Michael Rog supervises the Method Development and Validation group at the Lake Zurich Industrial Hygiene laboratory. He earned his B.S. in Biochemistry from the University of Illinois at Chicago and a Masters in Analytical Chemistry from Northeastern Illinois University.
Michael brings over 15 years of experience in the Pharmaceutical and Industrial Hygiene market segments, where he developed and validated dozens of analytical Industrial Hygiene methods for pharmaceutical compounds. During his time at Maxxam, Michael has led hundreds of projects that include the methodology expansion of ChemoAlert analysis, development and validation of OpiAlert, innovative techniques in method development for large molecules that include ADCs (Antibody Drug Conjugates), as well as development and validation of other small molecules at sub-nanogram levels.
As Director of Operations, Jason manages Maxxam’s 3 Industrial Hygiene laboratories across the United States. His mandate is to ensure their alignment with Maxxam’s quality and health and safety standards, as well as the adoption of our customer experience framework.
Jason brings over 20 years of multidisciplinary analysis experience that spans Paint, Coating, Pharmaceutical, Biopharmaceutical Diagnostic, and Industrial Hygiene market segments. He also has experience with research and development, quality control, re-validating products to modern standards and developing methodologies to analyze GMP regulated excipients and Active Pharmaceutical Ingredients.
Jason earned his B.A. in Chemistry from Saint Mary’s College of Winona Minnesota and his Doctorate in Analytical Chemistry from Northern Illinois University.
Mr. Meiners has more than 30 years of experience in Industrial Hygiene laboratory services with BV/Maxxam legacy companies. Matt has a B.A. in Chemistry from St. Olaf College, and is Board Certified in Industrial Hygiene (CIH). Matt is responsible for client relationship management, business development and technical consulting for the pharmaceutical business segment. His areas of expertise include industrial hygiene, occupational toxicology, API sampling/analysis, and process containment. Matt was one of the original principle authors of the Good Practice Guide, “Assessing the Particulate Containment Performance of Pharmaceutical Equipment”, published by the International Society of Pharmaceutical Engineers (2005). Matt has been an active participant and speaker for ISPE, the Occupational Toxicology Roundtable, the British Occupational Hygiene Society and the American Industrial Hygiene Association, and is widely regarded within Pharma as an expert resource in the areas of analytical chemistry, process containment assessment and pharmaceutical industrial hygiene.