Jose R. Deida-Soto

Jose R. Deida-Soto has a comprehensive work experience in the pharmaceutical industry. Jose R. currently serves as the Director of Quality Operations at Neolpharma S.A. de C.V, where they ensure compliance with regulatory requirements and oversees the overall quality program. Prior to this, they worked as the Technical Services Manager at Neolpharma, Inc., where they managed manufacturing and packaging operations for marketed products. Jose R. has also held roles as an Audit and Quality System Expert at Business Excellence Consulting, Inc., where they performed GMP compliance audits, and as a QA Compliance Manager at iPR Pharmaceuticals, Inc. Overall, Jose has a strong background in quality management, compliance, and technical operations in the pharmaceutical industry.

Jose R. Deida-Soto holds a Bachelor of Science degree in Chemistry from the University of Puerto Rico, Río Piedras. Jose R. has additional certifications as a Certified Quality Engineer from ASQ, a Chemist from CQPR, and an ISO 9001:2008 Lead Auditor with Medical Device Focus (ISO 13485:2003) from AQS Management Systems, Inc. (Exemplar Global Certified).