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Posted on 18 Nov, 2024
Overview
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Legal / Law
- Job Role - Regulatory Affairs - Officer / Executive
- Employment type - Full Time
- Work Mode - In Office
Job Description | Role and Responsibilities
- To prepare and compile dossiers for allotted countries (ROW) in CTD format (Countries worked on Anglo African countries , French West African countries ).
- End to End registration of new molecule in the market, license renewals and others.
Candidate Profile | Who Can Apply
- 5-6 years of experience in Pharma Formulation in Regulatory Affairs.
- B.Pharm / M.Pharm
- Good Communication skills, Time Management and IT skills
Education
- BSc - Any Specialization, B.Pharma - Any Specialization
- MSc - Any Specialization, MPharma - Any Specialization
- Any Doctorate - Any Specialization
Job Related Keywords
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