1 year temporary project management position related to the MDR transition
Regulatory Project Manager - MDR transition
International medical device company
- Crossfunction role to coordinate the RA resources related to the MDR transition
- Works internally with different key stakeholders in Europe and in the USA : RA, QA, R&D..
- To coordinate RA stakeholders to ensure deadlines are met on a timely manner
- To work on submissions and life cycle management activities.
- Previous significative experience in Regulatory Affairs in a pharmaceutical/medical device environment
- Experience in combination products would be a plus
- PMP certification would be a plus
- Fluent in English
- Must be detail oriented with good organizational skills with the ability to analyse regulatory documents
Project managament related to the MDR transition