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Medical Device Developer Jobs (NOW HIRING)

Bausch + Lomb

Medical Device Engineer I

Rochester, NY · On-site

$65K - $100K/yr

The Medical Device Engineer II supports the design and development of contact lenses within Bausch + Lomb's Vision Care R&D organization. This role serves as a product advocate on cross-functional ...

Bausch+Lomb Companies Inc.

$65K - $100K/yr

The Medical Device Engineer II supports the design and development of contact lenses within Bausch + Lomb's Vision Care R&D organization. This role serves as a product advocate on cross-functional ...

Kellton Tech

Medical Device Technician

Madison, WI · On-site

$38.80K - $48.90K/yr

Medical Device Technician Location: Madison, WI (Onsite) Scope of Work: Assemble and test medical ... Bachelor's degree in engineering or related scientific field. Associate's degree with 2+ years ...

Dexcom

Sr Medical Device Engineer

San Diego, CA · On-site

$110.90K - $152.40K/yr

This role offers an exciting opportunity for an enthusiastic polymer engineer who understands the technical and regulatory challenges of integrating new materials within the medical device field. You ...

Aequor Technologies

Quality Engineer (MED DEVICE)

Tempe, AZ · On-site

$70.10K - $90.50K/yr

Quality Engineer (MED DEVICE) The Quality Engineer in Medical Plastic Injection Molding is responsible for overseeing and ensuring the quality of existing and new products and processes within the ...

Dexcom, Inc.

Sr Medical Device Engineer

San Diego, CA · On-site

$110.90K - $152.40K/yr

This role offers an exciting opportunity for an enthusiastic polymer engineer who understands the technical and regulatory challenges of integrating new materials within the medical device field. You ...

Bausch+Lomb Companies Inc.

$65/hr

The Medical Device Engineer II, Usability, is responsible for planning and executing usability engineering activities for contact lens and lens care products in accordance with FDA, MDR, and other ...

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Medical Device Developer information

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$50K

$97.4K

$150K

How much do medical device developer jobs pay per year?

As of Jun 3, 2026, the average yearly pay for medical device developer in the United States is $97,383.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $107,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Medical Device Developer, you need a strong background in biomedical engineering, product design, and regulatory compliance, typically supported by a relevant degree. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is essential. Creative problem-solving, attention to detail, and effective teamwork are crucial soft skills in this field. These abilities ensure that innovative, safe, and compliant medical devices are developed efficiently to improve patient outcomes.

What are some common challenges Medical Device Developers face when working on new product designs?

Medical Device Developers often encounter challenges related to balancing strict regulatory requirements with innovative design. They must ensure products meet safety and efficacy standards set by agencies like the FDA, while also collaborating closely with cross-functional teams such as engineers, clinicians, and quality assurance. Addressing feedback from clinical trials and adapting to evolving technologies can also add complexity to the development process. Successful developers are adaptable, detail-oriented, and proactive in problem-solving to navigate these hurdles efficiently.

What does a Medical Device Developer do?

A Medical Device Developer is responsible for designing, developing, testing, and refining medical devices such as diagnostic equipment, implants, and monitoring tools. They collaborate with engineers, healthcare professionals, and regulatory bodies to ensure products are safe, effective, and compliant with industry standards. The role involves a combination of research, prototyping, validation, and documentation throughout the product life cycle. Medical Device Developers must stay updated on technological advancements and regulatory changes to create innovative and reliable healthcare solutions.

What is the difference between Medical Device Developer vs Medical Device Engineer?

AspectMedical Device DeveloperMedical Device Engineer
CredentialsTypically requires a degree in biomedical engineering, mechanical engineering, or related fields; certifications like Certified Biomedical Equipment Technician (CBET) are commonSimilar credentials; often holds engineering degrees and may have certifications in medical device design or quality assurance
Work EnvironmentResearch labs, product development teams, manufacturing facilitiesDesign, testing, and quality assurance in labs or manufacturing settings
Industry UsageUsed interchangeably in some companies; focuses on product development lifecycleMore technical focus on engineering aspects, testing, and compliance

While both roles require similar educational backgrounds and work environments, Medical Device Developers often focus on the overall product development process, including design and user needs, whereas Medical Device Engineers concentrate on technical design, testing, and ensuring compliance with standards.

More about Medical Device Developer jobs
What cities are hiring for Medical Device Developer jobs? Cities with the most Medical Device Developer job openings:
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Medical Device Developer jobs near you
Infographic showing various Medical Device Developer job openings in the United States as of May 2026, with employment types broken down into 10% Full Time, 89% Part Time, and 1% Contract. Highlights an 80% Physical, 5% Hybrid, and 15% Remote job distribution, with an average salary of $97,383 per year, or $46.8 per hour.

Software Medical Device Engineer

Stark Pharma Solutions Inc

Pleasanton, CA • On-site

Contractor

Posted 5 days ago

Job description

Location: Pleasanton, CA .  

The contract is for 1 year.  

RESPONSIBILITIES:
• Plan and execute migration of requirements and related data from legacy tools (e.g., DOORS, Jama, Excel, Jira) into new platforms, ensuring data integrity, traceability, and compliance.
• Administer, configure, and maintain enterprise requirements management tools, including hierarchies, templates, workflows, versioning, and baselining in alignment with the quality system.
• Develop and maintain a requirements management plan in collaboration with cross‑functional teams, defining the overall requirements structure and links to associated design control documents.
• Create and maintain standardized requirements templates, traceability frameworks, and governance models based on quality and regulatory requirements.
• Maintain the requirements database, develop scripts or automation as needed, and support integrations or add‑in tools to improve usability and efficiency.
• Provide training, documentation, and ongoing support to engineers, serving as the primary functional expert for requirements tools and best practices.
REQUIRED QUALIFICATIONS:
• Bachelor’s degree in Engineering, Computer Science, Biomedical Engineering, or a related discipline for requirements management.
• A minimum of 5 years with hands on experience administering or configuring enterprise requirements management tools to support regulated development environments (e.g., Codebeamer, DOORS, Jama, or comparable platforms). Ability to quickly learn and adopt new tools is expected.
• Hands‑on experience with requirements migration from legacy tools.
• Strong understanding of medical device product development and design control principles.
• Excellent verbal and written communication skills, with the ability to train and support engineers at all levels.
• Ability to work effectively in a collaborative environment.
PREFERRED QUALIFICATIONS:
• Experience acting as a tool administrator, configuration owner, or advanced power user in a regulated development environment.
• Experience defining or scaling requirements management frameworks for large or multi‑team programs.
• Familiarity with medical device development (FDA 21 CFR Part 820) with the ability to configure tools to support compliant workflows.
• Experience supporting software‑driven, connected, or mobile medical devices.
• Experience with different requirements management or lifecycle tools is valued; strong foundational understanding of requirements structures and traceability is more important than experience with a specific platform.
Abbott’s Heart Failure division is seeking a Requirements Tools Engineer to support medical device development by enabling and maintaining enterprise requirements management infrastructure. The role focuses on administering, configuring, and optimizing requirements tools, migrating data from legacy systems (e.g., DOORS, Jama, Excel, Jira), and ensuring data integrity, traceability, and regulatory compliance. The engineer collaborates with cross functional teams to define scalable requirements structures, templates, workflows, versioning, and baselining aligned with quality systems. Responsibilities also include developing requirements management plans, maintaining databases, supporting integrations or automation, and acting as the functional expert through training and ongoing support. The role requires 5+ years of hands on experience with enterprise requirements tools in regulated environments, strong knowledge of medical device design controls, and excellent communication skills. Experience with FDA 21 CFR Part 820, large scale programs, and software driven medical devices is preferred.