Enhance healthcare regulations as a Regulatory Affairs Specialist with Abbott in Mississauga, Canada. Contribute to regulatory applications and ensure compliance in the medical device sector.
Abbott is seeking a Regulatory Affairs Specialist to join their Medical Devices division. This on-site role requires staying updated on Canadian medical regulations and working closely with Health Canada. You’ll prepare robust regulatory applications, review engineering changes, and maintain essential communication across teams to adhere to compliance standards.
Key Responsibilities:
• Prepare regulatory applications aligned with organizational goals
• Review and approve engineering changes promptly
• Analyze regulatory guidelines and project assessments
• Ensure compliance with Canadian medical device regulations
• Interface directly with Health Canada for submissions
Requirements:
• Bachelor’s degree in Life Sciences or Engineering
• 3 to 5 years of regulatory experience
• Knowledge of Canadian medical device regulations
• Strong communication and organizational skills
• Ability to work in a matrixed environment
Contribute your expertise in regulatory affairs and compliance within Abbott's agile healthcare team.
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