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    Job · 12158308

    Amgen logo

    Sr Associate Clinical Supply Chain Support Office

    Amgen · Hyderabad · onsite · Posted 66d ago

    Undisclosed5–10 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    In this vital role, you will serve as Sr Associate, supporting the Design and Setup of the Clinical Supply Chain.
    Reporting to the Manager Clinical Supply Chain - Change Mgt, and directed by the Global Setup Leads, you will contribute to the execution and completion of key deliverables associated with setup activities of global supply chains for clinical trials, by leading information gathering across stakeholders such as RD, Regulatory Affairs, Site Supply Chain and Master data, and task close out.
    In close collaboration with the Global Setup Lead team, you will ensure reliable, compliant, and right-first-time process execution, transparent status reporting on progress, and pro-active identification of risks and mitigation strategies for closing out deliverables.
    The role is accountable for managing various deliverables such as:
    • Master data requests for product materials, BOM, and study related attributes in SAP.
    • Creation of the Clinical Artwork requests and facilitating prioritization of outstanding attributes in relation to the request form.
    • Creation and maintenance of Product Specification Files, and Depot Plans.
    Roles Responsibilities Master Data in ERP (SAP)
    • Central focus point for ERP (SAP) readiness:
    • Initiate clinical label material requests;
    • Requesting Finished Drug Product Materials, Bill of Materials (BOM), Work Breakdown Structure (WBS) elements, Custom Values and ensures timely availability to adhere to overall project timelines
    • Ensures setup of Study Design Tables.
    Setup Activities
    • Coordinate and prioritize artwork creation process via initiation and routing of clinical artwork creation request forms, facilitating discussions to resolve issues and following up on outstanding queries.
    • Creates and maintains Product Specification File Study throughout the life cycle of the clinical trial
    • Creates and maintains third party depot plans and cross docks to support global study footprint
    Reporting
    • Maintains Metrics for Global Setup lead team
    • Contributes to monthly Workforce planning cycle
    Qualifications
    • 5+ Years of experience with Bachelors Bachelor degree or equivalent in logistics, business administration or life science.
    • Typically relevant working experience, preferably in the biotechnology or pharmaceutical industry,
    • Typically relevant working experience in an international and regulated environment
    • Understanding of fundamentals of logistics /supply chain principles (especially BOM)
    • Experience in planning
    • Experience in project management techniques
    • Advanced experience in MS Office applications (Word, Excel)
    • Fluency in English, both in oral and written communication
    • High quality standards with regards to work
    • Ability to set priorities and timely escalation

    Sourced from naukri

    Skills

    SAPIssue ResolutionLIFESCIENCEclinical trialsRegulatory Affairspharmaceutical industryBiotechnologyLogisticsAPERPProject ManagementSupply ChainSupply Chain ManagementAdministrationbomPharmaceuticalworkforce planning

    About Amgen

    Amgen logo

    Amgen

    Biotechnology

    1.5k+

    employees

    1980

    46 years old

    Hyderabad, Telangana

    India

    About

    Amgen operates in the biotechnology sector, developing and delivering advanced medicines to address critical health challenges globally.

    Industries

    BiotechnologyBiotech & Life sciences

    Employee ratings

    173 reviews

    2.8/ 5

    Culture

    2.7

    Career growth

    2.5

    Work-life

    2.8

    Employees rate it well for

    Senior Management11Salary7Work Culture7Work Life Balance7Learning6

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