Posted:19 hours ago|
Platform:
On-site
Full Time
Job Description – Regulatory Affairs- Executive
No.of vacancy: 01
Role Summary:
The Regulatory Affairs professional will be responsible for preparing, reviewing, submitting, and maintaining regulatory documents to ensure compliance with national and international regulatory authorities. The role ensures smooth product registration, license renewals, and compliance with all statutory requirements.
Key Responsibilities:
1. Dossier Preparation & Submission
2. Product Registration & Approvals
3. Regulatory Compliance
4. Documentation Control
5. Communication with Authorities
6. Artwork & Label Review
7. Cross-Functional Coordination
Required Qualifications:
* B.Pharm / M.Pharm (preferred) with 4-5 years of experience in Regulatory Affairs
.* Strong understanding of regulatory guidelines (CDSCO, WHO, ASEAN, Africa, LATAM etc.).
* Knowledge of dossier formats (CTD/eCTD/ACTD).
* Experience in product registration and regulatory submissions.
Job Types: Full-time, Permanent
Pay: ₹30,000.00 - ₹35,000.00 per month
Benefits:
Work Location: In person
Medizest Pharmaceutical Pvt. Ltd.
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