Teams at Krystal Biotech

Support QA systems for gene therapy manufacturing: create and maintain GMP documentation, review and approve manufacturing and QC records, update SOPs, support FDA audit readiness, and ensure regulatory compliance and continuous QA improvement.

Support QA for gene therapy GMP manufacturing: produce and review GMP documentation, maintain quality systems, update SOPs, support FDA audit readiness, and ensure regulatory compliance for cGxP operations.

Lead clinical development from late preclinical through Phase 1-3 and post-approval, manage trial execution, regulatory interactions (IND/BLA/MAA), medical monitoring, data review, KOL engagement, publication strategy, and cross-functional collaboration to advance gene therapy programs to approval and commercialization.