Beta Release
4 - 9 Years
Not Disclosed
Full Time
Mumbai (All Areas) | Mumbai - Central & Harbour Suburbs | Mumbai - Western Suburbs | Navi Mumbai / Panvel

Views:595

Applicants:12

Posted on 17 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).

- Maintain international regulation, guidance and standards applicable to company products.

Candidate Profile | Who Can Apply

- 5-6 years of experience in Pharma formulation regulatory affairs for French west Africa, Anglo Africa, South East Asia.

- Excellent communication skills.

  • Candidate's can apply from Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
  • Candidate’s can apply from Functional Area Legal / Law
  • Candidate's current / Last Designation Executive - Regulatory Affairs
Overview
  • Industry - PHARMACEUTICAL / MEDICAL DEVICES / CRO
  • Functional Area - Legal / Law
  • Job Role - Regulatory Affairs - Officer / Executive
  • Job level - Executive Level
  • Employment type - Full Time
  • Work Mode - In Office
  • Other Employee Benefits - NA

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Education
  • Any Graduate - Any Specialization
  • Any Post Graduate - Any Specialization
  • Any Doctorate - Any Specialization
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