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Michael Carlson has extensive work experience in the field of analytical development and quality control. Michael is currently serving as the Head of Analytical and Quality Control at Northway Biotech since 2022.

Before joining Northway Biotech, Carlson held the role of Director of Analytical Development and Quality Control at Pharmasol Corporation from 2015 to 2022. In this position, they were responsible for managing the day-to-day technical and scientific operations of the Analytical Development and Quality Control department. Michael also optimized laboratory resources to meet manufacturing demands.

Prior to Pharmasol Corporation, Carlson worked at Bio-Concept Laboratories, Inc. as a Quality Control Manager in 2015. Michael managed the quality control group and ensured adherence to cGMP, ICH, and USP guidelines for raw materials and finished product analysis.

From 2009 to 2015, Carlson served as a QC Manager/ Supervisor at Allergan Medical, where they oversaw the day-to-day operations of the quality control group and conducted method transfers.

Earlier in their career, Carlson worked as a Laboratory Director and Owner at an Independent Testing Laboratory from 1989 to 2009. Michael was responsible for planning and managing the laboratory's operations.

At the beginning of their career, Carlson held the position of Quality Control (QC) Manager and Program Chemist at Gillette Company from 1977 to 1989. Michael managed the quality control laboratory and was involved in hiring and training analysts.

Michael Carlson holds a Bachelor's Degree in Chemistry from St. Anselm College. Michael also obtained a Master's Degree in Analytical Chemistry from the University of Massachusetts Lowell.