Staff Device Lifecycle Engineer

Small Molecules Packaging & Device Team, within MSAT organization of the Janssen Supply Chain of Johnson & Joshnson Innovative Medicine, is recruiting for a Staff Device Lifecycle Engineer. This position is located in Beerse, Belgium. Alternative locations may be considered in Titusville, NJ; Horsham, PA; Malvern, PA; Spring House, PA; and Gurabo, PR.

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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/.

Are you interested in joining a global and diverse team that is helping improve patient care and drive innovation? At Johnson & Johnson, we blend heart, science, and ingenuity to profoundly change the trajectory of health for humanity. Apply today for this exciting opening!

Device and Packaging solutions are becoming an increasingly meaningful component in delivering innovative medicines to our patients. The Staff Device Lifecycle Engineer will be working in a multi-functional setting, responsible for the ongoing lifecycle engineering and technical support for the device constituent for combination products in the JSC network. They will lead and support product and process quality improvement and reliability projects, and be the key point of contact to site and external operations, suppliers and quality for their area of responsibility.

Key Responsibilities:

• Device lifecycle engineering including process engineering, product engineering and support to site or external manufacturing network as necessary.

• Viewed as a device design owner for one or more products in the JSC portfolio. Conduct design controls post-launch, maintain design history file.

• Provide technical aspects of capacity scale-up to support global demand for the product lifecycle. Qualify additional capacity for sub-assembly and assembly processes per manufacturing network strategies

• Develop and qualify additional supplier capacity (multi-cavitation for plastic molded components, other process technologies as necessary) per quality systems requirements.

• Support assembly sites in solving technical issues as vital.

• Lead design change controls for devices. Perform technical assessments on combination product change controls.

• Lead or support projects as necessary to address issues with customer satisfaction, quality, manufacturing improvements and cost reductions.

• Provide audit support where required

• Lead or contribute to the improvement of processes and quality systems in support of combination products and the device constituents of combination products.