Validation Scientist Cleaning & Sterilization

Eli Lilly

Research Triangle Park, North Carolina, United States
Base: $66,000 - $171,600; bonus/equity: compyny bo...
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Cgmp manufacturing experience
Cleaning and sterilization validation
Temperature mapping studies
** Eli Lilly is seeking a Validation Scientist for Cleaning & Sterilization at its state-of-the-art facility in Research Triangle Park, North Carolina. The role requires expertise in validating manufacturing equipment and systems, with a strong emphasis on compliance with regulatory guidelines and maintaining product safety and quality. **

Job Summary

  • This role plays a critical part in ensuring the safety, efficacy, and quality of pharmaceutical products through advanced cleaning and sterilization validation strategies.
  • The position requires leading the design, execution, and documentation of validation studies while providing technical support for start-up activities at a state-of-the-art facility.
  • Eli Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k) pension, and performance-based bonuses to eligible full-time employees.

Matching Summary

Match Score: 75

** Eli Lilly is seeking a Validation Scientist for Cleaning & Sterilization at its state-of-the-art facility in Research Triangle Park, North Carolina. The role requires expertise in validating manufacturing equipment and systems, with a strong emphasis on compliance with regulatory guidelines and maintaining product safety and quality. **

Salary

Base: $66,000 - $171,600; Bonus/Equity: Company bonus depending on performance; Benefits: Medical, dental, vision, 401(k), pension, vacation

Skills & Requirements

Must-have

  • cGMP manufacturing experience
  • cleaning and sterilization validation
  • temperature mapping studies
  • regulatory compliance FDA EMA
  • validation protocol authoring

Nice-to-have

  • statistical data analysis skills
  • cross-functional team leadership
  • root cause investigation expertise
  • continuous improvement mindset
  • excellent written communication

Key Requirements

  • BS or MS in Microbiology or related field
  • 3-5 years pharmaceutical industry experience
  • Knowledge of cGMP regulations 21 CFR Parts 210 211
  • Experience with steam dry heat EtO sterilization methods

Work Rights

Not specified

Tailored Resume

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