13 Sep
|
Artevet Therapeutics
|
India
13 Sep
Artevet Therapeutics
India
Managing regulatory affairs of the organization & its subsidiaries / associates.
Liaising with regulatory bodies like State and Central FDA, DCI, etc.
Well conversant with Drug law/feed supplement regulation.
Co-ordination with factory, purchase department, marketing department.
Reviewing of technical documents like process validation, stability, etc.
Compilation of dossiers and handling dossier related queries.
Arranging and checking artworks for registration as per guidelines.
Compilation and preparation of tender documents.
Preparation of Drug Material File
Job Types: Full time, Permanent
Pay: ₹400,000.00 - ₹550,000.00 per year
Perks:
Provident Fund
Application Question(s):
Which is the highest degree you achieved
Are you ready to work in a veterinary pharmaceutical manufacturing company
Experience:
Regulatory: 1 year (preferred)
Work Location: In person
📌 Regulatory Affairs Executive Vile Parle (India)
🏢 Artevet Therapeutics
📍 India