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Quality Auditor 1

De Bilt | HBO | Dutch & English | QA | cGMP
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 they learn, develop and grow. At the production site De Bilt, chicken vaccines are produced using tissue culture. Our clients' vaccines are supplied worldwide and currently employ around 80 people at our site, of which around 40 are in the Production department. We work according to strict GMP (Good Manufacturing Practices) and SHE (Safety Health Environment) standards.

Your new role
As a Quality Assurance (QA) officer, you are responsible for the daily Quality Assurance support within our production location in De Bilt. You are the link between the operational production teams and the Qualified Person (QP) and in that role you give direction on the shop floor regarding Good Manufacturing Practices (GMP) compliance. You are involved in conducting deviation management and root cause research. You will work closely with fellow QA officer(s) and the QP to carry out all Quality Assurance activities efficiently and effectively. You report to the QA Lead De Bilt.
What you'll need to succeed
Our Animal Health division is committed to protecting and improving the health, welfare and performance of animals. Working closely with veterinarians, farmers, pet owners and governments, we develop an unrivalled range of veterinary pharmaceuticals, vaccines and health management solutions and services. We are one of the first companies to focus on biological R&D for animal health.

We ask:
  1. A completed and relevant HBO or WO education, preferably Biotechnology, Biochemistry or Microbiology;
  2. At least three years of relevant work experience within a production environment, preferably within the pharmaceutical industry;
  3. Demonstrable work experience with deviation management, change management and process validation;
  4. Extensive knowledge of GxP (good practice quality guidelines);
  5. Excellent command of the Dutch and English language;
  6. Living at a travelable distance from De Bilt and willing to travel to Boxmeer occasionally for consultation.
What you'll get in return
Hays Detachering | This is a project that will start with a contract for 12 months through Hays. Extensions to stay within the department are anticipated. In this position, you will get a competitive salary and your travel expenses are covered.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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Overzicht

Contractvorm
Contracting
Branche
Pharmaceutisch
Locatie
Utrecht
Vakgebied
Life Sciences
Salaris
4300
Referentie:
1049286
Sluitingsdatum
15 Jul 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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