Adyasha Mishra
About Adyasha Mishra
Adyasha Mishra is the Senior Manager of Regulatory Compliance, Global Quality at Bristol Myers Squibb, with a strong background in life sciences and good manufacturing practice.
Current Role at Bristol Myers Squibb
Adyasha Mishra serves as the Senior Manager of Regulatory Compliance, Global Quality, at Bristol Myers Squibb in New Brunswick, New Jersey. In this role, she oversees the implementation and maintenance of regulatory compliance standards and processes across the company's global sites. She partners with internal and external stakeholders to manage audits, inspections, and risk assessments, ensuring adherence to relevant guidelines and regulations.
Previous Experience at Bristol Myers Squibb
Prior to her current role, Adyasha held various positions at Bristol Myers Squibb. From 2021 to 2023, she worked as a QA Drug Product Manager in New Brunswick, New Jersey. Before that, from 2018 to 2021, she served as a QA Specialist - Drug Product Parenteral in the Greater New York City Area. These roles involved managing quality assurance processes and ensuring compliance with good manufacturing practice (GMP) standards.
Earlier Career at IBM
Before joining the biopharmaceutical industry, Adyasha Mishra worked at IBM as an Associate System Engineer from 2012 to 2013 in Bangalore, India. In this capacity, she focused on software development and system engineering tasks, contributing to various technical projects and initiatives.
Educational Background
Adyasha holds a Master's of Biotechnology from Penn State University, where she studied from 2013 to 2015. She also earned a Bachelor of Technology (BTech) in Biotechnology from Vellore Institute of Technology, completing her degree in 2012. Her early education took place at Sacred Heart Senior Secondary School in Chandigarh, India.
Professional Certifications and Skills
Adyasha Mishra is an ASQ Certified Quality Improvement Associate, a credential that underscores her expertise in quality improvement and regulatory compliance. Her strong background in life sciences and GMP, combined with her passion for advancing the science and technology of biopharmaceuticals, enables her to support continuous improvement and innovation initiatives within her organization.