Irvine, California, United States · On-site
$87k–$123k/yr
Innovation starts from the heart. At Edwards, we put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structur…
Skills: Python, Databricks, Minitab, Excel, Data Analysis
Irvine, California, United States · On-site
$150k–$165k/yr
Aerospace is at a turning point — costs are rising, supply chains are strained, and old ways of building can’t keep up. At Neon Aero, we’re breaking that mold. We move fast, think big, and combine start-up agility with a…
Skills: Full-cycle Recruiting, Technical Sourcing, Pipeline Management, Greenhouse, LinkedIn Recruiter
Irvine, California, United States · Remote OK
$90k–$140k/yr
Job Title: Vertical Key Account Manager Location(s): Remote- (West Coast preferred) Compensation: $90,000 with up to $140,000 OTE About this position Advantech has an immediate opening within our key account sales team, …
Skills: Account Management, Sales Negotiation, Business Development, Strategic Planning, CRM Software
Irvine, California, United States · Hybrid
Overview Our new global headquarters is conveniently located in Irvine, CA near John Wayne Airport in the Park Place development. For our onsite and hybrid employees you will be able to enjoy amenities such as access to …
Skills: Technical Sales, Solutions Architecture, Systems Engineering, Customer Relationship Management, Technical Presentation
Irvine, California, United States · On-site
About Rivian Rivian is on a mission to keep the world adventurous forever. This goes for the emissions-free Electric Adventure Vehicles we build, and the curious, courageous souls we seek to attract. As a company, we con…
Skills: Thermal Science, CFD Simulation, 1D Simulation, Heat Transfer, Thermodynamics
Irvine, California, United States · On-site
$146k–$201k/yr
WeAreIn for jobs that impact everyone's life. Build the future nobody’s dreamed of yet... are you ready to rethink the impossible? As a [Role Name] in our Research & Development team, you'll have the opportunity to merge…
Skills: Analog Mixed Signal Design, Linear Circuit Design, High Speed Design, Data Converters, ADC/DAC
Irvine, California, United States · Hybrid
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Skills: Java, Spring Boot, Microservices Architecture, AWS, NodeJS
Irvine, California, United States · Hybrid
$104k–$142k/yr
Brown and Caldwell has an exciting opportunity for a Process Mechanical Engineer to help lead major projects and deliver exceptional service to our well-established wastewater/biosolids clients. This position will be res…
Skills: Process Modeling, Data Analysis, Troubleshooting, Problem Solving, Process Performance Evaluation
Irvine, California, United States · Hybrid
$71k–$93k/yr
Langan provides expert land development engineering and environmental consulting services for major developers, renewable energy producers, energy companies, corporations, healthcare systems, colleges/universities, and l…
Skills: Civil Engineering Design, Site Planning, Grading, Stormwater Management, Drainage
Irvine, California, United States · Hybrid
$117k–$171k/yr
Langan provides expert land development engineering and environmental consulting services for major developers, renewable energy producers, energy companies, corporations, healthcare systems, colleges/universities, and l…
Skills: Civil Engineering, Land Development, Project Management, Permitting, Site Layout Design
Irvine, California, United States · Hybrid
$97k–$140k/yr
Langan provides expert land development engineering and environmental consulting services for major developers, renewable energy producers, energy companies, corporations, healthcare systems, colleges/universities, and l…
Skills: Civil Engineering, Land Development, Project Management, Site Layout Design, Grading And Drainage
Irvine, California, United States · On-site
$105k–$125k/yr
Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, he…
Skills: Safety Testing, Product Design, Technical Reporting, Test Planning, Client Communication
Irvine, California, United States · On-site
$221k–$270k/yr
Rise above. Are you ready to take human possibility to a new dimension with us? Supernal is an Advanced Air Mobility (AAM) company that’s developing an electric vertical take-off and landing (eVTOL) vehicle and the groun…
Skills: Mechanical Engineering, Flight Systems Engineering, FAA Certification, Composite Design, Aerospace Engineering
Irvine, California, United States · Hybrid
Overview Exciting client side opportunities in the Irvine, California area for those looking to take the next big step in their career within the Life Sciences industry! PM Group is currently engaged in the delivery of m…
Skills: Project Management, Project Control, Project Engineering, Planning and Scheduling, Procurement
Irvine, California, United States · On-site
$68k–$89k/yr
Langan provides expert land development engineering and environmental consulting services for major developers, renewable energy producers, energy companies, corporations, healthcare systems, colleges/universities, and l…
Skills: Field Investigation, Boring Logging, Sample Collection, Field Testing, Foundation Monitoring
Irvine, California, United States · Hybrid
$68k–$89k/yr
Langan provides expert land development engineering and environmental consulting services for major developers, renewable energy producers, energy companies, corporations, healthcare systems, colleges/universities, and l…
Skills: Civil Engineering Design, Land Development, AutoCAD, Civil 3D, Site Planning
Irvine, California, United States · On-site
$214k–$267k/yr
Position Summary: Lead the design and implementation of advanced AI solutions, primarily utilizing LLMs for natural-language interaction with enterprise data. This Principal Engineer role involves designing and building …
Skills: LLMs, RAG Systems, Python, Vector Databases, Graph Databases
Irvine, California, United States · On-site
$100k–$115k/yr
Previous Pharmaceutical/Biotech experience is mandatory for this role MMR Consulting is an engineering and consulting firm specializing in the pharmaceutical and biotechnology industries. Its services include Engineering…
Skills: Commissioning, Qualification, Validation, cGMP, Project Management
Irvine, California, United States · Hybrid
$75k–$95k/yr
Company Overview At Motorola Solutions, we believe that everything starts with our people. We’re a global close-knit community, united by the relentless pursuit to help keep people safer everywhere. We build and connect …
Skills: Spectrum Analyzers, Multimeters, Signal Generators, RF Testing, Data Network Testing
Irvine, California, United States · On-site
$110k–$176k/yr
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Skills: Finite Element Analysis (FEA), Thermo-mechanical Simulation, Ansys Mechanical, Ansys APDL, Python
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Support the lifecycle management of Class III medical devices by monitoring performance data and automating monitoring tools. Investigate field issues, implement design improvements, and ensure regulatory compliance through rigorous documentation and change control.
Requires a Bachelor's in Engineering/Science with 2 years of experience, or a Master's degree. Proficiency in Python, Databricks, and statistical tools is essential for data-driven device performance analysis.
Innovation starts from the heart. At Edwards, we put patients first. We invest a significant proportion of our revenue towards research and development to drive and develop groundbreaking medical innovations for structural heart disease. As part of our R&D Engineering team, you will work closely with our Quality and Manufacturing teams to develop the latest tools and technologies to address significant, unmet clinical needs that impact patients’ lives around the world.
Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It’s our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
The Engineer II, R&D Sustaining will support lifecycle management of on-market Class III medical devices by investigating field and manufacturing issues, developing automated tools to monitor device performance, implementing design and process improvements, supporting engineering change assessments, and ensuring continued product safety, performance, reliability, manufacturability, and regulatory compliance.
The role is ideal for an engineer who enjoys working across the boundary between device hardware and data systems, with data-driven investigations, cross-functional collaboration, and ownership of product performance after commercial release. The successful candidate will use engineering judgement, data analysis, algorithm development, design control principles, risk management practices, and verification and validation methods to support product improvements, automated monitoring, and high standards of quality and performance.
In this role you will be responsible for:
Product Performance Monitoring and Data Automation: Continuously monitor and assess device performance and quality metrics using device performance data maintained on a data platform. Develop scripts, dashboards, and automated workflows to identify trends, anomalies, and deviations from expected performance, and support timely decisions regarding device calibration, maintenance, or additional technical assessment.
Algorithm Development and Validation: Develop, implement, and validate analytical algorithms, including machine learning techniques where appropriate, to automate device performance monitoring, support root cause investigations, and generate objective evidence for engineering decisions. Ensure scripts, models, and associated outputs are documented, version controlled, verified, and validated in accordance with applicable quality system expectations.
Issue Resolution and Root Cause Investigation: Investigate and resolve device field issues by analyzing product performance data, customer feedback, and failure reports. Define and execute engineering studies and testing to determine root cause and support effective actions to minimize device downtime and customer impact. Collaborate with cross-functional teams to review and support CAPA and NCMR documents.
Design and Process Improvement: Collaborate with cross-functional teams, including R&D and manufacturing, to identify and implement design changes and process improvements that enhance device reliability, performance, and manufacturability.
Design Changes & Change Control: Support design and process changes for on-market medical devices, including design impact assessments, design documentation updates, requirements and specification updates, verification planning, implementation through change control processes, and assessment of potential impacts to labeling and risk.
Documentation and Compliance: Maintain accurate and comprehensive documentation of engineering changes, investigation records, technical reports, test records, risk documentation, and change control documentation. Ensure all activities comply with regulatory requirements and company standards. Collaborate with quality and regulatory to address regulatory requests
Cross-Functional Collaboration: Work closely with manufacturing, quality assurance, regulatory affairs, clinical development, medical affairs, sales, suppliers, and other engineering teams to support product lifecycle management and ensure effective implementation of engineering solutions.
Other Duties: Perform other duties as assigned
Bachelor's Degree in Engineering or Scientific field with 2 years of experience -OR- Master's Degree or equivalent in Engineering or Scientific field with industry/education internship, senior project, or thesis
Proficiency in engineering software, statistical tools, and scripting for data analysis, in particular Python on Databricks or comparable database/data analytics platforms, plus Minitab, and Excel.
Experience developing, validating, and maintaining Python scripts or similar automated data pipelines used for monitoring product performance, detecting anomalies, supporting investigations, or informing maintenance and recalibration decisions.
Familiarity with machine learning, statistical process monitoring, predictive analytics, or anomaly detection methods applied to engineering or device performance data.
Relocation is not provided for this role. Only candidates within a 50-mile radius of Irvine, CA will be considered.
Experience supporting on-market medical devices, preferably Class III implantable or electromechanical devices.
Working knowledge of medical device design controls, change control, CAPA, complaint investigations, and risk management.
Familiarity with ISO 13485, ISO 14971, FDA quality management system regulations, and applicable medical device regulatory expectations.
Experience developing or executing verification and validation protocols, engineering test methods, and technical reports.
Strong written and verbal communication skills with the ability to clearly document technical rationale and present findings to cross-functional stakeholders.
Solid problem-solving, organizational, analytical and critical thinking skills
Attention to detail and commitment to high quality documentation.
Ability to work effectively in a team-oriented, fast-paced, regulated environment while managing multiple priorities.
Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control
Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $87,000 to $123,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.
Global leader in the medical device industry with a patient-focused culture of innovation
Edwards Lifesciences (NYSE: EW), is the leading global structural heart innovation company, driven by a passion to improve patient lives. Through breakthrough technologies, world-class evidence and partnerships with clinicians and healthcare stakeholders, our employees are inspired by our patient-focused culture to deliver life-changing innovations to those who need them most. We thrive on discovery and expanding the boundaries of medical technology, serving patients in 100+ countries, with the help of our employees in areas including Clinical Affairs, Quality Engineering, Research & Development, Regulatory Affairs, Sales & Marketing, corporate functions and more. Contact Us We want to hear from you and engage in meaningful discussions. However, please note that we are not equipped to provide customer, candidate, or technical support through this platform. If you require assistance from those teams, please find their contact information here: https://www.edwards.com/aboutus/contactus If you’re a patient in need of medical advice, please contact your healthcare provider directly. We reserve the right to remove any comments that are off-topic, repetitive, or include hate speech, profanity, or offensive language. Additionally, we will not engage in discussions about competitor products, off-label use of Edwards products, or unsubstantiated/misleading claims that could cause harm. All Terms and Conditions of LinkedIn apply. For the Edwards Lifesciences privacy policy, visit https://www.edwards.com/legal/privacypolicy.
Offices: One Edwards Way, Irvine, CA 92614, US · 12050 S Lone Peak Pkwy, Draper, Utah 84020, US · 1919 Minnesota Crt, Mississauga, Ontario L5N 0C9, CA · Parque Industrial de Itabo, Carr. Sanchez, Km 18.5 Zona Franca Industrial de Haina, Haina, San Cristobal, DO · State Road 402 North, Km 1.4, Industrial Park, Añasco, 00610-1577, PR
Based on 831 listings with disclosed salaries, most engineering jobs in Irvine, CA pay between $60k–$188k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 978 open engineering positions in Irvine, CA listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Rivian, Edwards Lifesciences, mouhamedzz, CoStar Group, FieldAI, among others. Browse the listings above to see every active employer.
Yes — 268 of the 978 open engineering positions offer remote or hybrid work (39 remote, 229 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
