Principal Scientist, Investigations

Bristol Myers Squibb

Manati, Puerto Rico, US
Base: $106,520 - $129,080; bonus/equity: + incenti...
50% onsite
Parenteral product manufacturing experience
Root cause analysis execution
Cgmp regulatory compliance knowledge
Bristol Myers Squibb is seeking a Principal Scientist for Investigations in Manati, Puerto Rico. The role requires strong technical and managerial skills to support investigations in parenteral manufacturing, ensuring compliance and quality standards

Job Summary

  • The role provides technical leadership for the support of lead investigators team for Parenteral Manufacturing at the BMS Manati site.
  • The incumbent is accountable for ensuring investigations meet company expectations for robustness, quality, and timely completion in compliance with cGMPs.
  • Bristol Myers Squibb offers a wide variety of competitive benefits including health coverage, financial well-being protection, and flexible time off options.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking a Principal Scientist for Investigations in Manati, Puerto Rico. The role requires strong technical and managerial skills to support investigations in parenteral manufacturing, ensuring compliance and quality standards.

Salary

Base: $106,520 - $129,080; Bonus/Equity: Additional incentive cash and stock opportunities available; Benefits: Medical, dental, vision, 401(k), paid time off, and wellness programs

Skills & Requirements

Must-have

  • Parenteral product manufacturing experience
  • Root cause analysis execution
  • cGMP regulatory compliance knowledge
  • Technical report writing skills
  • FDA regulatory requirements expertise

Nice-to-have

  • Strategic and proactive mindset
  • Ability to challenge status quo
  • Cross-functional collaboration skills
  • Project management capabilities
  • Bilingual English/Spanish proficiency

Key Requirements

  • BS in Engineering/Science with 9 years experience OR Master's with 6 years
  • Broad knowledge of parenteral products specifically
  • Proficient knowledge of FDA regulatory requirements
  • Excellent technical writing and oral communication skills

Work Rights

Not specified

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