Position : QC / AR&D – Analyst to Senior Executive.
Qualification : M.Sc/M.Pharm/B.Sc/B.Pharm
Experience : 2 to 7 years in Pharma Industry.
Role & Responsibility:
v Having knowledge in current GLP requirement.
v Having adequate knowledge in all analytical instruments like HPLC, UPLC, GC and Dissolution tester etc.
v Having technical exposure on testing of in-process and finished product batches such as Assay, Related substances/compounds, Dissolution, Content Uniformity & etc as per Good documentation practices.
v Experience in Method validations, Method Verifications and Method Transfer for analytical methods of drug products such as 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.
v Experience in calibration of all analytical instruments like HPLC, UPLC, GC, Dissolution tester, UV-Visible spectrophotometer and etc.
v Having adequate knowledge in Preparation and review of analytical method validation/ method verification protocols, Method transfer/Routine/Stability documents for drug products such as Assay, Related compounds, Dissolution, Content Uniformity & residual solvents.
v Having adequate knowledge for the review of analytical raw data & trend of stability samples.
v Having good communication skills and planning of work.
v Ability to work in a multi-task environment.
v Ability to produce high quality outputs.
Venue Details:
Stabicon Life Sciences Pvt. Ltd.
Plot No. 28,Bommasandra Industrial Area, 4th Phase, Jigani hobli, Anekal Taluk, Bangalore - 560 100.
If Interested candidate can send confirmation on same date by mail; hrd@stabicon.com or call 91 80 27839259/9260
