Mentor, train, and supervise Regulatory Affairs teams, ensuring effective collaboration with other departments.Monitor and interpret changes in international regulations.Develop and implement regulatory strategy aligned with the company''s business objectives, in collaboration with other departments.Supervise the preparation and submission of registration files required for product market entry, ensuring compliance with international requirements.Establish and maintain effective relationships with competent regulatory authorities, representing the company during regulatory inspections and audits.Ensure product compliance with standards and regulations, collaborating closely with cross functional teams.University degree in sciences, pharmacy, biology, or a related field.Significant experience in Regulatory Affairs (for the pharmaceuticals and/or medical devices sectors).Minimum 10 years of experience in a similar role.Knowledge of European and US regulations.Strong team management and communication skills.Ability to work independently and make strategic decisions.Proficiency in English and French, both written and spoken.