Scientist, Drug Product Analytical Science And Technology (asat), Cell Therapy

Bristor Myers Squibb

Devens, MA, US
Devens - ma - us: $97,440 - $118,079; madison - gi...
50% onsite
Bioassay, flow cytometry, molecular biology
Analytical method transfer and validation
Cgmp environment experience
Provide bioassay, flow cytometry and/or molecular biology analytical expertise in support of QC lab investigations, including technical investigations and method remediations

Job Summary

  • Provide bioassay, flow cytometry and/or molecular biology analytical expertise in support of QC lab investigations, including technical investigations and method remediations.
  • Support transfer of commercial methods and method validation in compliance with global regulatory requirements, and responsible for the stewardship of methods in the Cell Therapy Quality organization.
  • Bristol Myers Squibb offers a wide variety of competitive benefits, services and programs that provide employees with resources to pursue their goals, both at work and in their personal lives.

Matching Summary

Provide bioassay, flow cytometry and/or molecular biology analytical expertise in support of QC lab investigations, including technical investigations and method remediations.

Salary

Devens - MA - US: $97,440 - $118,079; Madison - Giralda - NJ - US: $91,070 - $110,354; Seattle - WA: $100,180 - $121,396; Bonus/Equity: Additional incentive cash and stock opportunities (based on eligibility) may be available; Benefits: Health Coverage, Wellbeing Support, Financial Well-being and Protection, Work-life benefits

Skills & Requirements

Must-have

  • bioassay, flow cytometry, molecular biology
  • analytical method transfer and validation
  • cGMP environment experience
  • cell therapy product portfolio support
  • method lifecycle management

Nice-to-have

  • initiative, resourcefulness, flexibility
  • cross-functional project team representation
  • continuous improvement efforts

Key Requirements

  • Bachelor’s degree or equivalent
  • 6+ years relevant analytical experience
  • Experience in analytical method lifecycle
  • Experience in cGMP regulations
  • Understanding of FDA, EMA, ICH, USP, EP guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter