Associate Director, Regulatory Affairs CMC
Posted by employer 2 months ago
First seen on Joblaze 1 week 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
In this role, the Associate Director of Regulatory Affairs CMC is responsible for overseeing the regulatory strategy and submissions related to chemistry, manufacturing, and controls for CRISPR Therapeutics' products. The position requires expertise in regulatory guidelines and a strong background in CMC processes, making it ideal for candidates with significant experience in the biotech or pharmaceutical sectors. This role suits professionals who are adept at navigating complex regulatory environments and have a proven track record in managing submissions. CRISPR Therapeutics is focused on innovative gene-editing technologies, positioning the team at the forefront of biopharmaceutical advan
Joblaze insights
- Listed 7 days ago on Joblaze — tracked directly from CRISPR Therapeutics's career page.
- CRISPR Therapeutics has 17 other open roles including Associate Manager, CMC Operations, Director, LNP Discovery, Clinical Trial Associate.
Quick facts
- What seniority level is this role?
- CRISPR Therapeutics targets director candidates for this position.
- Is this full-time or contract?
- Full-time for this Associate Director, Regulatory Affairs CMC role at CRISPR Therapeutics.