Validation Engineer, Life Sciences — GMP & FlexAbroad

Capgemini Engineering

Diegem

Sur place

EUR 45 000 - 65 000

Plein temps

14 jours+
Générateur de candidature

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Passez les filtres ATS

Avantages offerts par ce poste

Continuous feedback and performance discussions
FlexAbroad opportunity
Access to a digital campus and training resources

Résumé du poste

Capgemini Engineering in Diegem, Belgium, is seeking a Validation Engineer to ensure compliance in pharmaceutical manufacturing. This role includes executing validation protocols, preparing documentation, and supporting regulatory inspections. You will work closely with cross-functional teams to optimize validation processes while maintaining high quality and regulatory standards.

The ideal candidate holds a Bachelor’s or Master’s degree and has 2-5 years of experience in validation. Join us to be part of groundbreaking projects and continuous professional growth!

Qualifications

  • 2-5 years of experience in validation within the pharmaceutical or life sciences industry.
  • Strong knowledge of GMP regulations, FDA/EMA requirements, and industry validation standards.
  • Experience with risk assessment methodologies and contamination control strategies.

Responsabilités

  • Executing validation protocols including IQ/OQ/PQ for equipment and process validation batches.
  • Developing and reviewing cleaning validation documentation.
  • Collaborating with engineering, production, and quality teams.

Connaissances

Fluency in Dutch
Fluency in English
Hands-on experience with IQ/OQ/PQ
Strong analytical skills
Excellent communication skills

Formation

Bachelor’s or Master’s degree in Engineering, Pharmaceutical Sciences, Chemistry

Description du poste

Capgemini Engineering in Diegem, Belgium, is seeking a Validation Engineer to ensure compliance in pharmaceutical manufacturing. This role includes executing validation protocols, preparing documentation, and supporting regulatory inspections. You will work closely with cross-functional teams to optimize validation processes while maintaining high quality and regulatory standards.

The ideal candidate holds a Bachelor’s or Master’s degree and has 2-5 years of experience in validation. Join us to be part of groundbreaking projects and continuous professional growth!

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