02 Aug
|
U Square Lifescience
|
India
02 Aug
U Square Lifescience
India
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
📌 Executive Regulatory Affairs Ahmedabad (India)
🏢 U Square Lifescience
📍 India