How you’ll spend your day
To participate in method development and routine analytical support to CRD for raw materials, intermediates, in process samples and drug substance.
Stability studies and Forced Degradation studies for drug substance as per ICH guidelines.
Calibration and Maintenance of sophisticated Instruments, such as HPLC, GC, IR, Karl Fischer and Melting point analyzer
Familiar with LCMS/MS, HPLC, GC, GCHS, FTIR, XRD, PSD, DSC and TGA Techniques.
Documentation as per GMP requirements.
Adhering to safety norms and safe culture in lab.
To ensure online data compilation and recording to have full compliance.
To contribute in maintaining analytical laboratory as per the GLP and safety requirements.
To contribute in providing necessary support to QC during validation batches as well as in routine (Need based in justifiable fashion).
To support in full-filling the regulatory/customer related tasks related to commercial/pipeline products (as per real need and assigned task).
To participate in departmental trainings/discussion programs.
Any other assignments allocated by manager as per time need.
Expertise in Structure elucidation and Identification and characterization of APIs, known and unknown impurities and intermediates by various spectroscopy techniques
Good knowledge of wet chemistry.
Conducting routine analysis of CRD samples as per set procedures.
Your experience and qualifications
MSc – Chemistry
Exp: 6 to 9 Yrs.
