Denise Diehr-New

Denise Diehr-New has over 20 years of experience in the pharmaceutical and laboratory industries, currently serving as the Manager of Computer and Equipment Validation at Hikma Pharmaceuticals since August 2014. In this role, Denise has effectively managed validation projects for various systems and ensured compliance with industry guidelines while mentoring staff on validation procedures. Prior experience includes roles at Boehringer Ingelheim, where Denise served as a GMP Specialist II and Scientist II, focusing on cGMP compliance, equipment validation, and regulatory documentation. Denise started in customer service management at VIOC, honing skills in employee supervision and public relations. Denise holds a Bachelor of Science degree in Wildlife Biology from Ohio University.