Olympus Corporation of the Americas is seeking an Analyst for International Regulatory Affairs to manage regulatory submissions and compliance strategies for medical devices in Latin America. The ideal candidate will have a background in regulatory affairs with at least three years of experience in the medical devices sector, complemented by strong project management skills and advanced English proficiency
Job Summary
As an International Regulatory Affairs Analyst II, you will be responsible for independently managing and executing regulatory submissions, compliance strategies, and lifecycle maintenance of medical devices in Latin American markets.
This role requires strong regulatory knowledge, project management skills, and the ability to collaborate cross-functionally and with external partners to ensure timely and compliant market access.
You will play a key role in identifying and implementing process improvements, supporting audits, and contributing to regional regulatory intelligence.
Matching Summary
Match Score: 85
Olympus Corporation of the Americas is seeking an Analyst for International Regulatory Affairs to manage regulatory submissions and compliance strategies for medical devices in Latin America. The ideal candidate will have a background in regulatory affairs with at least three years of experience in the medical devices sector, complemented by strong project management skills and advanced English proficiency.
Skills & Requirements
Must-have
International regulatory submissions
Medical device lifecycle management
LATAM regulatory compliance
Cross-functional collaboration
Regulatory change management
LATAM regulatory intelligence
Nice-to-have
Patient-focused technology
Integrity and empathy
Continuous process improvement
Digital tools for efficiency
Key Requirements
Bachelor's degree in Pharmaceutical, Life Science, Engineering, or related field
Minimum 3 years of direct experience in regulatory affairs