Quality Operations Specialist Analyst Jobs at Novartis in Hyderabad for QA QC regulatory professionals with GMP knowledge and pharmaceutical manufacturing experience roles available
Company Overview
Novartis is one of the world’s leading pharmaceutical organizations known for innovation, research excellence, and commitment to improving patient lives. With a strong presence in India, Novartis supports global healthcare systems through advanced drug development, manufacturing, and quality operations.
The company offers a collaborative work environment, global exposure, and strong career development opportunities for professionals in quality assurance and regulatory domains.
Job Location & Employment Type
- Location: Hyderabad
- Employment Type: Full-Time
Open Positions / Department Details
- Role: Specialist / Analyst – Quality Operations
- Department: Quality Assurance / Quality Operations
This role focuses on maintaining compliance with global quality standards and supporting manufacturing and QC-related processes within the pharmaceutical domain.
📊 Job Overview (Quick Details)
| Job Title | Specialist / Analyst – Quality Operations |
|---|---|
| Company | Novartis |
| Location | Hyderabad, India |
| Employment Type | Full-Time |
| Department | Quality Assurance / Quality Operations |
| Experience Required | Minimum 3 Years |
| Qualification | Pharmacy / Science / MBA / Engineering |
| Salary | As per company norms |
| Mode of Application | Online |
Key Roles & Responsibilities
The selected candidate will be responsible for ensuring product quality compliance and supporting key quality operations processes. Major responsibilities include:
- Deliver quality-related services aligned with cGMP standards and internal quality systems.
- Support regulatory workflows and ensure compliance across product lifecycle activities.
- Assist in QC release processes including preparation and review of inspection plans, specifications, and compliance documents.
- Manage documentation such as Certificates of Analysis (CoA), Certificates of Compliance (CoC), and inspection-related records.
- Contribute to testing monograph preparation and perform impact assessments where required.
- Prepare and manage risk evaluation reports, including nitrosamine risk assessments for global and country-specific requirements.
- Collect data and prepare reports or presentations for internal meetings and leadership discussions.
- Provide statistical support, performance tracking, and trend analysis for quality processes.
- Ensure adherence to regulatory guidelines, internal SOPs, and service-level agreements.
- Participate in audit readiness and provide support during internal and external inspections.
- Follow all GxP compliance requirements and internal quality policies.
- Work with digital tools and systems to enhance data-driven decision-making.
- Coordinate with global stakeholders and cross-functional teams to ensure smooth operations.
Eligibility Criteria
🎓 Education
Candidates must have one of the following qualifications:
- Bachelor’s or Master’s degree in Pharmacy or Science
- MBA or Engineering degree (relevant fields)
- Equivalent qualification from a recognized institute
💼 Experience
- Minimum 3 years of experience in:
- Quality Assurance (QA)
- Regulatory Affairs (RA)
- Pharmaceutical manufacturing (drug substances/products or medical devices)
🛠 Skills Required
- Strong understanding of Quality Management Systems (QMS)
- Knowledge of GMP and GxP guidelines
- Familiarity with Quality Control processes and analytical methods
- Experience in risk assessment and compliance documentation
- Good communication and presentation skills
- Ability to collaborate with global teams and stakeholders
- Basic IT and digital tool proficiency
- Strong problem-solving and analytical thinking
- Understanding of regulatory requirements and audit processes
- Knowledge of data integrity and operational excellence
Salary & Benefits
- Compensation: As per company norms
- Additional benefits may include health insurance, career development programs, and exposure to global pharmaceutical operations
Selection Process
The recruitment process generally includes:
- Online application submission
- Resume shortlisting
- Technical/functional interview
- HR discussion
- Final selection
How to Apply
Interested candidates can apply through the official online application portal of Novartis.
- Ensure your resume highlights QA/QC experience and regulatory knowledge
- Prepare for technical discussions related to GMP and quality systems
Important Dates
- Last Date to Apply: April 30, 2026
Why Apply for This Pharma Job?
This opportunity at Novartis offers professionals a chance to work with a globally reputed pharmaceutical company in the quality operations domain. The role provides exposure to international quality standards, regulatory frameworks, and advanced manufacturing practices.
Candidates will gain hands-on experience in compliance management, audit support, and quality systems, making it an excellent opportunity for long-term career growth in pharmaceutical quality assurance and regulatory affairs.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We do not provide recruitment services or charge any fees. Candidates are advised to verify details from the official company website before applying.
Final Call-to-Action
If you have experience in pharmaceutical quality operations and want to work with a global industry leader, apply now and advance your career in quality assurance with Novartis.
