Validation Engineers (France & Belgium)


Brussels
Contract
Negotiable
Quality
CR/602814_1784883427
Validation Engineers (France & Belgium)

Locations: France & Belgium
Contract Types: Short-Term and Long-Term Projects
Industry: Pharmaceutical Manufacturing

Overview

We are supporting multiple pharmaceutical clients across France and Belgium in the search for experienced French-speaking CQV and Validation Engineers. These opportunities are available on both long-term and short-term projects, supporting major capital investments, equipment qualification programmes, process validation activities, and manufacturing expansion initiatives.
Successful candidates will bring hands-on experience within GMP-regulated pharmaceutical environments, with a particular focus on non-sterile manufacturing equipment, systems, and processes.

Key Responsibilities

  • Execute Commissioning, Qualification and Validation (CQV) activities across pharmaceutical manufacturing facilities.
  • Prepare and review qualification documentation, including IQ, OQ, PQ protocols and reports.
  • Perform equipment qualification activities for manufacturing and process equipment.
  • Support process validation and cleaning validation programmes.
  • Ensure all validation activities comply with GMP and internal quality standards.
  • Collaborate with engineering, operations, quality assurance and project teams to deliver project milestones.
  • Manage deviations, investigations, CAPAs and change controls related to validation activities.
  • Participate in risk assessments and validation strategy development.
  • Support commissioning and start-up activities for new equipment and manufacturing systems.

Requirements

Essential

  • Bachelor's degree in Engineering, Pharmaceutical Sciences, Biotechnology or a related technical discipline.
  • Proven experience within pharmaceutical, biopharmaceutical or life sciences manufacturing environments.
  • Strong CQV and/or Validation experience.
  • Hands-on experience with non-sterile manufacturing equipment and processes.
  • Knowledge of GMP, FDA and EU regulatory requirements.
  • Experience writing and executing qualification and validation documentation.
  • Professional proficiency in French.

Preferred

  • Experience supporting capital projects, facility expansions or technology transfers.
  • Exposure to process validation, cleaning validation or equipment qualification.
  • Experience working within multinational project teams.
  • Additional English language skills.

What's on Offer

  • Multiple contract opportunities across leading pharmaceutical manufacturers in France and Belgium.
  • Long-term and short-term assignments available.
  • Opportunity to work on major pharmaceutical expansion and manufacturing projects.
  • Competitive contract rates and flexible project durations.
  • Collaborative international project environments.

FAQs

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That's why we recommend registering your resume so you can be considered for roles that have yet to be created. 

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