Regulatory Affairs & Quality Senior Specialist

Ferring Pharmaceuticals

Canada
Base: $80,000 – $119,000 cad annually; bonus/equit...
Not specified (assumed to be hybrid based on industry standards).
Health canada regulatory submissions
Cgmp standards compliance
Product registration and amendments
Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs and Quality to support regulatory and quality activities for its Canadian portfolio. The ideal candidate will have over five years of experience in regulatory affairs within the pharmaceutical or biotechnology sectors, with a strong focus on compliance and strategic input

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 family building support program and parental leave.

Matching Summary

Match Score: 85

Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs and Quality to support regulatory and quality activities for its Canadian portfolio. The ideal candidate will have over five years of experience in regulatory affairs within the pharmaceutical or biotechnology sectors, with a strong focus on compliance and strategic input.

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 registration and amendments
  • CMC submission support
  • Document lifecycle management
  • Change control and CAPA management

Nice-to-have

  • Mentoring junior team members
  • Strategic regulatory input
  • Cross-functional collaboration
  • Proactive problem solving
  • Entrepreneurial culture fit

Key Requirements

  • Bachelor's degree in Life Sciences or related field
  • 5+ years progressive regulatory affairs experience
  • Proven experience with Health Canada submissions
  • Strong understanding of change control processes

Work Rights

Not specified

Tailored Resume

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