Regulatory Affairs & Quality Senior Specialist

FERRING PHARMACEUTICALS AS

Canada
Base: $80,000 – $119,000 cad annually; bonus/equit...
**
Health canada regulatory submissions experience
Cgmp standards compliance knowledge
Product registration and amendment management
** Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs & Quality Assurance to support regulatory and quality activities for their Canadian portfolio. The ideal candidate will have over five years of experience in regulatory affairs within the pharmaceutical or biotechnology industries, particularly with Health Canada, and will be responsible for ensuring compliance and guiding cross-functional teams. **

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 including family building support policies.

Matching Summary

Match Score: 75

** Ferring Pharmaceuticals is seeking a Senior Specialist in Regulatory Affairs & Quality Assurance to support regulatory and quality activities for their Canadian portfolio. The ideal candidate will have over five years of experience in regulatory affairs within the pharmaceutical or biotechnology industries, particularly with Health Canada, and will be responsible for ensuring compliance and guiding cross-functional teams. **

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 experience
  • cGMP standards compliance knowledge
  • Product registration and amendment management
  • CMC submission support capabilities
  • Document lifecycle management skills

Nice-to-have

  • Mentoring junior team members
  • Strategic regulatory input provision
  • Cross-functional collaboration abilities
  • Proactive problem-solving mindset
  • Risk management implementation planning

Key Requirements

  • Bachelor's degree in Life Sciences, Pharmacy, Chemistry, or related field
  • 5+ years of progressive regulatory affairs experience in pharmaceuticals or biotechnology
  • Proven experience working with Health Canada preparing Canadian regulatory submissions

Work Rights

Not specified

Tailored Resume

Cover Letter