Posted yesterday
REGULATORY AFFAIRS INTERN
@ GE HEALTHCARE
Mississauga, Ontario
Requirements summary:
- The Regulatory Affairs Intern will gain hands-on experience supporting premarket and compliance activities within a collaborative Regulatory Affairs team.
- This role offers a unique opportunity to gain hands-on experience in the medical device industry.
- 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…
- Support regulatory inspections as required
- Establish plan and deliverables for timely submission of annual medical device licence and establishment licence renewal
- Required Qualifications:
Tools & skills
Source and dates
Employer career site / ATS feed · phenom
- 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.
GE HEALTHCARE
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Full company description
Every day millions of people feel the impact of our intelligent devices, advanced analytics and artificial intelligence. As a leading global medical technology and digital solutions innovator, GE HealthCare enables clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services, supported by its Edison intelligence platform. With over 100 years of healthcare industry experience and around 50,000 employees globally, the company operates at the center of an ecosystem working toward precision health, digitizing healthcare, helping drive productivity and improve outcomes for patients, providers, health systems and researchers around the world. We embrace a culture of respect, transparency, integrity and diversity and we work to create a world where healthcare has no limits.
- LinkedIn followers
- 2,823,823
- People associated on LinkedIn
- 59,965
- Reported office locations
- -, Chicago, US
- Business categories
- Home Improvement
- Health Care
- Apps
- Enterprise Resource Planning (ERP)
- IT Management
- Professional Services
- Medical
- IT Infrastructure
- Manufacturing
- Health Diagnostics
- Medical Device
- Internet
- Biotechnology
- Home Renovation
- Other recorded names
- GE HealthCare
- Specialties
- Healthcare and Biotechnology
- Profile identifies a recruitment agency
- No
- Reported total investment
- 5,524,660,836
Currency and observation date were not supplied; this is not a current valuation or a funding round.
Every day millions of people feel the impact of our intelligent devices, advanced analytics and artificial intelligence. As a leading global medical technology and digital solutions innovator, GE HealthCare enables clinicians to make faster, more informed decisions through intelligent devices, data analytics, applications and services, supported by its Edison intelligence platform. With over 100 years of healthcare…
| Field | Value |
|---|---|
| Industry | Hospitals and Health Care |
| Company size | 10,001+ employees |
| Headquarters | Chicago |
| Organization type | Public Company |
| Specialties | Healthcare and Biotechnology |
| Open jobs on Jobsy | 14 |
| View page |
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.