Regulatory Affairs Intern

GE HealthCare is hiring a Regulatory Affairs Intern in Mississauga. Posted November 10, 2026. Checked against the employer's posting on November 12, 2026.

Job Description Summary The Regulatory Affairs Intern will gain hands-on experience supporting premarket and compliance activities within a collaborative Regulatory Affairs team.

The intern will contribute to regulatory projects and help establish and implement best-practice processes and procedures that support efficient premarket activities and regulatory compliance.

Job Description GE HealthCare is seeking a highly motivated and detail-oriented Regulatory Affairs Intern to support our regulatory team in ensuring compliance with Canada Medical Devices Regulations.

This role offers a unique opportunity to gain hands-on experience in the medical device industry. Key responsibilities/essential functions include: • Create regulatory compliance / project plan to ensure all requirements are met for country submissions and liaise with relevant personnel to ensure appropriate, timely input is provided for submissions.

• Support regulatory compliance and optimization of quality system procedures relating to new product registration submissions through the development, maintenance and improvement of documented processes.

• Support regulatory inspections as required • Establish plan and deliverables for timely submission of annual medical device licence and establishment licence renewal • File and maintain regulatory deliverables Required Qualifications: • Bachelor’s Degree in a related field such as: Biomedical Engineering, Biology, Chemistry, Life Sciences, and completion of postgraduate Regulatory Affairs program OR Bachelor’s Degree and minimum of 1 year regulatory affairs experience in medical device industry or medical product regulation agencies, including knowledge and experience applying device laws and regulations.

• Strong analytical skills • Ability to work in a team environment with minimal supervision on projects and activities • Ability to prioritize, plan & evaluate deliverables • Knowledge & experience conducting scientific, regulatory, legal, or business research.

• Excellent verbal and written communication and presentation skills with the ability to communicate in English in an easy to understand manner Preferred Qualifications: • Experience in medical device industry.

• Knowledge of Quality Management Systems (QMS). • Experience working across cultures/countries/sites. • Demonstrated experience interfacing with regulatory agencies (e.

g. Health Canada, FDA). • Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment.