REQ-10029901
12月 12, 2024
India

摘要

-This is a universal job description meant to capture some of the primary duties of this role that are common across functions or divisions. It is not intended to represent all of the specific responsibilities of the position -Organizes, monitors and performs activities related to assigned area of responsibility. Ensures compliance of processes with national regulations as well as Novartis internal procedures and GxP requirements.

About the Role

Major accountabilities:

  • Interacts and collaborates with internal stakeholders -Actively supports project execution to ensure key milestones and quality are met -Communicates issues to teams and line management and propose corrective actions -Applies lessons learned -Coaching and technical training as peer / technical expert.
  • Act as mentor for junior associates -Understand resource contraints and identify cost saving opportunities -Work according to relevant guidelines at own workplace -Show positive work ethics and influences others.
  • Propose ideas for continuous process improvement in area of expertise as a member of a team and follow up on implementation.
  • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

  • QUOTIF (QUality On Time In Full delivery) -GMP Compliance (number of deviations, technical issues, audit / inspection findings) -HSE compliance (accidents, incidents, general condition of shop/facility, adherence to behaviour based safety programm)

Minimum Requirements:
Work Experience:

  • 3-4 years relevant experience.

Skills:

  • Capacity Planning.
  • Continual Improvement Process.
  • Material Requirements Planning (Mrp).
  • Materials Management.
  • Project Planning.
  • Supply Chain.
  • Wms (Warehouse Management Systems).

Languages :

  • English.

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A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
REQ-10029901

Intern - Clinical Trial Supply Management

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