Job Description

Summary

  • Provides effective operational and regulatory support to Novartis as well as to regional/global organizations for assigned regulatory submission and maintenance activities, including preparation and submission of regulatory dossiers, maintenance of regulatory databases and archives and artwork-related activities.

About The Role

Major accountabilities:

  • Coordinates and prepares high quality submissions of regulatory dossiers for assigned products -Achieve the CTA/NDA submission on the targeted date; -Achieve the approval of CTA, NDA and other related supplementary application on the targeted date; -Ensure license renewal Submission and approval on time; -Ensure CMC/BPI/PSUR/RMP in line with NMPA regulation and Novartis internal policies; -Ensure registration master file update -Assist to coordinate f2f meeting with CFDA/CDE for new project discussion -Communicate the questions referred by HAs timely and smoothly; -Timely update and communicate the registration status to the line manager -Timely order and tracking the registration sample, dossier, certificates…; -Start to establish good communication and relationship with key stake holders.
  • Get familiar and with company and department SOP and working procedures -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:

  • Timely accomplishment of assigned tasks in required quality.
  • Compliance with regulations and internal procedures -Relevant databases and archives up -to -date.

Minimum Requirements:

Work Experience

  • Functional Breadth.
  • Cross Cultural Experience.
  • Operations Management and Execution.
  • Project Management.

Skills:

  • Clinical Trials.
  • Collaboration.
  • Databases.
  • Detail Oriented.
  • Lifesciences.
  • Project Planning.
  • Regulatory Compliance.

Languages :

  • English.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.

Read our handbook (PDF 30 MB)


Job Details

Role Level: Not Applicable Work Type: Full-Time
Country: India City: Greater Hyderabad Area
Company Website: http://www.novartis.com/in-en Job Function: Others
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

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