Scientist/Sr. Scientist, Biochemical Assay Development
Sutro Biopharma, Inc. - South San Francisco, CA

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Sutro Biopharma, located in South San Francisco, is developing a new generation of antibody drug conjugate therapeutics and bifunctional antibody-based therapeutics for targeted cancer therapies. These therapeutics will significantly extend the clinical impact of current oncology therapeutic approaches and are beyond what can be envisioned with current cell-based expression technologies. Sutro's biochemical synthesis technology, which underpins these therapeutics, allows the rapid and systematic exploration of many protein drug variants to identify drug candidates. Once these product candidates are identified, production can be rapidly and predictably scaled up to commercial levels. Sutro has established a Good Manufacturing Practice (cGMP) facility for the production of clinical supplies of materials using its biochemical protein synthesis platform. Sutro Biopharma is collaborating with pharmaceutical and biotech companies in the discovery and development of novel protein therapeutics.

Sutro Biopharma, Inc. is looking for energetic and talented individuals to join its multidisciplinary research and development team. You will be working to maximize our technology and internal and collaborative product development initiatives in a fast paced environment.

We are seeking a Scientist/Sr. Scientist to join our Analytical Development group to support process development and manufacturing of recombinant bio-therapeutic proteins.

The candidate we are seeking will independently develop, validate and perform assays for biochemical characterization and quality control of recombinant proteins under regulated/non regulated environment. The candidate will be responsible for routine sample analysis using, but not limited to, ELISA, Biacore, q-PCR, UV-Vis and cell based assays to assess product quality and potency. The position will also include writing SOPs, protocols and reports as per FDA/ICH guidelines. The candidate will be responsible for analyzing, interpreting and presenting results at team meetings. The ideal candidate will have experience in drug development/QC environment and possess a strong work ethic. - 2 years ago - save job