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