Senior Manager, Project Engineer

Bristol Myers Squibb

Devens, MA, United States
Base: $139,480 - $169,013; bonus/equity: + incenti...
50% onsite
Cell therapy manufacturing projects
Automated systems commissioning and qualification
Gmp operations support
This role is responsible for executing cross‑functional projects that enable new capabilities, process enhancements, and technology deployments within the Devens Cell Therapy Facility

Job Summary

  • This role is responsible for executing cross‑functional projects that enable new capabilities, process enhancements, and technology deployments within the Devens Cell Therapy Facility.
  • Key responsibilities include leading FAT, SAT, installation, commissioning, and qualification of automated systems, and providing technical process support for cell therapy manufacturing operations.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

This role is responsible for executing cross‑functional projects that enable new capabilities, process enhancements, and technology deployments within the Devens Cell Therapy Facility.

Salary

Base: $139,480 - $169,013; Bonus/Equity: Additional incentive cash and stock opportunities may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • cell therapy manufacturing projects
  • automated systems commissioning and qualification
  • GMP operations support
  • single-use technologies and closed systems
  • cGMP manufacturing environment experience

Nice-to-have

  • transforming patients' lives through science
  • collaboration and communication skills
  • critical thinking and diligence
  • work-life balance and flexibility

Key Requirements

  • Bachelor’s degree in science or engineering
  • Minimum 4–6 years of industry experience
  • Demonstrated experience delivering manufacturing or capital projects
  • Experience with equipment startup and validation
  • Experience within a cGMP manufacturing environment
  • Ability to develop and execute design, engineering, and validation strategies

Work Rights

Not specified

Tailored Resume

Cover Letter