David Marks
Senior Project Executive, Process Engineering
David has over 30 years of experience with process systems and facilities in biotechnology, pharmaceutical, medical device, food and chemical industries. His professional experience is concentrated in the design of bioprocess systems and FDA-licensed commercial manufacturing facilities. Author of the Biotechnology Facilities chapter of Good Design Practices for GMP Facilities, 2nd Edition, David is a frequent speaker and consultant on bioprocess technology, facility design, and cGMP manufacturing topics. David is a contributing member of the ASME BioProcess Equipment (BPE) standard committee and has served for 10 years as chair of the design subcommittee.
