This Stability Associate role involves executing stability studies of plasma-derived biopharmaceuticals in a cGMP environment. Key responsibilities include planning and managing stability studies, inventory, and stability pulls, as well as preparing protocols, monitoring data, and writing stability reports. The position requires expertise in cGMP compliance, data trending, and technical documentation. Candidates should have a bachelor’s or master’s degree in a related scientific field, 1-3 years of regulated lab experience, familiarity with GLP/GMP, and strong communication skills. Preferred experience includes stability program knowledge. The role demands attention to detail, ability to work under pressure, and adherence to regulatory standards. Additional benefits include comprehensive health plans, 401K, paid time off, tuition assistance, and accessible location options. The company values integrity, innovation, and continuous improvement in a growing biopharmaceutical setting.