Controls Engineer

Exact Sciences • Madison, WI

5d • Onsite

About The Position

At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. The Controls Engineer/Senior Controls Engineer collaborates with internal and external partners to procure, install, commission, maintain, and optimize equipment and process control systems that support reagent manufacturing, material handling, and molecular diagnostic testing. This role is responsible for supporting and improving hardware and software control systems through activities such as system architecture and equipment design support, process control strategy development, troubleshooting, configuration management, performance monitoring, programming modifications, and operational support. Depending on level, the individual will contribute to or lead technical initiatives, partner with maintenance and metrology teams on repair and service activities, and drive continuous improvement efforts across Exact Sciences and Exact Sciences Laboratories. We are open to hiring at either the Engineer or Senior Engineer level depending on candidate experience.

Requirements

• Bachelor’s Degree in Engineering or field as outlined in the essential duties; or High School Diploma (GED) and 4 years of relevant experience as outlined in the essential duties.
• 3+ years of experience as a controls engineer.
• Proficient in Microsoft Office programs, such as: Word, Excel, PowerPoint, and Outlook.
• Demonstrated ability to perform the essential duties of the position with or without accommodation.
• Authorization to work in the United States without sponsorship.

Nice To Haves

• Experience with AVEVA InTouch and System Platform.
• 5+ years of experience as a controls engineer in a regulated environment.
• 3+ years of experience managing and executing projects of various sizes and scopes and communicating to cross functional stakeholders.
• Experience working in a cGMP/ISO 13485 compliant manufacturing environment.
• Experience leading cross functional and multi-site projects.
• Operational knowledge of industrial networking.
• Experience with Rockwell Automation systems.
• Familiarity with AutoCAD.

Responsibilities

• Conceive, specify, procure, and implement control system installation and modifications to support new manufacturing solutions, process automation, system integration, and monitoring, clinical laboratory test procedure automation, volume growth, and new product introduction based on stakeholder input and collaboration with internal and external partners.
• Support existing control system installations; including, but not limited to, hands-on troubleshooting, system set up and adjustment, integration of new equipment, repair, planned maintenance, and performance monitoring.
• Lead projects to analyze, troubleshoot, and improve systems, such as environmental monitoring, automated batch production in a cGMP environment, and clinical laboratory diagnostic sample testing automation in a CAP/CLIA environment, with guidance from senior team members and leadership.
• Use engineering knowledge to assist in the consolidation of project requirements and data for interface with functional specialist on cross-functional teams, to ensure stakeholder understanding of trade-offs amongst cost, schedule, quality, and risk.
• Participate in all aspects of project delivery from inception to turnover in accordance with accepted project management principles and internal engineering practices.
• Develop and maintain documentation, such as standard operating procedures, engineering standards, user requirements, design specifications, component specifications, and commissioning protocols, to ensure consistent, high-quality projects.
• Provide technical support, ensuring appropriate change control practices are followed.
• Lead or participate in investigations and troubleshooting of control systems and manufacturing processes associated with internal review, CAPA, audits, or complaints.
• 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.
• Maintain regular and reliable attendance.
• Ability to act with an inclusion mindset and model these behaviors for the organization.
• Ability to work designated schedule.

Benefits

• paid time off (including days for vacation, holidays, volunteering, and personal time)
• paid leave for parents and caregivers
• a retirement savings plan
• wellness support
• health benefits including medical, prescription drug, dental, and vision coverage

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED