Posted yesterday
REGULATORY AFFAIRS INTERN
@ GE HealthCare Technologies Canada
Mississauga, Ontario
Overview
GE HealthCare Technologies Canada is hiring a Regulatory Affairs Intern for a full-time role supporting the regulatory team on Canada Medical Devices Regulations compliance. The intern will help with premarket submissions, quality system procedures, regulatory inspections and licence renewals.
Responsibilities:
- Plan regulatory compliance and country submissions
- Support quality system procedures for product registration
- Support regulatory inspections
- Plan annual medical device and establishment licence renewals
- File and maintain regulatory deliverables
Requirements summary:
- Bachelor's degree in biomedical engineering, biology, chemistry or life sciences
- Postgraduate regulatory affairs program or one year regulatory experience
- Strong analytical skills
- Ability to work in a team with minimal supervision
- Excellent English communication and presentation skills
Source and dates
Employer career site / ATS feed · workday
- Employer posting date
- 2026-11-09
- First seen by our source
- 2026-11-10
- Source record updated
- 2026-11-10
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Quality assurance |
| Hours per week | 40 (estimated) |
| Work setting | Office |
| Position | Mostly sitting |
| Physical demands | physical low · computer high |
| Languages | English |
| Education | Bachelor’s degree (required) |
| Fields of study | Biomedical Engineering, Biology, Chemistry, Life Sciences |
Summary and details written by AI from the posting; the employer’s posting is the authority.
GE HealthCare Technologies Canada
| Field | Value |
|---|---|
| Open jobs on Jobsy | 12 |
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.
Additional Information
Relocation Assistance Provided: No
Journal
Only you can see this. Kept on this device, and in your account when you sign in.