QA Manager - Pharma - Compliance - FvP Rolle

Oversee FvP responsibilities for releases, deviations, OOS, and resulting corrective actions while managing customer and regulatory audits and CAPA tracking. Draft and revise quality agreements and process documentation, collaborating with QA, RA, and PV teams. Lead project budgets and coordinate between Zurich North office and client sites. Maintain internal and external contacts in German and English, communicating clearly with management and authorities. Requires GMP environment experience, audit management skills, and a pragmatic, solution-oriented compliance approach.