Levim Lifetech Pvt Ltd is hiring motivated and detail-oriented graduates for a 6-month Regulatory Affairs Internship in Taramani, Chennai. This opportunity is ideal for freshers and early-career professionals who want to build expertise in regulatory dossier preparation, labeling compliance, and cross-functional documentation within the pharmaceutical industry.
If you are planning to start a successful career in Regulatory Affairs, this internship provides hands-on experience and industry exposure at one of the promising pharma companies in Chennai.
Key Responsibilities
As a Regulatory Affairs Intern, you will gain practical experience in core RA operations, including:
- Supporting preparation, compilation, and review of regulatory submissions, dossiers, and applications.
- Assisting in data collection, document formatting, and regulatory documentation.
- Coordinating with QA, QC, Production, R&D, and Pharmacovigilance teams for required documents.
- Reviewing product artworks, labels, and packaging to ensure regulatory compliance.
- Performing administrative and regulatory documentation support as required.
Qualifications
Ideal candidates should have:
- Background in Pharmacy, Life Sciences, Chemistry, Biotechnology, or related fields.
- Strong attention to detail, documentation skills, and willingness to learn.
- Good communication and coordination skills.
- Ability to work with cross-functional teams.
Benefits
- Stipend: ₹10,000 – ₹15,000 per month
- Hands-on exposure to Regulatory Affairs processes in the pharma industry
- Opportunity to work with experienced professionals in a structured RA environment
- Practical understanding of dossiers, submissions, labeling, and QA compliance
- Certificate upon successful completion
Job Location
📍 Taramani, Chennai, Tamil Nadu, India
How to Apply
Interested candidates can share their updated resume at:
📧 gopinath@levim.in
