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!
...
