|Johnson & Johnson||Senior Manager, Regulatory Affairs DACH||Germany|
MDR implementation and suspension: what are the implications?
- Qualified as a German Lawyer with 20+ years of experience in the regulated health care industry
- 10 years with Johnson &Johnson Medical, before 10 years with Teleflex Medical
- Experienced in quality and regulatory affairs in pharmaceutical and mainly medical device industry
- Expert knowledge of regulatory requirements in the EU and ability to translate regulations into requirements to support CE-marking
- At J&J involved in the planning and implementation of MDR requirements since 2013
- Working experience abroad: 1 year in the US (Philadelphia) and 4 years in the UK (London)