Positionsnummer / Reference Number


Position / Job Title

RA Consultant - MDR Innovation Projects

Dauer / Project Length

6 months with an option to be extended

Aufgaben / Tasks

• Lead, participate and support the registration of innovative, completely new medical devices within the European and American Market

• Liaise with a multitude of internal stakeholders from various departments as well as the responsible authorities

• Facilitate a smooth and streamlined registration process, providing detailed documentation and regulation related knowledge

Qualifikationen / Qualifications

• Multiple years of experience in medical device Regulatory Affairs in combination with having participated in innovation projects

• Sound knowledge of the MDR, the 510k process as well as design control

• The ability to work well within a multicultural environment and communicate effectively cross departmental

• Immaculate English skills in both verbal and in writing

Weitere Informationen / Further Information

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