Senior Product Development Engineer II

Johnson & Johnson is currently seeking a Senior Product Development Engineer II to join our Abiomed Engineering team based in Danvers, MA.

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.

Learn more at https://www.jnj.com/ .


* Lead early-stage design & process development projects of novel hemodynamic support devices and accessories.


* Lead initiatives with engineers in research, product development, new product introduction and contract manufacturers or OEMs.

Collaborate to deliver designs with margin to performance requirements and demonstrated process capability in scalable manufacturing processes.


* Serve as Subject Matter Expert (SME) across platforms and lifecycle phases from research through sustaining teams


* Conduct voice of the customer and transform clinical observations into new device concepts and requirements


* Generate intellectual property through invention disclosures in pursuit of patients and trade secrets.


* Turn concepts into reality by rapidly prototyping using a variety of fabrication techniques.


* Test and iterate on your designs to develop an optimal solution.


* Bring solutions to market by collaborating with an exceptional cross-functional team.


* Conceptualize, design, prototype, procure, and build components and assemblies for products and testing/manufacturing fixtures.


* Lead the planning and execution of animal and cadaver labs throughout the development cycle.


* Conduct feasibility testing, analyze, and report on test results providing conclusions and recommendations.


* Perform failure investigations in the event of test failures with support from the technical team.



* BS in Mechanical Engineering or directly related scientific discipline.


* 8 years of related experience in medical device, 4 years in manufacturing or new product introduction.


* Strong problem-solving skills and demonstrated experience identifying root cause of device failures.


* Demonstrated ability to execute tasks in a timely manner under minimal supervision.


* Willingness to learn the interventional cardiology space - the devices and the clinical practice.


* Experience applying statistical techniques and analysis.


* Willingness & ability to travel internationally ~5% of the time.

Strongly Preferred Qualifications :


* Experience in FDA Class II and III medical devices.


* Experience in Solidworks 3D modeling, 2D drawing applying GD&T, PDM.

Able to model complex parts and assemblies and conduct basic structu...