Immanuel Moss serves as the Quality Assurance Validation Manager at Kiniksa Pharmaceuticals, providing leadership in lab and process equipment design, qualification, and maintenance/calibration. Responsibilities include supporting Data Integrity initiatives and overseeing computer systems Risk Based Assessments. Prior experience includes roles as Autoclave SME and Validation Lead at Thermo Fisher Scientific, Senior Validation Engineer at Regeneron and AstraZeneca, and various engineering positions in the military and pharmaceutical sectors. Immanuel holds a Bachelor’s degree in Physics from Kutztown University of Pennsylvania and possesses extensive experience in validation processes, equipment qualification, and regulatory compliance within the pharmaceutical and medical device industries.
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