Jobs · Engineering · Wisconsin

Engineer, Manufacturing

Experis · Madison, WI · 3 wk ago
On-siteEngineering$35–$41/hrContract

About the role

Manufacturing Engineer position located in Madison, WI (100% onsite) for a 12‑month contract. Shift is 8 am to 5 pm.

Responsibilities

  • Create SolidWorks designs and drawing files for new and existing products.
  • Create assembly files with complete Bill of Materials.
  • Create drawing files using correct tolerances, including GD&T.
  • Support the PLM Vault system and product lifecycle management requirements.
  • Help develop and create assembly procedures for new or modified designs.
  • Work with external vendors to have prototype parts quoted and ordered as needed.
  • Support the assembly, testing, and documentation of designs.
  • Lead or support Design Reviews, First Article Inspection Reports, and non‑conformance investigations as needed.
  • Support part and assembly documentation requirements for manufacturing and quality systems in accordance with FDA, GMP, ISO, CAP, CLIA requirements.
  • Apply defined procedures to execute and document changes to existing equipment.
  • Create, document, and execute protocols to support process or part changes.
  • Investigate problems, gather facts, analyze data, and draw accurate conclusions.
  • Troubleshoot and repair equipment.
  • Support failure analysis investigations, identify root cause analysis with support from more experienced team members, and develop solutions to resolve quality issues.
  • Support the building and testing of custom equipment.
  • Provide manufacturing support for the repair center.
  • Apply technical knowledge to identify opportunities and recommend improvements to existing equipment and processes.
  • Develop implementation plans and execute assigned tasks.
  • Lead less complex improvement projects.
  • Manage time and competing priorities with minimal guidance from leadership.
  • Communicate project status and resource needs; prepare and present reports.
  • Follow procedures and maintain detailed records in accordance with FDA, ISO, CAP, CLIA requirements.
  • Ability to work independently

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