• QA Associate - Batch…

    Actalent (St. Louis, MO)
    Job Title: QA AssociateJob Description The QA Associate is responsible for the rigorous review, verification, and archival of batch records and ... resolve discrepancies and maintain data integrity. Responsibilities + Perform comprehensive batch record reviews for completeness, accuracy, and compliance with… more
    Actalent (07/18/25)
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  • Associate , Quality Assurance

    Catalent Pharma Solutions (Kansas City, MO)
    …of experience providing analytical services for stand-alone and integrated biologics projects. The Associate , Quality Assurance ( QA ) is responsible for ... ** Associate , Quality Assurance ** **Position...scientific field with no experience + Preferred experience with batch record review, floor QA ,… more
    Catalent Pharma Solutions (07/16/25)
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  • Quality Assurance Specialist

    Catalent Pharma Solutions (Kansas City, MO)
    ** Quality Assurance Specialist** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission ... Pharma Solutions in Kansas City, MO is hiring a Quality Assurance Specialist. The Quality ...patient, consumer, and Catalent employee.** **The Role** + Performs batch record review, product release, and disposition… more
    Catalent Pharma Solutions (06/27/25)
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  • Quality Associate II

    Catalent Pharma Solutions (Kansas City, MO)
    ** Quality Associate II** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to ... Pharma Solutions in Kansas City, MO is hiring a Quality Associate II. The Quality ...and packaged finished product + Perform Component Inspection-primary/secondary + Pre- Batch Record and Post- Batch … more
    Catalent Pharma Solutions (06/28/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
    …technical oversight of downstream manufacturing operations at CDMOs, including review of batch records , deviation investigations, and change controls. + Lead or ... **Job Summary** **​** The Associate Director, MSAT - Downstream provides specialized technical...processing. + Collaborate closely with Upstream MSAT, Validation MSAT, QA , Regulatory, Process Development, Analytical Development, and CDMO technical… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Associate Director, MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Jefferson City, MO)
    …technical oversight of upstream manufacturing operations at CDMOs, including review of batch records , deviation investigations, and change controls. + Lead or ... to upstream processing. + Collaborate closely with Downstream MSAT, Validation MSAT, QA , Regulatory, Process Development, and CDMO technical teams. + Stay current… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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