Equipment Qualification Engineer – GMP & CQV (Life Sciences)

Capgemini; Diegem; Sur place; EUR 70 000 - 95 000; Plein temps

Avantages offerts par ce poste

Impact Together Week

Mentoring programs

Free learning platforms access

Résumé du poste

Capgemini Engineering in Belgium is seeking a Qualification/Validation professional to support the Equipment Requalification program at the Geel site, collaborating with Engineering, Quality, Manufacturing, and Validation teams to deliver GMP-compliant documentation.

You will execute IQ/OQ/PQ, contribute to CQV activities, manage deviation and CAPA processes, and ensure audit readiness. English and Dutch fluency are required.

Qualifications

• Minimum 3 years of experience in equipment qualification or validation in a pharmaceutical or biopharmaceutical setting.
• Experience with IQ/OQ/PQ protocols and CQV activities.
• Strong understanding of GMP/GxP documentation and regulatory standards.

Responsabilités

• Support equipment qualification and requalification in GMP environments.
• Prepare, execute, and review IQ/OQ/PQ documentation per GMP/GxP requirements.
• Contribute to CQV activities including utilities, facilities, and process equipment.
• Manage deviations, CAPA follow-up, and remediation plans.
• Assist with audit readiness and inspection support when needed.

Connaissances

IQ/OQ/PQ protocols

CQV methodologies

GMP/GxP documentation

Deviation management & CAPA

English and Dutch fluency

Description du poste

Capgemini Engineering in Belgium is seeking a Qualification/Validation professional to support the Equipment Requalification program at the Geel site, collaborating with Engineering, Quality, Manufacturing, and Validation teams to deliver GMP-compliant documentation.

You will execute IQ/OQ/PQ, contribute to CQV activities, manage deviation and CAPA processes, and ensure audit readiness. English and Dutch fluency are required.