Job Title: Senior Validation Engineer - Medical Devices Location: Silver Spring, MD (Onsite ... Knowledge of GMP, FDA, and quality system requirements * Strong collaboration, communication, and ...
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Job Title: Senior Validation Engineer - Medical Devices Location: Silver Spring, MD (Onsite ... Knowledge of GMP, FDA, and quality system requirements * Strong collaboration, communication, and ...
... Systems Engineer to join our team developing next-generation medical devices. In this role, you ... a quality management system. Key Responsibilities * Board-Level Schematic Generation: Design and ...
... Systems Engineer to join our team developing next-generation medical devices. In this role, you ... a quality management system. Key Responsibilities * Board-Level Schematic Generation: Design and ...
... Systems Engineer to join our team developing next-generation medical devices. In this role, you ... a quality management system. Key Responsibilities * Board-Level Schematic Generation: Design and ...
... Systems Engineer to join our team developing next-generation medical devices. In this role, you ... a quality management system. Key Responsibilities * Board-Level Schematic Generation: Design and ...
Aerospace Supplier Quality Engineer
Chantilly, VA · On-site
$57 - $106/hr
Aerospace Supplier Quality Engineer Full Time Employee Full-Time Chantilly, VA, US 4 days ago ... Quality Assurance experience in a regulated field (e.g., aerospace, automotive, medical devices)
Aerospace Supplier Quality Engineer
Chantilly, VA · On-site
$57 - $106/hr
Aerospace Supplier Quality Engineer Full Time Employee Full-Time Chantilly, VA, US 4 days ago ... Quality Assurance experience in a regulated field (e.g., aerospace, automotive, medical devices)
Aerospace Supplier Quality Engineer
Chantilly, VA · On-site
$57K - $106K/yr
Position Title: Aerospace Supplier Quality Engineer Requisition ID: 1856 Position Location ... Quality Assurance experience in a regulated field (e.g., aerospace, automotive, medical devices)
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Aerospace Supplier Quality Engineer
Chantilly, VA · On-site
$57K - $106K/yr
Position Title: Aerospace Supplier Quality Engineer Requisition ID: 1856 Position Location ... Quality Assurance experience in a regulated field (e.g., aerospace, automotive, medical devices)
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Columbia, MD · On-site
$75K - $125K/yr
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Quality Engineer
Columbia, MD · On-site
$75K - $125K/yr
About the Job A Quality Engineer ensures products and manufacturing systems consistently meet ... or medical devices). * Technical Skills: Deep understanding of Geometric Dimensioning and ...
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$77K - $99K/yr
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Quality Engineer
Alexandria, VA · On-site
$77K - $99K/yr
Overview As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance ... and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet ...
Quality Engineer
Alexandria, VA · On-site
$77K - $99K/yr
Overview As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance ... and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet ...
Quality Engineer
Alexandria, VA · On-site
$77K - $99K/yr
Overview As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance ... and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet ...
Quality Engineer
Alexandria, VA · On-site
$77K - $99K/yr
Overview As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance ... and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet ...
Quality Engineer
Glen Burnie, MD · On-site
$69K - $90K/yr
... devices from the realities of their harsh surrounding elements and environments. The Quality ... The Quality Engineer will work closely with cross-functional teams to ensure compliance, reduce ...
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Quality Engineer
Glen Burnie, MD · On-site
$69K - $90K/yr
... devices from the realities of their harsh surrounding elements and environments. The Quality ... The Quality Engineer will work closely with cross-functional teams to ensure compliance, reduce ...
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Alexandria, VA · On-site
$90 - $130/hr
Overview As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance ... and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet ...
Quality Engineer
Alexandria, VA · On-site
$90 - $130/hr
Overview As the Quality Engineer at MPR, you play a key role in ensuring the MPR quality assurance ... and medical devices. You'll serve as an internal QA resource ensuring our deliverables meet ...
Quality Engineer
Seabrook, MD · On-site
$71K - $92K/yr
... devices, instruments, and liquids. DORC uses cutting-edge technology, works closely with innovative ... such as medical technology. As a company wholly owned by a foundation, ZEISS is rooted in and ...
Quality Engineer
Seabrook, MD · On-site
$71K - $92K/yr
... devices, instruments, and liquids. DORC uses cutting-edge technology, works closely with innovative ... such as medical technology. As a company wholly owned by a foundation, ZEISS is rooted in and ...
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QA Manufacturing Engineer - Medical Device
Sterling, VA · On-site
$40 - $80/hr
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Quick apply
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$40 - $80/hr
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Be Seen First
QA Manufacturing Engineer - Medical Device
Sterling, VA · On-site
$40 - $80/hr
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Quick apply
Be Seen First
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Sterling, VA · On-site
$40 - $80/hr
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Tysons Corner, VA · On-site
$72K - $93K/yr
Good understanding of computer networking and ability to troubleshoot malfunctioning devices ... The package includes medical plans with company subsidies, a Health Savings Account (HSA) with a ...
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Quality Engineer (Video)
Tysons Corner, VA · On-site
$72K - $93K/yr
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Greenbelt, MD · On-site
$121K - $201K/yr
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Greenbelt, MD · On-site
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Greenbelt, MD · On-site
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Greenbelt, MD · On-site
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MEDICAL DEVICE MECHANICAL ENGINEER / SUBJECT MATTER EXPERT Cardiovascular Devices - Durability ... FDA Regulations and Guidance * 21 CFR Part 820 - Quality System Regulation, as applicable to device ...
MEDICAL DEVICE MECHANICAL ENGINEER / SUBJECT MATTER EXPERT Cardiovascular Devices - Durability ... FDA Regulations and Guidance * 21 CFR Part 820 - Quality System Regulation, as applicable to device ...
MEDICAL DEVICE MECHANICAL ENGINEER / SUBJECT MATTER EXPERT Cardiovascular Devices - Durability ... FDA Regulations and Guidance * 21 CFR Part 820 - Quality System Regulation, as applicable to device ...
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MEDICAL DEVICE MECHANICAL ENGINEER / SUBJECT MATTER EXPERT Cardiovascular Devices - Durability ... FDA Regulations and Guidance * 21 CFR Part 820 - Quality System Regulation, as applicable to device ...
MEDICAL DEVICE MECHANICAL ENGINEER / SUBJECT MATTER EXPERT Cardiovascular Devices - Durability ... FDA Regulations and Guidance * 21 CFR Part 820 - Quality System Regulation, as applicable to device ...
MEDICAL DEVICE MECHANICAL ENGINEER / SUBJECT MATTER EXPERT Cardiovascular Devices - Durability ... FDA Regulations and Guidance * 21 CFR Part 820 - Quality System Regulation, as applicable to device ...
Quality Engineer Medical Devices information
See Washington salary details
$51K - $58.6K
1% of jobs
$58.6K - $66.2K
3% of jobs
$66.2K - $73.8K
7% of jobs
$73.8K - $81.4K
13% of jobs
$81.8K is the 25th percentile. Wages below this are outliers.
$81.4K - $89.1K
18% of jobs
The median wage is $92.2K / yr.
$89.1K - $96.7K
19% of jobs
$103K is the 75th percentile. Wages above this are outliers.
$96.7K - $104.3K
17% of jobs
$104.3K - $111.9K
9% of jobs
$111.9K - $119.5K
6% of jobs
$119.5K - $127.2K
4% of jobs
$127.2K - $134.8K
2% of jobs
$51K
$95.2K
$134.8K
How much do quality engineer medical devices jobs pay per year?
As of Sep 5, 2026, the average yearly pay for quality engineer medical devices in Washington is $95,182.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,500.00 and $105,300.00 per year, depending on experience, location, and employer.
What does a quality engineer do in the medical device industry?
A Quality Engineer in the medical device industry is responsible for ensuring that products meet regulatory standards and quality requirements throughout their lifecycle. They develop and implement quality control processes, conduct risk assessments, lead investigations into product defects, and work closely with cross-functional teams to ensure compliance with regulations such as FDA and ISO 13485. Their work helps to guarantee the safety, reliability, and effectiveness of medical devices before they reach patients.
How does a quality engineer collaborate with cross-functional teams in the medical device industry?
Quality Engineers in the medical device field work closely with design, manufacturing, and regulatory teams to ensure products meet stringent quality and compliance standards. They participate in design reviews, help develop verification and validation protocols, and support the implementation of corrective actions. Regular communication with production and R&D teams is essential to identify potential risks early and to ensure that quality is built into every stage of product development. This collaborative approach not only improves product safety and efficacy but also streamlines regulatory submissions and audits.
What are the key skills and qualifications needed to thrive as a quality engineer in medical devices, and why are they important?
To thrive as a Quality Engineer in Medical Devices, you typically need a degree in engineering or a related field, combined with knowledge of quality assurance principles and regulatory requirements (such as ISO 13485 and FDA regulations). Familiarity with risk management tools, validation protocols, and quality management systems (QMS), as well as certifications like CQE (Certified Quality Engineer), are highly valuable. Strong analytical thinking, attention to detail, and effective communication skills enable you to identify issues, collaborate with cross-functional teams, and ensure compliance. These competencies are crucial for maintaining product safety, meeting regulatory standards, and supporting a culture of continuous improvement in the medical device industry.
What is the difference between Quality Engineer Medical Devices vs Quality Technician Medical Devices?
| Aspect | Quality Engineer Medical Devices | Quality Technician Medical Devices |
|---|---|---|
| Certifications | ISO 13485, Six Sigma, ASQ certifications | ISO 13485, basic quality certifications |
| Responsibilities | Designing quality systems, process improvements, root cause analysis | Inspecting products, conducting tests, recording quality data |
| Work Environment | Design and development labs, manufacturing plants | Manufacturing floors, quality control labs |
| Employer & Industry Usage | Medical device companies, OEMs, suppliers | Manufacturers, contract labs, quality departments |
In summary, Quality Engineer Medical Devices focus on developing quality systems, process improvements, and ensuring compliance, while Quality Technicians primarily perform product inspections and testing. Both roles are essential in maintaining high standards in the medical device industry but differ in scope and responsibilities.
What are popular job titles related to Quality Engineer Medical Devices jobs in Washington?
For Quality Engineer Medical Devices jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Quality Engineer Medical Devices jobs in Washington look for?
The top searched job categories for Quality Engineer Medical Devices jobs in Washington are:
What cities in Washington are hiring for Quality Engineer Medical Devices jobs?
Cities in Washington with the most Quality Engineer Medical Devices job openings:
Contractor
Re-posted 3 days ago
Job description
Job Title: Senior Validation Engineer – Medical Devices
Location: Silver Spring, MD (Onsite)
Duration: 06 months contract (High potential for extension)
Job Summary
We are seeking a Senior Validation Engineer to support equipment lifecycle management, facility changes, and commercialization activities within a medical device environment. This role will play a key part in ensuring equipment and systems are validated, compliant, and maintained in a validated state throughout their lifecycle.
The ideal candidate will have strong experience in validation documentation, equipment qualification, and cross-functional collaboration within regulated environments.
Key Responsibilities
Validation & Documentation
- Develop, review, and execute validation documents including:
- User Requirement Specifications (URS)
- Validation Determination Assessments (VDA)
- Installation, Operational, and Performance Qualifications (IQ/OQ/PQ)
- Requirements Traceability Matrix (RTM)
- Final/Summary Reports
- Support equipment lifecycle validation activities for commercial medical device operations
- Execute validation protocols and ensure compliance with regulatory standards
Required Qualifications
- Minimum 5+ years of experience in validation within medical device or regulated environments
- Strong experience with equipment lifecycle management and validation documentation
- Hands-on experience with IQ/OQ/PQ, URS, RTM, and validation reporting
- Experience supporting commercialization, facility changes, or system transitions
- Knowledge of GMP, FDA, and quality system requirements
- Strong collaboration, communication, and problem-solving skills