QA Validation Specialist - Flexible GMP for Cell Therapy in Stevenage

A biotech company in Stevenage is seeking a Quality Assurance professional to support the delivery of CAR T-cell products. The role involves ensuring GMP compliance within a multi-product facility, collaborating with cross-functional teams, and reviewing validation documentation. Candidates should have 1-2 years of experience in quality assurance within a regulated environment and a BSc in relevant fields. Strong communication and attention to detail are crucial in this role, which offers a collaborative and flexible work environment.
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