CQV Engineer: GMP Validation & Commissioning

Capgemini

Diegem

Sur place

EUR 45 000 - 65 000

Plein temps

14 jours+
Générateur de candidature

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Avantages offerts par ce poste

Learning assets access
Mentoring programs

Résumé du poste

Capgemini Engineering in Belgium is seeking a Commissioning, Qualification and Validation Engineer to join our pharmaceutical-focused teams in Diegem. You will develop and execute qualification and validation protocols for pharmaceutical equipment and systems, ensuring GMP compliance and regulatory alignment.

You will perform IQ/OQ/PQ testing, document results in detailed reports, collaborate with multidisciplinary teams, identify deviations, and participate in corrective actions.

Qualifications

  • IQ/OQ/PQ methodologies knowledge.
  • GMP regulations familiarity.
  • Fluent in English with good Dutch (written and spoken).
  • Completed at least one internship in pharma or regulated environment.

Responsabilités

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

Connaissances

CQV
GMP knowledge
IQ/OQ/PQ
Documentation

Formation

Engineering degree or equivalent in pharmaceutical engineering, biochemistry, process engineering or related field

Description du poste

Capgemini Engineering in Belgium is seeking a Commissioning, Qualification and Validation Engineer to join our pharmaceutical-focused teams in Diegem. You will develop and execute qualification and validation protocols for pharmaceutical equipment and systems, ensuring GMP compliance and regulatory alignment.

You will perform IQ/OQ/PQ testing, document results in detailed reports, collaborate with multidisciplinary teams, identify deviations, and participate in corrective actions.

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