Job description

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference. Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together. Job Description Company Overview Gilead Sciences, Inc. is a biopharmaceutical company committed to advancing innovative medicines that help prevent and treat life-threatening diseases. Our work is grounded in scientific rigor, collaboration, accountability, and a shared commitment to improving the lives of patients. Position Overview The Director, Quality Control Product Readiness leads the organization of QC Leads responsible for assigned commercial products and programs. The role establishes direction, governance, expectations, and resource priorities for the QC Lead function, ensuring consistent oversight of product readiness, analytical lifecycle activities, and transition from clinical to commercial QC. This leader coaches and develops the QC Leads, removes barriers, resolves cross-program issues, and serves as the escalation point in commercial QC. Focus Areas Product Readiness and Portfolio Execution Oversee clinical-to-commercial QC transitions and ongoing product readiness, ensuring clear criteria, stakeholder alignment, sustainable ownership, and resolution of readiness gaps. Manage portfolio priorities, testing capacity, resources, and execution risks; escalate systemic issues and sponsor recovery plans to support uninterrupted product supply. Analytical and Regulatory Lifecycle Oversight Provide technical guidance and decision frameworks for complex analytical issues, investigations, methods, specifications, reference standards, documentation, and related readiness gaps. Ensure scientifically sound health authority responses and governance of post-approval changes and regulatory commitments through implementation and closure. Leadership and Cross-Functional Partnership Build, lead, mentor, and develop a high-performing team of QC Leads responsible for product readiness and analytical lifecycle oversight. Define the QC Lead operating model, role expectations, decision rights, performance standards, and development pathways. Ensure appropriate assignment and capacity of QC Leads across the portfolio based on program complexity, risk, and business priorities. Establish scalable standards, metrics, and continuous improvement practices that strengthen consistency, product readiness, compliance, and execution across the QC Lead organization. Contribute to department strategy, workforce and resource planning, budgeting, succession planning, and long-range capability development. Qualifications BS degree with 12 years of relevant experience, MS degree with 10 years of relevant experience, or PhD with 2 years of relevant experience in Chemistry, Biochemistry, Pharmaceutical Sciences, Life Sciences, or a related field. Significant experience in pharmaceutical or biopharmaceutical Quality Control, including leadership of technical professionals responsible for commercialization, product lifecycle management, or external laboratory oversight. Demonstrated ability to lead and develop product-focused QC Leads, establish governance and operating standards, balance portfolio priorities, and drive accountability through others. Broad technical knowledge of analytical method validation and transfer, method lifecycle management, commercial specifications, laboratory investigations, sample management, and testing logistics. Experience providing leadership oversight for QC-related BLA or NDA content and responses to health authority questions. Strong knowledge of cGMP principles, data integrity expectations, and applicable global regulatory requirements for commercial analytical testing. Proven ability to influence senior cross-functional stakeholders, resolve complex escalations, manage competing portfolio priorities, and make risk-based decisions in ambiguous environments. Excellent scientific judgment, people leadership, coaching, organizational, written communication, and presentation skills. The salary range for this position is: $210,375.00 - $272,250.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*. For additional benefits information, visit: gilead.com * Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans. For jobs in the United States: Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex , age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations gilead.com for assistance. For more information about equal employment opportunity protections, please view the Know Your Rights poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law. Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team. Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion. For Current Gilead Employees and Contractors: Please apply via the Internal Career Opportunities portal in Workday.

Requirements

Must-haves

Company Overview
Position Overview
Product Readiness and Portfolio Execution
Oversee clinical-to-commercial QC transitions and ongoing product readiness, ensuring clear criteria, stakeholder alignment, sustainable ownership, and resolution of readiness gaps.
Manage portfolio priorities, testing capacity, resources, and execution risks; escalate systemic issues and sponsor recovery plans to support uninterrupted product supply.
Analytical and Regulatory Lifecycle Oversight
Provide technical guidance and decision frameworks for complex analytical issues, investigations, methods, specifications, reference standards, documentation, and related readiness gaps.
Ensure scientifically sound health authority responses and governance of post-approval changes and regulatory commitments through implementation and closure.
Leadership and Cross-Functional Partnership
Build, lead, mentor, and develop a high-performing team of QC Leads responsible for product readiness and analytical lifecycle oversight.
Define the QC Lead operating model, role expectations, decision rights, performance standards, and development pathways.
Ensure appropriate assignment and capacity of QC Leads across the portfolio based on program complexity, risk, and business priorities.
Establish scalable standards, metrics, and continuous improvement practices that strengthen consistency, product readiness, compliance, and execution across the QC Lead organization.
Contribute to department strategy, workforce and resource planning, budgeting, succession planning, and long-range capability development.
Demonstrated ability to lead and develop product-focused QC Leads, establish governance and operating standards, balance portfolio priorities, and drive accountability through others.
Broad technical knowledge of analytical method validation and transfer, method lifecycle management, commercial specifications, laboratory investigations, sample management, and testing logistics.
Experience providing leadership oversight for QC-related BLA or NDA content and responses to health authority questions.
Strong knowledge of cGMP principles, data integrity expectations, and applicable global regulatory requirements for commercial analytical testing.
Proven ability to influence senior cross-functional stakeholders, resolve complex escalations, manage competing portfolio priorities, and make risk-based decisions in ambiguous environments.
Excellent scientific judgment, people leadership, coaching, organizational, written communication, and presentation skills.
Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
For more information about equal employment opportunity protections, please view the Know Your Rights poster.
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT
Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Nice-to-haves

None flagged.

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: workday
Effort: long

Benefits

Benefits detected in the listing.

Dental

Vision

Paid Time Off