Looking for an experienced BIS specialist to lead ISI Mark and CRS certification projects for our international clients. You'll manage end-to-end BIS applications, coordinate with labs and BIS officers, and mentor junior team members. This is a senior role with direct client interaction. You'll own 8-12 concurrent projects and be responsible for maintaining our 98% first-time approval rate across your portfolio.
Post : CDSCO Regulatory Associate
Job Description
• Lead ISI Mark and CRS certification projects from application to grant
• Prepare and review all documentation for BIS portal submissions
• Coordinate product testing with BIS-recognized laboratories
• Manage factory inspections — preparing client teams and quality systems
• Liaise with BIS officers and handle queries during the review process
• Track regulatory changes (new QCOs, policy updates) affecting client products
• Mentor 2-3 junior specialists on your team
Candidate Profile
• 5+ years experience in BIS certification (ISI Mark or CRS)
• Strong understanding of QCOs and Indian Standards
• Experience managing multiple concurrent certification projects
• Excellent documentation skills — attention to detail is non-negotiable
• Clear communication — you'll work directly with international clients
• Self-driven — you own your projects end-to-end
Additional Information
Experience : 5+ years
Location : Gurugram, Work from office & WFH ( Flexible )
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Regulatory
End Date : 30th September 2026
CDSCO Regulatory Associate : Apply Online
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