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Posted on 18 Nov, 2024
- Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
- Functional Area - Regulatory Affairs / Corporate Affairs
- Job Role - Manager - Regulatory Affairs
- Employment type - Full Time
- Work Mode - In Office
- Prepare and compile dossiers for allotted countries (ROW) in CTD format.
- Arrange samples.
- Apply and review legal documents for Product.
- Coordinate for required information.
- Timely response on query and compile required materials.
ComplianceGlenmarkAjantaNat Aristo co Regulatory Affairs Pharmed Formulation Medley Shalina Macleods Cadila IPCA Lupin Dr. Reddys Al Sun kem Zydus Indoco JB Chemicals Pharma SouthUSV Africa Cipla
- Good Communication.
- Time Management.
- IT Competency.
- Relevant industry knowledge.
- B.Pharma - Any Specialization
- MSc - Any Specialization, MPharma - Any Specialization
- Any Doctorate - Any Specialization
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