Apply expert Canadian regulations knowledge at BD in Mississauga, leading medical device submissions, licensing, audits, and regulatory change management.

As a Staff Regulatory Affairs Specialist, you will support BD product market entry and maintenance for medical devices and natural health products. This approximately 21-month assignment requires robust regulatory strategy, project management, and communication skills. You will negotiate Health Canada approvals, assess post-market changes, and provide guidance to cross-functional teams. The position also contributes to continuous improvement, inspections, audits, and team capability through mentoring and training.

Key Responsibilities:
Drive regulatory change management and continuous improvement initiatives
Negotiate Health Canada approvals for device and drug applications




Interpret regulatory requirements for project teams and business leaders
Lead regulatory activities supporting audits, inspections, and CAPAs
Represent BD on regional and external committees as required

Requirements:
Minimum Bachelor of Science degree in life sciences or engineering
Seven-plus years within medical device Regulatory Affairs
Experience with Class III and Class IV medical devices
Expertise in Canadian medical device regulations
Solid submissions management and regulatory strategy skills

Use regulatory strategy, Health Canada submissions, and audit leadership to support BD products from Mississauga.

📌 Canadian Medical Device Regulatory Lead Mississauga
🏢 Becton Dickinson
📍 Mississauga