Validation Lead

Novartis UK

Indianapolis, IN, US
Base: $114,100 - $211,900 py; bonus/equity: perfor...
Onsite
Bachelor's degree in biomedical engineering or related field
Minimum 5 years experience in pharmaceutical manufacturing
Hands-on experience leading validation projects
This role involves shaping and owning the site's end-to-end validation strategy to ensure manufacturing stays inspection ready and compliant with current Good Manufacturing Practice

Job Summary

  • This role involves shaping and owning the site's end-to-end validation strategy to ensure manufacturing stays inspection ready and compliant with current Good Manufacturing Practice.
  • The position offers a competitive salary range between $114,100 and $211,900 per year, along with performance-based cash incentives and eligibility for annual equity awards.
  • Candidates will partner closely with cross-functional teams including Manufacturing Science and Technology, Engineering, and Quality Control to orchestrate the Validation Master Plan.

Matching Summary

This role involves shaping and owning the site's end-to-end validation strategy to ensure manufacturing stays inspection ready and compliant with current Good Manufacturing Practice.

Salary

Base: $114,100 - $211,900 per year; Bonus/Equity: Performance-based cash incentive and potential annual equity awards; Benefits: Comprehensive health, life, disability, 401(k) match, and generous time off package

Skills & Requirements

Must-have

  • Bachelor's degree in Biomedical Engineering or related field
  • Minimum 5 years experience in pharmaceutical manufacturing
  • Hands-on experience leading validation projects
  • Strong knowledge of GMP and risk assessments
  • Proven ability to write technical reports

Nice-to-have

  • Experience with product transfers and launches
  • Ability to coach teams and build standards
  • Proficiency in applied statistics and data analytics
  • Fluency in English and local site language
  • Experience with continuous improvement processes

Key Requirements

  • Bachelor's degree in Biomedical Engineering, Chemistry, Pharmacy, Chemical Engineering, or Pharmaceutical Technology
  • Minimum 5 years' experience in manufacturing, technical development, or quality within the pharmaceutical industry
  • Fluent in English and proficient in the local site language

Work Rights

Not specified

Tailored Resume

Cover Letter