Responsible Person (RP) / Fachtechnisch verantwortliche Person (FvP) (60-100%) Your Role Act as the Responsible Person (RP) / Fachtechnisch verantwortliche Person (FvP) in accordance with Swiss regulatory requirements (HMG, AMBV) and Swissmedic Technical Interpretation .17. Ensure compliance with applicable GMP requirements and regulatory commitments across manufacturing operations. Assess quality-critical issues and support decision-making related to product quality, compliance, and patient safety. Serve as the primary contact for Swissmedic and represent the company during inspections and regulatory audits. Act as an independent quality authority and trusted partner, balancing compliance, quality, and business needs.
Ophtapharm AG is an FDA/EU-GMP certified pharmaceutical manufacturer specializing in ophthalmic products.
