Sr Exec, Quality Assurance - IPQA
Sr Exec, Quality Assurance - IPQA
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
This is where you save and sustain lives
At Baxter we are deeply connected by our mission. No matter your role at Baxter your work makes a positive impact on people around the world. Youll feel a sense of purpose throughout the organization as we know our work improves outcomes for millions of patients.
Baxters products and therapies are found in almost every hospital worldwide in clinics and in the home. For over 85 years we have pioneered significant medical innovations that transform healthcare.
Together we create a place where we are happy successful and inspire each other. This is where you can do your best work.
Join us at the intersection of saving and sustaining liveswhere your purpose accelerates our mission.
2.1 To execute inprocess quality assurance activities as delegated by Supervisor and/or shift lead in each shift.
2.2 To perform the line clearance activity at various stages of packaging activity as defined in the Batch Packaging record.
2.3 To perform routine inprocess checks online documentation as defined in batch manufacturing records.
2.4 To check and ensure challenge test performed at defined frequency for applicable packaging equipments.
2.5 To collect the FP/stability sample/Retain Sample/other samples.
2.6 To verify sample / good destruction process and report any gap to Shift Lead or Supervisor.
2.7 To ensure the compliance and GDP of logbooks online documents records and other supporting documents related to products manufactured and packed in the plant and data integrity is ensured.
2.8 To perform Acceptance Quality Limit (AQL) of visually inspected product.
2.9 To verify and approve pallet planning approval in PCR system at dispatch area.
2.10 To ensure cGMP compliance during packing and visual inspection process.
2.11 To perform evaluate and carry out Visual Inspection qualification process.
2.12 To prepare and maintain visual inspection qualification kit and record.
2.13 To carry out stagewise BPR review for batch execution compliance.
2.14 To review and verification of user access management and Audit trail.
2.15 To perform and support in the CPV program.
2.16 To ensure the handover of shifttoshift activities and record in Shift charge Handover format/logbook.
2.17 To Perform impact assessment of breakdown maintenance and approve activity in MAXIMO and risk assessment review.
2.18 To participate in investigation in case of any complaints or nonconformity.
2.19 To communicate about any failure or abnormal notification to Supervisor & shift lead for timely escalation and resolution.
2.20 To raise Document Change Request (DCR) and Change Control Management (CCM) and track the same and ensure closure as per Standard Operating Procedure.
2.21 Any other responsibility assigned by shift lead and reporting manager.
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.
Recruitment Fraud Notice
Baxter has discovered incidents of employment scams where fraudulent parties pose as Baxter employees recruiters or other agents and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself review our Recruitment Fraud Notice.
Required Experience:
Senior IC
Employment Type
Full-Time
