Drive regulatory excellence with Adecco as a Regulatory Affairs Project Manager in Ottawa. This full-time contract role emphasizes IVD projects and global compliance in the medical device sector.

Adecco is searching for an experienced Regulatory Affairs Project Manager to support their international regulatory team. With 5–8 years of regulatory affairs experience in medical devices, you will lead cross-functional projects and develop regulatory strategies. This position requires solid project management skills and compliance knowledge with global standards throughout the product lifecycle.

Key Responsibilities:
• Lead regulatory workstreams for IVD medical device projects
• Collaborate on regulatory strategies for product registration




• Develop and maintain project plans and timelines
• Monitor project progress and implement mitigation strategies
• Support regulatory activities throughout product lifecycle

Requirements:
• Legally eligible to work in Canada
• Bachelor’s degree in a relevant field
• 5-8 years of experience in regulatory affairs
• 2-3 years of project management experience
• Strong understanding of global regulatory frameworks

Maximize your impact in healthcare innovation with Adecco, focusing on IVD and global regulations.
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📌 Regulatory Affairs Project Manager in Ottawa (Quebec City)
🏢 Adecco Canada
📍 Quebec City