MEDICAL DEVICE DEVELOPMENT MANUFACTURING. EVERYTHING IN-HOUSE.
Adam Johnson
President of Quality & Regulatory
Key Experience:
​Prior to joining VitaTek, Adam was Vice President of Regulatory, Quality, and R&D for pharmaceutical manufacturer Apex International.
Adam also spent 10 years at Smiths Medical (now ICU Medical) in increasing roles ending as Director of Regulatory Affairs and Quality Systems.
During his tenure at Smiths Medical, he lead regulatory and quality systems teams globally focusing on European MDR, FDA 510K submission, Medical Device Single Audit Program geographies (US FDA, Health Canada, Japan MHLW-PMDA, TGA Australia, ANVISA Brazil), and over 100 additional geographies. Adam offers over 20 years of managerial experience within the medical device, pharmaceutical, in-vitro diagnostics, and Research and Development space managing multiple size teams as well as project/program management.
Notable Achievements:
-
20+ Years of Regulator & Quality Experience
-
Gustavus Adolphus College with degrees in Chemistry, Biochemistry and Molecular Biology.
-
Attended graduate school with studies in Biochemistry, Biophysics, and Molecular Biology.