Bioprocess Technician – Production & Operations Support
Bioprocess Technician voor productie van vaccinantigenen bij een wereldwijde diergezondheidsorganisatie in Boxmeer, tijdelijke opdracht.
- Locatie
- Boxmeer
- Werkvorm
- op locatie
- Sluitingsdatum
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Eisen
- Teamplayer
- Kunnen werken onder druk en prioriteiten stellen
- MBO-3 of MBO-4 opleiding, bij voorkeur Biotechnologie, Procestechniek of vergelijkbaar
- Sterke focus op kwaliteit en veiligheid
- Goede communicatie in Nederlands en Engels
Wensen
- Ervaring in farmaceutische of biotech productieomgeving
- Kennis van aseptische technieken en cleanroomomgevingen
- Affiniteit met virologie, microbiologie en bioproces technologie
Volledige omschrijving
A global leader in animal health, committed to improving the wellbeing of animals, food safety, and sustainability. The organization develops and manufactures innovative medicines and vaccines for farm and companion animals, operating within a high-tech, biotechnological environment. Their site in Boxmeer forms part of an international network, producing essential veterinary products for the worldwide market, with a strong focus on quality, safety, and continuous improvement.
We are looking for a dedicated Bioprocess Technician to join our production team in Boxmeer. In this role, you will be a key contributor to the manufacturing of inactivated antigens for vaccines, working within a fast-paced, high-precision biotechnology environment. Your responsibilities will include supporting the production process, ensuring compliance with GMP and safety standards, and participating in process improvements to enhance efficiency and quality.
Responsibilities: Prepare and plan production activities for each manufacturing week, including media preparation. Independently execute production tasks such as cell culture, virus propagation, inactivation, fermentation control, centrifugation, filtration, and handling of bioreactors and vessels. Record all procedures accurately and complete batch documentation following strict protocols. Identify, report, and document deviations or irregularities in the production process.
Evaluate the product quality and process methods, suggesting improvements where appropriate. Support project teams in process optimization and participate in continuous improvement initiatives. Maintain technical knowledge related to valve controls and replacement parts, and train colleagues when necessary. Contribute to deviating process management by thoroughly documenting deviations and supporting root cause analysis. Work primarily day shifts but may be required to participate in on-call, weekend, or shift work as needed in the future.
Requirements: Completed MBO-3 or MBO-4 level education, preferably in Biotechnology, Process Technology, or a related field. Experience in a pharmaceutical or biotech production environment is preferred, but recent graduates are encouraged to apply. Familiarity with aseptic techniques and working in controlled environments such as cleanrooms is advantageous. Interest or affinity for virology, microbiology, and bioprocess technology, with willingness to undergo training.
Strong focus on quality and safety, with good communication skills in Dutch and English. Ability to work under pressure, prioritize tasks, and collaborate in a team.
Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.
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