Job Description

Summary

The Quality Operations Partner, AS&T Expert is responsible for managing all analytical aspects within responsible projects to ensure that the operational business is in compliance with cGMP (Current Good Manufacturing Practices), the Quality Assurance Agreement, regulatory requirements & the Novartis Quality Manual and is conducted according to the relevant Standard Operating Procedures. Ensures analytical Life Cycle Management for commercial products and ensures timely analytical implementation for new projects.

About The Role

Obligatory requirements:

  • Management and oversight of all analytical activities related within responsible projects.
  • Life-cycle management of analytical methods, including control of method performance, analytical method improvements, pharmacopoeia and health authority compliance (subject matter expert in health authority inspections)
  • Single point of contact for internal and external clients and contract laboratories, if applicable.
  • Ensure timely analytical implementation (Method Transfer and Method Validation) for (new) projects in the course of product transfers
  • Scientific analytical support for quality control, production, registration and marketing
  • Setup and monitoring of stability studies
  • Support overarching product investigations cross functional, e.g. QC, QA, Production, MS&T.
  • Implementation of GMP requirements. Compilation and review of documents (analytical protocols and reports, annual performance quality reports, ongoing process verification reports, registration documents)

Minimum Requirements

  • Education: M.Pharm/ MBA / M.Tech/MSc/Engineering/equivalent from a reputed institute.
  • Experiences: Minimum 8 years’ experience in Quality Assurance, Quality Control, AS&T, Regulatory or in the manufacturing of pharmaceutical drug substances or products/ medical device/ expertise in Learning management system
  • Problem Solving skills and stakeholder management
  • Basic awareness of GxP compliance requirements.
  • English fluent, written and spoken

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards

Commitment To Diversity And Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network.

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: Philippines City: Greater Hyderabad Area
Company Website: http://www.novartis.com/in-en Job Function: Quality Assurance & Control
Company Industry/
Sector:
Pharmaceutical Manufacturing

What We Offer


About the Company

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