Regulatory Affairs Specialist
vor 1 Monat
**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 approval-relevant 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 self-determined 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 medium-sized company
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