CQV Process Engineer

☞ Pauwels Consulting

View: 195

Update day: 16-11-2025

Location: Gosselies Hainaut

Category: IT - Software IT - Hardware / Networking Information Technology Executive management

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Job description

For one of our clients in the pharmaceutical industry in the Hainaut region, we are looking for a CQV (Commissioning/Qualification/Validation) Engineer

As a CQV Engineer, your main tasks will be :

  • Equipment commissioning and qualification (following the URS)
  • Equipment validation (IQ/OQ/PQ) + FAT/SAT
  • Management and creation of documentation (protocols, reports)
  • Contact with suppliers

Benefits

    • Challenging projects based on your interests and skills
    • Personal follow-up and clear, transparent communication both before and after commencement of employment
    • Possibility to follow extra training
    • Inspiring network events and legendary after work drinks
    • Strong network of industry leading clients
    • Expertise within IT, Engineering and Life Sciences
    • A flying start for every junior, growth opportunities and possibility to share gathered knowledge for more senior employee

    Have you got what it takes?

    As a CQV Engineer, you meet the following requirements:
    • Bachelor or Master’s Degree in a scientific field
    • At least 2 years of experience in a similar role in the pharmaceutical industry
    • Knowledge in GMP practices
    • Well organised, good communication and analytical skills
    Reference number: 35846
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    Deadline: 31-12-2025

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