CZ

Cathleen Zimmerman

Quality Assurance/regulatory Specialist at Armis Biopharma

Cathleen Zimmerman is a Quality Assurance/Regulatory Specialist at CHD Bioscience, Inc. since December 2012, with extensive experience in regulatory affairs, including expertise in the 510(k) process, QSR - 21 CFR 820, ISO 13485, CAPAs, design controls, MDRs, and cGMPs. Previous roles include positions as a Legal Assistant at Stewart Law Offices, a Regulatory Affairs position at Colorado State University, and various roles at Kelly Services, Cedar Supply/VinylPatioKits.com, Cetac Technologies, Transgenomic, Inc., On Assignment Lab Support, and Cabot Corporation. Academic qualifications include a Certificate in Regulatory Affairs from Colorado State University and a B.S. in Chemistry from Illinois State University.

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