Engineer Sr, Manufacturing / Sr. Equipment and Automation Engineer

Please Contact: To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Priyanka Mahant at email address Priyanka.mahant can be reached on # .

We have Contract role Engineer Sr, Manufacturing / Sr. Equipment and Automation Engineer for client at Madison WI. Please let me know if you or any of your friends would be interested in this position.

Position Details:

Engineer Sr, Manufacturing / Sr. Equipment and Automation Engineer- Madison WI

Location     : Madison WI 53719 (On-site)

Project Duration: 12 Months of contract

Shift              : 8:00 AM - 4:00 PM (Mon-Fri)

Pay Rate     : $52.00 per hour on W2

Position Overview:

·         Our Mission at Exact Sciences 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 Sr. Equipment and Automation Engineer, within the Corporate Operations department, is primarily responsible for leading design transfer efforts of new equipment from R&D, working with integrators to develop new machines for supporting production requirements, and provide manufacturing support for existing equipment.

·         This position will participate in a variety of engineering design functions, provide technical guidance to the production teams, 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 Exact Sciences.

·         This is an ideal role for a hands-on Electrical Controls 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:

·         Support internal automation machines using Allen Bradley controls.

·         Make software updates to support troubleshooting, improvement projects, and quality improvements.

·         Integrate machine software with cloud networking for Process Monitoring, dashboard creation and tracking metrics.

·         Lead or support new product introductions, design transfers, and product changes.

·         Create documentation records per regulatory and quality requirements.

·         Develop processes and procedures for new equipment.

·         Apply defined procedures to execute and document changes to existing equipment.

·         Identify, create, document, and execute protocols to support process or part changes.

·         Define improvement opportunities, investigate issues, gather facts, analyze data, and draw accurate data-driven conclusions.

·         Troubleshoot and repair equipment.

·         Lead failure analysis investigations, identify root cause analysis, and develop solutions to resolve quality issues in a timely manner.

·         Lead or support product non-conforming material reports, corrective and preventative actions, investigations, audits, or complaints.  Document in accordance with applicable regulatory requirements.

·         Provide subject matter expertise for custom equipment and processes.

·         Lead or support new product introductions, design transfers, and product changes.

·         Create documentation records per regulatory and quality requirements.

·         Lead continuous improvement projects.

·         Support the building and testing of custom equipment.

·         Provide manufacturing support for the repair center.

·         Identify opportunities, analyze data, and work with cross functional teams to implement solutions that improve production quality, capability, reliability, or reduce costs.

·         Develop project plans, delegate effectively, and execute assigned tasks.

·         Prioritize assignments and work independently with minimal guidance from leadership.

·         Provide clear and concise documentation and communication of project needs, scope, budget, and status to peers and leadership.

·         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 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 between Exact Sciences sites located in Madison, WI.

·         Other duties as assigned.

Minimum Qualifications:

·         Bachelor’s degree in Engineering with 5+ years of experience; or, in lieu of Bachelor's degree, Associates degree in Engineering, Technology, Electronics, or similar field with 7+ years of experience.

·         Effectively applies Engineering skills to complete assignments.

·         Demonstrated ability to identify opportunities for improvement, clearly define project scope, and complete projects on time and on budget.

·         Demonstrated ability to plan projects, balance multiple competing priority projects, and drove projects to successful completion.

·         Authorization to work in the United States without sponsorship.

·         Demonstrated ability to perform the Essential Duties of the position with or without accommodation.

Preferred Qualifications

·         5+ years of experience in engineering or relevant life sciences / medical device industry.

·         5+ years of experience working in manufacturing or engineering environments applying problem solving skills (e.g., Six Sigma, probability and statistics) and process improvement (e.g. Lean).

·         5+ years of experience working in an FDA/cGMP/CAP/CLIA regulated production environment.

·         5+ years of experience working with Electronic Quality Management Systems and Manufacturing Software Systems.

·         2+ years of experience managing projects.

To discuss this amazing opportunity, reach out to our Talent Acquisition Specialist Priyanka Mahant at email address Priyanka.mahant can be reached on # .