Assoc, Quality - IPQA
Baxter International · Ahmedabad · onsite · Posted 63d ago
Not disclosedFresherfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
- To take instructions from Supervisor and shift lead to perform the shift activity.
- To verify the correct raw material, primary packaging material, and Quantities are issued and dispensed as per the approved Batch records.
- To perform the line clearance activity at various stages of manufacturing and packaging activity as defined in the BMR.
- To perform routine In process checks, sampling, periodic verification, online documentation as defined in batch records and escalate any nonconformances to shift lead and supervisor and ensure appropriate actions (CAPA) in place.
- To collect In-process samples, finished product samples, and other samples timely submission into QC/micro.
- To review and verification of electronic records/Audit trails and printout of the equipment's like autoclave, sterilizer, filter integrity machine and any other equipment's etc.
- To ensure the respective documents to be destructed as per approved procedure.
- To ensure the compliance and GDP of logbooks, online documents, records, and other supporting documents related to products manufactured in the plant and data integrity is ensured.
- To ensure & provide support to Shift Lead or Supervisor in investigation, in case of any product complaints or non-conformities or Out of Specification.
- To execute the approved Corrective and Preventive Action (CAPA) with in define timeline.
- To raise Document Change Request (DCR) and Change Control Management (CCM) and track the same and ensure closure as per Standard Operating Procedure.
- To prepare and review the SOPs.
- To carry out stagewise BMR review for batch execution compliance.
- To track the CPV Program through provided exhibits and to prepare the Minitab files for required products based on production plan for the month. To collect the data related to CPPs/ CQAs and shall perform data analysisy. Report any abnormality gap to supervisor /Shift lead.
- To maintain the admin logins for all applicable equipments and to provide the new logins, activation & deactivation for users and periodic verification & access control of all users.
- Initiation of batch number in BaxLIMS after proper verification of manufacturing and expiry date and correction of entries if required.
- To approve the preventive maintenance activities in MAXIMO and risk assessment review and approval.
- To ensure the handover of shift-to-shift activities and record in Shift charge Handover format/logbook.
- To communicate about any failure or abnormal notification to Supervisor & shift lead for timely escalation and resolution.
- To Perform impact assessment of breakdown maintenance and approve activity in MAXIMO and risk assessment review.
- Material A.R.No. Stock Blockage or Un-blockage in System.
- To perform the periodic building inspection with Admin team.
- Any other responsibility assigned by shift lead and reporting manager.
Sourced from foundit
Skills
Document Change Request (DCR)corrective and preventive actionChange Control Management
About Baxter International
Baxter International
Healthcare
5k+
employees
1931
95 years old
Kolkata, West Bengal
India
₹20.4L PA avg
Avg at Baxter International
About
Baxter hires a range of talented and driven individuals with diverse skill sets and backgrounds, from scientists and researchers to industry professionals in manufacturing, engineering and technology,
Industries
HealthcareMedical EquipmentPharma
Employee ratings
10 reviews
3.8/ 5
Culture
3.9
Career growth
2.1
Work-life
3.5
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