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Mechanical, Piping, General Area Walkdown Engineer
Worley
Cameron, LA
…capital projects. As a Mechanical, Piping, General Area Walkdown Engineer, you will serve as a critical bridge between design, construction, commissioning, and operations by validating…
Added 1 min ago
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Senior GenAI Developer
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United States
- $50 to $60 USD / hour
As an AI / ML Engineer, you will be responsible for developing applications and systems that utilize artificial intelligence tools and cloud artificial intelligence services, ensuring…
Added 1 min ago
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Electrical Engineer
Actalent
Sunnyvale, CA
- $105 USD / hour
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Added 2 mins ago
Staff Electrical Engineer Multiport NPD
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Added 3 mins ago
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…measurable improvements in development speed, performance, reliability, and production…
Added 3 mins ago
Senior Test Infrastructure Engineer
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…Center products. We are looking to hire a Test Infrastructure Engineer to join NVIDIA’s Test Solutions Group and build the infrastructure foundation for manufacturing system of board and…
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Senior Software Engineer, Firmware
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NVIDIA Networking Unit is looking for an experienced firmware/software engineer proficient in C and C++ programming to join our team that works on NVIDIA NIC/DPU/Switches. You will be…
Added 3 mins ago
Senior Product Development Engineer
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Senior AI Engineer, Forward Deployed Engineering
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…our supply chain on Palantir Foundry and AIP. As a Senior AI Engineer and Forward Deployed Engineer, you will work directly with planners and supply-chain experts to turn their decision…
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We are seeking a Principal Software Engineer to architect and build core platform systems to accelerate Physical AI development, such as Autonomous Driving (AV) & Robotics. This is a…
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Critical Facilities Mechanical Engineer – Data Center
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Join NVIDIA’s innovative team as a DSX Infrastructure Integration Engineer and play a meaningful role in the future of AI Factory infrastructure. This position offers an outstanding…
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Senior IT Systems Engineer
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We are seeking a Sr. IT Systems Engineer to ensure the 24x7 availability and performance of our infrastructure through secure, scalable cloud solutions and automation. This is a hybrid…
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Software Engineering Manager, Cloud DNS Authoritative Name Serving
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Experience designing, building, and operating large-scale distributed systems, with a focus on scalability, fault tolerance, and reliability.
Added 8 mins ago
HPC Engineer
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The engineer will work across the HPC technology stack to troubleshoot issues, support infrastructure lifecycle activities, improve reliability and performance, and help ensure that…
Added 8 mins ago
CERTIFIED FACILITIES ENGINEER (EXPERT)
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…next level? We're seeking an experienced Certified Facilities Engineer (Expert) to serve as the go-to electrical systems expert responsible for maintaining, improving, and ensuring the…
Added 9 mins ago
Industrial & Systems Engineer, Continuous Improvement II
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…digital supply chain organization. As an Industrial & Systems Engineer (ISE) II, you’ll partner with site leadership to optimize labor, systems, and processes - delivering measurable…
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Sterile Engineer, Specialist (On-site)
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This Engineer position will provide on-site engineering support of the Rahway, NJ FLEx (Formulation, Laboratory & Experimentation) center, for sterile operations within Our Company's…
Added 9 mins ago
Building Automation System Engineer
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…the GWES Rahway Operations team. This role focuses on system reliability, troubleshooting, and execution of projects supporting HVAC…
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Continuous Improvement Engineer
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…safety, product quality, manufacturing efficiency, and machine…
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Software Engineer
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- $72,800 to $130,000 USD / year
As a Software Engineer within Optum Technology, you will join an innovative team dedicated to building high-quality, scalable applications that transform healthcare delivery. In this role,…
Added 10 mins ago
Software Engineer - Clinical Software
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The Software Engineer, Clinical Software Products contributes engineering work across Caris's clinical application portfolio: product delivery, reliability, and incremental modernization of…
Added 12 mins ago
Process Engineer, Wafer Preparation & Assembly (Starlink/Akoustis)
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We are looking for a hands-on Process Engineer to develop, optimize, qualify, and implement the full wafer-to-die preparation flow: wafer thinning and backside processing, dicing, die…
Added 12 mins ago
Process Engineer, Gold-To-Gold Interconnect & Flip Chip Assembly (Starlink/Akoustis)
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Added 13 mins ago
Senior Full Stack Product Engineer
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CubX is looking for a Senior Full Stack Product Engineer who can take a business need from concept to production.

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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