Jobs in the United States

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Added 4 mins ago
Software Development Engineer, Amazon Stores FinTech
Amazon.com Services LLC
Seattle, WA
- Resolve production issues, perform root cause analysis, and put lasting fixes in place.
Added 7 mins ago
O
Senior Application Software Engineer
Oracle
United States
- $86,100 to $187,000 USD / year
Troubleshoot complex production issues and drive root-cause analysis efforts.
Added 9 mins ago
Firmware Engineer
x Varian Medical Systems, Inc.
United States
Assists in investigating non-conformances (complaint investigations), determines root cause and assigns corrective action.
Added 9 mins ago
BI Analyst
PrePass
Remote, United States
Troubleshoot report refresh failures and data issues, partnering with data engineers on root-cause fixes.
Added 10 mins ago
Senior Data Scientist
Capgemini
Seattle, WA, WA
Network Operations Intelligence - Experience building AI-powered solutions for incident management, root cause analysis, predictive maintenance, anomaly detection, and operational…
Added 11 mins ago
P
Battery Test Engineer - Aeromechanical
Pivotal
Palo Alto, CA
- $135,000 to $155,000 USD / year
Author clear test plans, procedures, reports, nonconformance records, root-cause assessments, and design recommendations.
Added 14 mins ago
Advanced Package Development Engineer
Apple
CA
Drive failure analysis (FA), root-cause investigations, and issue resolution for wafer-level process excursions, defectivity, and reliability marginalities.
Added 14 mins ago
GD
Principal Software Engineer
Green Dot Corporation
United States
- $159,400 to $230,000 USD / year
Lead incident response and root cause analysis to improve system reliability.
Added 19 mins ago
Principal/Senior Plant Maintenance Engineer
Portland General Electric Company
Clatskanie, OR
Senior / Principal Plant Maintenance Engineer
Added 20 mins ago
Composites, Manufacturing Engineer II
Amro Fabricating Corporation
Huntington Beach, CA
Supports root cause analysis and implements corrective actions to resolve product or process issues.
Added 24 mins ago
Sr. Staff Identity & Access Management Engineer
Early Warning Services, LLC
United States
…platform, integration, authentication, and access issues; lead root cause analysis and implementation of sustainable corrective…
Added 25 mins ago
F
Build Your Robotics Career. Explore the Country as a Robotics Field Service Engineer or Technician
Formic
United States
- $25 to $32 USD / hour
Investigate recurring failures, participate in root cause analysis, and implement or recommend corrective actions
Added 29 mins ago
A
Test Equipment Design Engineer
Aerotek
Berkeley, CA
- $69.44 to $104.17 USD / hour
Perform hardware bring-up, validation, troubleshooting, and root-cause analysis.
Added 31 mins ago
Staff QA Engineer
DexCom Inc
San Diego, CA
You lead complex, high-risk quality investigations, including root cause analysis, CAPAs, NCMRs/MRB, Health Hazard Evaluations (HHEs), and other product and process risk assessments,…
Added 32 mins ago
CI
Sr. Customer Support Engineer
Celona Inc
United States
- $100,000 to $120,000 USD / year
…customer and field issues end to end: perform in-depth fault and root cause analysis, formulate technical action plans, and drive issues to resolution with clear, timely communication to…
Added 35 mins ago
Senior Engineer, Mechanical - Fixed Equipment & Piping Integrity
Calcasieu Pass Operations LLC
United States
Senior Engineer, Mechanical - Fixed Equipment & Piping IntegrityLocated:
Added 35 mins ago
Engineer, Electrical
Plaquemines LNG Operations LLC
Plaquemines Parish, LA
Root Cause Failure Analysis (RCFA): With expertise in relevant techniques to adequately lead RCFA exercises for failures relating to plant equipment and/or processes.
Added 36 mins ago
Senior RF Engineer II (Hardware)
Neros Technologies
Torrance, CA
Drive root cause analysis for complex RF/connectivity performance issues including interference, desense, link margin, spectral compliance, and system-level coexistence
Added 40 mins ago
Senior Product Development Engineer
International Motors, LLC
San Antonio, TX
Identify, investigate, and resolve product design, manufacturing, and field performance issues through structured root cause analysis and corrective actions.
Added 41 mins ago
Full Stack Java Developer
USA7 DXC Technology Services LLC
FORT WORTH, TX
Troubleshoot complex application and production issues and perform root cause analysis.
Added 46 mins ago
R
Staff Electronic Design Engineer
Rivian
Palo Alto, CA
- $186,000 to $232,000 USD / year
Added 46 mins ago
CC Rotating Equipment Engineer
CITGO Petroleum Corporation
Corpus Christi, TX
…to join our Reliability department. The Rotating Equipment Engineer position provides technical expertise and recommendations for rotating equipment mechanical integrity, repairs, and…
Added 47 mins ago
Senior Electrical Engineer (Power & Mixed-Signal)
Anduril Industries
Costa Mesa, CA
Root Cause Analysis: Perform root cause and failure analysis in support of engine test and field operations.
Added 47 mins ago
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Senior Backend Software Engineer, AI Observability & Evals Platform (NYC)
LangChain
New York, NY
- $180,000 to $240,000 USD / year
- Troubleshoot and resolve production issues, performing root-cause analysis and implementing long-term fixes.
Added 49 mins ago
Thermal Manager- Liquid Cooling Engineer
Flextronics International USA, Inc.
CA
Analyze thermal performance, identify improvement opportunities, and resolve thermal-related issues through root cause analysis.

SEDAA

R&D System Engineer

Plymouth, MN, United States

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Job details

Experience: Years Experience: 6+ years of related work experience with a complete understanding of specified functional area.
Posting language: English
Posted: Nov 2, 2026

Original job description

* LOCAL CANDIDATES TO WORK LOCATION OR OPEN TO RELOCATE NO C2C*

Job Title: R&D System Engineer Job Id: Sedaa48492 Location: Plymouth, MN, 100% Onsite role Rate: 70k to 80k annually This position is Non Exempt. Years Experience: 6+ years of related work experience with a complete understanding of specified functional area. Education: Bachelor's degree or an equivalent combination of education and work experience.

Duties:

Responsible for providing technical support in the creation and the development of new medical device products. Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Researches, develops, designs, and evaluates mechanical and electro-mechanical materials, components, assemblies, processes and/or equipment.
Performs analysis and/or interviews to determine the requirements and constraints of the system.
Analyzes user needs and provides input to stakeholders.
Conducts feasibility studies to verify capability and functionality.
Develops new concepts from initial design to market release.
Directs support personnel and coordinates project activities.
Writes and submits intellectual property (patents).
Maintains detailed documentation throughout all phases of research and development.
Reviews or coordinates vendor activities to support development.
Research various cost-effective, alternative approaches to current processes.

Looking for a senior engineer for R&D systems engineering in Electrophysiology division. Prior experience in medical devices and/or systems engineering a plus, especially prior experience related to establishing user needs and requirements for new product development. Experience with implantable/ class III devices, electromechanical devices, or echo imaging modalities (e.g., TEE, ICE) a plus.

* LOCAL CANDIDATES TO WORK LOCATION OR OPEN TO RELOCATE NO C2C*

Job Title: R&D Senior Mechanical Engineer Job Id: Sedaa48085 Location: Pleasanton CA, 100% Onsite role Rate: 100k to 130k annually

POSITION SUMMARY

Provides technical leadership in sustaining products for design, verification, investigation, reliability improvement of complex Class II and Class III medical devices, including Ventricular Assist Devices (VADs), extracorporeal blood pumps, oxygenators, and associated electromechanical systems. This individual serves as a subject matter expert responsible for leading complex technical investigations, driving product improvements, influencing engineering strategy, and solving challenging system-level problems throughout the product lifecycle. The role requires extensive collaboration across R&D, Quality, Regulatory, Manufacturing, Operations, and Supplier teams to ensure product safety, reliability, compliance, and performance.

RESPONSIBILITIES

Provide technical leadership across multiple sustaining engineering initiatives involving Class II and Class III medical devices.
Lead complex technical investigations associated with product performance, complaints, CAPAs, nonconformances, and field issues using structured root cause analysis methodologies.
Research, develop, test, and sustain mechanical and electromechanical systems used in ventricular assist devices, extracorporeal blood pumps, oxygenators, and related cardiovascular products.
Drive cross-functional efforts to identify, assess, and implement product, process, and reliability improvements throughout the product lifecycle
Apply experimental, analytical, empirical, and numerical methods to evaluate product performance, investigate failures, and support engineering decisions.
Develop test strategies, test methods, and protocols to evaluate system, subsystem, and component performance against product requirements.
Design, develop, qualify, and validate equipment and fixtures used for engineering verification, reliability testing, and failure analysis activities.
Identify technical risks and drive mitigation strategies throughout product development and sustaining activities.
Analyze complaint, post-market surveillance, manufacturing, and reliability data to identify trends and drive continuous improvement initiatives.
Create and review engineering drawings and specifications to ensure appropriate dimensioning, tolerancing, manufacturability, and assembly requirements.
Perform and review tolerance analyses and engineering stack-ups to assess product robustness and manufacturability.
Provide expertise in GD&T and mechanical system design principles.
Support design reviews and provide technical guidance to engineers across multiple disciplines.
Mentor and develop engineers through technical coaching, design reviews, and problem-solving activities.
Evaluate manufacturing processes including precision machining, injection molding, silicone molding, extrusion, laser welding, ultrasonic welding, bonding, and mechanical assembly methods.
Support supplier selection, qualification, and technical evaluations, including assessments of manufacturing capability, capacity, process controls, and quality systems.
Collaborate with regulatory, quality, and clinical teams to support submissions, audits, inspections, and responses to regulatory inquiries.
Ensure compliance with FDA regulations, international standards, company procedures, Quality Management System requirements, and applicable regulatory requirements.
Support company initiatives as directed by management and contribute to continuous improvement of engineering processes, product quality, and operational excellence.

MINIMUM QUALIFICATIONS

· Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or related engineering discipline. · 15+ years of progressively increasing engineering responsibility supporting Class II and/or Class III medical devices, including product development, sustaining engineering, verification and validation, manufacturing support, and risk management activities. · Demonstrated technical leadership of complex cross-functional programs and ability to influence technical decisions without direct authority. · Strong understanding of FDA Design Controls, 21 CFR Part 820, product lifecycle management, and medical device development processes. · Experience leading complex technical investigations and root cause analyses. · Expertise in mechanical design, tolerance analysis, GD&T, materials, manufacturing processes, and assembly methods. · Experience with risk management principles and methodologies, including FMEA analysis. · Strong written, verbal, presentation, and technical communication skills. · Ability to effectively communicate with engineers, management, auditors, regulators, suppliers, and customers. · Ability to travel approximately 10%, including domestic and occasional international travel.---

PREFERRED QUALIFICATIONS

· Master's degree in Mechanical Engineering, Biomedical Engineering, or related discipline · Experience with ventricular assist devices (VADs), extracorporeal blood pumps, oxygenators, cardiovascular implants, or other implantable Class III medical devices. · Experience supporting post-market surveillance activities, complaint investigations, CAPAs, and product reliability initiatives. · Experience with reliability engineering, accelerated life testing, fatigue analysis, and statistical data analysis. · Experience with medium- to high-volume medical device manufacturing environments. · Experience with CAD systems, Design of Experiments (DOE), SPC, Six Sigma, and project management methodologies. · Knowledge of ISO 13485, ISO 14971, EU MDR, and other applicable medical device standards and regulations. · Experience working with external manufacturing partners and global suppliers. · Exposure to multidisciplinary engineering fields including electrical systems, software-controlled devices, polymers, biomaterials, and biological systems.

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