FvP Associate

• Represent the Responsible Person at our site, in line with regulatory requirements.
• Ensure all processes comply with GDP guidelines and Swissmedic regulations.
• Perform technical release of medicinal products within the scope of applicable regulations.
• Monitor quality assurance and risk management processes in storage and transport areas.
• Train and support employees on quality-related topics.
• Collaborate with internal departments and external partners to ensure compliance.
• Manage documentation and report to authorities as required.

Profile

• Completed degree in pharmacy or natural sciences, or an equivalent qualification with several years of experience in the pharmaceutical sector.
• Professional experience in logistics, quality assurance, or as a Responsible Person/Deputy Responsible Person.
• Strong knowledge of GDP and Swissmedic requirements, with a keen understanding of technical processes.
• A pragmatic, assertive, and team-oriented approach, with the ability to convince others through practical relevance.
• Excellent communication skills to clearly convey knowledge and train employees.
• Fluent written and spoken German is essential; knowledge of French is a significant advantage.