Worldwide asian global leading manufacturer, developer and distributor of medical devices requieres: medical equipment regulatory affairs/quality assurance coordinatorensure that the company has all documents (licenses, importations permits, sops, certifications, or any other document) and that the activities are performed according to the local requirements of the countries for which the companyis responsible (mexico, cuba, caribe, dominican republic, guatemala, honduras, el salvador, nicaragua, costa rica, panama, colombia, peru, ecuador, bolivia & venezuela), allowing the commercialization of our medical devicesmain accountabilitiesquality assurance.get licenses (sanitary registrations for medical devices group products)assembling dossiers and submitting them to the local governmental institution responsible of it.local compliance for commercialization ofthe product in the respective countries.maintenance of current licenses.gathering documentation, according to local requirements, for amendments or renewals of licenseskeep licenses updated and valid for commercialization of the products according to the current portfolio.support to distributors for their licenses obtention our maintenancegathering documentation, according to local requirements, for amendments or renewals of licenseskeep licenses updated and valid for commercialization of the products according to the current portfolio.local compliance with regulationwe offervery competitive compensationbenefits superior to those established by lawinternational growth and continuous training