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This is whereyour 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 Team at Baxter: As a Sr. Manufacturing Engineer at Baxter plays a critical role in optimizing manufacturing processes and ensuring the efficient production of high-quality medical devices. This role requires a strong background in engineering principles, manufacturing processes, and project management. They work alongside diverse departments to drive continuous improvement initiatives, implement new technologies, and improve operational efficiency. In this role you will support several production 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 lead ongoing improvement efforts in support of departmental, site and corporate objectives for Safety, Quality, Delivery, Efficiency, and Cost Performance. What you'll be doing:Provide technical expertise and support to manufacturing teams for 10-12 medical device manufacturing assembly lines (e.g. Electronics, Machining, Plating, Manual Assembly), troubleshooting and resolving production issues.Develop and maintain manufacturing process documentation such as Manufacturing Process Specifications, Device History Records, Tooling/Equipment Specifications, Preventative Maintenance, and Calibration procedures through the Engineering Change Management (ECM) process.Conduct root cause analysis and implement corrective actions to address process deviations and equipment failures.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.Analyze and improve manufacturing processes to enhance efficiency, reduce waste, and increase productivity.Develop and implement process control strategies to ensure consistent product quality and compliance with regulatory standards.Lead and manage engineering projects from conception through implementation, ensuring they are completed on time and within budget.Collaborate with cross-functional teams, including production, quality assurance, and supply chain, to align project goals with business objectives.Prepare and maintain accurate documentation related to manufacturing processes, including work instructions, process flows, and validation protocols.Guarantee alignment with all relevant safety regulations, industry standards, and company policies.Identify and implement continuous improvement initiatives using Lean, Six Sigma, and other methodologies to enhance manufacturing performance.Monitor key performance indicators (KPIs) and develop action plans to achieve operational goals.Mentor and train junior engineers and manufacturing staff on best practices, process improvements, and new technologies.Foster a culture of learning and dev