Regulatory Affairs Intern

Descripción del puesto:

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