Pharma QA Job at Novartis | Quality Analyst | Pharma Graduates
Looking for QA Pharmaceutical Jobs with a global pharmaceutical leader? Novartis is hiring a Quality Operations Analyst in Hyderabad for professionals with experience in Quality Assurance, Quality Control, Regulatory Affairs, or pharmaceutical manufacturing. This opportunity is ideal for B. Pharm & M. Pharm candidates looking to build a rewarding Novartis Career in pharmaceutical quality operations and regulatory compliance.
- Job Title: Quality Operations Analyst
- Location: Hyderabad, India
- Department: Production / Manufacturing
About the Company
Novartis is one of the world’s leading pharmaceutical companies, dedicated to reimagining medicine to improve and extend people’s lives. Operating across multiple therapeutic areas and global markets, Novartis combines scientific innovation with operational excellence to deliver high-quality medicines to patients worldwide. A Novartis Career offers professionals the opportunity to work in a collaborative, innovation-driven environment focused on improving healthcare outcomes.
Job Description
The Quality Operations Analyst is responsible for supporting batch release activities, regulatory compliance checks, GxP documentation, and quality operations processes. This role plays a critical part in ensuring compliance with cGMP requirements, regulatory standards, and Novartis quality systems. These QA Pharmaceutical Jobs provide valuable exposure to quality management, batch document review, audits, CAPA management, and continuous improvement initiatives.
Key Responsibilities
- Perform batch release activities and regulatory compliance checks.
- Support product quality compliance and quality operations workflows.
- Review batch documentation and release-related records.
- Create and review GxP documents, SOPs, trend reports, and investigation reports.
- Ensure compliance with cGMP, regulatory requirements, and quality standards.
- Support CAPA management and process improvement initiatives.
- Escalate and investigate GxP and non-GxP compliance issues.
- Assist during internal and external audits.
- Prepare mismatch trend reports and quality documentation.
- Support preparatory activities for batch release processes.
Qualification & Experience
- Education
- B. Pharm
- M. Pharm
- Experience: 2–4 years in
- Quality Assurance
- Quality Control
- Regulatory Affairs
- Pharmaceutical Manufacturing
- Medical Device Industry
- Learning Management Systems
Required Skills
- Knowledge of cGMP and GxP requirements
- Batch release and batch document review
- Regulatory compliance understanding
- CAPA management and quality systems
- Proficiency in MS Office tools
- Documentation review and management
- Quality trend analysis and reporting
