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ExecutiveJobs Opening in Cadila Pharmaceuticals Ltd at Ankleshwar

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Executive

Cadila Pharmaceuticals Ltd
experience-icon 0 Years
salary-icon Not disclosed
qualification-icon Any Graduate
location-icon Ankleshwar
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Posted: 17 Dec 25
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Job Description

  • To   maintain and adherence of the GLP and safety procedures in laboratory.
  • To perform the        analysis as per work allocation and records the results in work sheet        (Protocols) for raw material / packing materials/intermediates /APIs/        Stability and etc.. as per current specification and method of analysis.
  • To work as        Analyst and maintain the CFR 21 part -11 compliance by following laid        down procedures.
  • To perform all        the HPLC related analysis and perform the online documentation for        In-process, intermediate, finished products & returned goods / raw materials        Hold time / Stability study / working standard analysis as per laid down        specification & test procedures , SOPs, as per work allocation and        report the analysis data in LIMS modules and report to Section – Head /        Or QC head.
  • To ensure that        every specification and method of analysis used of right        product/material code.
  • To follow the        instruction of Shift /Section In charge for analysis /planning.
  • To report QI/NQI/OOS/OOT / Deviation/ discrepancy in        laboratory analysis to QC- In charge and initiate of QI/NQI/OOS/OOT /        Deviation.
  • Responsible for performing calibration of laboratory        instruments as per schedule and laid down SOPs with documentation and        updation of instrument calibration status tag.
  • To record and ensure all the entries, and results are in        line with current specifications and STPs. 
  • To ensure the all column performance and column entry        are maintain in column logbooks.
  • To maintain        instruments log books properly as per analysis.
  • To acquire        training from concerned person to update the cGMP system update        technical knowledge.
  • To maintain reference / working standard/impurity        standard usage records.
  • To maintain instrument history record.
  • Joint analysis with A.R laboratory personnel during        analytical method transfer on HPLC.
  • Preparation of stability protocols and stability        reports. 
  • Toperformanalysis of stability samples as per        stabilityschedule
  • Daily monitoring and recording of temperature and        humidity of refrigerator / working standard chamber and laboratory area.
  • Perform holding time study of intermediates and        preparation of reports.
  • Inform and Investigate OOS results inRM/Intermediates/APIs 
  • Ensure CFR 21 part -11 compliance and follow good        chromatography practices during analysis, integration and reviewing of        on line and off line chromatographic analysis to
  • Maintain proper data integrity.
  • To ensure no spillage of lab. Chemicals /        solvents
  • To prepare mobile phase/solution for analysis as per        requirement to avoid wastage of lab chemicals and reagents/solvents.
  • To coordinate with store department to prior information        of urgent analysis of raw material.

Job Particulars

Role sales marketing executive
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2809576
Job Category Sales and Marketing
Locality Address
State
Country India

About Company

Cadila Pharmaceuticals Ltd
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