Executive Regulatory Affairs (Ahmedabad)

Executive Regulatory Affairs (Ahmedabad)

01 Aug
|
U Square Lifescience
|
Ahmedabad

01 Aug

U Square Lifescience

Ahmedabad

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)
🏢 U Square Lifescience
📍 Ahmedabad

Reply to this offer

Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.

Subscribe to this job alert:

Get the latest job offers by email for: executive regulatory affairs (ahmedabad) / ahmedabad

Subscribe to this job alert:

Get the latest job offers by email for: executive regulatory affairs (ahmedabad) / ahmedabad