Join BioScript Solutions as an Associate Manager in Pharmacovigilance Quality, where you will enhance safety reporting and compliance practices in a remote-friendly environment. This full-time position is based in the Greater Toronto Area.

In this role, you will oversee and enhance the pharmacovigilance compliance framework, driving quality initiatives and monitoring key performance metrics. A minimum of 5 years experience in pharmacovigilance or a regulated healthcare setting is required. You will also lead training development and address any deviations effectively.

Key Responsibilities:
• Maintain compliance with safety reporting frameworks
• Oversee quality reviews and monitoring metrics
• Lead investigations into pharmacovigilance deviations




• Develop and manage training programs for team members
• Implement process improvements in documentation

Requirements:
• Bachelor's degree in Health Sciences or related field
• 5+ years in pharmacovigilance or healthcare
• Knowledge of adverse event reporting requirements
• Experience with quality assurance practices
• Ability to manage training and guide staff

Elevate your expertise in pharmacovigilance quality with a team that values your contribution.
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📌 Associate Manager in Pharmacovigilance Quality (Manitoba)
🏢 BioScript Solutions group
📍 Manitoba