Sunrise Remedies Pvt. Ltd., a well-established pharmaceutical company. This role is ideal for candidates with B.Pharm or M.Pharm qualifications and 1–2 years of regulatory affairs experience seeking growth in global product registrations and dossier preparation.
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If you’re aiming to build a career in pharma regulatory affairs jobs in India, this opening in Santej, Ahmedabad offers hands-on exposure to international markets and regulatory compliance.
Job Overview
- Position: Regulatory Affairs Executive
- Company: Sunrise Remedies Pvt. Ltd.
- Location: Santej, Ahmedabad, Gujarat, India
- Qualification: B.Pharm / M.Pharm
- Experience: 1–2 Years
- Salary: Up to ₹2.40 LPA
- Job Type: Full-time
Key Responsibilities
As a Regulatory Affairs Executive, you will:
- Prepare and compile CTD/ACTD dossiers for international markets
- Coordinate regulatory documents such as COA, GMP, Stability data, FSC/CPP
- Manage regulatory submissions, renewals, and variations
- Review and maintain regulatory documentation and compliance records
- Ensure adherence to country-specific regulatory guidelines
- Collaborate with internal teams for smooth product registrations
This role is highly suitable for candidates searching for entry-level regulatory affairs jobs in pharma industry.
Required Qualifications & Skills
- Educational Qualification: B.Pharm or M.Pharm
- Experience: 1–2 years in Regulatory Affairs
- Strong understanding of CTD/ACTD dossier preparation
- Knowledge of international regulatory requirements
- Good documentation and coordination skills
- Attention to detail and compliance mindset
Salary & Benefits
- Competitive salary up to ₹2.40 LPA
- Opportunity to work on global regulatory submissions
- Hands-on experience in pharmaceutical regulatory affairs
- Career growth in international pharma markets
How to Apply
Interested candidates can apply by sharing their updated CV:
📧 Email: info@sunriseremedies.in
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