Demo

Quality Assurance Manager

LanceSoft
Cambridge, MA Full Time
POSTED ON 4/5/2025
AVAILABLE BEFORE 5/4/2025
  • Issue, review, and approve GMP documentation (e.g., batch records, SOPs, job aids, etc.) needed for internal manufacturing operations.
  • Review logbooks and reconcile documentation.
  • Assist with walkthroughs with senior Quality staff members.
  • Review labeling and packaging batch records and prepare documentation for release.
  • Review work orders, equipment qualification, and validation documentation for adequacy and compliance.
  • Review batch record documentation, ensure compliance and accuracy, and prepare for drug substance / product and / or critical material release.
  • Engage in daily onsite quality oversight and guidance and collaborate across functions, leveraging quality and manufacturing expertise to provide guidance on non-conformance / deviations, troubleshoot / problem solve, interpret data, and apply a risk-based approach for ongoing manufacturing operations and related quality events.
  • Represent QA in onsite operations from the thaw of starting material to drug substance / product filling and labeling.
  • Additional duties as assigned.
  • Minimum requirements :

    o Bachelor's Degree in Biology, Microbiology, Chemistry or related field

    o 4 years of experience in cGMP Quality Assurance in Biologics or Cell & Gene Therapy product manufacturing

    Preferred requirements :

    o Master's Degree in Microbiology, Biology, Chemistry or a related field

    o Working knowledge of cell or gene therapy product testing, manufacturing, or development

    • Demonstrated knowledge of current GMP regulations associated with pharmaceuticals, cell therapies, gene therapies, etc. in the field of responsibility.
    • Understanding and working knowledge of Quality Management System expectations, ability to interpret requirements, anticipate issues, make informed decisions, and respond rapidly to emerging quality situations. in the field of responsibility.
    • Local travel between manufacturing sites required.

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