Medical Job Opportunity for Clinicians at TÜV SÜD | Apply
This exciting medical job opportunity at TÜV SÜD offers experienced physicians the chance to contribute to clinical evaluations within the Clinical Centre of Excellence. As part of leading TÜV SÜD careers, this role blends regulatory expertise, innovation, and healthcare excellence across multiple international locations. If you are seeking a clinician job that combines medical practice with regulatory impact, this position provides a unique professional pathway.
Job Details:
- Position: Clinician for the Clinical Centre of Excellence
- Requisition ID: 3849
- Org Unit Code: PS-MHS-CCE-M
- Employment Type: Full-time or part-time/regular
- Working Model: Home-Office
- Work Area: Medical Devices & Healthcare
- Country/Region: Germany, India, Poland, Portugal, Spain
- Job Location: München, Madrid, Lisbon, Ahmedabad, Delhi, Warsaw
- Company: TÜV SÜD PS GmbH
About the Company
TÜV SÜD is a globally recognized leader in testing, inspection, certification, and technical services. With a strong presence across Europe and Asia, the organization plays a vital role in ensuring safety, quality, and sustainability across industries, including Medical Devices & Healthcare. Through continuous innovation and regulatory expertise, TÜV SÜD supports manufacturers in meeting international standards such as the European Medical Device Regulation (MDR).
Job Description
The Clinician for the Clinical Centre of Excellence is a specialized medical job within the Medical Devices & Healthcare work area. This job focuses on assessing clinical evaluations and supporting regulatory compliance under the European Medical Device Regulation (MDR).
This role offers the opportunity to work within international TÜV SÜD careers, contributing to high-quality technical documentation assessments while collaborating with multidisciplinary teams. The working model is Home-Office, with flexibility for full time or part time / regular employment.
Qualifications
- Physician with completed medical degree (current valid license 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 specializations
- Experience working with MS Office applications
- Excellent organizational and professional communication skills
Key Responsibilities
- 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 predictable services within defined timeframes
- Optionally providing support during audits of clinical processes of medical device manufacturers as a clinical expert (remote or on-site)
- Optionally continuing to practice medicine in part-time
