Baxter Job Vacancy for Assoc, Quality Assurance - IPQA

Baxter Job Vacancy for Assoc, Quality Assurance - IPQA

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. 

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