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Entry Level Medical Device Engineer Jobs in Reston, VA

Ability to explain signal processing for biosignals, finite element analysis, drug delivery systems, and medical device design principles while preparing students for biomedical engineering ...

This position is responsible for the interrogation, interpretation, and programming of all CIED ... Minimum two (2) years of healthcare/medical office experience required * Experience with ...

This position is responsible for the interrogation, interpretation, and programming of all CIED ... Minimum two (2) years of healthcare/medical office experience required * Experience with ...

Cardiac Device Specialist

Arlington, VA · On-site

$34.79 - $56.37/hr

This position is responsible for the interrogation, interpretation, and programming of all CIED ... Minimum two (2) years of healthcare/medical office experience required * Experience with ...

This position is responsible for the interrogation, interpretation, and programming of all CIED ... Minimum two (2) years of healthcare/medical office experience required * Experience with ...

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Entry Level Medical Device Engineer information

See Reston, VA salary details

$15

$32

$53

How much do entry level medical device engineer jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for entry level medical device engineer in Reston, VA is $32.58, according to ZipRecruiter salary data. Most workers in this role earn between $28.51 and $36.01 per hour, depending on experience, location, and employer.

How to become a biomedical engineer with no experience?

Entry-level biomedical engineers typically need a bachelor's degree in biomedical engineering, bioengineering, or a related field. Gaining experience through internships, volunteering, or project work can improve job prospects, and developing skills in CAD software, medical device design, and regulatory standards is beneficial.

What does an entry level medical device engineer do?

An entry level medical device engineer assists in designing, developing, and testing medical devices such as implants, diagnostic equipment, or surgical tools. They often work as part of a team under the supervision of experienced engineers, ensuring products meet regulatory standards and function safely and effectively. Responsibilities may also include documenting results, conducting research, and supporting manufacturing or quality assurance processes. This role provides hands-on experience with engineering principles in the healthcare industry and often serves as a starting point for more specialized or senior positions.

What is the difference between Entry Level Medical Device Engineer vs Quality Assurance Technician?

AspectEntry Level Medical Device EngineerQuality Assurance Technician
Required CredentialsBachelor's in engineering, biomedical or related fieldBachelor's in science, engineering, or related field; certifications optional
Work EnvironmentDesign labs, manufacturing facilities, R&D teamsManufacturing plants, quality control labs
Employer & Industry UsageMedical device companies, biotech firmsManufacturers, healthcare device companies

Entry Level Medical Device Engineers focus on designing and developing medical devices, while Quality Assurance Technicians ensure products meet quality standards. Both roles are essential in the medical device industry and often work closely to ensure product safety and compliance.

What Does an Entry-Level Medical Device Engineer Do?

As an entry-level medical device engineer, your duties include the research, design, and development of medical devices and healthcare products and equipment. An entry-level engineer works as part of a research and development team. You typically have specific tasks such as performing research on materials or testing a device in a laboratory setting or during a clinical trial. In addition to responsibilities related to design and development, entry-level engineers often document tests and trials, collect and organize data, and create drawings and plans using computer-aided design software.

What engineer makes $500,000 a year?

While most entry-level medical device engineers earn significantly less, senior or specialized engineers with extensive experience, advanced skills, and leadership roles can potentially reach or exceed $500,000 annually, especially in high-demand markets or with bonuses and stock options. Such compensation is rare at the entry level and typically requires many years of experience and proven expertise.

What engineers make $300,000 a year?

Highly experienced engineers in specialized fields such as petroleum engineering, aerospace engineering, or software engineering with senior roles and advanced skills can earn $300,000 or more annually. These positions often require extensive experience, advanced certifications, and leadership responsibilities, typically working in high-demand industries or companies. Entry-level medical device engineers generally do not reach this salary level.

Is BME a stressful job?

Entry level medical device engineers often work in regulated environments that require attention to detail and compliance, which can be stressful due to strict deadlines and quality standards. However, the job typically involves standard office hours and collaborative teamwork, which can help manage stress levels. Overall, stress varies based on workload, project complexity, and individual coping skills.

What types of projects and responsibilities can an entry level medical device engineer expect during their first year on the job?

As an entry level medical device engineer, you can expect to work closely with cross-functional teams—including design, quality, and manufacturing—to support product development and improvements. Your responsibilities may include assisting in prototyping, conducting testing and data analysis, and maintaining detailed documentation to ensure regulatory compliance. You’ll likely gain hands-on experience troubleshooting devices, collaborating in design reviews, and participating in validation activities. This role provides an excellent foundation for learning industry standards and building technical and teamwork skills essential for career advancement.

What are the key skills and qualifications needed to thrive as an Entry Level Medical Device Engineer, and why are they important?

To thrive as an Entry Level Medical Device Engineer, you need a bachelor's degree in biomedical, mechanical, or electrical engineering, along with a solid understanding of engineering principles and medical device regulations. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO standards is typically required. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help you stand out in this role. These competencies are critical for ensuring the safe design and development of innovative medical devices that meet regulatory standards and patient needs.
What are the most commonly searched types of Medical Device Engineer jobs in Reston, VA? The most popular types of Medical Device Engineer jobs in Reston, VA are:
What are popular job titles related to Entry Level Medical Device Engineer jobs in Reston, VA? For Entry Level Medical Device Engineer jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Entry Level Medical Device Engineer jobs in Reston, VA look for? The top searched job categories for Entry Level Medical Device Engineer jobs in Reston, VA are:
What cities near Reston, VA are hiring for Entry Level Medical Device Engineer jobs? Cities near Reston, VA with the most Entry Level Medical Device Engineer job openings:
Infographic showing various Entry Level Medical Device Engineer job openings in Reston, VA as of June 2026, with employment types broken down into 2% Locum Tenens, 3% As Needed, 75% Full Time, 16% Part Time, 2% Temporary, and 2% Contract. Highlights an 88% Physical, 5% Hybrid, and 7% Remote job distribution, with an average salary of $67,758 per year, or $32.6 per hour.
Medical Device and Technology - Junior to Mid-Level Associate

Medical Device and Technology - Junior to Mid-Level Associate

Hogan Lovells

Washington, DC • On-site

$235K - $310K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 11 days ago


Job description

The Washington, D.C. office of Hogan Lovells US LLP is seeking a junior to mid-level associate to join the Medical Devices group within our Food, Drug, Medical Device and Agriculture practice. This role offers the opportunity to work at the forefront of medical device regulation, advising clients across a broad spectrum of premarket and post-market compliance, enforcement, and strategic regulatory matters.
Our Medical Devices practice operates on a truly global platform, coordinating seamlessly with colleagues across major markets worldwide to help clients navigate complex and evolving regulatory frameworks. In the United States, we have been advising companies on FDA regulatory matters for decades, including helping bring innovative and first-of-their-kind medical technologies to market since the Medical Device Amendments of 1976. Our team regularly works on cutting-edge issues involving software as a medical device (SaMD), artificial intelligence and machine learning-enabled technologies, digital health platforms, and novel diagnostic tools, alongside more traditional device and in vitro diagnostic products.
The associate will play an integral role in advising clients on the full lifecycle of medical device regulation. This includes providing strategic guidance on FDA regulatory pathways; supporting the preparation and submission of premarket applications, including 510(k) notifications, Investigational Device Exemptions (IDEs), De Novo classification requests, and Premarket Approval Applications (PMAs); and assisting clients in navigating FDA review processes, including responding to deficiency letters and other agency inquiries. The associate will also work on post-market compliance matters, including quality system regulation issues, recalls and field corrective actions, adverse event reporting and vigilance obligations, and broader FDA enforcement and compliance strategies.
In addition to traditional regulatory work, the associate will be exposed to the rapidly evolving legal and policy landscape governing AI-enabled medical devices and digital health solutions, including issues relating to algorithm change management, real-world data and evidence, cybersecurity, and the intersection of FDA requirements with emerging state, federal, and international regulatory frameworks. The role will involve helping clients develop practical, forward-looking strategies for bringing innovative technologies to market while managing regulatory risk in a dynamic environment.
We are seeking candidates with a demonstrated interest in FDA regulatory law and medical device issues, and experience with FDA medical device matters is strongly preferred. This may include researching and analyzing regulatory questions, advising on regulatory pathways, or supporting the preparation of submissions and responses to the FDA. Prior experience at the FDA or within the medical device, pharmaceutical, or biotechnology industries is a plus, but is not required. A scientific, engineering, health, or biotechnology background is preferred but also not required. Candidates must be admitted to the District of Columbia Bar.
Successful candidates will have outstanding writing and analytical skills, strong academic credentials, and a commitment to excellence. They will be thoughtful and practical problem solvers with excellent judgment, strong communication skills, and the ability to convey complex regulatory concepts clearly and effectively. We value associates who are highly responsive, client-focused, and able to work both independently and collaboratively as part of a team. Intellectual curiosity, a willingness to take initiative and "figure it out," a strong work ethic, and a positive, team-oriented attitude are essential. The role also offers significant opportunities to develop meaningful client relationships and to grow within a collaborative and market-leading practice.
The expected base salary range for this role is $235,000 to $310,000 per year. This range reflects a good-faith estimate of pay at the time of posting; the actual compensation offered may vary depending on factors such as the candidate's qualifications. This position is eligible for additional forms of compensation, which may include annual performance bonuses and discretionary bonuses. Employees in this role are also eligible for benefits offered by the firm, subject to applicable plan terms and conditions, which currently include medical, dental, and vision insurance; a 401(k) retirement plan; and paid time off. Additional benefits may include relocation. Please review this link for more information regarding employee benefits in the United States.
We will consider for employment qualified applicants with arrest and conviction records in a manner consistent with the requirements of applicable law, including the San Francisco Fair Chance Ordinance and City of Los Angeles Fair Chance Initiative for Hiring Ordinance.
A resume or CV is a must for our application system. We also encourage you to include a cover letter to tell us why you are interested in this position and a law school transcript (or the equivalent). Candidates applying for this position must have a law degree from an ABA-accredited law school and be admitted to the District of Columbia Bar or eligible to waive into the Bar.
To apply please complete the on-line application, attaching a resume and law school transcript.
All search firm submissions should be sent to the attention of Suzanne Hudgens at JoinHoganLovellsDC@hoganlovells.com Submissions must include a resume and law school transcript.
This job description sets forth the responsibilities of this position and may be changed from time to time as shall be determined.
Hogan Lovells is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, age, national origin, disability, sexual orientation, gender identity or expression, marital status, genetic information, protected Veteran status, or other factors protected by law.
Hogan Lovells complies with federal and state disability laws and makes reasonable accommodations for applicants and candidates with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, please contact our Benefits Department at LeaveofAbsence_US@hoganlovells.com.