Regulatory Affairs Job The role of Regulatory Affairs Specialist in the Latin America region requires a professional to support regulatory filings. This involves ensuring compliance with local regulations, preparing and submitting necessary documents, and maintaining relationships with relevant authorities. Key Responsibilities: - Prepare and submit regulatory filings for products in the Latin America region. - Ensure compliance with local regulations and maintain up-to-date knowledge of regulatory requirements. - Collaborate with cross-functional teams to develop and implement regulatory strategies. Requirements: - Relevant degree in life sciences, law, or a related field. - Proven experience in regulatory affairs, preferably in the medical device industry. - Strong understanding of regulatory frameworks and procedures. - Excellent communication and interpersonal skills. What We Offer: - A dynamic and supportive work environment. - Opportunities for growth and development. - A competitive salary and benefits package.