Apply for Intelur Pharma Regulatory Affairs jobs 2026. Check eligibility, experience, global submissions, and application process for pharma professionals now.
Introduction
If you are an experienced regulatory professional aiming to work on global pharmaceutical submissions, this opportunity is highly relevant. The Regulatory Affairs Jobs at Intelur Pharma Science Pvt Ltd are designed for candidates with 3–5 years of experience in international markets. This role offers exposure to global regulatory frameworks such as US FDA, EU EMA, and CDSCO, making it ideal for career growth in regulatory affairs.
Job Overview
| Details | Information |
|---|---|
| Job Title | Regulatory Affairs – International Markets |
| Company Name | Intelur Pharma Science Pvt Ltd |
| Location | Bengaluru |
| Employment Type | Full-Time |
| Department | Regulatory Affairs |
| Experience Required | 3–5 Years |
| Education | B.Pharm / M.Pharm / Life Sciences |
| Salary | As per company standards |
Company Overview
Intelur Pharma Science Pvt Ltd is a growing pharmaceutical organization focused on regulatory services and global market compliance. The company specializes in supporting pharmaceutical businesses with international submissions, dossier preparation, and regulatory strategy. It provides professionals with opportunities to work on global projects and gain exposure to international regulatory standards.
Job Location & Employment Type
- Location: Bengaluru, India
- Employment Type: Full-Time
This role offers a professional work environment with exposure to global pharmaceutical regulatory operations.
Open Positions / Department Details
- Regulatory Affairs – International Markets
The role focuses on handling regulatory submissions and compliance across multiple global regions.
Key Roles & Responsibilities
- Manage end-to-end dossier planning and submission for international markets
- Prepare and review CTD and eCTD dossiers
- Ensure compliance with US FDA, EU EMA, CDSCO, and Rest of World (RoW) regulations
- Interpret and apply ICH guidelines in regulatory documentation
- Coordinate with cross-functional teams for regulatory strategy execution
- Track submission timelines and maintain regulatory records
- Support global regulatory compliance and documentation processes
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Pharmacy or Life Sciences
Experience
- 3 to 5 years of experience in Regulatory Affairs (International Markets)
Skills Required
- Strong knowledge of:
- US FDA, EU EMA, and CDSCO regulations
- ICH guidelines
- CTD/eCTD submissions
- Experience in global dossier preparation and submission strategies
- Good communication and documentation skills
- Ability to coordinate with multiple teams and manage timelines
Salary & Benefits
- Salary: As per company standards
Additional benefits include:
- Exposure to international regulatory markets
- Opportunity to work on global pharmaceutical submissions
- Career growth in Regulatory Affairs domain
- Collaborative and professional work environment
Selection Process
The selection process may include:
- Resume screening
- Technical interview
- HR discussion
Candidates with strong regulatory experience and international exposure will be preferred.
How to Apply
Interested candidates can apply by sending their updated CV along with a brief cover note to:
Make sure your resume highlights your experience in global regulatory submissions and dossier preparation.
Important Dates
Candidates are advised to apply early as hiring may close once suitable candidates are selected.
Why Apply for This Job?
The Regulatory Affairs Jobs at Intelur Pharma Science Pvt Ltd provide a strong platform for professionals aiming to build expertise in international regulatory markets. This role offers hands-on experience in global submissions, regulatory compliance, and dossier management. It is ideal for candidates seeking career advancement in regulatory affairs with exposure to multiple international guidelines.
FAQs
1. Who can apply for this job?
Candidates with B.Pharm, M.Pharm, or Life Sciences degrees and 3–5 years of regulatory experience can apply.
2. What is the salary offered?
Salary will be provided as per company standards and experience.
3. Is international regulatory experience required?
Yes, experience in US FDA, EU EMA, and CDSCO regulations is required.
4. How can I apply for this role?
You can apply by sending your CV to contact@intelurpharma.com.
5. What skills are needed for this job?
Candidates should have knowledge of CTD/eCTD submissions, ICH guidelines, and regulatory documentation.
Conclusion
The Regulatory Affairs Jobs at Intelur Pharma Science Pvt Ltd offer an excellent opportunity for professionals to work on global regulatory submissions and build a strong career in international pharmaceutical compliance. With the right exposure and growth opportunities, this role can help you advance in the regulatory domain.
Disclaimer
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