Elevate your career with Abbott as a Regulatory Affairs Specialist based in Mississauga, Ontario. Drive regulatory applications and adhere to guidelines while working on-site four days a week with remote flexibility.
In this position with Abbott's Medical division, you will play a vital role in preparing robust regulatory applications and reviewing engineering changes. You will collaborate with team members to ensure compliance with Canadian medical device regulations and health standards. Engaging with Health Canada and supporting product release processes will be essential responsibilities.
Key Responsibilities:
- Prepare regulatory applications to meet departmental goals
- Review and approve engineering changes for compliance
- Maintain up-to-date Canadian medical device regulations
- Communicate regulatory updates to relevant personnel
- Support product release requests and technical reports
Requirements:
- 3-5 years of regulatory affairs experience
- Knowledge of Canadian medical device regulations
- Strong organizational and communication skills
- Relevant degree in Life Sciences or Engineering
- Ability to work collaboratively in a diverse environment
Leverage your regulatory expertise at Abbott and support the healthcare advancements that matter most.
Regulatory Affairs Specialist at Abbott in Mississauga employer: Abbott
Abbott is an exceptional employer, offering a dynamic work environment in Ottawa where innovation meets healthcare excellence. With a strong commitment to employee development and diversity, Abbott provides numerous opportunities for career growth while fostering a collaborative culture that values every team member's contributions. Join us to be part of a globally recognized company that not only leads in medical science but also prioritizes the well-being and professional advancement of its employees.
