Cadila is looking for Experienced Professionals – Regulatory Affairs.
- Analytical method validation exposure along with RA experience (USBU).
- Topical ANDA submission exposure, Life cycle management/Post approval submission(USBU).
- Thorough knowledge of drug development and approval process.
- Prior regulatory experience with EU/Australia/New Zealand/WHO filings is a must.
- Experience in preparing requests and briefing documents for scientific advice/pre-submission meetings is preferable.
- Excellent verbal and written communication skills.
Qualification : M. Pharm /M.SC ( Regulatory Affairs)
Experience: 2 – 12 Years experience with RA
Positions: Executive, Sr. Executive, Assistant Manager, Dy. Manager, Manager
Job Location: Cadila Pharmaceuticals Limited, Dholka, Ahmedabad(Gujarat)
Candidate can share updated resume at email@example.com