CQV Engineer - GMP Validation & Commissioning

Capgemini Engineering; Diegem; On-site; EUR 45,000 - 65,000; Full time

Job summary

Capgemini Engineering is seeking a Commissioning, Qualification and Validation Engineer for the pharmaceutical industry. You will join expert teams ensuring compliance and quality of pharmaceutical facilities and equipment.

Responsibilities include developing and executing qualification/validation protocols, performing CQV activities, IQ/OQ/PQ testing, and collaborating with multidisciplinary teams. Requirements include an engineering degree in pharmaceutical engineering or related field,

Qualifications

• Knowledge of GMP and pharmaceutical regulations.
• Internship in pharma or regulated environment.
• English fluent with good Dutch skills in writing and speaking.

Responsibilities

• Develop and execute qualification/validation protocols for pharma equipment and systems.
• Perform CQV activities per GMP and pharma regulations.
• Execute IQ/OQ/PQ testing to verify installation, operation and performance.
• Collaborate with multidisciplinary teams to ensure facility compliance.
• Document test results and write detailed technical reports.
• Identify deviations and participate in corrective actions.

Skills

English fluency

Dutch proficiency

Education

Engineering degree in pharmaceutical/related field

Job description

Capgemini Engineering is seeking a Commissioning, Qualification and Validation Engineer for the pharmaceutical industry. You will join expert teams ensuring compliance and quality of pharmaceutical facilities and equipment.

Responsibilities include developing and executing qualification/validation protocols, performing CQV activities, IQ/OQ/PQ testing, and collaborating with multidisciplinary teams. Requirements include an engineering degree in pharmaceutical engineering or related field,