Descripción y detalle de las actividades
- Communicates and provides essencial information to the Quality Systems Supervisor.
- Provide support to Scantibodies Group facilities to expedite labelling and document control activities
- Establish and maintain a configuration management system compliant with regulatory, quality, company and customer (both internal and external) requirements.
- Create, update and inactive employee profile in quality system.
- High volume printing of requested labels.
- Inventory contol, cycle count of the labeling location, material request and purchase orders for the labeling area.
- Collaborate with cross-functional departments to ensure timely implementation of change requisitions and change orders.
- Document and generate in Quality system the approved templates for the labels of manufactured products at Scantibodies Group plants.
- 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
- High school 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..
Beneficios
- Beneficios de acuerdo a la LFT
**Número de vacantes** 1
**Área** Calidad
**Contrato** Permanente
**Modalidad** Presencial
**Turno** Diurno
**Jornada** Tiempo Completo
**Horario**
- Jornada completa
**Estudios** Preparatoria
**Disponibilidad p. viajar** No

📌 Document Control Specialist (Tecate)
🏢 Scantibodies
📍 Tecate