Emcure Pharmaceuticals for experienced professionals in Ahmedabad. If you have hands-on expertise in CTD/ECTD dossier preparation and global regulatory submissions, this role can elevate your pharma career.
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This Regulatory Affairs Officer job in Ahmedabad is ideal for candidates with 3–8 years of experience handling international markets such as Africa, LATAM, CIS, MENA, and Asia.
Job Overview
- Position: Officer – Regulatory Affairs (Emerging Markets)
- Location: Ahmedabad, Gujarat
- Qualification: B.Pharm / M.Pharm
- Experience: 3–8 Years
- Company: Emcure Pharmaceuticals
Key Responsibilities
- Prepare, review, and submit CTD, eCTD, and country-specific dossiers
- Handle registration and re-registration submissions for emerging markets
- Manage regulatory queries, variations, and lifecycle activities
- Perform gap analysis and regulatory strategy planning for new product filings
- Review technical documents, labeling, and artwork compliance
- Coordinate with cross-functional teams for documentation and submission timelines
- Ensure compliance with global regulatory guidelines across regions like Africa, LATAM, CIS, and MENA
Required Qualifications & Skills
- Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm)
- 3–8 years of experience in Regulatory Affairs (Emerging Markets)
- Strong knowledge of CTD/eCTD formats and dossier compilation
- Experience in handling international regulatory submissions
- Good understanding of product lifecycle management
- Excellent communication and coordination skills
Why Join Emcure Pharmaceuticals?
- Opportunity to work in global regulatory markets
- Exposure to international submissions and compliance
- Career growth in emerging markets regulatory affairs
- Work with a reputed Indian pharmaceutical leader
- Collaborative and growth-oriented work environment
Salary (Estimated)
- ₹6 LPA – ₹12 LPA (based on experience and expertise)
How to Apply
Interested candidates can share their updated CV along with current and expected CTC:
📧 Email: bhavik.parekh@emcure.com
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