🔶Cadila Pharmaceutical Ankleshwar jobs for Quality Control apply now
🔶Jr. Officer To Executive For Quality Control Department at Cadila Phar
Cadila Pharmaceutical Limited
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Job Highlights
Experience - :2 - 7 Years
Not mentioned
Location - ;Ankleshwar
CTC - :₹ 2,00,000 - 7,00,000 P.A
Department - :qa, api research, qc, QA Analysis, microbiology, api analysis, gc, stability, hplc
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Job Description
To maintain and adherence of the GLP and safety procedures in laboratory.
To raise the request for issuance of work data sheet / protocols.
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To maintain instruments log books properly as per analysis.
To acquire training from concerned person to update the cGMP system update technical knowledge.
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To perform the analysis as per work allocation and records the results in work sheet / protocol and maintain on line documentation.
To work as Analyst / Operator as a level of users and maintain the CFR 21 part -11 compliance by following laid down procedures.
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To perform all the HPLC related analysis of In-process, intermediate, finished products & returned goods / raw materials Hold time / Stability study /reference / 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.
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To follow the instruction of Shift /Section In charge for analysis /planning.
To report any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to QC- In charge.
Responsible for performing calibration of laboratory instruments as per schedule and laid down SOPs with documentation and updation of instrument calibration status tag.
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To record and ensure all the entries, and results are in line with current specifications and STPs.
To prepare standard operating procedures, work data sheets and other documents related to QC.
To ensure the all column performance and column entry are maintain in column logbooks.
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To record analytical data in work data sheets / protocols for raw material / packing materials/intermediates /APIs and etc... As per current specification and method of analysis.
Preparation, qualification and management of working standard for Raw materials Intermediates/APIs.
To maintain reference / working standard/impurity standard usage records.
Review of in-process analysis data and approval for further processing of the batch.
To maintain instrument history record.
Joint analysis with R&D personnel during analytical method transfer on HPLC.
Preparation of stability protocols and stability reports.
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To perform analysis of stability samples as per stability schedule
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.
To prepare/ check the protocols & reports for analytical method validation and analytical method transfer
Inform and Investigate OOS results in RM/Intermediates/APIs
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Initiation of change control / deviations / QI /NQI/ OOT related to QC.
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.
Required Candidate profile
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Ankleshwar & Bharuch based preferable
Industry TypePharma, Biotech, Clinical Research
Functional AreaProduction, Manufacturing, Maintenance
RoleQuality Assurance/Quality Control Executive
Employment TypeFull Time, Permanent
Education
B.Sc in Microbiology, Chemistry
MS/M.Sc(Science) in Chemistry, Any Specialization, Microbiology
Any Doctorate in Any Specialization, Doctorate Not Required
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🔶Jr. Officer To Executive For Quality Control Department at Cadila Phar
Cadila Pharmaceutical Limited
[ads id="ads1"]
Job Highlights
Experience - :2 - 7 Years
Not mentioned
Location - ;Ankleshwar
CTC - :₹ 2,00,000 - 7,00,000 P.A
Department - :qa, api research, qc, QA Analysis, microbiology, api analysis, gc, stability, hplc
[ads id="ads1"]
Job Description
To maintain and adherence of the GLP and safety procedures in laboratory.
To raise the request for issuance of work data sheet / protocols.
[ads id="ads1"]
To maintain instruments log books properly as per analysis.
To acquire training from concerned person to update the cGMP system update technical knowledge.
[ads id="ads1"]
To perform the analysis as per work allocation and records the results in work sheet / protocol and maintain on line documentation.
To work as Analyst / Operator as a level of users and maintain the CFR 21 part -11 compliance by following laid down procedures.
[ads id="ads1"]
To perform all the HPLC related analysis of In-process, intermediate, finished products & returned goods / raw materials Hold time / Stability study /reference / 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.
[ads id="ads1"]
To follow the instruction of Shift /Section In charge for analysis /planning.
To report any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to QC- In charge.
Responsible for performing calibration of laboratory instruments as per schedule and laid down SOPs with documentation and updation of instrument calibration status tag.
[ads id="ads1"]
To record and ensure all the entries, and results are in line with current specifications and STPs.
To prepare standard operating procedures, work data sheets and other documents related to QC.
To ensure the all column performance and column entry are maintain in column logbooks.
[ads id="ads1"]
To record analytical data in work data sheets / protocols for raw material / packing materials/intermediates /APIs and etc... As per current specification and method of analysis.
Preparation, qualification and management of working standard for Raw materials Intermediates/APIs.
To maintain reference / working standard/impurity standard usage records.
Review of in-process analysis data and approval for further processing of the batch.
To maintain instrument history record.
Joint analysis with R&D personnel during analytical method transfer on HPLC.
Preparation of stability protocols and stability reports.
[ads id="ads2"]
To perform analysis of stability samples as per stability schedule
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.
To prepare/ check the protocols & reports for analytical method validation and analytical method transfer
Inform and Investigate OOS results in RM/Intermediates/APIs
[ads id="ads2"]
Initiation of change control / deviations / QI /NQI/ OOT related to QC.
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.
Required Candidate profile
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Ankleshwar & Bharuch based preferable
Industry TypePharma, Biotech, Clinical Research
Functional AreaProduction, Manufacturing, Maintenance
RoleQuality Assurance/Quality Control Executive
Employment TypeFull Time, Permanent
Education
B.Sc in Microbiology, Chemistry
MS/M.Sc(Science) in Chemistry, Any Specialization, Microbiology
Any Doctorate in Any Specialization, Doctorate Not Required
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Apply here
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🔶Upload your Latest Resume - Click here
When we get job suitable to you we can contact you. Please upload your updated Resume
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Interview questions asked frequently in Technical Plant Interviews.
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