Description
The Quality Assurance Specialist will oversee cGMP manufacturing of advanced cell and gene therapy products, including batch-record review, raw-material disposition, product release, investigations, change controls, deviations, CAPAs, audits, validations, and quality-system support. The role requires a bachelor’s degree in life science and at least five years of direct QA experience in GMP manufacturing, with cell-based therapeutics experience preferred. It is scheduled for 8:00 a.m. to 5:00 p.m. with irregular hours, weekends, and nights, and offers a base salary of $120,988 to $142,405 per year plus health, vision, dental, and 401(k) benefits.
