Melis Tay has 10 years of experience in GMP Biotechnology and Biopharmaceutical industry, in areas of Manufacturing operations and Process Development & Engineering. Melis is experienced in areas of commissioning and validation, operations, management, technical transfer and regulatory filing audit. She participated in three start up projects — two 20,000L capacity multi-product biopharmaceutical facilities and a 2000L scale single use platform. Currently Melis is involved in the fourth startup project.