03 ene
Importante Empresa Del Sector
Xico
Worldwide Asian global leading manufacturer, developer and distributor of medical devices requieres:
Medical equipment regulatory affairs/Quality assurance coordinator
Ensure 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 devices
Main Accountabilities
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 of the product inthe respective countries.
Maintenance of current licenses.
Gathering documentation, according to local requirements, for amendments or renewals of Licenses
Keep Licenses updated and valid for commercialization of the products according to the current portfolio.
Support to distributors for their licenses obtention our maintenance
Gathering documentation, according to local requirements, for amendments or renewals of Licenses
Keep Licenses updated and valid for commercialization of the products according to the current portfolio.
Quality Assurance.
Local compliance with regulation
We offer
Very competitive compensation
Benefits superior to those established by law
International growth and continuous training
Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.