OfficerJobs Opening in Cadila Pharmaceuticals Ltd at Ankleshwar
FEATURED JOBOfficer
Cadila Pharmaceuticals Ltd
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Posted: 02 Jun 26
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.
• To work as Analyst and maintain the CFR 21 part -11 compliance by following laid down procedures.
• To perform the all activity related to working standard management.
• To perform wet analysis of In-process/ intermediate/ finished product/ returned goods / raw materials/ Hold time / Stability study / working standard analysis (Test like Sulphated Ash/Residue on ignition/Specific Gravity/Water content by KF/Assay by manual or potentiometer titration, LOD/ Different type of limit test/ Melting or boiling point/ particle size analysis by air jet sieve/ analysis by UV spectrophotometer / BD/TD, pH measurement etc) as per work allocation and records the results in work sheet (Protocol) as per current specification and method of analysis and maintain the on line documentation.
• If required report the analysis data in LIMS modules and report to Section – 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 maintain instrument history record.
• To report and raise any QI/NQI/OOS/OOT / Deviation/ discrepancy in laboratory analysis to Section - In charge.
• Responsible for performing calibration of laboratory instruments as per schedule and laid down SOPs with documentation and up-dation of instrument calibration tag.
• To record and ensure all the entries and results are in line with current specifications and STPs.
• To maintain instruments log books properly as per analysis.
• To acquire training from concerned person to update the cGMP system update technical knowledge..
• Preparation, qualification and management of working standard for Raw materials Intermediates/APIs .
• To maintain reference / working standard/impurity standard usage records.
• Daily monitoring and recording of temperature and humidity of refrigerator / cooling cabinet working standard chamber and laboratory area.
• Ensure CFR 21 part-11 compliance and follow the SOP/STP for analysis to maintain proper data integrity.
• Ensure that all documents / records required for Regulatory Compliance are maintained properly.
• To maintain the GLP and GMP practices & ensure standards procedures in Quality Control laboratory followed effectively.
• To ensure awareness about the MSDS for 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/contamination.
• To ensure no spillage of lab. Chemicals / solvents
• To draw required sample quantity only for analysis of material to avoid wastage of material.
• To prepare required solution for analysis as per requirement to avoid wastage of lab chemicals and reagents/solvents.
• To co – ordinate with cross function department for cGLP systems and its maintenance, up-dation.
• To co – ordinate with production department for on line analysis support requirement, planning/clubbing of analysis.
• To co – ordinate with EHS for safety and environment related activities and its management.
• Give necessary and transparent feedback to the supervisors for continuing the production activities effectively.
• Inform/ discuss with Section head of any breakdowns, deviations, quality issues etc.
• 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
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2900632
Job Category Manufacturing
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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