CQV Engineer: Pharma GMP Commissioning & Qualification

EFOR (formerly CVO-Europe); Wallonië; Sur place; EUR 55 000 - 85 000; Plein temps

Résumé du poste

Efor is a leading Life Sciences consulting group actively supporting pharmaceutical and biotech projects in Belgium.

As a CQV Engineer, you will contribute to commissioning and qualification of facilities, systems and equipment in GMP-compliant projects, from new facilities to upgrades.

You will define strategies, review protocols, coordinate stakeholders, and ensure milestones are met, with a strong emphasis on quality, teamwork and continuous development.

Qualifications

• Degree in Engineering, Pharmacy, Life Sciences or equivalent.
• Experience in Commissioning, Qualification & Validation (CQV) for pharma/biotech projects.
• Knowledge of GMP environments and qualification lifecycle (DQ/FAT/SAT/IQ/OQ/PQ).
• Ability to work within multidisciplinary project teams and liaise with Engineering, Quality, Production and suppliers.

Responsabilités

• Define and implement Commissioning & Qualification strategies.
• Prepare, review and/or execute DQ, FAT, SAT, IQ, OQ and PQ activities.
• Coordinate CQV activities across project phases and with stakeholders.
• Review qualification protocols and test results; ensure data integrity and deviation resolution.
• Prepare and approve qualification reports; ensure GMP compliance.

Connaissances

CQV experience

GMP awareness

English & French

Formation

Engineering, Pharmacy, Life Sciences or equivalent

Description du poste

Efor is a leading Life Sciences consulting group actively supporting pharmaceutical and biotech projects in Belgium.

As a CQV Engineer, you will contribute to commissioning and qualification of facilities, systems and equipment in GMP-compliant projects, from new facilities to upgrades.

You will define strategies, review protocols, coordinate stakeholders, and ensure milestones are met, with a strong emphasis on quality, teamwork and continuous development.