Sterling Pharma: A versatile CDMO you can depend on; Sterling combines a full-service offering with expert knowledge and technical agility to offer API development and cGMP contract manufacturing capabilities. They can support your projects through the entire product lifecycle from grams to tons.
Their 700+ strong team across our facilities in the UK and the US are capable of handling even the most hazardous chemical processes safely. Industry-leading compliance culture and performance are part of their day-to-day work, and they work hard to maintain the Sterling standards.
Dedicated to adding value through continuous improvement, they constantly explore new and improved ways of doing things as part of their Technology and Innovation Program.
With over 50 years of experience, their exceptionally talented team combines their unrivaled knowledge with first-class customer service to ensure high-quality project delivery every time. That’s the Sterling way!
Bio Highlights: Mark is the Senior Director, Global Commercial Operations for Sterling Pharmaceutical Solutions, and is responsible for the commercial activities across Sterling’s three sites (Germantown, WI, Cary, NC, and the United Kingdom). Mark began his professional career as a Microbiology Specialist at a contract manufacturing company focusing on consumer and Over the Counter products. Mark transitioned to the pharmaceutical side of the CMO industry in 2007 and has spent the last 12+ years in various roles of increasing responsibility, including project management, operations, and business development. Mark Millar received his Bachelor of Science degree from Royal Roads University and later completed his Project Management Professional certification.