CQV Engineer (m/f/d)

For our client in Alzey, we are looking for an experienced Senior CQV Engineer (m/f/d) to join a pharmaceutical project on an employee leasing basis

Your responsibilities

• Independently plan, coordinate and execute commissioning and qualification activities for pharmaceutical facilities, equipment and utilities
• Prepare, review and approve CQV documentation, including FAT, SAT, IQ and OQ protocols and reports
• Coordinate suppliers and project stakeholders, and manage deviations and outstanding items through to closure
• Ensure CQV activities and documentation meet GMP requirements

Your profile

• Degree in engineering, chemical engineering or a related field
• Extensive CQV experience in the pharmaceutical industry, ideally at least eight to ten years
• Proven ability to take independent responsibility for CQV workstreams on complex projects
• Strong knowledge of GMP requirements and the qualification of manufacturing equipment, cleanrooms or clean utilities
• Fluent English; German is not required