Torrent Pharmaceuticals – Hiring B.Pharm, M.Pharm, M.Sc – Submit Resume to HR Email

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Torrent Pharmaceuticals – Hiring B.Pharm, M.Pharm, M.Sc – Submit Resume to HR Email

Torrent Pharmaceuticals The flagship company of the Torrent Group, Torrent Pharmaceuticals Limited is a major player in the Indian pharmaceuticals sector with the vision of becoming a global entity. Torrent Pharma enjoys dominance in the niche therapeutic areas like, cardiovascular and central nervous system, gastro-intestinal, pain management and oral anti-diabetic segments. Torrent Pharma owes its success in the domestic market to its thrust on frontline research, strategic marketing and world-class manufacturing. It is among the largest spenders on R&D and has set up one of the most advanced research centers in the country at an investment of Rs. 200 crores so far. It has discovered and patented the AGE (Advanced Glycosylation End Product) Breaker Compound which has potential to treat heart diseases and diabetes related vascular complications. Its manufacturing facilities have received quality certifications from various international regulatory authorities. It is this success that Torrent Pharma attempts to replicate in the international market now. It has already established fully-owned subsidiaries in Australia , Brazil , Germany , Japan , Mexico , Philippines Russia and USA and has over 1000 product registrations in more than 50 countries worldwide


Torrent Pharmaceuticals Recruiting For Following:

  • Qualification: B.Pharm, M.Pharm, M.Sc
  • Experience : 01-06+years
  • Role:  Executive
  • DEPARTMENT: Regulatory Affairs
  • Job Location: Gandhinagar, Ahmedabad

Interested candidates may share their updated CVs on with subject captioned “Application for Quality-RA”

Job Description

  • Preparation of dossiers for US , Europe and ROW
  • Coordination with cross functional teams and review of technical documents
  • Preparation of deficiency responses and query response
  • Dossier preparation and submission in CTD/ eCTD format
  • Experience of review of Modules 1, 2 & 3 and other administrative documents
  • DCP/ MRP/National filing for various EU countries
  • ANDA submission and experience in 505 (b) (2) drug device
  • Formulation regulatory for Solid orals/ Topicals/ Ophthalmics/ Solutions
  • Experience in management of life cycle and post approval variations which includes CCf evaluations, variation preparation and filing

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