Quality Control and Compliance Expert

4 days ago


Pittsburgh, Pennsylvania, United States Krystal Biotech Full time
Key Responsibilities
  • Perform cGMP material inspection, testing and release.
  • Write methods for analytical testing of ancillary materials used in the manufacturing process.
  • Review analytical data for compliance with regulations, methods and other specifications or criteria.
  • Implement USP Quality Standards and verify USP Methods.

In addition to these key responsibilities, the successful candidate will also have the opportunity to develop a strong understanding of HPLC and other chemistry testing.

If you are a skilled Pharmaceutical Analyst with experience in quality control and compliance, we encourage you to apply for this challenging and rewarding position.



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