Top 1318 Medical device regulatory Jobs in Remote

Medical Device Risk Management Advisor (Part-Time, Remote)
FocusKPI Inc. —Remote
- Part-time
- Remote
- Mid-level
- Analysis skills
Regulatory Affairs Specialist — Medical Devices
Azaaki LLC —Remote
- $85 - $90 an hour
- Full-time
- Remote
- Background check
- 5 years
- Engineering
- Work from home
Quick Apply
12d
Regulatory Affairs Specialist (FDA medical device regulation) - REMOTE: Anywhere USA
FUJIFILM —Remote
- $73,759 - $91,200 a year
- Remote
- Mid-level
- Bachelor's degree
- Travel
- Health insurance
- Dental insurance
Regulatory Affairs Specialist
Medline Industries —Remote
- $79,000 - $119,000 a year
- Full-time
- Remote
- Bachelor of Science
- Mid-level
- Travel
- Health insurance
- 401(k)
Principal Regulatory Affairs Specialist
Saluda Medical —Remote
- Full-time
- Remote
- 7 years
- Microsoft Excel
- Analysis skills
Quick Apply
Senior Regulatory Affairs Specialist
Saluda Medical —Remote
- Full-time
- Remote
- Analysis skills
- Mentoring
- Senior level
Quick Apply
Software Development Process Engineer / Specialist (Medical Device)
Siemens Healthineers —Remote
- $109,920 - $151,140 a year
- Full-time
- Remote
- Computer Science
- Engineering
- Mid-level
- Disability insurance
- Health insurance
Quick Apply
Senior Regulatory Affairs Specialist
Oura —Remote
- $127,500 - $178,000 a year
- Remote
- 5 years
- Organizational skills
- Senior level
- Paid holidays
- Health insurance
10d
Manager, Medical Device Labeling and Operations
LivaNova —Remote
- $120,000 - $145,000 a year
- Full-time
- 8 years
- Bachelor's degree
- Travel
- Employee stock purchase plan
- Health insurance
Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote)
MicroVention, Inc. —Aliso Viejo, CA
- $145,000 - $155,000 a year
- Remote
- Microsoft Excel
- 5 years
- Bachelor of Science
Senior Regulatory Affairs Specialist
Siemens Healthineers —Remote
- $117,770 - $161,931 a year
- Full-time
- Remote
- Microsoft Outlook
- Mid-level
- Presentation skills
- Disability insurance
- Health insurance
Quick Apply
Medical Information Specialist
Med Communications —Remote
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Health insurance
Quick Apply
Contract Opportunity - Medical Device Auditors
SGS —Remote
- Contract
- Spanish
- Computer literacy
- English
Quick Apply
12d
Medical Device & Diagnostics - CRA 2 - US Remote
Fortrea —Remote
- Full-time
- Mid-level
- Office
- Travel
- Disability insurance
- Health insurance
Medical Writer - Clinical Compliance
Solventum —Remote
- $124,000 - $170,500 a year
- Full-time
- Microsoft Excel
- 5 years
- Mid-level
- Health savings account
- Disability insurance
12d
Medical Device Workflow & Validation Lead (Remote, Continental United States)
ICA.ai —Arlington, VA
- $130,000 - $160,000 a year
- Full-time
- Remote
- Analysis skills
- US work authorization
- Senior level
- Disability insurance
- Health insurance
Quick Apply
Senior Regulatory CMC Drug-Device Combination Product Lead
Biogen —Remote
- $111,000 - $149,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Analysis skills
- Paid parental leave
- Employee stock purchase plan
Medical Writer (Remote, US)
Maquet Cardiovascular LLC —Boston, MA
- $105,000 - $115,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- 3 years
- Commuter assistance
- Disability insurance
Medical, Legal and Regulatory (MLR) Coordinator
EVERSANA —Overland Park, KS
- Contract
- Remote
- Microsoft Outlook
- Customer service
- Computer literacy
Quick Apply
Regulatory & Clinical Specialist
LivaNova —Remote
- $85,000 - $95,000 a year
- Full-time
- Remote
- 3 years
- Master's degree
- Doctor of Philosophy
- Employee stock purchase plan
- Health insurance

I want to receive the latest job alert for medical device regulatory in remote

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Medical Device Risk Management Advisor (Part-Time, Remote)

FocusKPI Inc.
Remote

Apply Now

Job Details

Part-time

Qualifications

Usability testing
Feature validation testing
Conducting user feedback sessions
Good documentation practices (GDP)
Mid-level
Analysis skills
Quality assurance in testing
Quality risk management
Compliance documentation
Design controls
Biomedical regulatory compliance
FMEA
Product quality assurance
Usability feedback collection
Hazard analysis
Regulatory compliance analysis
Prototypes

Full Job Description

We are building an AI-powered platform to support medical device risk management and regulatory documentation (including ISO 14971 and design controls), and are looking for a few professionals to serve as ongoing product feedback advisors.

This is a flexible, part-time opportunity for experienced professionals who can periodically test new features, review workflows, and provide practical feedback based on real-world medical device and regulatory experience. Your input will directly shape how the product supports day-to-day work in regulated environments.

What You’ll Do

Test new features and prototypes periodically
Provide feedback on usability and regulatory alignment
Review risk management and documentation workflows
Suggest improvements based on real industry practice
Join occasional 30–45 minute feedback sessions

Time Commitment

Flexible, ongoing engagement
Approximately 1–2 hours per week or biweekly
Fully remote

Preferred Background

Medical device regulatory affairs or quality assurance
Experience with ISO 14971 risk management
Design controls / DHF documentation
510(k), De Novo, or PMA experience is a plus
Risk management file, FMEA, or hazard analysis experience

Consultants and industry professionals are welcome.

How to Apply

If you’re interested, please complete this short screening form so we can better understand your background:
https://forms.gle/jgj1ZN2jtAGGAbYQA

We’ll follow up with selected candidates to schedule an initial session and discuss next steps.

NOTICE: Please be aware of fraudulent emails regarding job postings, job offers and fake checks. FocusKPI's recruiting team will strictly reach out via @focuskpi.com email domain. If you have received fraudulent emails now or in the past, please report it to https://reportfraud.ftc.gov/ .
The domain @focuskpijobs.com is fraudulent and not related to FocusKPI. Please do not not reply or communicate to anyone with @focuskpijobs.com.

wK7jr54dly

Apply Now

Refine Your Search

medical device regulatory jobs in remote

Medical Device Risk Management Advisor (Part-Time, Remote)

Regulatory Affairs Specialist — Medical Devices

Regulatory Affairs Specialist (FDA medical device regulation) - REMOTE: Anywhere USA

Regulatory Affairs Specialist

Principal Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

Software Development Process Engineer / Specialist (Medical Device)

Senior Regulatory Affairs Specialist

Manager, Medical Device Labeling and Operations

Sr. Medical Writer Peripheral Vascular Med Device (U.S. Remote)

Senior Regulatory Affairs Specialist

Medical Information Specialist

Contract Opportunity - Medical Device Auditors

Medical Device & Diagnostics - CRA 2 - US Remote

Medical Writer - Clinical Compliance

Medical Device Workflow & Validation Lead (Remote, Continental United States)

Senior Regulatory CMC Drug-Device Combination Product Lead

Medical Writer (Remote, US)

Medical, Legal and Regulatory (MLR) Coordinator

Regulatory & Clinical Specialist

I want to receive the latest job alert for medical device regulatory in remote

Related Searches

Explore jobs in more locations

What You’ll Do

Time Commitment

Preferred Background

How to Apply

Job Seeker Tools

Employer Tools

Browse

Stay Connected