Miral Patel
Associate Director @Bristol Myers Squibb
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WORK HISTORY
Associate Director @Bristol Myers Squibb
Demonstrated strong leadership by developing and implementing a robust quality strategy for Cell Therapy and Oncology Therapeutic Areas, aligning with regulatory requirements and industry best practices.Led the drive for continuous quality process improvements by analyzing audit findings, assessment results, inspection outcomes, trends, and metrics.Championed the implementation of Quality by Design (QbD) principles, fostering a culture of proactive quality management throughout the project lifecycle.Took the lead in developing, implementing, and maintaining the quality strategy and evidence of quality activities.Collaborated closely with Research & Early Development (RED) and Global Development & Delivery (GDD) teams to integrate end-to-end quality principles and ensure alignment with project milestones.Established and nurtured strong partnerships with business stakeholders, demonstrating leadership in promoting shared understanding of quality objectives and ensuring seamless execution.Provided independent expert support, demonstrating leadership in analyzing complex quality challenges and proposing effective solutions to ensure quality and compliance.Led the presentation of key data on compliance, conformance issues, and risks, showcasing leadership in enabling data-driven decision-making and proactive risk management.
EDUCATION
University of Pennsylvania
Master's degree, Biotechnology
University of Illinois Urbana-Champaign
Bachelor's degree, Molecular Biology
SKILLS
ABOUT MIRAL PATEL
With over a decade of experience in biotechnology, I am a quality-driven leader who delivers innovation and excellence in cell therapy and oncology. As an Associate Director at Bristol Myers Squibb, I develop and implement robust quality strategies that align with regulatory requirements and industry best practices, fostering a culture of proactive quality management throughout the project lifecycle.In my current role, I lead the drive for continuous quality process improvements by analyzing audit findings, assessment results, inspection outcomes, trends, and metrics. I also champion the implementation of Quality by Design (QbD) principles, enabling the team to anticipate and mitigate potential quality risks. Additionally, I collaborate closely with Research & Early Development (RED) and Global Development & Delivery (GDD) teams to ensure the quality strategy and evidence of quality activities are integrated and consistent across the portfolio. I leverage my skills in electronic trial master file (eTMF), CRFs, and cell biology to support the execution and delivery of clinical trials. I am motivated by the mission of Bristol Myers Squibb to discover, develop, and deliver transformative medicines that help patients prevail over serious diseases.
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