Mariah Cornish
About Mariah Cornish
Mariah Cornish is the Associate Director of Global Regulatory Sciences - CMC at Bristol Myers Squibb, with over 15 years of experience in the pharmaceutical and biotechnology industry.
Company
Mariah Cornish works at Bristol Myers Squibb in Massachusetts, United States. She is currently serving as the Associate Director, Global Regulatory Sciences - CMC. Bristol Myers Squibb is a renowned pharmaceutical company known for its focus on developing innovative therapies for serious diseases. Mariah plays an integral role in the company's regulatory affairs, particularly in Chemistry, Manufacturing, and Controls (CMC).
Prior Title and Roles
Mariah Cornish has held significant roles in various companies focusing on regulatory affairs and CMC. Before her current position, she was the Associate Director, Global Regulatory Affairs - CMC at Takeda from 2019 to 2020, and before that, she served as Senior Manager, Global Regulatory Affairs - CMC at Shire for 11 months from 2018 to 2019. She also worked as Manager, Global Regulatory Affairs - CMC at Shire from 2013 to 2018 and at Ipsen as Regulatory Affairs Associate - CMC in 2013.
Education and Expertise
Mariah Cornish has a solid academic background in engineering and biomedical sciences. She holds a Master’s degree in Biochemical Engineering from Dartmouth College (2006-2008) and a Bachelor’s degree in Biomedical Engineering from Rensselaer Polytechnic Institute (2001-2005). Her extensive education has equipped her with profound knowledge and skills that she applies to her roles in regulatory affairs and CMC within the pharmaceutical and biotechnology industries.
Industry Experience and Contributions
With over 15 years of experience in the pharmaceutical and biotechnology sectors, Mariah Cornish specializes in regulatory affairs and Chemistry, Manufacturing, and Controls (CMC). She has played a key role in the regulatory approval of multiple biologics and pharmaceuticals and has extensive experience in managing regulatory submissions and interactions with global health authorities, including the FDA and EMA. Additionally, she has been pivotal in the development and implementation of global regulatory strategies for complex biologics and pharmaceuticals.
Mentorship and Professional Development
Throughout her career, Mariah Cornish has been deeply involved in mentoring and training junior regulatory affairs professionals, fostering the next generation of experts in the field. She actively contributes to industry conferences and workshops related to regulatory affairs and CMC, sharing her insights and expanding her knowledge base. Her contributions have supported the successful launch of several new drug applications (NDAs) and biologics license applications (BLAs).