XDES projects bemiddelt in technische functies voor de industriële sectoren: Pharma, Chemie, Petrochemie, Energie en Levensmiddelen.Job DescriptionThe scientist main responsibility is to ensure for the design, coordination and execution of assay development and validation. The required activities must be executed, documented and reported according to Good Clinical Laboratory Practice (GCLP) quality requirements. The scientist could supervise one or more technicians.Must be able to work on multiple simultaneous tasks with limited supervision. Quick learner, motivated self-starter. Excellent customer service, interpersonal, communication and team collaboration skills. Able to follow change management for internal guidelines.Job RequirementsM.Sc. or PhD in biological, biotechnology or medical sciences. Knowledge of (immunological) assay development and validation. Industry experience minimal 2 years. Hands-on experience with T-cell assays, ICS, ELISpot and/or virus neutralization assays. Experienced in immunology and/or oncology and clinical development of drugs or vaccines is an advantage. Communicative skills, fluent in English. Management skills to supervise and guide a small team of technicians is an advantage. Ability to plan tasks of self and others. Trained in GLP, GCLP or GMP is an advantage, but if not training will be provided in house.The right candidate is quality minded, flexible, proactive, can do mentality and a team player. It is important that the candidate can deal with the pressure of challenging deadlines and that he/she is active in the lab. A positive attitude is required. Some flexibility in working hours is required. Language proficiencies: English and Dutch spoken and written.Salary and BenefitsMarktconformContact UsVoor meer informatie neem je contact op met Peter Debrichy, bereikbaar op telefoonnummer 023 55 78 529 of via e-mail: – Klik op de solliciteer-button om te solliciteren – Kenmerk: 7196.