Costa Mesa, California
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Today
Roles & Responsibilities: Bachelor's degree in engineering, Computer Science, Life Sciences, or related field. 2-10+ years of experience in computerized systems validation within pharmaceutical, biotechnology, or life sciences industries. Direct experience with GxP equipment, IT systems, or manufacturing automation systems. FDA and cGMP regulations and documentation practices. GAMP 5 guidance. 21 CFR Part 11 and Annex 11. Computer system validation methodologies. Familiarity with risk-based
Full-time