Levim Lifetech is inviting applications from fresh graduates for the position of Regulatory Affairs Trainee at its Chennai office. This is an excellent opportunity for candidates looking to build a career in pharmaceutical regulatory affairs, including exposure to dossier preparation, compliance, and global submission processes.
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This trainee role offers hands-on experience in CMC (Chemistry, Manufacturing & Controls) and clinical regulatory documentation, making it ideal for candidates aiming for long-term growth in the pharma regulatory domain.
📍 Job Details
- Position: Regulatory Affairs Trainee
- Location: Taramani, Chennai, Tamil Nadu
- Duration: Up to 1 year (may convert to on-roll based on performance)
- Stipend: Up to ₹15,000 per month
- Job Type: Full-time Internship / Trainee
🧪 Key Responsibilities
- Support preparation and compilation of regulatory dossiers (CMC & Clinical)
- Assist in reviewing manufacturing, quality, and clinical data
- Track and follow up on regulatory submissions and approvals
- Handle regulatory queries, documentation, and compliance activities
- Monitor regulatory updates and guidelines (FDA, EMA, CDSCO)
- Coordinate with cross-functional teams and regulatory authorities
🎓 Qualifications
- Education: B.Pharm / M.Pharm / M.Sc (Life Sciences, Chemistry, Biotechnology)
- Experience: Freshers or candidates with minimal experience
- Basic understanding of Regulatory Affairs, CTD/eCTD, and pharma guidelines
- Good communication and documentation skills
💼 Benefits
- Exposure to global regulatory submission processes
- Hands-on experience in CMC & clinical documentation
- Opportunity for full-time employment based on performance
- Learning environment with industry experts
- Strong foundation for careers in Regulatory Affairs (RA), QA, Clinical Research
📩 How to Apply
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