• Manager, Shop Floor QA (Day Shift)

    Bristol Myers Squibb (Devens, MA)
    …with cross functional teams. + Must have sound knowledge and experience in FDA regulated cGMP warehousing, Quality , and compliance environments. Prefer to also ... have knowledge of GMP Manufacturing operations and processes. + Directs ...2+ year of QA shop floor experience. Experience in FDA /EMA regulations in biopharmaceuticals or cell therapy manufacturing is… more
    Bristol Myers Squibb (08/09/25)
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  • Lead Microbiology Technician

    Integra LifeSciences (Braintree, MA)
    GMP /GLP laboratory experience in a medical device, pharmaceuticals, Quality /Regulatory Compliance, or other regulated industry + Familiarity with application of ... FDA and/or ISO quality standards in a government regulated industry. + Knowledge of QC terms, tools, and methodologies. Detail-oriented. + Strong verbal and… more
    Integra LifeSciences (08/08/25)
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  • Proposal Manager - Gene Therapy Manufacturing Cdmo…

    Charles River Laboratories (Wilmington, MA)
    …of the sales proposal document production process to ensure the overall quality meets company and client standards * Research appropriate responses through supplied ... a CDMO with understanding of gene therapy processes from process development to GMP . Broad understanding of program flow from development, QC/QA, logistics and … more
    Charles River Laboratories (08/09/25)
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  • Sr. Operations Manager

    Abbott (Westford, MA)
    …+ Manufacturing experience with companies engaged in the manufacture of high quality , FDA regulated products. + Proven leadership skills, results oriented, ... Mark requirements. + Manufacturing management experience in manufacturing planning, documented systems, GMP , and quality . Please note that the salary range… more
    Abbott (06/24/25)
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  • Laboratory Operations Technician I

    Charles River Laboratories (Wilmington, MA)
    …related to laboratory operations and animal husbandry in a Good Manufacturing Practice ( GMP ) compliant laboratory setting. Tasks may include but are not limited to ... Perform physical environment cleanliness and upkeep and maintain recordkeeping to GMP standards and/or Standard Operating Procedures (SOPs) + Collaborate with… more
    Charles River Laboratories (07/29/25)
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  • Talent Pipeline - Laboratory Support Services…

    Cambrex High Point (Agawam, MA)
    …customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities ... Together with our customers, we aim to improve the quality of life for patients around the world. Start...support for laboratory functions in accordance with SOP's & GMP practices. This role is responsible for the cleanliness… more
    Cambrex High Point (05/20/25)
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  • Senior Validation Engineer

    AbbVie (Worcester, MA)
    …and/or renovation of biopharmaceutical process equipment, facilities, and utilities in an FDA / GMP regulated environment. The engineer will work in a ... required + Comply with all regulatory, corporate, and site quality system procedures, especially safety and cGMPs Qualifications Key...and communication skills as well as experience in a GMP environment are preferred + Must be able to… more
    AbbVie (07/26/25)
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  • Research Scientist - Regulatory Submission / CMC

    ThermoFisher Scientific (Boston, MA)
    …(Days) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards **Job Description** At Thermo Fisher Scientific, you'll ... digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities… more
    ThermoFisher Scientific (06/28/25)
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  • Pr. Electronics Production Engineer

    J&J Family of Companies (Danvers, MA)
    …engineers and multi-functional team members. + Ensure compliance with all applicable ** FDA , ISO 13485, and GMP ** requirements. **Required Qualifications:** + ... Working knowledge of **industry standards** such as IPC-A-610, J-STD-001, and FDA /ISO quality system regulations. + Excellent problem-solving, technical writing,… more
    J&J Family of Companies (07/24/25)
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  • QA Lead Technical Operations

    System One (Harvard, MA)
    …Contract, Potential for extension or conversion to permanent Responsibilities + Provides Quality Assurance (QA) support to Devens Site and reporting Manger through ... quality review and approval of Investigations and Corrective Actions....preferred. + Advanced Level of relevant experience in a GMP , GCP, or GXP with at least 8 years… more
    System One (08/03/25)
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