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

Key Responsibilities

• Executes the regular, tactical management of CMOs to ensure Gilead’s Oral Solid Dose (OSD) products are manufactured in accordance with the registered process and approved Master Production Record
• Enables timely resolution of complex issues associated with manufacturing and/or compliance, including handling of deviations, complaints, out-of-specification investigations, Material Review Board associated investigations, finished product trending, and change control
• Responsible for coordination of inter- and intra-company technical transfers. Proactively partners with Technical Development and internal Gilead manufacturing sites for successful technology transfer and validation of new or existing processes/products to the identified CMO(s)
• Foster and facilitate continuous improvement of production and business processes to reduce cost, improve quality, increase efficiency, and ensure sustainability.
• Represent manufacturing on one or more cross-functional Development or Commercial CMC teams, as needed, with responsibility for proactively managing product strategies across the life cycle from clinical supply, to commercial product launch, to routine supply, and then to either divestiture or sunset.
• Confer with vendors to analyze their operations, technical capabilities and capacity to assess factors affecting pricing to negotiate competitive cost consistent with quality, reliability, and schedule requirements.
• Facilitate production schedules based on downstream operational and program requirements; proactively communicate supply risks and schedule delays to project teams.
• Apply solid working knowledge of relevant regulatory guidance, including pharmaceutical GMPs and ICH guidelines.
• Participate in Quality Assurance–led regulatory and compliance audits, as needed.
• Support department leadership with resource planning and financial reporting activities.
• Communicate effectively with senior management through clear, concise written and verbal updates.
• Apply sound organizational and time management skills to manage multiple priorities effectively.

Basic Qualifications

• Bachelor’s degree (BA or BS) in Organic Chemistry, Chemical Engineering, or another relevant scientific discipline with at least 10+ years of relevant, progressively responsible experience managing external sites

OR

• Master's degree in Organic Chemistry, Chemical Engineering, or another relevant scientific discipline with at least 8+ years of relevant, progressively responsible experience managing external sites
• Strong working knowledge of pharmaceutical GMPs and ICH regulatory guidance.
• Demonstrated experience managing external suppliers, contract manufacturers, warehouses, or logistics providers.
• Proven ability to interact effectively with senior management and cross-functional teams.
• Exceptional verbal and written communication skills.

Preferred Qualifications

• Experienced in OSD drug product manufacturing and supply chain execution and oversight in the pharmaceutical industry
• Understanding of the contract manufacturing organization (CMO) landscape; knowledge of CMO capabilities and limitations for worldwide drug product manufacturing is a plus
• Experience in application of manufacturing principles governed by current Good Manufacturing Practices (cGMP). Working knowledge of worldwide regulatory requirements, including pharmaceutical ICH guidance
• Experience supporting regulatory inspections and audits in partnership with QA.
• Advanced expertise in vendor qualification, contract negotiation, and supplier performance management

The salary range for this position is: $182,070.00 - $235,620.00. 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:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* 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.