Having more than 30 years of pharmaceutical experience, David is knowledgeable in cGMPs and specializes in parenteral drug manufacturing, specifically with Quality and Research & Development. Prior to joining QuVa Pharma, David held leadership roles in Quality and Research & Development with Par, JHP Pharmaceuticals, and Hospira supporting the manufacturing of sterile injectables. David has additional leadership experience in quality roles with Johnson & Johnson, Pfizer, Pharmacia, and Upjohn supporting the pharmaceutical manufacturing of API, OTC, and prescription drugs. David has a strong background in operational excellence, driving continuous improvement in processes and people through coaching and training.
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