Company: Stabicon Life Sciences Pvt. Ltd
Department: QC / AR&D
Job Title: Executive
Experience: 2 – 5 years
Walk In date: 10 November-12th November
-Having knowledge in current GLP requirements. -Having adequate knowledge in handling of analytical instruments like HPLC, UPLC, GC and Dissolution testers.
-Having technical exposure on testing of various dosage forms for Assay, Related substances/compounds, Dissolution, Content Uniformity & etc as per Good Documentation practices
-Experience in method validations, method verification and method transfer for analytical methods of drug products for Assay, Related substances/compounds, Dissolution, Content Uniformity and residual solvents by using HPLC, GC and UV-Visible Spectrophotometer as per current ICH guidelines and Pharmacopoeia.
-Experience in calibration / Qualification of analytical instruments like HPLC, UPLC, GC, Dissolution tester, UV-Visible Spectrophotometer, etc.
-Having adequate knowledge in Preparation and review of analytical method validation/ method verification protocols, Method transfer/Routine/Stability documents for drug products for Assay, Related compounds, Dissolution, Content Uniformity & residual solvents.
-Having adequate knowledge in review of analytical raw data & trends of stability samples.
-Ability to work in a multi-task environment. -Ability to produce high quality outputs.
Stabicon Life Sdences Pvt. Ltd.
Plot No. 28,
Bommasandra Industrial Area,
4th Phase, Jigani hobli, Anekal Taluk,
Bangalore 560 100
Interested candidate can send confirmation either by mail to email@example.com or call at 91 80 27839259/9260 between 9.00 AM to 5.00 PM.