Associate Director, Quality Assurance Compliance

Gilead Sciences

Foster City, California, United States
Bay area: $182,070.00 - $235,620.00; other us loca...
Fully remote
Manage regulatory inspections logistics
Develop inspection readiness tools
Manage inspection related documentation
At Gilead, we’re creating a healthier world for all people by tackling diseases such as HIV, viral hepatitis, COVID-19 and cancer, working relentlessly to develop therapies that help improve lives and ensure access to these therapies across the globe

Job Summary

  • At Gilead, we’re creating a healthier world for all people by tackling diseases such as HIV, viral hepatitis, COVID-19 and cancer, working relentlessly to develop therapies that help improve lives and ensure access to these therapies across the globe.
  • As an Associate Director, Quality Assurance Compliance, you will manage inspection logistics, develop inspection readiness tools and training, lead global inspection readiness activities, and implement inspection strategies aligned with regulatory requirements.
  • The salary range for this position is: Bay Area: $182,070.00 - $235,620.00. Other US Locations: $165,495.00 - $214,170.00, with eligibility for bonus, stock-based incentives, PTO, and benefits.

Matching Summary

At Gilead, we’re creating a healthier world for all people by tackling diseases such as HIV, viral hepatitis, COVID-19 and cancer, working relentlessly to develop therapies that help improve lives and ensure access to these therapies across the globe.

Salary

Bay Area: $182,070.00 - $235,620.00; Other US Locations: $165,495.00 - $214,170.00; Bonus/Equity: discretionary annual bonus, discretionary stock-based long-term incentives; Benefits: medical, dental, vision, and life insurance plans

Skills & Requirements

Must-have

  • Manage regulatory inspections logistics
  • Develop inspection readiness tools
  • Manage inspection related documentation
  • Lead global inspection readiness activities
  • Implement comprehensive inspection plans
  • Ensure compliance with regulatory agencies
  • Leverage data analytics for inspection readiness

Nice-to-have

  • Create inclusion and develop talent
  • Empower teams and align goals
  • Collaborate with cross-functional groups
  • Translate complex data into narratives

Key Requirements

  • BS/BA degree and 10+ years related experience
  • MS/MA degree and 8+ years related experience
  • PhD degree and 5+ years related experience
  • Biotech or pharmaceutical industry experience required
  • Experience managing Health Authorities during inspection
  • Knowledge of domestic and global regulations
  • Working knowledge of AI concepts
  • Experience using digital quality systems

Work Rights

Not specified

Tailored Resume

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