Job Description
Location: Basel
Duration: 1 year/possible extension
An exceptional candidate holds a Bachelor's degree in a relevant scientific or technical field and brings a minimum of three years of comprehensive Quality Assurance experience deeply rooted in a regulated GMP/GDP environment. They are completely fluent in English (with German being a strong asset), allowing them to confidently author Master Quality Agreements, manage clinical trial complaint systems, and articulate compliance strategies during high-stakes Health Authority Inspections. Finally, this individual is a proactive problem-solver who will seamlessly support clinical studies by approving complex IMP Supply & Release Flowcharts while actively driving continuous improvement projects across the distribution network.
Responsibilities:
Regulatory Compliance: Act as the appointed Delegate of the Swiss Responsible Person (FvP), providing necessary final Quality decision-making
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Submit ApplicationJob Details
- Location basel stadt, basel city
- Job Type Full-time
- Category PLA
- Posted Date June 24, 2026
- Application Deadline August 03, 2026