Posted:4 days ago|
Platform:
On-site
Full Time
8-10 years of exps. in Pharmaceuticals
Preparation, Review and submission of Technical documents/Dossiers (CTD/eCTD) related to Regulatory affairs for third country Export of Pharmaceuticals Formulations.
* Preparation and Review of SOPs.* Compilation of Validation Protocols/Reports.* Preparation,Review,Submission of Technical and other Documents/Dossiers with Drug Controller General of India/CDSCO/State FDAs for-* Registration for import of pharmaceuticals Formulations and bulk drugs.* Import Licenses* Export Licenses* Manufacturing & Marketing licenses* WHO-GMP Certification* No Objection Certificates etc.* Liasioning with DCGI/CDSCO/state FDA offices/Directorate General of Foreign Trade /FICCI/PHD Chamber of Commerce etc.
Job Type: Full-time
Pay: ₹360,000.00 - ₹600,000.00 per year
Benefits:
Schedule:
Work Location: In person
Tyykem Private Ltd.
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3.6 - 6.0 Lacs P.A.
3.6 - 6.0 Lacs P.A.
