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Positive Patient Stories.

Randy Brenner
Randy Brenner
Chief Development and Regulatory Officer

Randy Brenner has been Paratek’s Chief Development and Regulatory Officer since June 2019. Since 2015, Mr. Brenner has been part of the Executive team leading the regulatory, quality and manufacturing activities for NUZYRA’s development and approval.

Prior to Paratek, Mr. Brenner was the Global Head of Regulatory Affairs at Shire Pharmaceuticals where he was responsible for all aspects of regulatory for a broad range of programs in multiple therapeutic areas and pharmaceutical technologies. Before that, Mr. Brenner was Head of Regulatory Affairs for the Emerging Markets and Established Products Business Units at Pfizer. In this role, he played an active part on the regional leadership teams and was responsible for the regulatory activities and staff leading the development, registration, launch, and life cycle of all of Pfizer's innovative products outside the United States and European Union as well as the Established Products business in all regions.

Prior to Pfizer, Mr. Brenner spent 14 years at Wyeth Pharmaceuticals, where he held multiple senior regulatory positions.

Education and Accomplishments
Mr. Brenner has a B.S. in Chemistry from Muhlenberg College and an M.S. in Pharmaceutical Sciences from Temple University.

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Our Stories

"Our culture is unique because we all come to Paratek with vast experience, and we work together to combine the decades of experience into one single purpose - to deliver NUZYRA to our patients."

Jen Schauble, Executive Director, Supply Chain

Our Stories

"Working on a product that has the potential to positively impact so many patient lives is very rewarding and gives me a great sense of purpose."

Stephen Viccica, Senior Director, Regulatory Affairs