Qa Operations Associate

Novartis

Millburn, New Jersey, USA
Base: $60,600.00 - $112,600.00pyear; bonus/equity:...
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Gxp conformity and compliance
Shopfloor quality oversight
Batch release activities
** Novartis is seeking a QA Operations Associate for its Millburn, New Jersey facility to ensure compliance with quality standards in the production of Radioligand Therapies. The position requires collaboration across departments to maintain GxP conformity while supporting continuous quality improvement initiatives. **

Job Summary

  • Help reimagine cancer care by shaping how our Radioligand Therapies (RLT) reach more patients—safely, reliably, and faster.
  • The QA Operations Associate manages Quality aspects and projects within area of responsibility as well as ensuring and supporting overall GxP conformity and Compliance with the Novartis Quality Management Systems for the Millburn manufacturing site.
  • US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.

Matching Summary

Match Score: 75

** Novartis is seeking a QA Operations Associate for its Millburn, New Jersey facility to ensure compliance with quality standards in the production of Radioligand Therapies. The position requires collaboration across departments to maintain GxP conformity while supporting continuous quality improvement initiatives. **

Salary

Base: $60,600.00 - $112,600.00/year; Bonus/Equity: performance-based cash incentive and annual equity awards eligibility; Benefits: comprehensive benefits package including health, life, disability, 401(k) with match, generous time off

Skills & Requirements

Must-have

  • GxP conformity and Compliance
  • shopfloor quality oversight
  • batch release activities
  • data integrity
  • cGMP adherence

Nice-to-have

  • continuous quality improvement
  • collaboration across boundaries
  • culture of safety and quality
  • digital saviness
  • dealing with ambiguity

Key Requirements

  • Bachelors' Degree or 3-5 years relevant experience
  • 2+ years GxP (Bio)pharmaceutical experience
  • 1+ years Quality Assurance experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter