Regulatory Affairs Executive
Dossier compilation in CTD and ACTD, technical review and query responses for global markets.
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Build your career with us.
Work on real submissions for regulated and emerging markets, learn from a founder-led team and grow with a company that is growing fast.
Why join VRS
Work that reaches patients worldwide.
Global exposure
Prepare dossiers for the US, EU, ASEAN, GCC, CIS and African markets.
Learn every module
Hands-on work across CTD modules, publishing, PV and GMP compliance.
Room to grow
Take on more responsibility as you build expertise in your area.
Founder-led team
Work closely with our founders and learn from experienced professionals.
Roles we hire for
Find where you fit in.
These are the roles we hire for regularly. Don't see yours? Send a general application and we'll keep your profile on file.
eCTD Publishing Specialist
Build, validate and publish eCTD and NeeS submissions and manage lifecycle sequences.
Pharmacovigilance Associate
Prepare PSURs, RMPs and PSMFs and support PV surveillance activities.
Analytical Documentation Executive
Prepare AMV, CDP, process validation and stability documentation with raw data.
Labelling & Artwork Associate
Prepare SmPC, PIL and label text and review packaging artwork for each market.
Trainee / Intern
For B.Pharm, M.Pharm and M.Sc graduates who want to start a career in regulatory affairs.
Hiring process
What happens after you apply.
- Application reviewOur team reviews your profile and resume.
- Introductory callA short call about your experience and interests.
- Technical interviewA discussion on regulatory or documentation work.
- OfferWe share the offer and your joining plan.
You can also email your resume to ronak_shah@vrshealthcare.in.
Apply now
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