Associate Director, Quality Assurance

Gilead Sciences

Base: $182,070.00 - $235,620.00; bonus/equity: dis...
Onsite
Oversee contract manufacturing organizations
Clinical development phase appropriate cgmp
Small molecule osd manufacturing experience
This role provides proactive quality oversight for assigned Gilead CXOs to ensure sustainable delivery of clinical products to patients

Job Summary

  • This role provides proactive quality oversight for assigned Gilead CXOs to ensure sustainable delivery of clinical products to patients.
  • The successful candidate must have direct experience overseeing contract manufacturing organizations and a proven track record in clinical development from first-in-human through commercialization.
  • Gilead offers a competitive salary range of $182,070.00 - $235,620.00 along with discretionary bonuses, stock incentives, and comprehensive benefits packages.

Matching Summary

This role provides proactive quality oversight for assigned Gilead CXOs to ensure sustainable delivery of clinical products to patients.

Salary

Base: $182,070.00 - $235,620.00; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives available; Benefits: Medical, dental, vision, life insurance, and paid time off

Skills & Requirements

Must-have

  • Oversee contract manufacturing organizations
  • Clinical development phase appropriate cGMP
  • Small molecule OSD manufacturing experience
  • Drug substance and drug product release
  • Regulatory compliance and inspection readiness

Nice-to-have

  • People management and leadership skills
  • Strong negotiation and influencing abilities
  • Global regulatory intelligence knowledge
  • Experience with acquired clinical assets
  • Championing quality risk management

Key Requirements

  • Bachelor's Degree plus 10 years experience OR Master's plus 8 years OR PhD/PharmD plus 5 years
  • Biopharmaceutical or Pharmaceutical industry experience required
  • Prior experience leading or overseeing contract manufacturing operations
  • Deep understanding of clinical OSD (DS and DP) manufacturing
  • Expertise in US and international cGMP principles

Work Rights

Not specified

Tailored Resume

Cover Letter