Your main responsibility is to design and execute experiments for the development and validation of immunological assays to be used in the analysis of samples from clinical trials, and to generate high-quality scientific reports to document your work.
Besides, you are responsible for the long-term life cycle management of the methods you’re the expert on, together with the key reagents, equipment and data analysis tools required for the assay to be performed.
You’re expected to maintain your technical edge by following relevant literature and knowledge in the field, or by performing experiments on a regular basis, to support assay development processes.
Your activities must be executed according to Good Clinical Laboratory Practice (GCLP) quality requirements. You’re responsible for instructing associate and assistant scientist on the scientific fundamentals of the assays you’re responsible for and to critically review to the data generated by them.
A great job opportunity at an international healthcare company.
Contactpersoon voor deze functie is Joost Storms, bereikbaar op telefoonnummer 023 55 78 529 of via e-mail : joost xdes.nl Kenmerk : 9421.