The Bioprocess Engineer role at Krystal Biotech involves supporting product manufacturing in a GMP facility, including monitoring process steps like buffer preparation, upstream and downstream activities, equipment maintenance, and collaboration with various teams. The position requires cleanroom expertise and aims to improve lives through gene therapy solutions.

The Quality Assurance Associate at Krystal Biotech will support quality systems and GMP processes, develop expertise in FDA regulations, and ensure compliance with documentation practices. Responsibilities include reviewing and approving records from manufacturing and quality control, assisting with QA efforts, and overseeing continuous improvement in QA functions.