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Biomedical Device Engineer Jobs (NOW HIRING)

Job Title: Biomedical Engineer Location: 101 W Dickman St, Suite 300, Baltimore, MD 21230 ... Device Assembly and Hands-on testing support * Operate basic mechanical assembly tools to support ...

Job Title: Biomedical Engineer Location: 101 W Dickman St, Suite 300, Baltimore, MD 21230 ... Device Assembly and Hands-on testing support * Operate basic mechanical assembly tools to support ...

Perform device location services and medical device inspection rounds. Maintain assigned equipment ... Bachelor's degree or equivalent in Biomedical Engineering, Electrical/Electronics Engineering ...

... Device Act (SMDA), and JC requirements; ability to conduct capital asset and infrastructure ... biomedical engineering, directly supporting specialized clinical technology, including service ...

... Device Act (SMDA), and JC requirements; ability to conduct capital asset and infrastructure ... biomedical engineering, directly supporting specialized clinical technology, including service ...

Support biomedical device development, modeling and simulation systems, equipment troubleshooting ... Engineering support in biomedical systems or simulation environments. * Security & Background Check:

Support biomedical device development, modeling and simulation systems, equipment troubleshooting ... Engineering support in biomedical systems or simulation environments. * Security & Background Check:

Support biomedical device development, modeling and simulation systems, equipment troubleshooting ... Engineering support in biomedical systems or simulation environments. * Security & Background Check:

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Biomedical Device Engineer information

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$41K

$94.8K

$140K

How much do biomedical device engineer jobs pay per year?

As of Jun 14, 2026, the average yearly pay for biomedical device engineer in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What are biomedical device engineers?

Biomedical device engineers are professionals who design, develop, test, and maintain medical devices and equipment used in healthcare. Their work bridges the fields of engineering, biology, and medicine to create technologies that improve patient care, such as prosthetics, imaging machines, and diagnostic tools. They collaborate with medical professionals to ensure devices are safe, effective, and meet regulatory standards. Biomedical device engineers may also be involved in research, product development, and troubleshooting equipment in clinical settings.

What is the difference between Biomedical Device Engineer vs Biomedical Equipment Technician?

AspectBiomedical Device EngineerBiomedical Equipment Technician
CredentialsBachelor's degree in biomedical engineering or related fieldAssociate's degree or certification in biomedical technology
Work EnvironmentDesign, develop, and test medical devices in labs or officesInstall, maintain, and repair medical equipment in hospitals or clinics
Industry UsageUsed by medical device companies, research institutions, and hospitalsPrimarily employed by healthcare facilities and service providers

Biomedical Device Engineers focus on designing and developing new medical devices, while Biomedical Equipment Technicians handle the installation, maintenance, and repair of existing equipment. Both roles require technical knowledge, but their daily tasks and work environments differ significantly.

What are the key skills and qualifications needed to thrive as a Biomedical Device Engineer, and why are they important?

To thrive as a Biomedical Device Engineer, you need a solid background in biomedical engineering, mechanical or electrical engineering, and a bachelor's or master's degree in a related field. Familiarity with CAD software, medical device regulations (such as FDA or ISO standards), and prototyping tools is crucial. Strong problem-solving abilities, attention to detail, and effective collaboration and communication skills help you innovate and work efficiently with multidisciplinary teams. These competencies ensure the safe, effective, and compliant development of medical devices that improve patient outcomes.

What are some common challenges Biomedical Device Engineers face when working on cross-functional teams?

Biomedical Device Engineers frequently collaborate with professionals from various disciplines, including clinicians, software developers, and regulatory experts. A common challenge is aligning the technical requirements of device design with clinical needs and strict regulatory standards. Effective communication and adaptability are essential, as team members may have differing priorities or levels of technical understanding. Overcoming these challenges often leads to innovative solutions and a more robust final product, making strong teamwork and problem-solving skills invaluable in this role.
What cities are hiring for Biomedical Device Engineer jobs? Cities with the most Biomedical Device Engineer job openings:
What states have the most Biomedical Device Engineer jobs? States with the most job openings for Biomedical Device Engineer jobs include:
Engineer, Medical Devices (JP12014)

Engineer, Medical Devices (JP12014)

3 Key Consulting

Thousand Oaks, CA โ€ข On-site

$37 - $41/hr

Other

Posted 27 days ago


Job description

Job Title:Engineer, Medical Devices (JP12014)
Location:Thousand Oaks, CA. 91320
Business Unit:PFS And Lyo Kit Platforms
Employment Type: Contract
Duration:1+ years with possible extensions or conversion to FTE
Rate: $37 - $41/hour W2
Posting Date:11/29/2023
Notes:ONSITE - candidate is expected to be in mechanical lab and support.
3 Key Consulting is recruiting anEngineerfor a consulting engagement with our direct client, a leading global biotechnology company.
Ideal Candidate: Force testing, good documentation and lab safety, technical writing, electronic data, Data verification i.e. what goes into reviewing technical documentation. Familiarity with Minitab and JMP. basic statistics, ANOVA and capability experience. Bachelor Degree and 2 years of experience. working in a mechanical lab. Familiarity with combination product development. Familiarity with design controls. specifically prefilled syringes.
Job Description:
The Device Engineer will participate in the design, development, and lifecycle management design control activities for commercialized drug delivery devices. This role includes technical operations support for combination product development to global launch, clinical and commercial manufacturing, failure investigation, design change evaluation, development and execution of test procedures, and continuous improvement initiatives.
Scope includes mechanical delivery devices, such as Prefilled syringes. The qualified candidate will be part of a sustaining device engineering team that ensures design history files of these mechanical delivery devices are maintained. The engineer will participate in cross functional teams, leading device design activities such as the development of product enhancements, analytical failure analysis and implementation of design solutions, assessment of proposed changes, support product launches, and defend inspection and ensure the follow through of commitments.
Essential skills and Responsibilities:
  • Adheres to strict documentation practices in a GMP regulated environment
  • Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments, plans and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devises new approaches to problems encountered.
  • Authors and reviews technical documentation including protocols, reports, and technical assessments
  • Analyze and trend generated data by applying relevant statistical techniques to enable senior staff to make informed decisions
  • Coordinates and executes laboratory testing to support characterization, verification, design transfer, and fill-finish efforts
  • Maintains combination product design history files for assigned products
  • Develops characterization test methods through fixture prototyping, reference sample creation, and GR&R analysis
  • Provides functional subject matter expertise to actively participate in cross-functional activities including system level root cause analysis, design changes, and change control assessments
  • Provide general laboratory support including inventory management, sample shipments, and cleanup.
  • Works with Scientists and Engineers, to assess and develop appropriate design and manufacturing specifications
  • Individual contributor with Leadership attributes to effectively represent device engineer within a large network/matrix organization
  • At a minimum familiar with the following standards and regulations:
  • Quality System Regulation - 21CFR820
  • Risk Management - ISO 14971
  • EU Medical Device requirements - Council Directive 93/42/EEC
Basic Qualifications:
Master degree
OR Bachelor degree and 2 years of experience
OR Associate degree and 6 years of experience
Preferred Qualifications:
  • Bachelor's Degree or higher in relevant engineering or scientific field (Mechanical, Biomedical, Bioengineering)
  • Minimum 1 year of scientific or engineering experience in a GxP regulated environment
  • Statistical Analysis software (Minitab or JMP)
  • Strong technical writing skills
  • CAD fixturing software (SolidWorks)
  • Instron force tester using BlueHill Universal
  • Experience with design controls; including (but not limited to) verification and design transfer
  • Understanding of risk assessments including hazard and probability analysis
  • Background in medical device development, commercialization, and knowledge of manufacturing processes (fill-finish)
  • Ability to work independently and dynamically across functional team
  • Excellent written and verbal communication skills
  • Ability to support complex workstreams under demanding timelines.
Top Must Have Skill Sets:
  1. Hands on Laboratory Experience in a GxP Setting (Science or Engineering Lab)
  2. Good Communication and Technical Writing Skills
  3. Data Analysis and Problem Solving

Day to Day Responsibilities:
  • The device engineer will support a senior engineer on a variety of projects related to laboratory testing, life cycle management, and product-based initiatives regarding prefilled syringes in both the commercial and developmental space.
  • The engineer will be expected to author protocols, reports, and further technical documentation while adhering to GMP standards. Laboratory testing will primarily include the use of an Instron force tester and vision systems.
  • The identified candidate must be able to lift up to 50 lbs for receipt and transferring of material.
  • Fill-Finish experience is a bonus but not mandatory.
  • The engineer will be evaluated on ability to complete a wide variety of supporting tasks for projects in a timely manner while maintaining a high standard of quality.

Employee Value Proposition:great opportunity for growth in career
Why is the Position Open?
Supplement additional workload on team.
Red Flags:
  • No previous industry or laboratory experience
  • Unfamiliar with Good Documentation Practices
Interview Process:
2-3 rounds of interviews.
Individual Interviews (x2) - WebEx or In-person
Panel Interview (x1) - WebEx
We invite qualified candidates to sendyour resume torecruiting@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.