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Executive - AMV

3.00 to 4.00 Years   Hyderabad   03 Feb, 2021
Job LocationHyderabad
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other Software
EmploymentTypeFull-time

Job Description

Roles and Responsibilities

  • To ensure the error free and online documentation.
  • To ensure only calibrated instrument / equipments are used for analysis.
  • To coordinate with supervisor in developing the methods for dissolution, assay by UV/HPLC and RS by HPLC
  • Preparation of validation protocols, validation report
  • Perform validation of test procedures like Dissolution, Assay, Related substances, Residue, water content, identifications and Chiral purity etc.,
  • Receipt and storage of samples / standards.
  • Labeling of standards, chemicals and reagents.
  • Receipt of log books and SOPs and QA
  • To ensure the GLP compliance is laboratory.
  • Supporting for the installation of Instruments / Equipments.
  • To ensure the working standards, reference standards, impurities and columns are maintained as per the GLP.
  • To ensure the archival of completed files.
  • Assist and / or perform analysis of samples for Dissolution, Assay by UV/HPLC and RS by HPLC water content by KF, LOD and Identification tests as per Analytical Test Method / Standard Test Procedure.
  • Analysis and review of Raw Material, Packaging Material, In process, Finished and Stability samples.
  • Coordinate and assist / perform Instrument calibration and preventive maintenance.
  • Environmental monitoring as per SOP.
  • Any other work allotted by supervisor.
Desired Candidate ProfileLooking for Immediate joiners & worked with pharmaceutical companies.Designation : ExecutiveExperience : 3-4 Years Qualification : B Pharmacy / M Pharmacy,

Keyskills :
testshplclodimpuritiespackagingvalidationanalyticalinstrument calibrationsupervisionentertainment writinganalysistest proceduresmonitoringglpassaystorageprotocolscalibrationwatercompliance

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