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.

Your team:

Our team members possess strong technical backgrounds, excellent analytical skills, and the ability to work multi-functionally. Their collective expertise is crucial for upholding high standards in product quality and safety, making them vital to the organization’s success.

Our engineering team is dedicated to quality. Delivering life-saving products is about getting them right, and our technical expertise and experience working in a manufacturing environment empower us to meet that challenge.

What you'll be doing:

Apply acquired engineering experience, training, and techniques to solve problems encountered in design, redesign, or troubleshooting.

May supervise and/or provide technical and safety guidance or direction to colleagues, technicians, designers, drafters, model makers, and others. May serve as project leader.

Meet with external customers and vendors to exchange information and assist with more difficult technical issues.

Participate in project planning and may advise portions of smaller projects or segments of large projects to include scheduling, supervising costs, resources, workforce load, etc.

Design and implementation of production fixtures/tools and inspection equipment as the need arises.

Capacity (equipment, labor, space) and maintenance planning and strategies.

Production efficiency, efficiency, downtime tracking and corrective actions.

Coordination of activities related to transfer of manufacturing to the new manufacturing site.

Cycle time estimation, tracking and development of production routers.

Development and maintenance of manufacturing process instructions (process sheets, MPS), routers and bill of materials.

Development and completion of process validation, while ensuring that changes made to specifications, methods, processes or procedures are verified or, where appropriate, validated in accordance with standard operating procedures and QSR item 820.75, prior to implementation.

Participates in CPE projects and in the validation and verification of products and processes in accordance with quality system procedures.

May lead or participate with management of organizational and group operations in CAPA activities by performing, determining and verifying corrective actions necessary to ensure continued compliance with division policy and procedures, federal regulations under Title 21 CFR Part 820 and ISO 13485:2003.

Responsible for monitoring, identifying trends, investigating and resolving issues related to manufacturing processes.

What you'll bring:

• Bachelor's degree in Engineering (Industrial, Mechanical, Biomedical, or related field
• Minimum 2 years of experience in a related position. (Medical industry preferred)
• Bilingual: Oral and written communication in Intermediate English.
• Experience in problem solving, project management, lean practices, six sigma desirable, line transfers.
• Experience with ISO/FDA and GMP regulated environments.

Desirable Experience:

• Basic knowledge in design programs (Autocad, SolidWorks)
• Experience in validations (IQ/ OQ, PQ)... TMV
• Basic knowledge in Statistics (CPk, Histograms, PPk, etc.)

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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