We are recruiting for an Associate Principal Scientist in Regulated Bioanalytics to serve as an advanced technical contributor responsible for the development, validation, and implementation of regulated bioanalytical methods to support quantitative analysis of therapeutic and biotherapeutic drug candidates.
Requirements
- Bachelor's (with 10+ years), Master's (with 6+ years) or Ph.D. (with 4+ years) in Chemistry, Analytical Chemistry, Molecular Biology, Immunology, Cell Biology, Biology, Biochemistry or a related Biological Sciences discipline and relevant experience.
- Advanced experience in regulated bioanalysis for PK and/or immunogenicity, including developing, qualifying, and validating ligand-binding and/or LCâMS assays.
- Strong knowledge of global regulatory expectations, including writing and reviewing documents for IND/BLA submissions.
- Ability to lead bioanalytical strategy for development programs, delivering high-quality data on time.
- Experience troubleshooting complex bioanalytical issues and adapting methods for challenging matrices and changing program needs.
- Clear scientific writing and communication skills to present data, interpret results, and support cross-functional decisions.
- Strong project management skills to run multiple studies and priorities in a fast-paced environment.
Benefits
- Comprehensive package of benefits including medical, dental, vision healthcare and other insurance benefits (for employee and family)
- Retirement benefits, including 401(k)
- Paid holidays, vacation, and compassionate and sick days