Vice President Global Regulatory Affairs - Medical Devices
Bausch + Lomb
Donielle Johnson is the Vice President, Global Head Regulatory Affairs-Medical Devices for Bausch + Lomb.
In this role, Donielle leads the global medical device organization that supports strategic priorities domestically and internationally ensuring access to innovative technology and compliant maintenance of business. She partners closely with stakeholders across Medical Devices and represent Bausch +Lomb in various internal and external forums with regulatory bodies, health authorities and trade associations. Donielle leads a dedicated team who collaborates with different stakeholders to ensure consistency in global medical device policy shaping activities.
Prior to joining Bausch + Lomb, Donielle was the Sr. Director of Regulatory Affairs for EMEA & Canada at Johnson & Johnson. In this role she was responsible for leading a team to ensure compliant and on-time launches of new products, lifecycle management and business transformation, driving J&Js EMEA policy shaping initiatives toward regulatory harmonization.
Prior to Johnson & Johnson, Donielle held several global roles with increasing responsibility at major medical device companies such as Philips, Abbott Vascular, and Medtronic. Leading teams through challenging premarket approvals, such as, PMAs, 510(k), Health Canada approvals, and CE Mark. Additionally, Donielle has extensive experience in lifecycle management and leading major manufacturing site change projects, resulting in several millions of annual savings for the company. Her career has spanned several countries including the U.S, Japan, and the Netherlands where she has lived since 2014.
Donielle is a chemist who is currently pursuing a second graduate degree in Global Health Policy at the London School of Hygiene and Tropical Medicine.
Disclosure information not submitted.
Monday, September 12, 2022
8:15 AM – 9:30 AM MST