Crystal Thaggard

About Crystal Thaggard

Over 20 years of experience in Biopharmaceutical/Pharmaceutical Quality Assurance and Quality Control. A highly motivated and focused quality management professional with demonstrated ability to deliver corporate projects across multiple functions and business lines. Successfully led and implemented new quality systems initiatives and refined existing processes by utilizing strong communication skills to facilitate a high level of collaboration among stake-holders at all organizational levels. Positively interacted with inspectors during regulatory and client audits.Delivered value to the organization by developing an auditable and robust electronic quality management software system, including configuration and validation, for electronic document management, training management, deviation management, corrective action management, and supplier quality management applications.• Electronic Quality Systems Implementation and Management• Document Control Management• Training Program Management• Hosting Regulatory and Client Initiated Audits• Technical Writing and Editing• Leader for Continuous Improvement Initiatives

Experience

1. Associate Director, Analytical Formulation Sciences Compliance

   KBI Biopharma

   Jun 2022 — Present

Skills

• Fda
• Quality Control
• Gmp
• Document Imaging
• Document Management
• Adobe Professional
• Capa
• Software Documentation
• Laboratory
• Biopharmaceuticals
• Glp
• Good Laboratory Practice (Glp)
• Quality Auditing
• Microsoft Office
• Quality Management
• Corrective and Preventive Action (Capa)
• Laboratory Skills
• Employee Training
• Validation
• Uv/Vis Spectroscopy
• Laboratory Information Management System (Lims)
• Lims
• Uv/Vis
• Sample Management
• Change Control
• Quality Assurance
• Pharmaceutical Industry
• Sop