Senior Medical Device Compliance Specialist

Strengthen compliance for BD’s medical technology portfolio as a Staff Regulatory Affairs Specialist, with at least four days weekly in-office in Mississauga.This approximately 21-month assignment leads compliance activities for medical devices and natural health products. You will maintain establishment licenses, manage regulatory changes, support inspections, and lead audit-related CAPAs. You will also mentor associates and coordinate cross-functional regulatory work.Key Responsibilities:
Lead regulatory compliance and establishment license activitiesCoordinate product recalls and audit supportAssist with Health Canada inspections and third-party auditsLead CAPAs arising from internal and external auditsMentor team members through knowledge sharing and trainingRequirements:
Expert Canadian medical device regulation knowledgeExperience maintaining establishment license complianceExperience preparing medical device license applicationsStrong regulatory strategy and submissions management skillsExcellent communication, collaboration, and organizational skillsUse compliance leadership, audit expertise, and regulatory judgment to help BD maintain medical device and natural health product access.
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