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Reference # : 17-00331 Title : ***Sr. CAPA Qualtiy Engineer
Location : Hudson, NH
Position Type : Contract
Experience Level : Start Date / End Date : 11/28/2016 / 05/26/2017  
Description
Duties
  • Review of past cleaning, maintenance and calibration documentation to assure compliance to GDP and internal procedures as part of CAPA remediation activities
  • Maintain documentation pertaining to review and correction activities for FDA reporting
  • Recommendation of alternate methodologies to streamline future processes while maintaining documentation accuracy
  • Implementation of new requirements/methods as required
Requirements
  • Familiar with documentation and GDP requirements in an FDA environment
  • Attention to detail, ability to communicate effectively via written and verbal reports
  • Ability to work independently with minimal daily direction