Quality Engineer

Boxmeer | Quality Engineer | GMP | Dutch
Your new company
Our client is a leading company in global biopharmaceuticals with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products. With 69,000 employees operating in more than 140 countries, they offer state-of-the-art laboratories, plants and offices that are designed to inspire their employees as we learn, develop and grow.

The Animal Health department is located at the Boxmeer site. There they develop new medicines specifically for animals. They produce, amongst others, vaccines that prevent bacterial, parasitic and viral infections at both pet as farm animals. They are one of the first companies that focuses on biological research for animal health.

Your new role
The Quality Engineer is responsible for classification of laboratory systems, whether computerized; Reviewing and writing qualification documents (URS, protocols / reports, etc.); Close contact with the internal customers; Verification of qualification documents produced by outside companies. Works with moderate work direction and is skilled and knowledgeable to the position.

As a Quality Engineer at MSD Boxmeer, you will be part of the Process Optimization, Equipment & Automation (PEA) team. You will play a key role in ensuring the qualification and validation of laboratory and production systems, with a strong focus on compliance, safety, and continuous improvement.

Key Responsibilities
  • Develop and maintain qualification and validation protocols and work instructions in line with internal and external regulations.
  • Lead and support projects involving new equipment, automation, and laboratory setups.
  • Analyze qualification and calibration data and produce technical reports.
  • Act as Subject Matter Expert (SME) during audits and technical discussions.
  • Ensure knowledge transfer and documentation within Integrated Process Teams (IPTs) and Centers of Excellence (CoEs).
  • Collaborate with internal stakeholders and external vendors to verify and validate documentation and systems.

Your Profile
  • HBO-level education with 5–7 years of experience in the pharmaceutical industry.
  • Strong knowledge of GMP and Data Integrity.
  • Skilled in project management and technical documentation.
  • Fluent in Dutch and English, both written and spoken.
  • Analytical mindset with a pragmatic and service-oriented approach.
  • Preferably certified in continuous improvement methodologies (e.g., Lean Six Sigma Green Belt)

What you'll get in return
Hays Detachering | This is a project that will start with a contract for 12 months through Hays. Extension to stay within the department is anticipated. At this position, you will get a competitive salary between 4200 – 5200 based on experience and your travel expenses are covered.

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Overzicht

Contractvorm
Tijdelijk
Branche
Gezondheidszorg & Medisch
Locatie
Provincie Noord-Brabant
Vakgebied
Life Sciences
Salaris
5200
Referentie:
1049528
Sluitingsdatum
1 Nov 2025

Spreek met een consultant

Spreek met Robbie Wootton, de recruiting expert die deze vacature in behandeling heeft, werkzaam in kantoor Amsterdam
Hays Amsterdam, Rijnsburgstraat 9-11

Telefoonnummer: 0202192042

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