Job Details

A company is looking for a Regulatory Affairs Specialist.Key ResponsibilitiesSupport regulatory registration efforts for medical devices in global healthcare spin-offsEvaluate product changes for rebranding and their impact on existing licenses with Health CanadaUpdate technical documentation and coordinate with international regulatory teams for timely submissionsRequired QualificationsBachelor's Degree or higher in Biology, Chemistry, Pharmacology, Biochemistry, or a related field2-3 years of experience in regulatory affairs within the medical device industryDirect experience with submissions to Health CanadaProven ability to author technical documentation and support international registrations