New 
USA - Manufacturing Engineer I - CTQ
 Equiliem | |
 United States, New York, Skaneateles | |
 Mar 14, 2025 | |
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Your Role at Baxter
This is where your expertise helps people! You are a problem solver. Complex projects or unexpected challenges are just opportunities to bring your considerable abilities to use. Whether working independently or with a trusted team, you are always ready to tackle a project and work hard to find solutions. Your talent is needed across a wide variety of industries. As a Manufacturing Engineer you have a wide array of career choices, but are motivated by the opportunity to work in a company that supports innovation, professional develop- ment, and a purposeful mission. Your Team We are a team of inquisitive individuals who embrace a col- laborative environment to take on sophisticated challenges that meet the needs of our patients. We often need to change directions and respond to issues to avoid disruptions in our fast-paced manufacturing environment. Together, we build and maintain a positive work environment. Our team is dedicated to quality. Delivering life-saving prod- ucts is about getting them right, and our technical expertise and experience working in a manufacturing environment em- power us to meet that challenge. When you join us, you will work with a team of committed in- dividuals who trust each other to deliver on the tasks at hand. We support innovation and out-of-the-box thinking bal- anced with collaboration across functions and other teams. Our leadership understands the need for continuous educa- tion and provides opportunities for further development. What You'll Be Doing Member of cross functional Electronics "Gemba" Team with responsibility for up to 8 medical device manufacturing assembly lines. Execute Process and Equipment Validation/Veri fication Strategies for new or changing manu- facturing process elements. Execute Engineering Builds and assist with Material Qualification Planning to support new Lindsey Skrupa Hiring Manager Andy Maltese View Team Members 3/10/25, 10:07 AM View Job Posting Details - Workday https://www.myworkday.com/baxter/d/inst/15***/9925***htmld 2/4 Material Quali fication Planning to support new or changing component requirements. Works with project teams and established work processes and proactively finds creative meth - ods to reach desired performance le vels. Represent manufacturing on R&D project core teams, responsible for deliverables, collaborat - ing with internal stakeholders and ensuring productivity. De velop and maintain manufacturing process documentation including but not limited to: Manufacturing Process Speci fications, Device History Records, Tooling/Equipment Speci fications, Pr e ventative Maintenance and Calibration procedures through Engineering Change Management (ECM) process. Perform and document root-cause analysis for Non-Conforming Material Reports. Summarize and report on departmental Safety, Quality, Deliver y, Productivity, and Cost perfor - mance measures. Use Lean/Six Sigma methodology to identify and drive Continuous Impr o vement Projects to enhance Safety, Quality, Deliver y, Productivity, and Cost performance measures. 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 Reporting Process. Review product designs with R&D, Sustaining, and AME engineers for optimized manufactur a - bility and ease of assembly, from raw material to finish products. Le verage Subject Matter Experts during prob - lem solving exercise. Pr ovide multiple what-if scenarios to find the best total cost solution with financial impacts and emphasis on deliver y timelines. Uses existing tools and best practices to report and track product and process metrics. Informs others proactively about de velopments or issues that affect their work, and their ability to meet commitments. What You'll Bring Bachelor's Degree in Engineering. 0-2+ years of experience Preferred: Experience in the Medical Device or a similar regulated industry. Knowledge or experience in SAP, CAD modeling, schematic drafting, and electrical design knowledge - edge is a plus. Knowledge or experience in computer based automated testing. | |