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Manager, Documentation and Regulatory Affairs
(This is really more of a Documentation Manager slot)
Responsible for the computerization filing of all documents for raw material databases and finished product databases with technical support for regulatory approval and specification approval which support the manufacturing, product development, and Quality functions. These include but are not limited to: MAPICS (master formulas, new and changes), manufacturing directions, bulk specifications, raw material specifications.
BS/BA (minimum in Chemistry, Biochemistry, Pharmacology, Biology, or other science related degree). At least 5 years in quality assurance in laboratory or regulatory positions in a dietary supplement company. Knowledge of dietary raw materials and dietary supplements. Knowledge of the cGMPs for dietary supplements (21CFR Part 111) and some knowledge
Warning: Avoid fraudulent jobs and phishing scams, some work from home jobs and any job that asks you to pay to apply! More Info
