**Descripción y detalle de las actividades**:- Communicates and provides essencial information to the Quality Systems Supervisor.
- Establish and maintain a configuration management system compliant with regulatory, quality, company and customer (both internal and external) requirements.
- Collaborate with cross-functional departments to ensure timely implementation of change requisitions and change orders.
- Document and generate in Quality system the approved templates of manufactured product.
- Maintain files of official recorded documents, archive and label documents for permanent storage in the vault,- Have communication and coordinate needs with departments.
- Responsible for reviewing procedures and facilitating procedures updates in the assignment process.Experiência y requisitos:- University certifcate completed.




- Required a minimum of 2 years of experience in quality areas or similar, preferably focused on medical manufacturing produc inspection, document control and/or document translation english to spanish and vice versa.
.Tipo de puesto: Jornada completa, Por tiempo indeterminadoSueldo: $****** - $****** al díaBeneficios:- Caja de ahorro- Servicio de comedor- Vales de despensaPago complementario:- Bono de asistencia- Bono de puntualidadTipo de jornada:- Lunes a viernes- RotativoEscolaridad:- Licenciatura terminada (Deseable)Experiência:- Control de Documentos: 2 años (Deseable)Idioma:- Inglés (Obligatorio)Lugar de trabajo: Empleo presencialFecha de inicio prevista: 13/02/2025

📌 Document Control Specialist (Tijuana)
🏢 Formula Plastics
📍 Tijuana