.At Johnson & Johnson, the largest healthcare company in the world, we come together for one purpose: to transform the history of health in humanity.Diversity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest healthcare company in the world.When You Join Johnson & Johnson, Your Move Could Mean Our Next Breakthrough.At Johnson & Johnson Medical Devices Companies, we are using our breadth, scale, and experience to reimagine the way healthcare is delivered and to help people live longer, healthier lives.In a radically changing environment, we are making connections across science and technology to combine our own expertise in surgery, orthopedics, and interventional solutions with the big ideas of others to design and deliver doctor and patient-centric products and solutions.We are in this for life.We are changing the trajectory of human health, YOU CAN TOO.**COMPANY**: Biosense WebsterWe are searching for the best talent for a **STAFF NEW PRODUCT INTEGRATION ENGINEER** to be located in **Juárez, México.****Purpose**:Responsible for research and development activities in support of new medical device technologies and preparing them for the market.**Duties & Responsabilities**:- Design and development activities as assigned by engineering management- Sourcing of parts and components from existing and new vendors- Developing ideas into marketable products.- Interfacing with physicians to ensure that developed products meet requirements- Development and execution of protocols to verify and validate designs- Directing the work of R&D technicians performing essential research and development activities.- Interfaces with quality and manufacturing engineering functions within the company to ensure that designs meet quality objectives and long-term requirements- Documentation of development activities- Performs other related duties and tasks, as needed.- Responsible for communicating business related issues or opportunities to next management level- Responsible for ensuring subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures- Performs other duties assigned as needed**Qualifications** Qualifications**:- An engineering degree in a related engineering discipline.- General knowledge of the medical device industry.- Familiarity with quality and regulatory systems including FDA's Quality System Regulation, ISO13485, etc
