Ron Lagerquist
About Ron Lagerquist
Ron Lagerquist is the SVP of Quality Assurance & Regulatory Affairs with nearly 30 years of experience in the field.
Ron Lagerquist SVP Quality Assurance and Regulatory Affairs
Ron Lagerquist holds the position of Senior Vice President for Quality Assurance and Regulatory Affairs. Leveraging nearly 30 years of experience in these fields, he leads initiatives to maintain high standards and ensure compliance with industry regulations. His role involves overseeing quality assurance processes, directing regulatory strategy, and ensuring that products meet all necessary compliance requirements. Having worked across multiple leading organizations, Ron brings a wealth of knowledge and expertise to his current position.
Ron Lagerquist Education and Expertise
Ron Lagerquist earned a Bachelor of Science degree in Biology from Humboldt State University. His academic background in biology provided a solid foundation for his career in quality assurance and regulatory affairs. Over nearly three decades, he has accrued extensive expertise in regulatory compliance, quality systems management, and strategic leadership. This educational background and professional experience make him well-equipped to navigate the complex regulatory landscapes in the healthcare and biotechnology industries.
Ron Lagerquist Leadership Roles at Allergan, Philips Oral Healthcare, and Baxter BioScience
Ron Lagerquist has held significant leadership roles at prominent companies such as Allergan, Philips Oral Healthcare, and Baxter BioScience. In these positions, he was responsible for leading quality assurance and regulatory teams, developing compliance strategies, and ensuring product safety and efficacy. His leadership has contributed to the successful navigation of regulatory approvals and the maintenance of high-quality standards, thereby fostering trust and reliability in the products and services offered by these companies.
Ron Lagerquist's 30 Years of Experience in Regulatory and Quality Assurance
Ron Lagerquist brings almost 30 years of experience in regulatory and quality assurance to his current role. His extensive career includes responsibilities such as overseeing regulatory submissions, ensuring product compliance with healthcare standards, and implementing robust quality assurance processes. This vast experience allows him to effectively address regulatory challenges and drive quality improvements, making him a valuable asset to any organization in the healthcare and biotechnology sectors.