Join BioScript Solutions as an Associate Manager in Pharmacovigilance Quality, where you will enhance safety reporting and compliance practices in a remote-friendly workplace. 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 environment 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. #J-18808-Ljbffr

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