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Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs & Quality to manage regulatory submissions and ensure compliance with Health Canada and cGMP standards. The ideal candidate will have over five years of regulatory experience, strong communication skills, and a proactive approach to complex regulatory matters.
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Job Summary
The role involves managing regulatory submissions, amendments, and periodic reports to ensure timely approvals in Canada.
Candidates will act as a mentor for junior team members while ensuring compliance with Health Canada requirements and cGMP standards.
The position offers a salary range of $80,000 – $119,000 CAD annually along with comprehensive benefits and family-building support.
Matching Summary
Match Score: 75
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Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs & Quality to manage regulatory submissions and ensure compliance with Health Canada and cGMP standards. The ideal candidate will have over five years of regulatory experience, strong communication skills, and a proactive approach to complex regulatory matters.
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Salary
Base: $80,000 – $119,000 CAD annually; Bonus/Equity: Not specified; Benefits: Comprehensive package including parental leave and family building support
Skills & Requirements
Must-have
Health Canada regulatory submissions
cGMP standards compliance
CMC submission support
Product lifecycle management
Document lifecycle management
Nice-to-have
Mentoring junior team members
Strategic risk management
Cross-functional collaboration
Proactive problem solving
Entrepreneurial culture fit
Key Requirements
Bachelor's degree in Life Sciences or related field
5+ years of progressive regulatory affairs experience