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Posted on 20 Dec, 2024
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - C Level / Top Management / Director
- Job Role - Other C Level / Top Management / Director
- Employment type - Full Time
- Work Mode - In Office
Job Description | Role and Responsibilities
- Should have an regulatory experience in Europe market new application submissions
- Preparation, review and submission of new applications through DCP, MRP, NP for EU.
- You will be responsible for preparation and review of m1 documentation in-line to the m2-5 documents.
- Direct Interaction with EU regulatory authorities.
Candidate Profile | Who Can Apply
Education
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
About Employer
Contact Details
Email - chaitalitawade@drreddys.com,
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