Manager, Manufacturing Engineering

Terumo Aortic - Sunrise, FL

Hiring: Manager, Manufacturing Engineering Company: Terumo Aortic Location: Sunrise, FL Job Posted Time: 2026-09-10 13:44:15 Target Skills & Keywords : Lean Manufacturing, Six Sigma, SolidWorks About the job Required Skills: •Direct compliance with the TMC Quality System and applicable engineering and process-control requirements, including process controls, calibration, maintenance, document and data control, and change control. •Plan and implement projects to develop, install, and qualify manufacturing processes for new products and improve existing processes in support of business-plan objectives. •Provide engineering leadership for the design, fabrication, development, installation, and qualification of equipment, including feasibility studies, project justification, documentation, and operator training. •Manage team workload, deployment, organizational structure, and skill and experience mix by evaluating resource supply against business demand. •Lead project improvements and troubleshooting for production equipment and coordinate cross-functional personnel and direct reports through project completion. •Identify cost-reduction opportunities, conduct financial and capital-justification analyses, and manage work schedules, expenditures, meetings, and monthly reporting. •Promote compliance with company policies, participate in performance-improvement teams, contribute ideas and processes for company improvement, and perform other assigned duties. •Incumbent must follow all established Environmental Health & Safety and Quality System policies, programs, rules and practices, including but not limited to product and patient safety, the health and safety of all associates as well as the environment and community at large. Qualifications: •Thorough knowledge of statistical techniques; DMAIC or Six Sigma certification is preferred. •Excellent analytical and problem-solving skills and experience with experimental design and analysis for process development, characterization, and optimization. •Knowledge of GMP and FDA regulations and FDA process-validation requirements, including protocol development and execution. •Knowledge of Lean manufacturing techniques; relevant training or certification is a plus. •Thorough knowledge of laboratory testing equipment, tools, and inspection systems. •Excellent written and verbal communication skills, including the ability to explain complex engineering problems to non-engineering personnel. •Computer-aided design expertise, particularly SolidWorks, is a plus. •Bachelor of Science degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Polymer Science, Materials Science, or a related field; an advanced degree (MS or PhD) is preferred. •Minimum of eight years of experience in a manufacturing environment implementing major manufacturing and automation projects. •Minimum of three years of supervisory experience. Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!