Associate Consultant - Biologist- Quality Control

Lilly

Indianapolis, Indiana, US
Base: $65,250 - $169,400; bonus/equity: compyny bo...
Gmp qc laboratory experience
Method transfer and validation leadership
Technical document authoring skills
The role involves leading method transfers, validations, and verifications for new molecules within the Parenteral Manufacturing laboratories

Job Summary

  • The role involves leading method transfers, validations, and verifications for new molecules within the Parenteral Manufacturing laboratories.
  • Employees are expected to champion site impact assessments for compendial updates and serve as local data stewards for global site impacts.
  • The position offers a comprehensive benefit program including medical, dental, vision, 401(k), and wellness benefits alongside a competitive salary range.

Matching Summary

The role involves leading method transfers, validations, and verifications for new molecules within the Parenteral Manufacturing laboratories.

Salary

Base: $65,250 - $169,400; Bonus/Equity: Company bonus eligible; Benefits: Medical, dental, vision, 401(k), vacation

Skills & Requirements

Must-have

  • GMP QC laboratory experience
  • Method transfer and validation leadership
  • Technical document authoring skills
  • Change control management
  • Regulatory inspection support

Nice-to-have

  • Strong influencing and interpersonal skills
  • Mentoring and coaching analysts
  • Researching new technologies
  • Collaboration with global analytical stewards

Key Requirements

  • BSc or MSc in scientific degree
  • 3+ years GMP QC laboratory experience
  • Experience supporting regulatory inspections

Work Rights

Not specified

Tailored Resume

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