Carmella Tallarida

Carmella has over 30 years of consulting and design experience in a lead process engineering role on numerous biotech, biopharmaceutical, and API projects. She has worked on conceptual, basic, and detailed design phases across various processes, on in-house capital projects, and as on-site facilities and maintenance support engineer for biopharma and API operations at manufacturing, pilot plant, and lab scales. Direct experience in GMP equipment commissioning, qualification, and validation.

At IPS, Carmella strives to use extensive, diverse knowledge to proactively lead projects, meet objectives, drive efforts, remain flexible, and determine the best path forward in partnership with, and for, the clients.