Meghan C.

Meghan C. has worked in various quality and research roles in the pharmaceutical and medical device industry. Meghan has experience in executing and verifying testing with a high quality of GMP and GLP, reviewing documentation to ensure compliance with quality policy standards, and identifying cytotoxic leachables from disposable plastic bioreactors. Meghan has held roles such as Quality Engineer, Operations Diagnostic Technician, Research Assistant, and Quality Systems Specialist in companies like LifeScan, Johnson & Johnson Vision, Abbott, National Center for Biotechnology Information (NCBI), and Bristol Myers Squibb.