Job opening in Cadila

Cadila is looking for Experienced Professionals – Regulatory Affairs.

Skills Required:

  1. Analytical method validation exposure along with RA experience (USBU).
  2. Topical ANDA submission exposure, Life cycle management/Post approval submission(USBU).
  3. Thorough knowledge of drug development and approval process.
  4. Prior regulatory experience with EU/Australia/New Zealand/WHO filings is a must.
  5. Experience in preparing requests and briefing documents for scientific advice/pre-submission meetings is preferable.
  6. 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 apeksha.langhanoja@cplbio.com

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