Global QMS Manager

Novartis

Hyderabad

Hybride

INR 2 000 000 - 3 200 000

Plein temps

14 jours+

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Résumé du poste

Novartis in Hyderabad, India is seeking a Global QMS Manager to drive compliance, quality systems, and continuous improvement across global release processes. You will partner with Quality, IT, and business functions to define requirements, validate changes, and support training for users worldwide.

You will act as the global SME for Batch Release Hub processes, ensuring regulatory adherence, system integrity, and efficient, compliant product release across regions.

Qualifications

  • Bachelor's degree or equivalent in Life Sciences, Pharmacy, Engineering or related field.
  • Experience with quality systems in regulated pharma/healthcare environments.
  • Strong knowledge of pharma regulations and compliance.
  • Proven ability to collaborate across functions and locations.
  • Experience with system changes, validation, and UAT.

Responsabilités

  • Ensure Batch Release Hub configurations comply with regulatory and quality requirements.
  • Govern system changes to support compliant batch release globally.
  • Maintain and improve business documentation aligned with configurations.
  • Collaborate with Quality and IT to enhance system reliability and performance.
  • Translate business needs into clear requirements for development and enhancements.
  • Coordinate training to build global user confidence and capability.
  • Support validation, UAT, data migration, and system integration.
  • Act as global SME and primary contact for Batch Release Hub processes.

Connaissances

Batch Release
Quality Management
Regulatory Compliance
Stakeholder Management
System Validation
User Acceptance Testing
GxP
Leadership
Continuous Improvement
QA/QC

Formation

Bachelor's degree in Life Sciences/Pharma/Engineering

Outils

QMS software

Description du poste

Job Description Summary

#LI-Hybrid

Location: Hyderabad, India

Relocation Support: This role is based in Hyderabad, India. Novartis is unable to offer relocation support: please only apply if accessible.

If you are passionate about driving quality excellence on a global scale, this is an opportunity to make a meaningful impact at Novartis. As Global QMS Manager, you will drive compliance, innovation, and continuous improvement across critical quality processes that support product release worldwide. Working with diverse stakeholders across Quality, Information Technology, and business functions, you will help shape how global systems operate, improve efficiency, and ensure adherence to regulatory expectations. This is an exciting opportunity to make a visible impact on a global scale while helping deliver high-quality medicines to patients around the world.

Job Description
Major Accountabilities
  • Ensure compliance of Batch Release Hub configurations with regulatory and quality requirements.
  • Govern system changes to support compliant and efficient batch release processes globally.
  • Maintain and continuously improve business documentation aligned with system configurations.
  • Partner with Quality and Information Technology teams to enhance system reliability and performance.
  • Translate business needs into clear requirements for system development and enhancements.
  • Support and coordinate training initiatives that help users build confidence and capability globally.
  • Support validation, user acceptance testing, data migration, and system integration activities.
  • Act as the global subject matter expert and primary contact for Batch Release Hub processes.
Essential Requirements
  • Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or a related field, or equivalent relevant experience.
  • Experience supporting or managing quality systems within a regulated pharmaceutical, healthcare, or related environment.
  • Strong knowledge of pharmaceutical regulations, quality standards, and compliance requirements.
  • Demonstrated ability to collaborate across functions and build strong stakeholder partnerships globally.
  • Experience supporting system changes, validation activities, and user acceptance testing.
  • Excellent communication, problem-solving, and stakeholder management skills.
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.

Skills Desired

Collaboration, Communication, Continuous Improvement, Data Integrity, Decision Making, Good Manufacturing Practices (GMP), Leadership, Managing Ambiguity, Operational Excellence, Quality Assurance (QA), Quality Compliance, Quality Control (QC), Quality Inspections, Quality Management Systems (QMS), Regulatory Compliance, Statistical Process Control (SPC), Supplier Quality Management

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