Amanda has over 20 years of diverse pharmaceutical experience in Operations Management, Validation, Technical Services and Quality Assurance at various Pharmaceutical companies including PLIVA, Inc., Barr Pharmaceuticals, G&W Laboratories and Tris Pharma, Inc. She has a BS in Mechanical Engineering, with a concentration in Manufacturing, from Clarkson University and completed her MBA at Simmons College in Boston.
VP Global Analytical Sales and Business Development
Mark has 25 years of senior pharmaceutical industry experience (Brand, Generic and OTC) in public and private companies both domestic and international. Mark is skilled in pharmaceutical manufacturing, laboratory and development activities and sales and marketing. Experienced in product portfolio management, including product launches and clinical development, from product selection to life cycle management. Mark has extensive FDA, DEA, SEC and SOX compliance expertise, supply chain management and business development management including merger and acquisition work.
Mark has held executive positions for drug development companies such as Keryx Biopharmaceuticals, been president of Alpharma’s Generic Division (now Actavis) and Halo Pharmaceutical a contract development and manufacturing organization.
Director, Raw Material & Gas Testing
Lee’s prime responsibilities include management of the entire analytical chemistry team. Prior to joining the Whitehouse Laboratories’ team, Lee served as Chemistry Director for Gibraltar Laboratories, overseeing their contract services operation. In addition, he brings 20+ years of experience in all aspects of analytical chemistry inclusive of HPLC, GC, AA and numerous other analytical instruments. He provides his team with a wealth of experience in a wide array of wet-chemistry techniques and procedures. His hands on laboratory experience is coupled with an extensive cGMP and quality system background. A Master’s Degree Chemist, Lee is well positioned to work intimately with clients to insure their testing needs are always met.
Danielle has over 12 years of QA/QC experience at various contract research organizations. She has a BS in Biochemistry and a MS in Forensic Science.
Michael serves as Manager of Container Testing & Container Closure Integrity Testing at Whitehouse Laboratories. Michael has been working at Whitehouse Labs as part of the USP / EP Container testing team gaining hands-on experience with routine container testing as found USP chapters <661> and <671>. In his role, Michael utilizes his knowledge and experience to assist clients with general container qualification as well as the choice, development, and validation of the most appropriate CCI test method for their product-package systems.
Charles Felter serves as the Microbiology Manager at Whitehouse Laboratories, including Biological and Microbiological analysis. Charles has 6+ years of experience in the pharmaceutical industry, in both quality assurance and laboratory operations, including analytical/chemical, bioanalytical/biopharmaceutical, microbiological, and biological analyses and validation. He is a certified Lead Auditor by RABQSA with experience leading internal/external audit programs and hosting client and regulatory audits. He is a graduate of Dartmouth College, with an AB in Biology.
Business Development, Analytical
Aaron has over 10 years contract research testing experience within the medical device and pharmaceutical industries. He has a passion for developing rapport and building partnerships with clients to meet project timelines, regulatory endpoints, and strategic business goals. Previous to AMRI, Aaron worked as a Key Account / Regional Account Manager for WuXi AppTec and a Global Account Manager for Heraeus Medical Components. Prior to his Business Development experience, Aaron held a variety of technical positions ranging from Research Scientist to Study Director. He has a BS in Biology from St. John’s University and completed his MBA at Hamline University in Minnesota.