Quality Assurance Supervisor

3 weeks ago


Piedmont, United States PL Developments Full time
  • Knowledge of FDA/cGMP guidelines
  • Computer literate in Microsoft Windows and Microsoft Office
  • Excellent analytical and problem-solving skills, with a focus on continuous improvement and process optimization
  • Oversee that all in-line checks for count, labeling, seal integrity and overall package quality are monitored accurately and within designated times as slated in our SOP
  • Review Batch Record for missing entries and errors
  • Review daily, line operations to assure compliance with cGMP's and SOP's
  • Review cleaning log books to assure the proper cleaning has taken place
  • Interact with company personnel as required to remedy problems related to packaging production or product quality and batch record reconciliation variances


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