Danielle Murray has been working at Merck for over 20 years. During this time, she supported multiple roles including bacterial vaccines manufacturing for clinical supplies, analytical lead for recombinant protein vaccines and regulatory affairs liaison for the Diabetes franchise. In 2014, Danielle transitioned to the Global Regulatory Affairs  - Chemistry Manufacturing and Controls (CMC) organization. 

Danielle has supported both Biologics and Vaccines programs within CMC, developing filing strategies for investigational products, worldwide marketing authorizations and post approval changes. Most recently, within the vaccines area Danielle manages a team supporting an array of Live Virus Vaccines, including efforts related to POD manufacturing. 

In her spare time, she enjoys baking, bowling and spending time with family.