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Research And Development Engineer Medical Device Jobs in Baltimore, MD

LifeSprout

R&D Engineer

Baltimore, MD · On-site

We are a medical device company creating revolutionary products for aesthetic and reconstructive ... The Research and Development Engineer is responsible for planning and executing product and process ...

Workforce Genetics

R&D Engineer

Baltimore, MD

$80K - $100K/yr

We are a medical device company creating revolutionary products for aesthetic and reconstructive ... Role Summary The Research and Development Engineer is responsible for planning and executing ...

M Force

Development Engineer

Westminster, MD · On-site

$85K - $95K/yr

The ideal Development Engineer has experience in product development, research and development ... medical, professional and executive disciplines and industry demands, we deliver tailored ...

GDIT

Capabilities Development Engineer

Hanover, MD

$212K - $287K/yr

... Research, Rapid Prototyping of proof of concept capabilities. it's your chance to step up to the ... Our benefits package for all US-based employees includes a variety of medical plan options, some ...

GDIT

Capabilities Development Engineer

Hanover, MD · On-site

$195K - $264K/yr

... Research, Rapid Prototyping of proof of concept capabilities. it's your chance to step up to the ... Our benefits package for all US-based employees includes a variety of medical plan options, some ...

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All JobsResearch And Development Engineer Medical Device JobsResearch And Development Engineer Medical Device Jobs in Baltimore, MD

Research And Development Engineer Medical Device information

See Baltimore, MD salary details

$19.9K

$96K

$150K

How much do research and development engineer medical device jobs pay per year?

As of Aug 23, 2026, the average yearly pay for research and development engineer medical device in Baltimore, MD is $95,957.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,000.00 and $116,300.00 per year, depending on experience, location, and employer.

What does a research and development engineer do in the medical device industry?

A Research and Development (R&D) Engineer in the medical device industry is responsible for designing, developing, and testing new medical devices and technologies. They work closely with cross-functional teams to ensure products meet regulatory standards, are safe for patient use, and address clinical needs. Their tasks may include prototyping, conducting experiments, analyzing data, and collaborating with manufacturing teams to bring products from concept to market. R&D Engineers also stay updated on technological advancements and regulatory changes to ensure innovation and compliance.

What are the key skills and qualifications needed to thrive as a research and development engineer in the medical device industry?

To excel as a Research and Development Engineer in Medical Devices, you need a solid background in biomedical engineering or a related field, strong problem-solving skills, and experience with product development cycles. Familiarity with CAD software, prototyping tools, regulatory standards like ISO 13485, and relevant certifications (such as Six Sigma) is highly valued. Excellent teamwork, creativity, and effective communication are crucial soft skills for collaborating across multidisciplinary teams and driving innovation. These competencies ensure the design and launch of safe, effective, and compliant medical devices that improve patient outcomes.

What are some common challenges faced by research and development engineers in the medical device industry?

Research and Development Engineers in the medical device industry often face challenges such as navigating complex regulatory requirements, managing tight project timelines while ensuring product safety and efficacy, and collaborating with cross-functional teams like quality assurance and clinical affairs. Additionally, adapting to rapid technological advancements and integrating feedback from clinicians and end-users into the design process can be demanding. These challenges require strong problem-solving skills, adaptability, and effective communication to deliver innovative and compliant medical devices.

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

AspectResearch And Development Engineer Medical DeviceQuality Assurance Engineer Medical Device
Primary FocusDesigning, developing, and testing new medical device productsEnsuring products meet quality standards and regulatory requirements
Required CredentialsEngineering degree, knowledge of product developmentEngineering or science degree, knowledge of quality systems
Work EnvironmentResearch labs, product development teamsManufacturing facilities, quality control departments
Industry UsageInvolved in innovation and product creationInvolved in compliance, validation, and process improvement

While both roles require engineering knowledge and are integral to the medical device industry, Research And Development Engineers focus on creating and testing new products, whereas Quality Assurance Engineers ensure these products meet safety and quality standards throughout production.

What are popular job titles related to Research And Development Engineer Medical Device jobs in Baltimore, MD?

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

What job categories do people searching Research And Development Engineer Medical Device jobs in Baltimore, MD look for?

The top searched job categories for Research And Development Engineer Medical Device jobs in Baltimore, MD are:

Research And Development Engineer Medical Device jobs near you
Infographic showing various Research And Development Engineer Medical Device job openings in Baltimore, MD as of August 2026, with employment types broken down into 100% Full Time. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $95,957 per year, or $46.1 per hour.

R&D Engineer

LifeSprout

Baltimore, MD • On-site

Full-time

Re-posted 2 days ago

Job description

About LifeSprout:
LifeSprout was founded in September 2015 as a Johns Hopkins University spinout. We are a medical device company creating revolutionary products for aesthetic and reconstructive medicine. Our synthetic biomaterial platform mimics the look and behavior of native tissue and is being developed into a suite of products to restore form and function for millions of patients with soft tissue loss from aging, cancer, and metabolic disease. The company is led by a management team experienced across business, clinical, and scientific disciplines.
Position Overview:
The Research and Development Engineer is responsible for planning and executing product and process development activities to support innovation, product performance, and readiness for verification and validation. This role contributes across the development lifecycle, including process development, formulation screening, assay development, troubleshooting and root cause analysis, technical documentation, and preparation and execution of design verification and validation activities. The ideal candidate combines strong experimental skills with structured problem-solving, clear technical communication, and the ability to work effectively in a cross-functional, GMP-regulated environment.
Responsibilities:
  • Design and conduct experiments, analyze data, and interpret results to guide technical decisions and next steps.
  • Plan and execute formulation screening studies to evaluate candidate materials, compositions, and processing conditions.
  • Perform process development activities to improve product performance, manufacturability, robustness, and scalability.
  • Prepare for and execute design verification and validation activities, including protocol development, test coordination, data analysis, and report generation.
  • Develop, optimize, qualify, and document assays and test methods to support research, development, and product characterization.
  • Perform troubleshooting and root cause analysis for technical issues arising during development, testing, or manufacturing support activities.
  • Prepare clear and accurate technical documentation, including study protocols, reports, experimental records, and summaries of findings.
  • Collaborate with cross-functional teams such as Quality, Regulatory, Manufacturing, and Process Engineering to ensure development activities align with program goals and applicable requirements.
  • Maintain development records in accordance with internal procedures, quality system requirements, and good documentation practices.
  • Present technical findings, recommendations, and development updates to internal stakeholders.

Qualifications:
  • Master’s or PhD degree in Engineering, Biomedical Engineering, Chemical Engineering, Materials Science, Pharmaceutical Sciences, or a related technical field; advanced degree preferred.
  • 2+ years of experience in research and development, product development, formulation development, process development, assay development, or a related technical area.
  • Preferred experience working with biomaterials, hydrogels, electrospinning, high-shear mixing, separations, and sterilization processes
  • Hands-on experience designing experiments, analyzing data, and drawing conclusions to support product or process decisions.
  • Knowledge of verification and validation principles, test method development, and structured technical problem-solving.
  • Strong technical writing skills, with experience preparing protocols, reports, and development documentation.
  • Ability to troubleshoot effectively and apply root cause analysis tools to resolve complex technical issues.
  • Strong interpersonal and cross-functional collaboration skills.
  • Familiarity with regulated development environments, quality systems, and documentation practices is preferred.

Working conditions and what we offer:
  • Onsite presence required for laboratory activities with occasional travel (<10%).
  • Fast paced, collaborative environment balancing development and release activities.
  • Competitive compensation, benefits, and professional development opportunities.
  • Opportunity to shape analytical strategy for an innovative biomaterials platform with clear patient impact.

Eligibility to work in the U.S. is required.

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