Associate Scientist/Engineer, Manufacturing Technology

Scorpion Therapeutics; Harvard (MA); On-site; USD 85,000 - 125,000; Full time

Job summary

Bristol Myers Squibb, based in Devens, MA, is seeking an Associate Scientist/Engineer to support commercial biologics manufacturing within the Manufacturing Science and Technology team. The role focuses on resolving process deviations, conducting root cause analyses, and aiding technology transfer to ensure robust, scalable production.

The candidate will contribute to process validation, lifecycle management, and regulatory readiness, working on large-scale cell culture and single-use biologics

Qualifications

• Bachelor's in engineering, life sciences, biochemistry, or related field.
• 3–5 years of experience in biopharmaceutical manufacturing, process engineering, or technical operations.
• Knowledge of biologics production, GMP standards, and process troubleshooting.

Responsibilities

• Troubleshoot process deviations and perform root cause analyses.
• Contribute to process validation and lifecycle management.
• Support regulatory inspections and audits.
• Assist with technology transfer in large-scale cell culture and single-use biologics operations.

Skills

Biopharma manufacturing

GMP knowledge

Data analysis

Process troubleshooting

Education

Bachelor's degree in engineering or life sciences

Job description

Role

Support commercial biologics manufacturing as an Associate Scientist/Engineer within Bristol Myers Squibb's Manufacturing Science and Technology team. Responsibilities include troubleshooting process deviations, conducting root cause analyses, contributing to process validation and lifecycle management, and supporting regulatory inspections and audits. The role emphasizes applying scientific knowledge and data analysis to improve process robustness, monitor performance, and facilitate technology transfer in large-scale cell culture and single-use biologics operations.

Qualifications

• Bachelor's in engineering, life sciences, biochemistry, or related field;
• 3–5 years of experience in biopharmaceutical manufacturing, process engineering, or technical operations;
• knowledge of biologics production, GMP standards, and process troubleshooting.

Preferred

• experience with process validation, process transfer, and regulatory support activities.

High-Value

• focus on biologics, GMP compliance, process troubleshooting, deviation investigation, data analysis, and cross-functional collaboration.

The position is based in Devens, MA, with an on-site work setup and a focus on solving complex process challenges to ensure reliable supply of therapies.