Quality Control Analyst I
Krystal Biotech, Inc.
September 12, 2026
Full-time
On-site
Pittsburgh, PA
Operations
Role: Quality Control Analyst specializing in analytical testing for drug product release in clinical and commercial settings. Responsibilities: perform finished product and stability testing; review and report analytical data; support investigations, CAPA, deviations, and method validation; manage documentation, record retention, and material handling; maintain QC lab equipment; participate in audits and QC projects. Requirements: Bachelorβs degree in life sciences; hands-on experience with techniques such as mammalian cell culture, ELISA, qPCR, Western and Southern blot; proficiency in Microsoft Office; ability to support investigations and adapt to changing priorities; strong scientific writing and communication skills. Preferred: environmental monitoring experience. High-Value: biopharma (gene therapy, biologics), QC release testing, analytical method validation, GMP compliance, clinical and commercial manufacturing support, cross-function collaboration in quality assurance. WorkSetup: not specified but implied to be laboratory-based.