**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 indeterminado
Sueldo: $650.00 - $750.00 al día
Beneficios:
- Caja de ahorro
- Servicio de comedor
- Vales de despensa
Pago complementario:
- Bono de asistencia
- Bono de puntualidad
Tipo de jornada:
- Lunes a viernes
- Rotativo
Escolaridad:
- Licenciatura terminada (Deseable)
Experiência:
- Control de Documentos: 2 años (Deseable)
Idioma:
- Inglés (Obligatorio)
Lugar de trabajo: Empleo presencial
Fecha de inicio prevista: 13/02/2025

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