Support Canadian regulatory submissions at GSK as a Regulatory Affairs Associate, using scientific judgment and collaboration in a hybrid Mississauga role.

This 12-month contract supports regulatory activities across GSK’s portfolio of vaccines, specialty medicines, and general medicines. You will contribute to submission planning, Health Canada communications, compliance, and project issue resolution. The position suits a scientific qualified with some regulatory affairs experience.

Key Responsibilities:

- Provide input into submission and activity planning
- Assist with NDS, SNDS, CTA, and NC preparation
- Ensure compliance with Health Canada, industry, and GSK guidelines
- Prepare internal reports and Health Canada responses
- Communicate project plans and issues with global and local teams

Requirements:

- Bachelor of Science in life science or relevant scientific field
- Some experience in regulatory affairs
- Understanding of Canadian Food and Drug Regulations
- Knowledge of submission requirements and processes
- Experience working with Veeva Vault

Bring regulatory knowledge, attention to detail, and collaborative communication to GSK’s Canadian regulatory affairs activities.

📌 Regulatory Affairs Associate Canada (Mississauga)
🏢 GSK
📍 Mississauga