Job DescriptionCandidate's key responsibility-should Independently be able to perform the development of analytical methods for injectable formulations like suspension, emulsion, peptides, and other simple & complex injectables.Should be able to work on handling chromatographic techniques- HPLC, TLC, SEC-HPLC, IC, GC and other physico-chemical techniques like UV-visible spectrophotometer, coulometer, FTIR, Raman, ATR, etc.Should be able to work on various dissolution techniques applicable for injectable formulations like USP type IV, Bottle rotating apparatus, Type II, selection and use of MWCO membranes, etc.Handling of UPLC, Plate- Assy techniques is desirable.Should be able to perform routine analytical activities independently.Should be conversant with cGLP and cGDP required for performing, documenting and review of routine development activities.Should be capable of transferring the analytical methods at QC Labs, CROs, etc.Should be able to perform validation & verification of analytical & compendial methods, cleaning validation, etc as and when requiredShould have understandings on Analytical Quality by design (QbD).Desirable to have multitasking capability along with ability to think out of the box.Required good interpersonal skills, effective verbal and written communication skills.Work ExperienceM.Sc. and M. Pharm candidates 6 years to 15 years.Ph.D. candidates minimum 3 years.EducationMasters in PharmacyPost Graduation in Science or ChemistryCompetencies
