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.
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:
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📧 Email: bhavik.parekh@emcure.com
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