Senior Technical SupervisorJobs Opening in Cadila Pharmaceuticals Ltd at Dholka
FEATURED JOBSenior Technical Supervisor
Cadila Pharmaceuticals Ltd
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Posted: 11 Jul 26
Job Description
To perform the in process checks for control on production for the process / product being manufactured.
To ensure Quality and cGMP compliance of the products being manufactured.
Parenteral Manufacturing :
• To give Area /Equipment clearance i.e. checking and approval of all manufacturing & filling.
To verify environmental condition i.e. Temperature, Relative Humidity & Pressure Differential condition in all for said areas are within acceptable range at all the time during operation throughout the shift.
To ensure daily verification of weighing balance with standard weights.
To ensure sterilization cycles completion as per loading pattern & SOP.
To ensure lyophilization cycles completion as per MMD-I & SOP.
• To perform filled volume & weight method and leak test as per MMD-I & SOP.
• To perform sampling of bulk and finished product for each batch at the end of the batch as per SOP entry into sampling log and submit the samples to QC for analysis.
• Record review,
To review the Batch Manufacturing Records for on line entries at each stage.
To review sequential log of machines.
To review environmental condition records.
To review of area cleaning logs.
• To release the batches for further processing.
• To review and checking Batch Manufacturing Records for reconciliation, correct entries, completeness, affixing of release status labels.
• Reporting to shift in charge to address the observations under
Deviations, unusual observation
Daily report of total activities performed
Parenteral Packing :
• To give line clearance i.e. checks and approval of all packing.
• To perform checking and approval of overprinting details on printed packing material like blisters, cartons, labels etc. As per Batch Packing record.
• To verify the correctness of primary and secondary packing materials of product being packed as per CMOF and MMD-II.
• To perform periodic checks of overprinting details, number of units per pack, absence of empty pocket etc.
• To perform spot-checking on inspected ampoules/ vials SOP.
• To verify challenge test for brevity inspection machine.
• Record review,
To review the Batch Packing Records for on line entries at packing stage.
To review sequential log of machines.
To review of area cleaning logs.
• To co-ordinate with packing supervisor in relation to the issue related to packing.
• Any job assigned time to time.
• Responsible for review, tracking and closing of deviation, change control and CAPA in LIMS.
• Responsible for participating in investigation along with cross functional team to find out actual root cause of incident or deviation.
• Responsible for review and assign number to Deviation, Change control, CAPA when required supporting documents is available in system.
• To ensure the completion, closing and effectiveness of CAPA given to the different regulatory and customer audit.
• Responsible to take follow up with cross functional team to approval & closing of deviation, change control, CAPA.
• To check the effectiveness of implemented change control and CAPA as required.
• Responsible for review of manufacturing investigation.
• Responsible for handling of Market complaints. Perform investigation and report preparation.
• Responsible for review of manufacturing investigation.
• Responsible for preparation and review of Risk assessment.
• Responsible for logging of conversion note.
• Responsible for preparation of Trend analysis report for QMS records as per SOP.
• Responsible for review change control, deviation and CAPA logs from system.
• Responsible for handling of recall procedures.
• To prepare and revise the departmental SOP and ensure training to all concerns.
• To perform mock recall and documented all the activity within timeline as mention in the schedule.
• To assist for any other jobs assigned from time to time.
• Responsible for FAR handling and sharing investigation report for register market complaints.
• To Perform Vendor Audits for Vendor Qualification as per requirement of RM/PM.
• Perform effective self-inspection as per schedule and ensure timely closing with proper CAPA or justification for the noncompliance found during self-inspection.
• To participate in all internal and external audits.
• To prepare compliance report of different customer and regulatory audits.
• To make sure that internal and external audit compliance report is prepared within given timeline.
Job Particulars
Education Any Graduate
Who can apply Freshers
Hiring Process Face to Face Interview
Employment TypeFull Time
Job Id2922395
Job Category Sales and Marketing
Locality Address
State Gujarat
Country India
About Company
Cadila Pharmaceuticals Ltd
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