Medical Device Regulatory Compliance Specialist

Support BD’s on-site healthcare operations in Mississauga through regulatory compliance, quality systems, and post-market medical device activities.This Staff Regulatory Affairs Specialist provides regulatory support for BD products entering and remaining in Canadian markets. The approximately 21-month assignment spans medical devices and natural health products, with responsibilities across compliance, licensing, quality systems, and inspections. You will collaborate with regional and cross-functional teams, assist with recalls and audits, and lead regulatory activities connected with product changes. The position also calls for detailed communication, adaptability, organization, and knowledge sharing with team members.Key Responsibilities:
Perform new product activation and post-market change assessmentsReview advertising and promotional materials for regulatory requirementsSupport recalls, Health Canada inspections, and corporate auditsAssist with SOP maintenance and internal audit activitiesMentor team members through knowledge, advice, and resourcesRequirements:
Life sciences or engineering Bachelor of Science degreeRegulatory Affairs experience in the medical device industrySeven-plus years of relevant regulatory experienceMedical device license application preparation experienceExcellent communication, collaboration, and attention to detailCombine compliance knowledge, quality systems experience, and team guidance to advance BD medical device regulatory work.
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