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Carestream

Manufacturing Engineer II

Carestream

. Provide hands-on technical support to diagnose and resolve production issues, minimize downtime, and ensure product quality .

Posted 9/15/2026full-timeRochester • New York • United StatesJuniorMid-Level💰 $78,300 - $95,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in hands-on technical support, root cause analysis, and implementing Lean and Six Sigma methodologies to enhance manufacturing processes and product quality. Proficient in managing engineering change activities and ensuring compliance with regulatory standards in a medical device manufacturing environment.

Highest-signal resume keywords
Lean ManufacturingSix Sigma MethodologiesRoot Cause AnalysisMechanical Engineering DegreeSAP or ERP Systems

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Root Cause AnalysisLean ManufacturingSix Sigma MethodologiesMechanical Drawing InterpretationDesign for Manufacturing (DFM)Failure Mode and Effects Analysis (FMEA)Cost Reduction TechniquesProductivity Improvement TechniquesEngineering Change ManagementQuality Compliance
Soft Skills
Analytical SkillsProblem-Solving SkillsWritten CommunicationVerbal CommunicationTeam Collaboration
Tools & Technologies
MS Office SuiteExcelWordSAPERP SystemsCAD ToolsNXCreoSolidWorksQuality Management Systems
Industry Keywords
Medical Device ManufacturingProduction IssuesProduct QualityRegulatory StandardsEnvironmental Standards

Tech Stack

Tools & technologies
ERP

About the role

Key responsibilities & impact
  • Provide hands-on technical support to diagnose and resolve production issues, minimize downtime, and ensure product quality
  • Build and maintain a thorough understanding of assigned product lines, including functionality, end use, and standard work
  • Monitor product line health with the quality group by extracting trends from production data
  • Lead root cause analysis and implement corrective and preventative actions for production defects
  • Support equipment maintenance and calibration activities
  • Communicate project status and production updates to audiences with different levels of technical understanding
  • Identify and implement cost reduction initiatives and productivity improvements
  • Collaborate with cross-functional teams on new product introductions and process improvements
  • Analyze engineering requirements and propose manufacturing processes, tools, or fixtures
  • Drive safety, quality, and throughput improvements using Lean and Six Sigma tools
  • Manage engineering change activities, including component obsolescence, annual reviews, and supplier changes
  • Ensure manufacturing processes comply with regulatory, safety, and environmental standards
  • Represent Carestream’s manufacturing organization in discussions with internal customers and outside vendors

Requirements

What you’ll need
  • Ability to work hands-on, on-site with core hours from 7am – 4pm, Monday – Friday
  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Electrical Engineering or a related field
  • Minimum of 2 years of relevant hands-on engineering experience
  • Strong analytical and problem-solving skills
  • Excellent written and verbal communication skills
  • Ability to work collaboratively in a team environment
  • Knowledge of typical quality expectations and compliance requirements
  • Ability to manage multiple tasks and prioritize effectively
  • Comfortable with computers and able to quickly learn new programs & tools as needed
  • Proficient in MS Office Suite, primarily Excel and Word
  • Experience in medical device manufacturing preferred
  • Experience with Lean Manufacturing and Six Sigma methodologies
  • Experience with SAP or ERP systems
  • Familiarity with CAD tools, preferably NX, Creo, SolidWorks
  • Ability to read mechanical drawings and understand GD&T symbols and tolerances
  • Comfortable navigating quality management systems within a medical device manufacturing facility
  • Experience with change management tools
  • Knowledge of cost reduction and productivity improvement techniques
  • Experience with cost reduction, Design for Manufacturing (DFM) and Failure Mode and Effects Analysis (FMEA) methodologies
  • Ability to walk and stand for extended periods
  • Ability to lift up to 30 pounds
  • Must be able to work immediately and in the future without Visa Sponsorship; Carestream is not offering sponsorship

Benefits

Comp & perks
  • Relocation assistance may be considered for candidates outside the Rochester area
  • Reasonable accommodations for individuals with disabilities during the application process