Travis McGrady

Having nearly 20 years of pharmaceutical experience, Travis is knowledgeable in cGMP’s and specializes in parenteral drug manufacturing, specifically within Quality and Manufacturing Operations. Prior to QuVa Pharma, Travis held leadership roles in both Quality and Manufacturing, with Par, JHP Pharmaceuticals supporting the manufacture of sterile and aseptically produced products. And most recently, Travis supported a rapidly growing Cell & Gene Therapy site, for Lonza, delivering a zero 483, pre-approval inspection, for two critical products. Travis has a passion for developing and creating high performing teams, across multiple business units, and delivering on the need for continuous improvement.