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Assistant ManagerJobs Opening in Cadila Pharmaceuticals Ltd at Ankleshwar

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Assistant Manager

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 Id2809312
Job Category Sales and Marketing
Locality Address
State
Country India

About Company

Cadila Pharmaceuticals Ltd
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