Your job responsibilities are listed below for your understanding and acceptance. In case of any system up-gradation in future, you will be simultaneously re-trained to understand the new implementation.
Sr. No. Responsibilities
Handling and monitoring of process validation/ cleaning validation plan and procedure.
Monitoring of Preventive Maintenance / Internal calibration and External calibration.
Review of calibration / validation / qualification documentation.
To investigate the market complaints, OOS (out of specification), OOT (out of trend), Deviation, Change control, Lab-incident, non-conformance, product recall, reprocess, online rejection, return etc. and to suggest and implement methods to avoid reoccurrence.
To verify URS, DQ, FAT, IQ, OQ, PQ and Requalification of the Equipments/Instruments of all supporting system/area.
To identify Corrective and Preventive Actions and ensure timely tracking and implementation of the same.
To monitor in process testing and release/reject of in process material as well as finish product.
Report all malfunctions to production executives to ensure immediate action.
Review current standards and policies.
Review of the investigation, including risk assessment, root cause analysis and impact assessment.
Keep records of quality reports, statistical reviews and relevant documentation.
Ensure all legal standards are met
Sr. No.Responsibilities
Ensure compliance with current Good Manufacturing Practice on the shop floor during manufacturing activities.
Conduct the self inspection and/or quality audit.
Communicate with external quality assurance officers during in office inspections.
Any other work assigned by reporting manager/seniors diligently and promptly.
📌 Senior Executive-QA (Vapi)
🏢 Advanced Vital Enzymes
📍 Vapi
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.