RESPONSIBILITIES
Planning and coordination of biocompatibility testing for medical devices
Communication i.a. with external laboratories, service providers and internal specialist departments for sample preparation and determination of extraction conditions
Evaluation of the test results and updating of existing biological evaluation reports, with focus on FDA requirements
Toxicological literature and database searches (e.g. PubMed or ECHA)
SKILLS & EXPERIENCES / INTERESTS
Advanced degree (Masters, Diploma, or PhD/MD) in life sciences (e.g. Toxicology, Biology, Biochemistry) or medical sciences (e.g. Dentistry, Medicine)
Experience in the creation of biological evaluations (plans & reports) of medical devices
Knowledge of norms and regulations relevant for biocompatibility of medical devices (ISO 10993, ISO 7405, ISO 14971, MDR)
Team player and open personality with high commitment and initiative
Knowledge of medical and technical English, advanced German is a plus
BENEFITS
Work in the St. Gallen rhine valley area in a diverse range of tasks in a globally operating company
Opportunities for professional training and development, modern workplace, as well as collaboration in a dynamic and motivated team
Attractive employment conditions, good social benefits, flexible working hours
Pleasant working atmosphere, team events and harmonic collegial environment
Have we piqued your interest?
We look foreward to receiving your complete application documents.