Incorporated in the year 1994, Syngene International is one of India"s premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities.
Qualification: M. Pharm/ M.Sc from reputed institutes with experience in Analytical R&D for Formulation Development
Technical Skills:
• Expertise in Analytical Method development, Method Validation, Method transfers and stability studies (expertise in Analytical R&D for Formulation development Solid Orals and parenteral formulation) by using HPLC, UPLC, GC with EMPOWER -3 as platform
•Working experience with Analytical method development for Pre-formulations, Excipient Compatibility Studies and Validation of Analytical Procedures
• Thorough understanding on Stability Studies inline with ICH and other compendia
• Excellent knowledge in cGMP, ICH , USP and regulatory requirements and good oral & written communication skills.
• Working experience in 21 CFR part 11 compliance environment, Data Integrity & GLPs
• Working experience for IND,ANDA and other regulatory filings will be an added avanatage
Experience Range: 3 to 5 Years
Walk in interview :
Date- 29th April
Venue: Hotel Minerva Grand,
Sarojini Naidu Road, Secundrabad
Interested Candidates can mail us at Tabassum.ansari@svngeneintl.com
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