In this role, you will be responsible for monitoring the quality of cleanroom environments and high-purity media systems, including WFI (Water for Injection) and process gases. Your work ensures compliance with GMP requirements and contributes directly to product quality and patient safety. This is a fully on-site, one-day assignment requiring gowning and work in controlled areas.
Key Responsibilities
Perform environmental monitoring activities in cleanrooms (gowning required)
Monitor high-purity media systems, including WFI and process gases
Take ownership of assigned production facilities and independently organize and execute sampling activities
Personally transport collected samples to Quality Control (QC) for analysis
Ensure accurate and GMP-compliant documentation of all monitoring activities
Collaborate closely with team members as areas of responsibility rotate regularly, requiring flexibility and strong coordination
Actively support a smooth handover when responsibilities shift within the team
Working Environment
Assignment areas change at a fixed rhythm, offering variety and exposure to different production facilities
Work is performed entirely on-site in regulated GMP environments
No home office possible due to operational requirements
Your profile
Experience or familiarity with cleanroom environments and GMP-regulated processes is an advantage
Ability to work independently, with a high sense of responsibility and accuracy
Strong teamwork and communication skills, especially in a rotating responsibility setup
German language skills required
* Willingness to wear cleanroom gowning and work in controlled production areas
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