Document Control Specialist

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**- Tiempo completo**Estudios** Preparatoria**Disponibilidad p. viajar** No