• Lead Specialist , Batch

    Catalent Pharma Solutions (Harmans, MD)
    ** Lead Specialist , QA - Batch Disposition ** **Summary:** _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on ... other viral vector-based therapies and vaccines._ The ** Lead Specialist , QA - Batch Disposition ** is responsible for providing Quality Assurance support… more
    Catalent Pharma Solutions (10/25/24)
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  • Supervisor, Records/ Batch

    ThermoFisher Scientific (Cincinnati, OH)
    …cleaner, and safer. We are currently seeking a dedicated and daring Quality Specialist III-Supervisor Batch Disposition to join our world-class manufacturing ... MFG/PKG needs, driving the team's daily work plan to ensure results are met. Lead the batch record disposition team to achieve site goals for delivery and… more
    ThermoFisher Scientific (11/09/24)
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  • Reconciliation Specialist (Tableting) 2nd…

    Mallinckrodt Pharmaceuticals (Hobart, NY)
    …to determine scope of impact, corrective actions and rationale to support product disposition . Lead and assist with production safety, compliance and improvement ... Job Title Reconciliation Specialist (Tableting) 2nd Shift ($36,467.00 - $70,967.00) Plus...including coaching and mentoring operators and technicians on proper batch record documentation. + Lead and participate… more
    Mallinckrodt Pharmaceuticals (09/09/24)
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  • Senior Quality Assurance Specialist

    J&J Family of Companies (Athens, GA)
    …Operating Procedures (SOPs) * Maintain accurate and complete documentation of all batch record review activities. * Give timely disposition to manufactured ... Senior Quality Assurance Specialist - 2406213647W **Description** Janssen Pharmaceuticals, Inc., a...belong. In this role you will provide Quality Assurance batch record review and release associated with the manufacture… more
    J&J Family of Companies (11/12/24)
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  • Senior Quality Specialist

    Verista (Boston, MA)
    …facility including start-up of assembly, packaging and label operations + Responsible for batch disposition activities. Review batch data, including batch ... support of analytical laboratory, materials management, and facility/engineering groups. + Lead QA efforts to establish new programs to support Drug Product… more
    Verista (11/13/24)
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  • Specialist , Quality Assurance

    Astellas Pharma (Seattle, WA)
    …Excel. + Experience authoring/revising Standard Operating Procedures. + Hands-on experience with batch record review and product disposition is preferred. + ... ** Specialist , Quality Assurance, Universal Cells** Are you a...so, we're seeking you, and your bold ideas, to co- lead and accelerate the development of our research programs… more
    Astellas Pharma (09/19/24)
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  • QA Specialist I - Operations

    PCI Pharma Services (Bedford, NH)
    …internal procedures and external standards. Primary responsibilities for this role includes Batch Record Review, Lot Disposition , and Quality System review. This ... shape the future of PCI. Job Summary: The QA Specialist will work with other departments to ensure the...and commercial products. **Job Duties** + Perform review of batch documentation for release of internal and external clinical… more
    PCI Pharma Services (10/17/24)
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  • Operations Compliance Specialist II - Third…

    Mallinckrodt Pharmaceuticals (Hobart, NY)
    …to determine scope of impact, corrective actions and rationale to support product disposition . Lead and assist with production safety, compliance and improvement ... Job Title Operations Compliance Specialist II - Third Shift Requisition JR000014264 Operations...+ Perform Change Controls + Identify, implement and execute SOP/Form/ Batch Record revisions + Lead and/or support… more
    Mallinckrodt Pharmaceuticals (11/06/24)
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  • Specialist II, Manufacturing Technical…

    Catalent Pharma Solutions (Harmans, MD)
    …** Specialist II, MTO** will provide support to Manufacturing Associates to meet batch record review/ disposition schedule to adhere to lot release dates. The ... ** Specialist II, MTO** **Summary:** _Our FDA-licensed, state-of-the-art CGMP...and revising GMP documents such as SOPs and Manufacturing batch records. **This is a full-time on-site position** **Catalent… more
    Catalent Pharma Solutions (10/17/24)
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  • Principal Specialist , Bio QC

    Boehringer Ingelheim (St. Joseph, MO)
    …2008 for, Reprocess/Rework, Destruction and Pre-licensure of final product to support USDA disposition , CBRs (Chinese Batch Records) for China release, and MBPs ... Prepare accurate international quality release paperwork (eg APHIS Form 2008s, Manufacturer's Batch Protocols, Chinese Batch Records, CofA's) for all finished… more
    Boehringer Ingelheim (09/04/24)
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