Job Profile :
- Dossier preparation as per the ACTD & CTD (Module I, II, III, IV and V) guideline.
- Technical documents like Raw Material and finished products specification, manufacturing process,
Product development report, stability reports, process validations preparation & review.
- Analytical method validation review as per the ICH guideline.
- Drug Master File review
- Technical query response to the various regulatory authorities.
Dosage – Oral solid, Liquid, Injectable, Ophthalmic, Topical
Market – ROW, Latam, African Countries
Pay: ₹240,000.00 - ₹600,000.00 per year
Work Location: In person
