Senior Associate Scientist, Analytical Development

Bristol Myers Squibb•Cambridge, MA

1d•$96,010 - $116,339•Onsite

About The Position

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. The ideal candidate possesses hands-on laboratory experience, a strong scientific foundation, and a commitment to data quality and compliance.

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).
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.

Nice To Haves

Experience or familiarity with mass spectrometry is a plus.
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) is a plus.
Experience with bioanalytical method validation (e.g., per FDA or EMA guidelines).
Working knowledge of statistical analysis tools (e.g., GraphPad Prism, JMP, or Excel-based analysis).
Experience with RNA characterization techniques (e.g., SEC, CE, RT-PCR, RNAseq).

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

Benefits

Medical, pharmacy, dental, and vision care.
BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
Flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees))
160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
Unlimited paid sick time
Up to 2 paid volunteer days per year
Summer hours flexibility
Leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs
Annual Global Shutdown between Christmas and New Years Day.