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SalaryBiosense Webster, Inc. is recruiting for an Engineer R&D 2 , located in Irvine, CA.
Atrial fibrillation (AFIB) is a quivering or irregular heartbeat (arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-related complications. 20 million people around the world suffer from AFIB each year.
Biosense Webster, Inc. is the global leader in the science of diagnosing and treating heart rhythm disorders. The company established its leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and navigation technology, as well as the first electrophysiology catheter. The introduction of the company’s CARTO® 3 System in 2009 revolutionized 3D mapping technology by increasing the accuracy, speed, and efficiency of the cardiac ablation procedure.
The Research & Development Engineer will be supporting project teams in the development of electrophysiology catheters and systems at Biosense Webster. Project support includes overall design, requirement development, design for manufacturing, test method development, and product verification and validation testing.
Key Responsibilities:
- Support engineering by researching, designing, developing, and testing according to established policies, procedures, government and compliance regulations, and customer requirements.
- Build prototypes and works with the lab to develop test fixtures.
- Perform failure analysis, verification testing and generation of test reports for modules or subsystems.
- Data analysis of various system logs, including generators and Carto 3 system
- Collaborate with multi-functional teams and external vendors
- Expected to assist in the writing of reports, work instructions, test methods and procedures.
- Limited travel to customer sites, domestic and international, to gather VOC, perform testing and/or perform troubleshooting activities.
- Support the design reviews and pre-validation assessments to ensure the safe and environmentally sound processes and designs.
- Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
Qualifications
Qualifications
Required:
- A minimum of a Bachelor’s Degree in Life Sciences, Engineering or closely related degree
- A minimum of 2 years of experience is required
- Experience within the medical device industry OR other highly regulated industry.
- Must possess strong interpersonal and communication skills, written and verbal
- Ability to travel up to 10% domestic and international is required
Preferred:
- Experience with preclinical testing and test method development is highly preferred
- Experience in system integration and system-level testing is highly preferred
- Experience with programming tools such as Python, Java, Matlab, or R
- Knowledge and experience in product development processes
- Experience with statistical analysis and design of experiments (DOE)
- Ability to tackle complex problems
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.careers.jnj.com .
The anticipated base pay range for this position is $70,000- $112,700
This job posting is anticipated to close on 3/27/2024. The Company may however extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.
