Danaher · Coralville, IA
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This role leads comprehensive internal and external GMP and quality audit programs, including planning, execution, and corrective action oversight. The position requires expertise in regulatory compliance, quality systems, and cGMP standards, with responsibility for maintaining FDA inspection readiness and communicating regulatory trends across the organization. Candidates need a life sciences or related degree, 4+ years of quality/audit experience in regulated environments, and willingness to travel up to 20%.
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