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
- Strong 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