QC Tech & Innovation Director

Gilead Sciences Inc.

La Verne (CA)

On-site

USD 191,000 - 248,000

Full time

3 days ago
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Benefits offered by this job

Medical, dental, vision insurance
Bonus programs
Stock-based incentives
Paid time off

Job summary

Gilead Sciences Inc. seeks a Director of QC Technology & Innovation in La Verne, CA. You will lead the site’s QC technology roadmap, drive automation, digital solutions, and advanced testing approaches to modernize analytical workflows.

You’ll oversee method transfers, troubleshooting, and continual improvement across small molecule and biologics testing within GMP. You will collaborate with Global Quality and site stakeholders to ensure robust, scalable testing capabilities, and you’ll guide

Qualifications

  • BS/MS/PhD with 8–12+ years in pharma/biopharma.
  • Experience in analytical method transfer, validation, and lifecycle management.
  • Experience implementing analytical technologies, automation, and digital lab solutions.
  • Knowledge of GMP, data integrity, and regulatory expectations for QC labs.
  • Strong cross-functional leadership and communication skills.

Responsibilities

  • Lead the site QC technology and innovation strategy aligned with Global Quality.
  • Develop roadmaps for automated, low-touch testing across the network.
  • Drive automation, digital solutions, and tooling to modernize QC workflows.
  • Oversee method transfer, validation, and implementation for new products and lifecycle changes.

Skills

QC analytics
Method transfer
Troubleshooting
Automation
Regulatory compliance
Cross-functional leadership
Analytical thinking

Education

BS in scientific discipline
MS in scientific discipline
PhD in scientific discipline

Job description

Gilead Sciences Inc. seeks a Director of QC Technology & Innovation in La Verne, CA. You will lead the site’s QC technology roadmap, drive automation, digital solutions, and advanced testing approaches to modernize analytical workflows.

You’ll oversee method transfers, troubleshooting, and continual improvement across small molecule and biologics testing within GMP. You will collaborate with Global Quality and site stakeholders to ensure robust, scalable testing capabilities, and you’ll guide

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