Quality Assurance Jobs at Novartis
A rare chance has emerged for experienced professionals in the pharmaceutical sector. Novartis Hyderabad is seeking a Specialist in Quality Operations. Novartis is inviting applications from Pharmacy candidates with a strong background in GMP Quality Assurance. Interested individuals should apply for the Quality Assurance Jobs at Novartis Careers in Hyderabad.
About Novartis
Novartis is a global healthcare company based in Switzerland, dedicated to reimagining medicine to improve and extend people’s lives. The organization focuses on innovative pharmaceuticals and is committed to providing high-quality products and services. With a strong presence in Hyderabad, Novartis plays a vital role in the pharmaceutical industry, ensuring compliance with stringent quality standards.
Job Details
- Position: Specialist, Quality Operations
- Reference Number: REQ-10086080
- Location: Hyderabad
- Application Deadline: 30 September 2026
Job Description
The Specialist in Quality Operations will be responsible for overseeing batch release processes, ensuring compliance with Good Manufacturing Practices (GMP), and maintaining high-quality standards in documentation and operations. The Quality Assurance Jobs require a thorough understanding of Quality Management Systems (QMS) and the ability to support audits and quality events effectively.
Key Responsibilities
- Manage batch release preparations and technical release verification.
- Ensure compliance with GxP documentation standards in Quality Assurance Jobs in Hyderabad.
- Handle deviations and quality events within the QMS in this QA Job.
- Support audits and provide necessary documentation at Novartis Careers
- Oversee Certificate of Analysis (CoA), Bill of Materials (BOM), and master data management.
Eligibility Criteria for the Quality Assurance Jobs
- 5–7 years of experience in GMP Quality Assurance, with a focus on batch release.
- Educational qualifications: B.Pharm / M.Pharm.
Required Skills for the Quality Assurance Jobs
- Strong knowledge of batch-release processes.
- Experience in technical release verification.
- Proficient in GxP documentation practices.
- Ability to manage QMS deviations and quality events.
- Familiarity with audit support processes.
