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      Specialist - Quality Operations

      REQ-10015156
      9月 03, 2024
      India

      摘要

      -Manages Quality aspects and projects within area of responsibility. -Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.  

      About the Role

      Major accountabilities:

      • Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance -Support exception investigations -Review and approval of production, QC, and AS and T records -MBR review -Support OpEx improvement projects Qualified Person – Executes batch release in compliance with registration -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:

      • On-time and GMP-compliant release of dosage forms -No complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand -Successfully support continuous improvement projects -Executes batch release in compliance with registration  

      Minimum Requirements:
      Work Experience:

      • Functional Breadth.
      • QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &.
      • Collaborating across boundaries.
      • cleanliness zones.

      Skills:

      QMS

      BMR/ BPR review

      Batch Release process

      Quality Management

      Regulatory compliance checks

       

      Languages :

      • English.

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      A female Novartis scientist wearing a white lab coat and glasses, smiles in front of laboratory equipment.
      REQ-10015156

      Specialist - Quality Operations

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