Senior Manufacturing Engineer

This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride.

Your Role at Baxter

As a Manufacturing Engineer II, you will lead and support the integration of manufacturing processes transferred from other Baxter sites while driving continuous improvement across existing operations. This role combines technical problem-solving, project leadership, and process optimization to improve product quality, manufacturing efficiency, and operational performance.

You will serve as a trusted engineering partner to manufacturing, quality, and supply chain teams, helping to ensure processes are scalable, compliant, and capable of meeting business and customer needs. Through your work, you will directly contribute to operational excellence and support Baxter's mission of improving outcomes for patients worldwide.

What You'll Be Doing

• Lead the transfer and integration of manufacturing processes from other Baxter facilities, ensuring successful implementation, validation, and operational readiness.
• Drive continuous improvement initiatives that increase productivity, improve first-pass yield, reduce scrap, and enhance overall manufacturing performance.
• Design, develop, and implement manufacturing tools, fixtures, inspection equipment, and process improvements that support safe and efficient production.
• Analyze manufacturing data, identify performance trends, investigate root causes, and implement corrective actions to improve quality and operational results.
• Plan and support manufacturing capacity strategies, including equipment, labor, space utilization, and maintenance considerations to meet business demands.
• Lead or contribute to process validation activities, including IQ, OQ, PQ, and related verification efforts, ensuring compliance with quality and regulatory requirements.
• Collaborate with suppliers, operations, quality, and cross-functional teams to solve complex technical challenges and successfully execute engineering projects.

What You'll Bring

• Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, or a related engineering discipline.
• 3-5+ years of experience in manufacturing engineering, process development, process transfer, or continuous improvement within a regulated manufacturing environment.
• Experience leading validation of end-to-end manufacturing processes.
• Experience with IQ/OQ/PQ methodologies is highly desired.
• Demonstrated ability to identify manufacturing issues, perform root cause analysis, and implement sustainable corrective actions.
• Experience working cross-functionally with operations, quality, suppliers, and technical stakeholders to deliver business results.
• Strong project management, organization, and prioritization skills with the ability to manage multiple initiatives simultaneously.
• Effective communication skills with the ability to provide technical guidance, influence stakeholders, and lead project activities.

Preferred Qualifications

• Experience within the medical device, healthcare, life sciences, or other highly regulated manufacturing industries.
• Knowledge of FDA Quality System Regulations (21 CFR Part 820), ISO 13485, CAPA processes, and quality system requirements.
• Experience supporting manufacturing transfers, new product introductions, or site expansion projects.
• Knowledge of Lean Manufacturing, Six Sigma, or other continuous improvement methodologies.
• Experience developing manufacturing documentation, process instructions, routings, and bills of materials.
• Ability to mentor technicians, engineers, or cross-functional team members while fostering a collaborative work environment.

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.

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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