Document Management Associate

Descripción y detalle de las actividades- Maintain Quality Records in appropriate location.- Capture Training logs/roster for the site.- Training Data base handling.- CAPA facilitator.- Responsible to archive quality records (Training files, Logs, TCR, etc).- Audit/verify documents are compliant with GDPs.- Responsible for the distribution of controlled copies and retrieval when needed.- Assess/Audit of current controlled documents are posted at site level.- Scan DHR documentation prior to ship product to LLC for digital archiving.- Prepare records for outside storage (Iron Mountain).- Responsible for shredding obsolete/unused documents for the site.- Responsible for the support on document translations.- Purchase appropriate consumables for records shipping.Experiência y requisitos- Must have: Visa B1/B2 & Passport.- Availability to travel - 30 % traveling request.- Experience with GMP and GDP, Clean room environment.- Medical device manufacturing environment.- Ability to communicate effectively internal and externally with co-workers, and department management in both written and verbal form.- Provide support on NHO preparation.- Provide support with QA departmental purchases.- Support Internal/External audits.- Support with admin tasks.- Support Environmental control activities such as providing cleaning logs to the employees, ID DI water samples, etc.Beneficios- Beneficios de acuerdo a la LFT- fondo de ahorro**Número de vacantes** 1**Área** Calidad**Contrato** Permanente**Modalidad** Presencial**Turno** Mixto**Jornada** Tiempo Completo**Horario**- Tiempo completo- Lunes a viernes**Estudios** Carrera trunca o en curso**Inglés **Hablado: Avanzado, Escrito: Avanzado**Edad** 18 - 65 años**Disponibilidad p. viajar** Si