Sr. Director, Supplier Strategy and Management (Small Molecule API and OSD)

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

• Overview
• The Senior Director, Supplier Strategy and Management, API & OSD is responsible for sourcing, contracting, supplier relationship management (SRM), supplier portfolio strategy, and market and risk intelligence. This role manages business relationships with multiple contract development and manufacturing organizations (CMO/CDMOs) supporting both the Clinical and Commercial product portfolios. This role has significant leadership experience in strategic sourcing, contracting and supplier strategies, has executive presence and uses their business savvy and technical experience to drive high performance from our partners. This role collaborates effectively with senior leaders shaping how critical investments deliver value to the organization while simultaneously driving alignment across senior stakeholders. This role will influence significant CMO spend - how it is prioritized, governed and optimized to accelerative innovation, strategic priorities and ultimately supply of product to patients.

This is an onsite role based at our global headquarters in Foster City, CA. We do offer a hybrid environment with three days on campus and two days optional work from home.

Key Responsibilities

• •Serves as senior SSM partner to leaders across External Quality, Global External Manufacturing, and Pharmaceutical Development and Manufacturing
• •Translates business priorities into actionable supplier portfolio strategies that deliver measurable value
• •Own end-to-end accountability for OSD and API modalities with measurable outcomes
• •Define and execute supplier portfolio strategies leveraging market intelligence and deep category expertise
• •Drive value beyond savings, including innovation, supplier performance, quality/compliance and risk mitigation
• •Build trusted relationships with Senior Leadership and influence decision making
• •Communicate supplier portfolio strategies and performance to stakeholders, ensuring alignment
• •Lead cross functional alignment across stakeholders
• •Champion SSM strategic initiatives that increase early engagement and stakeholder satisfaction
• •Lead supplier governance in alignment with overarching segmentation and governance strategy
• •Lead strategic supplier relationships at the executive level
• •Define supplier performance expectations across cost, quality, innovation and reliability
• •Leads and partners with stakeholders on contract negotiations, competitive bidding process, optimizing contract compliance, and SRM. Ensures standardized tools are leveraged and maximize value for the business

• •Leads supplier risk assessments and ensures mitigation plans are identified and executed. Escalate risks and drive resolution to risks
• •Responsible for execution, review, and approval of RFPs/RFQs/RFIs
• •Negotiate Confidentiality Agreements, Master Service and Supply Agreements, Addendums, PSAs and SOWs
• •Lead and participate in Operational Excellence / Continuous Improvement projects
• •Stay informed and knowledgeable of relevant CMO/CDMO offerings, capabilities, as they relate to potential or known Gilead products/modalities

Qualifications

• •15+ years of experience in pharma/biotech or manufacturing
• •10+ years managing outsourced manufacturing and supplier networks and/or supply chains
• •Experience working in small molecule API and OSD manufacturing plant
• •Strong understanding of CMC development and GMP regulations
• •Excellent verbal and written communication skills; outstanding presentation skills
• •Proven leadership and cross-functional influence skills
• •Proven success driving large scale initiatives
• •Strong executive presence with demonstrated ability to influence senior stakeholders
• •Experience negotiating complex supplier agreements
• •Strong verbal and written communication, problem-solving, and organizational skills
• •Ability to manage multiple complex programs
• •Ability to operate in fast-paced, ambiguous environment – solve highly complex problems through ingenuity and collaboration with stakeholders
• •Ability to work under uncertainty and to resolve conflict in a constructive manner
• •Ability to effectively lead in a highly matrixed, global organization
• •Up to 20% travel

The salary range for this position is: $243,100.00 - $314,600.00. 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 inv