Join BioScript Solutions as an Associate Manager in Pharmacovigilance Quality, where you will enhance safety reporting and compliance practices in a remote-friendly setting. 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 (Canada)
🏢 BioScript Solutions group
📍 Canada