More jobs:
Manager, Engineering - Cuffs & Fabrications
Job in
Skaneateles Falls, Onondaga County, New York, 13153, USA
Listed on 2026-06-17
Listing for:
Zvh
Full Time
position Listed on 2026-06-17
Job specializations:
-
Engineering
Manufacturing Engineer, Lean Manufacturing / Six Sigma, Quality Engineering, Operations Engineer -
Manufacturing / Production
Manufacturing Engineer, Lean Manufacturing / Six Sigma, Quality Engineering, Operations Engineer
Job Description & How to Apply Below
Manufacturing Engineering Manager
As a Manufacturing Engineering Manager at Baxter, you will play a critical role in driving manufacturing excellence across our Fabrications and Cuffs operations. You will lead engineering teams, optimize manufacturing processes, and advance continuous improvement initiatives that support high‑quality healthcare solutions.
What You’ll Be Doing- 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 leadership and team development capabilities.
- Excellent communication and collaboration skills.
- Analytical thinking and problem‑solving abilities.
- Project management and organizational skills.
- Ability to manage multiple priorities in a fast‑paced environment.
- Continuous improvement mindset with a focus on operational excellence.
- Combination of office, manufacturing, and laboratory…
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