Support GxP compliance at Sentrex Health Solutions with quality systems administration, Standard Operating Procedures, and pharmacovigilance reporting in Markham.
This full-time Pharmacovigilance Associate works within QA and PV, supporting the Quality Management System alongside adverse event operations. You will help drive compliance, improve process efficiency with internal teams, and maintain documentation for audit readiness. The hybrid arrangement requires office attendance two to three days weekly.
Key Responsibilities:
- Help administer the Quality Management System
- Create and review Standard Operating Procedures and Work Instructions
- Contribute to organizational compliance objectives and process efficiencies
- File and archive pharmacovigilance documents electronically
- Deliver pharmacovigilance training and reconcile cases
Requirements:
- Three-plus years of pharmaceutical setting experience
- Three-plus years in pharmacovigilance or relevant industry experience
- Familiarity with Health Canada GxP and GVP regulations
- Experience with QMS is an asset
- Ability to prioritize, multitask, and meet tight deadlines
Use quality systems, documentation, and pharmacovigilance expertise to strengthen compliant operations for Sentrex Health Solutions.
📌 Quality Systems Pharmacovigilance Specialist (Markham)
🏢 Sentrex Health Solutions
📍 Markham
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.