Mark Rohlfing

Mark Rohlfing has extensive work experience in the pharmaceutical industry. Mark started their career as a Microbiologist at Teva Pharmaceuticals in 1994, eventually transitioning to the role of Regulatory Compliance Auditor. In 2000, they joined Cell Pathways, Inc. as a GMP Auditor. Later that same year, they joined Almac Group as a Quality Control Manager. Mark then progressed within the company, serving as Director of Quality and currently holds the position of Vice President of Operations - Clinical Services.

Mark Rohlfing has a Master of Science (MS) degree in Biology from Villanova University and a Bachelor of Science (BS) degree in Biology and Chemistry from Millersville University of Pennsylvania. Additionally, they have obtained certifications from ASQ - World Headquarters, including the Certified Manager of Quality/Organizational Excellence (CMQ/OE), Certified Quality Auditor (CQA), and Certified Six Sigma Green Belt (SSGB).