Posted:2 months ago|
Platform:
Work from Office
Full Time
1. Develop analytical methods on GC-HS, and GC-MS for fine chemicals and their impurities
2. Document analysis procedures and the test results mainly for wet labs and spectrophotometric testing
2. Document product stability studies are completed satisfactorily and supported by correct product sample analysis
3. Establish a tracking mechanism for customer & field complaints and suggest corrective actions
1. You have experience of around 3 or more years in pharmaceutical industry
2. Educational Qualification - M.Sc./M.Pharm degree with strong interest in quality control & its documentation
3. You work accurately, technically minded and able to work independently after training in the matter entrusted to you. Experience in an API industry is an asset
Care Group
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