About Gilead Sciences

Gilead Sciences is a biopharmaceutical leader dedicated to creating a healthier world for all. For over 35 years, Gilead has pioneered therapies for HIV, viral hepatitis, COVID-19, oncology, and inflammatory diseases. Headquartered in Foster City, California, the company drives scientific innovation to improve lives globally. With a relentless focus on collaboration and determination, Gilead's teams develop life-changing medicines, ensuring access across diverse populations. As a Sr Director, Quality Control, you'll contribute to this mission by upholding the highest standards in biologics manufacturing.

Role Overview

The Sr Director, Quality Control position at Gilead Sciences in Foster City, California, is a pivotal leadership role within Clinical Biologics QC. This full-time position demands strategic oversight of cGMP-compliant release testing, stability programs, and process refinements across internal and external networks. Reporting to senior QC leadership, you'll foster continuous improvement, mentor high-performing teams, and ensure regulatory compliance for Gilead's innovative biologics portfolio, including therapies for HIV, oncology, and inflammatory diseases.

Strategic Impact

In this role, you'll shape end-to-end QC strategies, manage budgeting, and drive KPIs for analytical performance. Your expertise in biological testing methods will troubleshoot complex issues, supporting Gilead's bold ambitions in biopharma.

Key Responsibilities

As Sr Director, Quality Control, your core duties include:

• Overseeing development and implementation of Clinical Quality Control strategies for Gilead’s biologics products.
• Leading the cGMP QC team in release testing and stability programs for drug substances and products.
• Refining QC processes across internal manufacturing, CMOs, and contract labs to align with global cGMP and Gilead’s Quality Management System.
• Providing mentorship, staff development, and strategic planning, including budgeting and cost control.
• Acting as escalation point for high-impact QC issues, reviewing data, and ensuring method validation and transfers.
• Supporting CMO/CTL selection, regulatory filings, and direct interfaces with agencies like FDA.
• Leading cross-functional projects with senior management visibility, promoting SOP harmonization.

Qualifications & Requirements

Gilead seeks candidates with:

• Broad experience across Quality Control sub-functions, with deep knowledge of industry best practices.
• In-depth understanding of GMP principles, concepts, and standards in the US and internationally.
• Ability to develop innovative solutions to complex problems requiring ingenuity and independent judgment.
• Proven track record working with senior management on company-wide initiatives.
• Expertise in biological product testing, assays, troubleshooting, and remediation.
• Strong leadership skills to motivate teams and meet project timelines.

A bachelor's or advanced degree in a relevant scientific field, plus 15+ years in biopharma QC, is essential. Experience in clinical biologics and regulatory interactions is highly preferred.

Benefits & Perks

Gilead Sciences offers a premium compensation package for the Sr Director, Quality Control role:

• Estimated salary range of $280,000 - $380,000 USD annually, based on biopharma sector rates in Foster City with a competitive buffer.
• Comprehensive health, dental, and vision insurance.
• 401(k) matching, stock options, and performance bonuses.
• Generous paid time off, parental leave, and flexible work options.
• Wellness programs, onsite fitness, and employee assistance resources.
• Tuition reimbursement and professional development opportunities.

Career Growth

At Gilead, people leaders are central to employee experience. This role positions you for executive advancement, with opportunities to influence global QC strategies. Benefit from mentorship programs, leadership training, and cross-functional exposure in HIV, oncology, and inflammation R&D. Gilead's commitment to inclusion and empowerment ensures your growth aligns with ambitious career aspirations.

Why Join Gilead

Join Gilead Sciences to make a direct impact on therapies transforming lives. In Foster City, collaborate with top talent tackling health challenges like HIV treatments, oncology breakthroughs, and inflammatory disease solutions. Enjoy a culture of innovation, where your QC leadership drives compliance and excellence. Gilead values every team member's role in scientific discovery, offering stability, purpose, and rewards in a premier biopharma environment.

Role FAQs

Q: What is the work location?
A: This full-time role is based in Foster City, California, United States.

Q: Is prior biologics experience required?
A: Yes, extensive knowledge of clinical biologics QC, testing methods, and cGMP is essential.

Q: What leadership scope does this role offer?
A: Ultimate responsibility for staff development, team motivation, and departmental strategy.

Q: How does this role support regulatory compliance?
A: Through filings, agency interfaces, and oversight of internal/external QC networks.

Q: What makes Gilead unique for QC professionals?
A: Focus on innovative therapies for HIV, oncology, and inflammation, with a culture of continuous improvement.

Apply now to elevate your career at Gilead Sciences!