ComplianceOnline

Expert Profile


Susan Muhr Leister
Director Quality Assurance, Technical Resources International Inc

Dr. Susan Leister serves as the director of quality assurance at Technical Resources International Inc. with over 19 years of experience in the pharmaceutical and medical device industry. She is also adjunct faculty for both graduate and undergraduate studies at the University of Phoenix. In addition to a bachelor’s degree in biochemistry and molecular biology, she has an MBA, a doctorate in organizational management with a focus on leadership, and holds certifications from the American Society of Quality (ASQ) as a Certified Quality Auditor and a Six Sigma Black Belt.

Dr. Leister has broad experience in GCP, GLP, and cGMP. She serves the ASQ Section 509 Executive Committee as the industry and professional development committee chair; she also served as a judge for ASQ’s International Team Excellence Awards in 2013 and 2014, and has been serving for the past four years as a Maryland Performance Excellence Award Examiner.

Trainings by Expert

Performance Metrics
Category: All FDA Regulated Industry , Hitech, Aerospace and Manufacturing , Quality Management , Quality & Safety , Best practices , Audits, CAPA , Manufacturing Quality , Quality management tools , Food Safety & Quality , Life sciences QA/QC , QA/QC

FDA Inspection Preparedness
Category: Drugs and Chemicals (Pharma) , Medical Devices , Clinical Research , Biotechnology , Laboratory Compliance , All FDA Regulated Industry , FDA Audit and Inspection , GXP Pharmaceutical , GXP Medical Devices , Quality and Safety , Audits & Inspections , QMS, ISO 13485, CAPA , Laboratory , GCP & Other Best Practices , Quality & Safety , Drugs Regulations , Clinical Trial Regulations , Biotech Regulations , Risk Management & Controls , All FDA Regulated Functions , Audit & Inspection-Role , Internal Audit , Quality Audit , Medical Device Inspection , Lab Audit , Drugs Inspections , Documentation and Policy Management , Lifescience process & Procedures , Life sciences QA/QC , Research & Development , Device R & D , Finance, Sox & Internal control , Regulations & Guidances , Best Practices & GXPs , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

Risk Management and Risk Analysis
Category: Drugs and Chemicals (Pharma)