Step into the pivotal role of Regulatory Affairs Specialist at Johnson & Johnson in Markham, Ontario. Oversee compliance and regulatory strategies for complex medical devices to elevate healthcare solutions.

In this position, you will develop and execute regulatory strategies for Class III and Class IV medical devices, ensuring alignment with corporate and Health Canada requirements. Your expertise will guide internal stakeholders while you manage the entire product lifecycle from pre-market to post-marketing phases. Building strong relationships with Health Canada is crucial as you navigate submission strategies and compliance protocols.

Key Responsibilities:
• Develop Canadian regulatory strategies for medical devices
• Manage product lifecycle and promotional material approvals




• Provide regulatory guidance to business partners
• Maintain quality management system in line with regulations
• Support audits and inspections from health authorities

Requirements:
• Bachelor's degree in Life Science or related field
• 3-5 years in Medical Device Regulatory Affairs
• Knowledge of Food and Drugs Act regulations
• Solid communication and documentation skills
• Proven ability to foster strong partnerships

Leverage your regulatory expertise to make a meaningful impact at Johnson & Johnson in Ontario.
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📌 Regulatory Affairs Specialist in Ontario
🏢 Johnson & Johnson
📍 Ontario