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Regulatory Affairs Analyst
Dr. Reddy's Laboratories
Indiana, USA, United States of America
Not Disclosed
1 - 6 Years
Full Time
Views:108
Applicants:7
Posted on 24 Dec, 2024
In Office
Job Description | 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.
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
Qualifications
- Any Graduate - Any Specialization
- Any Post Graduate - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
Attention to Detail
Interpersonal Skills
Regulatory Affairs
Regulatory Submissions
Standard Operating Procedure (SOP)
