Join Adecco as an International Regulatory Affairs Project Manager in Ottawa, focusing on IVD medical devices and global compliance strategies. This temporary role is ideal for experienced professionals.
Adecco seeks a Regulatory Affairs Project Manager to manage projects within the medical device sector. You will be part of an international team, leveraging 5-8 years of regulatory affairs experience and 2-3 years in project management. Your role will involve developing regulatory strategies and ensuring adherence to international regulations throughout the product lifecycle.
Key Responsibilities:
• Lead project efforts for IVD medical devices
• Develop and document regulatory strategies
• Monitor project timelines and deliverables
• Support regulatory submissions and market authorizations
• Ensure compliance with international regulatory standards
Requirements:
• Must work legally in Canada
• Bachelor’s degree in a relevant discipline
• 5-8 years of experience in regulatory affairs
• 2-3 years leading regulatory projects
• Strong understanding of global regulatory frameworks
Enhance your skills and make an impact with Adecco in the evolving healthcare landscape.
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