Assist in QC stability testing, prepare and maintain stability records and summaries.
Involve in training and transfer of methods to and from QC and contract manufacturers as assigned.
Modify and validate analytical procedures to meet QC’s needs.
Support design and development of experimental protocols, SOP’s, etc., consistent with cGMP/GLP.
|Experience||0 - 4 Years|
|Salary||3 Lac To 5 Lac 50 Thousand P.A.|
|Industry||Health Care / Pharmaceuticals / Medical|
|Qualification||Vocational Course, Diploma, Professional Degree, B.Pharma, Post Graduate Diploma, M.Pharma|
|Key Skills||Pharmacist Pharmacy QC Chemist|
|Contact Person||Garima Roy|
|Address||715/31, Ashoka Enclave, Near Kanishka Tower,sector-31,|