Principal Engineer, Qc Automation, Cell Therapy

Bristol Myers Squibb

Devens, MA, United States
Base: $124,590 - $150,977; bonus/equity: + incenti...
50% onsite
State-of-art automation solutions
Gmp qc laboratory implementation
End-to-end integrated automation systems
This role is a subject matter expert leading the implementation of state-of-art automation solutions for QC bioanalytical methods and technologies in autologous and allogenic cell therapy programs

Job Summary

  • This role is a subject matter expert leading the implementation of state-of-art automation solutions for QC bioanalytical methods and technologies in autologous and allogenic cell therapy programs.
  • Work collaboratively with internal and external stakeholders to ensure automation designs meet compliance and business requirements, and to implement novel integrated automated systems.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.

Matching Summary

This role is a subject matter expert leading the implementation of state-of-art automation solutions for QC bioanalytical methods and technologies in autologous and allogenic cell therapy programs.

Salary

Base: $124,590 - $150,977; 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

  • state-of-art automation solutions
  • GMP QC laboratory implementation
  • end-to-end integrated automation systems
  • automation technical transfer
  • troubleshooting and problem solving
  • global regulatory and cGMP requirements

Nice-to-have

  • collaborative quality culture
  • continuous improvement efforts
  • cross-functional collaboration
  • mentoring and coaching skills
  • strategic thinking and problem-solving

Key Requirements

  • Bachelor’s degree or equivalent required
  • 5+ years of integrated automation experience
  • Experience in a GMP QC laboratory preferred
  • Demonstrated automation developer experience
  • Experience designing, programming, operating, and troubleshooting integrated automation systems
  • Experience with migration of bench techniques to automated systems
  • Experience with ELN and LIMS

Work Rights

Not specified

Tailored Resume

Cover Letter