Regulatory Affairs Manager - Karslruhe Area

Regulatory Affairs Manager (F/M) Karlsruhe Area



Medical Devices



I am currently searching for a Regulatory Affairs professional who has
already gained valuable industry experience, and is determined to further
progress their career at a fantastic Medical Device company based in the
Karlsruhe area.



The position:



·
Creation and maintenance of Technical
Documentation

·
Strong focus on the reviewing and analysis of
the Technical Documentation

·
Heavily involved with Regulatory Strategies

·
To provide experienced know-how in the area of
Regulatory Submissions

·
Maintaining and archiving relevant Medical
Device registrations, along with reviewing the current Technical Documentation
to ensure compliance with regulatory authorities



Your profile:



·
Completed studies in a relevant Life Science
field

·
2-3 Years practical work experience within RA
for Medical Devices

·
Clear understanding of current MDR

·
First-hand experience of the compilation of
Technical Documentation

·
Fluent German and English both written and
spoken



If you are, or know anyone that would be interested in this
position with the right amount of experience in the above areas, then please
either respond to this Job Ad or directly send your application to d.perkins@sciproglobal.de



GOOD LUCK!!!
  • Standort: Plattenburg

Medical Device Company

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