Regulatory Affairs Intern
About this internship
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Skills you'll use
What you'll do
- Work on dossier compilation, labelling review and submission support alongside the core team
- Apply Regulatory Submissions, CTD / eCTD Basics, Dossier Compilation, Labelling Review to live, production-facing problems
- Document your work clearly for reviewers and stakeholders
- Participate in reviews and act on the feedback you receive
- Collaborate across engineering, product, design or business as required
- Follow the team's quality, testing and documentation standards
Who can apply
- Pursuing or recently completed B.Pharm/M.Pharm/M.Sc (Life Sciences)/Pharm.D — 2026 freshers & final-year students welcome
- Working knowledge of Regulatory Submissions, CTD / eCTD Basics, Dossier Compilation (or a genuine willingness to learn them)
- Strong fundamentals in your discipline and clear problem-solving ability
- Care with detail and the discipline to document your work
- Clear written and verbal communication in English
- Based in or willing to work from Thane, Maharashtra
Perks & benefits
Interview & selection process
2 rounds — typical selection flow for this role:
- 1Application screening & resume shortlisting by the talent team
- 2Online aptitude / domain assessment
About Molbio Diagnostics
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