Overview In this role you will design and execute experiments to support discovery and development of next-generation immune-oncology therapeutics. You will work hands-on in analytical development, communicating results to advance candidates toward clinic and commercialization. You'll collaborate with cross-functional teams to optimize methods, analyze data, and prepare development reports and SOPs. This is a fast-paced, impact-driven position at a company focused on translating science into therapies for cancer patients. You will help shape analytical strategies and contribute to regulatory-ready documentation.
Compensation / Benefits- Annual bonus program
- Incentive stock option plan
- 401k plan with flat non-elective employer contribution
- Comprehensive medical insurance
- Dental and vision insurance
- Unlimited PTO
Responsibilities- Perform HPLC and UPLC assays (SEC and RP) with minimal supervision
- Execute CE-SDS and iCIEF analysis for protein therapeutics and contribute to method qualification and lifecycle management
- Perform ELISAs for potency assessment
- Conduct DLS/SLS analysis using UNcle instrument for formulation development
- Perform subvisible particulate matter analysis by HIAC
- Support formulation development and clinical in-use stability studies; transfer formulation knowledge internally
- Design, analyze, interpret, and report experiments; prepare development reports and method qualification documents
- Write and manage SOPs and test methods; maintain reagents and equipment; ensure GDP-compliant documentation
- Prepare presentations for team meetings and work with team leaders to prioritize high-impact work
Key requirements- Bachelor's degree with 4-6 years of relevant industry experience or Master's degree with 3-5 years
- Strong benchtop skills and experience with protein biologics/peptides
- Proficiency with HPLC and UPLC assays ( 3 years); SEC and RP are desired
- Experience with CE-SDS and iCIEF or related electrophoretic methods preferred
- Experience with ELISAs is desired; method qualification, comparability, stability, or formulation development experience preferred
- Ability to analyze complex data, troubleshoot, and communicate conclusions
- Proficiency with SOPs, GDP-compliant documentation, and ELN systems
- Independent work capability with proactive problem-solving; strong computer skills (Excel, PowerPoint)
- excellent communication
- team player
- organization
- HPLC and UPLC assays
- SEC and RP chromatography
- CE-SDS
