Mammotome associates know that every moment matters when it comes to advancing breast cancer diagnostics and surgical solutions. When you come to work at Mammotome, you’re collaborating with a global team of engineers, designers, communicators, strategists, and specialists to improve patient outcomes. If you want to be inspired to grow every day, join our diverse, hardworking, high-performing team. Be part of a company that’s a trusted leader in breast cancer diagnostics and support products you can feel passionate about! Mammotome is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we’re working at the pace of change to improve patient lives with diagnostic tools that address the world’s biggest health challenges. The Quality Engineering Co-op is responsible for supporting Design Assurance Quality Engineers with product improvement through implementation of quality management policies, procedures, specifications, test methods and measurement systems and working on compliance programs as it relates to new and existing products. T his position is part of the Quality Engineering and Regulatory Compliance department located in Cincinnati, OH and will be onsite. At Mammotome, our passion is driving innovative technologies that create efficiencies, while never forgetting that at the heart of every breast cancer journey is a patient. You will be a part of the Quality Engineering and Regulatory Compliance function and report to the Senior Manager, Design Assurance in Quality and Regulatory Compliance responsible for the execution and implementation activities for New Product Development, VAVE, and Sustaining Engineering projects. This team is responsible for compliance programs as it relates to new and existing products. If you thrive in a multifunctional, fast paced role and want to work to build a world-class organization—read on. In this role, you will have the opportunity to : + Re-evaluate risk levels, risk acceptance, and state of the art assessments based on Post Market Surveillance data and provide support for risk management plans, reports, and utilize risk management tools such as FMEAs for NPD, VAVE, and Sustaining projects. + Apply design controls and development processes to existing products. + Assist Supplier Quality with periodic review of supplier files and maintenance of the Approved Supplier List. + Support Regulatory compliance through assistance with documentation of Clinical Evaluations, Audit preparation, RegDesk and product registrations, as needed. + Participate in and assist with the coordination of elements of investigations regarding customer complaints. The essential requirements of the job include: + Matriculated student working toward a Bachelor’s degree (BS) in a technical field (Biomedical Engineering, Bio engineering, Mechanical Engineering, Material Science or related field equivalent) required. + Minimum GPA 3.0 within curriculum is required. + Co-Op Term commitment: January 2025 - May 2025. It would be a plus if you also possess previous experience in: + Previous Co-op experience in an engineering and/or quality assurance and regulatory function is strongly preferred. + Experience in medical device is preferred. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com . Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here (https://www.dol.gov/agencies/ofccp/posters) . We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.