Public Relations

• Act as the designated RP/FvP for assigned activities under Bachem’s Swiss establishment licence
• Ensure effective technical supervision
• Provide independent oversight of manufacturing, testing, batch disposition, storage and distribution activities under Swiss GMP/GDP requirements and Bachem’s Pharmaceutical Quality System
• Make or support independent quality and regulatory decisions for significant deviations, investigations, CAPAs, changes, product-quality defects and other critical quality events
• Ensure escalation and measures where product quality, patient safety or regulatory compliance may be affected, including quarantine, supply restrictions, withdrawal or recall
• Support inspections, establishment-licence activities and communication with stakeholders and health authorities
• Represent Quality in customer audits, quality meetings and critical product or supply discussions
• Contribute to key quality governance processes and promote a risk-based quality culture

Explore Responsible Person at Bachem. Review requirements and application details.