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

Views:2398

Applicants:22

Posted on 16 Mar, 2024

Job Description | Role and Responsibilities

1. Prepare and compile dossiers for allotted countries (ROW) in CTD format
2. Arrange samples
3. Apply and review legal documents for Product
4. Coordinate for required information
5. Timely response on query and compile required materials

Candidate Profile | Who Can Apply

1. Good Communication
2. Time Management
3. IT Competency
4. Relevant industry knowledge

  • Candidate's can apply from Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
  • Candidate’s can apply from Functional Area Regulatory Affairs / Corporate Affairs
  • Candidate's current / Last Designation Regulatory Affairs Officer
  • Candidates can apply from Location Mumbai (All Areas), Navi Mumbai / Panvel, Thane
Overview
  • Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
  • Functional Area - Regulatory Affairs / Corporate Affairs
  • Job Role - Officer / Executive - Regulatory Affairs
  • Job level - Executive Level
  • Role Reports to - Regulatory Affairs Compliance
  • Employment type - Full Time
  • Work Mode - In Office
  • Other Employee Benefits - NA

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