• Physician - Pathologist

    Veterans Affairs, Veterans Health Administration (West Roxbury, MA)
    …the American Association of Blood Banks (AABB) and the Food and Drug Administration ( FDA ). The Anatomic Pathology Division accessions approximately ... in a testing designated position are subject to urinalysis to screen for illegal drug use prior to appointment. Applicants who refuse to be tested will be denied… more
    Veterans Affairs, Veterans Health Administration (08/02/25)
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  • Regulatory Coordinator - Breast Oncology

    Dana-Farber Cancer Institute (Boston, MA)
    …Event reports, to the appropriate regulatory agencies including the Food and Drug Administration ( FDA ), Office of Biotechnology Activities (OBA), etc. + ... Ensure various regulatory reporting required are met; Study Sponsor, FDA , IRB etc. **Key Stakeholder Interfacing** + Establishing and...or all of the following areas: DFCI, DF/HCC, ICH/GCP, FDA policy / guidance / regulation; an understanding of… more
    Dana-Farber Cancer Institute (08/27/25)
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  • Post Market Surveillance Analyst III

    Abbott (Burlington, MA)
    …(EMS), and other regulatory requirements. Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company ... regulatory requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating… more
    Abbott (08/27/25)
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  • Operations Supervisor

    Biomat USA, Inc. (Fall River, MA)
    …compliance with all state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedure Manual, Occupational ... Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good...standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure Manual, OSHA, CLIA and… more
    Biomat USA, Inc. (08/21/25)
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  • Operations Supervisor

    Biomat USA, Inc. (Worcester, MA)
    …compliance with all state and federal regulations, US Food and Drug Administration ( FDA )-approved Standard Operating Procedure Manual, Occupational ... Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good...standards in accordance with Federal and State regulations, with FDA approved Standard Operating Procedure Manual, OSHA, CLIA and… more
    Biomat USA, Inc. (07/31/25)
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  • Principal Scientist

    Amgen (Cambridge, MA)
    …and chapters, and International Conference on Harmonization (ICH) / Food & Drug Administration ( FDA ) mentorship documents related to analytical method ... Provide analytical testing support to functions including but not limited to Drug Substance Technologies, Quality, and Manufacturing + Leverage latest advances in… more
    Amgen (07/12/25)
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  • Principal Scientific Advisor

    Charles River Laboratories (Wilmington, MA)
    …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...about. **Job Summary** We are seeking an experienced nonclinical drug development professional to serve as a Senior Principal… more
    Charles River Laboratories (09/08/25)
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  • Sr. Operations Manager

    Abbott (Westford, MA)
    …develop a high performing team. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, ... experience with companies engaged in the manufacture of high quality, FDA regulated products. + Proven leadership skills, results oriented, highly collaborative,… more
    Abbott (06/24/25)
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  • Coordinator, Global Strategic Resources

    Charles River Laboratories (Wilmington, MA)
    …worked on 80% of the drugs approved by the US Food and Drug Administration ( FDA ) in the past five years. We're committed to providing benefits that ... in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will...Council ('SGC') policies with regards to suppliers. + Supports administration of the SGC policies. + Creates and identifies… more
    Charles River Laboratories (08/19/25)
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  • Global Commercial Lead, AskBio-1005, Parkinson's…

    Bayer (Cambridge, MA)
    …the Regenerative Medicine Advanced Therapy (RMAT) designation by the US Food & Drug Administration ( FDA ) to slow disease progression and improve motor ... outcomes in patients with PD. A randomized, double-blinded study is currently being conducted in the US, EU and UK. Successful commercialization of this asset provides an exciting challenge as we enter this new and important therapeutic area, The cell therapy… more
    Bayer (08/27/25)
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