Senior Regulatory Affairs Consultant – EU MDR Contract
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ClinChoice is seeking a Sr. Regulatory Affairs Associate – CONSULTANT for a 12-month contract in Canada. The role collaborates with the regulatory team to manage TDs per EU MDR and other regulatory requirements, with duties spanning document creation, QA, and cross-functional coordination.
The ideal candidate has a life sciences degree and 2+ years in EU MDR regulatory affairs, plus strong English communication and MS Office skills. Remote/contract arrangements are indicated.
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