Quality Assurance Associate

Role: Quality Associate supporting GMP manufacturing and quality systems at Krystal Biotech's Pittsburgh headquarters. Responsibilities: develop and review GMP documentation, ensure regulatory compliance, oversee daily QA functions including record review, and assist with SOP updates. Requirements: Bachelor’s in Biology or related Life Science; 3+ years in biotech/pharma quality systems; strong knowledge of GMP, GLP, GCP, FDA audits, ICH standards; self-motivated with excellent communication skills. HighValue: GMP manufacturing, cGXP documentation, FDA audit experience, biotech/pharma industry, quality oversight. WorkSetup: onsite in Pittsburgh; no travel specified.