Advance your career with Abbott as a Regulatory Affairs Specialist in Mississauga. This on-site role involves regulatory applications, compliance, and communications with Health Canada.
Located at Abbott's Mississauga office, this position requires four days onsite with one remote day. As a Regulatory Affairs Specialist, you'll be integral in preparing regulatory applications and ensuring compliance with Canadian medical device regulations. You will interact directly with Health Canada and provide crucial support in product release processes while collaborating across teams to meet project objectives.
Key Responsibilities:
• Prepare regulatory applications to meet organizational goals
• Review and approve engineering changes with diligence




• Maintain current Canadian medical device regulations
• Interface with Health Canada for regulatory compliance
• Collaborate with cross-functional project teams as needed
Requirements:
• 3-5 years of regulatory affairs experience
• Knowledge of Canadian medical device regulations
• Robust communication skills at multiple organizational levels
• Ability to work in a matrixed environment
• Detail-oriented with strong organizational skills
Utilize your expertise in regulatory affairs to enhance Abbott's mission of improving health globally.
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📌 Regulatory Affairs Specialist in Mississauga
🏢 Thornton Tomasetti
📍 Mississauga