Quality Manager - High-Purity Mechanical Equipment

Join Barré as a Quality Manager today!

Barré (Wavre) is looking for a Quality engineer or Quality manager to lead our quality system for manufacturing of clean piping networks, high-quality machines and equipment for the biopharmaceutical industry (vaccine production) and for other high-purity production sites (cosmetics, nuclear medicine, animal medicine, data centers, semiconductors, among others).

Why join Barré?

Barré (Wavre) specializes in high-quality mechanical engineering. We design, produce, install and maintain in 3 sectors:

• Clean Piping (high-quality, high-purity clean piping networks).
• Air Processing (filtration and air treatment solutions; hoods, pass boxes, biosafety cabinets, laminar flow, RABs; for the most regulated vaccine production areas)
• Design and manufacture of custom-made stainless-steel machines, equipment and special parts for our customers' production sites.

Barré is in full development and growth, nominated for the Trends Gazelles of Walloon Brabant 2025. We are looking for candidates who are passionate about Quality, mechanics and the management of the QA/QC systems for our company.

The project

• As a Quality Manager, you will collaborate for various of the company's main tasks (ISO9001, operational procedures, QC production, QC installation, commissioning). This is, for our different types of activities.
• Your role is key to Barré S.A.'s strategic growth plan.
• The activities are located on the company's site, between the production workshop and the offices, and supervision of the activities on customer’s production sites.

Your mission

• Management of the QMS
• Support to Safety management system
• Management of 3 to 10 people
• Coordination of activities for project quality management (QA-QC)
• Suppliers, audits, instruments, tools, training … follow-up and management
• Action plan management
• Deviation management, root cause analysis
• Manage quality control for incoming goods and finished products
• Quality control of documentation for manufactured products

Your profile

• Civil, Electromechanical, Mechanical, Industrial, Quality Engineer, or equivalent (Bachelor's degree with relevant experience in Quality department)
• Experience in mechanical manufacturing QA/QC for high-purity sectors (Biopharma, Biotech, Cosmetic, Nuclear Medicine, etc.), or similar
• Clean Piping knowledge/familiarity or in mechanical equipment (from past experiences in pharmaceutical, nuclear, cosmetic industries)
• Basic knowledge of mechanical-technical environments
• ISO9001-expertise, and VCA-system basic knowledge in option
• Ability to integrate/work/manage a team/communicate
• Mastery of office automation tools
• Knowledge of languages: French and English; Dutch is a plus
• Differentiating factors:
  • Structure and organization, self-disciplined
  • Good level of energy and commitment
  • Leadership
  • Desire to learn and improve the current management system

Our recruitment process

• 
  Resume Review

  We look at your background, your skills, but above all, what you are eager to learn.

• First Call

  A quick chat to get to know each other, understand your motivation, and answer your questions.

• Team Interview

  Usually two interviews with several people from the company to gather different perspectives and see if there's a good fit.

• Fast decision-making

  f we're a good fit, we won't waste any time. You'll receive an offer and join the adventure.

Ready for the challenge?

Join Barré and help shape the industry of tomorrow!