Wilmington, Ohio
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Today
Responsibilities Job Description: Serve as a subject matter expert in and lead equipment, facility, and utility qualification for clinical and commercial pharmaceutical manufacturing and laboratory systems. Serve as technical lead for maintenance of GMP compliance through monitoring, review, assessment and qualification of activities. Ensure Validation systems (policies, procedures, reviews, VMPs) effectively meet current/changing industry demands. Oversee maintenance of validation systems and
Full-time
USD 135,000.00 - 150,000.00 per year
