Job description

Our Client, a Medical Device and Healthcare company, is looking for an Equipment and Automation Engineer 2 for their Madison WI location. Responsibilities: • Create Solid works 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 the part and assembly documentation requirements for the 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 and as part of a team within a matrix organization. • Uphold company mission and values through accountability, innovation, integrity, quality, and teamwork. • Support and comply with the company’s Quality Management System policies and procedures. • Ability to work designated schedule. • Ability to lift up to 50 pounds as needed • Ability to work in front of a computer screen and/or perform typing for approximately 80% of a typical working day. • Ability to comply with all applicable personal protective equipment requirements. • Other duties as assigned. Requirements: • Bachelor’s degree in Engineering with 2+ years of experience; or, in lieu of Bachelor's degree, Associates degree in Engineering, Technology, Electronics, or similar field with 4+ years of experience. • Prior experience with Solidworks designs, drawing creation and BOM managment. • Demonstrated ability to drive project to successful completion. • Demonstrated ability to perform the Essential Duties of the position with or without accommodation. • Preferred Qualifications • 2+ years of experience in engineering or relevant life sciences / medical device industry. • 2+ years of experience working in manufacturing or engineering environments applying problem solving skills and process improvements. Why Should You Apply? • Health Benefits • Referral Program • Excellent growth and advancement opportunities

Requirements

Must-haves

Our Client, a Medical Device and Healthcare company, is looking for an Equipment and Automation Engineer 2 for their Madison WI location.
Create Solid works 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 the part and assembly documentation requirements for the 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.

Nice-to-haves

Why Should You Apply?
Referral Program
Excellent growth and advancement opportunities

Application prep

Use the role’s language and application details while tailoring your materials.

Platform: jobdiva
Effort: medium