Technical SupervisorJobs Opening in Cadila Pharmaceuticals Ltd at Dholka
FEATURED JOBTechnical Supervisor
Cadila Pharmaceuticals Ltd
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Posted: 06 Jan 26
Job Description
• To perform the analysis of In-Process, Finish & Stability samples in Penicillin QC lab Dholka.
• To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed/implemented properly.
• To manage an accurate, reliable, efficient and timely testing of finished products, in process/ validation samples.
• To ensure the compliance of GLP in Quality Control Lab.
• To analyze the In-Process, Finish & Stability samples as per monthly calendar by chemical / instrument method.
• To receive the samples for analysis form stability chamber and their management in QC up to analysis completion.
• Responsible for preparation of stability protocol and grid if required.
• To review the instruments log books related to In-Process, Finish & Stability samples document if required.
• Responsible for initiation of OOS, OOT and incidences.
• Responsible for monitoring daily routine activity & follow good documentation practices.
• Timely provide the In-Process, Finish & Stability samples data without any delay.
• Responsible for timely complete the analysis as per In-Process, Finish & Stability samples management SOP.
• To maintain the column usage and records of impurities and working standard / reference standard during stability samples analysis.
• Responsible for cleaning & monitoring of laboratory.
• Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) for analysis.
• To review timely release of batch audit trail, system audit trail, message center.
• To review of logbooks of instrument, equipment’s, column, standards, impurities etc.
• To review the COA of product in LIMS after the completion of analysis.
• To review the status label updated for the instrument, equipment’s, glassware and workplace.
• To provide the training program to analyst as per the training calendar.
• To review the training about the changes in standard operating procedures (SOP), if required.
• To review and sign in raw date as per specifications & Test procedure.
• To review methods are prepared according to STP/SOP.
• To review proper integration and prior to E-signature of data.
• To investigate and file deviation, change control, Out of Specification (OOS), Out of Trend (OOT), Lab Incident, report whenever observed.
• To review the calibration and preventive maintenance data.
• To review working Standard and Reference standard qualification data.
• To ensure that the Quality control always kept clean and presentable at all time.
• To do all work as per the instruction of HOD.
• Ensuring GLP compliance & Analysis of FP/In process/Validation/Raw Material samples in Penicillin QC lab, Dholka.
• Ensuring GLP compliance & Analysis of FP/In process/Validation/Raw Material sample, Stability and Raw Material sampling in Penicillin QC lab, Dholka.
• To ensure the compliance of GLP in Quality Control Lab.
• To analyze the finished products, In-process and Raw Material sample by chemically / instrumental method.
• To receive the samples for analysis and making entry in Inward register.
• To maintain the Instruments log books related to FP analysis.
• To analyze the validation sample and compilation of documents.
• To enter the finished product results through LIMS.
• Follow cGMP in Laboratory. Responsible for online documentation.
• Responsible for taking of Continuations sheet (CS) and print out Record of analysis (ROA) through LIMS.
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2820606
Job Category Sales and Marketing
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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