Jubilant Life Sciences Ltd Recruitment February 2020 Officer – IPQA @ Mysore
Job Description
Monitoring of day to day GMP activities in production department.
Shall be responsible for identifying the gap in existing production system, facilities & equipment system, laboratory controls system, materials system, packaging & labeling system.
To ensure in-process quality testing performed in manufacturing & packing areas according to prescribed timelines, and accurately captures test results in batch production record.
To investigate the cause of any non-conformance and its corrective/preventive action
Ensure execution of process & cleaning Validation as per approved protocol.
Ensure that procedures and specifications are appropriate and followed.
Ensure Plant area & pharma room cleaning is done as per established procedure.
Ensure entry & exit procedure available in the clean room & followed by operating personnel during routine operations.
Ensure execution of process & cleaning Validation as per approved protocol Perform final review and approval of line clearance activities.
Ensure online recording of batch production record and ensuring that those are completed and signed.
Ensure applicable SOPs available in the work place & accessible to operating persons.
Ensure equipment's are cleaned with the specified time after use as per established procedure.
Ensure indented Raw materials, packing materials, solvents are received from warehouse and stored in designated place with appropriate label.
Ensure Plant area & pharma room cleaning is done as per established procedure.
Ensure entry & exit procedure available in the clean room & followed by operating personnel during routine operations.
TO APPLY CLICK HERE
FOR MORE JOB UPDATES
No comments:
Post a Comment