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Job Requirements of QA Documentation Specialist:
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Employment Type:
Full-Time
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Location:
Morris Plains, NJ (Onsite)
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QA Documentation Specialist
Description
We're looking for a QA Documentation Specialist working in the 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 operations.
- Issues labeling/tags for Apheresis from LKPK Traveler through Packaging.
- Enters/maintains information accurately in systems/applications (e.g., SAP, LIMS, Cell Chain, etc.) as necessary to support operations and overall life cycle of documents.
- Supports document control room and GxP document lifecycle management activities such as filing, archiving, and providing execution copies.
- Supports validation/qualification activities as needed (e.g., labeling associated with Cell Chain).
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Recommended Skills
- Filing
- Lifecycle Management
- Packaging And Processing Duties
- Sap Applications
- Apheresis
- Securitization
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Job ID: j4lif49
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