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.

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