Jose Andrade
About Jose Andrade
Jose Andrade is a Sr. Specialist in QA Operations at Bristol Myers Squibb, specializing in quality assurance for cell therapy development and operations.
Current Company
Jose Andrade currently works at Bristol Myers Squibb in New Jersey, United States. He holds the position of Sr. Specialist, QA Operations in the Quality Assurance Cell Therapy Development & Operations (CTDO) department. His role involves ensuring adherence to quality standards and regulatory requirements in cell therapy development.
Previous Positions
Before joining Bristol Myers Squibb, Jose Andrade worked at Cosette Pharmaceuticals, Inc. as the Quality Assurance Operations-Batch Release Lead from 2019 to 2021 in South Plainfield, NJ. Additionally, he has been associated with G&W Laboratories as a Quality Operation Auditor - Batch Release in South Plainfield, NJ. His earlier roles also include serving as a Complaint Management Analyst at MTF (Musculoskeletal Transplant Foundation) in Edison, NJ, and a Complaint Analyst III - Quality Systems at Accriva Diagnostics in Piscataway, NJ.
Long-term Experience at Hoffmann-La Roche Inc.
Jose Andrade has substantial experience at Hoffmann-La Roche Inc., where he worked from 1999 to 2010. He started as a Quality Assurance - Compliance Specialist - QA and later served as Quality Assurance Compliance - Compliance Associate. This period includes his involvement in ensuring compliance with regulatory standards and managing quality assurance practices within the organization.
Expertise in GMP and Quality Assurance
Jose Andrade has extensive experience in auditing Shop Floor activities to ensure compliance with current Good Manufacturing Practices (GMP). He specializes in identifying regulatory deficiencies and potential improvements in GMP manufacturing-related documentation. His strong background in batch record review and documentation is a key aspect of his expertise in the pharmaceutical industry.
Educational Background
Jose Andrade studied at Kean University, where he acquired foundational knowledge that supports his extensive career in quality assurance and regulatory compliance. His education plays a crucial role in his ability to manage complex situations and meet the stringent demands of the pharmaceutical industry.