Bhaumik Patel

Mr. Patel has 15 years’ experience in pharmaceuticals, medical devices, and combination products. Leading Armata’s Quality Assurance department, Mr. Patel is responsible for ensuring compliance with cGMP and GLP standards in the manufacturing and testing of Armata’s investigational phage products, as well as ensuring GCP compliance in the conduct of human clinical trials.  Prior to joining Armata, Mr. Patel worked at Haemonetics Corporation in the role of Site Quality Lead, maintaining the quality and regulatory compliance of the manufacture of donor-derived blood products. Previously, he worked at Teva Pharmaceuticals as Senior Quality Analyst managing the remediation of regulatory audit gaps. Mr. Patel began his career in Quality at Bimeda, Inc., a global manufacturer, marketer and distributor of animal health products and veterinary pharmaceuticals, where he led the implementation of an electronic quality management system, hosted several FDA audits (with no findings), and cultivated a One Team mindset.  Mr. Patel earned a Bachelor’s degree in Pharmacy from R.C. Patel College of Pharmacy with an emphasis on quality of pharmaceutical manufacturing processes.