Editha Simon, BPharm, MBA is Director of Quality Compliance at Jeiven Pharmaceutical Consulting, Inc. She is responsible for the review and approval of batch records before start of operations and after execution, on-site monitoring of manufacturing, packaging and labeling activities and release of clinical supplies. She manages several quality consultants involved in auditing of contract manufacturing and testing facilities. She reviews and maintains Standard Operating Procedures (SOPs) for compliance to GMPs, regulatory guidelines and company policies.
Editha joined Jeiven in March, 2005 as Quality Assurance Consultant. She has extensive experience in both large and small pharmaceutical companies having worked in different capacities in research and development, manufacturing and quality control.