Colorado Licensed QC Compliance Specialist

A company is looking for a QC Technical Compliance Specialist. Key Responsibilities Manage compliance tasks including change controls, CAPAs, and document updates within the QC laboratory Collaborate with leadership and document writers to ensure accuracy and efficiency in document revisions Serve as a Subject Matter Expert for technical reports and facilitate compliance with established timelines Required Qualifications, Training, and Education BS in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field required 6+ years of pharmaceutical cGMP laboratory experience with a BS; 3+ years with a Master's; or 2+ years with a PhD Experience in cGMP analytical testing of drug substances and products in a high-volume Quality Control laboratory Strong understanding of quality event records and regulatory guidelines Proficiency in quality risk management and operational excellence

Created: 2026-03-05