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Quality Engineer - GMP

Reading Metro Area, Pennsylvania

Post Date: 07/24/2017 Job ID: JN -072017-19607
  • BS in Engineering - 2-3 years experience in Medical Device or related industry
  • Work with Manufacturing, Engineering, and other Quality functions to coordination/review/approval/ GMP documents such as inspection and testing mechanisms, equipment, validation documents and risk assessments, supplier assessments,
  • Assists in review or approval of GMP documents from a Quality Engineering point of view.
  • Analyzes production limitations and standards.
  • Recommends revision of specifications when indicated.
  • Formulates or assists in formulating quality document procedures.
  • Support gap analysis and closure of gaps identified.
  • Support and promote improvement activities for production area(s).
  • Uses various statistical and non-statistical problem-solving tools as part of analysis of data, issues, or improvement opportunities.

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