Janice
Quality or Design Assurance Technician for Medical Device or Pharmaceutical Industry  Deephaven Minnesota Status: Offline
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Summary

Provided pharmaceutical and medical device quality assurance functional support, Quality Auditing experience, Conduct investigations, documentation review. Analytical Chemistry laboratory, GLP/GMP testing in Pharma Medical Device

Experience

ISO 13485 regulations auditor, FDA CFR21, parts 210, 211, 820, GMP, Access database, auditing, data review,analytical chemistry, design assurance, cleanroom experience, gap analysis,


Details

  • Salary:
  • Date: August 4 2017
  • Location: Deephaven, MN

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