Tony Pavell has over 17 years of experience primarily focused in validation and technology services. Pavell is currently Senior Manager of Validation and Process Improvement at APP Pharma focusing on aseptic processing, process and systems validation. Pavell has been involved with the start up/commissioning and validation of six sterile manufacturing facilities. Pavell’s experience includes directing production operations, technology transfer of products and processes into the facility, management of all site related validation activities and management of the site calibration program. Pavell has held an Operations position with Catalent, Technical Services and Validation positions with MKCS Inc, Cardinal Health, Lloyd’s Register Serentec, Novo Nordisk, Glaxo Wellcome, and Burroughs Wellcome. Pavell is a member of the International Society of Pharmaceutical Engineers and the Parenteral Drug Association. Pavell received a Master of Science in Molecular Biology and Biotechnology from East Carolina University.