Medical Device Engineering Technician – Process & Quality

Carestream Health

Town of Greece (NY)

On-site

USD 48,000 - 58,000

Full time

14 days+
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Job summary

Carestream Health is seeking an Engineering Technician to provide technical support to the Engineering and Manufacturing teams in a regulated electromechanical medical device assembly environment. You will assist with manufacturing builds, process improvements, validation, troubleshooting, and production readiness, ensuring quality and compliance.

The role requires strong analytical and hands-on skills, fielding limited travel, and adherence to GDP and quality systems, including ISO 13485,

Qualifications

  • High school diploma or equivalent with 4+ years production/engineering technician experience, or an Associate's degree in STEM with 1+ years of experience.
  • Proficient in Microsoft Office applications (Excel, Word, Outlook, Teams).
  • Ability to troubleshoot electromechanical assemblies and identify root causes using structured problem-solving methods.
  • Understanding of GDP and document control requirements.

Responsibilities

  • Follow engineering direction to perform hands-on evaluation, repair, rework, and modification of electromechanical assemblies.
  • Execute engineering test plans and collect data to support verification and validation activities.
  • Collaborate with production lines to understand processes and enable troubleshooting and continuous improvement.
  • Assist with product/process development, including manufacturing transfers and new product introductions.
  • Create and maintain SOPs and train operators on procedures.
  • Support IQ/OQ/PQ validation, data collection, and CAPA activities.

Skills

MS Office
Root cause analysis
GDP knowledge
Troubleshooting
Data collection

Education

High school diploma + 4+ years manufacturing experience
Associate's degree in STEM

Tools

ERP systems (SAP)

Job description

Carestream Health is seeking an Engineering Technician to provide technical support to the Engineering and Manufacturing teams in a regulated electromechanical medical device assembly environment. You will assist with manufacturing builds, process improvements, validation, troubleshooting, and production readiness, ensuring quality and compliance.

The role requires strong analytical and hands-on skills, fielding limited travel, and adherence to GDP and quality systems, including ISO 13485,

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