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 workplace 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.

📌 Associate Manager In Pharmacovigilance Quality Winnipeg (Canada)
🏢 BioScript Solutions group
📍 Canada