REQ-10025245
12月 03, 2024
India

摘要

The Associate Supply Chain Manager (SCM) is responsible for Demand and Supply Planning from Clinical Finished Good (CFG) to Drug Substance (DS) ensuring demand fulfillment for assigned projects. The SCM acts as key contributor to the Clinical Supply & Operations Planning (CS&OP) process in TRD/GCS and provides transparency on supply constraints and manages related aspects accordingly within TRD.

About the Role

Major accountabilities:

  • 1. Creates and maintains the end-to-end supply plan from CFG to DS
    2. Harmonizes the supply strategy within GCS and contributes to the supply strategy of CHAD/PHAD/Biologics
    3. Leads the Clinical Demand Planning Meeting (CDPM) ensuring alignment between demand and supply.
    4. Ensures demand fulfillment and coverage of supply and regulatory aspects by contributing to GCS agenda at TRD Sub team CMC meeting. Represent GCS at TRD Sub-team on supply chain aspects.
    5. Optimizes the inventory strategy at PP and CFG level together with CTSM.
    6. Actively contributes to the portfolio manufacturing schedule alignment (from DS to CFG)
    7. Defines most cost-efficient ordering levels from CFG to DS, minimizing waste and allowing flexibility to accommodate demand variability.
    8. Drives Long term demand and capacity planning (LTDCP) coordinating with the CSPL, DPPL, DSPL and TPL.
    9. Adheres to SCM KPI for project and unit.
    10. Data and Digital savviness in SC domain. Manages Ordering and master data requirements in SAP within the scope of the role.
    11. Drive the Change control strategy for clinical supplies from GCS perspective.
    12. Provides impact assessment on clinical supplies and contribute to the regulatory submission strategy.
    13. Integrates Comparator supply strategy into the TRD procurement, blinding & release planning.
    14. GCS Process order check.

Key performance indicators:

  • Quality (GMP), quantity, and timelines for all assigned tasks/projects -Compliance with Novartis standards, in particular, ethics, health, safety, and environment (HSE), and information security (ISEC) standards.
  • Unit KPIs (e.g. FPFV (first patient first visit), LTA (lost time accident), FTR (first time right), Rework Rates, Recalls)

Minimum Requirements:
Work Experience:

  • Professional experience (ca. 3-5 years) in GMP environment and analytics.
  • (e.g., Quality Control).

Skills:

  • Continual Improvement Process.
  • Master Data.
  • Material Requirements Planning (Mrp).
  • Materials Management.
  • Production Planning.
  • Project Management.
  • Supply Chain Planning.
  • Supply-Chain Management.
  • Wms (Warehouse Management Systems).

Languages :

  • English.

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Development
Innovative Medicines
India
Hyderabad (Office)
Research & Development
Full time
Regular
No

Accessibility and accommodation

Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

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REQ-10025245

Associate Supply Chain Manager

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