Top 2682 Medical device quality Jobs

Design Quality Engineer, Software Medical Device
Senseye —Austin, TX
- $100,000 - $125,000 a year
- Full-time
- Mid-level
- Commuter assistance
- Disability insurance
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Quality Engineer - Medical Device
Proven Recruiting —San Diego, CA
- $50 - $75 an hour
- Full-time
- Engineering
- Mid-level
- 3 years
- Health insurance
- Dental insurance
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9d
Sr Quality Engineer – Medical Device only Locals
Grove Technical Resources —Salt Lake City, UT
- $50 - $60 an hour
- Contract
- Engineering
- Mentoring
- In-person
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R&D Manager - Medical Device & Life Science
Weiss-Aug MedPharma —Fairfield, NJ
- $120,000 - $150,000 a year
- Full-time
- Microsoft Excel
- Customer service
- 5 years
- Health savings account
- Disability insurance
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Quality Systems Manager – Medical Device Manufacturing
Weiss-Aug MedPharma —Fairfield, NJ
- Full-time
- Engineering
- Assembly
- Manufacturing
- Health savings account
- Disability insurance
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Quality Compliance/Labeling Specialist (Medical Device)
Adecco —Cupertino, CA
- $57 - $67 an hour
- Contract
- Mid-level
- Military encouraged
- Fair chance
- Commuter assistance
- Paid holidays
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Quality Auditor - Pharmaceutical/Medical Device
SQA Services —Chicago, IL
- $1,300 a day
- Contract
- 5 years
- Residential
- Travel
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Contract Opportunity - Medical Device Auditors
SGS —Remote
- Contract
- Computer literacy
- English
- Mid-level
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Medical Device Quality Inspector - 3rd Shift
Incipio Devices —Huntington, IN
- $17 - $20 an hour
- Full-time
- In-person
- Entry level
- Health insurance
- Dental insurance
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Bilingual Spanish /English Afternoon Quality Control Supervisor
Pivot Staffing, LLC —Sterling Hts, MI
- From $21 an hour
- Full-time
- Mid-level
- Analysis skills
- Organizational skills
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Manufacturing Engineer II
Hamilton Medical, Inc. —Reno, NV
- $65,000 - $120,000 a year
- Full-time
- 5 years
- Research
- Mid-level
- Disability insurance
- Health insurance
SENIOR PROCESS ENGINEER / SCIENTIFIC MOLDING ENGINEER
Moldworx LLC —Chandler, AZ
- $125,000 - $150,000 a year
- Full-time
- Engineering
- Analysis skills
- Mentoring
- Health savings account
- Paid holidays
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Manufacturing Test Technician II – Night Shift
Enercon Technologies —Gray, ME
- Full-time
- Mid-level
- High school diploma or GED
- Continuous improvement
- Wellness program
- Disability insurance
Quality Systems Engineer - Supplier Quality
AuST Manufacturing —West Valley City, UT
- Full-time
- Mid-level
- Analysis skills
- Bachelor's degree
- Health savings account
- Health insurance
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Quality Engineer
INTERCONNECT SOLUTIONS COMPANY LLC —Fountain Valley, CA
- $98,000 - $105,000 a year
- Full-time
- Engineering
- ERP systems
- Mid-level
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Quality Inspector – Sheet Metal Fabrication – Direct Hire –$45-65K
Schulte Staffing Solutions —Peabody, MA
- $45,000 - $65,000 a year
- Overtime
- Mid-level
- Forklift
- Continuous improvement
- Health insurance
- Paid time off
Quick Apply
Quality Control Technician
Optim LLC —Sturbridge, MA
- $45,000 - $50,000 a year
- Full-time
- 5 years
- Databases
- High school diploma or GED
- Health insurance
- Dental insurance
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Operational Quality Assurance Specialist
Centese, Inc. —Omaha, NE
- $25 - $28 an hour
- Full-time
- Criminal background check
- US work authorization
- Organizational skills
- Health insurance
- Dental insurance
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NSI P1 Quality Technician
Northern Stamping Inc —Cuyahoga Heights, OH
- $55,000 - $60,000 a year
- Full-time
- Mid-level
- High school diploma or GED
- Analysis skills
Quality Manager - Bemis Health Care
Bemis Manufacturing Company —Sheboygan Falls, WI
- Writing skills
- Engineering
- 3 years
Quick Apply

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Design Quality Engineer, Software Medical Device

Senseye
Austin, TX

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Job Details

Full-time
$100,000 - $125,000 a year

Benefits

Commuter assistance
Stock options
Disability insurance
Health insurance
Dental insurance
401(k)
Paid time off
Snacks provided
Vision insurance
Flexible schedule
Life insurance

Qualifications

Quality management standards in production
IT quality control
FDA 21 CFR Part 11
GMP
Quality assurance experience within IT
Quality risk management
Quality control documentation
Compliance documentation
Design controls
Biomedical regulatory compliance
Clinical quality assurance standards
Design (software development lifecycle)
ISO 13485
Product design documentation
IT risk management

Full Job Description

About Us

Senseye is a NeuroTechnology Company in Austin, TX on the cusp of revolutionizing Mental Health. Over the past 6 years we have invested millions of dollars in R&D to build our platform allowing us to measure cognitive activity via the eye through mobile phones. Through multiple iterations and use cases we are now focused on building the world’s first Objective Mental Health Diagnostics on top of our core technology. Our first diagnostic is for PTSD and is entering clinical trials now, followed soon by additional indications for Anxiety and Depression. As the world struggles with a mental health crisis, it is not hyperbolic to suggest that an objective diagnostic platform, that gives clinicians a safe and objective accurate approach to identifying and monitoring mental health disease, will redefine how mental health services are provided and will enable access to treatment for hundreds of millions of sufferers. The Senseye platform has the potential to be the technology that drives this change.

Senseye is developing AI-enabled software medical devices to help make mental health assessment more objective, starting with PTSD. We are looking for a Design Quality Engineer for our software medical device (SaMD) who can partner closely with engineering, clinical, regulatory, and product teams to build practical, audit-ready quality processes for SaMD development.

Role Description

This is a hands-on role for someone who understands design controls, software lifecycle documentation, risk management, and regulated product development — and who wants to help shape the quality system rather than simply maintain one. This is an intersection role: it requires both medical-device design-controls/quality experience and hands-on software / SaMD lifecycle experience — not one or the other.

Requirements

This role requires both of the following, not either/or:

4+ years in medical-device design quality, design assurance, or quality engineering for regulated software (design controls + software lifecycle).
2+ years hands-on with SaMD, SiMD, or medical-device software (including digital health / diagnostics software).
Hands-on experience with design controls, risk management, software validation, traceability, and quality-system documentation.
Working knowledge of ISO 13485, ISO 14971, IEC 62304, FDA QMSR / 21 CFR Part 820, and 21 CFR Part 11.
Comfort working directly with software teams using tools such as Jira, GitHub, Confluence, and eQMS systems.

Responsibilities

Own and improve SaMD design-control deliverables, including user needs, design inputs/outputs, traceability, design reviews, verification/validation evidence, and DHF readiness.
Partner with software, data science, clinical, and regulatory teams to apply IEC 62304, ISO 14971, ISO 13485:2016, FDA QMSR / 21 CFR Part 820, and applicable software quality practices.
Support AI/ML model lifecycle quality practices, including documentation, risk controls, change control, validation evidence, and total-product-lifecycle thinking.
Help define pragmatic QMS processes for a fast-moving regulated startup, including software development, non-product software validation / CSA, supplier controls, CAPA, and audit readiness.
Contribute to cybersecurity, usability/HFE, post-market, complaint, and quality-metrics activities in partnership with subject-matter experts

Nice to Have

AI/ML-enabled medical-device experience.
Familiarity with IMDRF GMLP principles.
Cybersecurity documentation experience for medical devices.
Usability / human factors engineering experience.
FDA submission, audit, notified-body, CAPA, or post-market experience.
Experience in a startup or early-stage regulated product environment.

Why this role is compelling

You will help shape the quality foundation for an AI-enabled SaMD product, not just maintain inherited procedures.

You will work cross-functionally with engineering, clinical, regulatory, product, and data science teams.
You will have direct impact on design controls, software lifecycle quality, risk management, and audit readiness.
You will join at a stage where quality decisions still materially shape how the product and QMS scale.

Benefits

The freedom and trust to define your role as we design, build, and ship our products
Competitive salary and stock option plan
Flexible paid time off (vacation, sick leave, and public holidays)
Flexible schedules
Company health care plan
- Medical, dental, and vision insurance
- Short and long term disability insurance
- Life insurance policy
401k
Commuter benefits for parking, public transit, carshares, etc.
Mothers' room
Fully stocked kitchen
Opportunities for continuing education

The compensation for this role is $100,000 - $125,000 annually.

Senseye is dedicated to building a community of employees that are diverse, passionate, and engaged. We are committed to equal opportunity regardless of race, color, ancestry, religion, gender, gender identity, parental or pregnancy status, national origin, sexual orientation, age, marital status, disability, or veteran status. When we're safe, healthy, and balanced we can accomplish phenomenal things together.

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medical device quality jobs

Design Quality Engineer, Software Medical Device

Quality Engineer - Medical Device

Sr Quality Engineer – Medical Device only Locals

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Contract Opportunity - Medical Device Auditors

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Quality Inspector – Sheet Metal Fabrication – Direct Hire –$45-65K

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Quality Manager - Bemis Health Care

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