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: M.Pharm, M.Sc
- Experience : 01-06+years
- Role: Executive
- DEPARTMENT: QC
- Job Location: Gandhinagar, Ahmedabad
Interested candidates may share their updated CVs on adrijasingh@torrentpharma.com/vilshashah@torrentpharma.com with subject captioned “Application for Quality Control (BE Study)”.
Job Description
- To undertake Quality control checks for documentation during clinical phase of bio study
- To monitor for compliance with study protocol during bio study
- To check protocol, ICF, CRF and other documents for a bio study
- To verify the corrective actions taken against observations during quality audit and to ensure their implementation
- To support in the process of enhancing the quality of clinical data
- To check and verify instrument/system related documentation
- To prepare the SOPs and monitor their periodic updation
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