DePuy Synthes, a member of Johnson & Johnson’s Family of Companies, is recruiting an Engineer, Enabling Technologies located Warsaw, IN. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comprehensive orthopaedic business in the world! DePuy Synthes Companies will offer an unparalleled breadth and depth of products, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, craniomaxillofacial, power tools and biomaterials.
Engineer, Enabling Technologies
Work closely with Marketing and our surgeon customers to define user needs
Participate in the full product development lifecycle for digital solutions that range from concept generation, prototype evaluation, development, risk analysis, product verification/validation, and market launch
Work with Project Management colleagues to define timelines for development activities and provide regular updates on the status of those activities
Generate reports and other technical documentation to support the product development process
Present technical information to internal and external partners to facilitate decision-making
Develop an in-depth knowledge of our product lines and detailed knowledge of various musculoskeletal pathologies
Know and follow all applicable laws and policies and maintain the highest level of professionalism, ethics, and compliance at all times
Diligently participate in our compliance program-related activities as denoted by their supervisor or Chief Compliance Officer
Bachelor’s Degree in Biomedical Engineering, Mechanical Engineering, Systems Engineering, Physics, Electrical Engineering, or other relevant technical field.
Demonstrated ability to prioritize tasks and manage a varied workload
Strong communicator in both formal and informal settings
Must have strong analytical and problem-solving skills by applying knowledge of mathematics, science and engineering
Ability to identify, formulate, and solve engineering problems despite imperfect information and resource constraints
This position will be based in Warsaw, IN and may require up to 15% travel, domestic and international.
Proficient in business-related computer applications eg Microsoft Office
Previous co-op or work experience is highly preferred
Experience with medical device regulations as well as GMP (Good Manufacturing Practices), QSR (Quality Systems Regulations) and relevant ISO (International Organization for Standardization) standards
Experience with computer programming including knowledge of flow control, parameter passing, and debugging
Proficiency in higher-level programming and computational tools, eg Python, Matlab
Working knowledge of statistics and hypothesis testing eg t-tests
Exhibits behaviors of a “T-shaped” engineer, where engineering fundamentals are applied (and reapplied) to develop deep expertise to solve specific problems
Experience working in a multidisciplinary team