Tim Myott has over 35 years’ experience in the pharmaceutical industry holding various positions in Manufacturing, Research and Development, Regulatory Affairs and Quality Assurance.  He has worked for companies such as DuPont, PerkinElmer, Wyeth, Millennium/Takeda, Cubist, and Merck.  Tim’s work includes developing drugs such as Cardiolite and Neurolite and launching Zerbaxa.  Tim is currently the Vice President of QA for Maplight Therapeutics and oversees all GMP, GCP, and GLP activities.  In addition to his work in the pharmaceutical industry, Tim held the position of adjunct professor in the Middlesex Community College Biotech program, where he developed courses in GMP Compliance and Pharmaceutical Processes and Systems.  Tim holds a BS from Franklin Pierce College and is an American Society of Quality Certified Quality Auditor (CQA).  Tim is also a long-time member of the Parental Drug Association.