Michael Inderwies
About Michael Inderwies
Michael Inderwies is a Quality Assurance Specialist in Development Operations at Bristol Myers Squibb, with a background in quality assurance from Teva Pharmaceuticals and a Bachelor's degree in Management Science from Kean University.
Current Role at Bristol Myers Squibb
Michael Inderwies is currently working as a Quality Assurance Specialist in Development Operations at Bristol Myers Squibb in Summit, New Jersey. In his current role, he is responsible for the release of raw materials and lab test reports related to batch processing. His duties include conducting evaluations of quality impact from deviations, performing investigations, and reviewing and approving Master Formulas. Additionally, he issues Certificates of Analysis, ensuring adherence to rigorous quality standards.
Previous Experience at Teva Pharmaceuticals
Before joining Bristol Myers Squibb, Michael Inderwies worked at Teva Pharmaceuticals as a Quality Assurance Analyst in Research and Development. He held this role from 2004 to 2018, accumulating 14 years of experience in Elizabeth, New Jersey. At Teva, he was involved in tasks such as reviewing and releasing specifications, which bolstered his proficiency in quality assurance and regulatory compliance within the pharmaceutical industry.
Educational Background
Michael Inderwies studied at Kean University, where he earned a Bachelor's degree in Management Science. His academic background has provided him with a robust foundation in management principles, critical thinking, and problem-solving skills, all of which are essential for his career in quality assurance within the pharmaceutical sector.