Baxter Job Vacancy for Assoc, Quality Assurance - IPQA
Post Name:Assoc, Quality Assurance - IPQA
Location: Ahmedabad, Gujarat
Email id:Americas_TTA@baxter.com
Selection Process: The selection will be on the basis of Interview.
Job Description:Walk-in interview at Baxter , Ahmedabad, Gujarat, India!
Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission.
- To take instructions from Sub-department Manager to manage shift activity.
- To do analysis of headspace oxygen and dissolve oxygen during in process monitoring.
- To verify primary raw material, primary packing material at the time of material issuance and material dispensing against Technical Package or Standard Material Requirement Form and approve the process step.
- To perform routine IPQA monitoring like volume check, critical control step verification during manufacturing of the product, sampling and periodic verification activities and if any non-conformity or abnormal observation in terms of noncompliance to Good Manufacturing Practice (GMP) observed, bring to the notice of Shift Manager and Sub-department Manager.
- To verify sample, good destruction process and report any gap to Department Head and take corrective and preventive action in coordination with respective Department Head.
- To carry out reconciliation and physical verification of the returned goods.
- To ensure that finished product samples are collected from defined location and submit it to QC after visual inspection.
- To ensure logbooks, online documents, records, analysis report and other supporting documents related to products manufactured in the plant.
- To ensure provide support to Sub-department Manager in investigation, in case of any product complaints or non-conformities or Out of Specification.
- To execute the Corrective and Preventive Action (CAPA) defined by Quality Management System (QMS), as per instruction of Sub-department Manager.
- To raise Document Change Request (DCR) and Change Control Management (CCM) and track the same and ensure closure as per Standard Operating Procedure.
- To help Sub-department Manager in preparation, review, implement and update SOP’s according to current regulations systems.
- To give non-compliance reports to the respective departments in case of internal quality audits and report it to Sub-department Manager and Department Head.
- To provide line-clearance for routine manufacturing activity and dispensing activity, monitor each line & sample collection at regular interval.
Post a Comment