Specialist in the clinical evaluation of medical devices (m/f/d)

Reference code: 18424 Company: TÜV Rheinland LGA Products GmbH

We share the enthusiasm for forward-looking solutions with over 28,000 people around the globe. At TÜV Rheinland you can contribute your knowledge independently and continue to develop in person. We are a team of highly qualified experts who face responsible challenges to enrich life with valuable achievements. And we all love what we do. If you want to bring your talents in a meaningful way, you will come to TÜV Rheinland. Let us take advantage of these diverse possibilities and make ourselves together on new goals. About us

TÜV Rheinland LGA Products GmbH is a leading provider of services in the field of auditing and certification of products.

It expects a comprehensive integration and corresponding further training which is of course ours. We support you in qualifying for the clinical expert and promote your professional training and further development. You will receive your expertise in the state of science through regular training.

In your role as a specialist for the clinical evaluation of medical devices (w/m/d) You provide medical aspects of product-related documentation submitted by manufacturers and assess the results of clinical trials and clinical evaluations of medical devices. You coordinate cooperation with external specialist specialists at project level and act as an interface between medical product experts and specialist specialists. You will support the medical and professional assessment of incidents with medical devices in the market. You contribute to the improvement and maintenance of quality management procedures, create medical professional training and perform these. You will also accompany the implementation of consultation procedures for medical devices containing a medical component.

Complete study of human medicine as well as valid approval as a doctor or Doctor and completed specialist training, ideally in orthopaedic/unfall surgery, cardiology or cardiosurgery, supplemented with profound knowledge in the application of invasive medical devices in the patient. Promotion and experience with clinical studies, scientific work and the production of publications are desirable. Ideally experience with process processes and in the preparation of medical advice. willingness to participate in the MDR (EU) 2017/745 medical device regulation as well as in relevant standards and guidelines of this area. German and English knowledge at level C1 in word and writing, joy in the analysis of complex facts and interest in developing new medical technologies.

Qualified applicants are welcome regardless of the desired working time model - the position can be occupied in full time or part time.

Training offers - from coaching and mentoring programs to the 'Women ́s Network'. Employee talks - Regular exchange at eye level. Well insured - accident insurance, occupational disability insurance, discounted insurance. Health protection measures - occupational sports groups, seminars, precautionary measures and more. Benefits - discounts for employees, e.g. in the sports studio or when buying a car. .