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    Job · 20488632

    HYDERABAD · FULLTIME

    Manager, Inventory Planning & Coordination

    Bristol-Myers Squibb

    Bristol-Myers Squibb

    Hyderabad · onsite · Posted 13d ago

    Sourced fromNaukri
    Undisclosed2–7 yrsfulltimeHyderabad

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    Section · 01

    About this role

    Position Summary
    Serves as the operational inventory management and distribution coordination expert within Global Clinical Supply Chain. Responsible for maintaining global inventory visibility, ensuring supply readiness, and coordinating global clinical supply distribution activities to support uninterrupted delivery of investigational product (IP) to patients. Through close partnership with Clinical Supply Leads (CSLs), Trial Supply Managers (TSMs), Logistics, depots, and external partners, the Inventory Planning Coordinator (IPC) drives effective inventory management, identifies and mitigates supply risks, and enables efficient operational execution across the clinical supply chain to support clinical trial success.


    Duties/Responsibilities
    • Works cross-functionally as part of a dynamic matrix team to plan delivery of clinical drug supply to ensure sufficient supply availability for new and ongoing studies.
    • For drug supply planning, the TSM initiates the planned depot transfers, based on product-specific demand required for the established time period(s). The Inventory Planning Coordinator utilizes this information to coordinate and follow up on depot shipments to ensure sufficient supplies are at the local depots in accordance with the MRB (Must Reach By) date.
    • Leads operational coordination between Logistics, Shipment Execution, Warehouses, and Depot providers to ensure timely execution of approved inventory movements
    • Inventory planning management includes responsibility for monitoring expiry dates and ensuring replacement supply is available at the local depots as well as proactively identifying and communicating upcoming inventory concerns/risks to responsible TSM.
    • Owns operational tracking and prioritization of QP (Qualified Person) release activities utilizing key milestone dates provided by the TSM.
    • Ensures country/study approval of product for assigned programs/studies as part of depot planning.
    • Supports execution and tracking of approved manual allocations and inventory movements.
    • Maintains visibility of approved inventory movement plans and escalates execution risks or delays affecting implementation.
    • Communicates changes to the Shipment Execution Team. Advises TSM of drug supply constraints and recommends alternative strategies to influence the ability of CSC to meet existing or anticipated demands.
    • Coordinates deployment of approved Use Date Extensions at depots and maintains completion tracking, escalating deployment risks as necessary.
    • If applicable, for program level supplies, prepares Product Information Listings and Batch Listing extract files as required for study database locks and regulatory filings.
    • Participates on key task forces and acts as a change lead for improvement initiatives and procedural updates. Seeks continuous improvement, recommends and implements ways to improve the efficiency of clinical supply chain processes.
    • Serves as the operational owner for inventory execution, distribution coordination and depot readiness activities. Escalates issues requiring supply strategy, forecasting, allocation or study-level supply decisions to the responsible TSM and/or CSL.
    • Acts as a change agent and operational subject matter expert, contributing to process improvements, system enhancements, and initiatives that advance clinical supply chain capabilities and operational excellence.


    Reporting Relationship
    • Senior Director or Director, Clinical Supply Team Lead


    Qualifications
    • Minimum 2 years experience in Supply chain or Pharma industry.
    • Minimum 1 year Clinical Development with global experience.
    • An equivalent combination of education and experience may substitute.
    • Moderate knowledge of the global drug development process and global regulatory requirements with respect to investigational new drugs.
    • Strong analytical and cross-functional negotiation skills.
    • Strong project management skills and handling multiple projects simultaneously.
    • Strong knowledge of Inventory planning and management, and Supply Chain Functionality.
    • Moderate knowledge of import / export requirements.
    • Strong knowledge of industry technology.
    • Oral and written communication skills (fosters open communication).
    • Demonstrated teamwork and collaboration skills.
    • Takes initiative and displays a strong sense of urgency.


    Education/Experience/ Licenses/Certifications
    • BA/BS in Science, IT or Business, preferably with focus on IT / Digitization / Supply Chain.
    • Travel: N/A


    Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

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    Section · 02

    Skills

    drug developmentExportdata privacyNegotiation Skillslosbsinventory planningclinical developmentregulatory filingsShipmentLogisticsdeploymentProject ManagementInventory ManagementCommunication SkillsPharmaForecasting

    Section · Company

    About Bristol-Myers Squibb

    Bristol-Myers Squibb

    Bristol-Myers Squibb

    Pharma

    375

    employees

    1887

    139 years old

    New York

    United States

    ₹19.1L PA avg

    Avg at Bristol-Myers Squibb

    About

    We are a global biopharmaceutical company whose mission is to discover, develop and deliver innovative medicines that help patients prevail over serious diseases. At Bristol Myers Squibb, we work every day to transform patients’ lives through science. We combine the agility of biotech with the reach and resources of an established pharmaceutical company to create a global leading biopharma company powered by talented individuals who drive scientific innovation. We have the brightest people in the industry and believe that their diverse experiences and perspectives help to bring out our best ideas, drive innovation and achieve transformative business results. Each day, our employees around the world work together for patients – patients are at the center of everything we do. They inspire us. They are the reason we come to work each day. We are proud of the advancements we have made in oncology, hematology, immunology, and cardiovascular disease, and we are dedicated to helping patients prevail over serious diseases through our diverse and promising pipeline and new scientific platforms. We are pursuing therapies at the forefront of scientific discovery with the goal of bringing an exciting new generation of life-changing treatments to patients. We aspire to be at the center of a vibrant healthcare innovation ecosystem, where academic research centers, biotech, and biopharma companies all contribute to continued scientific advancement.

    Industries

    PharmaBiotech & Life sciences

    Employee ratings

    10 reviews

    3.7/ 5

    Culture

    2.6

    Career growth

    2.2

    Work-life

    3.1

    Employees rate it well for

    Work-Life Balance38Compensation & Benefits37

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