Regulatory Affairs Specialist 3

Drive and implement global regulatory strategies and roadmaps, ensuring alignment with product marketing strategies and requirements in high surveillance countries. Lead regulatory planning and execution across the product lifecycle, including submissions, product registrations, and compliance protocols. Monitor and manage regulatory risks and product safety by conducting risk assessments and driving corrective actions in collaboration with cross-functional teams.

2+ years of experience in Regulatory Affairs, Quality Compliance, or Product Development within the medical devices industry. Bachelor's or Master's degree in Biomedical Engineering, Health Sciences, Pharmaceutical, Business Administration, Law, or a related field. Knowledge of regulatory requirements, product registrations, risk management, and strong analytical skills.

This is an in-office role with an administrative shift, requiring full-time presence in the company’s facilities at least 3 days per week.