About Gilead Sciences

Gilead Sciences is a leading biopharmaceutical company dedicated to creating a healthier world for all people. For over 35 years, Gilead has pioneered breakthroughs in treating HIV, viral hepatitis, COVID-19, cancer, and inflammatory diseases. Headquartered in Foster City, California, the company develops life-changing therapies that improve lives and ensure global access to innovative treatments. Gilead's relentless drive against major health challenges is powered by a collaborative team of scientists, leaders, and innovators committed to bold ambitions.

Role Overview

The Director, Quality Control Microbiology - Biologics/Small Molecules, is a pivotal leadership role overseeing microbiological operations for clinical and commercial programs at Gilead Sciences. Based in Foster City, California, this position demands strategic vision to develop QC strategies across biologics and small molecules, from cell banks to environmental monitoring. The ideal candidate is an approachable mentor fostering continuous improvement, regulatory compliance, and cross-functional collaboration in a GMP environment.

Key Responsibilities

Strategic Leadership

Lead the development and implementation of comprehensive QC microbiological strategies, including specifications for cell banks, products, raw materials, and facilities. Ensure seamless application from clinical stages to commercial lifecycle, driving innovation in microbial analysis technologies.

Team Development

Provide guidance and motivation to direct reports, building strong leaders capable of critical decision-making. Mentor staff for timely project completion while maintaining an approachable demeanor.

Operational Oversight

Manage daily operations including sterility, endotoxins, bioburden testing, microbial identification, particulate matter, and environmental monitoring. Coordinate with internal teams, CMOs, and third-party labs for sample submissions and trend reporting.

Compliance and Innovation

Drive qualification of USP microbial methods for in-process, release, and stability testing. Author/review procedures, support quality events, and implement aseptic techniques to prevent cross-contamination. Represent Gilead as a microbiology subject matter expert during regulatory inspections.

Qualifications & Requirements

Basic Qualifications

PhD with 8+ years, Master’s with 10+ years, Bachelor’s with 12+ years, Associate’s with 14+ years, or High School Diploma with 16+ years of relevant pharmaceutical industry experience.

Preferred Qualifications

4+ years in a GMP Microbiology Lab, expertise in microbiological testing, aseptic processing, sterile handling, and environmental monitoring. Proficiency with GMP systems like LIMS, QMS, SAP, Empower, and JMP. Strong knowledge of regulatory guidelines and laboratory instrumentation.

Benefits & Perks

Gilead Sciences offers a premium compensation package, including a competitive salary estimated at $230,000-$320,000 annually based on biopharma sector rates in Foster City, with performance bonuses. Employees enjoy comprehensive health coverage, 401(k) matching, generous PTO, and wellness programs. As a people leader, you'll access leadership development resources in an inclusive environment.

Career Growth

At Gilead, career progression is a priority. This director role positions you for executive leadership in quality control, with opportunities to influence global programs in HIV, oncology, and inflammatory diseases. Benefit from mentoring programs, cross-functional projects, and continuous learning to evolve Gilead's culture of empowerment and innovation.

Why Join Gilead

Join a team making direct impacts on life-changing therapies. Gilead's mission-driven culture values collaboration, determination, and inclusivity. In Foster City, contribute to cutting-edge biologics and small molecules, interfacing with regulators and driving scientific advancements in critical health areas like HIV treatments, oncology innovations, and solutions for inflammatory diseases.

Role FAQs

What experience is required?

A PhD with 8+ years in pharma is preferred, with GMP microbiology lab expertise essential.

Is relocation support available?

Gilead supports talented candidates relocating to Foster City, California.

What makes this role unique?

Strategic oversight of both biologics and small molecules in a high-impact, compliant environment at a global leader.

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