Regulatory Affairs Intern at Glenmark Pharmaceuticals
Glenmark Pharmaceuticals is hiring a Regulatory Affairs Intern in Pune for a 6-month, fully mentored internship. This is real, reviewed work on live projects — not a training sandbox or a certificate mill. About the internship You will join the regulatory affairs team and work alongside people who do this professionally every day. From week one you own a scoped piece of work, take it through review, and see it ship. Day-to-day responsibilities • Compile and format regulatory submission documents. • Track submission timelines and agency queries. • Review labelling and product information for compliance. • Maintain regulatory records and version control. • Document your work clearly so the next person can pick it up. • Take part in stand-ups, planning and review sessions with the team. Tools and technologies you will use Regulatory Affairs, Dossier Preparation, CTD Format, Regulatory Guidelines, Documentation, Compliance, Labelling Review, Submissions, Medical Terminology, Attention to Detail — plus the internal tooling Glenmark Pharmaceuticals uses day to day. What you will learn How products get and keep approval — dossiers, submissions, agency queries and lifecycle maintenance. Team structure You report to a senior team member who acts as your mentor, inside a pod of 6-10 people. Weekly 1:1s track progress and a mid-internship review tells you exactly where you stand. What we expect from you Curiosity, ownership and clear communication. You are not expected to know every tool listed — you are expected to have solid fundamentals, ask good questions, and document what you do. Details: ₹10,000/month stipend · 6 months · Work From Home (Remote) · 1 opening · Pune. If you want to start a career in regulatory affairs in Pune, apply now. Responsibilities: Compile and format regulatory submission documents.; Track submission timelines and agency queries.; Review labelling and product information for compliance.; Maintain regulatory records and version control.; Document your work so the next person can pick it up. Requirements: Education: pursuing or completed B.Pharm/M.Pharm/B.Sc/M.Sc in Life Sciences, Pharmacy or a related discipline; Graduation year: 2025, 2026 or 2027 batch; Minimum 60% / 6.0 CGPA (relaxable for candidates with strong practical projects); Technical skills: working knowledge of Regulatory Affairs, Dossier Preparation, CTD Format, Regulatory Guidelines; Soft skills: clear written communication, ownership, willingness to document work; Experience: none required — freshers welcome; prior projects or certifications are a plus.