Job at a glance
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Mammotome, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
At Mammotome, our expertise and compassion for breast care makes us the indispensable partner to physicians, clinicians and patients. Our drive for developing innovative technology is rivaled only by our compassion for the people we serve, from the clinicians and surgeons who demand consistently precise solutions, to the patients and families seeking peace of mind. When you join our company, you join in the fight against breast cancer.
Working at Mammotome means you will have the opportunity to collaborate with a diverse, hardworking, high-performing team committed to improving patient outcomes. As a trusted leader in breast cancer diagnostics, we invite you to join us and support products you can feel passionate about! Learn about the Danaher Business System which makes everything possible. The Staff Development Engineer is responsible for leading complex medical device development and manufacturing initiatives from concept through sustaining.
The role solves advanced technical challenges, leads cross-functional projects, and recommends best practices that improve products, processes, and services. This position reports to the Director, Engineering and is part of the Engineering team located in Cincinnati, Ohio and will be an on-site role. In this role, you will have the opportunity to : Lead device development and strategic engineering initiatives in collaboration with suppliers, manufacturing engineers, design engineers, and other cross-functional stakeholders.
Lead advanced design for manufacturing and assembly analyses and work with the design team to incorporate findings into product concepts. Qualify complex components, manufacturing processes, and assembly systems using appropriate validation methodologies and support design reviews to mitigate potential risks. Lead product and process improvement initiatives, develop engineering standards and best practices, and perform structured problem solving to address complex technical challenges.
Influence product strategy, technology roadmaps, and business planning activities while providing technical leadership, mentorship, and engineering expertise across the organization. The essential requirements of the job include: Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a technical discipline. Demonstrated progression of engineering experience in product development, manufacturing, or related technical disciplines.
Preferred candidates will possess 10 or more years of relevant engineering experience, including 6 or more years supporting product development and manufacturing activities. Experience developing products within regulated or highly technical industries and applying quality and regulatory requirements throughout the product lifecycle. Prior experience in medical device development, including design for manufacturability and regulatory compliance, is preferred.
Demonstrated experience leading technical initiatives, engineering projects, or cross-functional teams and solving complex technical challenges. Experience leading design, development, validation, and product lifecycle activities within a regulated or highly technical environment, including application of structured problem-solving and engineering project management methodologies. Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel up to 30% domestically and internationally; typical assignments may require overnight, out-of-town stays of 2