We are looking for a Senior RA (Regulatory Affairs) Program Lead, Strategic Programs – MDR (medical device regulations)
The Senior RA Program Lead, Strategic Programs – MDR is a critical position responsible for ensuring the consistent application of regulatory interpretation and implementation for programs such as the EU MDR and associated secondary legislation within the Cardiovascular & Specialty Solutions (CSS) Business Units.
With a good knowledge of Regulatory Affairs in the EU, this role will proactively coordinate and track the alignment of country-specific activities and liaise with relevant cross-functional stakeholders to support regulatory MDR Project deliverables for CSS.
Interested in this position? Please send your CV to: Sarah.firstname.lastname@example.org...