Assoc, Quality Control - QMS
Date de publication :
20 novembre 2024Taux d'activité :
100%Type de contrat :
Durée indéterminée- Lieu de travail :Ahmedabad
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To review, update, report and inform Supervisor as & when deviation is initiated.
To ensure that the recording of NCR is done in line with standard operating procedure
To ensure the implementation of GMP, GDP practices and review of issues and impact of the same, if any, & take corrective actions.
To carry out GLP rounds in the Quality Control lab.
To work as a Good Manufacturing Practice (GMP) inspector in the plant
To train/update the team members on various regulatory guidelines
To identify, monitor the deviation/abnormalities in process/documents/systems are captured and resolve them according to Quality management System.
To ensure that all the deviations and OOS are reported to QA within required time frame.
To prepare, review, Implement and update SOP’s according to current regulations systems.
To conduct Technical committee meeting on CCN impact assessment.
To conduct monthly corrective and Preventive Action Meeting.
To review the CAPA summary report and ensure that all CAPA are closed within time frame.
To review Change Control Note and NCR report before sending to Quality Committee for final closure and ensure the timely closure of Change Control Note and NCR
To train/update the personnel for the various aspect of current Good Manufacturing Practices.
To investigate and close the QMS elements in timely manner.
Reasonable Accommodations
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
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