Senior Development Engineer, INTO - Raritan New Jersey

Company: Disability Solutions
Location: Raritan, New Jersey
Posted On: 05/03/2024

At J&J, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat, and cure disease inspires us. We bring together the best minds and pursue the most promising science. We collaborate with the world for the health of everyone in it. Interventional Oncology (INTO), a cross-sector research and development group, is charged by the Executive Committee of J&J with meaningfully altering the course of cancer. Johnson & Johnson's Interventional Oncology is recruiting for a Senior Development Engineer. This position can be located in Raynham, Cambridge, or Boston, Massachusetts; Raritan, New Jersey; Cincinnati, Ohio; Spring House, PA. Remote locations within the US may be considered on a case-by-case basis and if approved by the company. The Senior Development Engineer will be responsible for supporting technical efforts for the INTO Engineering Sciences team. They will support technical aspects of the solution strategy for projects within one or more programs, each of which will focus on medical device technology but could also include a molecular entity, a drug/device combination, digital and electromechanical solutions, or other combinations of products necessary to deliver against the agreed-upon Target Product Profile (TPP) for cancer treatment. They will work with multi-functional teams to develop solutions in a timely and efficient manner. They will provide technical feedback, ensuring delivery of new products by serving as a technical enabler for cross-sector initiatives. The Senior Development Engineer will collaborate with internal business partners to help shape, develop, and execute projects (including development of TPP) as well as leverage external partnerships to drive growth of the business. Responsibilities:

• Deliver projects concerned with critical healthcare challenges, involving exploration of subject area, generation of novel concepts, and diligence on external technologies, including execution of in-vitro or in-vivo experiments as needed
• Lead technical product development of programs through charter, including gathering voice-of-customer, identification of specifications, requirements management, risk management, testing and evaluation, and generating evidence to support regulatory submissions
• Engage appropriate team members, including external academic and industry partners, to address technical challenges and risks
• Assist with the identification of external new technologies, products and capabilities aligned to business strategy and priorities
• Author technical reports and lead activities to strategically build and protect intellectual property associated with inventive output
• Partner with multi-functional team to support transaction activities (including licensing, partnerships, co-development, preclinical or clinical evaluations)
• Deliver oral and written presentations in support of approval for execution and funding of existing pipeline projects as well as new opportunities
• Maintain strong connections with J&J sector colleagues, as well as J&J Legal, Finance, HCC, Regulatory, Clinical, Quality, and other functional groups to support, review, and execute product development projects
• Build external relationships via trade shows, conferences, networking, and other new sources of information, intelligence, and insights
• Build knowledge of targeted disease states and procedural approaches through direct observation and primary and secondary research More...

      

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