Senior Specialist, Qc Analytical, Cell Therapy A2 Shift

Bristol Myers Squibb

Devens, MA, US
Base: $43.84 - $53.12 ph; bonus/equity: + incentiv...
50% onsite
Bachelor's degree in science
4+ years analytical testing experience
Cell and molecular biology techniques
Bristol Myers Squibb is seeking a Senior Specialist for QC Analytical in Cell Therapy on the A2 shift at its Devens, MA facility. The role involves supporting QC testing and method validation, alongside troubleshooting and mentoring responsibilities within a dynamic and meaningful work environment

Job Summary

  • This role involves supporting QC testing for in-process, final product, and stability samples within the cell therapy department.
  • The position requires performing method transfer/validation, routine troubleshooting, and comprehensive data verification under GMP requirements.
  • Bristol Myers Squibb offers competitive benefits including health coverage, financial protection plans, and flexible paid time off options.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Senior Specialist for QC Analytical in Cell Therapy on the A2 shift at its Devens, MA facility. The role involves supporting QC testing and method validation, alongside troubleshooting and mentoring responsibilities within a dynamic and meaningful work environment.

Salary

Base: $43.84 - $53.12 per hour; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), and paid time off included

Skills & Requirements

Must-have

  • Bachelor's degree in science
  • 4+ years analytical testing experience
  • Cell and molecular biology techniques
  • GMP regulatory compliance knowledge
  • Data verification and review skills

Nice-to-have

  • Advanced LIMS and ELN proficiency
  • Strong technical writing abilities
  • Mentoring and training capabilities
  • Fast-paced team collaboration
  • Continuous improvement mindset

Key Requirements

  • Bachelor's degree required
  • 4+ years relevant QC experience
  • Experience with flow cytometry and qPCR
  • Knowledge of cGMP regulations
  • US work authorization required

Work Rights

Not specified

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