C&Q Engineer

DPS Group Global; Geel; Hybrid; EUR 60,000 - 90,000; Full time

Job summary

DPS Group Global in Belgium is seeking several Commissioning & Qualification / CQV Engineers to support pharmaceutical investment projects, guiding testing through commissioning, qualification, start-up and handover. You will prepare and execute CQV activities, develop CQV documentation, and support FAT/SAT, IQ/OQ, while coordinating with Engineering, Quality, Validation and Operations.

The ideal candidate holds a Bachelor's or Master's in Engineering or Life Sciences, has CQV/validation

Qualifications

• 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.

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

Skills

Technical documentation

Communication

English

GMP awareness

Education

Bachelor's/Master's in Engineering or Life Sciences

Tools

FAT

SAT

IQ/OQ

Job description

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.