Aufgaben

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 as part of the interfaces with other departments, offering support of and close exchange with colleagues

Supporting the development of internal position papers for certain (groups of) medical devices to ensure and maintain consistency of assessments of clinical evaluations within TÜV SÜD

Delivering high-quality, reliable and predictable services within defined timeframes

Optionally providing support during clinical audits of medical device manufacturers as a clinical expert (might require a certain level of travel)

Optionally continuing to practice medicine part-time

Possibility of attending medical conferences

Qualifikationen

Physician with completed medical degree

Four years of clinical practice in health care services or related sectors including two years in usage, development or testing/evaluation of medical devices or clinical studies/investigations or clinical evaluation of medical devices

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 and programs

Excellent organisational and professional communication skills

Beschäftigungsart

Vollzeit / Unbefristet

Arbeitsmodell

Standort

Home Office

Land

Deutschland

Einsatzbereich

Medizintechnik & Gesundheitswesen

Berufserfahrung

Berufserfahrene mit 6-10 Jahren Erfahrung

Gesellschaft

TÜV SÜD Product Service GmbH