Quality Assurance Specialist

Jobdescription For one of our clients, an international pharmaceutical company, we are seeking a Quality Assurance Operations Specialist. General Information: Start date: 01.09.2026 Latest possible start date: 01.10.2026 End Date: 31.08.2028 Workplace: Schachen, Luzern Home office: Possible, 2 days per week Workload: 100% Working hours: Standard About the work: The Global Development Quality OPS team is responsible to drive or support compliance-based programs and results which include support cross functional projects, solving simple problems, current Good Manufacturing Practices (cGMP) quality initiatives, quality system improvements, quality directives, compliance metrics and monitoring, SOP management, and site procedures at Schachen Site. Task & Responsibilities: Participate in the release or rejection of GMP materials and components either through direct batch release support or involvement with critical program issues. Perform documentation, system or any other GMP record review in relationship with the QOS activities Conduct all work meeting high standards for quantity, integrity, quality, and GMP compliance "Day in the job": 3 times per week the day starts at 8:30 with a team meeting to discuss ongoing activities. During the day, the person will work on records review Requirements: University degree (bachelor or higher) is preferred Experience in a regulated environment is an advantage Previous experience in a similar role German C1 is must have, English business proficient is highly expected Sounds interesting? Apply now - we're looking forward to receiving your applications! Walentyna Dobrowolska