The Quality Assurance Associate at Krystal Biotech will support GMP manufacturing processes, oversee quality system documentation, ensure compliance with FDA regulations, and assist with continuous improvement within the company’s QA functions.

Krystal Biotech is seeking a Bioprocess Engineer to support product manufacturing at the Pittsburgh GMP facility. Responsibilities include performing process steps, documenting data, maintaining equipment, collaborating with various departments, and participating in training. The ideal candidate is detail-oriented, self-motivated, and has experience in cleanroom facilities and downstream processing.