About this opportunity
Monte Rosa Therapeutics, Inc lists this Regulatory Affairs Manager, FDA Submissions opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Monte Rosa Therapeutics, Inc is seeking an experienced regulatory affairs professional in Boston, MA. Responsibilities include coordinating regulatory workflows, compiling submissions to the FDA, and providing ongoing support to project teams.
The ideal candidate holds a Bachelors/Masters in a scientific discipline with at least 8 years of relevant experience. Strong knowledge of CMC requirements and excellent organizational skills are essential. The position involves direct interaction with regulatory agencies and is critical to the success of regulatory initiatives.
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.