Senior Associate Scientist, Analytical Development

About the role

Bristol Myers Squibb is seeking a motivated and detail-oriented Senior Associate Scientist to join our Analytical Development team. In this role, you will support routine and non-routine analytical testing activities critical to the advancement of our in vivo non-viral drug discovery and development pipeline.

Responsibilities

• Perform routine analytical assays including ELISA, HPLC, and other analytical methods in support of research, process development, and quality control activities
• Execute and document laboratory experiments according to established SOPs, protocols, and Good Laboratory Practice (GLP) standards
• Analyze, interpret, and summarize experimental data with accuracy; prepare clear and concise lab reports and technical summaries
• Maintain laboratory equipment including calibration, troubleshooting, and coordination with vendors for preventive maintenance
• Prepare reagents, buffers, and standards required for analytical testing; manage inventory of laboratory consumables and supplies
• Support method development and optimization efforts under the guidance of senior scientists
• Ensure compliance with all safety regulations, environmental health and safety (EHS) guidelines, and BMS corporate policies
• Contribute to cross-functional teams, collaborating with colleagues in research, process development, and formulations

Requirements

• Bachelor's degree in Biochemistry, Chemistry, Biology, Pharmaceutical Sciences, or a related scientific discipline
• 1–5 years of hands-on laboratory experience, preferably with RNA and/or LNPs, including academic research, internships, or industry roles
• Proficiency with ELISA, Western blotting, cell-based assays, UV-Vis spectroscopy, or qPCR
• Proficiency with HPLC operations, including method execution, column management, and chromatography data system use (e.g., Empower, OpenLabs, Chromeleon)
• Experience or familiarity with mass spectrometry is a plus
• Demonstrated ability to work independently and manage multiple priorities in a fast-paced environment while maintaining accuracy and attention to detail
• Demonstrated ability to analyze data and present results to the team and the larger research community

Preferred Qualifications

• Experience in a pharmaceutical or biopharmaceutical industry setting
• Familiarity with ICH guidelines, GLP/GMP principles and regulatory submission requirements
• Experience with LIMS (Laboratory Information Management Systems)
• Experience with bioanalytical method validation (e.g., per FDA or EMA guidelines)
• Experience with RNA characterization techniques (e.g., SEC, CE, RT-PCR, RNAseq)