Advance your career with Bausch Health as a Regulatory Affairs Associate (CMC) in Laval, Québec. This 12-month hybrid contract emphasizes a balance of onsite collaboration and remote flexibility.
The ideal candidate will hold a Health Sciences degree and possess at least one year of relevant experience in regulatory affairs within pharmaceuticals. You will update CPIDs, prepare L3 submissions to support compliance, and engage with key stakeholders. Proficiency in VEEVA and TRACKWISE software will be beneficial.
Key Responsibilities:
• Maintain and update CPIDs and regulatory dossiers
• Evaluate and determine change control requirements
• Prepare L3 submissions for compliance with Health Canada
• Communicate with internal and external partners effectively
• Stay informed on all Health Canada regulations
Requirements:
• A B.Sc or master’s degree in Health Sciences
• One year of pharmaceutical regulatory experience
• Knowledge of industry guidelines and dr...