Senior Lab Automation Engineer – GXP/CSV Specialist

Biopharma Careers; Harvard (MA); On-site; USD 99,000 - 121,000; Full time

Benefits offered by this job

Wellbeing support

Retirement plan

Insurance (medical, dental, vision)

Flexible Time Off

11 company holidays

Job summary

Bristol Myers Squibb in Devens, MA is seeking a Senior Engineer - Lab Automation to lead documentation, configure and support computerized systems, and ensure compliant operation of lab automation on the manufacturing floor.

You will mentor staff, coordinate multiple projects, work with cross-functional teams on data integrity, cyber security, and 21 CFR Part 11, and provide on-call support for 24/7 operations within a dynamic biopharma environment.

Qualifications

• Bachelor's degree in Life Sciences, Chemistry, Engineering, IT or related field with 5+ years in pharma lab ops or informatics.
• Hands-on experience configuring automation software and system integrations (e.g., Hamilton Venus).
• Experience with lab workflows, data integrity, cyber security, and validation (21 CFR Part 11, GAMP 5).

Responsibilities

• Execute and manage documentation and processes supporting lab automation assets.
• Configure, maintain, and support computerized systems and software on the lab floor.
• Support system implementations, upgrades, IQ/OQ, and validation activities.
• Lead multiple projects and provide SME guidance to cross‑functional teams.
• Provide end‑to‑end support for changes, incidents, problems, and asset management.

Skills

Automation software configurations

Hamilton Venus

Lab instrumentation knowledge

Data integrity & cyber security

Project leadership

Documentation practices

Cross-functional communication

CSV/GMP/FDA/GAMP/ISO/ICH knowledge

Education

Bachelor's degree in Life Sciences/Engineering/IT

Tools

Hamilton Venus

HighRes BioSolutions

Cellario

GXP lab software

Job description

Bristol Myers Squibb in Devens, MA is seeking a Senior Engineer - Lab Automation to lead documentation, configure and support computerized systems, and ensure compliant operation of lab automation on the manufacturing floor.

You will mentor staff, coordinate multiple projects, work with cross-functional teams on data integrity, cyber security, and 21 CFR Part 11, and provide on-call support for 24/7 operations within a dynamic biopharma environment.