A company is looking for a Principal Quality Systems Compliance Specialist.
Key Responsibilities
Own the Quality Systems metrics process and lead root cause analysis investigations
Facilitate investigations into quality issues and develop corrective and preventive actions
Collaborate cross-functionally to support regulatory inspections and manage the Material Review board
Required Qualifications
Bachelor of Science or equivalent combination of education and industry experience
8+ years of experience in a biopharmaceutical / pharmaceutical environment
Expert knowledge of root cause analysis and cGMP processes
Ability to make compliance-related decisions with minimal supervision
Experience with computerized programs such as AssurX (eQMS)
Quality System Specialist • Chandler, Arizona, United States