A lifelong worker in the field of cancer research, discovery, and development. A bachelor’s in science (chemistry) and obtaining an executive MBA during a time of managing a $50 million dollar product line with 220 personnel. Starting a company in Massachusetts to make clinical materials for AIDS, cancer, neurological disorders, anti-drug addiction, compounds to counter infectious diseases, antiviral research, and novel separations technologies for chiral molecules. Building out three facilities for cGMP work, the last one, 165,000 sq. ft. facility, still in operations, designed for up to 52 cGMP rooms and 6 cGMP manufacturing suites for small molecules. Real expertise in drug discovery, development and, cGMP process scale-up and compliance. Completely understand the needs of an API manufacturing facility and build processes that are scalable, environmentally acceptable, and safe. 3 FDA inspections with no 483's, ISO certification, DEA registration, DoD compliance, NCI contractor and inventor. Has also broad-based experience in start-up companies and how to make them operational and profitable. 7 years of Team set-up, management, and implementation for 165-person company (Pharm-Eco) and lecturer on cGMP and Teams within the Pharmaceutical Industry. What Job does your product or service do? How good is the team running your company? How good is your technology?