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Regulatory Affairs Specialist

vor 3 Monaten

Sankt Wendel, Saarland, Deutschland Fresenius Medical Care Vollzeit

Your assignments:

  • Obtain and sustain global registrations for product portfolio as per Regulatory Strategy and product roadmap
  • Compile global registration file (STED) per product and customize/ supplement in preparation of local submission where necessary
  • Communicate / collaborate with relevant global interfaces
  • Support site registrations and tender procedures
  • Provide regulatory design input and submission strategy guidance to sustaining and development project teams to ensure creation of approvalrelevant documents

Your profile:

  • Completed studies in a scientific/technical field or comparable training with professional experience
  • Sound professional experience in the field of Regulatory Affairs, preferably for medical devices in global markets
  • Business proficient in English (written and spoken)

Our offer to you:

There is a lot for you to discover at Fresenius, because we have a lot to offer.

No matter in which field you are an expert (M/F/d) and how much experience you bring with you - for your professional future with meaning:

  • The opportunity to work on a mobile basis, individually in consultation with your manager
  • Whether in front of or behind the scenes you will help to make better and better medicine available to more and more people around the world
  • Individual opportunities for selfdetermined career planning and professional development
  • A corporate culture in which there is enough room for innovative thinking to find the best, not the fastest, solution together
  • A large number of committed people with a wide range of skills, talents and experience
  • The benefits of a successful global corporation with the collegial culture of a mediumsized company