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Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs and Quality Assurance to support regulatory compliance and quality activities for its Canadian portfolio. The ideal candidate will have over five years of regulatory experience in the pharmaceutical or biotechnology industry, specifically with Health Canada, and will be responsible for managing submissions and mentoring junior team members.
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Job Summary
This role supports the regulatory and quality activities for Ferring Canada's portfolio ensuring timely approvals and ongoing compliance.
The successful candidate will act as a mentor for junior team members while managing complex regulatory matters independently.
Ferring offers a comprehensive benefits package including an inclusive support program for employees building families.
Matching Summary
Match Score: 75
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Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs and Quality Assurance to support regulatory compliance and quality activities for its Canadian portfolio. The ideal candidate will have over five years of regulatory experience in the pharmaceutical or biotechnology industry, specifically with Health Canada, and will be responsible for managing submissions and mentoring junior team members.
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Salary
Base: $80,000 – $119,000 CAD annually; Bonus/Equity: Not specified; Benefits: Comprehensive benefits package including family building support
Skills & Requirements
Must-have
Health Canada regulatory submissions
cGMP standards compliance
Product lifecycle regulatory strategy
CMC submission support
Document lifecycle management
Nice-to-have
Mentoring junior team members
Proactive problem-solving skills
Cross-functional collaboration
Entrepreneurial culture fit
Key Requirements
Bachelor's degree in Life Sciences or related field
5+ years of progressive regulatory affairs experience