Manager, Engineering - Cuffs & Fabrications

Manufacturing Engineering Manager

At Baxter, we are deeply connected by our mission. Every role at Baxter contributes to improving outcomes for patients around the world. As a Manufacturing Engineering Manager, you will play a critical role in driving manufacturing excellence across our Fabrications and Cuffs operations by leading engineering teams, optimizing manufacturing processes, and advancing continuous improvement initiatives that support high-quality healthcare solutions.

This is an exciting opportunity for a motivated engineering leader who thrives in a collaborative manufacturing environment and is passionate about developing teams, improving operational performance, and delivering meaningful impact through innovation and quality.

• Lead and support a team of Manufacturing Engineers, Manufacturing Technicians, and Toolmakers in daily operations and long-term professional development.
• Foster a collaborative, inclusive, and high-performing team culture focused on accountability, innovation, and continuous improvement.
• Provide coaching, mentorship, and technical leadership to support employee growth and organizational success.
• Oversee the design, implementation, documentation, and optimization of manufacturing processes within the Fabrications and Cuffs departments.
• Improve production efficiency, reduce waste, enhance product quality, and support operational performance goals.
• Utilize Lean Manufacturing, Six Sigma, and other continuous improvement methodologies to identify and implement process enhancements.
• Manage engineering projects from initiation through implementation, ensuring alignment with safety, quality, delivery, and cost objectives.
• Develop project plans, allocate resources, monitor progress, and support risk mitigation activities to ensure successful project execution.
• Balance multiple priorities while ensuring projects are completed on time and within budget.
• Partner closely with R&D, Quality, Regulatory Affairs, Supply Chain, and Manufacturing Operations teams to ensure manufacturing processes meet product specifications and compliance requirements.
• Facilitate effective communication and alignment across departments to support operational and business objectives.
• Serve as a key technical resource and contributor to cross-functional initiatives.
• Ensure manufacturing processes comply with Baxter quality standards, cGMP requirements, FDA regulations, ISO standards, and internal procedures.
• Conduct audits, inspections, and process reviews to identify and resolve quality or compliance concerns.
• Support a culture of quality, safety, and operational excellence throughout the organization.
• Support departmental budget management and resource planning activities.
• Monitor engineering performance metrics and identify opportunities for operational improvement.
• Prepare reports and presentations that communicate engineering performance, project updates, and improvement initiatives.
• Stay current with emerging manufacturing technologies and industry trends to help drive innovation and best practices.
• Support Baxter's Environmental Health & Safety (EHS) programs and proactively contribute to a zero-harm workplace culture.
• Ensure compliance with all applicable safety procedures, company policies, and regulatory requirements.
• Participate in identifying and implementing measures that improve employee and environmental safety.

• Bachelor's degree in Mechanical, Industrial, Manufacturing Engineering, or a related engineering discipline.
• 5+ years of manufacturing engineering experience, preferably within the medical device, pharmaceutical, or healthcare industry. 2–3 years of leadership or supervisory experience.
• Experience leading process optimization, manufacturing improvement, or engineering project initiatives.
• Strong technical knowledge of manufacturing processes, engineering principles, and regulated manufacturing environments.
• Proven experience leading cross-functional teams and managing complex engineering projects.
• Experience with Lean Manufacturing, Six Sigma, and continuous improvement methodologies.
• Knowledge of FDA, ISO, cGMP, and other regulatory requirements.
• Strong…