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 • Robust understanding of global regulatory frameworks

Enhance your skills and make an impact with Adecco in the evolving healthcare landscape. #J-18808-Ljbffr

📌 International Regulatory Affairs Project Manager (Montreal)
🏢 Adecco Canada
📍 Montreal