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Compliance Manager/Auditor
To obtain a position working as a Microbiology Business Analyst and Project Manager in a pharmaceutical/biotech validation environment, oriented toward management advancement. Over 20 years of experience in the Pharmaceutical Industry, 16+ years of those years are with GxP (GMP, GLP, GCP) systems compliance/QA and 21 CFR Part 11. Experience includes GxP system implementation projects, documentation/SOP writing/review.
Quality Assurance Director
About Me
Industry: |
Healthcare & Medical |
---|---|
Occupation: |
Quality Assurance Director |
Education level: |
Master |
Will Relocate: |
Yes |
Location: |
Wilmington, DE |