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.