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Medical Device Developer Jobs (NOW HIRING)

Bracco

Medical Device Assembler I

Eden Prairie, MN · On-site

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...

Bracco

Medical Device Assembler I

Eden Prairie, MN

$18.25 - $22.50/hr

The Medical Device Assembler I is responsible for performing a variety of production tasks related ... Instructions (WI), Engineering Prints and Bills of Materials (BOM). Primary Duties ...

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 ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

First Databank

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Newspapers

Medical Device Coder

Indianapolis, IN · On-site

$18 - $24/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst

Medical Device Coder

Carmel, IN

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Health

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

Hearst Communications, Inc.

Medical Device Coder

Carmel, IN · On-site

$17.75 - $23.75/hr

Partnering with our information system developer and healthcare institution customers, you'll help ... Evaluates medical device content to ensure the accuracy of HCPCS mappings. * Follows up with ...

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Showing results 21-40

All JobsMedical Device Developer Jobs

Medical Device Developer information

See salary details

$50K

$97.4K

$150K

How much do medical device developer jobs pay per year?

As of Aug 10, 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 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.

What are the key skills and qualifications needed to thrive as a medical device developer?

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.
More about Medical Device Developer jobs
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What job categories do people searching Medical Device Developer jobs look for? The top searched job categories for Medical Device Developer jobs are:
Medical Device Developer jobs near you
Infographic showing various Medical Device Developer job openings in the United States as of August 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 80% In-person, and 20% Hybrid job distribution, with an average salary of $97,383 per year, or $46.8 per hour.

Quality Engineer Medical Device

Egg Medical Inc

Roseville, MN • On-site

$100K - $115K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 23 days ago

Job description

Summary

We are seeking a Quality Engineer to add to our team! This position will support the management of our quality system while actively contributing to new product design and development initiatives. This role combines core quality engineering responsibilities with technical involvement in engineering projects to ensure our innovative medical devices meet the highest standards of safety, reliability, and regulatory compliance. 

Key Responsibilities

  • Quality System Support: Develop, implement, and maintain elements of the Quality Management System (QMS) to ensure ongoing compliance with FDA regulations, ISO 13485, and other applicable standards.
  • New Product Development & Design Control: Collaborate with R&D, engineering, and cross-functional teams on new design projects; support design inputs/outputs, risk assessments (e.g., FMEA, ISO 14971), design verification and validation activities, and design reviews/transfer to manufacturing.
  • Risk Management & Technical Reviews: Perform and document risk analyses, participate in technical design reviews, and ensure design controls are effectively applied throughout the product lifecycle.
  • Non-Conformance & Corrective Actions: Investigate non-conformances, lead root cause analysis, and implement corrective and preventive actions (CAPA) to drive continuous improvement and prevent recurrence.
  • Documentation & Compliance: Maintain accurate quality records, support internal/external audits, and contribute to regulatory submissions as needed.
  • Continuous Improvement: Identify opportunities to improve quality processes, product designs, and overall efficiency; partner with engineering and other teams on quality initiatives

Qualifications

  • Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Quality Engineering, or a related field.
  • 3+ years of experience as a Quality Engineer in a regulated industry, preferably medical devices.
  • Experience with FDA regulations, ISO 13485, and other medical device quality standards.
  • Proficiency in quality tools and methodologies (e.g., FMEA, SPC, CAPA).

Compensation & Benefits

  • Full-time position with salary range from $100,000-$115,000, depending on experience.
  • Additional bonus/incentive compensation available.
  • Company laptop provided.
  • Insurance available on the 1st of the month following date of hire, including: health, dental and vision insurance, plus pre-tax or Roth 401k available after 30 days.
  • PTO accrues starting at 15 days, plus 11 company paid holidays.

Company Description

Egg Medical is an innovative leader in radiation safety protection technology. Our mission is to protect healthcare professionals from occupational radiation exposure while enabling the delivery of exceptional patient care.