USPL is seeking a Specialist, QA Documentation in North Brunswick, NJ. The role focuses on writing, distributing, collecting, storing, and maintaining essential documentation to support GMP and regulatory compliance.
This position reports to the Quality Assurance Manager and aligns with the Head of Quality Assurance. Responsibilities include updating SOPs, ensuring the correct document versions, and coordinating with various departments to understand process documentation needs and regulatory
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QA Documentation Specialist
US PharmaLab Inc. · North Brunswick, NJ, USA ·
- Pay:
- 65.000 - 75.000
- Job type:
- Full Time