide support to the drug-device combination product testing in our Research and Development group. Duties will include development and execution of analytical assays in support of drug-device combination product testing, tabulation of data, assistance in data analysis and report writing, and assistance with animal tool development. | 5/31/2017 |
| 1497 | Indivior Richmond, VA Regulatory Associate, Ad/Promo Reviewer BS biomedical science or related field Exp: 1-3 yrs |
The Regulatory Associate, Ad / Promo Reviewer is a skilled regulatory manager with strong understanding of the FDA regulations associated with Ad / Promo 21 CFR Part 202.1 (Prescription Drug Advertising) and possesses excellent review and editing ability. The have the managerial skills regarding the production of instructions for the safe and effective use of drug products for human consumption, understand prescription drug labeling and have an understanding of DTC ads, Reminder ads, Testimonials, Internet advertisements, Press Releases which are related to commercial communication about Indivior Inc. drug products. The manager ensures the advertisement and promotional pieces and in line with product labeling and are of quality and compliance with FDA regulations throughout the drug product label life cycle. They should also have the ability to relate the prescribing information into Advertising and Promotional material and be willing to work within a commercial environment with other functional contributors within the Promotional Review Committee. | 5/31/2017 |
| 1498 | Inova Diagnostics San Diego, CA Chemist I BS biological or related science Exp: 0-2 yrs |
Major manufacturing duties include assistance with the activities required to produce ELISA calibrators, controls and conjugates. | 5/31/2017 |
| 1499 | Inovio Pharmaceuticals San Diego, CA College Intern: IT BS technology field Exp: 1 yr coursework |
The intern will be responsible for IT Administration tasks in addition to desk-side application support. | 5/31/2017 |
| 1500 | Inovio Pharmaceuticals San Diego, CA Research Associate I, Analytical Sciences BS biological sciences Exp: 1 yr |
The Research Associate position handles samples from Inovio s human clinical trials and processes whole blood to isolate the mononuclear cells. The Research Associate performs day-to-day laboratory duties and is incorporated into a collaborative team of scientists that determines the vaccine induced immune responses. | 5/31/2017 |
| 1501 | Inovio Pharmaceuticals Plymouth Meeting, PA Clinical Trial Associate BS / MS biology, immunology, bioengineering, or related Exp: 0-1 yrs |
Set-up and maintain Trial Master File (TMF) including project documentation files, investigator files, study books, and project databases on more complex projects. Assist in the preparation of informational documents and communications for designated projects, including internal and external correspondence. Work with Clinical Project Manager to collect relevant study information on timelines, progress and resources. Implements and maintains project processes and tracking systems. Generates and distribute status reports to management and other clinical team members. Coordinate and supports clinical team, consultant and vendor meetings. Assesses meeting requirements and plan appropriately (e.g., arrange meeting room, schedules teleconference, distributes meeting agenda, prepares and distributes meeting minutes, etc.). Complete assigned tasks in accordance with GCP, ICH guidelines and regulatory requirements for clinical trial management. Work with Clinical Data Management on assigned projects Assist in vendor and site audits as needed. Plan and participate in conduct of Investigator Meetings | 5/31/2017 |
| 1502 | IntegenX Pleasanton, CA Data Scientist BS / MS technical field with emphasis on bio-informatics Exp: 1 yr |
Work with extended team to drive overall improvements in signal processing pipeline and translate improvements into customer benefits. | 5/31/2017 |
| 1503 | IntegenX Pleasanton, CA Research Associate BS molecular biology or chemistry Exp: 1-5 yrs |
Contributes to Assay Development including assay optimization and methods development to achieve robust genomic test performance on challenging clinical samples. Conducts studies as assigned, performs data analysis and reports results. Manage and maintain required reagents and equipment needed to carry out assignment. Collaborate closely with other teams in the department to complete highest priority work as directed. Complies with all company safety, training, and quality regulations (e.g., ISO compliance, GLP / GMP requirements, etc.) and procedures. | 5/31/2017 |
| 1504 | Integra Cincinnati, OH Surgical Set Technician AS / BS technical discipline Exp: 1-3 yrs |
Attain and maintain surgical set inspection certification per quality certification requirements. Under general supervision, perform 100% Quality Assurance inspections on loaner pool surgical sets for quality and functionality of component parts, including instruments and implants, per standard operating procedures, protocols and work instructions. Perform data entry and system interface transactions to maintain accurate inventory reporting. Perform appropriate surgical set dispositions for tracking of set processing. Work both autonomously and in a team environment, consistent with all work instructions to complete surgical set processing with a high degree of accuracy and within quality standards. Under general supervision, perform surgical set processing assembly and refurbishment within targeted turnaround time to ensure loaner pool surgical sets are readily available for use. Develop a strong knowledge of product lines and component parts. Maintain a clean and organized work environment and adhere to safe work practices. Report defective materials or atypical situations to the Surgical Set Manager Conduct inventory cycle counts as required. Assist in training new Surgical Set Technicians. Contribute to a positive and professional team environment and treat others with respect. Works with integrity and upholds organizational values and brand promises. Perform other duties as required, directed, or assigned. | 5/31/2017 |
| 1505 | Integra Plainsboro, NJ Quality Assurance Engineer BS science or engineering Exp: 1-3 yrs |
Investigates events and / or complaints reported for material and / or finished goods manufactured at ILS Plainsboro. Tracks, follows-up and assists in the timely closure of Events / Complaints. Ensures that issues are investigated thoroughly and CAPAs are proposed as applicable. Provides hands-on guidance and training to all personnel performing activities within the Quality system. Ensure documentation is complete before closure. Assist QA Systems team as needed to investigate Nonconformances. Assist QA Systems team as needed to ensure proper implementation of CAPAs. Participates in the development and / or revision of Quality System SOPs. Makes effective written and verbal presentations, as needed. Prepares and distributes monthly and quarterly metrics reports (written and graphic) to plant management regarding the status of NCs, CAPAs, Effectiveness Checks, and Complaints and participates in the development of quality performance measures. Applies statistical methods appropriate to the types of data and variances involved in assessing Complaint Data for trending and risk management. Maintains a thorough understanding of the following regulations and guidelines: U.S. Food and Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian Medical Device Regulations (CMDR), Integra Corporation's policies and procedures, and other applicable regulatory agency requirements. Compares quality system within Integra with other external sources to identify areas for improvement | 5/31/2017 |
| 1506 | Integra York, PA Product Development Engineer Tech BS technical discipline Exp: 1-3 yrs |
This position is responsible for sustaining engineering activities / projects and support for new product development for lighting and other Specialty Surgical Solutions products. This includes contribution to design, assembly, product testing, prototype maintenance, part specifications development, and manufacturing documentation. It also includes leading small projects and providing technical direction. This position requires a hands-on engineering background requiring strong problem solving skills within a team, Design, Marketing and Manufacturing environment. | 5/31/2017 |
| 1507 | Integral Molecular Philadelphia, PA Research Associate BS biology, bioengineering, or related Exp: 1-2 yrs |
This position will involve conducting laboratory research and supporting general R&D operations at Integral Molecular. The position will involve both research and production of biomedical research products. You will be working with a dedicated group of scientists on the development and commercialization of biomedical technologies. Projects may involve cell culture, virology, DNA preparation, liquid handling automation, and cell-based assays (western blot, ELISA, immunofluorescence, flow cytometry). | 5/31/2017 |
| 1508 | Oncobiologics, Inc. Cranbury, NJ Engineer I/II, Manufacturing Support BS / MS in Chemical Engineering, Life Sciences Exp: 0-2 yrs |
The Engineer I / II, Manufacturing Support, is a new position, created to provide strong leadership as Oncobiologics continues its rapid growth. The Engineer I / II, Manufacturing Support, will be responsible for the introduction of all biosimilar candidates from process development to the Biologics Manufacturing Center. | 5/15/2017 |
| 1509 | Ora, Inc. 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. Placement at the CTA I, CTA II or Sr. CTA level will be determined based on the candidate s qualifications. | 5/15/2017 |
| 1510 | Organovo San Diego, CA Lab Technician I BS in biology, physiology, molecular and cellular biology, microbiology, or closely related field Exp: 0-2 yrs |
Under leadership and supervision of senior staff performs duties related to cell and tissue culture and analysis per established protocols. | 5/15/2017 |
| 1511 | Organogenesis CANTON, MA Clinical Research Associate I BS in a life science Exp: 1-3 yrs |
The CRA I will assist clinical affairs in creating, reviewing and preparing documents, maintaining the Trial Master File for each study and preparing any documentation needed for regulatory filings and / or IRB submissions. S / he will have a proven ability to independently prioritize and manage multiple tasks and projects with competing priorities and deadlines, screen and prioritize communications and opportunities from external sources. The ideal candidate will be dynamic, articulate, high-energy, organized, and able to support cross-functional coordination in a fast paced environment. | 5/15/2017 |
| 1512 | Organogenesis CANTON, MA Production Associate I Apligraf BS in biology or related science Exp: 0-2 yrs |
Responsible for manufacturing Apligraf according to established Master Batch Records and Operating Procedures. Responsible for the preparation of all media and sanitizing agents used in the Production areas. Responsible for adherence to all Operating Procedures, protocols, policies, regulatory requirements, GMP, and safety guidelines. Responsible for assuring batch records are complete and are compliant with all protocols. Responsible for proper operation of all clean room equipment. Responsible for maintaining all required records and adherence to established guidelines for quality control procedures, GMP s, and safety. | 5/15/2017 |
| 1513 | Organogenesis CANTON, MA Design Engineer I BS in Engineering Exp: 0-5 yrs |
Use of diverse engineering skills to design, approve, and test new product designs. Projects will focus on, but will not be limited to, conducting reliability assessments, evaluating existing products, and monitoring design developments to maintain quality compliance and assist in engineering, testing, and validation. Supports new product development and establish quality and reliability of the finished product. Participates in projects to improve product yield increase capacity and / or reduce overall production cost. Supports various aspects of design, prototyping, fabrication and testing with consideration given towards end product requirements (patient safety and efficacy). | 5/15/2017 |
| 1514 | Organogenesis LA JOLLA, CA Quality Control Analyst I - Microbiology BS in a Biology, Chemistry Exp: 1 yr |
The major purpose of this position is the performance and reporting of microbiological testing for product release as well as environmental monitoring of all areas of the manufacturing facility, water sample collection and testing, compilation and entry of environmental monitoring data. The position ensures that the company goals for timely product testing are accomplished by being directly involved in the production of test results for product release and investigations. Other responsibilities or tasks as deemed necessary from time to time by the area s supervisor. | 5/15/2017 |
| 1515 | Osiris Therapeutics Columbia, MD Biotechnology Manufacturing Associate BS Exp: 1-2 yrs |
Responsible for hands-on execution of all activities in the Biosurgery manufacturing area, which encompasses the processing and packaging of tissue products for transplantation and for use in surgical procedures. All duties are performed in compliance with GMP / GTP, American Association of Tissue Banks Standards, and Osiris Standard Operating Procedures (SOPs). The candidate should have a commitment to high standards of quality. | 5/15/2017 |
| 1516 | Osiris Therapeutics Columbia, MD QA Document Control Specialist BS in biology or related science Exp: 1-2 yrs |
Reporting to the QA Project Management Specialist, the primary purpose of this position is to work within the Quality Assurance department in several key roles relating to document control functions. | 5/15/2017 |
| 1517 | OvaScience Waltham, MA Research Associate BS / MS in cell biology, molecular biology or related field Exp: 1 yr |
Supporting projects at the bench level using a variety of cell biology techniques and methodologies | 5/15/2017 |
| 1518 | Miltenyi Biotec Sunnyvale, CA Manufacturing, Science and Technology 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 the process development, qualification and manufacturing of T-cells and other cell therapy products within a GMP environment. The unique duties of this position will consist of supporting the development of scalable cell culture processes as well as the manufacturing of primary human cells including activities that involve graft engineering for cellular therapies. Furthermore, you will be responsible for completing successful qualifications and material flow 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. This position will primarily involve routine GMP cell processing and facility / equipment support with research and development work on an as needed basis. Overall, your keen ability to carry out key cell processing and manufacturing procedures will champion the continued development of Miltenyi Biotec products and growing success. | 5/15/2017 |
| 1519 | Oxford Immunotec, Inc. Memphis, TN Validation Specialist BS Exp: 1 yr |
The Laboratory Validation Specialist assists the Automation Engineer and Tech Transfer Manager with the validation and verification of new equipment and processes in the laboratory. The Validation Specialist also assists in the transfer of newly developed assays from the development stage to routine practice in the laboratory in a manner that is consistent with the goals of Oxford Diagnostic Laboratories and with the Quality Management System. Critical to the role is ensuring compliance with regulatory standards, laws and requirements of requisite agencies by employing appropriate systems / processes. | 5/15/2017 |
| 1520 | Oxford Immunotec, Inc. Boston, MA Manufacturing Associate BA / BS in a biological field Exp: 1 yr |
The Manufacturing Associate is responsible for the production of the various ELISA, Rapid Assay, and Western Blot products and their components which includes preparation of kit components (buffers and serum controls) and assembling of kits. | 5/15/2017 |
| 1521 | Oxford Immunotec, Inc. Memphis, TN Lab Assistant I BS in a biological, chemical, or physical science Exp: 1 yr |
Within the standards of Oxford Immunotec, Inc., the Laboratory Assistant performs pre-analytical tasks associated with the T-SPOT test, assures the quality of the specimens, ensures the work area is clean and stocked with supplies | 5/15/2017 |
| 1522 | Patheon Greenville, SC Scientist I - Process R&D BS in Chemistry or related field Exp: 1-2 yrs |
Conduct laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Utilizes judgment in making adaptation and modifications on all assignments. - | 5/16/2017 |
| 1523 | Patheon Greenville, SC Validation Associate III MS Exp: 1 yr |
The primary purpose of this position is to provide direct quality support (e.g. compliance, regulatory assessment, validation) to the business unit, clients and corporate management. For activities / projects with moderate complexity, perform quality functions to ensure accurate and timely completion with frequent decision making required. Create, review, approve, track and present documents required for compliance with pharmaceutical regulations. Identify areas of non-compliance and assist in the resolution of major issues. Perform activities across key quality functions as needed to ensure full support of business units. - | 5/17/2017 |
| 1524 | Patheon St. Louis, MO EH&S Associate BS in Life / Physical Science, Environmental Engineering, Safety, or Industrial Hygiene - Exp: 1-4 yrs |
Employee will be responsible for providing technical EHS support to relevant stakeholders across all aspects of the Site. | 5/15/2017 |
| 1525 | Pace Analytical Services, LLC Greenfield, IN Analytical Scientist - Enzymes MS in Microbiology, Molecular Biology, Chemistry, or related scientific degree Exp: 0-2 yrs |
This candidate will provide resources for analytical development in enzymes. They will be working in an analytical lab testing current products and working to develop new methods. Some experience with method development or validation would be preferred, but we would also consider a candidate with the drive and willingness to learn. | 5/15/2017 |
| 1526 | Pace Analytical Services, LLC Maplewood, MN Regulatory Coordinator BS in Chemistry, Biochemistry, Biology or related 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. | 5/15/2017 |
| 1527 | Pace Analytical Services, LLC Maplewood, MN Microbiologist - Product Development BS in Microbiology or a related science Exp: 1-3 yrs |
This candidate will perform microbiological testing as part of a product development group that deals with food safety. | 5/15/2017 |
| 1528 | Pace Analytical Services, LLC Maplewood, MN Chemist BS in Chemistry or related science Exp: 0-1 yr |
Candidate will perform wet chemistry techniques to support marketed inhalation devices. Will also support shipping of chemicals and compounds domestically and overseas. | 5/15/2017 |
| 1529 | Pace Analytical Services, LLC Maplewood, MN Chemist - HPLC BS in Chemistry or related science Exp: 1-3 yrs |
Candidate will perform analytical testing to support product development on an inhalation device. Analytical lab experience is necessary, specifically with HPLC. Fresh grads with chromatography research experience will be considered. | 5/15/2017 |
| 1530 | Pacific Biosciences of California, Inc. Menlo Park, CA Research Associate BS in Chemistry Exp: 6 months- 5 yrs |
The candidate will be required to carefully execute the desired transformation and perform multiple preparative chromatography isolation / purifications of targeted compounds, along with their analytical characterization. | 5/15/2017 |
| 1531 | Pacira Pharmaceuticals, Inc. San Diego, CA QC Analyst I/II - Temporary BS in Chemistry Exp: 1 yr |
Assist in write-up and review of Worksheet Validation Protocols.Execute Worksheet Validation Protocols.Assist in completing deviations related to the Worksheet Validation | 5/15/2017 |
| 1532 | Pacira Pharmaceuticals, Inc. San Diego, CA QC Analyst 1 - Temporary BS in Chemistry Exp: 1 yr |
Conduct laboratory tests in compliance with established internal Standard Test Methods, compendial methods and vendor partners supplied methods. | 5/15/2017 |
| 1533 | Pacira Pharmaceuticals, Inc. Parsippany, NJ Contract Associate BS Exp: 1 yr |
The primary purpose of this position is to manage the KOL contracting process including reviewing contracts for certain key terms, acting as a liaison with other departments, obtaining appropriate departmental review, ensuring compliance with FMV and AKS requirements, and managing the document routing system to ensure appropriate routing of contracts. In addition, this position will assist the legal and compliance department with gathering and maintaining data for external reporting purposes and other coordination and special projects as needed. | 5/15/2017 |
| 1534 | Par Pharmaceutical Irvine, CA Chemist II MS in chemistry, chemical engineering or related field Exp: 1 yr |
Conducts laboratory analyses: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer / solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc. | 5/15/2017 |
| 1535 | Paragon Baltimore, MD Associate Scientist II/III - Virus Process Development Ms in Biology, Chemistry, Life Sciences or related field Exp: 1-3 yrs |
This individual functions with supervision as an Associate Scientist and is actively engaged in upstream and midstream process and product development within a dynamic project team. Displays strong technical knowledge, initiative and scientific commitment, and makes significant scientific and technical contributions within the virus and fermentation groups. | 5/15/2017 |
| 1536 | Paragon Baltimore, MD Associate Scientist II Ms in Biology, Chemistry, Life Sciences or related field Exp: 1-3 yrs |
This individual functions independently and productively as an Analytical Scientist and is actively engaged in process and product development within a dynamic project team. Displays strong technical knowledge, initiative and scientific commitment, and makes significant scientific and technical contributions within Process Development Group. | 5/15/2017 |
| 1537 | Paragon Baltimore, MD Quality Control Analyst I/II BS in a Life Sciences Exp: 1-2 yrs |
This role is responsible for Environmental Monitoring sampling, analyzing, and aseptic monitoring 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. | 5/15/2017 |
| 1538 | Nuventra, Inc. Durham, NC Quality Control Internship BS Exp: NA |
Function as a flexible resource for Nuventra s scientific, project management, business operations, and business development staff.Serve as a member of project teams to assure that functional deliverables are supplied on time, on budget and according to quality standards. | 5/15/2017 |
| 1539 | Thermo Fisher Scientific Pleasanton, CA Intern II BS Exp: 1 yr |
Work in a team based environment to develop, prepare and revise testing validation procedures / protocols to ensure that product manufactured meet internal company standards. | 5/15/2017 |
| 1540 | Thermo Fisher Scientific Pleasanton, CA Intern II, Engineering BS Exp: NA |
Lead a process improvement project; Install and qualify equipment;Support process improvement projects with experiments, data analysis and recommendations;Help troubleshoot OpenArray equipment and processes;General laboratory operation and maintenance tasks. | 5/15/2017 |
| 1541 | Thermo Fisher Scientific Pleasanton, CA Engineering Intern BS / MS in Mechanical, Chemical or Bio Engineering Exp: NA |
Engineer will support new Capillary Electrophoresis consumables development. This individual will work with a multi-disciplinary team to develop new concepts, and / or modify and test editing concepts. | 5/15/2017 |
| 1542 | Miltenyi Biotec Cambridge, MA Regulatory Affairs Intern BS in regulatory affairs, the life sciences or chemistry Exp: NA |
As an intern with the Miltenyi Biotec Regulatory Affairs Team, you will have the exciting opportunity to gain hands-on learning experience supporting regulatory objectives to ensure products meet worldwide regulatory requirements for product approval and post-marketing compliance. You will work on projects and documentation related to regulatory submissions and compliance. Additionally, you will apply your excellent writing skills in developing standard operating procedures and impact workflow processes as they relate to regulatory objectives. Overall, your efforts will drive Miltenyi Biotec s continuing business success and give you the opportunity to build your resume with a skill set that is in high demand industry-wide. | 5/15/2017 |
| 1543 | MPI Research Mattawan, MI Research Technician 2 - Surgical Services BS Exp: 1-2 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.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.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. | 5/10/2017 |
| 1544 | MPI Research Mattawan, MI Research Associate - Discovery PK BS / MS 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.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. | 5/10/2017 |
| 1545 | 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. | 5/10/2017 |
| 1546 | 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).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).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). | 5/10/2017 |
| 1547 | MPI Research Mattawan, MI QC Associate - Laboratory Sciences QC BS / MS 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. | 5/10/2017 |
| 1548 | NGM Biopharmaceuticals, Inc. South San Francisco, CA Research Associate/Senior Research Associate - Molecular Biology / Protein Engineering BS / MS in molecular biology, cell biology, or a related discipline Exp: 1 yr |
The successful candidate will play an integral role as a key team member of a group focused supporting our therapeutic candidate discovery efforts. | 5/10/2017 |
| 1549 | Novan, Inc. Durham, NC Associate Scientist 1 BS / MS in chemistry, chemical engineering, or related discipline. Exp: 0-2 yrs |
The Associate Scientist 1 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 interpretation of data when appropriate. The Associate Scientist 1 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. | 5/10/2017 |
| 1550 | Novartis Fort Worth, TX QA Analyst I - FWN BS Exp: 1 yr |
To perform activities that ensure required quality and safety standards are being met for our products. Knowledge of Systems required to perform job function such as: Inventory systems, release systems, Laboratory management system, Change Control, Update Databases, Non conformance or deviation management system, Release of intermediates and finished goods, Approve shipments under quarantine, Ownership of Documents related to job function, Support Audits, Logbook processing, After Market / Production Support, Resolve Holds, Support MBR Review, Issue MBRs and Support Investigations. | 5/10/2017 |
| 1551 | Navigate BioPharma Svcs., Inc. Carlsbad, CA Clinical Lab Technician I BS in technology science or health-related field Exp: 1 yr |
Provide Support to technical laboratory staff and our onsite physicians. Primary responsibilities include initial intake and registration of patient specimen, handling of patient specimens, data entry and quality assurance of patient information, and slide making. Prepare and stains smears of blood and bone marrow on glass microscope slides. Although this isn t considered a high throughput lab, each sample has its own set of protocols and requirements. | 5/10/2017 |
| 1552 | Navigate BioPharma Svcs., Inc. Carlsbad, CA Clinical Data Entry Specialist BS Exp: 1 yr |
Under direct supervision, this position will be responsible for the accurate entry of clinical trial data information into computer database(s) and electronic worksheets. The Data Entry Specialist will perform manual entries from information from multiple source materials. This position requires exceptional attention to detail and ability to follow study specific procedures and adherence to data management compliance. Duties may also include peer-to-peer quality review to ensure data integrity and contribution to process improvement. | 5/10/2017 |
| 1553 | Novartis Lake Forest, CA Regulatory Affairs Analyst BS Exp: 0 yr |
Provide project and administrative support for customers within Global Regulatory Affairs, as well as regional and country regulatory affiliates. | 5/10/2017 |
| 1554 | Novavax, Inc. Gaithersburg, MD Research Associate I BS in biological science, molecular biology, immunology Exp: 0-2 yrs |
Play a key role in performing technical laboratory processes, including training on existing assays and clinical testing related activities as per schedule and under manager discretion in a GxP environment. | 5/10/2017 |
| 1555 | Novavax, Inc. Gaithersburg, MD QA Specialist, I/II, Materials 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 use in GMP manufacturing. | 5/10/2017 |
| 1556 | Novavax, Inc. Gaithersburg, MD Medical Writer I (In - house) BS Exp: 1 yr |
The Medical Writer is responsible for providing clinical / regulatory document support and advanced scientific writing expertise to the clinical and regulatory teams to generate high quality submission-ready documents. Specifically, the individual will write clinical study reports (CSRs), clinical study protocols (CSPs) and amendments, Informed Consent Forms (ICFs), and Investigator Brochures (IBs) and amendments for a variety of therapeutic areas. He / she will work with external groups (e.g., Regulatory Affairs and Operations, Biostatistics, Clinical Development, Preclinical, etc.) to ensure accurate and timely completion / delivery of documents and information for clinical / regulatory submissions. The work will be overseen (reviewed and edited, as necessary) by a senior staff member, however, the Medical Writer is expected to drive the project, track deliverables, and ensure timely completion. | 5/10/2017 |
| 1557 | Novo Nordisk Lebanon, NH Manufacturing Technician BS Exp: 0 yr |
Manufacturing Technicians have primary responsibility to support the manufacturing processes for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines. | 5/10/2017 |
| 1558 | Novo Nordisk Lebanon, NH Manufacturing Coordinator BS Exp: 1 yr |
This position will provide operational support for manufacturing team and act as a liaison for production in designated operational area. This role will also provide support to other operational areas within manufacturing as required. | 5/10/2017 |
| 1559 | Novozymes Blair, NE QC Analyst, Global Quality Control BS in Chemistry or closely related field Exp: 0 yr |
As a QC Analyst, you will be challenged to work closely with other analysts under the direction of the QC Team Leader in our new state of the art facility. You will perform assays with accuracy and precision then calculate and record data in form / records, LIMS and SAP databases. You will also provide reports of analytical data, ensure compliance to method controls and conduct tests to effectively support OPS. You will perform basic troubleshooting techniques as outlined in SOPs and perform routine instrument maintenance and calibration. | 5/10/2017 |
| 1560 | Novozymes Fayetteville, AR Research Associate, Animal Health - AR BS / MS in Biology, Chemistry, Animal Health, Nutrition, Food Science or other applicable scientific discipline Exp: 0-5 yrs |
You will be responsible for supporting animal studies, performing basic microbiology, and data collection and analysis. In addition, you will have the opportunity to communicate the results to key stakeholders with varying levels of scientific training. You will challenge conventions by developing innovative and sustainable products that help our customers produce more with less to create a brighter tomorrow. | 5/10/2017 |
| 1561 | Novus Biologicals Minneapolis, MN Research Associate 1 or 2 BS / MS in biology Exp: 0-5 yrs |
The responsibilities of this position are to purify proteins to restock the supply of existing products and modify existing protocols for larger scale production of proteins. This position normally receives no instructions on routine work and general instructions on new assignments. | 5/10/2017 |
| 1562 | Novus Biologicals Missouri, MO Field Applications Scientist BS / MS degree in biology, chemistry, biochemistry, bioengineering, or a related life science field Exp: 1 yr |
The candidate will be a key member of a team of Field Applications Scientists responsible for providing pre- and post-sales applications and technical support for several products. The ideal candidate is both an experienced bench level scientist / application scientist with a strong background in proteomics / immunoassays, as well as an experienced customer support specialist. | 5/10/2017 |
| 1563 | Novus Biologicals Minneapolis, MN Technical Service Associate 1 or 2 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. | 5/10/2017 |
| 1564 | Nurix, Inc. San Francisco, CA RESEARCH ASSOCIATE, DISCOVERY BIOLOGY BS in biological sciences or related field Exp: 1-4 yrs |
The successful candidate will support active drug discovery projects and assist with building important reagents and cell lines. The ideal candidate will have a strong desire to learn new techniques and the ability to incorporate new methodologies into their work. This individual will interpret, summarize and present findings to the internal team. | 5/10/2017 |
| 1565 | NuVasive Dayton, OH Manufacturing Engineer BS in engineering Exp: 1 yr |
Take ownership of project success for new and existing families of production.Coordinate cross-functional teams to execute and document the manufacturing launch of new / legacy products.Determine manufacturing processes required to accurately and efficiently make spinal implants, from raw material to final cleaning and shipment. | 5/10/2017 |
| 1566 | Ocular Therapeutix, Inc. Bedford, MA QC Analytical Chemist BS Exp: 1-3 yrs |
The QC Analytical Chemist will perform a variety of QC testing to assess the strength, identity and purity of test samples and / or materials. Incumbent will work as a member of team to effectively plan and perform QC analytical testing using established (official and / or in-house) test procedures. | 5/14/2017 |
| 1567 | Sun Pharmaceuticals Industries, Inc. Cranbury, NJ In - Process QA Inspector BS Exp: 1-2 yrs |
This role verifies and line clearance for dispensing, manufacturing and packaging activity. Perform batch record review, random sampling and in-process testing and final AQL visual inspection of finished bulk product. Performs manufacturing and packaging record review, random sampling and in-process testing, and final AQL inspection of packaged finished product. | 5/14/2017 |
| 1568 | Olympus Redmond, WA Manufacturing Engineer I BS / MS in Mechanical, Industrial, Electrical or Bio-medical Engineering Exp: 1 yr |
The Manufacturing Engineer is responsible for improving existing manufacturing processes and methods as well as assisting in the transition of new products from development phase to manufacturing. The incumbent will also assist the Director, Operations, in improving production control systems, standard operating procedures, safety, quality control and training. | 5/14/2017 |
| 1569 | Olympus Center Valley, PA Olympus Intern - Fall 2017 BS Exp: NA |
Olympus America is seeking interns to participate in a 13 week program designed to expose university-enrolled students to a holistic real-world work experience through the completion of company learning sessions and finite, interest-based tasks and projects. An intern will experience specific assignments based on his or her field of study in connection with one of four program tracks: Communications / Corporate Services / Graphic Design, Compliance, Legal & Corporate Governance, Finance / Operations / Economics and Life Science / Technology. | 5/14/2017 |
| 1570 | Nuventra, Inc. Cambridge, MA Pharmacokineticist MS in pharmaceutical sciences Exp: 0-2 yrs |
The successful candidate will possess an understanding of clinical PK and PK / PD concepts and applications; knowledge of drug metabolism, physiology, and animal PK studies is a plus. Excellent writing, communication, and mathematical skills are requisite to success in this position. | 5/10/2017 |
| 1571 | NuVasive San Diego, CA Intern, Development Engineering BS in Mechanical Engineering, Biomedical Engineering, or similar curriculum Exp: NA |
Creation and layout covering all phases of new product development from concept layout to production. | 5/10/2017 |
| 1572 | Novus Biologicals Littleton, CO Antibody Production Intern BS Exp: NA |
The Summer Intern will be assisting the Laboratory in antibody production and validation. The Intern will be exposed to a broad range of responsibilities. Projects may include antibody purification, antibody testing, protein gel preparation, Western blot testing, buffer and kit component production. | 5/10/2017 |
| 1573 | Thermo Fisher Scientific South San Francisco, CA Intern - isothermal amplification and advanced DNA templating BS / MS Exp: NA |
We are seeking an intern to join our Ion Torrent chemistry R&D group and participate in driving our next generation of sequencing technologies. This may include work in isothermal DNA amplification strategies as well as innovations to our general workflow, such as novel approaches to templating hydrogels on the Ion chip. While we are a chemistry group, the members of our group have diverse scientific backgrounds and work at the interface of chemistry, biology, and material science, while engaging with the software and chip teams. As such, this internship is open to candidates from chemistry, biology, engineering, material science, or related backgrounds, and the exact responsibilities may vary depending on a candidate s particular strengths. | 5/10/2017 |
| 1574 | Thermo Fisher Scientific South San Francisco, CA Bioinformatics Intern MS in computer science, computational biology, biostatistics, bioinformatics, or similar Exp: NA |
We're seeking a highly skilled individual with experience analyzing data, building models, algorithms, and software for analysis of next-generation DNA sequencing data. The successful candidate will be part of a multi-disciplinary team developing applications for Ion Torrent DNA sequencing instruments. The candidate will prototype, adopt, improve, develop, optimize and validate algorithms and analysis software to analyze DNA / RNA sequencing data for oncology, epidemiology, pharmacogenomics, metagenomics, and other applications; for example, to detect low frequency variant in blood, to detect gene fusions, to detect deleterious deletions, to detect copy number variations, to detect drug resistance mutations, to detect bacteria species id in blood, etc. | 5/10/2017 |
| 1575 | Thermo Fisher Scientific South San Francisco, CA R&D Intern BS in material science, chemical engineering, physics, chemistry, biomedical engineering or equivalent Exp: NA |
This is a technology development project that seeks to push the boundaries of next generation sequencing (NGS). Powered by semiconductor chips, Ion Torrent sequencing technology is simpler, faster, and more cost-effective and scalable than other benchtop next-generation sequencing technologies. By leveraging principles in polymer science, surface chemistry and MEMS, we are developing a platform that will deliver high-throughput genomic data with unprecedented accuracy. We are looking for a highly motivated individual that will take this challenge head on and work with the team to push the technology from concept to development, and subsequently through to commercialization. | 5/10/2017 |
| 1576 | Novartis Melville, NY Summer Intern Maintenance/Engineering BS Exp: NA |
Work with multiple groups on a project or request. Support Engineering projects in the field. Provide vendor training in site procedures. Implementation of 5S manufacturing concepts in Maintenance / Engineering areas. | 5/10/2017 |
| 1577 | Noven Pharmaceuticals, Inc. New York, NY Clinical Pharmacology Intern BS Exp: NA |
We are seeking an undergraduate or graduate student in life sciences who is interested in applying pharmacokinetics / pharmacodynamics and translational science in drug development. This individual will work in our Clinical Pharmacology Department and will support the group in the decision-making for advancing molecules through critical stages of development. During the internship, she / he will be assigned an interesting and stimulating project and will get hands-on experience in clinical pharmacology. She / he will be included in the group s strategic meetings as well as in cros s-functional team meetings and will have a chance to present her / his work in several occasions during the duration of the internship. | 5/10/2017 |
| 1578 | Grifols Clayton, NC Purification Technician I/II AS / BS biology, chemistry, engineering, or related Exp: 1 yr |
Process fractionated plasma intermediates to sterile bulks. Predominant activities will include: high levels of housekeeping to conform to GMP standards, assembling, disassembling and cleaning of equipment before and after use, assist with process control and manipulations. | 5/16/2017 |
| 1579 | Grifols Clayton, NC IGIV - C Technician I/II/III/Senior 1 AS / BS biology, chemistry, engineering, or related Exp: 1 yr |
Isolation of IgG protein by processing plasma intermediate material II +III paste through the dissolution and filtration stage, chromatography purification stage, and ultrafiltration / diafiltration stage, to formulation and sterile bulking as well as preparation of buffers. | 5/16/2017 |
| 1580 | Grifols Clayton, NC Aeseptic Filling Core Technician I/II/III AS / BS biology, chemistry, engineering, or related Exp: 1 yr |
Performs a variety of operations involving the support of aseptic filling of plasma products, primarily operation of highly automated fill equipment inside the aseptic environment. Major duties will include operation of the fill / stoppering equipment to dispense sterile product into glass containers, calibration of critical loadcells before, during and after each fill, environmental monitoring of the aseptic environment during each fill, loading and unloading of sterile products from freeze dryers, and operation of the continuous particulate monitoring system during each fill. The responsibilities include the monitoring and troubleshooting of the fill process through the use of computer terminals and electronic trends and data to ensure proper functioning of the equipment. Responsibilities also include high levels of mechanical aptitude during setup and troubleshooting of the equipment. Trouble-shooting may include adjustment of photo-optic sensors and mechanical adjustments to the fill line. Predominant activities will include: high levels of housekeeping to conform to cGMP standards, cleaning and sanitizing aseptic filling areas to maintain the quality of the product, assembling and disassembling of equipment before and after use, and performing operations during fills by following proper procedures. Position will also be required to operate of all fill line equipment outside of the aseptic filling environment such as vial rinsers, depyrogenation tunnel, oversealers, cage loaders, cage rinsers, etc. Job responsibilities also include detailed and accurate documentation in batch production records. Must be able to determine availability of components and assign accordingly. May also be required to assist in training of co-workers. Must be able to perform in the aseptic filling areas while maintaining the integrity and cleanliness of these areas by utilizing aseptic gowning requirements and techniques. | 5/16/2017 |
| 1581 | Grifols Raleigh, NC Summer Intern - Bioanalytics BS biochemistry, microbiology ,biology, or related Exp: 2 yrs coursework |
This position is in the Biochemistry development group of the BioAnalytics department, which is located at Centennial Campus, North Carolina State University. The incumbent will work on developing immunoassays to support manufacturing projects. He / she will be expected to analyze, interpret and report the results of experimental studies and should work well in a multifunctional team environment. | 5/16/2017 |
| 1582 | Grifols Clayton, NC R&D Intern - Alpha 1 BS biochemistry, chemistry, chemical / biomedical engineering Exp: 2 yrs coursework |
This internship will conduct studies to test the effects of process conditions, excipients, and other parameters on product quality and stability as a part of a new process development team. Project responsibilities will include the preparing a supply of material for formulation development studies, concentration studies, yield analysis, analytical studies using techniques such as: differential light scattering, potency analysis, SE-HPLC, total protein analysis, | 5/16/2017 |
| 1583 | Grifols Research Triangle Park, NC Summer Intern BS scientific discipline Exp: 2 yrs coursework |
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. | 5/16/2017 |
| 1584 | Grifols Emeryville, CA Regulatory Affairs Associate I BS life sciences Exp: 1 yr |
The Regulatory Affairs Associate I will be responsible for preparing technical files and international product master files (e.g. STED), to support global regulatory submissions for the registration of IVD systems (assays, instruments, software). | 5/16/2017 |
| 1585 | Halozyme San Diego, CA Regulatory Information Management Specialist - Contract BS technical discipline Exp: 0-2 yrs |
The successful candidate will support the Regulatory Affairs function by coordinating, tracking, and archiving regulatory documentation including regulatory submissions, correspondence, questions, commitments, and partner information within Veeva Registrations [Halozyme s Regulatory Information Management System (RIMS)]. The Regulatory Information Management Specialist will maintain Halozyme s Nonclinical Protocols and Reports Database within SharePoint as well as maintain the department s physical files. The Regulatory Information Management Specialist will also provide formatting, author training and publishing support for the nonclinical protocols and reports. | 5/16/2017 |
| 1586 | Health Decisions Durham, NC Clinical Research Associate - West Coast BS / BA scientific or health-related field Exp: 1-2 yrs |
The CRA will be responsible for performing site monitoring activites for assigned clinical studies in accordance with the Task Order, protocol, standard operating procedures (SOPs), ICH guidelines and all applicable regulatory requirements. | 5/17/2017 |
| 1587 | HeartFlow Redwood City, CA Imaging Algorithms Engineer MS computer science or related Exp: 1 yr |
This position is for a developer working in HeartFlow s Image Analysis team who will work on a variety of software development tasks, including implementing new algorithms, refactoring existing algorithms, developing deep learning infrastructure, designing and implementing algorithmic tests for existing algorithms, and building interactive tools. In addition to performing the primary development activities listed above, the candidate may be responsible for general bug fixing, enhancements, test suite development, user support and participation in all other activities defined in the company s product development process and as requested by their manager. | 5/17/2017 |
| 1588 | Medtronic Mounds View, MN MDR/Vigilance Specialist MS health, clinical technical, or scientific field Exp: 1 yr |
This position is expected to work cross-functionally to ensure maintenance and review of events and complaints, reporting of Medical Device Reports (MDRs), ADE data, or adverse reaction data, as set forth by the FDA and other regulatory agencies. Requires follow-up internally and externally to assure complete and accurate event files, complaint detail, and product performance information. Supports and represents complaint handling in internal and external audits and inspections. | 5/17/2017 |
| 1589 | Medtronic North Haven, CT Product Engineer BS mechanical engineering or related Exp: 0-3 yrs |
The position will be in the New Product Development (NPD) team in the Advanced Surgical Technologies group. The Manufacturing Engineer will be responsible for assisting in the development, qualification, launch and commercialization of surgical instruments and devices. This position will assist senior and principal level Manufacturing Engineers who work directly with Design and Development Engineers in the development of new products. The Manufacturing Engineer will assist in the development of the commercialization strategy for the product. The commercialization strategy entails the development of component tooling, assembly tooling as well as validation and qualification of the product. These strategies will be developed during the Concept and Feasibility (NPD) stages followed by the execution of these strategies during the Development, Qualification and Launch phases. The Manufacturing Engineer will work under the direction of a Senior or Principal Advanced Manufacturing Engineer (AME) and report directly to the AME manager. The Position is in a fast-paced, collaborative environment that is supportive of program initiatives and compliant with the company s best practices, Tenets and Philosophy. | 5/17/2017 |
| 1590 | Medtronic Brooklyn Center, MN Technician I AS electrical / mechanical engineering or related Exp: 0-2 yrs |
The Technician s primary responsibility will be providing critical customer support on production impacting situations for laser welders, resistance welders, and test equipment. This position performs a variety of routine and non-routine tasks in a chemical, electrical, electronics, imaging, mechanical, quality, or other technical areas. The Technician completes complex tests requiring judgment in determining work methods, interpreting test results and writing clear and accurate test result reports. May build and test mechanical models, electrical circuits and assemblies. May have responsibility for minor projects, and assists on assignments that are moderately complex to complex in nature where judgment and initiative are required in resolving problems and making recommendations. | 5/17/2017 |
| 1591 | Medtronic Fridley, MN Technician AS technical discipline Exp: 1-2 yrs |
The Analysis Technician will perform analysis of returned explanted product. The position will require interface with fellow technicians, customer support and vigilance personnel, design and reliability engineers, and potentially with legal personnel. Information obtained during analysis will be entered into the Global Complaint Handling (GCH) Data Base System. | 5/17/2017 |
| 1592 | Medtronic Jacksonville, FL Associate Quality Engineer BS engineering Exp: 0 yrs |
This position has the responsibility and authority to provide Quality Engineering representation and support to select business teams facilitating front-end design, design transfer to manufacturing, and / or process improvements to obtain optimum product reliability, safety, effectiveness and compliance. | 5/17/2017 |
| 1593 | Medtronic Northridge, CA Internal Quality Auditor MS technical discipline Exp: 1 yr |
The Internal Quality Auditor is an important individual contributor role in the Quality System department. This person is responsible to conduct internal audits of Medtronic Diabetes Group s quality system to identify compliance gaps and opportunities for improvement. The incumbent will have demonstrated thorough understanding of 21 CFR Part 820, ISO 13485 and other global quality system requirements, and be able to audit those efficiently and effectively. This role also provides support through cross-functional collaboration in preparation for and hosting of external audits by regulatory agencies and Notified Bodies. This position reports to the Quality Improvement Director. | 5/17/2017 |
| 1594 | Medtronic Brooklyn Center, MN Associate Product Engineer BS mechanical engineering Exp: 0-3 yrs |
This position is in the Sourcing Continuity Engineering function within Sourcing department. This position entails developing technical solutions for components sourced from suppliers. This position supports MECC where components from suppliers are received and used. This position involves working closely with several other functions, including Manufacturing, Supplier Quality, Reliability, and Regulatory. | 5/17/2017 |
| 1595 | Helix San Carlos, CA Curation Analyst, Partner Science Team BS molecular biology or related Exp: 1 yr |
As a Curation Analyst, you will gain data curation experience and familiarity with personalized genomics as you conduct primary literature analysis. You will gain experience in how genomic products are built and have a real impact on our partner product and process development efforts. And, as a bonus, you ll get to work in a fast-paced, fun and exciting start-up environment and learn from some of the most brilliant minds in the industry. | 5/17/2017 |
| 1596 | Helix San Diego, CA Research Associate BS biology, genetics, chemistry, biochemistry, or related Exp: 1-3 yrs |
As an RA at Helix, you will work in a dynamic and fast-paced environment to develop robust, scalable genetic testing processes to be used in cutting-edge clinical genetics applications. | 5/17/2017 |
| 1597 | Helmer Scientific Noblesville, IN Electrical Engineer I BS electrical engineering or related Exp: 0-5 yrs |
Provides electrical engineering support to Sustaining Engineering department through the development, documentation and production support for Helmer product portfolio. Develop specs and electrical engineering requirements based on directions given by Team Leader. Have fundamental knowledge from educational background, while tasks are managed or directed by others. | 5/17/2017 |
| 1598 | Hill-Rom Skaneateles Falls, NY Engineer I, Electrical BS electrical engineering or related Exp: 0-2 yrs |
Applies basic Electrical Engineering principles to problem solving such as component selection, machine, process or failure investigations Understand fundamental electrical troubleshooting methods Communicate to senior staff and technologists on designs and resolutions Familiar with analytic tools such as MathCAD, Orcad, PSpice, etc. Generate clear and concise electrical protocols based on electrical knowledge and guidance from staff Create and identify test methods Contribute and run design based problem solving on advanced electrical circuits | 5/17/2017 |
| 1599 | Hill-Rom Skaneateles Falls, NY Engineer I, Mechanical BS mechanical engineering Exp: 0-2 yrs |
Familiar with design tools such as ProE, etc. Exposure to simulation and engineering analysis techniques and tools such as ANSYS Comfortable with lab test equipment and in a test environment Generate clear and concise mechanical protocols based on mechanical knowledge and guidance from senior staff Familiar with rapid prototyping techniques and tools and able to build prototypes Support manufacturing floor when needed, particularly for failure analysis Support design control processes as required by the QMS with guidance from senior staff Applies basic mechanical engineering principles to problem solving such as component selection, machine, process or failure investigations Understand fundamental mechanical troubleshooting methods Exposure to DFMA techniques Communicate to senior staff and technologists on designs and resolutions | 5/17/2017 |
| 1600 | Hologic San Diego, CA Research Associate BS molecular biology, chemistry, biochemistry, or related Exp: 1-3 yrs |
Hologic is seeking a RESEARCH ASSOCIATE responsible for designing and performing experiments while collaborating and communicating effectively. | 5/17/2017 |
| 1601 | Hologic Erie, PA Field Service Engineer, Diagnostics BS / BA scientific discipline Exp: 0-2 yrs |
Conducts advanced troubleshooting to repair, test and qualify instruments located at assigned territory sites. Provides 24 / 7 coverage to customers within 24 hours of notification. Schedules and manages preventive maintenance and unscheduled visits to instrument sites. Determines correct inventory levels of repair parts with supply lines. Documents repair / resolution of customer calls in CRM system and escalates issues to management as needed. Works with Product Application Engineers to resolve quality issues and advise of issues and developments. Keep management advised of issues and developments. Ensure instrumentation is in compliance with regulatory requirements and quality control standards. | 5/17/2017 |
| 1602 | Hologic San Diego, CA Intern, Biostatistics BS technical discipline Exp: 2 yrs coursework |
Perform ad-hoc analyses andtabulations on complex but structured data sets Assist review of tables andlistings to be included in clinical study reports and submissionsAssist development and review ofstatistical analysis plan and sample sizing calculations | 5/17/2017 |
| 1603 | Hologic Sunnyvale, CA Intern, Software Quality Assurance BS technical discipline Exp: 2 yrs coursework |
As a valued member of the Breast & Skeletal Health R&D team, an intern will be responsible for developing a software quality assurance inventory tool. | 5/17/2017 |
| 1604 | Horizon Pharma Lake Forest, IL Intern, Pharmacovigilance BS pre-pharmacy or related Exp: 1 yr coursework |
The Horizon Pharma Internship Program offers aspiring professionals an opportunity to build a strong foundation of business acumen, technical skills, and knowledge about the pharmaceutical industry. We are committed to providing program participants with experience-based learning, multidimensional assignments, targeted training, and continual coaching and development | 5/17/2017 |
| 1605 | Horizon Pharma Lake Forest, IL Intern, Regulatory Affairs MS regulatory science, molecular biology, biomedical sciences, engineering, or related Exp: 1 yr coursework |
The Horizon Pharma Internship Program offers aspiring professionals an opportunity to build a strong foundation of business acumen, technical skills, and knowledge about the pharmaceutical industry. We are committed to providing program participants with experience-based learning, multidimensional assignments, targeted training, and continual coaching and development. | 5/17/2017 |
| 1606 | Pfizer Rocky Mount, NC Manufacturing Quality Engineer - R2 Night Shift (ID: 1053962) BS scientific discipline Exp: 0-2 yrs |
The Manufacturing Quality Engineer provides oversight and guidance in R2 SVP manufacturing operations, ensuring continuous facility and GMP compliance. The MQ Quality Engineer will coach manufacturing personnel on proper GMP and SOP compliance and empower them to identify and escalate quality issues, to ensure quality product. | 5/17/2017 |
| 1607 | Pfizer McPherson, KS Operations Specialist - Tech Transfer (ID: 1045375) BS engineering or technical related field Exp: 1-3 yrs |
The Ops Specialist Tech Transfer is a role within McPherson Operations supporting new product introductions as a key member of tech transfer teams. This role provides a single point of contact to project teams for all Operations related implementations, including new products to plant through network strategy transfers, new development projects (Co-Dev), market growth opportunities, or process improvements, etc. | 5/17/2017 |
| 1608 | Medtronic North Haven, CT Biomedical Engineer BS / MS in mechanical / biomedical engineering or biological science Exp: 1-2 yrs |
Incumbent provides technical support for new and ongoing product development efforts, clinical liaisons and other business partners as appropriate. Develops and refines analytical test methods for competitive and internal comparative product analyses. Develops, executes and refines bench top, ex vivo and acute and chronic in vivo studies. Prepares technical reports and communicates to internal and external audiences. Member of new product development core teams providing guidance for early stage products and appropriate test development. Interfaces with quality to facilitate comprehensive product analyses. Manages all aspects of new product surgical training labs for surgeons. Manages collaborations internally (team to team) and participates in external collaborations(academic collaborators, clinical research organizations). Presents research findings at national and international conferences. | 5/3/2017 |
| 1609 | Medtronic Northridge, CA Field Clinical Research Specialist MS Exp: 1 yr |
The Field Clinical Research Specialist supports multiple activities in the conduct of clinical research studies and operational projects in compliance with applicable regulatory standards, IRB policies and procedures and Medtronic internal requirements. This position works with minimal supervision in consort with study and department management to perform complex and diverse project duties. | 5/3/2017 |
| 1610 | Medtronic North Haven, CT Associate Regulatory Prooduct and Operations Specialist BS in a scientific or engineering field Exp: 0-2 yrs |
The Regulatory Affairs Associate is responsible for assistance with management of the Regulatory Affairs department activities, supporting US FDA and EU submissions and the support in managing international regulatory registrations with the Regional Business Units (RBU), which includes global regulatory strategies and impact assessments, initial registrations, re-registrations and notifications / registrations of changes that may impact the regulatory approvals. | 5/3/2017 |
| 1611 | MPI Research Mattawan, MI Research Technician 1/Research Associate 1 - Safety Pharmacology 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. | 5/3/2017 |
| 1612 | MPI Research Mattawan, MI Research Technician 1/Research Associate 1 - Neurobehavioral Sciences In - Life 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. | 5/3/2017 |
| 1613 | MPI Research Mattawan, MI Research Technician 1 - Surgical Services - In - Life 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. | 5/3/2017 |
| 1614 | MPI Research Mattawan, MI Research Technician 1 - Surgical 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. | 5/3/2017 |
| 1615 | MPI Research Mattawan, MI Research Technician 1 - 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. | 5/3/2017 |
| 1616 | NantKwest Culver City, CA Regulatory Operations Associate BS Exp: 1-4 yrs |
Under the supervision of the Regulatory Operations Associate Director, this position is responsible for providing support for all submission-related activities including, submission project management, production of submission-ready documents, performing technical submission reviews, and maintaining an electronic archive for regulatory documents. This position will also assist the Regulatory Affairs team with any special projects as assigned. | 5/3/2017 |
| 1617 | NantKwest San Diego, CA Senior Research Associate MS in biological sciences Exp: 1 yr |
The successful candidate will work as part of the Immunology Research team at NantKwest Inc., to support the development the next generation products for adoptive cell therapy based on our Natural Killer (NK) cell platform. We are a growing company that offers competitive salaries and benefits. We are seeking a motivated Senior Research Associate to assist in developing our novel technology for use against cancer indications. The applicant will have previous experience in working an immunology laboratory (preferably working with primary cells and cell lines) and will be responsible for supporting the efficient operation of the laboratory and performing scientific studies to support immunology and oncology research and development projects. | 5/3/2017 |
| 1618 | Natera San Carlos, CA Clinical Laboratory Scientist I BS / BA in Medical Technology, Biological Sciences, or related field Exp: 1-4 yrs |
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. | 5/3/2017 |
| 1619 | Natera Austin, TX 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. | 5/3/2017 |
| 1620 | Neogen Corporation Lincoln, NE Lab Assistant BS Exp: 0 yr |
Within the lab, the responsibilities include sample tracking, lab maintenance, data entry, and inventory assistance. Contribute to established protocols with suggestions to improve current processes. | 5/3/2017 |
| 1621 | Neogen Corporation Lincoln, NE Lab Assistant, Sample Reception BS Exp: 1 yr |
Within the lab, the responsibilities include sample tracking, lab maintenance, extensive data entry, and inventory assistance. As well as contributing to established protocols with suggestions to improve current processes. This position handles agricultural samples, which can have some odor. | 5/3/2017 |
| 1622 | Neogen Corporation Lincoln, NE Laboratory Technician I, DNA BS in a science discipline (chemistry, microbiology, biochemistry, immunology, animal science) Exp: 1-2 yrs |
Within the lab, the responsibilities include quality control for sample tracking, extracting DNA from multiple sample types from a variety of species, and performing final quantification to ensure proper yield has been achieved. Contribute to established protocols with suggestions to improve. | 5/3/2017 |
| 1623 | Neogen Corporation Lincoln, NE Laboratory Tech I, Processing, 2nd Shift BS in a science discipline (chemistry, microbiology, biochemistry, immunology, animal science) Exp: 1-2 yrs |
Within Processing Lab will have routine exposure to robotics, low and high volume amplification reactions, and hood work utilizing single and multichannel pipettes. Must contribute to an established processing workflow with welcomed ideas for process improvements. | 5/3/2017 |
| 1624 | Neogen Corporation Lincoln, NE QA/QC Technician Level II BS Exp: 1-2 yrs |
Tasks also include the setup of performance studies on critical raw materials, components or products to measure performance, shelf life or product characteristics. Technicians provide assistance in troubleshooting and performing investigations on out-of-specification results. An ideal candidate will be detail oriented self-motivating and proficient in the ability to learn and apply knowledge to carry out tasks. Experience with ELISA and general lab equipment is preferred. | 5/3/2017 |
| 1625 | Nephron Pharmaceuticals West Columbia, SC Micro Analyst 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. | 5/3/2017 |
| 1626 | Neurona Therapeutics South San Francisco, CA Lab Assistant BS in biology, biotechnology or a related field Exp: 0 yr |
The Laboratory Assistant will perform operations that will aid in maximizing the research productivity of the laboratory staff. Day-to-day functions include reagent preparation, cleaning and autoclaving of equipment and materials, solid and liquid waste disposal, inventory management and other duties to support daily operations of the R&D teams. Neurona Therapeutics is an early stage biotechnology company based in South San Francisco focused on the development of neuronal stem cell-based therapies for neurological disease. This is a fantastic opportunity to join a small team and take part in building an exciting, science-driven company. | 5/3/2017 |
| 1627 | 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. | 5/3/2017 |
| 1628 | NewLink Genetics Ames, IA NewLink Genetics Corporation BS / MS in Organic Chemistry or Chemistry Exp: 1 yr |
The Research Associate in Medicinal Chemistry will assist in the synthesis of target compounds and will be responsible for maintenance of lab equipment. The candidate will be supervised by a Senior Scientist. | 5/3/2017 |
| 1629 | NGM Biopharmaceuticals, Inc South San Francisco, CA Research Associate/Senior Research Associate - Protein Characterization BS / MS in chemistry or a life science discipline Exp: 1 yr |
The successful candidate will be responsible for developing and performing methods in the biophysical characterization of proteins, as well as the operation and maintenance of analytical instrumentation. | 5/3/2017 |
| 1630 | NITTO DENKO Avecia Milford, MA Quality Assurance Specialist BS / BA in science Exp: 1-5 yrs |
Plays a key role in the cGMP compliance activities at the Milford site by preparing the site for FDA Pre-approval Inspections (PAI) and continuously works with other departments to maintain and monitor compliance with cGMPs. | 5/7/2017 |
| 1631 | NITTO DENKO Avecia Cincinnati, OH QA Documentation Specialist BS / BA in science Exp: 1-3 yrs |
Writes SOP s, protocols, validation plans and compliance documents for cGMP program.Acts as departmental resource for cGMP software programs.Oversees qualification of instruments, equipment, facility, clean rooms and computer hardware / software.Sets-up and organizes tracking program for equipment used in cGMP work. | 5/7/2017 |
| 1632 | Nova Biomedical Waltham, MA Technical Support Product Specialist BS in Chemistry / Biology Exp: 0-3 yrs |
Answer both general and technical questions related to the operation and maintenance of our analyzers. | 5/7/2017 |
| 1633 | Norwich Pharma Norwich, NY Chemist I BS in Chemistry, Biochemistry, Microbiology or Biology or related discipline Exp: 0-3 yrs |
Perform routine sample analysis requiring general laboratory skills such as weighing, pipetting, titration, and basic operation of laboratory instrumentation | 5/7/2017 |
| 1634 | Neurocrine Biosciences, Inc. San Diego, CA Summer Intern, Pharmaceutical Development BS in Chemistry, Biology Exp: NA |
The part-time student Intern (<29 hrs per week) will be involved in a range of research and general laboratory support efforts, primarily in the area of Pharmaceutical Development. | 5/3/2017 |
| 1635 | Neurocrine Biosciences, Inc. San Diego, CA Summer Intern, Chemistry BS Exp: NA |
The part-time student Intern (<29 hrs per week) will be involved in a range of research and general laboratory support efforts, primarily in the area of organic chemistry. | 5/3/2017 |
| 1636 | Thermo Fisher Scientific Carlsbad, CA Molecular Biology Intern BS in molecular biology, biochemistry or equivalent disciplines Exp: NA |
The successful candidate will work towards system optimization, focusing on critical reagents of the Chef and S5 system with the objective of meeting product requirements for customer use. The candidate will apply molecular biology laboratory skills to execute Ion Torrent DNA sequencing protocols, collect and analyze the data. This position entails working with a team of experienced scientists and interaction with software and engineering teams. The abilities to meticulously document and communicate results to diverse audiences are important aspects of this role. | 5/3/2017 |
| 1637 | Thermo Fisher Scientific Carlsbad, CA Intern II BS / MS Exp: NA |
The position will focus on sample preparation for next generation sequencing platforms and is located in Carlsbad. | 5/3/2017 |
| 1638 | Thermo Fisher Scientific South San Francisco, CA Intern - Bioinformatics BS / MS Exp: NA |
Experience with DNA and RNA analysis of next-generation sequencing data. Experience with data analysis with R / Matlab. Experience with pipeline and / or software development , with Python, Java, C++, etc.Ability to plan and organize experiments | 5/3/2017 |
| 1639 | MPI Research Mattawan, MI Research Associate (Intern) - Biomarkers and Investigative Pathology BS Exp: 1-2 yrs |
The Biomarkers and Investigative Pathology (BIP) Research Associate is responsible for assisting with conducting analyses for research studies, including sample and instrument preparation. May assist in the conduct of method validation analyses using investigational pathology platforms, such as, immunohistochemistry, immunoassay biomarkers, and / or flow cytometry. | 5/3/2017 |
| 1640 | MPI Research Mattawan, MI Research Technician 1 (Intern) - Small 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. | 5/3/2017 |
| 1641 | Nordson Corporation Chippewa Falls, WI Intern, Manufacturing Engineering (Summer) BS in Industrial Engineering or Manufacturing Engineering Exp: NA |
Perform engineering work requiring application of standard techniques, procedures, and criteria in carrying out a sequence of related engineering tasks. Independently evaluates, selects, and applies standard engineering techniques, procedures, and criteria, using judgment in making adaptations and modifications. | 5/7/2017 |
| 1642 | Nordson Corporation East Providence, RI Engineering/Operations Intern BS in engineering Exp: NA |
The Engineering / Operations Intern will be responsible for entry-level fundamental engineering and operations tasks. The intern will work in both our inventory and Engineering Services departments alongside department managers and personnel to obtain part weights / UOM and obtain product trade and compliance documentation. Results of these efforts will be recorded in spreadsheets to be uploaded into SAP. The internship will provide the student with exposure to a manufacturing environment while allowing them to create an impact on the organization. | 5/8/2017 |
| 1643 | Catalent Kansas City, MO Associate, Quality Assurance - 2nd Shift BS scientific discipline Exp: 0-2 yrs |
Under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians / assistants. Comply with divisional and site Environmental Health and Safety requirements. | 5/8/2017 |
| 1644 | Catalent Madison, WI Associate Scientist Raw Materials, Quality Control MS biotechnology Exp: 1 yr |
This position requires a variety of skills necessary for biotech company operations. Perform routine testing of process samples, raw materials, finished products and stability samples, while adhering to SOPs and GLPs, and working in a cGMP compliant environment. Analyze and interpret results in written and oral format. . Additionally, this position will support Preventative Maintenance and basic Laboratory maintenance activities while maintaining a GMP quality system. Other duties will include data review / archiving, database entry / review and contributions to process improvement initiatives. This position will support the raw material program techniques employed include raw material sampling, identity testing via RAMAN light scattering, compendial testing and management of outsource partners. | 5/8/2017 |
| 1645 | Genospace Cambridge, MA Software Engineering Intern BS / MS technical background Exp: 1 yr coursework |
As a Software Engineering Intern you will gain an understanding of how to develop web based tools that further new discovery in the treatment of disease. More specifically, you will learn how Genospace applications are architected and be able to launch, operate and interact with your own development environment. Initially the intern will be tasked with testing and bug fix assignments on existing Genospace applications. As proficiency is gained an appropriate standalone project will be assigned that should be completed by the end of the program. During the internship Genospace will provide basic training in clinical and genomic informatics. | 5/8/2017 |
| 1646 | GenScript Piscataway, NJ Analystical Biochemist (ID: 421) MS 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. 2. Primarily focus on development of molecular biology and synthetic biology, including gene synthesis, vector design / construction, gene expression, plasmid purification, gel electrophoresis or DNA analysis. 3. Analyze samples using a variety of instruments, including High Performance Liquid Chromatography (HPLC), Liquid Chromatography Mass Spectrometry (LC-MS) and Gas Chromatography (GC). 4. Analyze, record, report and summarize the laboratory results and conclusions. 5. Responsible for maintaining and troubleshooting analytical instrumentations, solutions, reagents, and supplies | 5/8/2017 |
| 1647 | GenScript Piscataway, NJ Lab Technician (ID: 253) BA / BS biology or related Exp: 1 yr |
Sequencing technician will be responsible for: 1.Preparing and purifying DNA samples, 2.Performing PCR amplification, 3.Operating automated DNA sequencer, 4.Interpreting sequencing data using computer-based approaches, 5.Developing protocols and updating databases. | 5/8/2017 |
| 1648 | Ginkgo Bioworks Boston, MA Research Assistant, Sample Management AS / BS biology or related Exp: 1 yr |
Sample intake and distribution within Ginkgo. Generation of a company wide sample repository. Maintain and keep track of sample quality. Storage / retrieval QC Assist lab staff with basic bench level molecular biology | 5/8/2017 |
| 1649 | Ginkgo Bioworks Boston, MA Lab Assistant AS / BS biology or related Exp: 1 yr |
Prepare solid and liquid microbial media on a daily basis, including standard items as well as custom recipes. Perform glassware washing and sterilization on a daily basis. Prepare special reagent solutions as needed. Maintain and keep track of lab chemical and reagent inventories. Supply chain management of laboratory consumables. | 5/8/2017 |
| 1650 | Ginkgo Bioworks Boston, MA Automation Padawan BS biology or related Exp: 3 yrs coursework |
You will be working in the foundry with a mix of operations and development in collaboration with Ginkgo jedis. Our foundry encompasses high throughput genetic engineering of microbes as well as high resolution analytics to assess cell performance; you will be responsible for helping to transition and adapt protocols and new unit operations to run on Ginkgo's automated platforms. Most importantly, you should be passionate about making biology easier to engineer. | 5/8/2017 |
| 1651 | Ginkgo Bioworks Boston, MA Build Team Padawan BS / MS biology, biochemistry, bioengineering, molecular biology, or related Exp: 1 yr |
Core to our organism engineering pipeline is the construction of our engineered strains using state-of-the-art molecular biology techniques and automation platforms. We are looking for highly talented and motivated students to join our Build team. Interns on the Build team help maintain, improve, and innovate the high-throughput genetic engineering of microbes. | 5/8/2017 |
| 1652 | Ginkgo Bioworks Boston, MA Fermentation Padawan BS / MS chemical engineering, microbiology, or related Exp: 1 yr |
Assist with setup and operation of Sartorius ambr250 and ambr15 automated bioreactor systems Assist with processing and analysis of fermentation samples Apply Design of Experiment methods for strain and process optimization Prepare fermentation SOPs Communicate results to fellow employees, within the Fermentation team and across functional groups | 5/8/2017 |
| 1653 | Ginkgo Bioworks Boston, MA Foundry Operations Co - op BS biology or related Exp: 1 yr coursework |
Co-op students at Ginkgo will be responsible for learning and performing a particular set of operations within Bioworks1. Foundry operations include genetic engineering and molecular biology, enzyme screening, metabolomics, proteomics, fermentation, and purification. Our approaches are designed to scale 100-1000X via software and automation. You ll be exposed to the cutting edge and be expected to not only perform operations but report on daily activities to a mixed team of software developers, biological and chemical engineers, and biologists. The ability to adapt in a rapidly changing technological environment will be required. | 5/8/2017 |
| 1654 | Ginkgo Bioworks Boston, MA Organism Engineering Padawan BS / MS biochemistry, metabolic engineering, molecular biology, or related Exp: 1 yr |
Assisting OEs with routine bench work tasks, such as molecular cloning, genome engineering etc. Communicating and interacting with other teams, i.e. interacting with the Build team to use our high-throughput pipeline and automated processes, etc. Lead certain projects assigned by OEs according to your experience | 5/8/2017 |
| 1655 | GSK Warren, NJ Clinical Quality Documentation Specialist BS technical discipline Exp: 1 yr |
Conduct and report (document) the QA review of clinical study documents and / or their repositories | 5/8/2017 |
| 1656 | GSK Upper Merion, PA Associate/Senior scientist BS chemical engineering, biology, chemistry, or related Exp: 1 yr |
The Associate / Senior Scientist leads the manufacture of clinical supply of investigational biopharmaceutical molecules. Specifically, hands-on cGMP mid to large scale purification of bulk drug substance for use in early phase clinical trials. | 5/8/2017 |
| 1657 | GSK King of Prussia, PA Laboratory Technician, Downstream Process Development AS chemistry or related Exp: 1 yr |
Maintain adequate supplies of raw materials and in-process materials for use by the DPD scientific staff: Prepare buffers and reagents requested by DPD scientists by either following a preset recipe or by developing a recipe based on buffer specifications provided by the scientist. Document all buffer prep and calibration information in official electronic lab notebooks for clear traceability and accountability. Order materials through appropriate systems and contact vendors as necessary to obtain product details and delivery schedules. Take accountability for accurate delivery of analytical samples to appropriate locations. | 5/8/2017 |
| 1658 | GSK Upper Merion, PA Associate Scientist BS / MS biotechnology or pharmaceutical science Exp: 0-5 yrs |
The candidate will participate in the development, qualification, and implementation of various analytical methods including methods testing for product quality and quantification of excipients for all GSK biopharm assets. The candidate is expected to engage with project teams and other stakeholders on strategy development and method development / testing plans for various projects under different stages of development. The candidate may also be responsible for contributing to relevant CMC sections of regulatory submissions. | 5/8/2017 |
| 1659 | GSK Upper Merion, PA Scientist: Mass Spectrometry BS / MS chemistry, biochemistry, chemical engineering, or related Exp: 0-3 yrs |
The candidate will be primarily responsible for developing mass spec based methods (e.g. LC / MS and LC / MS / MS) and multi-dimensional LC multi-attribute methods (MAM) for the characterization and comparability evaluation of complex therapeutic proteins including identification and quantification of product variants such as posttranslational modifications and product & process related impurities. The candidate could also be expected to develop other analytical and / or biochemical methods and participate in testing for supporting of biopharmaceutical process development and manufacturing. | 5/8/2017 |
| 1660 | GSK King of Prussia, PA Cell Culture Development Sr. Scientist/Associate Scientist BS / MS biology, chemical / biomedical engineering or related Exp: 0-2 yrs |
The candidate will be responsible for lab-based experimentation including but not limited to setting up / running bioreactors, culturing cells, media / feed preparation, combining data from multiple equipment / experiments. The candidate will interact with scientists / engineers within the group and also with colleagues in downstream process development, analytical methods development, clinical manufacturing groups involved in the process scale-up and technology transfer of manufacturing processes for the production of Pre-clinical, Phase 1 3 clinical supplies. The candidate must be a highly motivated self-starter, with excellent verbal and written communication skills, and the ability to work effectively individually and in team and matrix environments. The candidate must also be flexible to work in other areas of the Biopharm Process Development (BPD) organization such as downstream process development. | 5/8/2017 |
| 1661 | GSK Rockville, MD Scientist/Scientific Associate MS biology or related Exp: 1 yr |
Key member with expertise in molecular virology and molecular biology, particularly RNA virology, in diverse team of vaccine scientists, to design, characterize, optimize, evaluate and select vaccine candidates, and support platform technology development | 5/8/2017 |
| 1662 | Good Start Genetics Cambridge, MA QA Specialist II AS biology, chemistry, or related Exp: 1 yr |
The Quality Assurance Specialist will assist the Director of Quality in maintaining the laboratory s quality assurance and quality improvement programs and will ensure compliance with all state and federal regulatory requirements. | 5/8/2017 |
| 1663 | Goodwin Biotechnology Plantation, FL Upstream Manufacturing Technician AS biological or physical science Exp: 0 yrs |
Assists Upstream Manufacturing and Cell Culture Operations with Manufacturing in accordance with Master Batch Records and in compliance with GMP regulations and guidelines. Monitors Manufacturing Processes, Operates Analytical Laboratory Equipment and provides Operational Support for USP-MFG activities. Compiles electronic / laboratory notebooks, maintains laboratory equipment, and equipment logs and monitors supplies. | 5/8/2017 |
| 1664 | Gore Santa Clara , CA Environmental Monitoring/Microbiology Associate BS biology or related Exp: 1 yr |
As a leading manufacturer of vascular grafts, endovascular and interventional devices, surgical meshes for hernia repair, and sutures, we are looking for a highly-motivated Environmental Monitor to join our Environmental Monitoring and Control (EM&C) team in Santa Clara, CA. | 5/8/2017 |
| 1665 | Gore Avondale, PA Test Engineer - Radio Frequency/Microwave Cable MS Electrical Engineering Exp: 1 yr |
In this role, you will provide Electrical Engineering support for GORE s Radio Frequency (RF) / Microwave cable and assembly products. You will work closely with other engineers globally, including Product Design, Process, and Applications and with manufacturing to support existing operations. You will have commitments ranging from support of production test equipment, test method development, support of customer specification review, input on product design, and support of equipment investment plans. Over time, you will develop broader expertise in signal integrity in support of high-data-rate digital cable and assemblies. | 5/8/2017 |
| 1666 | Integer Alden, NY Chemical Engineer I BS chemical engineering or related Exp: 0-2 yrs |
Apply principals of chemistry and engineering to perform experiments. Designs chemical equipment and devises processes for manufacturing chemicals and products. Control movement, storing, and packaging of solids, liquids and gases. Prepares written and oral reports and provides recommendations to others. Provides support in areas where needed. May troubleshoot problems with chemical manufacturing processes. | 5/8/2017 |
| 1667 | Integer Chaska, MN Laser Technician BS technical discipline Exp: 0-3 yrs |
Performs non-routine assignments and provides technical support to engineers often having similar duties and standards. Performs complex troubleshooting; repairs, modifies and maintains systems and / or equipment. Analyzes data, evaluates systems and processes and makes decisions regarding modifications, if necessary. Depending on location, may use CAD software and assist with blueprints and tool design. May derive and carry out testing methods and / or interpret drawing and specifications. | 5/8/2017 |
| 1668 | Integer Plymouth, MN Lead Technician - Calibration BS technical discipline Exp: 0-3 yrs |
The primary purpose of this job is to perform non-routine assignments and provide technical support with a high variety and complexity. Develops, designs, installs, and maintains new processes, tests, and / or control systems. Has critical company knowledge of processes / systems and is responsible for projects and deadlines. Acts as a lead technician in a group. | 5/8/2017 |
| 1669 | Integer Plymouth, MN Maintenance Intern BS / MS technical discipline Exp: 1 yr coursework |
Do you want to learn more about business and technology At Integer we are committed to being the definitive leader in critical technologies by infusing integrity, innovation and operational excellence into the medical device and commercial markets. We understand that sometimes it takes a fresh face and a new take on things to complete a project or solve a problem. Our internship program allows you to gain hands on experience while participating in critical business projects aligned with department and company goals. | 5/8/2017 |
| 1670 | Integer Alden, NY Manufacturing Engineer Intern BS / MS technical discipline Exp: 1 yr coursework |
Do you want to learn more about business and technology At Integer we are committed to being the definitive leader in critical technologies by infusing integrity, innovation and operational excellence into the medical device and commercial markets. We understand that sometimes it takes a fresh face and a new take on things to complete a project or solve a problem. Our internship program allows you to gain hands on experience while participating in critical business projects aligned with department and company goals. | 5/8/2017 |
| 1671 | Integer Raynham, MA Quality Engineer I BS technical discipline Exp: 0-2 yrs |
Identifies and evaluates procedures to ensure the production of quality product. Develops new and unique approaches to complex problems and can advance technology beyond previous achieved levels. Applies engineering concepts to resolve acute or chronic problems. Conducts studies to understand capability for process and / or measurement systems. Provides management with technical guidance as required. Identifies and develops appropriate documentation for process improvement and project implementation. Maintains liaison with individuals and units within or outside the organization with responsibility for acting independently on technical matters pertaining to their filed. | 5/8/2017 |
| 1672 | Integer Plymouth, MN Quality Engineer I BS technical discipline Exp: 0-2 yrs |
The primary purpose of this job is to perform work which involves conventional engineering practice. Ensures GB internal and external customer expectations are met or exceeded. | 5/8/2017 |
| 1673 | FujiFilm College Station, TX Manufacturing Technician I/II/III - Downstream MS biology, microbiology, chemistry, biochemistry, engineering, or related Exp: 1 yr |
The Downstream Manufacturing Technician III will work directly with a range of purification technologies including continuous flow centrifugation, sucrose gradient separation, filtration technologies (TFF and depth), chromatographic separations (GE AKTA systems), and viral inactivation following aseptic technique in a cGMP environment. | 4/30/2017 |
| 1674 | FujiFilm College Station, TX Process Development Technician III MS science Exp: 1 yr |
The Process Development Technician III is responsible for laboratory testing for the product monitoring process, in-process analytical testing, equipment performance and maintenance, assisting in process verification / validation and executing development initiatives using laboratory and processing equipment in lab production scale-up environments for the Upstream, Downstream, or Virology groups. | 4/30/2017 |
| 1675 | FujiFilm Research Triangle Park, NC Scientist I, Analytical Development MS scientific discipline Exp: 1 yr |
The successful candidate will primarily be responsible for the development and qualification of qPCR assays for the characterization and testing of recombinant protein drugs. | 4/30/2017 |
| 1676 | FujiFilm Research Triangle Park, NC Scientist I, Cell Culture/Fermentation Development MS engineering or life sciences Exp: 1 yr |
The successful candidate will contribute to the team-based execution of projects in the discipline of biomanufacturing process development. The products to be manufactured are recombinant biopharmaceutical proteins and the indivudual should have demonstrated expertise in upstream process development with an understanding of tech transfer and manufacturing. This position will contribute to the execution of projects in various stages of process development or tech transfer to manufacturing utilizing platform processes as approprriate during process development. | 4/30/2017 |
| 1677 | FujiFilm Research Triangle Park, NC Production Technician BS / BA technical discipline Exp: 1 yr |
The successful candidate will execute Development and Production processes as well as the accompanying documentation. | 4/30/2017 |
| 1678 | G&W Laboratories Sellersville, PA Regulatory Affairs Associaet BS scientific field Exp: 1 yr |
This position is responsible for managing the regulatory aspects of projects / products for pre-approval and post-approval submissions to FDA s Office of Generic Drugs. This includes the preparation and submission of annual reports, supplements, amendments and original ANDAs. This person participates in project team meetings by providing regulatory support to ensure compliance with all FDA requirements and provides product approval strategies with limited oversight from Regulatory Affairs Senior Manager. A strong science background with experience in compiling and reviewing Chemistry, Manufacturing, and Controls (CMC) submissions is required. Experience with the Common Technical Document (CTD) format is preferred | 4/30/2017 |
| 1679 | Catalent Woodstock, IL Validation Engineer BS science in engineering or scientific discipline Exp: 1 yr |
Validation empowered representative on cross-functional project teams. Validation Project Manager for cross-functional project teams. Researches governmental regulatory requirements on each assigned project to ensure that each study subject is challenged to meet required specifications. Prepares scientifically sound Validation Study Protocols that incorporate the defined specifications into acceptance criteria and assessment procedures. Schedules the execution of Validation studies with the appropriate department. Prepares detailed, concise documentation dossiers on completed studies that summarize the studies experimental results and specifications and their conformance to defined acceptance criteria. Perform test plans as required by Equipment Change Orders. Maintains close contact with Business development, Engineering, and Manufacturing groups to assure effective communication on challenges and opportunities related to validation. Provides technical support to Business Development, Engineering, Manufacturing, Quality Assurance, Quality Control, and Regulatory Affairs as needed. Assists the Validation department in developing policies, programs, SOPs, and Quality standards to meet current industry, corporate Quality, and external Regulatory requirements. Supports the facility in internal and external inspections. Works directly with management, contract customers, and / or contract engineers. Maintain effectiveness of the Quality System components relevant to this position. Other duties as assigned. | 4/30/2017 |
| 1680 | Catalent Woodstock, IL Process Engineer BS engineering, chemistry, pharmacy, or related Exp: 1-5 yrs |
The Process Engineer position interfaces with Operations, Quality, Engineering, and Product Development to identify and implement robust solutions that realize efficiencies, enhance capability, and reduce overall execution costs. | 4/30/2017 |
| 1681 | Catalent Madison, WI cGMP Manufacturing Associate Scientist MS scientific discipline Exp: 1 yr |
This position requires a variety of skills necessary for cGMP BioManufacturing operations. The position is expected to possess a thorough understanding of cGMP upstream manufacturing / downstream purification and conduct work within cGMP guidelines. The position is responsible for performing manufacturing operations according to standard operating procedures and batch instructions under limited supervision. Responsible for performing solution preparation, cell culture and\or purification operations. | 4/30/2017 |
| 1682 | Catalent Winchester, KY QC Analyst BS chemistry, biology, chemical engineering, or life science Exp: 0-5 yrs |
A QC Analytical chemist is an entry level position for individuals who use their understanding of science to perform the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. Their work is hands on in an analytical lab and requires analytical testing, computer operating, record keeping, and report writing abilities. This position performs the quality testing needed for raw material, in-process, finished goods, stability, and cleaning validation analysis. | 4/30/2017 |
| 1683 | Catalent Woodstock, IL BFS Technician AA / AS technical discipline Exp: 1 yr |
The position is entry level and responsible for learning the basic BFS theory, personal protective equipment, tool use, and comprehension of processes and methods such as: BFS start-up, machine and tank sterilization process, filter integrity test methods, temperature recorder function, reading set-up drawings and batch record documentation. This position is responsible for aseptic gowning certification as prerequisite to entering the Aseptic BFS Suite. In addition, position is required to inspect and package product as Production Associate 1. New hire is not intended to stay in this position long term. Once training and qualification is completed at this level, employee advances to BFS Technician Level 1. | 4/30/2017 |
| 1684 | Catalent Morrisville, NC Laboratory Associate BS chemistry or related Exp: 0 yrs |
Execute laboratory work plan / schedule developed by supervisor or senior team member. 80% of time. Edits technical documents, such as test methods, with direct guidance from a supervisor or senior level scientist 2 % of time. Performs parallel review of laboratory documentation.5 % of time. Demonstrates laboratory techniques as part of training. 5 % of time. Participates in assigned improvement projects. 5 % of time. All other duties as assigned. 3 % of time | 4/30/2017 |
| 1685 | GE Del Rio , TX Technician I - Biomedical BS electrical, biomedical or mechanical engineering Exp: 1 yr |
Responds to service calls to evaluate, diagnose, and perform repair and planned maintenance (PM) on customers basic biomedical equipment. Drives customer satisfaction through service excellence.Position is located in Del Rio, Tx. | 4/30/2017 |
| 1686 | GE Marlborough, MA Engineering Associate - Life Sciences BS engineering / technology Exp: 1 yr coursework |
This Engineering Associate works on projects related to the Engineering / Technology function depending on their prior coursework and degree program. | 4/30/2017 |
| 1687 | GE Waukesha, WI QA Leader BS / MS technical discipline Exp: 1 -3 yrs |
This position is responsible for maintaining and improving the Site Quality Management System. It entails working directly with all functions at the site in the participation of these programs. Specifically, responsible for supporting QMS implementation, site documentation requirements, Quality Management Reviews and general QMS activities. | 4/30/2017 |
| 1688 | Ocimum Biosolutions Indianapolis, IN Inside Sales Executive MS sciences or bioinformatics Exp: 0-4 yrs |
Generate Leads or qualify marketing leads generated from conferences, trade shows, web and existing accounts Execute lead generation program to increase attendance at upcoming events, conferences, trade shows and to create awareness of LIMS solutions Pro-actively cold call and profile target accounts Maintenance and updating sales database, setting alarms for follow-up, lead tracking and lead hand-off Maintain metrics for call volumes, emails and leads generated Work with marketing to build contacts and build target list for marketing campaigns Work with Business Analyst team and field sales team to generate new business and building sales pipeline Support LIMS Marketing by providing content for brochures, website, white papers, case studies, etc. Effective use of Social media Linkedin, Facebook, Blogs, Google etc, for LIMS promotional activities Develop personal knowledge of the science, laboratory processes, business process, SDLC, and technology utilized in Life science and Pharma LIMS targeted markets. Required to work in US, Europe or ROW time zones as required. | 4/30/2017 |
| 1689 | Genentech Vacaville, CA Intern - Pharma Technical Operations - Facilities Services: Instrument Services BS technical discipline Exp: 1 yr coursework |
Facility Services enables Vacaville Operations to excel in the manufacture of high quality bulk pharmaceuticals by providing a safe and secure work environment and ensuring the optimal performance of our dynamic facility and complex equipment. | 4/30/2017 |
| 1690 | Genentech San Francisco, CA Intern - Pipeline and Portfolio Planning - CPAC Portfolio Reporting and Analytics BS / MS science or related analytical field Exp: 1 yr coursework |
Objectives and scope of position: The CPAC team is accountable for portfolio-related analytics and analytical methodologies (such as risk assessment and valuation), business and financial planning, internal & external reporting and partnering / BD support. The CPAC Analytics intern role supports various portfolio analytics and reporting processes and / or initiatives and / or tools across late stage and the REDs. The position will help to identify areas of improvement for portfolio reporting and propose and implement new methodologies and processes for data collection and visualization | 4/30/2017 |
| 1691 | Genentech San Francisco, CA Intern - Early Clinical Development - Clinical Imaging MS computer science, engineering, or related Exp: 1 yr coursework |
Group (CIG) Machine / Deep Learning pilot team is seeking a graduate student summer intern to join an ongoing effort to demonstrate the value of Machine / Deep Learning on clinical imaging to drug discovery and development. Responsibilities will include data preparation, model development, and evaluation. | 4/30/2017 |
| 1692 | Genentech San Francisco, CA Intern - Research Biology - Early Discovery Biochemistry BS biology or related Exp: 1 yr coursework |
Intern will meet with supervisor or a regular basis and the progress will be continuously evaluated. At the start of internship goals will be set and the intern will be evaluated on how he / she performed in achieving these goals. Lab head, Domagoj Vucic, as well as principal scientific researchers Eugene Varfolomeev and Tatiana Goncharov, both with PhD in molecular biology will be working with and mentoring intern. | 4/30/2017 |
| 1693 | Genewiz South Plainfield, NJ Intern Developer, Information Technology BS computer science or related Exp: 1 yr coursework |
Assists with coding, testing and troubleshooting the company s Online Ordering & Management System Responds in a timely manner to incidents and requests submitted by end-users and assigned by management Assists with additional IT projects as needed | 4/30/2017 |
| 1694 | Genewiz South Plainfield, NJ Intern, Quality Assurance BS life sciences Exp: 1 yr coursework |
Assist in maintaining current employee training records, including sending document requests to HR or employees Assist QA Archivist with preparation and distribution of various quality documents (logbooks, training lists, etc.) Assist senior QA personnel with filing / archiving Assist with in-process of new employees: welcome email, adding them to tracking system, assigning relevant training, providing / collecting training documentation, name badge prep and distribution Help with preparation for customer audits: reserving conference rooms, arranging lunch, intranet post for site-wide notification, etc. | 4/30/2017 |
| 1695 | Genewiz South Plainfield, NJ Laboraty Technician AA / AS scientific discipline Exp: 1 yr |
Prepare DNA template, including: preparation, amplification and PCR purification. Be aware of data extraction and analysis procedures Check inventory and replenish consumable supplies Prepare buffers and related solutions Communicate with customers by phone and e-mail in a friendly and professional manner. Strictly follow SOPs and Manager s direction in training, sample handling, project processing, and documentation Assist and maintain the cleanliness of work area. Additional responsibilities as assigned | 4/30/2017 |
| 1696 | Genewiz San Francisco, CA Laboratory Technician AA / AS scientific discipline Exp: 1 yr |
Prepare DNA template, including: preparation, amplification and PCR purification. Be aware of data extraction and analysis procedures Check inventory and replenish consumable supplies Prepare buffers and related solutions Communicate with customers by phone and e-mail in a friendly and professional manner. Strictly follow SOPs and Manager s direction in training, sample handling, project processing, and documentation Assist and maintain the cleanliness of work area. Additional responsibilities as assigned | 4/30/2017 |
| 1697 | Genewiz San Francisco, CA Laboratory Technician, Molecular Biology AA / AS scientific discipline Exp: 1 yr |
Prepare DNA template, including: preparation, amplification and PCR purification. Be aware of data extraction and analysis procedures Check inventory and replenish consumable supplies Prepare buffers and related solutions Communicate with customers by phone and e-mail in a friendly and professional manner. Strictly follow SOPs and Manager s direction in training, sample handling, project processing, and documentation Assist and maintain the cleanliness of work area. Additional responsibilities as assigned | 4/30/2017 |
| 1698 | Genewiz Boston, MA Laboratory Intern BS life sciences Exp: 1 yr coursework |
Assist in sample sorting and properly distribute them Assist with processing bacterial colonies as needed Maintain laboratory cleanliness Perform routine maintenance on lab equipment Prepare supplies and assist Associate Scientists or Laboratory Technician | 4/30/2017 |
| 1699 | GenMark Carlsbad, CA Research Associate I - Temp BS chemistry, biochemistry, molecular biology or related Exp: 1-5 yrs |
This position will execute a range of data analysis techniques, molecular biology procedures, reagent preparation, and bioanalytical procedures and laboratory duties. | 4/30/2017 |
| 1700 | Genomic Health Redwood City, CA Desktop Engineering Intern BS technical discipline Exp: 1 yr coursework |
The ideal candidate will be responsible for assisting Desktop Engineering team with daily tasks, testing and deployment of Windows 10 operating system. This will include any documentation and components that are required for image deployment. Majority of time will be spent helping with Windows 10 deployment, computer imaging, labeling, logistics and preparation work for OS Image deployment. | 4/30/2017 |
| 1701 | Genomic Health Redwood City, CA Clincal Operations Intern BS scientific field Exp: 1 yr coursework |
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. | 4/30/2017 |
| 1702 | Genomic Health Redwood City, CA Translational Sciences Operations Intern BS technical discipline Exp: 1 yr coursework |
The Intern will be an individual contributor who will report to the Associate Director, Translational Sciences Operations and provides support to the departments reporting to the Chief Medical Officer, including but not limited to Clinical Operations, Biostatistics, Data Management, Pathology, and Oncology Development. This intern position will focus on supporting the Oncology Development and Pathology Department relative to the Oncotype SEQ products. Secondarily, this intern will also be directly responsible for supporting Translational Sciences Operations. | 4/30/2017 |
| 1703 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Fremont, CA Protein Analytical Chemist MS Exp: 1-2 yrs |
Perform analytical (UV / Vis, FTIR, Raman, TOC, conductivity) and compendial testing (pH, osmo, turbidity, appearance), as well as wet chemistry practices in a GMP environment | 4/27/2017 |
| 1704 | Eurofins Lancaster Laboratories Professional Scientific Services, LLC Summit, NJ Process Analytics Scientist BS Exp: 1 yr |
Experience transferring and executing analytical assays in a biologics industry laboratory. Demonstrated experience in the analysis of therapeutic proteins with at least one of the following : HPLC-Based Methods; Gel-Based Methods; CE-Based Methods; Cell-Based Assays; Compendial Assays | 4/27/2017 |
| 1705 | Laboratory Corporation of America Westborough, MA Quality Control Coordinator - Molecular Genetics BS in Biological / Chemical Science Exp: 1-5 yrs |
The QC Coordinator will be responsible for reagent preparation and testing for use in a high throughput molecular genetics clinical testing laboratory. | 4/27/2017 |
| 1706 | Medtronic North Haven, CT Associate Quality Engineer BS in a Science / Engineering field Exp: 0-2 yrs |
Perform evaluations of new and existing products consisting of a wide variety of physical characteristics. Responsible for the benchmarking of finished goods performance characteristics. | 4/27/2017 |
| 1707 | Medtronic Santa Ana, CA R - D Engineer MS in relevant engineering field, preferably Mechanical Engineering, Biomedical Engineering, or Materials Science Exp: 0 yr |
Contribute to the product development by designing, developing, and implementing test methods and equipment to conduct tests on materials, components, and devices to meet development and regulatory requirements. Works under the general supervision of a more experienced engineer or engineering manager. | 4/27/2017 |
| 1708 | Medtronic Portsmouth, NH Quality Engineer MS in Engineering MS in Engineering MS in Engineering Exp: 0 yr |
This position has the responsibility and authority to perform Quality Engineering functions including inspection and testing, calibration, procedure writing, and statistical analysis of quality data. The Quality Engineer must be able to prioritize activities and allocate resources for greatest effectiveness. The Quality Engineer must deal with both concrete and abstract problems on a daily basis. | 4/27/2017 |
| 1709 | Medtronic Portsmouth, NH Assoc R - D Engineer BS in Mechanical Engineering,Biomedical Engineering, or equivalent Exp: 0 yr |
Completes tasks or objectives with direction or assistance from experienced engineers. Can work individually or in a team environment to complete objectives.Consistently generates innovative and unique solutions to market needs and submits idea disclosures. | 4/27/2017 |
| 1710 | Medtronic Northridge, CA Quality Systems Specialist - Tech Comm MS Exp: 1 yr |
The Quality Systems Specialist will work within the Technical Communication team to analyze documents and labels for completeness and accuracy, then administer final documents and labels for review and approval to ensure compliance with corporate and department procedures and guidelines. Incumbents will work cross-functionally to drive the timely review, changes and approval of documents / labeling according to project schedules through the interaction with documentation authors, graphic designers, reviewers and approvers. | 4/27/2017 |
| 1711 | Medtronic NA, NA Associate Manufacturing Engineer BS in Engineering Exp: 0-2 yrs |
You will support the day to day operations and strategic projects to the business providing daily support of finished good stapling manufacturing with specific regard to safety, product quality, service, process improvement, and customer feedback. You will participate in cross functional teams to accomplish project specific goals, root cause analysis, and developing and implementing robust corrective and preventive action plans. | 4/27/2017 |
| 1712 | Magellan Diagnostics Inc. North Billerica, MA Product Support Specialist BS in a life science and / or medical technology Exp: 1-3yrs |
Your role is to be an expert in the functioning and application of Magellan Diagnostics' products and to participate in the team that provides technical product support as well as product training to external and internal customers, including nurses, doctors, and laboratory technicians as well as sales, marketing and other personnel. The Product Support team is also responsible for laboratory investigations required to assess and understand customer complaints, for tracking and closing complaint investigations, and for working with Quality Assurance to properly escalate complaints in the quality management system. | 4/27/2017 |
| 1713 | Mersana Therapeutics Cambridge, MA Associate Scientist, Analytical BS / MSdegree in chemistry Exp: 1-2 yrs |
Under guidance from the senior scientists perform RP / IEX / SEC HPLC, LC / MS, CE / cIEF and spectrophotometry based testing of research materials including small molecules, polymers and biologics. | 4/27/2017 |
| 1714 | Mayne Pharma Group Greenville, NC Analytical Chemist I BS / MS Exp: 0 yr |
This position requires the ability to perform established routine and non-routine laboratory techniques in a GMP environment. | 4/27/2017 |
| 1715 | Microbiotix, Inc. Worcester , MA Associate Scientist (Medicinal Chemistry) BS in chemistry Exp: 1-3yrs |
We are currently seeking a synthetic organic chemist for a position as an Associate Scientist at Microbiotix, Inc. This scientist should have demonstrable bench synthesis experience, communicable either through publication or personal recommendation. He / She will join several active projects in the antibacterial, antiviral, and antiparasitic areas in the hit-to-lead and lead optimization stages. The Associate Scientist will be tasked primarily with performing multi-step synthesis, compound isolation and characterization, but there will be opportunities to contribute to design and route scouting. Additionally, there will be a high probability of publication from this position. Motivated, energetic problem-solvers with a strong work ethic are highly desired for this position. | 4/27/2017 |
| 1716 | MicroConstants Inc. San Diego, CA Quality Control Technician BS / BA Exp: 0 yr |
Performs and maintains documentation and compliance standards with adherence to USFDA, OECD and MHLW Good Laboratory Practices regulations as required.Perform calibration and / or maintenance of pipettes and other laboratory equipment.Assist in the maintenance of reference standards. | 4/27/2017 |
| 1717 | Micropoint Santa Clara, CA Quality Control Associates MS in chemistry, biology, or related scientific field Exp: 0 yr |
We are looking for highly motivated QC Associates (two openings) to join our quality team. 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. | 4/27/2017 |
| 1718 | MicroVention TERUMO Tustin, CA Industrial Engineer I BS / MS in Engineering Exp: 1-3yrs |
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. | 4/27/2017 |
| 1719 | MilliporeSigma St. Louis, MO Associate Scientist BS in Biological Sciences, Chemical or Biochemical Engineering Exp: 1 yr |
The candidate for this position will be part of the upstream process development team working at the bench-top bioreactor scale and supporting SAFC s cell line and media development groups in St Louis, MO. The candidate will in addition have a significant role in the development of new upstream processes. The candidate will participate in the design of the experiments, data analysis and presentation of the results to the internal project teams. He / she will be responsible to execute the planned experiments and record the experimental data. The work will include different bioreactor types at the bench-top scale supporting internal and customer projects. | 4/27/2017 |
| 1720 | MilliporeSigma Kankakee, IL Quality Systems Specialist BS in a Quality or Science discipline preferred Exp: 1 yr |
Oversee the CAPA system to ensure effective corrective and preventive actions are implemented to prevent reoccurrence. | 4/27/2017 |
| 1721 | MilliporeSigma St. Louis, MO Associate Analytical Scientist BS in Chemistry, Biochemistry or related field Exp: 0-5 yrs |
The ideal candidate will execute analytical methodologies of general to moderate scope and complexity to enable process development and transfer methods to cGMP Quality Control groups for a wide range of bio-organic and bio-pharmacuetical products. | 4/27/2017 |
| 1722 | EMD Serono Billerica, MA Research Associate, In Vivo Pharmacokinetics BS in Biology, pharmacology Exp: 1 yr |
The research associate is a laboratory-based role within Discovery DD. You will contribute to project progression by performing pharmacokinetics studies with NCEs, primarily in rats and mice. | 4/27/2017 |
| 1723 | Moderna Cambridge, MA (Contract) Research Associate BS / MS Exp: 0-2 yrs |
Moderna is seeking a contract research associate for a position based at their Cambridge, MA site. The individual in this role will support mRNA nanoparticle formulation design and evaluation. He / she will be responsible for preparation and characterization of mRNA nanoparticle formulations for research studies. Knowledge of chemistry, nucleic acid formulations, and drug delivery is desired. The successful candidate must be willing to meet technology development and research goals on aggressive timelines working in a multi-disciplinary environment | 4/27/2017 |
| 1724 | Moderna Cambridge, MA Manufacturing Associate BS 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. He / she will apply existing and new knowledge of bioprocess unit operations and cGMPs to enable technical success with stringent adherence to a Quality System that respects global regulatory expectations. The successful candidate will be able to document and communicate their technical and operational observations clearly and efficiently. They will be able to operate pilot-scale bioprocessing equipment and interact fluidly with peers and supervisors in the Pilot Plant, and cross-functionally with Quality Control, Quality Assurance, Logistical and Process Development Technology Transfer counterparts. | 4/27/2017 |
| 1725 | Momenta Cambridge, MA Research Associate, Analytical Development BS / MS in Analytical Biochemistry or related discipline Exp: 0-3 yrs |
The Research Associate, Analytical Development will assist in developing / qualifying test procedures as well as perform a variety of analytical techniques to support cell line and bioprocess development, reference product characterization and drug substance / drug product testing for a pipeline of protein-based biotherapeutics, including biosimilars. | 4/27/2017 |
| 1726 | MPI Research Mattawan, MI Research Technician 2 - DART BS Exp: 1-2 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. | 4/27/2017 |
| 1727 | MPI Research Mattawan, MI Research Technician 2 - Animal Services BS Exp: 1-2 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. | 4/27/2017 |
| 1728 | MPI Research Mattawan, MI Research Technician 1/Research Associate 2 - Second Shift Operations 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. | 4/27/2017 |
| 1729 | Luminex Corporation Austin, TX Reagent Mfg Associate I BS in a Chemistry, Life Sciences, or Medical Technology related field Exp: 1 yr |
The Reagent Manufacturing Associate I is primarily responsible for delivering manufacturing requirements against production schedule within a focused manufacturing operation and / or product segment. Work schedule may include alternate shifts. The Reagent Manufacturing Associate I also participates in manufacturing processes to support new product design transfer, stability program, process development, equipment validations, process validations, and investigations and resolution of product / process issues. The position is responsible for performing maintenance and calibration of Manufacturing measuring and monitoring devices as well as maintaining the integrity of work areas. | 4/30/2017 |
| 1730 | NanoString Seattle, WA Manufacturing Research Associate I BS in Molecular Biology, Biochemistry or Chemistry Exp: 1-2 yrs |
We are seeking a Research Associate (Level I) to join our Production group. In this entry-level role you will learn and perform both manual and automated production processes for the manufacture of reagents needed for the multiplexed detection and quantification of mRNA transcripts from biological samples. | 4/30/2017 |
| 1731 | Myriad Genetics, Inc. Mason, OH Lab Technician I BS / MS 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. | 4/30/2017 |
| 1732 | Miltenyi Biotec, Inc. Cambridge, MA Regulatory Affairs Intern BS / MS in regulatory affairs, the life sciences or chemistry Exp: NA |
As an intern with the Miltenyi Biotec Regulatory Affairs Team, you will have the exciting opportunity to gain hands-on learning experience supporting regulatory objectives to ensure products meet worldwide regulatory requirements for product approval and post-marketing compliance. You will work on projects and documentation related to regulatory submissions and compliance. Additionally, you will apply your excellent writing skills in developing standard operating procedures and impact workflow processes as they relate to regulatory objectives. Overall, your efforts will drive Miltenyi Biotec s continuing business success and give you the opportunity to build your resume with a skill set that is in high demand industry-wide. | 4/27/2017 |
| 1733 | Thermo Fisher Scientific Pleasanton, CA Intern II BS / MS in engineering Exp: NA |
Plan, design and implement efficient business and systems solutions for optimization of process improvement database system. Document business requirements and business process flows. Participate / drive requirements and design workshops.Plan, design and implement efficient business and systems solutions for optimization of process improvement database system. Document business requirements and business process flows. Participate / drive requirements and design workshops. | 4/30/2017 |
| 1734 | Thermo Fisher Scientific South San Francisco, CA Chemical and Material Science Engineering Sr. Intern BS in either chemical engineering, material science engineering, or related engineering degree Exp: NA |
As a Sr. Intern at Thermo Fisher Ion torrent, you will be helping characterize the Ion torrent DNA sequencing S5 chip. | 4/30/2017 |
| 1735 | Thermo Fisher Scientific Pleasanton, CA Intern I BS / MS Exp: 1 yr |
Work in a team based environment to develop, prepare and revise testing validation procedures / protocols to ensure that product manufactured meet internal company standards. | 4/30/2017 |
| 1736 | NanoString Seattle, WA Application Lab Intern BS in the life sciences Exp: NA |
Your job as a summer intern is to help develop the protocols needed to make the new DNV single nucleotide variant (SNV) detection panel compatible with low-input samples such as whole blood and core needle biopsies. You will work with the team scientists to design mutant DNA-specific PCR primers to amplify rare mutant alleles and run experiments to fine tune and optimize the conditions. Toward the end of the project, you will have opportunities to test this new technology on circulating cell-free DNA extracted from whole blood from healthy individuals to prove the clinical utility of the new DNA SNV assay. | 4/30/2017 |
| 1737 | NanoString Seattle, WA Biostatistics Intern BS Exp: NA |
As an intern in the biostatistics department, you will contribute to building software tools that facilitate harnessing biological information from data generated by our nCounter hardware. | 4/30/2017 |
| 1738 | Exactech Gainesville, FL Internship - Supply Chain BS industrial engineering Exp: 3 yrs coursework |
Supply Planning: Master Scheduled Workbench (MSW) Data Review and update Work with Packaging team on capacity to update MSW. This would include being the liaison between the packaging supervisor regarding time study and the associated data entry in MSW. Work with Internal MFG on capacity to update MSW for items that are solely MFG in Gainesville. This would include being the liaison between the MFG supervisors / leads regarding time study and the associated data entry to MSW. Working with Internal MFG, 01FLBR Site team and IT on capacity set-up and update MSW of dual sourced knee products. Working with Internal MFG, 01FLSA Site team and IT on capacity set-up and update MSW of dual sourced shoulder products. Assist in the completion of the MSW work instruction. Demand Planning / Finance Assist with development of the Forecast Accuracy Metric | 4/24/2017 |
| 1739 | Exosomed Cambridge, MA Laboratory Technologist BS / MS biological 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. | 4/24/2017 |
| 1740 | Ferring Pharmaceuticals Parsippany, NJ Technician, QC Microbiology - 2nd Shift BS / MS microbiological laboratory science Exp: 1-4 yrs |
Work in a cGMP-compliant manner in support of production, facilities, Clean Utilities and general microbial testing on second shift. Participate in assay transfer processes and qualification of equipment. Create / Revise equipment qualification protocols, test methods, and procedures as required. Work independently with minimal supervisory guidance. Apply aseptic clean room practices during execution of all work tasks. Must have prior clean room aseptic sampling experience in water and environmental monitoring. | 4/24/2017 |
| 1741 | Fibrogen San Francisco, CA Summer Intern - GCP Operations BS technical discipline Exp: 1 yr coursework |
The Summer Intern will have the opportunity to learn about Good Clinical Practice (GCP) Operations and Inspection Readiness for global regulatory agency inspections. This position will learn the foundation of gap analysis to assess and mitigate risks and strengthen the company for regulatory inspections. The intern will have the opportunity to create a lasting impact on training and record standardization and management at FibroGen. | 4/24/2017 |
| 1742 | Fibrogen San Francisco, CA Summer Intern - Regulatory Operations BS pharmaceutical sciences Exp: 1 yr coursework |
The summer intern will work directly with the Director of Regulatory Operations Department . The intern will be exposed to the Regulatory Operations role including (databases, systems, publishing tools, such as Global Submit) used to support the day-to-day regulatory submissions to Health Authorities. | 4/24/2017 |
| 1743 | Fibrogen San Francisco, CA Summer Intern - Cell Biology BS cell biology, molecular biology, biotechnology, or related Exp: 1 yr coursework |
The summer-based project will primarily involve developing, optimizing, and validating one or more electrochemiluminescent immunoassays (which are similar in principle to ELISA assays) to support cell-based inhibitor screens and target validation studies for drug discovery. Additional tasks could include cell-based studies relevant to the immunoassay targets. | 4/24/2017 |
| 1744 | Idex Corporation Oklahoma City, OK Manufacturing Engineer BS engineering Exp: 6 months - 2 yrs |
The Manufacturing Engineer is responsible to develop, implement and maintain methods, operation routings and processes in the manufacture, fabrication, assembly and testing of parts, sub and final assemblies. This position also interfaces with and serves as intermediary between the engineering design, quality inspection and production implementation functions with respect to new product introductions. Applicant must have the ability to continually improve the quality, manufacturability and value of current products utilizing Standard Work, Flow, 5S, Kanban, SMED, and other Lean tools, estimate manufacturing costs, determine time standards, and make recommendations for tooling and process requirements of new and existing product lines. Will maintain records and reporting systems for coordination of manufacturing operations ensuring robust processes are in place. | 4/24/2017 |
| 1745 | FivePrime San Francisco, CA IT Systems Analyst BS sciences, information systems, or related Exp: 0-3 yrs |
This position will collaborate with stakeholders across business units and technology service providers to develop and implement computerized systems and workflows to enable robust and efficient operations. This is an excellent opportunity for a computer systems inclined individual to start an exciting career in Information Technology. This position reports to Vice President of Strategy Technology Operations. | 4/24/2017 |
| 1746 | Fluke Biomedical Everett, WA Manufacturing Engineer BS manufacturing engineering plastics engineering or related Exp: 0-2 yrs |
As a Manufacturing Engineer I 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. | 4/24/2017 |
| 1747 | Fluke Biomedical Everett, WA User Experience Research Intern BS / MS user research or cognitive science Exp: 3 yrs coursework |
In this position, you will work closely with members of Fluke s Industrial Group, primarily in the UI Design team. The division encompasses mechanical, electrical, and software engineering; interaction, industrial, and graphic design; prototype fabrication, technical writing, and product planning. The division s product teams collaborate with sales and marketing staff for all of Fluke s global brands and products. As an intern at Fluke, you will start and complete a user research project of appropriate scope and complexity. The UI Design staff will support you throughout the process. You will work both in a team setting and indepen-dently, and will be expected to present your work for critique. This project will occupy the majority of your time. You will walk away with professional experience and you may decide that Fluke is the right place for you. | 4/24/2017 |
| 1748 | Fluke Biomedical Plymouth, MN Electro - optics Systems Engineer Intern BS engineering, physics, or related Exp: 3 yrs coursework |
For this internship the student will be expected to work on a limited-scope project focused on exploring new technologies and developing prototypes under the direction and supervision of an IG engineer. More specifically, the work will involve designing and setting up measurements to evaluate prototype thermal imaging cameras, making careful measurements and analyzing the results. These activities should be well documented and presented at the end of the internship. This internship is located in Plymouth, Minnesota location. | 4/24/2017 |
| 1749 | Fluxion Biosciences San Francisco, CA Inside Sales Representatives BS sciences Exp: 1-3 yrs |
The Inside Sales Rep will be responsible for increasing revenue and lead creation by focusing on proactively prospecting and qualifying targeted leads using telephone and email with the goal of converting leads to new opportunities and sales. The Inside Sales Rep will also provide sales support to the fields sales and product marketing teams. | 4/24/2017 |
| 1750 | Allergan Campbell, CA Quality Control Analyst Chemistry BS natural sciences Exp: 1 yr |
The Quality Control (QC) Analyst (Chemistry) will primarily provide analytical support for the manufacture, release, and stability testing of drug substance produced at Allergan DSO. Contributes to the completion of milestones associated with specific projects. Failure to obtain results or erroneous decisions may result in minor program delays and result in the allocation of additional resources. The employee must conduct their work activities in compliance with all Allergan international requirements and with all applicable regulatory requirements. Allergan internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements and objectives. | 4/24/2017 |
| 1751 | Allergan Campbell, CA Quality Control Analyst, Microbiology BS natural sciences Exp: 1 yr |
The Quality Control (QC) Analyst (Microbiology) will primarily provide analytical support for the manufacture, release, and stability testing of drug substance produced at Allergan DSO. Contributes to the completion of milestones associated with specific projects. Failure to obtain results or erroneous decisions, may result in minor program delays and result in the allocation of additional resources. The employee must conduct their work activities in compliance with all Allergan international requirements and with all applicable regulatory requirements. Allergan internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements and objectives. | 4/24/2017 |
| 1752 | Allergan Branchburg, NJ Quality Control Technician II BS technical discipline Exp: 1-3 yrs |
Performs Quality Control inspection of incoming components, materials, supplies, and outsourced finished goods. Performs inspection of in-house finished goods / final packaged product. Documents results of inspection into inspection record and determines acceptability of item for LifeCellTM use or further processing. Performs necessary electronic and physical transactions, and appropriately segregates materials and product. Provides technical support to cross-functional teams to ensure effective operations. Initiates Nonconformance Reports (NCRs) and Supplier Issues (SIs). Ensures proper equipment functionality and appropriate levels of supplies. | 4/24/2017 |
| 1753 | Freudenberg Carpinteria, CA Packaging and Support Engineer BS mechanical engineering, packaging engineering, or related Exp: 1-3 yrs |
Prepare assembly drawings, recipes and inspection criteria for product packaging, labeling and device production. Support and develop validation protocols and reports (IQ / OQ / PQ) and provide objective evidence that equipment, processes, test methods and product meet requirements and are compliant with applicable regulations. Provide support for sustaining projects initiated by Engineering and / or Quality departments. Provide daily sustaining support for packaging related issues in Production and Packaging departments. Create packaging related SOP s and Work Instructions. Provide training for appropriate personnel performing packaging activities. Oversee transfer of products into production and resolve issues as they arise. Organize, plan and implement global changes to product packaging and labeling. Serve as the subject matter expert for all product packaging to include product configuration, labeling and associated manufacturing procedures and test methods. Process EO s for product obsolescence to include planning the depletion of inventory and identify and process the obsolescence all affected components, tooling and documentation. Oversee and manage complete packaging development process, including the creation of packaging designs, prototype development, and performance testing. Troubleshoot new and existing packaging problems involving designs, materials and processes and provide creative, timely, and cost-effective solutions. Work with the manufacturing department to insure packaging designs are optimized for manufacturability. Complete assigned Quality Notifications. Maintains adherence to Company policies, safety / ergonomic standards and good housekeeping practices | 4/24/2017 |
| 1754 | Fresenius Kabi Grand Island, NY Manufacturing Engineer BS engineering or technical background Exp: 0-3 yrs |
Under the guidance of the Manager of Engineering or Senior Manufacturing Engineer, the primary responsibility of this position is for design modifications to existing high-speed pharmaceutical manufacturing equipment and tooling in order to improve quality, optimize performance and minimize defects. | 4/24/2017 |
| 1755 | Fresenius Kabi Boston, MA Associate Scientist BS 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. | 4/24/2017 |
| 1756 | Fresenius Kabi Melrose Park, IL Associate Scientist BS biological sciences Exp: 1-2 yrs |
Responsible for performing routine testing of in-process and finished product samples. Monitors environmental conditions in the production and lab areas. Summarizes environmental monitoring and product test results. Provides project support to Scientist and Lead Scientist. Prepares media and reagents and equipment. | 4/24/2017 |
| 1757 | Fresenius Kabi Grand Island, NY Validation Engineer BS science or engineering Exp: 1-3 yrs |
Responsible for providing technical support to operations in terms of equipment / system initial validation and equipment / system requalifications. Will participate in equipment improvement teams charged with enhancing the compliance and performance of plant systems, while considering the regulatory requirements for change control. Individual must also perform HEPA filter integrity / velocity testing and participates in critical area (class 100) airflow pattern testing. The individual must have a comprehensive understanding of cGMPs and become certified to enter Controlled Areas of the plant (Grade D, C and up to B / A). The ability to write reports clearly, concisely and accurately; accurately record data and a basic understanding of statistical analysis is also required to perform these duties. Weekends and Off-shift hours are periodically required. | 4/24/2017 |
| 1758 | Fresenius Kabi Grand Island, NY AQL Specialist (2nd Shift) BS life sciences or related 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. | 4/24/2017 |
| 1759 | Fresenius Kabi Lake Zurich, IL Drug Assessment Intern BS chemical, biomedical, or mechanical engineering Exp: 2 yrs coursework |
Evaluate potential new drug targets and therapies. Assist with technical assessment of feasibility projects. Support NPA (New Product Approval) preparation and and approval. Analysis and recommendation of potential new business areas. Business case development. Product Analysis. Market Research. | 4/24/2017 |
| 1760 | Frontage Exton, PA Associate Scientist, Analytical Services BS chemistry or related Exp: 1-2 yrs |
Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines. Assists method development Performs method validation under supervision Reports and resolves any unexpected issues under supervision Complies with all relevant cGMP and / or GLP regulatory requirements while carrying out assigned studies | 4/24/2017 |
| 1761 | Frontage Lexington or New Haven, MA Scientist, Biological Services BS / MS scientific discipline Exp: 0-2 yrs |
Perform biologics method transfer, method development, method validation, and sample analysis according to FDA guidance, Frontage SOP and industry practice. Perform immunoassay techniques (ELISA, MSD or other ligand binding based assays, and / or RIA applicable to Pharmacokinetic and Immunogenicity studies) with proficiency Prepare and handle various cell lines, tissue culture media and other reagents for cell-based assays Perform RNA, DNA isolation, PCR and qPCR assays. Provide assistance to project management to ensure meeting the requirements of project quality and timelines. Maintenance of instruments, and address technical and instrumental issues Assist the Principal Investigator with study conduct Maintain study documentation Meet regulatory compliance requirements Maintain a safe work environment | 4/24/2017 |
| 1762 | Frontage Exton, PA Associate Scientist, Analytical Services BS chemistry Exp: 1-2 yrs |
Performs routine sample analysis and a variety of tasks to support product |