Quality Assurance, Cgmp, Validation, GMP Operations, Regulatory Requirements, Sops

change requests , capas , manufacturing processes , Process campaigns, Deviation investigations, Root Cause Analysis, Operational readiness activities, MBR development revision, Rejected material management, 5-Why's, ishikawa, Technology transfers, Continuous improvement initiatives, Deviation assessments, Manufacturing equipment, Data integrity principles

Quality Assurance, Risk Assessment, Electronic Quality Management Systems, GMP compliance, Microsoft Office Applications, Analytical problem-solving