Manager Job in Cadila Pharmaceuticals Ltd at Ankleshwar
FEATURED JOBManager
Cadila Pharmaceuticals Ltd
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Posted: 06 Sep 26
Job Description
Principal Tasks &Responsibilities
Quality Control analysis :
• To maintain and adherence of the GLP and safety procedures in laboratory.
• To raise the request for issuance of work data sheet / protocols.
• Allocate the work to analyst as per planning.
• 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 any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to QC- In charge.
• To 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.
• To maintain instruments log books properly as per analysis.
• To provide training to concerned person to update the cGMP system update technical knowledge.
• To ensure that analytical data in work data sheets / protocols for raw material /intermediates /APIs and etc... As per current specification and method of analysis.
• To ensure reference / working standard/impurity standard usage records.
• Review of in-process, Intermediate, Raw material, analytical data and approval for further processing of the batch.
• To ensure that the maintain of instrument history record.
• To ensure Daily monitoring and recording of temperature and humidity of refrigerator / working standard chamber and laboratory area.
• To be plan 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
• Initiation of change control / deviations / NQI / QI/OOT related to QC.
• Ensure that all documents / records required for Regulatory Compliance are maintained properly.
• Review of SOP’s for regulatory compliance and actual practice.
• To prepare list of chemical which required for HPLC analysis and inform for indents.
• To ensure the analytical documents like specification, protocol, STP, are prepared as per SOP.
• Ensure timey report and completion of reports of NQI, OOS, OOT, deviation, customer / market complaint investigation and change control.
• Ensure all issues related to completed batches are resolved and documents are submitted to QA.
• To maintain instruments logbooks properly as per analysis.
• To maintain the GLP and GMP practices & ensure standards procedures followed in Quality Control laboratory effectively.
• To review the Standard Operating procedures, work sheets/protocols of Hold time / stability / validation / qualification and other relevant documents of Quality control department.
• To ensure awareness about the MSDS to all concern persons.
• To educate and train the workmen for safe handling of chemicals, gas, cylinder and laboratory instruments to prevent the accidents.
• To ensure the storage of laboratory chemicals and test samples at proper place with segregation to prevent accidents.
• To ensure no spillage of lab. Chemicals / solvents
• To coordinate with QA department for cGLP system
• To coordinate with production department for on line analysis by proper planning/clubbing of analysis.
• Give necessary for the supervisors for continuing the Production activities effectively.
• Inform / Discuss with Department Head for any breakdowns, Deviations, quality issues, etc. for investigation and documentation.
• Prepare and submit reports as required.
• To ensure the storage of lab chemicals and test samples at proper place with segregation to prevent accidents.
Job Particulars
Role head quality
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2951538
Job Category Quality Control
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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