Senior PV Process Quality Lead — CAPA & Inspection Readiness

Bristol-Myers Squibb Company is seeking an experienced Pharmacovigilance Quality Manager in Denham, UK. You will lead investigations of GVP deviations, drive quality risk initiatives, and ensure our pharmacovigilance systems are inspection-ready.

The ideal candidate has over 10 years in pharmaceuticals, with significant experience in GVP management. You will work closely with cross-functional teams to uphold the highest standards of quality and compliance within the organization.

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