Elevate your regulatory career with Adecco as an IVD Regulatory Affairs Manager in Ottawa. Focus on project leadership and strategic compliance in the medical device field.

Adecco is recruiting a Regulatory Affairs Project Manager for a contract role emphasizing IVD medical devices. Ideally, you will have 5-8 years of regulatory experience and robust project management abilities. By joining the international regulatory team, you will ensure compliance and lead vital regulatory projects that contribute to market success.

Key Responsibilities:
• Coordinate regulatory workstreams for medical device projects
• Collaborate with international teams on strategies
• Track project timelines, milestones, and risks
• Facilitate meetings and communicate updates
• Support ongoing regulatory processes and submissions

Requirements:
• Eligible to work in Canada
• Bachelor’s degree in Life Sciences or related field
• 5-8 years of Regulatory Affairs experience
• 2-3 years managing cross-functional projects
• Knowledge of Health Canada Medical Devices Regulations

Join Adecco to drive innovative regulatory solutions in the dynamic medical device industry.
#J-18808-Ljbffr

📌 Ottawa IVD Regulatory Affairs Manager (Quebec City)
🏢 Adecco Canada
📍 Quebec City