Validation Lead

Novartis UK

Indianapolis, IN, USA
Base: $114,100 - $211,900; bonus/equity: performan...
Onsite
Site's end to end validation strategy
Validation master plan
Risk assessments and validation documentation
As our Validation Lead in Indianapolis, you will shape and own the site’s end to end validation strategy—process, cleaning, primary packaging, and ongoing process verification—so manufacturing stays inspection ready and continuously compliant with current Good Manufacturing Practice

Job Summary

  • As our Validation Lead in Indianapolis, you will shape and own the site’s end to end validation strategy—process, cleaning, primary packaging, and ongoing process verification—so manufacturing stays inspection ready and continuously compliant with current Good Manufacturing Practice.
  • You’ll partner closely with Manufacturing Science and Technology, Engineering, Information Technology, Quality Control, and Analytical Science and Technology to orchestrate the Validation Master Plan, monitor meaningful performance indicators, and proactively manage risk.
  • Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

Matching Summary

As our Validation Lead in Indianapolis, you will shape and own the site’s end to end validation strategy—process, cleaning, primary packaging, and ongoing process verification—so manufacturing stays inspection ready and continuously compliant with current Good Manufacturing Practice.

Salary

Base: $114,100 - $211,900; Bonus/Equity: performance-based cash incentive and annual equity awards; Benefits: health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits

Skills & Requirements

Must-have

  • site's end to end validation strategy
  • Validation Master Plan
  • risk assessments and validation documentation
  • equipment, utilities, and analytical method qualification
  • product transfers and launches

Nice-to-have

  • coaching teams
  • turning complex technical challenges
  • bold innovation through collaboration
  • unleash their full potential

Key Requirements

  • Bachelor’s degree in Biomedical Engineering, Chemistry, Pharmacy, Chemical Engineering, or Pharmaceutical Technology
  • Minimum 5 years’ experience in pharmaceutical industry
  • Hands-on experience leading and managing validation projects
  • Fluent in English

Work Rights

Not specified

Tailored Resume

Cover Letter