"Hurry Up! Dream Job Alert: Senior Expert Role at Novartis, Hyderabad"
"Hurry Up! Dream Job Alert: Senior Expert Role at Novartis, Hyderabad"

Senior Expert Role at Novartis For Chemistry & Chemical Engineering – Apply Online

Senior Expert, Science & Technology (EPM Specialist)

Hyderabad, Telangana, India

About the job

Summary

5! The typical number of projects you will participate in as the new EPM Specialist based at Novartis Hyderabad site. As part of the Global Drug Development (GDD) team, this role is essential in ensuring the development of the highest quality small molecule drug substances throughout the life cycle of each project, required to support clinical trials.

About The Role

Your responsibilities include, but are not limited to:

  • Leading and facilitating operational excellence in the External Partner Management (EPM) unit of Chemical and Analytical Development (CHAD) in their new group in Hyderabad/Genome Valley.
  • Owning and leading process improvement activities related to externalized process R&D, including analytical services and supplies of chemical intermediates and APIs.
  • Managing data and readouts related to externalized activities (business, KQI, KPI, etc.).
  • Facilitating regular Portfolio and Business Review meetings and other frequent business activities.
  • Supporting/leading the setup of databases and document flow processes within the EPM unit.
  • Supporting documentation/workflows related to externalized business (non-GMP/GMP).
  • Contributing to evaluation, selection, and onboarding processes of new external partners.
  • Actively managing interactions between internal and external partners to ensure a constructive and well-functioning collaboration.
  • Participating in scientific/technical exchange with internal stakeholders and external partners.
  • Reviewing technical and GMP-relevant documents.
  • Owning, developing, and maintaining team SharePoint.

What You’ll Bring To The Role

  • Desirable: PhD/MSc in chemistry, chemical engineering, or equivalent and a minimum of 3 years’ experience in the pharmaceutical industry in chemical development and/or commercial.
  • Successfully demonstrated expertise in a specific scientific/technical area.
  • Experience in operational excellence and Six Sigma certification is a plus.
  • Excellent knowledge of data management and software/tools such as Office package (e.g. Excel, SharePoint, MSTeams), SAP, planning tools, etc.
  • Personal inclination for IT solutions and data management is a plus.
  • Proven experience in a GMP environment (equipment/facilities, manufacturing, analytics, deviation handling, change control, documentation, etc.).
  • Fluent English (oral and written).
  • Strong coordination and communication skills, collaborative spirit, self-driven attitude, high level of learning agility are key attitudes.
  • Experience and knowledge in the procurement of APIs, intermediates, raw materials, and services, including management of RFPs and RFIs, is a plus.

For more details and to apply, visit the original notification.

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