CQV Engineer

EFOR; Geel; Sur place; EUR 120 000 - 150 000; Plein temps

Résumé du poste

EFOR invites a senior CQV professional to join a high-caliber team in Belgium on one of the largest fast-track brownfield projects. You will lead CQV execution for complex process equipment, contribute to URS and risk assessments, and collaborate with an expert team of CQV consultants.

Ideal candidates bring 10+ years in CQV within biopharma GMP settings, plus hands-on experience with reactors, filters, storage tanks, and containment solutions. Kneat or digital CQV platforms are advantageous.

Qualifications

• Must have extensive CQV experience with senior-level autonomy.
• Experience leading URS and risk assessments for complex process equipment projects.
• Strong familiarity with GMP biopharma environments is a plus.

Responsabilités

• Lead and support CQV execution for complex process equipment projects.
• Contribute expertise to URSes and risk assessments (urgent starts needed).
• Collaborate with a multidisciplinary team of senior CQV consultants.

Connaissances

CQV experience

URS & risk assessments

Autonomy

Senior-level expertise

Process equipment knowledge

Biopharma GMP familiarity

Outils

Kneat

Digital CQV platforms

Description du poste

Are you ready for your next challenge? Join a high-caliber team working on one of the largest fast-track brownfield projects in Belgium!

We are searching for senior professionals with proven expertise in Commissioning, Qualification & Validation (CQV) for process equipment projects. This opportunity focuses on upgrading and modifying existing facilities as part of a €500 million undertaking. All our current team members have more than 10 years of relevant CQV experience, and we are seeking like-minded experts to join us.

What You’ll Do:

• Lead and support CQV execution for complex process equipment projects
• Contribute expertise to URSes and risk assessments (urgent starts needed!)
• Collaborate with a multidisciplinary team of senior CQV consultants

Your Qualifications:

• Extensive CQV experience (10+ years is preferred), ideally on large-scale process equipment projects and brownfield environments
• Hands-on knowledge with reactors, centrifuges, filters (including filter dryers), dryers, storage tanks, and containment solutions is highly advantageous
• Strong background in the biopharmaceutical sector and GMP environments is a plus
• Familiarity with Kneat or digital CQV platforms is an asset
• Senior-level expertise and autonomy are key; you’ll be working alongside seasoned CQV professionals

Why Join Us?

• Be part of a project of unprecedented size and technical ambition in the region
• Fast-track, stimulating environment with leading-edge digital CQV practices
• Immediate impact: support risk assessments and URSes as the project ramps up

Are you a CQV expert ready to take the next step?