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Posted:2 days ago| Platform:
On-site
Full Time
Key Responsibilities: Dossier preparation (CTD / ACTD / eCTD) Regulatory submissions & documentation Coordination with QA, QC, R&D, and Production Handling product registrations, renewals & variations Compliance with WHO, USFDA, EU, TGA, etc. Skills Required: In-depth knowledge of regulatory formats & global guidelines Excellent communication & documentation abilities High attention to detail and ability to manage deadlines Apply Now : Contact: 7820082233 Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Schedule: Day shift Morning shift Education: Master's (Required) Experience: Dossier preparation : 3 years (Required) Language: English (Required) Work Location: In person
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0.3 - 0.35 Lacs P.A.
0.3 - 0.35 Lacs P.A.
