At TÜV SÜD we are passionate about technology. Innovations impact our daily lives in countless ways, and we are dedicated to being a part of that progress. We test, we audit, we inspect, we advise. We never stop challenging ourselves for the safety of society and its people. We breathe technology, we strive for professional excellence, and we leave a mark. We take the future into our hands. We are TÜV SÜD.

Tasks

Assessing clinical evaluations as part of technical documentation assessments according to the requirements layed down in the European Medical Device Regulation (MDR)
Preparing deficiency reports in case of non-conformities with the requirements of the MDR
Serving as an internal point of contact for clinical matters as part of the interfaces with other departments, offering support and close exchange with colleagues
Delivering high-quality reliable and predicatable services within defined timeframes
Optionally providing support during audits of clinical processes of medical device manufacturers as a clinial expert (remote or on-site)
Optionally continuing to practice medicine in part-time

Qualification

Physician with completed medical degree (current valid licence not mandatory)
Four years of clinical practice in health care services or related sectors in the area of Cardiac surgery
Two years of experience in usage, development or testing/evaluation of medical devices or clinical studies/investigations or clinical evaluation of medical devices
Experience with MDR, regulatory aspects of medical devices, clinical evaluation for medical devices / medical writing is a plus.
Experience with scientific literature searches or peer review in the medical context
Fluent in written and spoken English. German is a plus.
Interest in intercultural cooperation in an international team of clinicians with different medical backgrounds and specialisations
Experience working with MS Office applications
Excellent organisational and professional communication skills

At TÜV SÜD, we have employees from more than 100 different countries collaborating together. People of different backgrounds, skills, and pursuing different life goals. Our strength comes from these countless and varied perspectives.

We are committed to be an inclusive and diverse workplace by welcoming people of all backgrounds. We want Diversity & Inclusion (D&I) to be a foundation of our company and create an environment where all our employees can trust they will be treated with respect, regardless of gender, nationality, ethnic background, faith, beliefs, disabilities, age, sexual orientation, or identity. As such, our employees are expected to behave at all times in a manner consistent with TÜV SÜD Code of Ethics and Company values.

We firmly believe embedding D&I in the heart of what we do will inherently contribute to the success of TÜV SÜD. Click here to find out more about Diversity at TÜV SÜD.

Work Area: Medical Devices & Healthcare

Country/Region: Germany, India, Poland, Portugal, Spain

Job Location: München, Delhi, Ahmedabad, Madrid, Lisbon, Warsaw

Working Model : Home-Office

Employment Type: Full time or part time / regular

Company: TÜV SÜD Produkt Service GmbH

Org Unit Code: PS-MHS-CCE-M

Requisition ID: 5696

TÜV SÜD

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