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Medical Device Development Jobs (NOW HIRING)

Research Fellow, Medical Device Toxicologist

OR ยท On-site +1

$150K - $200K/yr

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We have a significant global research, development, manufacturing and commercial footprint of ... The Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical ...

Minimum of four years experience in medical device development, manufacture and/or testing, with demonstrated knowledge of US, Canada and EU medical device regulatory requirements, experience with ...

Medical Device Assembler

Buffalo, NY ยท On-site

$17.75 - $19.75/hr

  • Retirement

  • PTO

Assemble medical device sub-assemblies and finished products following work instructions. * Perform ... Training and Development opportunities: Because we foster a culture of continuing education. Let ...

Medical Device Solderer

Irvine, CA ยท On-site

$22 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The environment encourages skill development with modern equipment, opportunities to learn new ... a sterile medical device production setting. Job Type & Location This is a Contract to Hire ...

New

Medical Device Rep

Boca Raton, FL ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Senior Device Development Engineer

Valley, AL ยท On-site

$83K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a Senior Device Development Engineer to join our New Technologies, Combination ... medical, dental, vision, life and disability), paid time off, and family support benefits. For ...

New

Medical Device Rep

Baton Rouge, LA ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Medical Device Rep

Albuquerque, NM ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Medical Device Rep

Austin, TX ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Medical Device Rep

Carlsbad, CA ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Medical Device Rep

Santa Barbara, CA ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Medical Device Rep

Sarasota, FL ยท On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Showing results 41-60

Medical Device Development information

See salary details

$29K

$53.4K

$81K

How much do medical device development jobs pay per year?

As of Aug 13, 2026, the average yearly pay for medical device development in the United States is $53,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $60,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in medical device development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

What is the difference between Medical Device Development vs Medical Device Quality Assurance?

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.
More about Medical Device Development jobs

What cities are hiring for Medical Device Development jobs?

Cities with the most Medical Device Development job openings:

What states have the most Medical Device Development jobs?

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

Infographic showing various Medical Device Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $53,418 per year, or $25.7 per hour.

Sr. Manager, Medical Device Cyber Security

Tempus

Chicago, IL โ€ข Hybrid

$150K - $210K/yr

Full-time

Re-posted 8 days ago


Job description

Passionate about precision medicine and advancing the healthcare industry?

Recent advancements in underlying technology have finally made it possible for AI to impact clinical care in a meaningful way. Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical information about the right treatments for the right patients, at the right time.

The Role

As the Medical Device Cybersecurity Senior Manager, you will own the medical device cyber security program at Tempus AI. You will act as the crucial bridge between enterprise-wide security strategy and product-level medical device technical execution. You will partner closely with R&D, Product Management, Regulatory Affairs, and Quality to integrate security into the device lifecycle ("shift-left"), ensure adherence to FDA cybersecurity guidelines, and enabling Pre-Market submissions as well as Post-Market surveillance of Tempus Medical Devices.

What You'll Do
  • Program Management & Strategy Execution:

    • Develop, implement, and continuously mature the Medical Device Cybersecurity roadmap, policies, and Standard Operating Procedures (SOPs), aligning them with the overarching enterprise data security strategy.

  • Product Security & Engineering Partnership:

    • Partner with R&D and engineering teams to embed secure-by-design principles and Secure Software Development Life Cycle (SSDLC) practices into medical device development.

    • Define and manage the strategy for Software Bill of Materials (SBOM) generation and maintenance across all device product lines.

    • Coordinate with Cloud Security, Application Security, and Vulnerability Management Information Security teams to integrate their services into Tempus Medical Devices.

  • Regulatory Compliance & Quality Assurance:

    • Ensure device design and lifecycle management align with FDA pre-market and post-market cybersecurity guidelines.

    • Author, review, and maintain cybersecurity documentation required for regulatory submissions (e.g., 510(k), De Novo, PMA).

    • Coordinate with the Quality Management team to integrate cybersecurity into the enterprise Quality Management System (QMS).

  • Leadership & Mentorship:

    • Mentor, and develop the Medical Device Cybersecurity Analyst(s), guiding their daily tactical execution, vulnerability assessments, and professional growth.

    • Serve as the primary Subject Matter Expert (SME) for Medical Device Cybersecurity across the organization and provide education to cross-functional teams on the program.

  • Threat & Vulnerability Management:

    • Oversee the continuous monitoring, vulnerability scanning, and patching strategies for deployed medical devices.

    • Manage engagements with penetration testing conducting assessments on Tempus hardware and embedded systems

Qualifications
  • 7+ years of technical experience in information security in the tech or healthcare industry.

  • Deep understanding of FDA Cybersecurity Guidance (Pre-market and Post-market), ISO 14971, and ISO 13485

  • Proficiency in threat modeling methodologies (STRIDE, PASTA) and secure architecture design.

  • Industry-recognized certifications such as CISSP, HCISPP, CISM, or relevant SANS certifications are preferred.

  • Ability to manage several programs at once and work proactively to align multi-disciplinary stakeholders.

  • Excellent written and verbal communication skills, including the ability to act as translator among diverse teams of biologists, medical professionals, engineers, operators, and data scientists.

#LI-HR1

#LI-Hybrid

CHI: $150,000-$210,000

The expected salary range above is applicable if the role is performed from Illinois and may vary for other locations (California, Colorado, New York). Actual salary may vary based on qualifications and experience. Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and other benefits depending on the position.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.