NPD ENGINEER I

Biosense Webster is recruiting for an NPD Engineer I located in Irvine, CA! At Biosense Webster, Inc.
we have one goal — to ensure those with cardiac arrhythmias can live the lives they want.
This means transforming the latest advancements in electrophysiology into a suite of tools that empowers physicians with a range of treatments for the best outcomes! Quality products and approaches are achievable only through collaboration with the smartest minds in electrophysiology.
For more than 30 years, we’ve been the global market leader in the science and technology of cardiac arrhythmia treatment, working with thousands of electrophysiologists to identify and develop diagnostic and treatment tools.
And through onsite training, online courses and our global education centers, we work together to set new standards every day.
Learn more about Biosense Webster at www.
iosensewebster.
om and follow us on LinkedIn.
Are you interested in making a difference in a thriving diverse company culture, that celebrates the uniqueness of our employees and is committed to inclusion Apply today! Key Responsibilities.
Develop and apply key problem-solving abilities to identify and resolve basic-to-complex issues in critical production processes, helping the company run more efficiently.
Perform engineering analysis and testing of new product designs, assembly and test processes Develop tools, jigs and fixtures for test and assembly of our ground-breaking arrhythmia catheters Create preliminary sketches of design concepts Create technical 2D drawings for mechanical components per ASME Y14.
or electrical schematics per IEEE Perform measurements and analysis, build engineering samples, develop and complete engineering testing Design DOEs, write test protocols (e.
., characterization, benchtop, V&V, pre-clinical), implement testing and generate engineering test reports Support technical reviews (design reviews, technical assessments) Responsible for communicating business related issues or opportunities to next management level Identifies, designs and develops vital equipment related to new product assembly and testing process Performs equipment verification and validation Studies the existing processes to implement improvements on new products Responsible for creating and establishing equipment specifications Assists technicians and engineers about unusual problems to find root cause and a mitigation to the problem Responsible for procuring and designing equipment that meets safety and environment requirements Performs activities of process/product validation Performs statistical analysis using Minitab or similar software Can supervise, coordinate, and technically revise the work of a limited group of technicians.
Responsible for following 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 Carries out ad-hoc tasks as the need arises Qualifications Qualifications Education.
A minimum of Bachelor’s degree is required in the fields of.
Engineering, Mechatronics or Mechanical Engineering are preferred Experience and Skills.
Required.
Knowledge of good manufacturing practices and documentation, preferably in the medical industry Ability to participate in a technical team Strong management of statistical procedures Knowledge of computer programs Proficiency in the creation and interpretation of 2-D technical drawings using ASME Y14.
and IEEE standard s Experience in writing technical test and validation reports Preferred.
Preferably knowledge or experience in the medical industry Ability to use PLC programming such as Rs Logix, CCW will be considered a plus Ability to output electrical diagrams will be considered a plus Ability to use CAD software such as SolidWorks will be considered a plus Ability to perform statistical analyses Other.
Oral and written communication in Spanish and English, preferably The anticipated base pay range for this position is $ to $ The Company maintains highly competitive, performance-based compensation programs.
Under current guidelines, this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan.
The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporation’s performance over a calendar/ performance year.
Bonuses are awarded at the Company’s discretion on an individual basis.
Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, pension plan, disability plan, vacation pay, sick time, holiday pay, and work, personal and family time off in accordance with the terms of the applicable plans.
Additional information can be found through the link below.
For additional general information on company benefits, please go to.
https://www.
areers.
nj.
om/employee-benefits This job posting is anticipated to close on April 19th, The Company may however extend this time-period, in which case the posting will remain available on https://www.
areers.
nj.
om to accept additional Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.
areers.
nj.
om.