Tamara Marsh
About Tamara Marsh
Tamara Marsh is a Group Leader in Process Development at Sana Biotechnology, Inc., with a PhD in Molecular and Cell Biology. She has significant experience in transferring processes to GMP manufacturing and has previously worked as a Scientist/Embryologist at UCSF.
Work at Sana Biotechnology
Tamara Marsh has been serving as the Group Leader for Process Development at Sana Biotechnology, Inc. since 2019. In this role, she is responsible for strategizing and overseeing the entire manufacturing process. Her contributions include designing and establishing a GMP manufacturing facility, which involves creating Standard Operating Procedures (SOP) and Batch Records. Marsh's leadership ensures that the manufacturing processes align with regulatory standards set by the FDA and EMA.
Education and Expertise
Tamara Marsh studied Molecular and Cell Biology, achieving her PhD from the University of California, San Francisco, and the University of Belgrade, Serbia. Her academic journey spanned from 2002 to 2009, during which she developed a strong foundation in molecular biology. This educational background supports her extensive experience in transferring processes from development labs to GMP manufacturing environments.
Background
Before joining Sana Biotechnology, Tamara Marsh worked at the University of California, San Francisco (UCSF) from 2009 to 2015. During her six years there, she served as a Scientist/Embryologist in the Center for Reproductive Sciences and the Center for Stem Cell Research within the Department of Obstetrics, Gynecology, and Reproductive Sciences. This experience contributed to her expertise in process development and compliance in the biotechnology field.
Achievements
Tamara Marsh has played a significant role in the establishment of a GMP manufacturing facility at Sana Biotechnology. Her work includes the creation of Standard Operating Procedures (SOP) and Batch Records, which are essential for maintaining compliance with industry regulations. Additionally, she has a strong background in training and managing manufacturing teams, ensuring adherence to FDA and EMA regulations.