Senior Reliability Engineer

Waukesha, WI - USA

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

The job posting is outdated and position may be filled

Job Summary

Job Description Summary

The Senior Reliability engineer will be an integral part of the central DFR (Design for Reliability) program team within the STO org partnering with GEHC modality engineers reliability leaders and external vendors (ASQ etc.) to support the development and deployment of the standard GEHC DFR methodology applying relevant reliability concepts processes standards and tools. Activities include providing Sub Matter Expertise (SME) in assessing and quantifying tech (reliability) risks in New Product Introduction (NPI) as well as existing IB. Focusing on preventative measures while providing tech support (in areas like root cause analysis test protocols FMEAs V&V etc.) to product engineers to address recurring quality/reliability failures is key. Creating and managing effective dashboards to show overall DFR status highlighting progress around reliability planning and execution on several key programs/project milestones including technical design reviews will be critical.

Job Description

Roles and Responsibilities

Collect and analyze reliability data (field performance data service costs complaints data etc.) to identify quality/reliability trends and explore opportunities for improvement in current IB or in new product designs (NPIs).
Lead /Participate to support product engineers on RCA (Root Cause Analysis) and FMEA activities to facilitate design analysis and brainstorming of key failure modes.
Drive root cause analysis with an emphasis on identifying physics of failure. Develop and execute reliability testing protocols including accelerated life testing environmental testing and stress testing to assure products meet project objectives on time.
Create reliability test strategies and estimate resources to meet project or product goals. Guide engineers through creation and execution of reliability plans -especially around new product designs
Provide troubleshooting and CAPA expertise/assistance for unusual or persistent product problems thru the application of suitable L6S (Lean Six Sigma) tools & methodologies Ensure reliability testing and documentation meet all relevant internal and external standards and is consistent with guidelines for medical devices to assure regulatory compliance (FDA IEC 60601 etc.)
Effectively communicate to Quality Supply chain and Engineering teams regarding application and use of reliability processes strategies and tools.
Coach and train the next generation of GEHC product engineers on DFR methodology - concepts processes standards and tools.

Required Qualifications

Bachelors degree in engineering or STEM discipline.
Certified Reliability Engineer (CRE-ASQ) or a Masters Degree in Reliability Engineering.
4 of reliability engineering experience in a highly regulated manufacturing/process-oriented industry
Proficiency in reliability analysis tools and software (e.g. Weibull ReliaSoft etc.) and familiarity with medical device standards (e.g. ISO 13485 FDA regulations).
Proven ability to develop timely and effective technical solutions for challenging design/engineering problems.
Subject matter expert in Reliability Engineering concepts and tools
Working knowledge of product development processes and product qualification steps
Prior Program or Project management experience (Agile methodology etc.)
Ability to create long lasting relationships with stakeholders building trust through effective communication and strong interpersonal connections.
Strong influencing skills to manage change/conflicts/unforeseen events.
Strong technical aptitude including applicable engineering tools and systems.

Desired Characteristics

Six Sigma black belt certification
Masters degree in engineering or STEM discipline
Experience working in a highly regulated industry preferably with time spent directly in product design development certification testing verification & validation activities.
Knowledge of medical device regulations test standards
Familiarity with the broad GEHC product portfolio and demonstrated cross-functional and multi-product knowledge.
Proven ability to work cross-functionally and with global virtual teams.
Passion for people development and willingness to take risks.
Proven mentoring and coaching abilities; demonstrated ability to motivate & inspire others.
Demonstrated ability to deliver results while working on multiple projects simultaneously balancing resources timing and quality of outcomes.

Additional Information

GE HealthCare offers a great work environment professional development challenging careers and competitive compensation. GE HealthCare is anEqual Opportunity Employer . Employment decisions are made without regard to race color religion national or ethnic origin sex sexual orientation gender identity or expression age disability protected veteran status or other characteristics protected by law.

GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19 some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.

Relocation Assistance Provided: No

Required Experience:

Senior IC

Job Description SummaryThe Senior Reliability engineer will be an integral part of the central DFR (Design for Reliability) program team within the STO org partnering with GEHC modality engineers reliability leaders and external vendors (ASQ etc.) to support the development and deployment of the sta...

Job Description Summary

Job Description

Roles and Responsibilities

Collect and analyze reliability data (field performance data service costs complaints data etc.) to identify quality/reliability trends and explore opportunities for improvement in current IB or in new product designs (NPIs).
Lead /Participate to support product engineers on RCA (Root Cause Analysis) and FMEA activities to facilitate design analysis and brainstorming of key failure modes.
Drive root cause analysis with an emphasis on identifying physics of failure. Develop and execute reliability testing protocols including accelerated life testing environmental testing and stress testing to assure products meet project objectives on time.
Create reliability test strategies and estimate resources to meet project or product goals. Guide engineers through creation and execution of reliability plans -especially around new product designs
Provide troubleshooting and CAPA expertise/assistance for unusual or persistent product problems thru the application of suitable L6S (Lean Six Sigma) tools & methodologies Ensure reliability testing and documentation meet all relevant internal and external standards and is consistent with guidelines for medical devices to assure regulatory compliance (FDA IEC 60601 etc.)
Effectively communicate to Quality Supply chain and Engineering teams regarding application and use of reliability processes strategies and tools.
Coach and train the next generation of GEHC product engineers on DFR methodology - concepts processes standards and tools.

Required Qualifications

Bachelors degree in engineering or STEM discipline.
Certified Reliability Engineer (CRE-ASQ) or a Masters Degree in Reliability Engineering.
4 of reliability engineering experience in a highly regulated manufacturing/process-oriented industry
Proficiency in reliability analysis tools and software (e.g. Weibull ReliaSoft etc.) and familiarity with medical device standards (e.g. ISO 13485 FDA regulations).
Proven ability to develop timely and effective technical solutions for challenging design/engineering problems.
Subject matter expert in Reliability Engineering concepts and tools
Working knowledge of product development processes and product qualification steps
Prior Program or Project management experience (Agile methodology etc.)
Ability to create long lasting relationships with stakeholders building trust through effective communication and strong interpersonal connections.
Strong influencing skills to manage change/conflicts/unforeseen events.
Strong technical aptitude including applicable engineering tools and systems.

Desired Characteristics

Six Sigma black belt certification
Masters degree in engineering or STEM discipline
Experience working in a highly regulated industry preferably with time spent directly in product design development certification testing verification & validation activities.
Knowledge of medical device regulations test standards
Familiarity with the broad GEHC product portfolio and demonstrated cross-functional and multi-product knowledge.
Proven ability to work cross-functionally and with global virtual teams.
Passion for people development and willingness to take risks.
Proven mentoring and coaching abilities; demonstrated ability to motivate & inspire others.
Demonstrated ability to deliver results while working on multiple projects simultaneously balancing resources timing and quality of outcomes.