CQV Engineer — GMP-Driven Pharma & Biotech Projects

EFOR (formerly CVO-Europe); Wallonië; On-site; EUR 55,000 - 85,000; Full time

Job summary

EFOR in Belgium is seeking CQV Engineers to contribute to ambitious pharmaceutical and biotechnology projects, including new facilities, revamps, capacity expansion, and equipment optimization. You will work on commissioning and qualification of facilities and systems in GMP-compliant environments.

Depending on your experience, you may define CQV strategies, prepare and execute DQ, IQ, OQ, PQ activities, and coordinate across Engineering, Quality, Production, suppliers and contractors to ensure

Qualifications

• Scientific or technical degree: Engineering, Pharmacy, Life Sciences or equivalent.
• Initial experience or several years in Commissioning, Qualification & Validation.
• Experience in pharmaceutical or biotechnology industry.
• Good understanding of GMP environments and requirements.
• Hands-on knowledge of DQ/FAT/SAT/IQ/OQ/PQ lifecycle.
• Expertise in one or more pharmaceutical systems or equipment types.
• Ability to work in multidisciplinary project teams with Engineering, Quality, Production, suppliers and contractors.
• Strong analytical skills, autonomy, attention to detail, quality-driven mindset.
• Good command of English and French.

Responsibilities

• Define and implement Commissioning & Qualification strategies.
• Prepare, review and/or execute DQ, FAT, SAT, IQ, OQ and PQ.
• Coordinate commissioning and qualification activities across project phases.
• Review qualification protocols, test results and raw data.
• Identify, investigate and resolve deviations.
• Prepare and/or approve qualification reports.
• Ensure GMP compliance throughout the project lifecycle.
• Coordinate stakeholders including Engineering, Quality, Production, suppliers and contractors.
• Manage CQV activities aligned with milestones and timelines.

Skills

CQV Engineering

Commissioning

Qualification

Validation

GMP

English and French

Education

Engineering degree (Life Sciences/Pharma)

Tools

DQ

FAT

IQ

OQ

PQ

Job description

EFOR in Belgium is seeking CQV Engineers to contribute to ambitious pharmaceutical and biotechnology projects, including new facilities, revamps, capacity expansion, and equipment optimization. You will work on commissioning and qualification of facilities and systems in GMP-compliant environments.

Depending on your experience, you may define CQV strategies, prepare and execute DQ, IQ, OQ, PQ activities, and coordinate across Engineering, Quality, Production, suppliers and contractors to ensure