John Jarrett

Consulted for multiple companies, managing projects for bioreactor development and providing paperless validation support. Collaborated with clients and internal teams on Kneat-related activities, including user acceptance testing and migration of protocols.

Project managed C&Q contracts for various cell therapeutic companies, leading internal and client teams through project execution. Responsible for scope development, schedule and budget management, and generating technical documentation.

Managed global regulatory affairs projects, focusing on business improvement and data analysis. Defined and executed cross-functional improvement projects, optimizing processes and reducing cycle times for drug development.

Drove strategic planning for oncology therapeutic area and designed the Medical Material Review Process. Collaborated with legal, medical, and compliance groups to launch and manage the process and system.

Performed and optimized genetic characterization assays for regulatory filings and managed cell culture technology development. Conducted bench-scale antibody purification to support clinical and commercial product release.

Responsible for GMP cell bank manufacturing, including NC/CAPA ownership and cross-functional collaboration. Contributed to process improvement studies and authored controlled and technical documents.

Led GMP vial, syringe, and lyophilized product filling operations, scheduling and training staff. Optimized fill processes, implementing two significant improvements to fill lines.

Earned a Bachelor of Science in Biology, gaining a comprehensive understanding of biological principles and research methodologies. Developed strong analytical and problem-solving skills through scientific coursework and laboratory work.

Completed a Master of Fine Arts in Creative Writing, developing advanced skills in narrative construction and literary analysis. Focused on honing writing craft and critical thinking through rigorous academic study.