- Lilly (Pasadena, CA)
- …methods + Introduce and maintain innovative technologies with respect to peptide therapeutics, including developing and implementing assays and maintaining critical ... instruments. + Perform data analysis. Critically evaluate data and results and troubleshoot experiments. + Demonstrable ability to function independently, work within a team-oriented lab environment, and work within cross-functional project teams. + Maintain… more
- Amgen (Thousand Oaks, CA)
- …to have experience, knowledge and understanding of small molecule, peptide , and/or oligonucleotide development and commercial lifecycle maintenance, product ... stability programs, CMC regulatory filings, risk assessment, and Amgen Quality Management Systems. Amgen offers the opportunity to be at the interface between research, global development and manufacturing to ensure that our molecules become medicines. Many of… more
- Catalent Pharma Solutions (San Diego, CA)
- …Catalent's San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an ... array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of… more
- Genentech (South San Francisco, CA)
- …assessment and specifically their implementation in immunopeptidomics or MAPPs (MHC-associated peptide proteomics) assays. The intern will use advanced cell biology ... techniques, flow cytometry and high-resolution mass spectrometry to investigate how culture microenvironments influence antigen processing and presentation kinetics. This is a unique opportunity to apply deep immunological expertise to translational drug… more
- Gilead Sciences, Inc. (Oceanside, CA)
- …CH2/HOS stability, aggregation, or PK. + Proficiency with intact/subunit MS, peptide mapping, CE-SDS, SEC-MALS, cIEF and UPLC/HPLC techniques. + Knowledge of ... therapeutic antibody glycosylation, Fc engineering strategies, and effector-function silencing frameworks. + Familiarity with ICH Q5E/Q6B and analytical method qualification for glycan assays. + Experience with MS analysis tools (Protein Metrics, Peaks etc.)… more
- Catalent Pharma Solutions (San Diego, CA)
- …Catalent's San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an ... array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of… more
- Catalent Pharma Solutions (San Diego, CA)
- …Catalent's San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an ... array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of… more
- Catalent Pharma Solutions (San Diego, CA)
- …Catalent's San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic. This facility offers an ... array of services that support oral and injectable dosage forms that include preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution. Our San Diego location is the home of… more
- Danaher Corporation (San Francisco, CA)
- …expertise in one or more of the following is essential: intact mass analysis, peptide mapping, and PTM analysis. + An advanced degree (Ph.D. or MS) in Analytical ... Chemistry, Biochemistry, or a related field is preferred. We also enthusiastically welcome candidates with a BS and 10+ years of directly relevant industry experience. + Experience with scientific programming in Python or R is a plus + Must be legally… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …The ideal candidate will also have some prior experience with biologic, peptide or oligonucleotide products. + Proven track record in late-stage development ... investigational filings, marketing applications (NDA/MAA), global submissions, and post-marketing lifecycle management as the CMC Regulatory lead. + Regulatory experience in handling-controlled substance applications will be a plus. **Skills:** + Comprehensive… more