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Cae Engineer Medical Device Jobs (NOW HIRING)

Sr. CAE Engineer

Plymouth, MI

$125.80K - $157.20K/yr

Rivian provides robust medical/Rx, dental and vision insurance packages for full-time employees ... device, recruiting system usage/interaction, security and preference information. Rivian may use ...

Sr. CAE Engineer

Plymouth, MI ยท On-site

$125.80K - $157.20K/yr

Rivian provides robust medical/Rx, dental and vision insurance packages for full-time employees ... device, recruiting system usage/interaction, security and preference information. Rivian may use ...

Sr. CAE Engineer

Plymouth, MI ยท On-site

$125.80K - $157.20K/yr

Rivian provides robust medical/Rx, dental and vision insurance packages for full-time employees ... device, recruiting system usage/interaction, security and preference information. Rivian may use ...

Compliance Test Engineer/Medical Device Compliance Engineer Location: Plano, TX Duration: 12 Months 100% Onsite Duties: Coordinate and work with external test houses for compliance testing of medical ...

At Roush, we fuse technology and engineering to provide product development solutions to customers ... Our Full-Time benefits include medical, dental, vision, life insurance, earned sick time, STD, LTD ...

Industrial Engineer | Med Device

Raynham, MA

$72.90K - $95.60K/yr

Key Skills Required: 3+ years of Medical Device or regulated manufacturing experience Strong SAP / MRP / PP&L experience Supply Chain Planning & Inventory Management Windchill or PLM systems exposure ...

Test Engineer - Medical Devices (Cardiovascular Domain) Job Title: Test Engineer / Senior Test ... Understand device design, system architecture, and core technologies to support effective test ...

At Roush, we fuse technology and engineering to provide product development solutions to customers ... Our Full-Time benefits include medical, dental, vision, life insurance, earned sick time, STD, LTD ...

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Showing results 1-20

Cae Engineer Medical Device information

See salary details

$33

$42

$50

How much do cae engineer medical device jobs pay per hour?

As of May 28, 2026, the average hourly pay for cae engineer medical device in the United States is $42.90, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $46.39 per hour, depending on experience, location, and employer.

What is the difference between Cae Engineer Medical Device vs Mechanical Engineer Medical Device?

AspectCae Engineer Medical DeviceMechanical Engineer Medical Device
Required CredentialsBachelor's in Engineering, CAD/CAE certificationsBachelor's in Mechanical Engineering, CAD certifications
Work EnvironmentDesign labs, R&D departments, manufacturingDesign labs, manufacturing, testing facilities
Industry UsageUsed for simulation, validation, and testing of medical devicesUsed for device design, structural analysis, and prototyping

While both roles involve engineering skills in the medical device industry, a Cae Engineer Medical Device specializes in computer-aided engineering simulations to validate device performance, whereas a Mechanical Engineer Medical Device focuses on designing and developing the physical components of medical devices. Both roles often collaborate but serve distinct functions within the product development process.

Infographic showing various Cae Engineer Medical Device job openings in the United States as of May 2026, with employment types broken down into 33% As Needed, and 67% Full Time. Highlights an 99% Physical, and 1% Hybrid job distribution, with an average salary of $89,228 per year, or $42.9 per hour.
Senior Systems Engineer, Medical Device Technical Lead

Senior Systems Engineer, Medical Device Technical Lead

3 Key Consulting

Newbury Park, CA โ€ข On-site

$110.60K - $151.40K/yr

Full-time

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Senior Systems Engineer, Medical Device Technical Lead

3 Key Consulting is recruiting a Senior Systems Engineer, Medical Device Technical Lead for a consulting engagement with our direct client, a leading global biotechnology company.

Job Description:

Candidates must have experience in the biotechnology, pharmaceutical, or medical device industry. Candidates must have at least 5 years' experience in systems engineering. Candidates must have great communication skills and can lead meetings and work teams. Candidates must have a strong background in documenting requirements and providing traceability documentation for FDA approval using DOORS, Requisite Pro, or other similar requirements management software. Practical experience in configuration management and change control process/requirements, CCB (change control board), CIT (change implementation team) concepts experience is preferred.

The Systems Engineer (SE) works as part of cross-functional program teams to deliver technical content, performance, intellectual property, and quality deliverables of a combination product development program. The Systems Engineer understands and captures the user needs into system requirements and participates in the functional decomposition and allocation to subsystems. The Systems Engineer ensures that the quality targets are satisfied, identifies technical risks, and assists risk retirement activities on the program. The Systems Engineer maintains close interaction with customers to understand and enhance the ability to deliver on customer satisfaction through high product quality.

Top Must Have Skill Sets:

Systems Engineering past work experience. Ability to communicate effectively and lead large teams in development of technical deliverables required for design control deliverables. Past experience in writing SOPs, Guidance & technical documents is preferred but not required. Proficient in Microsoft Excel especially in writing macros in excel.

Day to Day Responsibilities:

Work cross-functionally with individuals and project teams in Marketing, Operations, and Development. Create and assess product requirements to determine technical coverage and proper integration different subsystems. Create and execute to project plans and schedules. Develop, execute, and review requirements documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects. Responsible for writing technical and guidance documents that provides guidance to team members in following design control and business processes within client. Develop Toolsets using Microsoft excel to enable easier on boarding of other engineers onto client processes. Work and Lead cross functional teams in development of common practices and write technical guidance documents to enable consistency across various combination product teams.

Basic Qualifications:

BS in Engineering and previous experience in a medical device industry. 10 years current experience with engineering processes and procedures.

Preferred Qualifications:

6+ years of progressive experience as an engineer or scientist within the appropriate field of study (Systems Engineering). Creative problem solver and solution developer when presented with conflicting requirements, business demands and technical risks/issues. Experience in combination product development.

Why is the Position Open?

Planned Project.

Red Flags:

No degree. No systems engineering experience.

Interview Process:

Video Conference with Hiring Manager. Selected candidates would then have a panel 1:1 video conference with additional team members. Candidate must be comfortable with video (webcam) online interview process.