About this opportunity
Bristol Myers Squibb lists this Global Regulatory CMC Lead for Cell Therapy opportunity in princeton, New Jersey. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Bristol Myers Squibb’s Global Regulatory Sciences - CMC team seeks an Associate Director to lead content development and review of CMC submissions across global markets. You will guide manufacturing change controls, support HA submissions, and coordinate with GPS/CTDO teams to ensure regulatory success.
In this role, you will manage complex projects, provide strategic input on regulatory expectations, and interact with health authorities as part of cross-functional teams.
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Worksite address
princeton, NJ, 08543, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.