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Medical Device Development Jobs in Washington (NOW HIRING)

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Medical Device Development information

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$32.8K

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$91.7K

How much do medical device development jobs pay per year?

As of Jun 10, 2026, the average yearly pay for medical device development in Washington is $60,501.00, according to ZipRecruiter salary data. Most workers in this role earn between $48,100.00 and $68,000.00 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.
What are popular job titles related to Medical Device Development jobs in Washington? For Medical Device Development jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Medical Device Development jobs in Washington look for? The top searched job categories for Medical Device Development jobs in Washington are:
What cities in Washington are hiring for Medical Device Development jobs? Cities in Washington with the most Medical Device Development job openings:
Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in Washington as of June 2026, with employment types broken down into 2% As Needed, 80% Full Time, 10% Part Time, and 8% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $60,501 per year, or $29.1 per hour.
Senior Scientist / Engineer (Oncology / Medical Device)

Senior Scientist / Engineer (Oncology / Medical Device)

Lexical Intelligence LLC

Rockville, MD

$93K - $127K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 6 days ago

Job description

Senior Scientist / Engineer (Oncology / Medical Device)


Lexical Intelligence provides software and services related to processing large-scale biomedical information sources. Our Natural Language Processing (NLP) and analytics software is used by policy and decision makers to evaluate and prioritize current and emerging areas of research.


We are looking for a Senior Scientist / Engineer (Oncology / Medical Device) to work within the Advanced Research Projects Agency for Health (ARPA-H), Health Science Futures (HSF) Mission Office. The Senior Scientist / Engineer will have experience in medical device development (hardware and software), oncology and cancer biology, and biomedical research and engineering. The Senior Scientist / Engineer will have a firm understanding of R&D program management, diagnostic device development, and regulatory affairs in diagnostics. The Senior Scientist / Engineer shall be able to work well within a team of program managers, scientists, engineers, and government stakeholders. The selected applicant will be subject to a pre-employment background and reference check.


Required Qualifications

  • 8+ years of relevant industry experience in biotechnology, biopharmaceutical, or diagnostics companies
  • PhD or other advanced degree(s) in Biomedical Engineering, Oncology, Cancer Biology, Biochemistry, Cell Biology, Mechanical Engineering, Chemical Engineering, or related fields
  • Demonstrated expertise in medical device development, including both hardware and software components
  • Strong oral and written communication skills, with the ability to convey complex technical information to both technical and non-technical audiences
  • Proficiency in Microsoft PowerPoint and Excel, including the ability to create presentations and spreadsheets in real time during high-pressure meetings using keyboard shortcuts
  • Must be able to obtain a federal government Public Trust clearance
  • Must be authorized to work in the United States


Preferred Qualifications

  • Prior experience at diagnostics startups or mid-cap companies with exposure to regulatory affairs in diagnostics
  • Experience supporting executives managing large-budget R&D programs
  • Background in both basic and applied research environments
  • Demonstrated ability to conduct thorough technical evaluations of the R&D landscape, including identifying research gaps and critical unmet needs
  • Experience monitoring and tracking program performance metrics
  • Strong logical and critical thinking skills with the ability to critically review scientific and technical data
  • Professional curiosity, continuous drive for learning, and the ability to independently manage and prioritize assigned tasks


Responsibilities

  • Assist, support, and provide advice to the ARPA-H Program Manager to further the development and progress of new and existing R&D programs
  • Conduct thorough technical and scientific evaluations of the current R&D landscape to identify gaps in research portfolios and address critical needs aligned with the ARPA-H mission to accelerate better health outcomes
  • Monitor and track performer progress toward established program metrics and milestones
  • Read and synthesize complex scientific information and develop team and executive-level briefings tailored for both technical and non-technical audiences
  • Critically review scientific and technical data using strong logical and analytical thinking skills
  • Integrate into an existing team to support current ARPA-H efforts while also operating independently in support of technical R&D initiatives
  • Perform programmatic administrative tasks, including collecting, sorting, analyzing, and writing internal reports and briefings on relevant health-related topics
  • Support the development, funding, and management of new and existing R&D programs in oncology and medical device development
  • Participate in CONUS travel (approximately 10-20%) as needed to fully support the Program Manager and program activities


Responsibilities also include ensuring compliance with organizational security and privacy policies, protecting sensitive data and systems, reporting security incidents, and participating in required cybersecurity training. The role may also involve implementing best practices related to access control, data handling, and risk mitigation within the scope of assigned duties.

All candidates will be required to undergo a background check and must be authorized to work in the United States.


Salary and Benefits

We offer a competitive salary and a generous benefits package, including at no cost: full health and dental for you and your dependents, retirement and HSA accounts, short- and long-term disability insurance, life and accident insurance, paid time off, and 11 federal holidays.


Location

Washington, D.C. Metro Area


Equal Employment Opportunity Policy

Lexical Intelligence, LLC, provides equal employment opportunities to all employees and 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.


This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.


Lexical Intelligence, LLC | 2001 Veirs Mill Rd #546 | Rockville, MD 20851

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