QC / AR&D - Executive
Stabicon Life Sciences Pvt Ltd
2 - 5 yrs
Bengaluru
Walkin Interview
10th
November - 12th November 2 PM
Job Description
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
Verifications 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.
Having good communication skills and planning of
work.
Ability to work in a multi-task environment.
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.
Interested candidate can send confirmation
either by mail to hrd@stabicon.com or call at 91 80 27839259/9260 between 9.00
AM to 5.00 PM.
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