Equipment/Automation Engineer I
$50,700–$101,300 year
On-siteMadison, Wisconsin, United States
Job Summary
Develop process and procedures for building new equipment, apply defined procedures to execute and document changes to existing equipment, and investigate problems by gathering facts, analyzing data, and drawing accurate conclusions. Assist with troubleshooting and repairing equipment, support investigation of Non-Conforming Materials Reports to resolve quality issues, and support the building and testing of custom equipment. Participate as a team member on complex improvement projects, communicate project status, and prepare written and oral reports while following FDA, ISO, CAP, and CLIA requirements. Execute assigned tasks, manage time and competing priorities, and travel approximately 10% of working time for vendor site visits.
Required Qualifications
- Bachelor's degree in Engineering or related field
- Associates degree in Engineering, Technology, Electronics, or similar field with 2 years of experience
- Basic knowledge of engineering theories, practices and procedures
- Authorization to work in the United States without sponsorship
- Ability to work independently and as part of a team within a matrix organization
- Ability to work designated schedule
- Ability to work nights and/or weekends, as needed
- Ability to work overtime, as needed
- Ability to lift up to 50 pounds for < 5% of a typical working day
- 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
- Ability to travel approximately 10% of working time for occasional training, out of state vendor site visits, and travel between Exact Sciences sites
- Regular and reliable attendance
Desired Qualifications
- Experience in engineering or relevant life sciences / medical device industry
- Experience working in manufacturing or engineering environments applying problem solving skills (e.g., Six Sigma, probability and statistics) and process improvement (e.g. Lean)
- Experience working in an FDA/cGMP/CAP/CLIA regulated production environment
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