You are hereSubmit CV/resume for future consideration as Assistant Manager - Third Party Manufacturing @ Novartis | B.Pharm, B.Sc, M.Pharm, M.Sc can apply

Submit CV/resume for future consideration as Assistant Manager - Third Party Manufacturing @ Novartis | B.Pharm, B.Sc, M.Pharm, M.Sc can apply


A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post: Assistant Manager - Third Party Manufacturing

To ensure manufacture of good quality products at Third Party Manufacturing units as per the agreed Production plan at the most optimum cost, and in 100% compliance with Novartis GMP requirements

Job Description:
* Product Supply & TPM Operating rhythm

  • Ensure timely supply of Product from TPMs to meet the Monthly dispatch requirement
  • Execute TPM operating rhythm to ensure hassle free operations
  • Ensure timely submission of reports from TPMs as part of the operating rhythm
  • Provide support to other functions like QA, R&D, Packaging Development and Direct Procurement.
  • Identify opportunities for process improvement and cost savings

* TPM Performance Management

  • Monitor Key Performance Indicators (KPI) to evaluate TPM Performance and drive KPI as a culture at TPMs.
  • Design and implement TPM performance evaluation model

* Product Costing and COGS Budgeting

  • Develop cost sheet for all products and benchmark with the best in the industry
  • Support COGS budgeting by co-coordinating with the other functions
  • Update the BOM of all products on timely basis

* New Product Development & Technology transfer to TPMs

  • Work closely with Innovations team, R&D, QA and TPMs for new product development
  • Engage in new TPM selection , screening and finalization
  • Technology transfer of products from R&D to commercial production stage

* Quality System Implementation

  • Focus on TPMs for improvement of Quality Systems in manufacturing
  • Support to QA & Compliance for audits of TPMs

* Corporate Citizenship

  • Liaison with TPMs to ensure compliance with Novartis CC guidelines
  • Ensure closure of CAPA of audit action points

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