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Medical Device Startup Jobs (NOW HIRING)

Quality Technician

Burlingame, CA · On-site

$35 - $40/hr

Neptune Medical, is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the ...

Quality Engineer - Medical Device

Newark, DE · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Location: Delaware Largescale Medical Device client facing a ... Participate in production line startup and manufacturing support as needed. Skills: Required: * 3 ...

Pramand is a fast-paced medical device startup operating across multiple hydrogel-based platforms; the successful candidate will bring a hands-on, builder's mindset, a bias toward execution, and the ...

Marketing Manager

Bedford, MA · On-site

$110K - $175K/yr

Pramand is a fast-paced medical device startup operating across multiple hydrogel-based platforms; the successful candidate will bring a hands-on, builder's mindset, a bias toward execution, and the ...

Senior Quality Engineer

Alameda, CA · On-site

$120 - $180/hr

Previous role at a fast-paced medical device startup. How We Work * We are intentional. We prioritize and are thoughtful about how we use others' time. * We care for others. We prioritize safety both ...

Minimum 5 years of medical device R&D experience * Hands‑on catheter prototyping and testing ... Startup and/or small‑company experience preferred * Proficiency with SolidWorks including: * 3D ...

Device Technician

Boca Raton, FL · On-site

$25 - $28/hr

Experience with medical devices, medical device assembly, and repair. * Ability to support equipment installation and startup in a field-based, travel-intensive environment. * Comfort working in ...

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing ... Startup and/or small-company experience preferred * Proficiency with SolidWorks including: * 3D ...

Sustaining Engineer

Santa Clara, CA · On-site

$107K - $132K/yr

A demonstrated desire to work in a small medical device startup. * A willingness to work hard, with a driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.

New

Sustaining Engineer

Menlo Park, CA

$107K - $132K/yr

A demonstrated desire to work in a small medical device startup. * A willingness to work hard, with a driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.

Sustaining Engineer

Sunnyvale, CA · On-site

$107K - $132K/yr

A demonstrated desire to work in a small medical device startup. * A willingness to work hard, with a driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.

New

Sustaining Engineer

Menlo Park, CA · On-site

$90 - $105/hr

A demonstrated desire to work in a small medical device startup. * A willingness to work hard, with a driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.

Sustaining Engineer

San Mateo, CA · On-site

$104K - $128K/yr

A demonstrated desire to work in a small medical device startup. * A willingness to work hard, with a driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.

New

Sr. Quality Engineer

San Francisco, CA · On-site

$104K - $141K/yr

Medical device startup experience. * Experience supporting Class II and/or Class III medical devices. * Experience with process validation methodologies. * Excellent project management and ...

Sustaining Engineer

Mountain View, CA

$107K - $132K/yr

A demonstrated desire to work in a small medical device startup. * A willingness to work hard, with a driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.

New

Sustaining Engineer

Palo Alto, CA · On-site

$107K - $132K/yr

A demonstrated desire to work in a small medical device startup. * A willingness to work hard, with a driven outlook and with a strong desire to succeed as an engineer, as a team, and as a company.

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How much do medical device startup jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for medical device startup in the United States is $36.72, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $45.91 per hour, depending on experience, location, and employer.

What is a medical device startup?

A medical device startup is a company in its early stages that focuses on developing, manufacturing, and bringing innovative medical devices to market. These startups often work on new technologies or improvements to existing devices, aiming to address unmet medical needs or improve patient outcomes. They typically operate in a high-regulation environment and may seek funding from investors, grants, or partnerships to support research, development, and commercialization efforts. Success in this field requires multidisciplinary expertise, including engineering, regulatory affairs, and clinical knowledge.

What are jobs at a medical device startup?

Jobs at a medical device startup include roles in research and development, sales, information technology, software development, and customer service. Working at a medical device startup in research and development, you collaborate with teams to design studies, perform research, and devise training materials for products. Your end goal is to help develop new products. As a sales representative, you promote and sell medical equipment, educate clients on the benefits of products, and respond to questions and concerns. Software and IT jobs at a medical device startup involve responsibilities like troubleshooting technical problems, diagnosing and repairing computer systems, creating databases, evaluating processes, and maintaining and utilizing medical imaging equipment.

What are the key skills and qualifications needed to thrive in a medical device startup?

To thrive in a medical device startup, you need a solid background in biomedical engineering, product development, and regulatory compliance, often supported by relevant degrees or experience in healthcare technology. Familiarity with FDA regulations, CAD design software, and project management tools like Jira or Asana is typically required. Strong collaboration, adaptability, and entrepreneurial problem-solving are essential soft skills in this dynamic environment. These skills and qualities are vital for navigating rapid innovation cycles, ensuring regulatory approval, and driving successful product launches in a competitive market.

What are the common challenges faced when working in a medical device startup environment?

Working in a medical device startup often involves navigating a fast-paced, dynamic environment where priorities can shift rapidly. Team members typically wear multiple hats, balancing product development with strict regulatory requirements and limited resources. Collaboration across engineering, clinical, and business teams is essential, as everyone works together to meet ambitious milestones and bring innovative products to market. Despite these challenges, the role provides unique opportunities to make a tangible impact and grow professionally within a close-knit, innovative team.

What is the difference between Medical Device Startup vs Medical Device Engineer?

AspectMedical Device StartupMedical Device Engineer
Required CredentialsTypically requires engineering degree, certifications varyRequires engineering degree, often with specific certifications in biomedical or mechanical engineering
Work EnvironmentFast-paced, innovative startup setting, often small teamsDesign, develop, and test medical devices, usually in corporate or R&D labs
Employer & Industry UsageStartups in medical device industry, early-stage companiesEstablished companies, R&D departments, or startups
Common Search & Comparison IntentUnderstanding roles in startups, career optionsJob responsibilities, qualifications, career path

Medical Device Startup roles focus on innovation, product development, and often require versatile skills in a dynamic environment. Medical Device Engineers are specialized professionals responsible for designing and testing devices, typically within established or startup companies. While both roles require engineering credentials, startups emphasize adaptability and entrepreneurial spirit, whereas engineers focus on technical expertise and product quality.

What cities are hiring for Medical Device Startup jobs?

Cities with the most Medical Device Startup job openings:

What are the most commonly searched types of Medical Device Startup jobs?

The most popular types of Medical Device Startup jobs are:

What states have the most Medical Device Startup jobs?

States with the most job openings for Medical Device Startup jobs include:

Infographic showing various Medical Device Startup job openings in the United States as of August 2026, with employment types broken down into 59% Full Time, 8% Part Time, 8% Temporary, and 25% Contract. Highlights an 100% In-person job distribution, with an average salary of $76,384 per year, or $36.7 per hour.

Quality Technician

Neptune Medical

Burlingame, CA • On-site

$35 - $40/hr

Full-time

Medical, Vision, Life, Retirement

Re-posted 4 days ago


Job description

Neptune Medical, is an innovative, venture capital funded medical device startup headquartered in Burlingame, CA. We have already commercialized novel medical devices using our technology. Now the team at Neptune is building something truly unique: a fully flexible medical robot that enables doctors to reach deep into human anatomy. Triton Robotic Endoscopy will disrupt flexible endoscopy and set a new standard in outcomes for decades to come.
TITLE: Quality Technician
POSITION SUMMARY: The Quality Technician will support manufacturing operations by ensuring in-process and finished medical devices meet established quality requirements, specifications, and regulatory standards. This role is responsible for identifying and documenting quality issues on the production floor, supporting investigations and root cause analysis, managing nonconforming materials, and collecting process and product data to drive continuous improvement.
The technician works closely with Manufacturing, Quality Engineering, and cross-functional teams to ensure rapid response to quality concerns and compliance with applicable quality system regulations (e.g., FDA 21 CFR Part 820, ISO 13485).
ROLES AND RESPONSIBILITIES
Manufacturing Quality & Inspection
  • Perform incoming, in-process, and final inspections of components, subassemblies, and medical devices in accordance with approved procedures, drawings, and sampling plans
  • Ensure product compliance with specifications, GMP, and regulatory requirements
  • Accurately document inspection and test results in device history records (DHRs) and other quality records
  • Maintain traceability of materials and finished goods throughout production

Nonconformance & Investigation Support
  • Identify, document, and segregate nonconforming materials
  • Support containment activities, including line clearance, product holds, and sorting/rework activities
  • Assist in root cause investigations and corrective and preventive actions (CAPA)
  • Collaborate with Quality Engineers to analyze trends and recurring issues

Data Collection & Continuous Improvement
  • Collect and analyze in-process quality data to support process monitoring and improvement initiatives
  • Provide input on quality metrics, yield trends, and defect data
  • Partner with Manufacturing and Engineering teams to implement process improvements and error-proofing solutions

Equipment & Testing
  • Operate, maintain, and calibrate inspection and test equipment (e.g., calipers, microscopes, gauges)
  • Support equipment calibration and environmental monitoring programs as needed
  • Perform basic product or material testing in accordance with validated methods

Documentation & Quality Systems Support
  • Review Device History Records (DHRs) and other quality documentation for completeness and accuracy
  • Maintain quality records in compliance with document control procedures and regulatory requirements
  • Support audits (internal/external) by providing documentation and participating in audit activities
  • Ensure adherence to Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP)

Cross-Functional Collaboration
  • Work closely with Production, Manufacturing Engineering, and Quality Engineering to ensure timely resolution of quality issues
  • Communicate quality concerns clearly and escalate issues as appropriate
  • Support training of production personnel on quality requirements and procedures

REQUIRED QUALIFICATIONS:
  • High school diploma or equivalent required; Associate degree or technical certification preferred
  • 3-5+ years of experience in Quality Assurance/Quality Control in a manufacturing environment (medical device industry strongly preferred)
  • Working knowledge of FDA Quality System Regulation (21 CFR Part 820) and/or ISO 13485
  • Experience with inspection methods, sampling plans, and interpreting engineering drawings and specifications
  • Proficiency in Microsoft Office and electronic quality management systems

PREFERRED QUALIFICATIONS:
  • Experience in a regulated medical device or life sciences environment
  • Familiarity with nonconformance systems, CAPA, and root cause analysis tools (e.g., 5 Whys, Fishbone)
  • Hands-on experience with dimensional and visual inspection equipment
  • Understanding of validation activities (IQ/OQ/PQ)
  • Experience supporting audits and regulatory inspections

Neptune Medical is located in Burlingame, CA, near the Millbrae Caltrain and BART Station.
Our job titles may span more than one career level. The starting hourly rate for this role is between $35-$40/hour depending on experience. The actual base pay is dependent upon many factors, such as: education, training, transferable skills, work experience, business needs, and location. The base pay range is subject to change and may be modified in the future. This role may also be eligible for equity, benefits and 401(K) with matching.
Neptune Medical provides equal employment opportunities to all applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.