Jackie Elbonne
About Jackie Elbonne
Jackie Elbonne is the Senior Vice President, Quality and Chief Quality Officer with over 25 years of experience in the pharmaceutical and biotechnology industries.
Jackie Elbonne: Senior Vice President, Quality and Chief Quality Officer
Jackie Elbonne serves as the Senior Vice President, Quality and Chief Quality Officer. In this pivotal role, they oversee all aspects of quality assurance and regulatory affairs. With extensive responsibilities, they ensure compliance with global quality standards across all company operations. They bring their expertise to advance quality management systems, focusing on maintaining and elevating quality standards.
Jackie Elbonne Education: PhD in Biochemistry
Jackie Elbonne holds a PhD in Biochemistry from the University of London. This advanced education provides a solid foundation for their extensive career in the pharmaceutical and biotechnology industries. Their academic background equips them with the scientific knowledge essential for overseeing quality management systems and navigating complex regulatory frameworks.
Jackie Elbonne's Experience in the Pharmaceutical Industry
With over 25 years of experience in the pharmaceutical and biotechnology industries, Jackie Elbonne has a wealth of expertise. Their career includes significant roles in quality assurance and regulatory affairs. This extensive background helps them manage comprehensive quality programs and ensures regulatory compliance in global markets.
Jackie Elbonne: Leadership in Quality Assurance
Throughout their career, Jackie Elbonne has held various leadership roles focused on quality assurance and regulatory affairs. Their leadership ensures that quality management systems are robust and compliant with industry standards. They have been involved in numerous global regulatory inspections and audits, enhancing their expertise in maintaining high-quality standards.
Jackie Elbonne's Contributions to Quality Management Systems
Jackie Elbonne has a strong background in quality management systems and compliance. They have been instrumental in advancing quality standards within the biotechnology sector. Their work focuses on ensuring that quality systems are thoroughly implemented and maintained, contributing to the overall integrity and reliability of pharmaceutical products.