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EXECUTIVE / SR. EXECUTIVE - REGULATORY AFFAIRS

Is
AhmedabadOn-siteMid level3–5 yrs
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Subscribers got this job on 3 October 2026. New jobs reach them at 8 am and 6 pm, 5 days before they open here. Get the next one first

The job in short

Regulatory affairs dossier preparation for pharmaceutical products.

Details

Found
25 d ago · posted 2026-10-03
Location as listed
Ahmedabad, GJ, India
Role
Regulatory Affairs Specialist
Source
The company’s own careers site

Full description

EXECUTIVE / SR. EXECUTIVE - REGULATORY AFFAIRS No of Position : Two Designation : Executive / Sr. Executive - Regulatory Affairs Experience : B.Pharm/M.Pharm with minimum experience of 3 to 5 years Company : Pharmaceutical Company Salary : Depend on candidates experience & Industry Standard 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

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