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Medical Device Development Jobs (NOW HIRING)

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Medical Device Tester II

Plano, TX · On-site

As a Medical Device Tester II, you will be part of the Quality Assurance department supporting ... Collaborate with cross-functional engineering teams to support product development and testing ...

New

Tekhawks LLC

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Systems Engineer - Medical Device/Design controls - 100% Remote

New Brunswick, NJ · Remote

$30 - $35/hr

Qualifications • Strong experience in Systems Engineering, Biomedical Engineering, or a related technical discipline. • Experience in medical device development, including design controls and ...

Tekhawks LLC

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Systems Engineer - Medical Device/Design controls - 100% Remote

New Brunswick, NJ · Remote

$30 - $35/hr

Qualifications • Strong experience in Systems Engineering, Biomedical Engineering, or a related technical discipline. • Experience in medical device development, including design controls and ...

SlingShot Connections

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Medical Device Assembler

San Clemente, CA · On-site

$20.25 - $22.27/hr

Contribute to safe, effective product development from concept through production * Work under ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

ICU Medical

Senior Engineer, R&D

Salt Lake City, UT · On-site

$101K - $138K/yr

As a subject matter expert (SME) in medical device development, the Senior R&D Engineer will lead key projects of significant complexity while applying sound engineering principles, experimental ...

ICU Medical

Senior Engineer, R&D

Salt Lake City, UT · On-site

$101K - $138K/yr

As a subject matter expert (SME) in medical device development, the Senior R&D Engineer will lead key projects of significant complexity while applying sound engineering principles, experimental ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 Design Controls required * Experience with ...

AngioSafe

Medical Device R&D Engineer

San Jose, CA · On-site

$115K - $175K/yr

Minimum 5 years of medical device R&D experience * Hands-on catheter prototyping and testing experience required * Experience working within ISO 13485 Design Controls required * Experience with ...

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How much do medical device development jobs pay per year?

As of Jun 5, 2026, the average yearly pay for medical device development in the United States is $53,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $60,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Medical Device Development, and why are they important?

To thrive in Medical Device Development, you need expertise in engineering or life sciences, a solid understanding of regulatory requirements, and often an advanced degree such as a master's or Ph.D. in a relevant field. Familiarity with CAD software, prototyping tools, and knowledge of FDA or ISO regulatory standards is typically required. Strong problem-solving abilities, collaboration, and effective communication distinguish top professionals in this field. These skills ensure the development of safe, innovative, and compliant medical devices that meet both user needs and regulatory standards.

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

AspectMedical Device DevelopmentMedical Device Quality Assurance
CredentialsEngineering degrees, certifications like RAPS or regulatory trainingQuality certifications, ISO 13485, regulatory compliance training
Work EnvironmentDesign labs, R&D teams, product development settingsManufacturing sites, quality control labs, compliance departments
Industry UsageDesigning and creating new medical devicesEnsuring devices meet quality and regulatory standards

Medical Device Development focuses on designing and creating new medical devices, involving engineering and product innovation. Medical Device Quality Assurance ensures these devices meet safety, quality, and regulatory standards through testing and compliance processes. Both roles are essential in the medical device industry but serve different functions in the product lifecycle.

What are some common challenges faced by professionals in medical device development, and how can they be addressed?

Professionals in medical device development frequently encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and managing cross-functional collaboration between engineering, clinical, and regulatory teams. Addressing these challenges requires staying updated on evolving regulations, fostering open communication among diverse team members, and implementing robust quality control processes. Proactively engaging with regulatory bodies and regularly reviewing project milestones can help streamline development and reduce the risk of costly delays.

What is medical device development?

Medical device development is the process of designing, creating, testing, and bringing medical devices to market. This process involves multiple stages, including concept development, prototyping, preclinical and clinical testing, regulatory approval, and manufacturing. The goal is to ensure that new devices are safe, effective, and meet regulatory standards before they are used by healthcare professionals or patients. Teams in medical device development often include engineers, scientists, regulatory specialists, and quality assurance professionals.
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What states have the most Medical Device Development jobs? States with the most job openings for Medical Device Development jobs include:
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Medical Device Development jobs near you

Senior Mechanical Engineer - Medical Device

Micro Leads Inc

Somerville, MA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Life

Posted 7 days ago

Job description

Location: Somerville, MA

Senior Mechanical Engineer – Medical Device

Overview:

Micro-Leads is a fast-paced early-stage company developing an injectable medical device to treat people with chronic pain with greater efficacy. Our company has extensive expertise in precision implantable medical devices for nerve stimulation and neuromodulation.

Role Summary:

The primary role of this position is to design and build injectable electrodes for needle delivery and implantable pulse generator housings for next-generation neurostimulator devices. The individual will design electrodes for stimulation and nerve recordings.  In addition, the candidate will prototype, build, and conduct mechanical integrity and related tests. The individual will also develop manufacturing processes and work with vendors to manufacture components.

The candidate must have significant background in medical device development, implantable electrodes, process development, and verification and validation. The individual should be hands-on and have direct experience working with vendors and design transfer to contract manufacturers.

Responsibilities:

  • Mechanical design of implantable electrodes for neuromodulation 
  • End-to-end development of assembly and manufacturing processes
  • Design of processes for thin substrate laminations and bonding techniques
  • Design of microscale assembly techniques, including scaling to manufacturability
  • Develop micro-molding, thermoforming, and lamination methods for thin substrates and catheters
  • Create 3D assemblies and technical drawings of electrodes and implantable housings using SolidWorks and AutoCAD
  • Identify, source, and manage vendors to obtain hardware components on a schedule (e.g. procuring materials, services from machine shops or 3D printing houses, contract manufacturing)
  • Develop mechanical testing structures and set up accelerated lifetime tests
  • Manage engineering personnel as necessary (e.g. junior engineers, technicians, co-ops)
  • Adhere to Micro-Leads quality management system, understands essential regulatory requirements, and follows standard operating procedures
  • Maintain design control requirements related Micro-Leads’ QMS including developing design inputs/outputs, risk management, verification and validation

Minimum qualifications:

  • B.S. in Mechanical or Biomedical Engineering, M.S. Preferred
  • 2-4 years of related professional experience post-Bachelor’s Degree

Desired qualifications & experience:

  • Successful candidates must be able to multi-task and work effectively as part of a small team
  • Successful candidates will have excellent benchtop capability including the dexterity to manipulate small structures under a stereomicroscope
  • Familiarity with standard tooling for rapid prototyping (e.g. drill presses, saws, welding, soldering, CNC mills)
  • Experience with precision microscale assembly of silicone electrodes using processes such as injection molding, casting, micro-fluidic molding, etc.
  • Experience with Class III implantable systems and hermetic manufacturing methods
  • Experience with precision microscale assembly of silicone electrodes using processes such as injection molding, thermoforming, lamination, micro-molding, etc.

Benefits:

  • Medical Insurance
  • Dental Insurance
  • Vision Insurance
  • Stock Options

Company Description

Micro-Leads is a fast-paced early-stage company developing an injectable medical device to treat people with chronic pain with greater efficacy. Our company has extensive expertise in precision implantable medical devices for nerve stimulation and neuromodulation.