Regulatory Affairs Specialist - Health Canada Submissions

Medtronic; Brampton; On-site; CAD 74,000 - 92,000; Full time

Job summary

Medtronic Canada is seeking a regulatory affairs specialist for a 6-month contract to support submissions and registrations. You will coordinate document packages, liaise with internal teams, and help ensure timely Health Canada approvals.

The role emphasizes attention to regulatory changes, cross-functional collaboration, and initiative in maintaining compliant labeling and documentation across programs. This position offers exposure to a global medical technology leader.

Qualifications

• Requires a Bachelor Degree with 2+ years in regulatory affairs.
• Alternative: advanced degree with 0 years experience.
• Ability to coordinate documentation for regulatory submissions.

Responsibilities

• Coordinate and prepare regulatory submission document packages.
• Compile materials for submissions, renewals and registrations.
• Recommend labeling and protocol changes for compliance.
• Monitor and improve regulatory tracking and controls.
• Stay current with regulatory procedures and changes.
• May interact with regulatory agencies on defined matters.
• Suggest strategies for Health Canada approval timelines.

Skills

Regulatory submissions

Documentation coordination

Project coordination

Regulatory affairs knowledge

Education

Baccalaureate degree in a related field

Advanced degree (MS/PhD) in a related field

Job description

Medtronic Canada is seeking a regulatory affairs specialist for a 6-month contract to support submissions and registrations. You will coordinate document packages, liaise with internal teams, and help ensure timely Health Canada approvals.

The role emphasizes attention to regulatory changes, cross-functional collaboration, and initiative in maintaining compliant labeling and documentation across programs. This position offers exposure to a global medical technology leader.