Jobannonce: IVD Regulatory Affairs Specialist
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Agilent Technologies Denmark, Glostrup
Are you an individual with knowledge in IVD or Medical Devices, looking for a new challenge in your career? A job where your actions will have an impact improving quality of life. Then we are looking for you!
Come and join us in a highly collaborative environment where we fight cancer together! You will be part of our two most profitable divisions, Pathology' and 'Reagent Partnerships and be exposed to innovative IVD products across different regulatory classifications including hardware, software and immunochemistry technologies.
We are searching for an upbeat and driven Regulatory Specialist to play a key role in implementing Regulatory QMS procedures in compliance with the EU IVDR, and help to acquire NB certification for our extensive IVD portfolio.