Director, Quality

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

The Director Quality Assurance, US market, a member of the Global Product Distribution & Affiliates (GPD&A) group, is responsible for supporting distribution of Gilead products within the US market. The Director QA acts as Designated Representative (DR) for Gilead Sciences Inc. and works with internal & external stakeholders to ensure quality requirements are met and compliance to Good Distribution Practice (GDP) is adhered to for Gilead products, throughout the US distribution network to patients.

Key Responsibilities:

• Act as Designated Representative (DR), for Gilead Science Inc., responsible for ensuring compliance with National Association or Boards of Pharmacies (NABP) Verified-Accredited Wholesale Distributors (VAWD) requirements as well as all relevant regulations pertaining to current best practice
• Responsible for maintaining the California Board of Pharmacy (CA BoP) Wholesale Drug Permit (license) by ensuring all licensee requirements are met
• Work with trade operations colleagues to establish and maintain an engagement program for quality with Gilead's US trading partners/customers
• Coach and mentor direct report(s) & manage workload prioritization to ensure local QA activities are performed to meet timelines and quality & compliance expectations, as well as ensuring that key performance indicators are monitored and reported, and key project timelines & milestones are tracked.
• Perform vendor site owner responsibilities in relevant Gilead system relating to Gilead's US trading partners/customers
• Responsible for providing guidance on interpretation and application of existing and new US requirements pertaining to product distribution.
• Act as the QA SME relating to DSCSA compliance and provide strategic support for operational processes relating to implementation of DSCSA requirements
• Act as prescription Drug Marketing Act (PDMA) Quality representative in Gilead's Sample Compliance Committee (SCC)
• Act as Deputy Designated Representative (dDR) for Asegua (a subsidiary of Gilead Sciences Inc), supporting the DR to ensure compliance with state pharmacy state and federal laws and regulations pertaining to current best practice
• Lead/Support market actions, including recall, of Gilead products distributed in US market
• Support shipping & distribution-related complaints process for US market & investigations into suspect product, as required.
• Manage QMS records such as deviations (internal & external), CAPAs & Change Controls related to QA Operations supporting US market distribution.
• Collaborate with Global QA teams as well as working cross-functionally with Trade Operations personnel, Global Supply Chain and other relevant colleagues supporting all aspects of US product distribution
• Host NAPB or CA BoP audits of Gilead and interacts closely with external regulators/stakeholders as well as supporting external FDA audits and internal audit programs
• Participate in developing/approving Standard Operating Procedures (SOPs) and other types of documentation to ensure quality objectives are met.
• Participate in the development & delivery of training programs relevant to GDP, PDMA & DSCSA compliance as they relate to activities covering US market
• Conduct/Participate in gap analyses and risk assessments of processes & procedures against relevant GDP, PDMA & DSCSA guidelines as well as corporate standards.
• Participate in, or where relevant lead, local and corporate projects, and process improvement initiatives, as required.

Knowledge, Experience & Behaviours:

• 10+ years of relevant experience in the pharmaceutical industry with a pharmacy degree or equivalent.
• Deep knowledge and experience in quality assurance in a highly regulated manufacturing environment.
• Experience in US market to include supporting/hosting FDA inspections.
• Demonstrates proficiency in Good Distribution Practices (GDP), Prescription Drug Marketing Act (PDMA), and Drug Supply Chain Security Act (DSCSA) requirements as well as risk management principles
• Demonstrates a highly developed knowledge of compliance requirements, and an understanding of current global and regional trends in compliance,
• Capable of assessing and communicating the impact of relevant requirements to the business.
• Ability to engage and manage multiple stakeholders to achieve the objective.
• Demonstrates excellent influencing and negotiation skills.
• Excellent verbal, written and interpersonal skills are required.
• Organized with systematic approach to prioritization.

Gilead Core Values:

• Integrity (always doing the right thing)
• Teamwork (collaborating in good faith)
• Excellence (working at a high level of commitment and capability)
• Accountability (taking personal responsibility)
• Inclusion (encouraging diversity)

The salary range for this position is: $210, $272, 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:

• 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

for assistance.

For more information about equal employment opportunity protections, please view the

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