Cell Therapy Manufacturing Technician
Cell Therapy Manufacturing Technician voor een biotech-organisatie in Hoofddorp, 40 uur per week, tijdelijk dienstverband.
- Locatie
- Hoofddorp
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Sluitingsdatum
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Eisen
- MLO/MBO/HBO qualification (MBO Level or higher) with a background in Life Sciences
- Familiarity with aseptic procedures and working in full gowning requirements
- Proficient in Microsoft Word, Excel, and data analysis
- Ability to work independently in a fast-paced environment, adapt to changing priorities, and collaborate well within a team
- Strong communication skills in English; knowledge of Dutch is not required
- Hands-on, proactive attitude with excellent attention to detail
- Experience with cGMP manufacturing in a biotech or pharmaceutical environment
Wensen
- Knowledge of blood processing methods (e.g., Vapro A/B or LITOP A/B)
Volledige omschrijving
A leading organization in the biotechnology sector dedicated to advancing cell therapy solutions. The company is committed to innovation, quality, and the development of life-changing treatments through expert manufacturing practices. We are seeking a dedicated Cell Therapy Manufacturing Technician to join our client's dynamic team. In this role, you will support the production and quality of cell therapy products, working in a highly regulated, aseptic environment to ensure the delivery of safe and effective treatments.
Responsibilities: Support daily manufacturing operations in both production support and manufacturing teams. Perform tasks such as processing blood products, preparing growth media, and handling batch documentation in line with SOPs and cGMP standards. Conduct visual inspections of final products and cryopreserve excess cells as needed. Assist with transfer and documentation of samples to quality control. Support cleanroom activities, including maintaining environment cleanliness and materials decontamination.
Help troubleshoot equipment and process issues, contributing to continuous improvement initiatives. Draft and revise manufacturing batch records, SOPs, and work instructions to enhance processes and ensure compliance. Participate in investigations for deviations and assist in change management procedures. Work in rotating shifts, including weekends and evenings, to support manufacturing schedules.
Requirements: MLO/MBO/HBO qualification (MBO Level or higher) with a background in Life Sciences. Experience with cGMP manufacturing in a biotech or pharmaceutical environment. Familiarity with aseptic procedures and working in full gowning requirements. Knowledge of blood processing methods (e.g., Vapro A/B or LITOP A/B) is a plus. Proficient in Microsoft Word, Excel, and data analysis. Hands-on, proactive attitude with excellent attention to detail.
Ability to work independently in a fast-paced environment, adapt to changing priorities, and collaborate well within a team. Strong communication skills in English; knowledge of Dutch is not required.
Other Information: Because this role involves working with blood products, KITE strongly recommends candidates to be vaccinated against Hepatitis B. You may already be vaccinated or be willing to get vaccinated.
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