John Condon

Manager Gmp Quality Assurance @ Deciphera Pharmaceuticals

About John Condon

John Condon is the Manager of GMP Quality Assurance at Deciphera Pharmaceuticals, where he has worked since 2019. He has over a decade of experience in Quality Assurance, previously serving as a Senior Quality Assurance Associate at Alkermes from 2014 to 2019.

Work at Deciphera Pharmaceuticals

John Condon has been serving as the Manager of GMP Quality Assurance at Deciphera Pharmaceuticals since 2019. In this role, he oversees quality assurance operations, ensuring compliance with Good Manufacturing Practices (GMP). His responsibilities include conducting audits of suppliers, vendors, and Contract Manufacturing Organizations (CMOs), as well as managing deviation investigations. Condon's position is critical in maintaining the integrity of quality systems within the organization, contributing to both commercial and clinical programs.

Previous Experience at Alkermes

Prior to his current role, John Condon worked at Alkermes as a Senior Quality Assurance Associate from 2014 to 2019. During his five years at Alkermes, he gained extensive experience in quality assurance processes and compliance. His work involved ensuring that quality standards were met across various projects, which laid a strong foundation for his subsequent role at Deciphera Pharmaceuticals.

Education and Expertise

John Condon studied at Massasoit Community College, where he earned an Associate of Arts degree in Liberal Arts and Sciences/Liberal Studies from 1998 to 2000. His educational background supports his expertise in quality assurance, particularly in the areas of Supplier/Vendor/CMO audits and deviation investigations. Condon has developed Quality Management Systems (QMS) that cater to both commercial and clinical environments, showcasing his comprehensive understanding of quality operations.

Background in Quality Assurance Operations

With over a decade of experience in Quality Assurance operations, John Condon has focused on both commercial and clinical programs. His background includes implementing change control and continuous improvement initiatives, which are essential for maintaining high-quality standards in pharmaceutical manufacturing. Condon's extensive experience enables him to effectively manage quality assurance processes and contribute to the overall success of the organizations he has worked for.

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