T. J. Kuhn | GxP Zone

Good Practice for the Pharmaceutical Industry from the Quality Assurance Perspective

About T. J. Kuhn

Mr. Kuhn was trained as an analytical chemist at SUNY Geneseo. He began his career in the pharmaceutical industry at Merck Manufacturing Quality Operations in 1998 where he worked in several laboratory and validation capacities. After five years in the cGMP area, he has spent six years in Clinical Quality Assurance roles at Eisai, sanofi-aventis, and most recently at Celgene where serves as Clinical Quality Assurance with a focus on computer systems and vendor audits.

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