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Quality Final Acceptance Inspector - 10AM - 6PM

Req ID: J2294315

  • Ubicación
    West Chester, Pensilvania, United States of America
  • Categoría Grupo de Calidad
  • Publicado martes, 9 de noviembre de 2021
  • Tipo Tiempo completo
  • Tipo de Empleo Empleado Permanente

Descripción del Trabajo

OVERALL RESPONSIBILITIES:

Responsible for performing basic Device History Record review, including document verification and work order release to ensure quality standards are met and following prescribed steps to document issues and follow-up on corrective actions.

POSITION DUTIES & RESPONSIBILITIES:

  • Perform basic Device History Record review, including document verification and work order release to ensure quality standards are met and following prescribed steps to document issues and follow-up on corrective actions.
  • Maintain a high level of concentration and attention to detail in order to ensure that products are manufactured,  labeled, and packaged according to internal quality requirements.
  • Communicate issues arising from daily activities that should be reviewed by a supervisor.
  • Performs other related duties, as required.
  • Know and follow all laws and policies that apply to one’s job, and maintain the highest levels of professionalism, ethics and compliance at all times.
  • Diligently participate in compliance program-related activities as denoted by the  supervisor or the Chief Compliance Officer.

EDUCATION & EXPERIENCE REQUIREMENTS:

  • High school diploma or equivalent. Associates degree is preferred.
  • Experience with record review in medical device or pharmaceutical industry preferred.
  • High level of concentration and attention to detail is required.
  • Experience with Microsoft PC applications, preferred.
  • Experience with MRP / ERP systems, preferred.
  • 20/30 vision using both eyes with the ability to perform color verification.
  • Lifting weight up to 20 pounds on regular basis and up to 50 pounds on occasional basis.
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