• Distribution Specialist II

    Gilead Sciences, Inc. (Frederick, MD)
    …of cancer immunotherapy, you will assist in the commissioning and operation of a GMP warehouse and inventory management system. In this exciting new area of cancer ... immunotherapy, the Technician will assist in the maintenance of a GMP /Non- GMP warehouse and inventory management system. In this role, the Technician will… more
    Gilead Sciences, Inc. (12/16/25)
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  • Sr. Spclst, Engineering

    Merck (West Point, PA)
    …we collaborate to discover the next medical breakthrough. The Senior Specialist, GMP Process Operations, serves as a technical expert and operational leader within ... Senior Specialist applies deep technical knowledge of bioreactor systems and GMP compliance to ensure successful production of clinical materials, effective… more
    Merck (12/11/25)
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  • Engineer - Fume & CSQ Prd Quality Assurance

    Lilly (Indianapolis, IN)
    …systems design and validation, change control proposals, procedure revisions, GMP drawings, commissioning and qualification, and maintenance. This position is ... essential for maintaining GMP compliance and providing support to internal / external...and Qualification (C&Q) and Computer System Validation (CSV) of GMP assets including review and approval of associated Engineering/… more
    Lilly (12/04/25)
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  • Principal Engineer, Assay and Data Automation

    Bristol Myers Squibb (Seattle, WA)
    …strong technical background in automation design, development, and deployment within both GMP and non- GMP labs. This individual will foster effective ... automation platforms for bio-analytical methods that are performed in GMP and non- GMP labs. + Effectively communicate experimental results to influence program… more
    Bristol Myers Squibb (01/03/26)
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  • Fsq Technician

    Actalent (Union City, CA)
    …safety and quality requirements daily, leading by example in Good Manufacturing Practices ( GMP ) for others, working cohesively as a team to drive the improvement of ... checks as required * Ensures all stakeholders follows Good Manufacturing Practices ( GMP ), good housekeeping, and company policies and procedures * Performs hold and… more
    Actalent (12/24/25)
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  • Senior Technician, Filling Operations (Onsite)

    Merck (Rahway, NJ)
    …Laboratory, and Experimentation (FLEx) Center to support drug product development and GMP clinical supply of sterile dosage forms. Positions will support development ... feedback on product and process development. These roles require adherence to GMP procedures, strong attention to detail in completing GMP documentation,… more
    Merck (12/13/25)
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  • QA Specialist II - Operations

    PCI Pharma Services (Bedford, NH)
    …Visual Inspection activities for clinical and commercial drug product in a GMP facility. The work scope includes on-the-floor Quality oversight of manufacturing ... aseptic processes, performing AQL visual inspection of finished drug product vials, GMP documentation and Batch Record review, line clear and product changeover… more
    PCI Pharma Services (01/01/26)
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  • QA Document Control Specialist

    Actalent (Shawnee Mission, KS)
    …Document Control Specialist Key Responsibilities: + Maintain document control for GMP documents, ensuring accuracy and compliance with paper-based data integrity ... raw data form sheets in a controlled manner. + Organize and manage GMP documentation, including filing, tracking, and retrieving completed records such as batch… more
    Actalent (12/31/25)
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  • Associate Project Manager: Biopharmaceutical…

    Eurofins US Network (Lancaster, PA)
    …of biological substances and products. **Job Description** **Role Overview** The GMP Testing Project Manager is responsible for planning, coordinating, and ... overseeing Good Manufacturing Practice ( GMP )-compliant testing projects within a regulated laboratory environment. This role ensures timely delivery of testing… more
    Eurofins US Network (12/30/25)
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  • Associate Data Review Scientist: Biochemistry

    Eurofins US Network (Lancaster, PA)
    …quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. + Review simple and complex routine and non-routine ... analytical procedures; ensure all work is performed according to GLP/ GMP requirements and apply GLP/ GMP in all areas of responsibility + Experience in a… more
    Eurofins US Network (12/30/25)
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