Beta Release
1 - 5 Years
Not Disclosed
Full Time
Kalyan - Dombivali | Mumbai (All Areas) | Navi Mumbai / Panvel | Thane

Views:211

Applicants:6

Posted on 8 Feb, 2024

Job Description | Role and Responsibilities

- 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

Candidate Profile | Who Can Apply
  • Good Communication.
  • Time Management.
  • IT Competency.
  • Relevant industry knowledge.
Overview
  • Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
  • Functional Area - Regulatory Affairs / Corporate Affairs
  • Job Role - Manager - Regulatory Affairs
  • Employment type - Full Time
  • Work Mode - In Office

Job Related Keywords
Education
  • B.Pharma - Any Specialization
  • MSc - Any Specialization, MPharma - Any Specialization
  • Any Doctorate - Any Specialization
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