eBay Classifieds » All ads » Jobs » Biotech, R&D, & science » 

document control in Boston

(1-24 of 57 ads)
View as:
Categories
    Ads
    1. ADME Analytical Development Scientist - BS/ MS

      Seeking Bioanalytical methods development expertise to join drug development team. Activities: Develop and qualify LC-MS/MS methods for the quantification of small molecules from biological matrices in support of pre-clinical and clinical programs.. Author and validate ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    2. Lead Environmental Health and Safety (EHS) Specialist IMGN115

        The Opportunity The Lead Environmental Health and Safety Specialist will provide primary support for the Environmental, Health and Safety (EHS) program at the ImmunoGen Norwood facility and may be called upon to provide assistance at other company facilities. Job ...

    3. Manager - Pharmacovigilance/Drug Safety

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Partner Operations Manager, Study Management ...

    4. Medical Device Engineer - possible remote (21 CFR 820 / ISO13485)

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Engineer, Medical Device Industrialization Job ID: ...

    5. Laboratory Equipment Qualification

      Here at ProPharma Group, we work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. We build successful long-term relationships with clients by providing leading industry ...

    6. Medical Device Engineer - possible remote (21 CFR 820 / ISO13485)

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Engineer, Medical Device Industrialization Job ID: ...

    7. QA/QC Specialist I

      QA/QC Specialist I Needed in Lexington, MA Every day, Kelly Services connects professionals with opportunities to advance their careers. We currently have a contract opportunity with a global leader in the biotechnology industry in Lexington, MA.ASSIGNMENT LENGTH: 1 year ...

    8. Prescription Drug Promotion Submission Director - Regulatory Affairs

      Lead regulatory review and submission of required documentation for FDA approval of promotional and marketing materials. Activities: *** Support a dynamic, cross-functional team actively developing new therapeutic treatments. *** Develop strategies to ensure regulatory ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    9. QA Regulatory Affairs Specialist

      QA / Regulatory Affairs Specialist This Position pays Market + Full Benefits Description Job Summary: This QA/RA Specialist is responsible for maintaining and ensuring that the company quality system meets FDA requirements for class I medical devices (IVD and ASR). The QA ...

    10. Manufacturing Supervisor

      Manufacturing Supervisor - External Control (Lexington, MA)The successful candidate will be responsible for supervising External Control and Verification Panel Manufacturing process from material receipts through shipments including, but not limited to: production scheduling ...

    11. Associate I, QA Doc

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Quality Documentation Associate I Job ID: 6732 ...

    12. Document Management Coordinator

        Hello,   My name is Josh and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Document Management Coordinator  for a prominent Fortune 500 client of ours.  This position is located in Lexington, MA.  Details for the positions ...

    13. Safety Operations Lead - Pharmacovigilance (PV), Consultant

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Partner Operations Manager, Study Management Safety ...

    14. Partner Operations Manager

          Hello,   My name is Carlane and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Partner Operations Manager position  for a prominent client of ours.  This position is located in Cambridge, MA. Details for the position are ...

    15. Equipment Validation Specialist

      Job Description QA Equipment Validation Specialists are part of the Quality organization and report directly to the QA Validation Manager. Lead all validation activities for commissioning of a cell therapy facility in both supervised and unsupervised areas. Work closely with ...

    16. Clinical Supply Associate

        Supervise, plan and coordinate the clinical supplies activities within the clinical trials research projects. Ensure that goals and objectives of projects are accomplished within established time frames and budget guidelines. Ensure compliance with Good Manufacturing ...

    17. Laboratory Technician

        Hello,   My name is Josh and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Laboratory Technician for a prominent Fortune 500 client of ours.  This position is located in Walpole MA.  Details for the positions are as follows ...

    18. How to Become Clinical Research Associate  :  FREE WORKSHOP

      How to Become Clinical Research Associate : Program Awareness Workshop (FREE ENROLLMENT)   Dear Candidate, LEARNING's FOR JOB (HOME-BASED)   We thank you for your application and interest in our Online Training and Internship program. Below are the learning you will ...

    19. Document Control Specialist - CMC

      TITLE: CMC DOCUMENT CONTROL SPECIALIST ASSIGNMENT LENGTH: 9+ MONTHS LOCATION: Lexington, MA PAY RATE: ~$25-27/hrDescription Responsible for the maintenance of required CMC documentation for the company.The Document Control Specialist will be required to identify and map the ...

    20. Regulatory CMC Manager/Sr. CMC Manager IMGN100

        The Opportunity ImmunoGen, Inc. is in search of an organized and motivated team player to join our growing Regulatory Affairs department. This individual will be responsible for preparing CMC and Quality related agency correspondence and regulatory applications to support ...

    21. 97355 – Clinical Supplies Associate

          •             Supervise, plan and coordinate the clinical supplies activities within the clinical trials research projects. •             Ensure that goals and objectives of projects are accomplished within established time frames and budget guidelines. •             ...

    22. Pilot Manufacturing Associate

      Hello,   My name is Domenic and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Pilot Manufacturing Associate for a prominent client of ours.  This position is located in Cambridge, MA. Details for the position are as follows: ...

    23. Clinical Data Associate II

      The Sr. Clinical Data Associate will provide leadership and comprehensive data management expertise in the development and maintenance of data collection tools and processing of clinical data for longitudinal observational rare disease registries in support of scientific, ...

    24. Associate Director - Translational Modeling & Simulation - Andover, MA

      Seeking solid project manager to work closely with Drug Development Research, Preclinical and Clinical Development, Biostatistics, and Regulatory developing predictive models using the Physiologically-Based Pharmacokinetic approach. Activities: *** Designing, analyzing, ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute