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QA Documentation Specialist
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- The Opportunity Description We're looking for a QA Documentation Specialist, working in Pharmaceuticals and Medical Products industry in 220 East Hanover Avenue, Morris Plains, New Jersey, 07950, United States.
- Job description:Maintains and follows CGT procedures for MBR creation, issuance, receipt, reconciliation, filing and archiving.
- Prints and issues batch records, in-process labels, and final product labels to support labeling/tags for Apheresis from LKPK Traveler through Packaging.
- Enters/maintains information accurately in systems/applications (e.g. SAP, LIMS, Cell Chain, etc.)
- Supports document control room and GxP document lifecycle management activities such as filing, archiving, providing execution copies, etc.
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