Principal Scientist, Investigations

Bristol Myers Squibb

Manati, Puerto Rico, US
Base: $106,520 - $129,080; bonus/equity: + incenti...
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Parenteral product manufacturing experience
Root cause analysis execution
Fda regulatory requirements knowledge
** Bristol Myers Squibb is seeking a Principal Scientist for Investigations in Manati, Puerto Rico, to lead investigations in parenteral manufacturing while ensuring compliance with quality standards. The ideal candidate will have extensive experience in pharmaceutical operations, particularly with parenteral products, and possess strong leadership and technical skills. **

Job Summary

  • This role provides technical and managerial leadership to support lead investigators for parenteral manufacturing at the BMS Manati site.
  • The incumbent is accountable for ensuring investigations meet company expectations for robustness, quality, and timely completion of root cause analyses.
  • Bristol Myers Squibb offers competitive benefits including health coverage, financial protection plans, and flexible time off policies.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Principal Scientist for Investigations in Manati, Puerto Rico, to lead investigations in parenteral manufacturing while ensuring compliance with quality standards. The ideal candidate will have extensive experience in pharmaceutical operations, particularly with parenteral products, and possess strong leadership and technical skills. **

Salary

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

Skills & Requirements

Must-have

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

Nice-to-have

  • Strategic and proactive mindset
  • Global investigation community collaboration
  • Ability to challenge status quo
  • Multi-disciplinary team leadership
  • Risk management assessment skills

Key Requirements

  • BS in Engineering/Science with 9 years experience OR Master's with 6 years
  • Broad knowledge of FDA regulatory requirements and cGMPs
  • Proficiency in English and Spanish communication

Work Rights

Not specified

Tailored Resume

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