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Medical Device Development Jobs in Washington (NOW HIRING)

Ametek

Sr. Mechanical Engineer

Germantown, MD · On-site

$106K - $140K/yr

Contribute to the design and development of a medical device platform, including enclosure design, cabling, and patient-contacting electrode systems. * Generate mechanical designs, assemblies ...

Ametek

Sr. Mechanical Engineer

Germantown, MD · On-site

$106K - $140K/yr

Contribute to the design and development of a medical device platform, including enclosure design, cabling, and patient-contacting electrode systems. * Generate mechanical designs, assemblies ...

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All JobsMedical Device Development JobsMedical Device Development Jobs in Washington

Medical Device Development information

See Washington salary details

$32.8K

$60.5K

$91.7K

How much do medical device development jobs pay per year?

As of Aug 6, 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 July 2026, with employment types broken down into 1% As Needed, 75% Full Time, 21% Part Time, and 3% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $60,501 per year, or $29.1 per hour.

Medical Device & Technology Associate Attorney

Direct Counsel

Washington, DC • On-site

$235K - $310K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 14 days ago

Job description

Medical Device & Technology Associate Attorney

Direct Counsel is seeking a Medical Device & Technology Associate Attorney to join a prestigious Am Law firm in Washington, D.C.

This is an exceptional opportunity for an attorney interested in FDA regulatory law and medical device regulation to join a nationally recognized Food, Drug, Medical Device & Agriculture practice. The team advises medical device, biotechnology, pharmaceutical, and digital health companies on the full lifecycle of FDA regulatory compliance, including premarket submissions, post-market obligations, enforcement matters, and emerging issues involving artificial intelligence and software-based medical technologies.

Responsibilities

  • Advise clients on FDA regulatory requirements governing medical devices and related technologies.

  • Counsel clients on regulatory pathways for medical devices, including 510(k) notifications, Investigational Device Exemptions (IDEs), De Novo requests, and Premarket Approval Applications (PMAs).

  • Assist with FDA submissions, agency communications, and responses to deficiency letters and regulatory inquiries.

  • Advise on post-market compliance matters, including quality system regulations, recalls, adverse event reporting, and FDA enforcement issues.

  • Counsel clients on regulatory considerations affecting software as a medical device (SaMD), digital health technologies, artificial intelligence (AI), machine learning, cybersecurity, and diagnostic products.

  • Research and analyze evolving FDA regulations and related state, federal, and international regulatory developments.

  • Develop practical regulatory strategies that support innovative product development while managing compliance risks.

  • Collaborate with clients and multidisciplinary legal teams on sophisticated regulatory matters throughout the product lifecycle.

Qualifications

  • J.D. from an ABA-accredited law school.

  • Active membership in, or eligibility for admission to, the District of Columbia Bar.

  • Demonstrated interest in FDA regulatory law and medical device regulation.

  • Experience with FDA medical device matters is strongly preferred.

  • Experience at the FDA or within the medical device, pharmaceutical, or biotechnology industries is a plus.

  • Scientific, engineering, health sciences, or biotechnology background is preferred but not required.

  • Excellent legal research, analytical, drafting, and communication skills.

  • Strong academic credentials and the ability to thrive in a collaborative, fast-paced, client-focused environment.

Compensation & Benefits

  • Salary: $235,000-$310,000, commensurate with experience and qualifications.

  • Comprehensive benefits package, including:

    • Medical, dental, and vision insurance

    • 401(k) retirement plan

    • Paid time off

    • Annual performance and discretionary bonus eligibility

    • Relocation assistance, where applicable