Beta Release
4 - 8 Years
Not Disclosed
Full Time
Mumbai (All Areas) | Mumbai - Western Suburbs | Thane

Views:609

Applicants:14

Posted on 30 Mar, 2024

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