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IPC Specialist (Quality Assurance)

Rameda
6th of October, Giza
Posted 6 years ago
261Applicants for3 open positions
  • 85Viewed
  • 14In Consideration
  • 41Not Selected
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Job Details

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Job Description

  • Ensure line clearance & cleaning checks of the batch manufacturing process
  • Reviews documentation associated manufacture of products on the manufacturing floor during production.
  • Work closely with manufacturing to address any production issues on shift and ensure appropriate documentation.
  • Coordinates and assembly of batch record documentation to assist with disposition.
  • Reviews and approves completed manufacturing related documents for batch record disposition.
  • Performs in process control sampling & testing.
  • Coordinates activities associated with deviation resolution and CAPAs to facilitate investigations and assure timely closure.
  • Ensures adherence of appropriate cGMP regulations and quality standards.
  • Perform or support any other tasks necessary to maintain the product quality and site cGMP compliance, as needed.
  • Ensures that all activities in his unit or section are done according the relevant cGMP and ISO standards (ISO 9001/2008 , ISO 14001/2004 , OHSAS 18001/2007).

Job Requirements

  • Bachelor pharmacy (Fresh or experienced are welcomed)
  • Bachelor science (With minimum experience 1 year as IPC specialist in pharmaceutical industry)
  • Males only due to night shifts.

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