Senior QA Records Specialist: Deviation & Change Control

A leading technology and clinical staffing firm is looking for a Quality Assurance Records Senior Specialist in Louisville, CO. The successful candidate will be responsible for investigating quality events, managing change control records, and overseeing continuous improvement initiatives to enhance GMP efficiency. Candidates should possess a Bachelor's degree in a relevant field and have 8+ years of experience in deviation investigations and writing reports in a GMP environment. #J-18808-Ljbffr