Intelur Pharma Science Pvt Ltd. for professionals experienced in international markets regulatory affairs. If you have expertise in US FDA, EU EMA, CDSCO, and dossier submissions, this role could be your next big career move.
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This Regulatory Affairs role in Bengaluru is ideal for candidates with 3–5 years of experience who want to work on global submissions and compliance strategies in the pharmaceutical sector.
🏢 Job Overview
- Company: Intelur Pharma Science Pvt Ltd.
- Role: Regulatory Affairs – International Markets
- Location: Bengaluru, India
- Experience: 3 to 5 Years
- Job Type: Full-Time
🛠️ Key Responsibilities
- Manage end-to-end dossier planning and submission for global markets
- Prepare and review CTD/eCTD dossiers for regulatory submissions
- Ensure compliance with US FDA, EU EMA, CDSCO, and RoW regulations
- Interpret and implement ICH guidelines in regulatory documentation
- Coordinate with cross-functional teams for global regulatory strategy
- Track submission timelines and maintain regulatory records
🎓 Qualifications & Skills Required
- Bachelor’s or Master’s degree in Pharmacy / Life Sciences
- 3–5 years of experience in Regulatory Affairs (International Markets)
- Strong knowledge of:
- US FDA, EU EMA, CDSCO guidelines
- ICH Guidelines
- CTD/eCTD submissions
- Experience in global dossier preparation and submission strategies
- Good communication and documentation skills
🎁 Benefits of Working with Intelur Pharma
- Exposure to international regulatory markets
- Opportunity to work on global pharmaceutical submissions
- Career growth in Regulatory Affairs domain
- Collaborative and professional work environment
📩 How to Apply
Interested candidates can apply by sending their updated CV along with a brief cover note to:
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