This innovative biotech focuses on the development of genetically targeted therapies to improve the lives of patients with rare diseases. The organizaiton is looking to bring a Senior Manager/Associate Director, Quality Assurance onto the team who will support external GMP manufacturing activities as they move through phase II. They are impressively backed by a clinical stage parent-company and have received 65 million in initial financing. The parent company's focus ranges from pre-clinical to late stage development in therapeutic areas including oncology, cardiology, dermatology and endocrinology. This unique opportunity will provide excellent exposure to different therapeutic areas with an organization that is reinventing biotech.
Reports into: VP Quality Assurance
-Perform external GMP manufacturing activities
-Support tech transfer
-CMO oversight including external audits, batch record review
-Interface with GMP manufacturing and internal QA team
-B.S. or advanced scientific degree
-Strong hands on GMP manufacturing experience
-Small molecule background
-Direct experience working in a virtual environment with contract manufacturers
Offices are located in San Francisco. This position has the potential to be fully remote with 50% travel.
Sthree US is acting as an Employment Agency in relation to this vacancy.