Executive - QA
Lupin · Not specified · onsite · Posted 41d ago
Not disclosed6–9 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Job Description
Compliance to the instructions given in Batch records of various products.
Ensuring the compliance of the SOPs and cGMP requirements at shop floor.
Ensuring no mix-ups, contamination and cross contamination of the products during all stages of manufacturing means of Line Clearance and continuous monitoring the process.
Performing In-process Checks at different stages of manufacturing for various products and ensuring the compliance.
Sampling at different stage of manufacturing or as per the requirement.
Stage wise review of batch records and compliances if any, to facilitate timely release.
Preparation, execution and compilation of process validation (Process performance qualification) and cleaning validation & cleaning verification.
Review of master batch manufacturing record and batch packing record in SAP
Active participation in execution of Qualification and calibration activity.
Periodic review and preparation of APQR.
Handling of CAPA, Change controls, OOS, OOT, Laboratory Incidence, Market complaint & Deviations through QAMS.
Co-ordination & execution of Self Inspection and compilation of self-inspection observations.
Active participation in investigation related to product / system failure.
Ensuring the awareness of cGMP and its requirement to the technicians/concerns through continuous interaction/SOP training.
Active Participation in Batch Release Activity.
Handling eDMS activities.
Active participations in all the IPQA activities.
Work Experience
6-9 years
Education
Graduation in Pharmacy
Competencies
Job Description
Compliance to the instructions given in Batch records of various products.
Ensuring the compliance of the SOPs and cGMP requirements at shop floor.
Ensuring no mix-ups, contamination and cross contamination of the products during all stages of manufacturing means of Line Clearance and continuous monitoring the process.
Performing In-process Checks at different stages of manufacturing for various products and ensuring the compliance.
Sampling at different stage of manufacturing or as per the requirement.
Stage wise review of batch records and compliances if any, to facilitate timely release.
Preparation, execution and compilation of process validation (Process performance qualification) and cleaning validation & cleaning verification.
Review of master batch manufacturing record and batch packing record in SAP
Active participation in execution of Qualification and calibration activity.
Periodic review and preparation of APQR.
Handling of CAPA, Change controls, OOS, OOT, Laboratory Incidence, Market complaint & Deviations through QAMS.
Co-ordination & execution of Self Inspection and compilation of self-inspection observations.
Active participation in investigation related to product / system failure.
Ensuring the awareness of cGMP and its requirement to the technicians/concerns through continuous interaction/SOP training.
Active Participation in Batch Release Activity.
Handling eDMS activities.
Active participations in all the IPQA activities.
Work Experience
6-9 years
Education
Graduation in Pharmacy
Competencies
Compliance to the instructions given in Batch records of various products.
Ensuring the compliance of the SOPs and cGMP requirements at shop floor.
Ensuring no mix-ups, contamination and cross contamination of the products during all stages of manufacturing means of Line Clearance and continuous monitoring the process.
Performing In-process Checks at different stages of manufacturing for various products and ensuring the compliance.
Sampling at different stage of manufacturing or as per the requirement.
Stage wise review of batch records and compliances if any, to facilitate timely release.
Preparation, execution and compilation of process validation (Process performance qualification) and cleaning validation & cleaning verification.
Review of master batch manufacturing record and batch packing record in SAP
Active participation in execution of Qualification and calibration activity.
Periodic review and preparation of APQR.
Handling of CAPA, Change controls, OOS, OOT, Laboratory Incidence, Market complaint & Deviations through QAMS.
Co-ordination & execution of Self Inspection and compilation of self-inspection observations.
Active participation in investigation related to product / system failure.
Ensuring the awareness of cGMP and its requirement to the technicians/concerns through continuous interaction/SOP training.
Active Participation in Batch Release Activity.
Handling eDMS activities.
Active participations in all the IPQA activities.
Work Experience
6-9 years
Education
Graduation in Pharmacy
Competencies
Job Description
Compliance to the instructions given in Batch records of various products.
Ensuring the compliance of the SOPs and cGMP requirements at shop floor.
Ensuring no mix-ups, contamination and cross contamination of the products during all stages of manufacturing means of Line Clearance and continuous monitoring the process.
Performing In-process Checks at different stages of manufacturing for various products and ensuring the compliance.
Sampling at different stage of manufacturing or as per the requirement.
Stage wise review of batch records and compliances if any, to facilitate timely release.
Preparation, execution and compilation of process validation (Process performance qualification) and cleaning validation & cleaning verification.
Review of master batch manufacturing record and batch packing record in SAP
Active participation in execution of Qualification and calibration activity.
Periodic review and preparation of APQR.
Handling of CAPA, Change controls, OOS, OOT, Laboratory Incidence, Market complaint & Deviations through QAMS.
Co-ordination & execution of Self Inspection and compilation of self-inspection observations.
Active participation in investigation related to product / system failure.
Ensuring the awareness of cGMP and its requirement to the technicians/concerns through continuous interaction/SOP training.
Active Participation in Batch Release Activity.
Handling eDMS activities.
Active participations in all the IPQA activities.
Work Experience
6-9 years
Education
Graduation in Pharmacy
Competencies
Sourced from foundit
Skills
Market ComplaintSAPLaboratory IncidenceQAMSprocess validationootcleaning validationAPQRCGMPSOPsSamplingCAPAEDMSoosIPQAdeviationsline clearanceProcess Performance Qualificationchange controlsIn-process ChecksSelf-inspectionqualification and calibration activity
About Lupin
Lupin
Pharma
20.9k+
employees
1968
58 years old
Mumbai, Maharashtra
India
About
Global pharmaceutical leader, reporting over ₹20,000 crore in FY24 revenue and a leading global manufacturer of generic medicines with a product footprint in more than 100 countries.
Industries
PharmaBiotech & Life sciencesManufacturing
Employee ratings
7,366 reviews
4.1/ 5
Culture
3.9
Career growth
3.4
Work-life
3.8
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