MES Engineer
Bristol Myers Squibb
July 02, 2026
On-site
Devens, MA
IT
Summary
The MES Engineer is responsible for the configuration, implementation, and support of Manufacturing Execution System (MES) solutions within the Devens Cell Therapy Facility (Emerson Syncade MES), focusing on recipe authoring, troubleshooting, and system maintenance to ensure reliable and compliant operation.
Responsibilities
- Configure, modify, and maintain MES recipes to meet business requirements.
- Document and test changes following governance procedures.
- Provide hands-on support for MES issues affecting manufacturing.
- Collaborate with IT and operations to troubleshoot and resolve incidents.
- Participate in rotational on-call support.
- Develop working knowledge of assigned manufacturing processes.
- Assist investigations and contribute to recipe improvements.
- Support creation of training materials; guide new MES users/recipe authors.
- Contribute to design, testing, documentation, and deployment of moderate-complexity MES solutions.
Compliance & Documentation
- Ensure MES compliance with cGMP, 21 CFR Part 11, Annex 11, and internal quality standards.
- Maintain technical documentation, test records, and validation deliverables.
Qualifications
- Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field.
- 1–3 years of MES experience in Biologics, Pharmaceutical, or Cell/Gene Therapy.
- Exposure to Emerson Syncade MES (or comparable MES) preferred.
- Understanding of cGMP and computerized system validation.
Skills
- Strong problem-solving and attention to detail.
- Effective communication; cross-functional collaboration.
- Interest in recipe authoring, troubleshooting, and continuous improvement.
Compensation/Benefits (as stated)
- Devens, MA: $89,390–$108,315.
- Health coverage; wellbeing support; 401(k); disability/life insurance and other listed protection benefits; paid time off.
Application
- If the role doesn’t perfectly match your resume, apply anyway.
The MES Engineer is responsible for the configuration, implementation, and support of Manufacturing Execution System (MES) solutions within the Devens Cell Therapy Facility (Emerson Syncade MES), focusing on recipe authoring, troubleshooting, and system maintenance to ensure reliable and compliant operation.
Responsibilities
- Configure, modify, and maintain MES recipes to meet business requirements.
- Document and test changes following governance procedures.
- Provide hands-on support for MES issues affecting manufacturing.
- Collaborate with IT and operations to troubleshoot and resolve incidents.
- Participate in rotational on-call support.
- Develop working knowledge of assigned manufacturing processes.
- Assist investigations and contribute to recipe improvements.
- Support creation of training materials; guide new MES users/recipe authors.
- Contribute to design, testing, documentation, and deployment of moderate-complexity MES solutions.
Compliance & Documentation
- Ensure MES compliance with cGMP, 21 CFR Part 11, Annex 11, and internal quality standards.
- Maintain technical documentation, test records, and validation deliverables.
Qualifications
- Bachelor’s degree in Engineering, Computer Science, Life Sciences, or related field.
- 1–3 years of MES experience in Biologics, Pharmaceutical, or Cell/Gene Therapy.
- Exposure to Emerson Syncade MES (or comparable MES) preferred.
- Understanding of cGMP and computerized system validation.
Skills
- Strong problem-solving and attention to detail.
- Effective communication; cross-functional collaboration.
- Interest in recipe authoring, troubleshooting, and continuous improvement.
Compensation/Benefits (as stated)
- Devens, MA: $89,390–$108,315.
- Health coverage; wellbeing support; 401(k); disability/life insurance and other listed protection benefits; paid time off.
Application
- If the role doesn’t perfectly match your resume, apply anyway.