Associate Systems Verification Engineer - Simulated Use

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Job Description - Associate Systems Verification Engineer - Simulated Use

Associate Systems Verification Engineer - Simulated Use - 2406191588W

Description

Johnson & Johnson

is currently seeking an

Associate Systems Verification Engineer - Simulated Use

in

Santa Clara, CA

.

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/.

For more than 130 years, diversity, equity & inclusion (DEI) has been a part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Rooted in Our Credo, the values of DEI fuel our pursuit to create a healthier, more equitable world. Our diverse workforce and culture of belonging accelerate innovation to solve the world’s most pressing healthcare challenges.

We know that the success of our business – and our ability to deliver meaningful solutions – depends on how well we understand and meet the diverse needs of the communities we serve. Which is why we foster a culture of inclusion and belonging where all perspectives, abilities and experiences are valued and our people can reach their potential.

At Johnson & Johnson, we all belong.

The

Associate System Verification Engineer - Simulated Use

will own, manage, and develop test equipment and systems for the Johnson & Johnson Surgical Robotics system. The individual should have strong communication skills as they will work closely with engineers from all functional teams; including R&D, systems, quality engineering, and external vendors. The engineer will document the test equipment and systems in accordance with FDA design control processes (21 CFR820.30) and IEC 62304. They will operate the system during clinical labs, troubleshoot and resolve known issues, document novel issues that arise during system use, perform SW installation and smoke testing, and provide complex engineering test support for R&D applications. This is an exciting opportunity for someone with an interest in medical robotics to gain deep technical and industry knowledge, while providing a critical service to the OTTAVA program.

Core Job Responsibilities:

Design and develop test protocols.

Support other engineer in test development.

Execute system stability, reliability, and verification tests, including wet lab tests on excised tissue.

Design, prototype, qualify, and document test fixtures and equipment.

Develop software test scripts (primarily in Python).

Work closely with system, R&D, and quality engineering to ensure equipment meets internal customer needs. Communicate plans to technical and non-technical leadership.

Document issues that arise with the system or responsible subsystem, and resolve by working across hardware, electrical, and software teams.

Maintain the configuration and records of the responsible subsystem used for development and verification.

A pre-identified candidate is being considered for this role. However, all applications will still be considered.

Qualifications

B.S. in Engineering or other applicable technical degree.

At least a year of relevant work experience is required, inclusive of internships or co-op.

Possesses breadth of knowledge across engineering fields (electrical, mechanical, software), with domain expertise in at least one area.

Highly organized; strong project management ability and communication skills.

Proficient in technical writing and good documentation practices

Comfortable working with excised tissue.

Ability to travel up to 10%, international and domestic.

Preferred Qualifications:

Experience in test system design, implementation, manufacturing, and qualification/maintenance.

Medical device or similar regulated industry (e.g. automotive, aerospace) experience.

Experience developing and executing test method validation and equipment qualification.

Robotics or electro-mechanical experience.

Additional Information:

The anticipated pay range for this position is

$70,000 to 112,700

This position is not eligible for overtime.

Employees are eligible for the following time off benefits:

Vacation - up to 120 hours per calendar year

Sick Time - up to 40 hours per calendar year

Holiday Pay, including Floating Holidays - up to 13 days per calendar year

Work, Personal, and Family Time - up to 40 hours per calendar year

For additional general information on Company Benefits, please go to:

_https://www.careers.jnj.com/employee-benefits_

This job posting is anticipated to close on June 18, 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.

A pre-identified candidate is being considered for this role. However, all applications will still be considered.

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

.

Primary Location

NA-US-California-Santa Clara

Organization

Auris Health, Inc. (6267)

Job Function

R&D Software/Systems Engineering

Req ID:

2406191588W
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