Immunology Technician Development and Qualification

Werkgever CheckMark Labrecruitment
Plaats Regio Utrecht
Provincie Utrecht
Dienstverband Voltijd (> 36 uur)
Contract Vast
Plaatsingsdatum maandag 9 juli 2018
Sluitingsdatum maandag 6 augustus 2018

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You are responsible for carrying out, developing and qualifying immunological assays. The results and methods are essential for the clinical development of drug products.

As Immunology Technician Development and Qualification you will work in the translational research team that executes, optimizes and qualifies state-of-the-art bioassays.

- By working in the translational team you contribute to the data package supporting the conduct of clinical trials to test the safety and efficacy of therapeutic antibody products
- You will work with a scientist on one or multiple project(s). At the department in a team of scientists and research associates dedicated to developing state of the art bioassays that are used to demonstrate the quality and characteristics biopharmaceutical products
- These methods include, but are not restricted to cell culture, flow cytometry,(FACS), ELISA, and functional cellular assays
- As Immunology Technician Development and Qualification you execute these assays make sure data is generated, analyzed and interpretet
- If applicable, you make sure that all quality requirements are met (qualification) and may assist in the transfer of a method


Opleiding HBO
Ervaring Ervaren (3 - 8 jaar)
For this vacancy as Immunology Technician Development and Qualification we are looking for a skilled and experienced research technician with a track record in (tumor) immunology who meets the following profile:

- You have a bachelor (HLO) or Master (MSc) degree in a Life Science field. This is not a PhD-level position
- With at least 2 years of work experience, you are skilled in cell culture, flow cytometry (FACS), ELISA and functional cellular assays
- Advanced flow cytometry skills in FlowJo Software and using FACS formulas is considered a plus

- Being quality-minded, you know how to adhere and/or to update quality procedures (e.g. GLP or GCP) 
- You can organize your work efficiently, draw conclusions from results and are able to collaborate smoothly in a team
- You are fluent in English

Aanvullende informatie

- Full-time availability is required
- Year contract at the company, with possibility for extension


Neem voor meer informatie contact op met Coen Smiers // 0182-590218 // 06 218 999 66
Vacaturenummer: 5903


The company is specialized in the creation and development of differentiated human antibody therapeutics for the treatment of cancer.

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