Compliance Specialist II - Regulatory Affairs
Core
Ensure products and operations comply with Canadian and international regulatory requirements, supporting product onboarding and business continuity.
Role type
mid-level IC regulatory affairs specialist
Builds
compliant product launches and operational processes for life sciences and medical device customers
Domain
Life Sciences / Medical Devices / Chemical Compliance
Required skills
regulatory assessments, permit/license maintenance, regulatory change monitoring, audit support, SOP development, cross-functional collaboration
Preferred skills
French language proficiency, experience with Health Canada Medical Device regulations, chemical compliance framework knowledge
Technologies
Microsoft Office
Responsibilities
Conduct regulatory assessments for new products, review product inquiries for compliance, maintain regulatory permits and licenses, monitor regulatory changes and assess business impact, support internal and external audits, develop and maintain SOPs
Seniority
Mid-level, hands-on IC