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Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Associate Director, End-to-End Commercial Supply Planner - Supply Chain

Supply Chain ManagementConfirmed live in the last 24 hours
Full-timeFoster City, CA, USAHybrid

About the Job

Requirements

  • At least 10 years of relevant experience in a related field and a Bachelor of Science or Bachelor of Arts; or at least 8 years of relevant experience and a Master of Arts or Master of Business Administration; or at least 5 years of relevant experience and a Doctor of Pharmacy or PhD.
  • Experience in a pharmaceutical operations or current Good Manufacturing Practice environment.
  • Experience purchasing custom chemicals, planning pharmaceutical development activities, and managing third-party synthesis of intermediates or Active Pharmaceutical Ingredients.
  • Ability to develop solutions to complex problems requiring ingenuity and innovation.
  • Strong verbal and written communication skills, including the ability to write structured, clear, concise messages with well-supported conclusions.
  • Strong negotiation skills.
  • Organizational and time-management skills, including working knowledge of project-management tools and techniques.
  • Ability to interact effectively with senior management.
  • In-depth understanding and application of relevant principles, concepts, practices, and standards, and in-depth knowledge of industry practices.
  • Working knowledge of relevant regulatory guidance, including pharmaceutical Good Manufacturing Practices and ICH Q7A.
  • Ability to apply organizational policies and interpret, execute, and recommend modifications to department policies and procedures.
  • Familiarity with the technologies, strengths, and weaknesses of fine chemical and pharmaceutical manufacturers worldwide may be required.
  • In-depth understanding of the financial aspects of Supply Chain operations.
  • In-depth knowledge and proficiency across multiple Supply Chain practices, with ability to coordinate and communicate across competing demands.

Responsibilities

  • Develop and execute supply plans for commercial small-molecule and biologics products, partnering with regional commercial supply-chain leads to incorporate demand-planning trends, market dynamics, and promotional activities into global supply plans.
  • Understand regional demand-planning trends, market-access changes, promotional campaigns, and product lifecycle events with regional commercial supply-chain leads.
  • Integrate demand signals from regional planning teams into end-to-end supply plans for Active Pharmaceutical Ingredients, Drug Substance, Drug Product, and Finished Goods.
  • Facilitate regular communication and alignment sessions with regional leads to validate assumptions, reconcile forecast discrepancies, and adjust supply plans.
  • Develop, maintain, and execute detailed commercial supply plans across Active Pharmaceutical Ingredients, Drug Substance, Drug Product, and Finished Goods, integrating demand insights, manufacturing capacities, end-to-end lead times, and minimum remaining shelf-life requirements at batch release and market delivery.
  • Review part setups, effective dates, and other master data for Active Pharmaceutical Ingredient planning.
  • Monitor new-product supply setup updates.
  • Manage Active Pharmaceutical Ingredient retest and expiry review.
  • Review and manage months of hand (MoH) across Active Pharmaceutical Ingredients.
  • Manage system forecasted purchase orders, including allocation of intercompany notifications.
  • Review demand and Drug Product supply-plan outliers.
  • Review the Drug Product five-year supply plan and Active Pharmaceutical Ingredient four-year supply plan.
  • Review Active Pharmaceutical Ingredient inventory health.
  • Create the first draft of the supplier relationship management Active Pharmaceutical Ingredient change-analysis slide and provide the Active Pharmaceutical Ingredient change-analysis slide.
  • Review shipping quantities and requirements.
  • Review lot-level restrictions for Drug Product firm orders.
  • Provide four-year budget volumes during the latest estimate process.
  • Use SAP ERP and Kinaxis Rapid Response to build, monitor, and scenario-test supply plans, proactively managing demand changes, supply constraints, expiry risk, and shelf-life-driven trade-offs related to production timing, inventory positioning, and allocation decisions.
  • Work with internal and external manufacturing sites to align production schedules and batch strategies with demand trends, lead-time realities, and minimum remaining shelf-life expectations at release and in market, minimizing write-off risk while supporting commercial priorities and service-level commitments.
  • Optimize global inventory positioning with regional supply leads, balancing customer service and cost efficiency.
  • Enable informed allocation decisions in constrained-supply scenarios through demand-trend analysis.
  • Partner with Commercial Operations, Quality, Manufacturing, and Finance to ensure supply plans support business objectives.
  • Maintain partnerships with regional market leads to provide visibility into supply status, risks, and escalations and support product availability in market.
  • Support change-management initiatives affecting supply plans because of commercial or regulatory changes.
  • Track and report supply-planning metrics, including supply-plan adherence, inventory levels, and service performance.
  • Provide timely updates and escalations to leadership and stakeholders based on supply-demand alignment.
  • Provide leadership, direction, and management to a team in support of Supply Chain strategy.
  • Supervise, train, guide, and conduct performance management for department personnel.
  • Create and maintain a positive working environment to support productivity, employee engagement, and performance.
  • Exercise independent judgment in developing methods, techniques, and evaluation criteria for obtaining results.
  • Develop and implement policies and procedures for Supply Chain operations, ensuring relevant regulatory requirements are met.
  • Develop and implement strategies and goals for specific products or projects.
  • Create and communicate supplier, subcontractor, or vendor agreements and opportunities to the organization.
  • Implement and maintain material and production control systems, policies, processes, and procedures to ensure approved materials flow on time to meet production requirements.
  • Serve as liaison between the company and governmental or audit agencies as required.
  • Review and implement changes to controlled documents as needed and author sections of regulatory documents when required.
  • Negotiate large contracts involving substantial financial amounts; monitor cost, schedules, and performance of major contracts; and drive cost savings through negotiation and other sourcing methods.
  • Execute supplier agreements with Legal and internal clients as needed to ensure contract terms and conditions comply with corporate and purchasing guidelines.
  • Conduct formal business reviews with key suppliers, subcontractors, or vendors; manage contract performance against cost, service, quality, schedule, and flexibility goals.
  • Manage outsourced manufacturing activities as needed.
  • Compile information from periodicals, catalogs, and other sources to stay informed about relevant market and competitor information.
  • Coordinate multiple production schedules as needed.
  • Create inclusion by modeling inclusive leadership and embedding diversity in team management.
  • Develop talent by understanding employees’ skills, experience, aspirations, and potential; coaching them on performance and future potential; and ensuring they receive feedback and insight to grow and develop.
  • Empower teams by aligning goals, purpose, and organizational objectives, holding teams accountable, removing barriers, and connecting them to the broader organization.

About the Company

Gilead Sciences

Makes medicines for HIV, liver disease and cancer

Gilead Sciences is a biopharmaceutical company that discovers, develops and sells medicines for HIV, viral hepatitis and other liver diseases, cancer and inflammatory conditions. Its HIV business covers both treatment, led by the once-daily pill Biktarvy, and prevention, including Descovy and Yeztugo, a lenacapavir injection given twice a year. In cancer, its Kite unit makes CAR T-cell therapies from patients' own immune cells, and Trodelvy is an antibody-drug conjugate for breast cancer. Gilead earns revenue by selling its drugs to wholesalers, specialty pharmacies, hospitals and governments worldwide after regulatory approval. The company was founded in 1987 and is headquartered in Foster City, California.

Company size
10,001+
Company stage
IPO
Headquarters
Foster City, CA
Founded
1987

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