[Emploi] CellProthera job opportunity : Quality Control Engineer

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CellProthera is a biotech company based in Mulhouse (FR) developing innovative cell therapy products based on a proprietary cell processing technology platform. A multi-center Phase I/IIb clinical trial is currently on-going in Europe to test the therapy product Protheracytes® (ATMP) in patients having suffered from severe acute myocardial infarction.


Under supervision of the Director of Quality and Regulatory Affairs and in close collaboration with the Quality Assurance team, you are actively working at the development of standards, methods and procedures for inspecting, testing and assessing the accuracy, efficacy and reliability of our stem cell based process and product:
• Develop test protocols to characterise and identify stability of key elements of the processes and cell therapeutic product
• Write, set-up and follow-up new QC tests with external laboratories
• Compile data for documentation of test procedures and prepare reports
• Write and update Standards Operating Procedures and QMS documentation (deviations/change control/CAPA/OOS) in GMP environment


Skills and experience
Degree in Biotechnology, Biology, Pharmacy or equivalent level
3-5 years’ experience in the industry, preferably pharma, biotech or equivalent
Experience in Quality Control
Familiarity with laboratory techniques and QC test methods
English fluent. French conversational is a plus
Strong analytical skills


Ability to work in autonomy and in a demanding regulatory environment
Rigorous, dynamic, result-oriented and hands-on hard-worker
Well-structured, self-motivated and solutions oriented
Applicants should also be entitled to work within the European Economic Area (EEA).

The position is located in Mulhouse, France. If you are interested in this job, please contact Paula Lee (plee@cellprothera.com)