Senior Engineer, IT Laboratory & Quality Systems, Devens Biologics Digital Plant
Bristol Myers Squibb
August 13, 2026
Remote friendly (Devens, MA)
United States
IT
Duties:
- Ensure secure administration of documentation and benchtop equipment, lab, and quality systems.
- Provide end-to-end management in BMS systems for changes, incidents, problems, and asset management within defined timeframes.
- Assess system reliability; serve as plant subject matter expertise (SME).
- Ensure application configurations, data integrity, and cybersecurity meet regulatory compliance.
- Identify technology efficiencies; collaborate to develop methodologies.
- Maintain alignment with BMS directives and industry validation guidelines.
- Support Quality/Manufacturing during audits and inspections.
Requirements:
- Bachelor’s (or foreign equivalent) in Mechanical Engineering, Computer Engineering, or related field; 5 years progressive experience as a Validation Engineer (or related).
- 5 years experience in:
- Applying Lean/OpEx to optimize SDLC in regulated industries.
- Using LIMS, LES, ELN, and document management for benchtop equipment.
- Administering Waters NuGenesis and Empower.
- GMP, SOPs, GDocP; FDA/EU regulations.
- IT/network concepts, LDAP/Active Directory, databases, servers, user account management, operating systems.
- Supporting regulatory audits (researching responses; creating information/presentations).
Benefits (if applicable): annual discretionary bonus; healthcare, wellbeing support, 401(k), disability/life/insurance, and paid time off.
Apply: Use req. number R1603228 online or email resume to resume.com@bms.com. Up to 20% domestic travel; hybrid telecommuting allowed as determined by employer.
- Ensure secure administration of documentation and benchtop equipment, lab, and quality systems.
- Provide end-to-end management in BMS systems for changes, incidents, problems, and asset management within defined timeframes.
- Assess system reliability; serve as plant subject matter expertise (SME).
- Ensure application configurations, data integrity, and cybersecurity meet regulatory compliance.
- Identify technology efficiencies; collaborate to develop methodologies.
- Maintain alignment with BMS directives and industry validation guidelines.
- Support Quality/Manufacturing during audits and inspections.
Requirements:
- Bachelor’s (or foreign equivalent) in Mechanical Engineering, Computer Engineering, or related field; 5 years progressive experience as a Validation Engineer (or related).
- 5 years experience in:
- Applying Lean/OpEx to optimize SDLC in regulated industries.
- Using LIMS, LES, ELN, and document management for benchtop equipment.
- Administering Waters NuGenesis and Empower.
- GMP, SOPs, GDocP; FDA/EU regulations.
- IT/network concepts, LDAP/Active Directory, databases, servers, user account management, operating systems.
- Supporting regulatory audits (researching responses; creating information/presentations).
Benefits (if applicable): annual discretionary bonus; healthcare, wellbeing support, 401(k), disability/life/insurance, and paid time off.
Apply: Use req. number R1603228 online or email resume to resume.com@bms.com. Up to 20% domestic travel; hybrid telecommuting allowed as determined by employer.