C&Q Engineer
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For multiple pharmaceutical investment projects, we are looking for several Commissioning & Qualification / CQV Engineers.
You will support projects from equipment and system testing through commissioning, qualification, start-up and handover.
Your responsibilities
- Prepare and execute commissioning and qualification activities
- Develop and/or review commissioning and qualification documentation
- Support and execute FAT and SAT activities
- Prepare, execute and follow up IQ/OQ and related qualification activities
- Coordinate closely with Engineering, Quality, Validation and Operations
- Identify and follow up deviations, punch-list items and technical issues
- Ensure proper documentation, traceability and GMP compliance
- Support system and equipment start-up
- Coordinate final handover to Operations
Your profile
- Bachelor's or Master's degree in Engineering, Life Sciences or another relevant technical discipline
- Experience in Commissioning, Qualification, Validation or CQV
- Previous experience within pharmaceutical or biotech manufacturing
- Good knowledge of GMP requirements
- Experience with equipment and/or utility qualification is highly desirable
- Hands-on experience with FAT, SAT, IQ and OQ
- Strong technical documentation and communication skills
- Professional proficiency in English
- Willing to work approximately 2 to 3 days per week on-site in Geel
What we offer
You will join an ambitious, long-term investment programme within a large international pharmaceutical manufacturing environment, working alongside a multidisciplinary team of experienced engineers and project professionals.