William Nordling
About William Nordling
William Nordling is the Associate Director of Process Engineering, CSO-OSD at Bristol Myers Squibb in New Brunswick, NJ, with extensive experience in drug product life cycle and solid dose manufacturing.
Current Role at Bristol Myers Squibb
William Nordling currently serves as the Associate Director of Process Engineering, CSO-OSD at Bristol Myers Squibb. Based in New Brunswick, New Jersey, he started this role in September 2023. His responsibilities include leading process engineering initiatives and overseeing operations related to oral solid dosage manufacturing. This position builds on his extensive background in solid dose manufacturing and pharmaceutical engineering.
Previous Roles at Bristol Myers Squibb
Before his current role, William Nordling held several positions at Bristol Myers Squibb. From 2019 to 2023, he worked as the Process Engineering Manager in Clinical Supply Operations for Oral Solid Dosage Manufacturing. Prior to that, he served as a Consultant in ExM Manufacturing Science & Technology from 2018 to 2019. These roles were also based in New Brunswick, NJ, where he has contributed significantly to various engineering and manufacturing processes.
Career at Teva Pharmaceuticals and Actavis
William's experience in the pharmaceutical industry includes positions at Teva Pharmaceuticals and Actavis (now Allergan). At Teva Pharmaceuticals, he was the Manager of Manufacturing Science and Technology focusing on process and product robustness for 8 months in 2016-2017. His tenure at Actavis spanned 11 years, where he held roles as a Scientist/Process Engineer, Project Manager, and Manager of Global Pharmaceutical Technology. These roles were primarily based in North Brunswick, NJ, and Elizabeth, NJ.
Educational Background in Pharmaceutical and Chemical Engineering
William Nordling holds a Master's of Science in Pharmaceutical Engineering and a Bachelor's of Science in Chemical Engineering from the New Jersey Institute of Technology. He completed his M.S. between 2006 and 2009, and his B.S. from 1997 to 2001. His academic background has provided a strong foundation for his extensive career in drug product lifecycle management and solid dose manufacturing.
Experience at Barr Pharmaceuticals
William Nordling began his career at Barr Pharmaceuticals as a Validation Engineer, working there for three years from 2002 to 2005. Based in Pomona, NY, he was responsible for validation tasks that ensured the integrity and quality of pharmaceutical products. This early role in his career helped him develop a strong foundation in pharmaceutical validation and technology processes.