A global pharmaceutical company is looking to hire a Senior Quality Assurance Manager on a permanent basis. Working from their site in Zug, the successful candidate will play a key role in ensuring regulatory compliance and product quality across several Swiss legal entities.Role Responsibilities:
Acting as Deputy QP (FvP), including batch disposition, recalls, and ensuring GDP compliant distribution
Leading and maintaining the local Quality Management System (QMS) in line with GMP/GDP standards
Serving as primary quality contact for Swissmedic, cantonal authorities, and external partners
Conducting management reviews, self-inspections, and release of reworked batches/products
Acting as Person Responsible for Regulatory Compliance (PRRC) under the Swiss Medical Devices Ordinance
Managing responsibilities related to narcotics and controlled substances according to Swiss regulations
Handling deviations, complaints, CAPA activities, and product recalls
Approving and maintaining quality-relevant documentation (SOPs, PQRs, Technical Quality Agreements)
Supporting supplier qualification and overseeing training activities
Required Skills & Experience:
University degree in pharmacy or a scientific discipline (e.g., chemistry, biology)
8+ years of experience in the pharmaceutical industry, including minimum 5 years in Quality Assurance
Proven experience as Swiss QP (FvP) or Deputy QP (minimum 3 years)
In-depth knowledge of regulatory requirements (TPA, MPLO, GDP, GMP, BetmG)
Strong decision-making and communication skills, able to act independently and responsibly
Fluency in English and German (spoken and written); French is a plus
Experience in liaising with Swissmedic and international regulatory authorities is an advantage
This role is open to EU/EFTA citizens or those who hold a valid Swiss Work Permit.For additional information, and a confidential discussion, please apply now with an updated CV.
