Verified recordBiotechnology Research

Tao Ling

Lead Quality Operations, Cmc, Gmp at Praxis Precision Medicines, Inc

Based in San Francisco, United States

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Seniority

Other

Department

Other

Location

San Francisco

Industry

Biotechnology Research

Company size

180

Contact information

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Email

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t•••••••@praxismedicines.com

Phone

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Background

About Tao Ling

Strategic Operational QA Expert with over 15+ years of experience in quality assurance, regulatory compliance, and risk management, I specialize in enhancing operational efficiency, ensuring GxP adherence, and maintaining inspection readiness across clinical and commercial pharmaceutical stages. My expertise lies in developing proactive quality strategies that drive compliance, optimize processes, and mitigate risk, enabling organizations to deliver high-quality, safe, and effective products to global markets. Whether leading quality system improvements, streamlining audit processes, or strengthening cross-functional collaboration, I thrive in fast-paced environments that demand precision, strategic thinking, and a commitment to excellence. I’m passionate about building scalable quality frameworks that improve compliance and operational efficiency while fostering a culture of continuous improvement and accountability. I excel at turning regulatory challenges into opportunities, refining deviation and CAPA management processes, and implementing data-driven quality solutions that align with industry best practices. Through collaborative leadership, strategic vision, and an unwavering focus on quality, I empower organizations to exceed regulatory expectations, minimize risk, and drive long-term success in pharmaceutical and biotech operations. Transformational Results: Boosted operational efficiency by 15%, reduced rework by 10%, and improved productivity by implementing innovative quality systems. Reduced audit findings by 30% through the implementation of a risk-based monitoring approach and proactive CAPA management. Accelerated project timelines by 20% and improved product development quality outcomes by building strong relationships with CDMOs. Increased quality process efficiency by 15% by successfully initiating and delivering process validation and root cause analysis projects. Led high-impact initiatives that lowered deviations by 20% and enhanced quality metrics by improving compliance with SOPs. Let’s connect to discuss how my expertise and proactive, data-driven approach to quality assurance can strengthen compliance, optimize processes, and drive long-term success for your organization!

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