REQ-10026688
Oct 21, 2024
India

About the Role

Major accountabilities:

1. Handling of Audit CAPA actions, Deviations and Investigations.

2. Preparation of annual audit plans

3. Monitoring and maintain of KQI's and KPI's.2.

4. Maintenace of Shrepoints and Repositories. ·

5. Responsible to update the information on SharePoint/ trackers, review the applicable documents for correctness and archival of necessary documents on SharePoint. ·

6. Provide Administrative support in preparation of Quality Management Review meeting slide deck & metrics reporting. ·

7. Preparation, approval, and management of QAA's.

8. Develop and maintain process SOPs, working procedures and process maps. ·

9. Provide support for GMP External Audits and inspection management activities (HA and Self Inspection Audits).

10. Maintain Approved supplier list for GxP vendors.

11. Preparation of UQAP (Unified Quality Audit Program), Audit preparation support and QARP (Quality assurance responsible Person) Role for audit CAPA Management.

Minimum Requirements:

M.Pharm/ equivalent from a reputed institute.

• Min 4-6 yr Experience in Quality Assurance, Regulatory or in the manufacturing of pharmaceutical drug substances or products/ Medical device.

• Basic awareness of GxP compliance requirements.


Work Experience:

  • QMS Knowledge w.r.t. deviations, Investigations, handling of CAPA.

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

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.

Role Requirements

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

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Operations
Innovative Medicines
India
Hyderabad (Office)
Quality
Full time
Regular
No
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REQ-10026688

Analyst - Quality Operations

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