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Debra Porti is an Industry professional with more than 25 years of experience ranging from the bench to clinical trials to full cGMP manufacture. Her experience encompasses R&D, cGMP Clinical trials, Manufacturing and Quality. She is responsible for all aspects of Quality and Operations at the site, including compliance, operational efficiencies, inspections, validation, logistics, quality assurance and quality control.

Ms. Porti’s experience includes management in facilities producing non-sterile APIs, sterile injectable products, over-the-counter (OTC), and neutraceutical products. With vast knowledge and experience in both national and international requirements, she has served as Senior Management in Quality and Operations at various companies.

Her prior employment includes Kedrion Biopharma, Grifols Therapeutics, Talecris Biotherapeutics, Precision Pharma Services and North Shore LIJ Health System.