QA Auditor

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Irfa******

  • United States 

  • Last Update: 29.06.2019 at 12:00

Job Type
Full Time
Start
ASAP
Duration
6 Month +
Place
Greenville, NC, US
Country
United States
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Category

Management

Description

  • Experience in quality reviews of manufacturing and packaging batch records for bulk and finished packaged product for final disposition of lots
  • Ability to review approved manufacturing and packaging investigations/deviations to determine final QA disposiiton
  • Attentive to detail, able to recognize critical attributes, steps and functions relating to manufacturing processes and/or laboratory activities
  • Knowledgeable of cGMPs and application of good documentation practices within pharmaceutical industry

    • Seniority Level

    Associate

    Industry

      • Research
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