Contribute to medical device regulation at Percucision in Montréal as a Junior Regulatory Affairs Associate. Support FDA submissions and maintain compliance for innovative products. This entry-level role focuses on regulatory activities for medical technologies aimed at market entry in Canada, the U.S., and internationally.

You will assist with FDA 510(k) submissions, regulatory strategy development, and close collaboration among multidisciplinary teams. Your work will be crucial in achieving compliance and clearance for our revolutionary medical devices. Key Responsibilities:

- Prepare and submit FDA and Health Canada regulatory applications
- Assist with documentation and submission planning for FDA clearance




- Collaborate with internal teams and regulatory consultants
- Maintain regulatory documentation and follow-up with authorities
- Conduct research on medical-device regulations and standards Requirements:
- Bachelor's degree in relevant scientific discipline
- 2+ years in regulatory affairs, preferably in medical devices
- Experience with regulatory submissions for medical technologies
- Solid communication and project management skills
- Proficient in English and French Drive impactful regulatory strategy and device compliance as part of Percucision's team.

📌 Junior Regulatory Affairs Associate at Percucision (Montreal)
🏢 Percucision
📍 Montreal