Tressa Randall
Vice President Regulatory Affairs and Quality
Professional Overview
Tressa Randall is an experienced pharmaceutical executive with a track record of driving regulatory compliance and quality assurance initiatives. As the Vice President of Regulatory Affairs and Quality at Faraday Pharmaceuticals, Inc., she leverages her deep industry expertise to ensure the company's product portfolio meets stringent regulatory standards while upholding the highest quality benchmarks.
Experience Summary
Current Role
Serving as the Vice President of Regulatory Affairs and Quality at Faraday Pharmaceuticals, Inc., Tressa is responsible for overseeing all aspects of the company's regulatory compliance and quality management systems. She leads a team of subject matter experts in navigating the complex regulatory landscape, strategically guiding Faraday's product development and commercialization efforts to achieve timely approvals and successful market launches. Under her leadership, Faraday has maintained an impeccable regulatory standing, earning the trust of industry stakeholders and regulatory agencies.
Career Progression
Tressa's career in the pharmaceutical industry spans over 15 years, during which she has held progressive leadership roles in regulatory affairs and quality assurance. Prior to her current position, she served as the Director of Regulatory Affairs at Acme Pharmaceuticals, where she spearheaded the successful registration of multiple drug products in both domestic and international markets. Tressa's ability to navigate complex regulatory frameworks and drive continuous quality improvements has been instrumental in advancing the companies she has served.
Academic Background
Tressa holds a Bachelor of Science degree in Pharmaceutical Sciences from the University of Washington, where she graduated with distinction. She is also a certified regulatory affairs professional (RAC) and a member of the Regulatory Affairs Professionals Society (RAPS), actively contributing to industry best practices and thought leadership.
Areas of Expertise
- Regulatory strategy and compliance
- Quality management systems and process optimization
- Product registration and lifecycle management
- Cross-functional collaboration and stakeholder management
- Leadership and team development
Professional Impact
During her tenure at Faraday Pharmaceuticals, Tressa has spearheaded the successful registration of three novel drug products, achieving first-cycle approvals from the U.S. Food and Drug Administration (FDA) and regulatory bodies in key international markets. Her strategic approach to regulatory affairs and quality management has been instrumental in maintaining Faraday's reputation as a reliable and innovative pharmaceutical partner.
Conclusion
Tressa Randall's extensive expertise in regulatory affairs and quality assurance, combined with her proven leadership skills, make her a valuable asset to Faraday Pharmaceuticals and the broader pharmaceutical industry. Her commitment to upholding the highest standards of compliance and quality continues to drive innovation and ensure the safe and effective delivery of Faraday's products to patients worldwide.
