Medical Device Job at TÜV SÜD
Looking for a Medical Device Job that takes your medical expertise beyond traditional hospital practice? TÜV SÜD is hiring a Urologist / General Surgeon for its Centre of Clinical Evaluation. This opportunity combines clinical knowledge with medical-device evaluation and regulatory compliance under the European Medical Device Regulation (MDR). Doctors exploring TÜV SÜD Careers, Clinical Evaluation Jobs, and specialized Medical Jobs India can consider this unique clinical-to-corporate career opportunity.
About TÜV SÜD:
TÜV SÜD is a global organization providing testing, inspection, certification and technical services across multiple industries. Its healthcare and medical-device activities support the assessment of products against applicable safety, quality and regulatory requirements. For doctors exploring careers beyond conventional clinical practice, TÜV SÜD Careers can provide opportunities to apply medical expertise to areas such as clinical evaluation, technical documentation and medical-device regulation.
Job Details:
- Job Name: Urologist / General surgeon for the Centre of Clinical Evaluation (f/m/d)
- Job Location: München, Delhi, Ahmedabad, Madrid, Lisbon, Warsaw
- Working Model: Home-Office
- Employment Type: Full-time or part-time / regular
- Org Unit Code: PS-MHS-CCE-M
- Requisition ID: 6287
Job Description:
The Urologist / General Surgeon will be responsible for assessing clinical evaluations as part of technical documentation assessments in accordance with the European Medical Device Regulation (MDR). This role includes preparing deficiency reports for non-conformities, serving as an internal point of contact for clinical matters, and delivering high-quality services within defined timeframes.
Key Responsibilities:
- Assessing clinical evaluations as part of technical documentation assessments according to the requirements laid 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, 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 part-time.
Eligibility Criteria for this Medical Device Job:
- Completed medical degree as a physician.
- A current valid medical licence is not mandatory for the position.
- Significant clinical-practice experience in healthcare or a related sector.
- At least 2 years of experience involving medical-device use, development, testing/evaluation, clinical studies/investigations, or medical-device clinical evaluation.
- Experience with MDR and medical-device regulatory requirements is advantageous.
- Clinical evaluation or medical-writing experience is considered an advantage.
- Experience conducting scientific literature searches or medical peer review.
- Fluent written and spoken English.
- German language skills are advantageous.
- Strong organizational and professional communication abilities.
- Ability and interest in working within an international, multicultural clinical team.
- Experience using Microsoft Office applications.
Skills Required for this Medical Device Job:
- Clinical Evaluation of Medical Devices
- European Medical Device Regulation (MDR)
- Clinical & Surgical Expertise
- Medical Device Safety & Compliance
- Scientific Literature Review
- Medical & Regulatory Writing
- Technical Documentation Assessment
- Professional Communication & Cross-Cultural Collaboration
