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. 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 (w/m/d) you evaluate medical aspects of product-related documentation submitted by manufacturers. You assess the results of clinical trials and clinical evaluations of medical devices. You coordinate cooperation with external specialist specialists at project level and form the interface between medical device experts and specialist specialists. You will support the medical and professional assessment of incidents with medical devices in the market. You help to improve and maintain quality management procedures, create and maintain medical professional training. You shall accompany the implementation of consultation procedures in medical devices containing a medical component.

Complete study of human medicine and valid approbation as a doctor are provided as well as completed further training to the specialist, preferably in an area of orthopaedic/unfall surgery, ophthalmic surgery, surgery, or gynecology and well-founded knowledge of the use of (invasive) medical devices in the patient are required. Promotion, experience with clinical studies, scientific work and the creation of publications are desirable Ideally experience with process processes and in the preparation of medical advice Ready to work into the MDR (EU) 2017/745 medical device regulation, as well as the applicable standards and guidelines documents for this topic Knowledge of German and English at C1 level in word and writing Joy in the analysis of complex facts and interest in developing new medical technologies

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. .