Canadian Regulatory Affairs Officer
3 days ago
Mississauga, Peel Region, Canada
CV Warehouse
Full-time
€70,000 - €110,000 Contract
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Support Canadian compliance through Health Canada submissions, product registration, and detailed regulatory documentation. Help maintain requirements across products, processes, and records.
This Regulatory Affairs Officer supports compliance activities across the Canadian market. You will prepare filings, coordinate registrations, and interpret Health Canada regulations. The work also connects with Quality, R&D, Operations, Marketing, external partners, consultants, and regulatory agencies.
Key Responsibilities
- Prepare, review, and submit Health Canada regulatory filings
- Coordinate product registrations, licenses, renewals, and amendments
- Maintain technical files and compliance records
- Support teams with regulatory interpretation and guidance
- Liaise with agencies, consultants, and external partners
Requirements:
- Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or related field
- Two to five years of regulatory affairs experience
- Understanding of Health Canada regulations and sector frameworks
- Excellent attention to detail and technical writing skills
- Quality systems experience, including ISO 13485 or GMP, is an asset Apply regulatory expertise, technical writing, and Health Canada knowledge to support compliant products across Canada.
Key Responsibilities
- Prepare, review, and submit Health Canada regulatory filings
- Coordinate product registrations, licenses, renewals, and amendments
- Maintain technical files and compliance records
- Support teams with regulatory interpretation and guidance
- Liaise with agencies, consultants, and external partners
Requirements:
- Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or related field
- Two to five years of regulatory affairs experience
- Understanding of Health Canada regulations and sector frameworks
- Excellent attention to detail and technical writing skills
- Quality systems experience, including ISO 13485 or GMP, is an asset Apply regulatory expertise, technical writing, and Health Canada knowledge to support compliant products across Canada.