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

Bristol Myers Squibb

Devens, MA, US
Devens - ma - us: $115,790 - $140,307; madison - g...
50% onsite
Molecular biology analytical expert
Cgmp environment
Method transfer and validation
Function as a molecular biology analytical expert supporting the Cellular Therapy product portfolio, with a strong foundation in development, transfer, validation, and life-cycle management of test methods in a cGMP environment

Job Summary

  • Function as a molecular biology analytical expert supporting the Cellular Therapy product portfolio, with a strong foundation in development, transfer, validation, and life-cycle management of test methods in a cGMP environment.
  • Provide molecular biology analytical expertise in support of QC lab investigations, including technical investigations, root cause analysis, and corrective/preventive actions, as well as authoring technical documents and leading project-related tasks.
  • Partner with development organizations and represent the function on cross-functional project teams, while also training and mentoring others on molecular biology techniques and fostering a collaborative quality culture.

Matching Summary

Function as a molecular biology analytical expert supporting the Cellular Therapy product portfolio, with a strong foundation in development, transfer, validation, and life-cycle management of test methods in a cGMP environment.

Salary

Devens - MA - US: $115,790 - $140,307; Madison - Giralda - NJ - US: $108,210 - $131,129; Seattle - WA: $119,030 - $144,241

Skills & Requirements

Must-have

  • molecular biology analytical expert
  • cGMP environment
  • method transfer and validation
  • method lifecycle management
  • viral vector and cell therapy drug products
  • regulatory submissions

Nice-to-have

  • positive and successful collaborative quality culture
  • initiative, resourcefulness, and flexibility
  • work that transforms the lives of patients

Key Requirements

  • 8+ years relevant analytical experience
  • Advanced molecular biology methodologies
  • Analytical method lifecycle experience
  • cGMP regulations experience
  • Strong technical writing experience
  • Ability to travel

Work Rights

Not specified

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