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Medical Device Research And Development Jobs in Washington

StarKist Co.

Director, Research & Development

Reston, VA · On-site

$190 - $250/hr

Director, Research & Development Regular Full-Time Reston, VA, US 3 days ago Requisition ID: 1310 ... medical conditions, or any other classification protected by federal, state and local laws and ...

Google

Medical Device Regulatory Specialist

Washington, DC · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience monitoring regulatory developments and composing white papers or policy briefs ... care delivery, research to catalyze the use of artificial intelligence for the screening and ...

Ametek

Sr. Mechanical Engineer

Germantown, MD

$106K - $140K/yr

... Research & Development team focused on innovative medical devices. In this onsite role in ... Contribute to the design and development of a medical device platform, including enclosure design ...

Ametek

Sr. Mechanical Engineer

Germantown, MD · On-site

$106K - $140K/yr

... Research & Development team focused on innovative medical devices. In this onsite role in ... Contribute to the design and development of a medical device platform, including enclosure design ...

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Medical Device Research And Development information

What is medical device research and development?

Medical device research and development (R&D) is the process of designing, creating, testing, and improving medical devices used for diagnosing, treating, or preventing health conditions. This field combines engineering, biology, and medicine to develop innovative tools ranging from simple instruments to complex implantable devices. Professionals in this area work on everything from concept development and prototyping to clinical trials and regulatory approval. Their work ensures that medical devices are safe, effective, and meet strict regulatory standards before reaching patients.

What are some typical challenges faced by professionals in medical device research and development, and how can these be managed?

Professionals in Medical Device Research and Development often encounter challenges such as navigating complex regulatory requirements, balancing innovation with safety, and coordinating cross-functional teams. Managing these challenges involves staying current with FDA and international regulations, fostering open communication between engineering, clinical, and regulatory teams, and maintaining rigorous documentation throughout the development process. Strong project management skills and a collaborative mindset are key to overcoming these obstacles and ensuring successful product development.

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

To thrive in Medical Device Research and Development, you need a solid background in engineering or life sciences, along with experience in product design and knowledge of regulatory standards. Familiarity with CAD software, prototyping tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong problem-solving skills, creativity, and effective teamwork set standout professionals apart in this field. These skills and qualities are crucial to ensure innovative, safe, and compliant medical devices that meet both clinical needs and regulatory requirements.

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

AspectMedical Device Research And DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications in R&DQuality certifications, regulatory training
Work EnvironmentLabs, design teams, product developmentInspection facilities, compliance departments
Employer & Industry UsageManufacturers, biotech firms, innovation labsRegulatory agencies, manufacturing companies
Search & Comparison IntentInnovation, product development, prototypingCompliance, testing, product validation

Medical Device Research And Development focuses on designing and developing new medical devices, emphasizing innovation and prototyping. In contrast, Medical Device Quality Assurance ensures products meet safety and regulatory standards through testing and compliance. Both roles are essential in the medical device industry but serve different stages of the product lifecycle.

What are popular job titles related to Medical Device Research And Development jobs in Washington?

For Medical Device Research And Development jobs in Washington, the most frequently searched job titles are:

What job categories do people searching Medical Device Research And Development jobs in Washington look for?

The top searched job categories for Medical Device Research And Development jobs in Washington are:

What cities in Washington are hiring for Medical Device Research And Development jobs?

Cities in Washington with the most Medical Device Research And Development job openings:

Medical Device Research And Development jobs near you
Infographic showing various Medical Device Research And Development job openings in Washington as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Medical Device & Technology Associate Attorney

Direct Counsel

Washington, DC

$235K - $310K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 25 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