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QA Document Control Specialist I
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- Pacific BioLabs is an independent CRO offering cGMP/GLP testing services in toxicology, biocompatibility, pharmacology, analytical chemistry, and microbiology.
- PBL has immediate openings for full or part time Document Control Specialist I in the Quality Assurance Department.
- The general responsibility of the QA Document Control Specialist I assisting Quality Management in administering the company's systems for document control.
- A large part of the Document Control Specialist's job consists of maintaining the company's Operations Procedures and the company's Form/Worksheet Control System.
- Overall, the Document Control Specialist role presents the employee with an opportunity to contribute substantially to the company's ongoing success as a quality testing laboratory.
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