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

Benefits:
- 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)
🏢 Artevet Therapeutics
📍 Vile Parle