Drive Health Canada submissions and approvals for BD medical devices as a Staff Regulatory Affairs Specialist, based at the Mississauga Derry Road West location.

This approximately 21-month assignment focuses on regulatory support for market entry and product maintenance. You will prepare device and drug applications, negotiate approvals, and provide regulatory interpretation. The role also supports quality systems, audits, inspections, and cross-functional training.

Key Responsibilities:
Prepare regulatory submissions for device and drug applications
Negotiate effective approvals with Health Canada
Provide regulatory guidance to project teams and leaders
Maintain quality systems procedures and improvement activities
Represent BD on regional and external committees

Requirements:
Minimum Bachelor of Science degree required
Regulatory Affairs experience within the medical device industry
Seven or more years of relevant experience
Advanced science degree preferred
Regulatory Affairs postgraduate certificate preferred

Bring submission management, regulatory strategy, and communication skills to support BD approvals and product maintenance through Health Canada.

📌 Health Canada Regulatory Submissions Specialist Mississauga
🏢 BD
📍 Mississauga