Elevate your career with Abbott as a Regulatory Affairs Specialist based in Mississauga, Ontario. Drive regulatory applications and adhere to guidelines while working in office four days a week with remote flexibility.
In this position with Abbott's Medical division, you will play a vital role in preparing robust regulatory applications and reviewing engineering changes. You will collaborate with team members to ensure compliance with Canadian medical device regulations and health standards. Engaging with Health Canada and supporting product release processes will be essential responsibilities.
Key Responsibilities:
• Prepare regulatory applications to meet departmental goals
• Review and approve engineering changes for compliance
• Maintain up-to-date Canadian medical device regulations
• Communicate regulatory updates to relevant personnel
• Support product release requests and technical reports
Requirements:
• 3-5 years of regulatory affairs experience
• Knowledge of Canadian medical device regulations
• Strong organizational and communication skills
• Relevant degree in Life Sciences or Engineering
• Ability to work collaboratively in a diverse environment
Leverage your regulatory expertise at Abbott and support the healthcare advancements that matter most.
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