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Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs & Quality to support regulatory and quality compliance for their Canadian portfolio. The ideal candidate will have extensive experience in regulatory affairs, particularly with Health Canada, and will mentor junior team members while ensuring product quality and compliance.
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Job Summary
The role involves managing and supporting regulatory submissions including product registrations, amendments, supplements, and periodic reports for Ferring Canada's portfolio.
Candidates must ensure timely approvals and ongoing Regulatory & Quality compliance of approved products considering Health Canada requirements and cGMP standards.
This position offers a salary range of $80,000 – $119,000 CAD annually complemented by a comprehensive benefits package and inclusive family building support.
Matching Summary
Match Score: 75
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Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs & Quality to support regulatory and quality compliance for their Canadian portfolio. The ideal candidate will have extensive experience in regulatory affairs, particularly with Health Canada, and will mentor junior team members while ensuring product quality and compliance.
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Salary
Base: $80,000 – $119,000 CAD annually; Bonus/Equity: Not specified; Benefits: Comprehensive benefits package including parental leave and family building support
Skills & Requirements
Must-have
Health Canada regulatory submissions
cGMP standards compliance
Product lifecycle management
CMC submission support
Document lifecycle management
Nice-to-have
Mentoring junior team members
Cross-functional collaboration
Proactive problem solving
Strategic regulatory input
Key Requirements
Bachelor's degree in Life Sciences or related field
5+ years progressive regulatory affairs experience