Medline Canada is seeking a Director of Quality Assurance & Regulatory Affairs to lead regulatory compliance and quality assurance activities. The ideal candidate will have extensive experience in the medical device or pharmaceutical industry, coupled with strong leadership and communication skills
Job Summary
This role reports to the Sr. Director, International Regulatory at Corporate and is responsible for overseeing all quality and regulatory activities at Medline Canada.
The position requires implementing GMP compliance across facilities and directing QA/RA employees in Guelph and Terrebonne to ensure efficient operations.
Medline Canada offers a competitive benefits package including LTD & Insurance, DPSP match, fitness subsidies, and career growth programs.
Matching Summary
Match Score: 85
Medline Canada is seeking a Director of Quality Assurance & Regulatory Affairs to lead regulatory compliance and quality assurance activities. The ideal candidate will have extensive experience in the medical device or pharmaceutical industry, coupled with strong leadership and communication skills.
Salary
Base: $143,400.00 - $215,000.00 Annual; Bonus/Equity: Not specified; Benefits: Competitive compensation plan including LTD, Insurance, DPSP match, and more
Skills & Requirements
Must-have
10 years medical device or pharma experience
5 years people management experience
Expert knowledge of Health Canada regulations
GMP compliance implementation
Regulatory application submission to Health Canada
Nice-to-have
SAP software proficiency
ISO regulation alignment
Mentoring and staff development skills
Strategic communication with senior leadership
Collaborative work environment experience
Key Requirements
Bachelor of Science degree
Minimum 10 years progressive experience in medical device/pharma
At least 5 years managing people
Excellent written and verbal English communication
Proficiency in Microsoft Office (SAP asset)
Work Rights
Canadians and permanent residents will be given priority