Senior Associate Scientist LNP Analytical Testing - Cambridge MA

VetJobs; Cambridge (MA); On-site; USD 87,000 - 105,000; Full time

Benefits offered by this job

Stock options

Incentive pay

Job summary

Bristol Myers Squibb in Cambridge, MA, is seeking a laboratory professional to perform analytical assays and support process development, stability, and quality control. The role emphasizes ELISA, HPLC, RNA-related techniques, and data interpretation within a GLP framework.

The candidate will work on multi-disciplinary teams, maintain critical equipment, prepare reagents, and ensure strict adherence to safety and regulatory guidelines. On-site role with competitive compensation.

Qualifications

• Bachelor's degree in Biochemistry, Chemistry, Biology, Pharmaceutical Sciences, or 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.
• Familiarity with RNA characterization techniques (e.g., SEC, CE, RT-PCR, RNAseq).
• Demonstrated ability to 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.
• Familiarity with ICH guidelines, GLP/GMP principles, and regulatory submission requirements.
• Experience with LIMS and Benchling 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).
• We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Responsibilities

• Perform routine analytical assays including ELISA, HPLC, and other analytical methods in support of research, process development, stability, 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

Skills

ELISA

Western blotting

Cell-based assays

qPCR

RNA characterization

Data analysis

Statistical analysis tools

Education

Associates

Bachelor's degree in Biochemistry, Chemistry, Biology, Pharmaceutical Sciences, or related scientific discipline

Tools

HPLC

Chromatography data systems

Empower

OpenLabs

Chromeleon

LIMS

Benchling

GraphPad Prism

JMP

Excel

Job description

Job Description

Job Description

Job Description

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

Key Responsibilities

• Perform routine analytical assays including ELISA, HPLC, and other analytical methods in support of research, process development, stability, 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

Auto req ID

486741BR

Minimum Education Required

Associates

Additional Qualifications/Responsibilities

• Bachelor's degree in Biochemistry, Chemistry, Biology, Pharmaceutical Sciences, or 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.
• Familiarity with RNA characterization techniques (e.g., SEC, CE, RT-PCR, RNAseq).
• Demonstrated ability to 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.
• Familiarity with ICH guidelines, GLP/GMP principles, and regulatory submission requirements.
• Experience with LIMS and Benchling 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).
• We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway.

Compensation Overview

Cambridge - MA - US: $86,510 - $104,833

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully – carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.

City*

Cambridge

State*

Massachusetts

Job_Category

Health/Medical other

Job Code

Pharmaceutical Pharmaceutical

Affiliate Sponsor

Bristol Myers Sqibb BMS