Jobs in Milton

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Within 25 km of Milton

Added 9 hours ago
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REGULATORY AFFAIRS INTERN
GE HealthCare
Mississauga, ON
Added 10 hours ago
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GE HealthCare

REGULATORY AFFAIRS INTERN

Mississauga, ON, Canada

Full-time

Within 25 km of Milton · About 21.5 km from the city centre

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Job details

Job type: Full-time
Posted: Nov 10, 2026

Original job description

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

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More about this job

Responsibilities

The intern will support premarket and compliance activities, including creating project plans for country submissions and maintaining quality system procedures. They will also assist with regulatory inspections and the renewal of medical device and establishment licences.

Requirements

Candidates must hold a Bachelor's degree in a relevant scientific or engineering field and have completed a postgraduate Regulatory Affairs program. Alternatively, applicants may have a Bachelor's degree with at least one year of experience in the medical device industry or regulatory agencies.

Skills

Regulatory compliance
Medical device regulations
Project planning
Quality management systems
Regulatory submissions
Analytical skills
Scientific research
Communication
Presentation skills
Documentation
Process improvement
Regulatory inspections
Health Canada regulations
FDA regulations

Visa sponsorship

Not detected in the job text

Keywords

Regulatory Affairs
Medical Devices
Compliance
Premarket
Quality Management Systems
QMS
Health Canada
FDA
Biomedical Engineering
Biology
Chemistry
Life Sciences
Licence Renewal
Regulatory Submissions
Process Improvement
Documentation
Project Management

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