Director Quality & Pharmacovigilance

E.A. Associates

Canada

On-site

CAD 175,000 - 200,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

A leading healthcare organization in Canada seeks a Director of Quality & Pharmacovigilance to oversee quality assurance services and ensure compliance with regulations. Ideal candidates will have over 10 years of leadership experience in healthcare or pharma, with expertise in quality systems and regulatory compliance. This full-time role offers a competitive salary with significant responsibilities in shaping organizational quality culture.

Qualifications

  • 10+ years’ experience in healthcare, pharma, or regulated industries.
  • Experience leading Quality Functions across multiple disciplines.
  • Proven expertise in QMS, CAPA, GxP audits, and Health Canada compliance.

Responsibilities

  • Develop and maintain a Quality Management System (QMS).
  • Ensure compliance with external regulations.
  • Manage departmental budgets and quality assurance functions.
  • Direct and implement quality auditing programs.
  • Collaborate with Senior Leadership on quality issues.

Skills

Leadership
Quality Management System (QMS)
Pharmacovigilance
Regulatory Compliance
Strategic Mindset
Communication
Bilingualism (French/English)

Education

Bachelor's or Master's degree in a Life Science discipline

Job description

Base pay range

CA$175,000.00/yr - CA$200,000.00/yr

This range is provided by E.A. Associates. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

🚀 Exciting Leadership Opportunity in Quality & Patient Safety!

Are you ready to lead with purpose and shape the future of quality and pharmacovigilance in a growing, mission-driven organization? We’re searching for an exceptional leader who’s passionate about driving excellence, elevating compliance, and ensuring patients remain at the heart of everything our client does.

The Director, Quality & Pharmacovigilance reports directly into the CEO and oversees the delivery of quality assurance and pharmacovigilance services for day-to-day operations (i.e. GMP Operations, Pharmacovigilance, Patient Support Programs, Nursing and Clinics, and Pharmacies). This role is responsible for designing, planning, implementing, directing and evaluating quality assurance and pharmacovigilance functions, and the quality management system as a whole, for product and service delivery across the client company. The Director, Quality & Pharmacovigilance is also responsible for establishing and maintaining a culture of continual improvement, and for promoting collaboration across all business units. This individual will work collaboratively with Senior Leadership, Directors and Managers in the evaluation of product quality assurance and business operations and will identify, recommend and implement necessary changes.

Primary Duties and Responsibilities
  • Develop, implement and maintain a Quality Management System (QMS) that ensures ongoing compliance with external regulations, internal company quality standards, and customer requirements.
  • Develop and maintain the Pharmacovigilance function to ensure ongoing compliance with external regulations, internal company quality standards, and customer requirements as they apply to the reporting of Safety incidents and data.
  • Formulate and administer policies and standard operating procedures (SOPs) relating to the quality assurance and pharmacovigilance functions that will ensure compliance, foster a culture of continual improvement, and encourage innovation.
  • Define, develop and implement both short- and long-term strategies, goals, objectives and tactics relating to the quality assurance and pharmacovigilance functions.
  • Ensure that all functions that interact with the QMS (i.e., Warehousing & Importation, Pharmacovigilance, Patient Support Programs, Nursing and Clinics, and Pharmacies) are operating in conformance with all applicable quality standards and regulations.
  • Ensure that Adverse Events and other reportable events are reported in accordance with both regulatory requirements and contractual obligations.
  • Use quality event investigations (e.g. deviations), incidents, corrective and preventive action (CAPA) investigations, and their associated processes, to drive quality improvements and respond to process and service issues.
  • Develop and implement an effective training program for internal departments and functions that have quality assurance and pharmacovigilance responsibilities.
  • Implement an internal quality auditing program covering all quality and pharmacovigilance related activities (including applicable vendors and subcontractors).
  • Ensure all applicable programs, systems, and facilities are ’inspection ready’ at all times.
  • Develop and propose key quality, compliance and performance indicators.
  • Analyze the performance of quality assurance and pharmacovigilance functions, document resolutions, identify problem areas, and devise / deliver solutions to enhance quality control and prevent recurrence.
  • Keep the Senior Leadership team appraised of all quality assurance and pharmacovigilance issues as appropriate.
  • Direct and manage departmental budgets and goals for the quality assurance and pharmacovigilance functions.
  • Manage government interactions requiring governmental approvals, including liaison with Health Canada and other regulatory agencies as appropriate.
What You Bring
  • Bachelor’s or Master’s degree in a Life Science discipline.
  • 10+ years’ experience in healthcare, pharma, or regulated industries, leading quality and/or pharmacovigilance functions.
  • Experience leading Quality Functions across multiple disciplines (i.e., GMP operations, Patient Support Programs, Distribution).
  • Proven expertise in QMS, CAPA, GxP audits, and Health Canada compliance.
  • Strategic mindset with hands‑on execution capability.
  • Strong communicator with exceptional emotional intelligence.
  • Bilingualism (French/English) is an asset.
Seniority level

Director

Employment type

Full-time

Job function

Quality Assurance

Industries: Pharmaceutical Manufacturing and Biotechnology Research

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Director of Quality
Director of Quality

Confidential • Montreal

On-site
CAD 110,000 - 140,000
Director, Quality & Pharmacovigilance — Lead Patient Safety
Director, Quality & Pharmacovigilance — Lead Patient Safety

E.A. Associates • Canada

On-site
CAD 175,000 - 200,000
Senior Director, Regulatory & Quality
Senior Director, Regulatory & Quality

TalentSphere Staffing Solutions • Vancouver

On-site
CAD 150,000 - 175,000
Competitive wages
Health, dental, and medical benefits
Performance-based bonuses
+3
Spécialiste senior, Assurance qualité et conformité
Spécialiste senior, Assurance qualité et conformité

Bausch Health Companies Inc. • Laval (administrative region)

On-site
CAD 79,000 - 105,000
Director Quality Science & Technology
Director Quality Science & Technology

agilent • Charlottetown

Hybrid
CAD 131,000 - 205,000
Remote work option
Bonus and stock eligibility
Laboratory Director – Analytical Testing Laboratory
Laboratory Director – Analytical Testing Laboratory

Pathogenia Lab • Montreal (administrative region)

On-site
CAD 180,000 - 240,000
Director of Quality & Compliance – Pharma
Director of Quality & Compliance – Pharma

Confidential • Montreal

On-site
CAD 110,000 - 140,000
Directeur(trice), Assurance qualité
Directeur(trice), Assurance qualité

Vetio Animal Health • Montreal (administrative region)

On-site
CAD 90,000 - 130,000
Salaire compétitif
Avantages sociaux complets
REER collectif
+3
Senior Director Regulatory Affairs (Canada)
Senior Director Regulatory Affairs (Canada)

MedAccess Recruiters • Toronto

On-site
CAD 180,000 - 240,000
Quality Assurance Associate
Quality Assurance Associate

Insight Global • Toronto

On-site
CAD 90,000 - 110,000