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Industrial Engineer II – TPR
Terumo Medical Corporation. Design, analyze, and improve integrated manufacturing systems and production processes .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in designing and improving integrated manufacturing systems, applying Lean and Six Sigma methodologies, and conducting thorough production workflow analyses. Proficient in project management and capable of delivering continuous improvement initiatives within regulated manufacturing environments.
Highest-signal resume keywords
Lean ManufacturingSix SigmaStatistical Process ControlProject ManagementIndustrial Engineering Principles
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Production Workflow AnalysisRoot Cause AnalysisCapacity AnalysisProcess DocumentationPerformance Trend EvaluationTime And Motion StudiesQuality System PoliciesProcess StandardizationWaste ReductionTakt Time Analysis
Soft Skills
CommunicationCollaborationMentoringProblem SolvingTechnical Guidance
Tools & Technologies
Microsoft OfficeAutoCADMinitabVisio
Certifications & Qualifications
Continuous Improvement CertificationStatistical Analysis CertificationProject Management Certification
Industry Keywords
Regulated ManufacturingFDA RegulationsISO StandardsEnvironmental Health And SafetyMedical Device ManufacturingPharmaceutical ManufacturingBiotechnology
About the role
Key responsibilities & impact- Design, analyze, and improve integrated manufacturing systems and production processes
- Conduct production workflow analysis and time and motion studies
- Apply Lean, Six Sigma, statistical process control, and root cause analysis methods
- Provide engineering support to resolve process-related issues and optimize production lines and equipment
- Monitor key performance indicators and implement corrective actions to minimize downtime
- Establish and maintain process controls with Quality and Operations
- Investigate nonconformances and implement corrective and preventive actions
- Develop capacity analyses and design or improve facility and production layouts
- Recommend equipment and technology enhancements
- Collect, validate, and analyze production data to identify trends and improvement opportunities
- Communicate actionable recommendations through reports and presentations
- Plan and execute moderately complex process improvement, facility expansion, technology implementation, and new product introduction initiatives
- Manage project scope, timelines, budgets, risks, and cross-functional deliverables
- Develop and maintain process documentation, procedures, work instructions, and training materials
- Deliver continuous improvement training and provide technical guidance and mentoring
- Collaborate with Operations, Quality, R&D, Supply Chain, suppliers, and other stakeholders
- Follow Environmental Health & Safety and Quality System policies, programs, rules, and practices
Requirements
What you’ll need- Bachelor’s degree in Industrial Engineering or related engineering discipline from an accredited institution
- Minimum of six years of progressively experience in industrial engineering, manufacturing engineering, operational excellence, or a related field
- At least three years supporting a regulated manufacturing environment such as medical device, pharmaceutical, or biotechnology
- Demonstrated experience independently analyzing and improving manufacturing processes
- Experience leading moderately complex cross-functional initiatives involving productivity, capacity, quality, cost, facility layout, or technology implementation
- Knowledge of industrial engineering principles and practices
- Knowledge of Lean manufacturing, Six Sigma, 5S, waste reduction, root cause analysis, and process standardization
- Knowledge of statistical process control, Pareto analysis, time and motion studies, takt time analysis, and performance trend evaluation
- Knowledge of manufacturing operations within regulated industries
- Knowledge of FDA regulations, ISO standards, environmental health and safety requirements, and internal operating procedures
- Knowledge of project management principles
- Proficiency in Microsoft Office applications, including Excel, Word, PowerPoint, and Project
- Proficiency in AutoCAD, Minitab, and Visio
- Professional proficiency in English and Spanish
- Ability to work effectively in a regulated, onsite manufacturing environment and enter controlled areas requiring established gowning and safety practices
- Professional certification or formal training in continuous improvement, statistical analysis, or project management is preferred
Benefits
Comp & perks- Annual bonus
- Paid vacation
- Paid holidays
- Health benefits
- Dental benefits
- Vision benefits
- 401(k) with matching contributions
- Tax advantage savings accounts
- Legal plan
- Voluntary life and AD&D insurance
- Voluntary long-term disability
- Short term disability
- Critical illness and accident insurance
- Parental leave
- Personal leave
- Tuition reimbursement
- Travel assistance
- Employee assistance program