Associate Director, Master Production Planner

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 At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers. We set and achieve bold ambitions in our fight against the world's most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. As an Associate Director, Master Production Planner at Gilead you are responsible for translating global supply strategies into an integrated, feasible, and optimized master production schedule (MPS) across the internal and external manufacturing network. This role acts as the primary conduit between Global Network Planning and Site Supply Chain Planning, ensuring that long‑range strategies and demand signals convert into executable and stable production plans. The role governs planning outside and inside the 4‑month planning time fence, driving proactive risk mitigation in the 6-24‑month horizon and protecting execution stability within the frozen window. Responsibilities Global‑to‑Site Planning Integration Translate global demand signals, inventory policies, and supply network strategies into feasible, detailed site‑level production schedules. Lead integration between Global Network Planning and Site Planning teams to ensure alignment on feasibility, constraints, and assumptions. Reconcile the Global Supply Plan (GSP) with Site Rough‑Cut Capacity Plans (RCCP), resolving discrepancies prior to execution. Master Production Scheduling (MPS) Leadership Own and govern the 24‑month master production schedule for DS, DP, and FG across internal and external manufacturing nodes. Build batch sequences, production cycles, campaign structures, and capacity allocations. Ensure MPS stability within the 4‑month frozen window while enabling appropriate agility outside it. Lead scenario modeling and recommend adjustments in response to supply risks, capacity shifts, regulatory changes, and demand variability. Planning Outside the 4‑Month Time Fence (Owning the 6-24‑Month Horizon) The Associate Director governs all planning activities beyond the 4‑month frozen/planning time fence, ensuring feasibility and alignment well ahead of execution.

Responsibilities include:

Owning the 6-24‑month unconstrained planning horizon, translating global strategies into forward‑looking production plans. Conducting advanced long‑range capacity modeling to identify constraints, maintenance windows, QC load, labor availability, and network balancing needs. Running structured scenario analyses for launch acceleration, demand shifts, supply disruptions, regulatory changes, and market expansions. Driving early alignment between Global Network Planners and Site Planners to validate assumptions and address issues before the frozen zone. Partnering with Procurement and Materials teams to confirm long‑lead material readiness and supplier feasibility. Validating feasibility for lifecycle initiatives such as tech transfers, new SKUs, artwork/label updates, and new market entries. Leading long‑range planning forums with Global Planning, Site Planning, External Manufacturing, Quality, Regulatory, and Technical Operations. Identifying long‑range risks and establishing mitigation strategies ahead of the 4‑month window. Planning Time Fence Governance (4‑Month Frozen Window) Maintain governance for all plan changes within the 4‑month frozen window. Ensure major planning decisions (campaign timing, capacity adjustments, material commitments) are resolved before entering the frozen horizon. Protect execution stability by minimizing late changes and deviations within the fixed window. Manage any required exceptions through established supply governance forums. Internal Manufacturing & Network Coordination Serve as the central planning interface to internal manufacturing sites, ensuring alignment between global supply strategies and site‑level operational plans. Partner closely with internal Site Supply Chain, Manufacturing Operations, and Master Scheduling teams to confirm production feasibility, capacity availability, and alignment with maintenance, labor, and equipment constraints. Coordinate with internal network governance to ensure synchronized DS, DP, and FG flows across internal nodes. Monitor schedule adherence at internal sites, capturing deviations, understanding drivers, and ensuring timely corrective actions. Provide internal manufacturing sites with 6-24‑month long‑range visibility to support staffing plans, capital/asset planning, material readiness, and QA/QC workload forecasting. External Manufacturing & Network Coordination Serve as the central planning interface to the Global External Manufacturing (GEM) organization, ensuring aligned communication of production needs, capacity requirements, and schedule assumptions. Partner with GEM to validate slot reservations, campaign timing, yield expectations, testing sequences, and release timelines across the external network. Collaborate with GEM to maintain synchronized production calendars and ensure visibility across DS, DP, and FG flows. Monitor schedule adherence and network performance through GEM, supporting proactive escalation and issue resolution. Provide GEM with 6-24‑month long‑range visibility to enable proactive contracting, supplier readiness, and risk mitigation. Inventory, Materials, and Lifecycle Integration Align MPS with material availability, safety stock policies, and procurement strategies. Support lifecycle readiness including artwork changes, regulatory updates, tech transfers, and market expansions. Maintain appropriate inventory levels to support service targets while minimizing E&O exposure and working capital. Performance Management & Continuous Improvement Track and report KPIs including: MPS attainment Schedule adherence across internal and external nodes Capacity utilization Supply reliability / OTIF Inventory health Ensure adherence to Plan Stability and Performance‑to‑Plan metrics, and manage any exceptions diligently through established governance processes. Partner with Digital/IT teams to improve planning tool capabilities (SAP, IBP, OMP, Kinaxis) and data quality. Lead continuous improvement initiatives to enhance planning discipline, cycle time reduction, and cross‑functional integration. Qualifications Required Bachelor's degree in Supply Chain, Operations, Engineering, Life Sciences, or related field with 10+ years of relevant experience OR Masters degree in Supply Chain, Operations, Engineering, Life Sciences, or related field with 8+ years of relevant experience OR PhD in Supply Chain, Operations, Engineering, Life Sciences, or related field with 5+ years of relevant experience Supply chain planning experience, with strong exposure to network and site planning required Deep understanding of GMP operations, internal and external manufacturing, batch‑based production, and global distribution flows. Proficiency with ERP and advanced planning systems (SAP, IBP, OMP, Kinaxis). Strong influencing skills across global, matrixed organizations. Preferred

APICS CPIM/CSCP

certification or MBA (advanced degree) Experience with commercial biologics or sterile injectables. Experience with

S&OP/S&OE

processes and supply governance frameworks. Key Capabilities Strong ability to translate strategy into executable plans. Excellent communication, alignment, and stakeholder engagement skills. Highly analytical with advanced scenario planning capability. Effective at navigating complex networks and competing priorities. Calm, structured, and decisive during supply escalations.

People Leader Accountabilities:

Create Inclusion

• knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams. Develop Talent
• understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose. Empower Teams
• connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account.

They provide the support needed to remove barriers and connect their team to the broader ecosystem. The salary range for this position is:

Bay Area:

$182,070.00

• $235,620.

00.

Other US Locations:

$165,495.00

• $214,170.

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. Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.