Detalles de la oferta

Descripcin y detalle de las actividadesThis position executes and coordinates Engineerinctior the organization in sterile and non sterile processes. The position requires a dynamic, hard-working professional with a desire to worst-paced, large corporate organization. In addition to exceptional communication skills, a roll-up your sleeves entrepreneurial attitude is expected. Lead and coordinate Corrective and Preventive Actions (CAPr Customer complaints, and process non-conformities.Develop and define measurement equipment and test methods to evaluate and perform component or process inspections. Define effective control plar warehouse to operations delivery of raw materials processes. Define, and lead continuous improvement projeccused on improvement, and costreductions.Perform periodic audits of the accuracy and cleanliness of component storage locations and communicate results with appropriate warehouse personnel.Support the implementation and improvemenr Good Manufacturing Practices (GMPs).Serve as an ISO-13485 Lead Internal Auditor, participating in the Internal Audit Program.Ensure compliance with domestic and international regulations associated with product lines and processesExperiência y requisitosIndustrial, Electrical, etc3-5 years of Control/Engineering experienceMedical Devices Importante empresa (pharmaceuticaod or personal CareSupervisory Importante empresa desireInternal / Lead Auditor ISO 13485:2016MDSAP knowledge / experienceOffice Windows:Word, Excel, Power Point, etc.Strong leadershipeffective communicationManagement skills / Decision MakingSix Sigma (BB/GB) Lean Manufacturing Importante empresa


Fuente: Jobtome_Ppc

Requisitos

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