Technical Responsible Person (FvP) / Senior Quality Assurance Specialist (m/f/d)

We are looking for a Technical Responsible Person (FvP) / Senior Quality Assurance Specialist to join the Quality Department of Bausch & Lomb Swiss AG in Zug. The role focuses on implementing and maintaining the company's Quality Management System, guaranteeing compliance with Swiss and European regulations, and handling batch release activities for the Swiss market during an eight‑month parental‑leave cover. Day‑to‑day duties involve ensuring quality and compliance across the Pharma, Surgical and Vision Care units, acting as the FvP for import and wholesale distribution, and releasing medicinal products and medical devices for Switzerland. You will manage non‑conformances, CAPAs and complaints, conduct internal audits, oversee training, and communicate with Swiss health authorities to keep product registrations up to date. Additional tasks include supporting pharmacovigilance and materiovigilance, reporting Quality Performance Indicators, qualifying suppliers and service providers, and taking responsibility for advertising compliance. The position requires a university degree in Life Sciences, Pharmacy, Chemistry or a comparable scientific field, and formal qualification to work as an FvP under Swiss law (I‑SMI.TI.17). Candidates must have several years of experience in the pharmaceutical industry, preferably as a (deputy‑)FvP in a senior compliance or quality role, and possess solid knowledge of GMP, GDP and MDR requirements. Strong analytical, problem‑solving and decision‑making abilities, as well as very good German (C1) and fluent English, are essential. Experience with sterile medicinal products, project‑management background and prior work in a similar industry are considered advantageous. The assignment is full‑time (100 %) for eight months, offering an attractive compensation package, pension contributions, 25 days of annual leave plus additional time off, a collaborative team environment, and opportunities for training, career development and a fitness subsidy. What the role asks for: - University degree in Life Sciences, Pharmacy, Chemistry or equivalent - Qualified as FvP per Swiss requirements (I‑SMI.TI.17) - Several years pharma experience as (deputy‑)FvP, senior level - Strong knowledge of GMP, GDP, MDR and regulatory standards - Very good German (minimum C1) and fluent English - Excellent problem‑solving and decision‑making skills - Experience with sterile medicinal products, nice to have - Project‑management experience, nice to have