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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-timeCork, IrelandNo salary listedHybrid

About the Job

Requirements

  • Extensive experience in a related field and a BS/BA, MA/MBA, PharmD, or PhD.
  • Experience in a pharmaceutical operations or cGMP 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 produce clear, concise, well-supported written conclusions.
  • Strong negotiation skills.
  • Organizational and time-management skills, including working knowledge of basic project-management tools and techniques.
  • Ability to interact effectively with senior management.
  • In-depth understanding of relevant principles, concepts, practices, standards, and industry practices.
  • Working knowledge of relevant regulatory guidance, including pharmaceutical GMPs and ICH Q7A.
  • Ability to apply organizational policies and recommend modifications to department policies and procedures as needed.
  • Familiarity with 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, enabling coordination and communication across competing demands.

Responsibilities

  • Partner with regional commercial supply chain leads to understand demand-planning trends, market-access changes, promotional campaigns, and product lifecycle events.
  • Integrate regional demand signals into end-to-end supply plans for active pharmaceutical ingredients, drug substance, drug product, and finished goods.
  • Hold regular alignment sessions with regional leads to validate assumptions, reconcile forecast discrepancies, and adjust supply plans.
  • Develop, maintain, and execute commercial supply plans that integrate demand insights, manufacturing capacities, 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 reviews.
  • Review and manage MoH across active pharmaceutical ingredients.
  • Manage system FPOs, including allocation of ICNs.
  • 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 SRM 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 LE.
  • Use SAP ERP and Kinaxis Rapid Response to build, monitor, and scenario-test supply plans, managing demand changes, supply constraints, expiry risk, and shelf-life-driven trade-offs related to production timing, inventory positioning, and allocation.
  • Coordinate with internal and external manufacturing sites to align production schedules and batch strategies with demand trends, lead times, and minimum remaining shelf-life expectations, while minimizing write-off risk and supporting service commitments.
  • Optimize global inventory positioning with regional supply leads to balance customer service and cost efficiency.
  • Analyze demand trends to support allocation decisions in constrained supply scenarios.
  • 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.
  • Support change-management initiatives that affect supply plans because of commercial or regulatory changes.
  • Track and report supply-plan adherence, inventory levels, and service-performance metrics.
  • Provide timely updates and escalate issues to leadership and stakeholders based on supply-demand alignment.
  • Provide leadership, direction, and management of a team to support execution of Supply Chain strategy.
  • Supervise, train, guide, and manage the performance of department personnel.
  • Create and maintain a positive working environment that supports productivity, employee engagement, and performance.
  • Use independent judgment to develop methods, techniques, and evaluation criteria for achieving results.
  • Develop and implement policies and procedures for Supply Chain operations, ensuring regulatory requirements are met.
  • Develop and implement strategies and goals for specific products or projects.
  • Create and communicate supplier, subcontractor, and vendor agreements and opportunities to the organization.
  • Implement and maintain material and production-control systems, policies, processes, and procedures to ensure approved materials flow in time to meet production requirements.
  • Liaise with governmental and audit agencies as required.
  • Review and implement changes to controlled documents and author sections of regulatory documents as needed.
  • Negotiate large contracts, monitor their costs, schedules, and performance, and drive cost savings through negotiation and other sourcing methods.
  • Execute supplier agreements with Legal and internal clients as needed to ensure compliance with corporate and purchasing guidelines.
  • Conduct formal business reviews with key suppliers, subcontractors, and vendors, and 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 track relevant market and competitor information.
  • Coordinate multiple production schedules as needed.
  • Create an inclusive team environment and model inclusion in team management.
  • Assess employees’ skills, experience, aspirations, and potential; coach them on current performance and future development; and ensure they receive feedback and guidance to grow.
  • Align team goals with organizational objectives, hold the team accountable, remove barriers, and connect the team 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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