Support Canadian regulatory pathways for advanced medical devices with Health Canada knowledge and submission experience in Markham, Ontario.

As a Regulatory Affairs Specialist, you will support DePuy Synthes Orthopaedics within Johnson & Johnson’s planned business separation. Your responsibilities span submission strategies, product licensing, inspections, and post-market activities. You will collaborate across functions while communicating regulatory changes.

Key Responsibilities:

- Coordinate Canadian submission strategies and regulatory pathway activities
- Maintain relationships with Health Canada and business partners
- Support recalls, special access processes, and submission updates
- Monitor regulatory trends, policies, and proposed requirements




- Support Health Canada, MDSAP, and external inspections

Requirements:

- Degree in life science, engineering, or physical science required
- Canadian medical device regulatory experience preferred
- Three to five years’ relevant regulatory experience preferred
- Solid documentation and technical writing capability required
- Leadership, analytical, and problem-solving skills required

Bring Canadian regulatory affairs experience, submission expertise, and collaborative leadership to Orthopaedics products in Markham.

📌 Canadian Medical Device Regulatory Specialist (Markham)
🏢 Brighter Signals
📍 Markham