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. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.


Baxter's 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 lives--where your purpose accelerates our mission.


Production QMS

Outline: Production Documentation

Key Responsibilities:


. Handling of Production change control activities and cross functional change impact assessment.

Handling of Production document change request and cross functional DCR impact assessment. Execution of CA/PA records and perform effectiveness check of implemented actions. Perform risk assessment for Production QMS elements as per impact assessment. NCR/SNCR, Market complaint and Laboratory investigation and prepare report. Production documentation related to QMS elements, SOP, Audit compliance. Regulatory observation compliance. Work for Audit readiness. Execution of other project assigned time to time.

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

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