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Mint Pharmaceuticals

Pharmacovigilance Leader

Mississauga, ON, Canada

Full-time

Apply on LinkedIn About employer

Applications open in a new tab.

Job details

Job type: Full-time
Apply by: Dec 12, 2026
Posting language: English
Posted: Nov 12, 2026

Original job description

Pharmacovigilance Leader (Level commensurate with experience)

Mississauga, Ontario, Canada

Full Time (Hybrid)

About Mint Pharmaceuticals: Mint Pharmaceuticals is a Canadian pharmaceutical company recognized for its commitment to quality, compliance, innovation, and patient safety. Through our growing portfolio and strategic partnerships, we strive to make healthcare more accessible while upholding the highest standards of pharmaceutical excellence.

As we continue to expand, we are seeking exceptional leaders who are passionate about advancing healthcare, driving operational excellence, and building high-performing teams that make a lasting impact on patients, customers, and the healthcare community.

Position Summary

Reporting to the Vice President, Quality & Pharmacovigilance, Pharmacovigilance Leader will provide strategic leadership and operational oversight of Mint's global Pharmacovigilance system. This incumbent will serve as the company's Pharmacovigilance Subject Matter Expert and primary PV contact for business partners, vendors, and internal stakeholders.

The incumbent will drive compliance, inspection readiness, safety surveillance, signal management, aggregate reporting, Risk Management Plans (RMPs), foreign action notifications, Access to Information requests, and continuous improvement initiatives across the Pharmacovigilance function.

Key Responsibilities

Leadership & Compliance

Lead and oversee Mint's Pharmacovigilance program.
Maintain and continuously improve the PV Quality Management System.
Provide strategic PV guidance to senior leadership.
Ensure ongoing inspection readiness and regulatory compliance.
Support product launches, acquisitions, licensing agreements, and business development activities.

Safety Operations

Oversee adverse event, literature, medical inquiry, and product quality complaint processing.
Ensure timely submission of ICSRs and regulatory safety reports.
Maintain oversight of safety databases, coding practices, and reconciliation activities.
Ensure compliance with regulatory reporting timelines and data integrity requirements.

Signal Management & Risk Management

Lead signal detection, evaluation, and benefit-risk assessments.
Develop and maintain Risk Management Plans (RMPs).
Evaluate emerging safety issues and implement risk mitigation strategies.
Collaborate on safety communications and product labeling updates.

Health Authority Interactions

Oversee PSURs, PBRERs, Annual Summary Reports, and aggregate safety reporting.
Serve as the primary Pharmacovigilance contact for Health Canada.
Lead inspections, audits, regulatory inquiries, and agency responses.
Monitor evolving Canadian PV requirements and implement changes as needed.

Regulatory Intelligence & PV Governance

Manage Foreign Action Notifications and regulatory intelligence activities.
Support Access to Information requests and regulatory transparency initiatives.
Establish and maintain Safety Data Exchange Agreements and Pharmacovigilance Agreements.
Develop and maintain PV Business Continuity and Disaster Recovery Plans to ensure uninterrupted operations and regulatory compliance during business disruptions.

People Leadership

Lead, mentor, and develop a high-performing Pharmacovigilance team.
Support talent development, succession planning, and training initiatives.
Foster a culture of compliance, accountability, collaboration, and continuous improvement.

Qualifications

Degree in Pharmacy, Nursing, Medicine, Dentistry, or related healthcare discipline.
Qualified Healthcare Professional (QHP) designation preferred.
5-10 years of Canadian Pharmacovigilance, Drug Safety, Medical Information, or related pharmaceutical industry experience.
Minimum 5 years of leadership experience within Pharmacovigilance or a regulated healthcare environment.
Strong working knowledge of Health Canada, FDA, EMA, and ICH Pharmacovigilance requirements.
Experience with safety databases such as Veeva Vault Safety, Argus Safety, or ARISg is preferred.
Bilingual English/French is considered an asset.

Why Join Mint?

Opportunity to build and shape a growing global Pharmacovigilance function.
High visibility role with direct interaction with senior leadership and health authorities.
Collaborative and dynamic environment where your contributions make a measurable impact.
Competitive compensation package and professional development opportunities.
Hybrid work environment based in Mississauga, Ontario.

Apply Today

If you are a passionate Pharmacovigilance leader looking to make a meaningful impact on patient safety while helping shape the future of a growing Canadian pharmaceutical company, we would love to hear from you.
Apply through LinkedIn or submit your resume to poonamp@mintpharma.com

Compensation & Benefits

Salary Range: Commensurate with level.

Apply on LinkedIn About employer

More about this job

Responsibilities

Lead Mint's global pharmacovigilance program, quality system, safety operations, signal and risk management, aggregate reporting, and regulatory compliance. Serve as the primary pharmacovigilance contact for Health Canada and business partners while leading inspections, regulatory interactions, and the development of a high-performing team.

Requirements

Requires a degree in Pharmacy, Nursing, Medicine, Dentistry, or a related healthcare discipline, with a Qualified Healthcare Professional designation preferred. Candidates should have 5–10 years of relevant Canadian industry experience, at least five years of leadership experience, and working knowledge of Health Canada, FDA, EMA, and ICH requirements; experience with Veeva Vault Safety, Argus Safety, or ARISg is preferred.

Skills

Pharmacovigilance Leadership
Pharmacovigilance Compliance
Pharmacovigilance Quality Management Systems
Adverse Event Processing
Individual Case Safety Reports
Signal Detection and Management
Benefit-Risk Assessment
Risk Management Plans
Aggregate Safety Reporting
Health Authority Interactions
Regulatory Intelligence
Inspection and Audit Readiness
Safety Database Oversight
Safety Data Exchange Agreements
Team Leadership and Development
Business Continuity Planning

Benefits

Professional Development Opportunities

Visa sponsorship

Not detected in the job text

Keywords

Pharmacovigilance
Drug Safety
Health Canada
FDA
EMA
ICH
Veeva Vault Safety
Argus Safety
ARISg
Qualified Healthcare Professional
Adverse Events
Individual Case Safety Reports
Literature Monitoring
Medical Information
Product Quality Complaints
Signal Detection
Benefit-Risk Assessment
Risk Management Plans
PSURs
PBRERs
Annual Summary Reports
Foreign Action Notifications
Access to Information Requests
Safety Data Exchange Agreements
Pharmacovigilance Agreements
Regulatory Intelligence
Inspection Readiness
Business Continuity Planning
Disaster Recovery Planning

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