Jacqueline Stief

Jacqueline has 13 years of experience in the pharmaceutical and cell therapy industry with deep expertise in quality management, including experience in building a quality and compliance program for an autologous cell therapy product from the ground up. Throughout her career, Jacqueline has managed site quality assurance and quality control under a variety of regulatory environments including the US and EU.

In her previous role as Sr. Director of Quality Operations at Adaptimmune, Jacqueline was responsible for the oversight of Quality Batch Release Operations for US/EU, Quality Control Analytical testing, and Quality Control Microbiology. She was also responsible for developing the Quality modules of the GxP quality system and implementing the Quality policies, and standard operating procedures to establish a compliant manufacturing site at the Philadelphia location. Prior to this role, Jacqueline worked at MedImmune, a subsidiary of AstraZeneca, in the quality unit responsible for maintaining compliance for vaccine manufacturing.

Jacqueline has her Bachelor of Science in Biology from the Shippensburg University of Pennsylvania.