Associate Director, Regulatory Affairs – CMC Small Molecules
Posted by employer 4 days ago
First seen on Joblaze 1 day ago
Last verified on the company career page 1 day ago
Not disclosed in this posting: compensation, years of experience, work arrangement, visa sponsorship.
Joblaze summary
The Associate Director of Regulatory Affairs for CMC Small Molecules at Monte Rosa Therapeutics is responsible for overseeing regulatory submissions and ensuring compliance with industry standards. This role requires expertise in chemistry, manufacturing, and controls, along with a strong understanding of regulatory guidelines. It is suited for a mid to senior-level professional with a background in pharmaceutical development and regulatory affairs. The position is part of a growing team focused on advancing innovative therapies.
Joblaze insights
- Listed yesterday — first seen on Joblaze September 25, 2026. Last confirmed on Monte Rosa Therapeutics's careers page September 25, 2026.
Quick facts
- What seniority level is this role?
- Monte Rosa Therapeutics targets director candidates for this position.
- Is this full-time or contract?
- Full-time for this Associate Director, Regulatory Affairs – CMC Small Molecules role at Monte Rosa Therapeutics.