Equipment/Automation Engineer I

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries

Position Overview Our Mission at Abbott Cancer Diagnostics is to eradicate cancer and the suffering it causes – through tests that help prevent it, detection that finds it earlier, and guidance for its successful treatment. Come join our team and make a difference in other people’s lives.

The Equipment/Automation Engineer I, within the corporate operations department, is primarily responsible for manufacturing support for existing equipment, and helping to launch new equipment into Production. This position will participate in a variety of engineering design functions, provide technical guidance to the production teams, triage failures, manage improvements, and ensure our machines are properly supported throughout their life.

This position will work cross functionally with multiple departments to ensure that the business objectives and our customer needs are met. This position supports a collaborative environment that promotes positive teamwork where all members are working for the good of Abbott Cancer Diagnostics.

This is an ideal role for a hands-on engineer with good communication skills looking to make an impact in the fight against cancer. Essential Duties Include but are not limited to the following: Develop process and procedures for building new equipment.

Apply defined procedures to execute and document changes to existing equipment. Investigate problems, gather facts, analyze data, and draw accurate conclusions. Assist with troubleshooting and repairing equipment. Support investigation of Non-Conforming Materials Reports to resolve quality issues.

Support the building and testing of custom equipment. Participate as a team member on more complex improvement projects. Execute assigned tasks; manage time and competing priorities with guidance from leadership. Communicate project status; prepare and present written and oral 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. Regular and reliable attendance. 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. Other duties as assigned