Priscilla Pingrey is a seasoned biopharmaceutical leader specializing in cGMP operations, aseptic processing, facility design, and technology transfer. As Director of Engineering Programs at SynerG, she provides strategic leadership and project management in GMP readiness, contamination control, and technology transfer across commercial, clinical, and viral vector manufacturing environments.

Priscilla has successfully led initiatives in GMP readiness, environmental monitoring, and technology transfer, delivering innovative, compliant, and efficient solutions that strengthen manufacturing performance.

Before joining SynerG, Priscilla held key leadership roles at Stemedica Cell Technologies and Vista Biologicals, where she managed cGMP manufacturing of cell therapies, established aseptic processing platforms, and supported global technology transfer programs. Her expertise spans project management, risk assessment, aseptic controls and continuous improvement, fostering operational excellence and sustainable compliance.

Priscilla earned her B.S. in Biological Studies from San Diego State University and holds certifications from the Parenteral Drug Association (PDA) in Manual Aseptic Processing and Media Fill Design, as well as Management & Leadership certification from SDSU. She is highly skilled in GMP documentation, facility startup, staff training, and inspection readiness.

Her ability to navigate complex regulatory landscapes, lead high-performing teams, and implement innovative manufacturing strategies makes Priscilla a trusted advisor and valued partner to SynerG’s clients.