GMP Cell Therapy Documentation Specialist

A global biopharmaceutical leader in Massachusetts seeks a Specialist for Technical Documentation in Cell Therapy Manufacturing. The role involves authoring and revising SOPs to ensure compliance with cGMP standards. Ideal candidates should have at least 3 years in biotechnology or pharmaceutical manufacturing and skills in technical writing and collaboration. The position offers competitive pay between $43.84 - $53.12 per hour, with additional benefits including comprehensive health coverage and 401(k) plan. #J-18808-Ljbffr