Sr Eng, Manufacturing Process (Night Shift)

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 role at Baxter:

We are responsible to improve their assigned lines to meet the efficiency requirements in agreement with Baxter’s Key Performance Metrics, we are also responsible to optimize the product Flow of the Lines and implement the change requirements via SUS, MODs, NCMRs, CAPAs, etc. Also, we perform various engineering, leadership duties in support of operation processes, in order to achieve the daily goals in terms of EHS and Quality compliance as well as Productivity.

Your Team:

Our Team is full of technical skills and knowledge, we are engineers with experience of many industries with knowledge in Mechanical, Hydraulic, Mechanical, Pneumatic and Problem Solving. Our mission is bring our knowledge of preventive, corrective and predictive maintenance as well as build a positive and productive relationship with all members of the Team, fostering a culture of innovation and continues improvement

What you'll be doing

– Other duties may be assigned:

• Implement and document the evidence of the monitoring and control activities of the manufacturing process, in order to sustain quality levels and EHS requirements for every day’s production.
• Establishment of the manufacturing sequence to achieve production goals daily.
• Responsible for the quality of the operation product process, which may include the ownership of resolving quality problems using the CAPA methodology, implement processes validation and qualification, develop and implement process controls using statistical techniques such as design of experiments.
• Responsible to document and keep up to date the job Instructions, visual aids, and related quality system procedures. Able to enter Information and modify Routings and BOMs on JDE
• Manage the implementation of product changes through fabrication, purchasing, and assembly due to engineering changes and new product instructions.
• Drive continuous improvement and lean manufacturing methodologies into the manufacturing process including material flow and line balancing, workstation arrangements to meet required production rates and improve efficiency of the painting process. Participate in Lean Manufacturing Initiatives.
• Responsible for EHS compliance in their assigned lines, this means, implement projects to improve ergonomics in each workstation to prevent injury. Lead Planning & coordination of EHS training.
• Design and validate the DHRs for the parts or product they are responsible for.
• Responsible for ensuring that our manufacturing processes stays in sync with FDA Quality System Regulation as well as Baxter Quality System Requirements. Develop & implement programs & practices to assure 100% compliance with applicable Federal, State, Local and Baxter regulations & practices. Comply & provide all Corporate Requirements.
• Responsible for leading teams and advising the technical efforts of others.
• Create and continuously improve the systems for the elimination of downtime in manufacturing areas.
• Support the manufacturing process, with projects to improve the Quality, Cost and Lean manufacturing.
• Coordinate and supervise the design, construction, and assembly of machinery. Support manufacturing in the installation of new process equipment.

What you'll bring

Bachelor of Engineering preferred.

Proven experience in manufacturing process, 3-4 years, medical field desirable.

Intermediate English.

Experience with Manufacturing process engineer activities, programming, rack design, line balancing, time studies

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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