Document Management Associate

Descripción y detalle de las actividadesMaintain 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.Experiencia y requisitosExperience with GMP and GDP, Clean room environment.Medical device manufacturing environment.Proficient with Microsoft programs and other basic computer applications.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.BeneficiosBeneficios de acuerdo a la LFTfondo de ahorroNúmero de vacantes: 1Área: CalidadContrato: PermanenteModalidad: PresencialTurno: MixtoJornada: Tiempo CompletoHorario:Tiempo completoLunes a viernesEstudios: Carrera trunca o en cursoInglés: Hablado: Avanzado, Escrito: AvanzadoEdad: 18 - 65 añosDisponibilidad para viajar: Si#J-18808-Ljbffr