Become a pivotal member of Medtronic as a Regulatory Affairs Specialist. Focus on ensuring compliance and accelerating approvals for cutting-edge medical devices.
You will lead the preparation of regulatory submissions and engage with agencies to facilitate timely approvals. This role involves collaboration with various experts to navigate challenges and recommend compliance strategies. Your efforts will directly impact patient care by ensuring that high-quality products meet regulatory standards.
Key Responsibilities:
• Coordinate document preparation for regulatory applications
• Identify compliance needs for product changes
• Collaborate with teams to tackle regulatory inquiries
• Conduct audits and maintain systems for regulatory tracking
• Foster relationships with regulatory agencies for effective communication
Requirements:
• Bachelor’s degree required
• Minimum of 2 years in regulatory affairs
• Experience with Health Canada is a plus
• Proficient in project management and analytical tasks
• Strong verbal and written communication skills
Utilize your regulatory expertise to enhance healthcare impact at Medtronic.
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