Coordinador De Asuntos Regulatorios

Sobre nuestro cliente Manage regulatory submissions tracking process in Mexico and Panama, establishing timelines for product maintenance submissions Descripción - Manage regulatory submissions tracking process in Mexico and Panama, establishing timelines for product maintenance submissions.
- Closely supervise regulatory consultants and/or local distributors in Latin America, regarding the regulatory activities of medical devices .
- Interact with local regulatory bodies where needed or through local in-country consultants to discus project feasibility, strategies to achieve fast-track approvals and assess the impact of change control for the regional marketing authorizations.
- Analyze, translate, prepare, or adapt the technical documentation in accordance with the legislationin force for the registration, variations, processes, and certifications of good manufacturing practices, according to the reference documents, meeting the established deadlines Perfil buscado - Academic background: Bachelor's degree or equivalent in health sciences, chemical pharmaceutical discipline, or related (Essential) with an active registration in the respective Regional Council.
- Solid knowledge of the legislation for medicines and medical devices in the applicable countries - Fluency in English - At least 5 years of previous Regulatory experience in medical devices industry.
- Qué Ofrecemos - Benefits that are up to the market standard - A permanent contract with the company - The opportunity to work in a company in the life science industry We invite all suitable candidates to apply for this exciting opportunity to contribute to the life science industry in Mexico.