Mokhlis Sadihom
About Mokhlis Sadihom
Mokhlis Sadihom serves as the Quality Control Laboratory Manager at QuVa Pharma, Inc. in Bloomsbury, New Jersey, a position he has held since 2017, bringing over two decades of experience in quality assurance and analytical chemistry.
Work at QuVa Pharma
Mokhlis Sadihom has been serving as the Quality Control Laboratory Manager at QuVa Pharma, Inc. since 2017. Located in Bloomsbury, New Jersey, he oversees quality control operations, ensuring compliance with industry standards and regulations. His role involves managing laboratory processes, conducting quality assessments, and leading a team of professionals dedicated to maintaining product integrity.
Previous Experience in Quality Control
Before joining QuVa Pharma, Mokhlis Sadihom worked at G&W Laboratories as a Quality Control Laboratory Supervisor for ten years, from 2007 to 2017. His earlier experience includes positions at Johnson & Johnson and Pfizer, where he held roles as QA Scientist III and Group Leader. His extensive background in quality assurance spans over two decades, contributing to his expertise in laboratory management.
Educational Background in Chemistry
Mokhlis Sadihom holds a Master's degree in Analytical Chemistry from the University of London, which he completed from 1995 to 1997. He also earned a Bachelor's degree in Biochemistry from Alexandria University, studying from 1981 to 1985. His academic qualifications provide a strong foundation for his work in quality control and laboratory management.
Career Progression in the Pharmaceutical Industry
Mokhlis Sadihom's career in the pharmaceutical industry began at GSK, where he worked as an Analyst from 1999 to 2001. He then transitioned to Roche as an Analytical Development Chemist for one year before moving to Pfizer and Johnson & Johnson. His diverse experience across multiple leading pharmaceutical companies has equipped him with a comprehensive understanding of quality assurance processes.