Lead Canadian regulatory strategy at BD as a Staff Regulatory Affairs Specialist, supporting medical devices and natural health products in office in Mississauga.

This approximately 21-month assignment supports market entry and maintenance for BD products. You will manage regulatory activities, prepare Health Canada submissions, interpret requirements, and guide teams. The position also shares expertise through mentoring and training.

Key Responsibilities:

- Lead compliance activities and establishment license maintenance
- Classify products and prepare Health Canada submissions
- Manage regulatory changes and continuous improvement initiatives
- Assess post-market changes and review advertisements and promotions
- Support recalls, audits, inspections, and regulatory CAPAs

Requirements:

- Bachelor of Science in life sciences or engineering
- Seven or more years of medical device regulatory experience
- Class III and Class IV device experience
- Expert knowledge of Canadian medical device regulations
- Medical device license application experience

Apply regulatory expertise, Health Canada submissions knowledge, and strategic leadership to advance BD product compliance in Mississauga.

📌 Staff Medical Device Regulatory Affairs Specialist (Mississauga)
🏢 BD
📍 Mississauga