Novartis Recruitment 2026 | Regulatory Affairs Associate | Freshers & Experienced Apply Online
Are you looking for a career in Regulatory Affairs with one of the world’s leading pharmaceutical companies? Novartis has announced a new recruitment drive for the position of Regulatory Affairs Associate at its Hyderabad Office. This is an excellent opportunity for candidates interested in regulatory submissions, compliance, life sciences, and pharmaceutical registration activities.
If you have strong communication skills, knowledge of regulatory compliance, and an interest in global pharmaceutical regulations, don’t miss this opportunity to build your career with Novartis.
Novartis Regulatory Affairs Associate Recruitment 2026 – Overview
| Particular | Details |
|---|---|
| Company Name | Novartis |
| Job Role | Regulatory Affairs Associate |
| Job Location | Hyderabad |
| Employment Type | Full Time |
| Job Category | Regulatory Affairs |
| Experience | Freshers & Experienced (As per company requirements) |
| Qualification | Life Sciences/Pharmacy or Related Discipline |
| Application Mode | Online |
| Job ID | REQ-10083967 |
| Last Date to Apply | 24 July 2026 |
| Official Website | https://www.novartis.com |
About Novartis
Novartis is a global healthcare company headquartered in Switzerland, dedicated to reimagining medicine to improve and extend people’s lives. The company develops innovative medicines across multiple therapeutic areas and operates in more than 140 countries. Novartis offers excellent career opportunities, continuous learning, and an inclusive work environment for professionals in pharmaceutical research, regulatory affairs, clinical development, and manufacturing.
Job Summary
The Regulatory Affairs Associate will provide operational and regulatory support for product registration, submission of regulatory dossiers, maintenance of regulatory databases, regulatory documentation, artwork coordination, and lifecycle management activities.
The selected candidate will work closely with regional and global regulatory teams to ensure timely submissions and compliance with regulatory requirements.
Key Responsibilities
Selected candidates will be responsible for:
- Prepare and coordinate regulatory submissions for assigned products.
- Support CTA and NDA submissions within defined timelines.
- Ensure timely submission and approval of license renewals.
- Maintain CMC documentation according to regulatory requirements.
- Support PSUR, RMP, and other regulatory maintenance activities.
- Update and maintain regulatory master files.
- Coordinate meetings with regulatory authorities for project discussions.
- Respond to Health Authority queries promptly.
- Track registration samples, certificates, and submission documents.
- Maintain regulatory databases and documentation.
- Ensure compliance with company SOPs and regulatory guidelines.
- Report adverse events, technical complaints, and special safety cases within required timelines.
- Support distribution of marketing samples wherever applicable.
Required Skills
Candidates should possess the following skills:
- Regulatory Compliance
- Clinical Trials Knowledge
- Regulatory Documentation
- Project Planning
- Database Management
- Attention to Detail
- Collaboration Skills
- Communication Skills
- Operations Management
- Project Coordination
- Documentation Management
- Cross-functional Teamwork
Educational Qualification
Candidates with qualifications in the following disciplines are encouraged to apply:
- B.Pharm
- M.Pharm
- Pharm.D
- MSc Life Sciences
- Biotechnology
- Biochemistry
- Microbiology
- Life Sciences
- Other relevant healthcare disciplines
Candidates having knowledge of pharmaceutical regulatory processes will have an added advantage.
Preferred Experience
Novartis is looking for candidates having experience in:
- Regulatory Affairs
- Pharmaceutical Documentation
- Clinical Trials
- Regulatory Submissions
- Product Registration
- Project Management
- Regulatory Compliance
Fresh graduates with relevant academic knowledge and strong learning ability may also be considered depending on business requirements.
Key Performance Indicators (KPIs)
The successful candidate will be expected to:
- Complete assigned regulatory tasks on time.
- Maintain high-quality regulatory documentation.
- Ensure compliance with regulatory requirements.
- Keep regulatory databases updated.
- Support timely product registrations.
- Maintain excellent communication with stakeholders.
Language Requirement
- English (Mandatory)
Strong written and verbal communication skills are essential.
Why Join Novartis?
Working at Novartis offers several career advantages, including:
- Global pharmaceutical work environment
- Career growth opportunities
- Exposure to international regulatory processes
- Professional training and development
- Hybrid and collaborative work culture (role dependent)
- Competitive salary package
- Employee wellness programs
- Learning and certification opportunities
- Inclusive workplace
- Opportunity to work on innovative medicines
Expected Salary
Although Novartis has not officially disclosed the salary for this position, based on similar Regulatory Affairs Associate roles in Hyderabad, candidates may expect:
| Experience | Expected Annual Salary |
|---|---|
| Freshers | ₹4.5 – ₹7 LPA |
| Experienced | ₹7 – ₹12 LPA |
Salary may vary depending on qualifications, experience, and company policies.
Selection Process
The selection process may include:
- Online Application Screening
- HR Interview
- Technical Interview
- Managerial Interview
- Final HR Discussion
- Offer Release
Documents Required
Applicants should keep the following documents ready:
- Updated Resume
- Educational Certificates
- Government ID Proof
- Passport-size Photograph
- Experience Certificates (if applicable)
- Skill Certifications (if any)
How to Apply for Novartis Regulatory Affairs Associate Recruitment 2026?
Follow these simple steps:
- Visit the official Novartis Careers website.
- Search for Job ID: REQ-10083967.
- Open the Regulatory Affairs Associate job posting.
- Review the eligibility criteria and job description.
- Click on Apply Now.
- Create or log in to your Novartis career account.
- Fill in the online application form.
- Upload your updated resume and required documents.
- Verify all details carefully.
- Submit your application before 24 July 2026.
APPLY ONLINE
Important Details
| Particular | Information |
|---|---|
| Company | Novartis |
| Position | Regulatory Affairs Associate |
| Location | Hyderabad |
| Employment Type | Full Time |
| Job ID | REQ-10083967 |
| Last Date | 24 July 2026 |
Frequently Asked Questions (FAQs)
1. What is the job role offered by Novartis?
Novartis is hiring for the Regulatory Affairs Associate position.
2. Where is the job location?
The position is based in Hyderabad.
3. What is the last date to apply?
The application closes on 24 July 2026.
4. What qualifications are preferred?
Candidates from B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, Microbiology, and related fields are generally suitable for this role.
5. Is prior experience mandatory?
The job description emphasizes regulatory and operational skills. Relevant experience is preferred, though candidates meeting the required qualifications should review the official posting for eligibility.
6. Which skills are required?
Key skills include Regulatory Compliance, Clinical Trials, Collaboration, Database Management, Project Planning, and Attention to Detail.
7. Is this a full-time position?
Yes, this is a full-time role.
8. What is the Job Requisition ID?
The Job Requisition ID is REQ-10083967.
Conclusion
The Novartis Regulatory Affairs Associate Recruitment 2026 offers an exciting opportunity for pharmacy and life sciences professionals to build a rewarding career in global regulatory affairs. If you have a passion for regulatory compliance, documentation, clinical development, and pharmaceutical product registration, this role provides excellent exposure to international regulatory standards while working with one of the world’s leading healthcare companies.
Candidates are encouraged to apply online before the application deadline and prepare well for the recruitment process.
APPLY ONLINE
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