Job Title: Regulatory Affairs Specialist You will play a critical role in ensuring the successful marketing of our products in the Latin America region. Key Responsibilities - To develop and implement effective regulatory strategies that meet regional requirements. - To maintain strong relationships with local authorities to ensure compliance and obtain necessary approvals. - To coordinate with cross-functional teams to ensure timely product launches. Required Skills and Qualifications - Advanced degree in a life science or related field. - Minimum 5 years of experience in regulatory affairs, preferably in the medical device industry. - Proven track record of successfully navigating complex regulatory environments. - Excellent communication and project management skills. Benefits A competitive compensation package, opportunities for professional growth and development, and a dynamic work environment. About the Role This is a unique opportunity to join a global leader in the medical technology industry and contribute to the success of our business in the Latin America region.