Senior Manager, Quality & Responsible Person overseeing pharmaceutical quality operations in Geneva, Switzerland. Leading quality oversight for compliance and safety in pharmaceutical manufacturing.
Responsibilities
Act as the Responsible Person (RP) in accordance with Article 11 of the Swiss Ordinance on Establishment Licenses
Own and continuously improve the Quality Management System (QMS) for the Swiss entity
Ensure full GMP/GDP compliance for import, wholesale distribution, export, and foreign trade activities
Provide end-to-end GMP quality oversight of Contract Manufacturing Organizations (CMOs)
Hold final authority for quality-related decisions to protect patient safety and regulatory compliance
Lead Swissmedic inspections and manage internal and external audits
Champion a Right-First-Time and continuous improvement culture across internal teams and partners
Lead, mentor, and develop a team of quality professionals
Requirements
Advanced degree in Pharmaceutical Sciences, Pharmacy, Chemistry, Biochemistry, or Biology
Recognized qualification as Responsible Person or Qualified Person
Senior-level Quality experience within the pharmaceutical industry
Strong expertise in GMP/GDP, sterile and oral dosage forms preferred
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