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RssCompliance 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

Wilmington, DE

About Me

Industry:

Healthcare & Medical

Occupation:

Quality Assurance Director
 

Education level:

Master

Will Relocate:

Yes

Location:

Wilmington, DE