Top 55 Of quality assurance medical devices Jobs in Remote

Biomedical Engineering Quality Assurance Lead (QAL)
SME Careers by SuperAnnotate —Remote
- Contract
- Remote
- Management
- English
- Mid-level
Senior Manager, Global Quality Assurance
Medexus Pharma —Remote
- Remote
- Microsoft Excel
- Master's degree
- Analysis skills
Engineer I, Software Quality
FUJIFILM —Remote
- Remote
- Microsoft Excel
- Bachelor of Science
- Office
Quality Systems Implementation Specialist
RQM+ —Remote
- Ability to walk for extended periods
- Engineering
- Mid-level
Quick Apply
Quality and Regulatory (QA/RA) Consultant - Independent Contractor
Cook Device Solutions —Remote
- $100 - $175 an hour
- Part-time
- Remote
- Computer literacy
- Bachelor's degree
- Travel
- Flexible schedule
Quick Apply
Senior Manager, Clinical Quality Assurance
Gan & Lee Pharmaceuticals —Remote
- Full-time
- Writing skills
- English
- Analysis skills
Quick Apply
Associate Director, Clinical Quality Assurance Auditor
Cytokinetics —Remote
- $195,300 - $227,850 a year
- Full-time
- Remote
- Bachelor's degree
- Travel
- Senior level
Senior Software Quality Assurance (SQA) Engineering Lead
iRhythm Technologies, Inc. —Remote
- $138,000 - $180,000 a year
- Full-time
- Remote
- Java
- 8 years
- Product management
Quick Apply
10d
DX Head of Regions Quality Management and Regulatory Affairs
Siemens Healthineers —Remote
- $240,000 - $330,000 a year
- Full-time
- Remote
- 11+ years
- English
- Analysis skills
- Disability insurance
- Health insurance
Quick Apply
Document Control & Quality Systems Administrator
Noctrix Health —Remote
- $120,000 - $140,000 a year
- Full-time
- Remote
- 3 years
- Continuous improvement
- Neurology
Quick Apply
11d
Staff Quality Specialist
Katalyst Healthcares & Life Sciences —Parsippany-Troy Hills, NJ
- Contract
- Remote
- 7 years
- Engineering
- Business Administration
Quick Apply
Sr Mgr, QA/Quality Engineer, Device & Combination Products
ESPERION THERAPEUTICS INC —Ann Arbor, MI
- $166,500 - $175,000 a year
- Remote
- Laboratory experience
- Microsoft Office
- Travel
- Paid holidays
- Health insurance
Quick Apply
Manager, Customer Quality
Advanced Sterilization Products —Remote
- $114,100 - $190,500 a year
- Remote
- Nursing
- Supervising experience
- Travel
7d
Sr. Manager, Quality Systems
TG Therapeutics —Remote
- Email
- Remote
- 5 years
- Mentoring
- US work authorization
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
Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge Management
BeiGene —Remote
- $172,000 - $232,000 a year
- Full-time
- 6 years
- Microsoft Outlook
- Computer literacy
- Health savings account
- Employee stock purchase plan
Senior Global Supplier Quality Professional II
Kindeva Drug Delivery Careers —Remote
- $104,000 - $137,800 a year
- Full-time
- Remote
- 8 years
- Project management
- Senior level
- Health insurance
- Dental insurance
Quick Apply
11d
Complaint Handling Specialist
FUJIFILM —Remote
- $73,759 - $82,000 a year
- Mid-level
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Contract Opportunity - Medical Device Auditors
SGS —Remote
- Contract
- Spanish
- Computer literacy
- English
Quick Apply
12d
Director, (GCP) Quality Assurance
Tempus —Chicago, IL
- $160,000 - $200,000 a year
- Full-time
- Remote
- Microsoft Word
- Microsoft Excel
- 5 years
- Health insurance

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Biomedical Engineering Quality Assurance Lead (QAL)

SME Careers by SuperAnnotate
Remote

Apply Now

Job Details

Contract

Qualifications

Rubric-based evaluation
Document control experience within engineering industry
English
Compliance documentation
Managing product quality assurance teams
Rubric-based test scoring

Full Job Description

In this hourly, remote contractor role, you will work as a Biomedical Engineering Quality Assurance Lead (QAL) to oversee quality, consistency, and trainer performance across biomedical engineering AI training projects. You will review AI-generated biomedical engineering content and trainer/QA work, evaluate output quality against project guidelines, provide precise written feedback, and ensure that all contributors follow the expected quality standards. You will assess work for technical accuracy, biomedical reasoning, calculation correctness, standards awareness, regulatory awareness, unit consistency, safety considerations, clarity, formatting, instruction-following, and adherence to project-specific rubrics. You will spot recurring quality issues, communicate updates to trainers and QAs, support onboarding, maintain documentation, and help activate contributors who are not working consistently. This role requires strong biomedical engineering expertise, strong English communication skills, excellent attention to detail, structured communication, and the ability to manage quality workflows across remote technical teams. This role is with SME Careers, a fast-growing AI Data Services company and subsidiary of SuperAnnotate, delivering training data for many of the world’s largest AI companies and foundation-model labs. Your biomedical engineering quality leadership will directly help improve the world’s premier AI models by ensuring that biomedical engineering training data is accurate, logically sound, clearly explained, well-documented, safety-aware, and aligned with client expectations. Selection process involves an AI interview, a domain-specific task, and an interview with a recruiter. Important: There is no immediate project for this role; however, if qualified, you will be among the first experts we reach out to when relevant opportunities arise. This will also provide you with access to future projects available through our expert network.

requirements

Bachelor’s or Master’s degree in Biomedical Engineering, Bioengineering, Medical Engineering, Biomechanical Engineering, Electrical Engineering with biomedical focus, Mechanical Engineering with biomedical focus, or a closely related field.

Strong grasp of the English language to follow project guidelines, communicate with teams, and provide clear technical feedback in English.

3+ years of professional experience in biomedical engineering, medical devices, biomechanics, biomaterials, bioinstrumentation, clinical engineering, R&D, regulatory documentation, technical review, engineering education, or related workflows.

Strong understanding of core biomedical engineering topics such as biomechanics, biomaterials, medical devices, bioinstrumentation, biosignals, imaging systems, physiological systems, tissue engineering, rehabilitation engineering, and biomedical data analysis.

Ability to evaluate biomedical engineering content against detailed rubrics and identify issues such as incorrect assumptions, flawed calculations, missing units, unsafe recommendations, weak biological/clinical reasoning, hallucinated standards, regulatory overclaims, or incomplete explanations.

Familiarity with common biomedical engineering tools or workflows such as MATLAB, Python, LabVIEW, SolidWorks, CAD/CAE tools, signal processing workflows, medical device documentation, ISO/FDA-related documentation, clinical engineering workflows, or biomedical data analysis tools is preferred.

Experience leading or supporting remote teams of trainers, annotators, reviewers, engineers, technical writers, or QAs is strongly preferred.

Comfortable working in fast-moving remote environments using tools such as Discord, Google Sheets, Google Docs, trackers, dashboards, and project management systems.

Highly detail-oriented and organized, with the ability to maintain style guides, FAQs, trackers, onboarding materials, honeypots, calibration tasks, and other quality documentation.

Experience with AI training, data annotation, large language models, prompt/response evaluation, technical content QA, biomedical content QA, or rubric-based LLM evaluation is a strong plus.

responsibilities

Quality monitoring: Spot-check biomedical engineering items, identify quality issues, provide ongoing feedback through DMs, and escalate recurring or critical issues.

Technical review: Evaluate AI-generated biomedical engineering explanations, medical-device reasoning, biomechanics calculations, biomaterials discussions, bioinstrumentation workflows, biosignal explanations, diagrams/descriptions, and problem-solving steps for correctness and clarity.

Trainer and QA communication: Update trainers and QAs on Discord about new item guidelines, project changes, workflow updates, quality expectations, and biomedical-engineering-specific review standards.

Question handling: Respond to trainer/QA questions clearly and promptly, especially around engineering assumptions, units, formulas, biological context, device safety, regulatory considerations, standards references, and rubric interpretation.

Trainer/QA activation management: DM contributors who are inactive or not working, encourage activation, track follow-ups, and flag availability issues when needed.

Documentation: Create and maintain biomedical engineering project documentation, including style guides, trackers, FAQs, quality notes, examples, honeypots, calibration tasks, and onboarding materials.

Onboarding and training: Schedule and run onboarding/training calls with trainers and QAs to explain project expectations, workflows, rubrics, quality standards, and biomedical-engineering-specific review requirements.

Quality alignment: Ensure all trainers and QAs apply biomedical engineering guidelines consistently and understand updates as projects evolve.

Risk and safety review: Flag unsafe, misleading, or overconfident biomedical engineering recommendations, especially where medical devices, patient safety, clinical workflows, biological systems, diagnostics, imaging, rehabilitation tools, or regulatory claims may be affected.

Process improvement: Identify recurring quality gaps, propose workflow improvements, and help build scalable QA processes for biomedical engineering AI training projects.

Apply Now

Refine Your Search

of quality assurance medical devices jobs in remote

Biomedical Engineering Quality Assurance Lead (QAL)

Senior Manager, Global Quality Assurance

Engineer I, Software Quality

Quality Systems Implementation Specialist

Quality and Regulatory (QA/RA) Consultant - Independent Contractor

Senior Manager, Clinical Quality Assurance

Associate Director, Clinical Quality Assurance Auditor

Senior Software Quality Assurance (SQA) Engineering Lead

DX Head of Regions Quality Management and Regulatory Affairs

Document Control & Quality Systems Administrator

Staff Quality Specialist

Sr Mgr, QA/Quality Engineer, Device & Combination Products

Manager, Customer Quality

Sr. Manager, Quality Systems

Manager, Medical Device Labeling and Operations

Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge Management

Senior Global Supplier Quality Professional II

Complaint Handling Specialist

Contract Opportunity - Medical Device Auditors

Director, (GCP) Quality Assurance

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