- 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.
Great opportunity to join an amazing team and take the lead on challenging projects.
Head of Regulatory Affairs - Medical devices
Significant experience in Regulatory Affairs (for the pharmaceuticals and/or medical devices sectors). Mentor, train, and supervise Regulatory Affairs teams, ensuring effective collaboration with other departments. Establish and maintain effective relationships with competent regulatory authorities,...
Head of Regulatory Affairs - Medical devices
Significant experience in Regulatory Affairs (for the pharmaceuticals and/or medical devices sectors). Mentor, train, and supervise Regulatory Affairs teams, ensuring effective collaboration with other departments. Establish and maintain effective relationships with competent regulatory authorities,...
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