Strengthen compliance for BD’s medical technology portfolio as a Staff Regulatory Affairs Specialist, with at least four days weekly in-office in Mississauga.

This approximately 21-month assignment leads compliance activities for medical devices and natural health products. You will maintain establishment licenses, manage regulatory changes, support inspections, and lead audit-related CAPAs. You will also mentor associates and coordinate cross-functional regulatory work.

Key Responsibilities:

- Lead regulatory compliance and establishment license activities
- Coordinate product recalls and audit support
- Assist with Health Canada inspections and third-party audits
- Lead CAPAs arising from internal and external audits




- Mentor team members through knowledge sharing and training

Requirements:

- Expert Canadian medical device regulation knowledge
- Experience maintaining establishment license compliance
- Experience preparing medical device license applications
- Robust regulatory strategy and submissions management skills
- Excellent communication, collaboration, and organizational skills

Use compliance leadership, audit expertise, and regulatory judgment to help BD maintain medical device and natural health product access.

📌 Senior Medical Device Compliance Specialist (Mississauga)
🏢 BD
📍 Mississauga