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Engineering Medical Device Jobs (NOW HIRING)

Quality Engineer - Medical Device

Newark, DE · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Location: Delaware Largescale Medical Device client facing a ... Technical Review & Support • Review engineering drawings and specifications to confirm accuracy ...

... days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance ... Evaluate and integrate relevant engineering advances for improving or solving problems Understand ...

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

The ideal candidate will combine strong engineering fundamentals with hands-on technical ability ... Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing ...

Lead iOS (Swift) Software Engineer - Medical Device Startup We're partnering with a well-funded, fast-growing startup to hire a Lead iOS/Swift Software Engineer. This is a high-impact, full-time role ...

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

The ideal candidate will combine strong engineering fundamentals with hands-on technical ability ... Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing ...

Medical Device Technician

Madison, WI · On-site

$38K - $48K/yr

Medical Device Technician Location: Madison, WI (Onsite) Scope of Work: Assemble and test medical ... Bachelor's degree in engineering or related scientific field. Associate's degree with 2+ years ...

Job Title Medical Device Service Engineer Requisition JR000015824 Medical Device Service Engineer ... Collaborate with engineering, quality, and product teams to escalate issues and support continuous ...

Be Seen First

We are seeking a Medical Device Assembler to support the build and integration of capital medical ... Read and interpret assembly drawings; use computers for basic programming, menu navigation, and ...

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Engineering Medical Device information

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How much do engineering medical device jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for engineering medical device in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

What are engineering medical device professionals?

Engineering medical device professionals are specialists who design, develop, test, and improve medical devices used in healthcare. They combine principles of engineering, biology, and medicine to create equipment such as pacemakers, imaging machines, and prosthetics that help diagnose, treat, or manage medical conditions. Their work ensures devices are safe, effective, and comply with regulatory standards. These professionals often work closely with doctors, patients, and regulatory agencies throughout the product development process.

What are the key skills and qualifications needed to thrive as a Medical Device Engineer, and why are they important?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant degree and knowledge of FDA regulations. Familiarity with CAD software, prototyping tools, and quality management systems is typically required, along with certifications like Six Sigma or ISO 13485. Strong problem-solving abilities, teamwork, and effective communication are standout soft skills in this role. These competencies are crucial for designing safe, innovative devices that meet regulatory standards and improve patient outcomes.

What are some typical challenges faced by engineers working in the medical device industry?

Engineers in the medical device industry often face challenges related to strict regulatory compliance, such as meeting FDA or ISO standards. Additionally, they must ensure that devices are safe, effective, and user-friendly, requiring frequent collaboration with cross-functional teams like clinical, quality assurance, and manufacturing. Balancing innovation with patient safety while managing tight project timelines is also a common aspect of the role. Overcoming these challenges can be rewarding, as it directly contributes to improving patient outcomes.

What is the difference between Engineering Medical Device vs Biomedical Engineer?

AspectEngineering Medical DeviceBiomedical Engineer
Required CredentialsEngineering degree, possibly certifications in medical device designEngineering or biomedical degree, certifications in healthcare technology
Work EnvironmentDesign labs, manufacturing facilities, regulatory agenciesHospitals, research labs, healthcare companies
Employer & Industry UsageMedical device companies, biotech firms, regulatory bodiesHospitals, medical research institutions, healthcare technology firms

Engineering Medical Device professionals focus on designing, developing, and testing medical devices, often working in manufacturing or regulatory settings. Biomedical Engineers have a broader scope, integrating engineering principles with biological sciences to improve healthcare solutions, including medical devices. While both roles require engineering backgrounds, Engineering Medical Device specialists typically concentrate on product development, whereas Biomedical Engineers may work on research, clinical applications, or device integration.

More about Engineering Medical Device jobs
What cities are hiring for Engineering Medical Device jobs? Cities with the most Engineering Medical Device job openings:
What are the most commonly searched types of Engineering Medical Device jobs? The most popular types of Engineering Medical Device jobs are:
What states have the most Engineering Medical Device jobs? States with the most job openings for Engineering Medical Device jobs include:
What job categories do people searching Engineering Medical Device jobs look for? The top searched job categories for Engineering Medical Device jobs are:
Infographic showing various Engineering Medical Device job openings in the United States as of June 2026, with employment types broken down into 52% Full Time, 45% Part Time, and 3% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.

Quality Engineer - Medical Device

IT MINDS L.L.C.

Newark, DE • On-site

$70K - $90K/yr

Contractor

Posted 22 days ago


Job description

Role: Quality Engineer – Medical Device

Location:  Delaware

Largescale Medical Device client facing a remediation project here on site in Delaware.

What is the project the contractor will be working on?

•              We are seeking experienced Quality and/or Manufacturing Engineers to support a large-scale production documentation and remediation initiative at our client’s Newark, Delaware manufacturing site. These professionals will play a critical role in strengthening risk management practices, supporting transfer to manufacturing activities, and driving process validation and equipment qualification efforts.

o             This engagement will begin with comprehensive documentation gap assessments across multiple production lines, followed by remediation and implementation activities to ensure manufacturing readiness and compliance.

-            

Quality Engineer (Remediation)

Documentation Gap Analysis

•              Perform detailed reviews of production line documentation, including:

o             Process documentation

o             Work instructions

o             Training records

o             Validation documentation

o             Specifications and technical drawings

•              Identify documentation gaps, inconsistencies, and compliance risks.

•              Partner cross-functionally with manufacturing, quality, and engineering teams to prioritize findings.

Remediation & Implementation

•              Develop and execute remediation plans following gap assessments.

•              Update and create SOPs, work instructions, and validation documentation as needed.

•              Support transfer-to-manufacturing activities through structured risk mitigation.

•              Ensure documentation aligns with regulatory and internal quality standards.

Risk Management & FMEA

•              Lead and/or support:

o             Process FMEAs

o             Risk assessments tied to manufacturing transfer

o             Risk mitigation planning and documentation

•              Apply strong risk management principles to process validation and equipment qualification activities.

Process Validation & Equipment Qualification

•              Support process validation activities including:

o             IQ/OQ/PQ execution

o             Equipment qualification documentation

o             Validation protocol review and approval

•              Ensure alignment between validation activities and risk management outputs.

Technical Review & Support

•              Review engineering drawings and specifications to confirm accuracy and alignment with production processes.

o             Ability to read and interpret drawings is required (drafting not required).

•              Support sampling plan assessments:

o             Evaluate sampling plans and statistical justifications

o             Determine appropriate sample sizes and rationale

•              Participate in production line startup and manufacturing support as needed.

Skills:

Required:

•              3–6+ years of experience in Quality Engineering (QE) and/or Manufacturing Engineering within Medical Devices

•              Strong experience leading or supporting:

o             Process FMEAs

o             Risk management initiatives

o             Process validation activities

•              Experience reviewing and remediating manufacturing documentation.

•              Working knowledge of equipment qualification (IQ/OQ/PQ).

•              Ability to interpret engineering drawings and technical specifications.

Desired:

•              Experience with instrumentation and electronics (strong plus for the Delaware site).

•              Experience assessing sampling plans and statistical justifications (preferred but not required).

•            

•              Exposure to:

o             Plastics manufacturing

o             Chemistry-based processes or test strip formulation

o             Experience supporting multi-site environments.

Best Regards,

 

Satya Satish J | Technical Recruiter | IT Minds LLC |