Scientist, Investigations Team, S12 Msat

Bristol Myers Squibb

Summit West, NJ, US
Base: $82,420 - $99,879; bonus/equity: + incentive...
Hybrid (50% onsite)
Root cause analysis tools
Cgmp environment experience
Deviation investigation execution
Bristol Myers Squibb is seeking a Scientist for their Investigations Team in Summit West, NJ, to lead manufacturing and quality control investigations related to CAR T operations. The role involves conducting root cause analysis, collaborating with cross-functional teams, and developing corrective actions to improve processes

Job Summary

  • The Scientist/Investigator is responsible for leading manufacturing and QC investigation reports in support of S12 CAR T operations.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being programs, and flexible time off.
  • The role requires working with cross-functional teams to propose effective corrective and preventive actions while ensuring compliance with global regulatory requirements.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Scientist for their Investigations Team in Summit West, NJ, to lead manufacturing and quality control investigations related to CAR T operations. The role involves conducting root cause analysis, collaborating with cross-functional teams, and developing corrective actions to improve processes.

Salary

Base: $82,420 - $99,879; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off

Skills & Requirements

Must-have

  • Root cause analysis tools
  • cGMP environment experience
  • Deviation investigation execution
  • CAPA process implementation
  • Technical writing skills

Nice-to-have

  • Lean manufacturing principles
  • Six Sigma methodology
  • Statistical analysis software
  • CAR-T manufacturing experience
  • Electronic Quality systems (eQRM)

Key Requirements

  • Bachelor's Degree in science or engineering
  • Minimum 3 years cGMP environment experience
  • 1+ years hands-on investigation experience
  • 1+ years root-cause analysis experience

Work Rights

Not specified

Tailored Resume

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