• Salt Lake City, UT
    2 days ago

    Job Description

    Our client is looking for someone to join the manufacturing team supporting engineering and production activities for an active product development program. This position is ideal for an early-career engineer who enjoys hands-on manufacturing support, documentation management, and collaboration with cross-functional teams. Responsibilities include supporting change control activities, maintaining manufacturing and engineering documentation, assisting with investigations and troubleshooting efforts, participating in manufacturing builds, and executing studies designed by senior engineers. The role provides strong mentorship and development opportunities while offering direct exposure to production operations and regulated medical device environments.

    Required Skills:

    • 1-4 years of experience within the medical device industry (Class II or Class III devices).
    • Experience supporting manufacturing, quality, or engineering activities in a regulated environment.
    • Exposure to documentation control, change control processes, manufacturing records, or related engineering documentation.

    Nice to Have:

    • Class III medical device experience.
    • Experience supporting investigations, process studies, or data analysis activities.
    • Hands-on collaboration with manufacturing operators or production teams.
    • Education: Engineering degree required.
    • Support daily manufacturing and production engineering activities.
    • Maintain manufacturing and engineering documentation.
    • Manage engineering change control (ECO/ECN) processes.
    • Support production builds and product development activities.
    • Investigate manufacturing issues and assist with troubleshooting.
    • Collaborate with Manufacturing, Quality, and Engineering teams.
    • Execute process studies and engineering experiments.
    • Analyze manufacturing data and identify process improvements.
    • Support process validation and verification activities.
    • Ensure compliance with medical device manufacturing standards and procedures.
    • Maintain accurate manufacturing records and documentation.
    • Support continuous improvement initiatives to improve product quality and production efficiency.
    • Work closely with manufacturing operators to resolve production challenges.
    • Support investigations, corrective actions, and process optimization.
    • Assist senior engineers with engineering projects and technical activities.

    Numbers & Facts

    LocationSalt Lake City, UT

    Skills

    • Change Controlunmatched
    • Change Managementunmatched
    • Continuous Improvementunmatched
    • Corrective Actionunmatched
    • Cross-Functionalunmatched
    • Data Analysisunmatched
    • Document Managementunmatched
    • Documentationunmatched
    • Engineeringunmatched
    • Engineering Managementunmatched
    • Identify Issuesunmatched
    • Maintain Complianceunmatched
    • Manufacturingunmatched
    • Manufacturing Analysisunmatched
    • Manufacturing Engineeringunmatched
    • Medical Equipmentunmatched
    • Medical Protocolsunmatched
    • Medical Treatmentunmatched
    • Mentoringunmatched
    • Process Developmentunmatched
    • Process Engineeringunmatched
    • Process Improvementunmatched
    • Process Manufacturingunmatched
    • Process Validationunmatched
    • Product Developmentunmatched
    • Product Programsunmatched
    • Production Supportunmatched
    • Quality Engineeringunmatched
    • Quality Managementunmatched
    • Record Keepingunmatched
    • Support Documentationunmatched
    • Technical Supportunmatched
    • Validation Testingunmatched

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