Vaccine Manufacturing Technician, De Bilt, Utrecht

Location: De Bilt, Utrecht  |  Sector: Pharmaceuticals  |  Start Date: 7/16/2025  |  Job ref: 55592


About the company

Join a global healthcare leader known for its mission-driven work in human and animal health. At the De Bilt site, our team focuses on producing poultry vaccines that make a real difference across more than 100 countries. These vaccines not only contribute to animal welfare but also enhance global food safety. With a workforce of around 80 dedicated professionals, the De Bilt facility is expanding to meet growing global demand. This year, a new state-of-the-art production building will be brought online, further strengthening our commitment to innovation and quality.

About the Role

As a Bioprocess Technician, you are at the heart of vaccine manufacturing. You’ll work hands-on in various production steps that require precision, care, and compliance with strict Good Manufacturing Practice (GMP) and safety guidelines. From working with biological materials in cleanrooms to operating advanced equipment, your contribution is vital in delivering safe, high-quality vaccines.

This is an excellent opportunity to develop a career in biotech manufacturing, especially for those who enjoy practical, hands-on work in a highly regulated environment. You will receive structured internal training to help you become an all-round operator capable of working across different stages of production.
 

Key Responsibilities

  • Support the production of vaccines in GMP-compliant cleanroom environments.

  • Execute and document procedures such as cell preparation, infection, harvesting, filling, freezing, and storage of vaccines.

  • Operate specialized equipment and aseptic processes in Class A and B cleanrooms.

  • Strictly follow SOPs, work instructions, and GMP documentation standards—your signature represents quality and accountability.

  • Carry out supportive tasks like equipment setup, cleaning procedures, and preparation of cleanroom environments.

  • Identify and escalate process deviations and actively participate in troubleshooting and resolution.

  • Contribute to a collaborative team culture where mistakes are seen as learning opportunities and no colleague is left to fail.

  • Continuously seek to improve processes through small improvements or project participation.

  • Contribute to updating work instructions and procedures in coordination with process owners.
     

    Requirements

  • MBO level 3 or 4 diploma, or a relevant higher vocational (HBO/HLO) degree; OR relevant work experience in a GMP-regulated production environment (e.g., food, pharma, feed).

  • Proficiency in Dutch (speaking, reading, and writing).

  • Experience with GMP processes and/or aseptic techniques (e.g., cell culture) is preferred.

  • Willingness to work in a high-biological containment production setting.

  • Able to follow procedures meticulously and work independently.

  • Open to ongoing internal training and development.

55592

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About us

Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.

SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.

Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.

Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.