Clinical Research department in Teva supports Protocols, Bioanalysis, CDISC, Final Reports, eTMF, Data Management. It also provides bioanalysis to support Teva studies in various other countries. Teva India Clinical Research team does monitoring to support Teva Israel/ Europe & US for studies and we also do Medical Writing, Coding and Publication along with Patient based studies.
Multiple Openings
Analytical Research
• Finished product testing and analytical method development and analytical method validation by HPLC, GC, 1C, UV, etc.
• Development of analytical methods, analytical method validation and transfers, analysis of finished product R&D samples.
Qualification & Experience : M.Sc./M.Pharm./Ph.D. with minimum 4-20 years of experience.
Scientific Publisher/Principal Scientific Publisher ARD/FRD
• Preparation of documents and facilitation of documentation management in R&D.
• Preparation and review of technical documents for Formulation & Analytical teams.
• Preparation of high impact presentations including graphs, charts & statistical analysis of data.
• Continuously improve documentation systems to increase efficiency & compliance.
• Excellent in oral and written communication.
Qualification & Experience : Bachelor’s / Master’s degree in a scientific discipline with minimum 5-15 years of experience. Candidate should be having experience in Analytical development/Formulation development for this role.
Job Location : Ambernath
Interested candidates may email their CV to Prince.dubey@teva.co.in
Walk in Interview
Date : 25th March 2023
Venue : Plot No K-7, Additional M.I.D.C, Ambernath, Maharashtra 421506
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