Associate Director – Qc – Iapi Analytical Sciences

Workday Lilly

Indianapolis, Indiana, US
$123,000 - $180,400; bonus eligible; comprehensive...
Analytical control strategy stewardship
Method development and transfers
Analytical techniques (chromatography, mass spectroscopy)
The Quality Control (QC) Associate Director (AD) Analytical Sciences is responsible for leading the Indianapolis API QC Analytical Sciences team by establishing key capabilities needed to support site operations, QC, and commercialization work within IAPI

Job Summary

  • The Quality Control (QC) Associate Director (AD) Analytical Sciences is responsible for leading the Indianapolis API QC Analytical Sciences team by establishing key capabilities needed to support site operations, QC, and commercialization work within IAPI.
  • Develop and execute a comprehensive technical capability strategy to ensure site competencies in fields including but not limited to analytical stewardship, chromatography, Mass Spectroscopy, and Process Analytical Technology.
  • Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $123,000 - $180,400.

Matching Summary

The Quality Control (QC) Associate Director (AD) Analytical Sciences is responsible for leading the Indianapolis API QC Analytical Sciences team by establishing key capabilities needed to support site operations, QC, and commercialization work within IAPI.

Salary

$123,000 - $180,400; Bonus eligible; Comprehensive benefit program

Skills & Requirements

Must-have

  • analytical control strategy stewardship
  • method development and transfers
  • analytical techniques (chromatography, Mass Spectroscopy)
  • cGMP lab experience
  • data analysis and documentation skills

Nice-to-have

  • technical leadership and mentoring
  • cross-functional collaboration
  • new technology implementation
  • continuous optimization of methods
  • innovative analytical solutions

Key Requirements

  • Bachelor’s degree in a science field
  • 5 years of relevant cGMP lab experience
  • 2+ years supervisory experience
  • Knowledge of cGMPs and quality systems
  • Experience in method development and validation

Work Rights

Not specified

Tailored Resume

Cover Letter