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.

Summary

The Senior Manufacturing Engineer s to the Senior Manager Manufacturing Engineering. In this role you will support several manufacturing assembly lines within the Final Assembly Department. You will partner with cross – functional operations team members (i.e. Production Supervisor, Quality Assurance Engineer, and Materials Planning) to effectively identify, investigate and resolve manufacturing process related issues. In addition, you will drive continuous improvement initiatives in support of departmental, site and corporate objectives for Safety, Quality, Delivery, Productivity, and Cost Performance.

Key Responsibilities:

• Member of cross functional Final Assembly “Gemba” Team with responsibility for 10-12 medical device manufacturing assembly lines.

• Develop and maintain manufacturing process documentation including but not limited to: Manufacturing Process Specifications, Device History Records, Tooling/Equipment Specifications, Preventative Maintenance and Calibration procedures through Engineering Change Management (ECM) process.

• Perform and document root-cause analysis for Non-Conforming Material s.

• Summarize and on departmental Safety, Quality, Delivery, Productivity, and Cost performance measures.

• Use Lean/Six Sigma methodology to identify and drive Continuous Improvement Projects to enhance Safety, Quality, Delivery, Productivity, and Cost performance measures.

• Develop and execute Process and Equipment Validation/Verification Strategies for new or changing manufacturing process elements.

• Develop and execute Engineering Builds and assist with Material Qualification Planning to support new or changing component requirements.

• Perform and document Impact Assessments and Corrective Actions for Equipment Remediation’s associated with out of tolerance calibration results.

• Proactively identify and address safety related issues through Near Miss ing Process.

Qualifications

Required Background:

• A Bachelor’s degree, or equivalent, in relevant Engineering discipline accompanied by five to seven years of solid work experience in a related field.

Preferred Background:

• Experience in the Medical Device or a similar regulated industry.
• SAP, CAD modeling, Schematic drafting, PLC programming, and/or Visual Basic programming experience is a plus.

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The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

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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.

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