CQ Engineer
We are currently searching for a CQE to support a Global Leader in the Pharmaceutical and Biotechnology industry, Headquartered in Switzerland. This project is initially for 6 months, with the possibility of extension or long-term engagement
Key Responsibilities:
Document Reviews:
- Review and verify Electro & Pneumatic Schematics
- Analyze PID / P&ID Schematics
- Validate Main Component Lists
- Ensure accurate System and Safety Labeling
- Maintain and ensure all documentation meets current Good Manufacturing Practice (cGMP) standards
- Perform calibration of various sensors to ensure accuracy.
- Conduct air velocity mapping within equipment
- Conducting Operational Qualification (OQ) tests
Qualifications:
- Strong attention to detail and analytically skills
- Excellent documentation and communication skills
- Familiarity with industry standards and regulatory requirements
*Please note, only those with the right to work in Switzerland will be considered. Permit sponsorship is unfortunately not possible
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