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Medical Device Development Jobs (NOW HIRING)

Crown Medical, Inc.

Medical Device Rep

Albuquerque, NM · On-site

$82K - $113K/yr

We are a fully integrated company with internal resources dedicated to the development and promotion of medical supplies and device products. We believe that our proven products and customer focused ...

Kelly Services

Medical Device Assembler

Irvine, CA · On-site

$24/hr

Johnson & Johnson is rapidly expanding and is immediately hiring qualified Medical Device Assemblers to support production demand and new product development. Position Summary: As a Medical Device ...

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Medical Device Development information

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$29K

$53.4K

$81K

How much do medical device development jobs pay per year?

As of Jul 21, 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.
More about Medical Device Development jobs
What cities are hiring for Medical Device Development jobs? Cities with the most Medical Device Development job openings:
What states have the most Medical Device Development jobs? States with the most job openings for Medical Device Development jobs include:
What job categories do people searching Medical Device Development jobs look for? The top searched job categories for Medical Device Development jobs are:
Medical Device Development jobs near you
Infographic showing various Medical Device Development job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $53,418 per year, or $25.7 per hour.

Contract Medical Device Lead Auditor

DQS

Schaumburg, IL • On-site

Part-time

Re-posted 6 days ago

Job description

Your role
Medical Device Lead Auditor
DQS Inc. has an immediate contract opportunity for a Medical Device Lead Auditor. Working closely with your schedulers, you will visit client locations and perform the audits as specified. Position is home based with extensive travel.
Job Responsibility:
  • Knowledge of principles and methods for management systems audits.
  • Experience with internal, 2nd or 3rd party ISO-9001, ISO 13485, and/ or GMP auditing.
  • Preference given to RAB-QSA or Exemplar Global Lead Auditor or Auditor qualification.
  • Ability to develop an audit scope and audit plan and manage audit team activities.
  • Ability to present the audit team conclusions to the customer and review customer resolution of any nonconformities.
  • Must be able to assess customer needs and meet UL DQS service and customer satisfaction standards.
  • Work independently and project a professional image appropriate to the work environment.
  • Extensive travel.

Your profile
  • Bachelor's degree in a physical or life science or electrical, mechanical or biotechnology engineering required
  • Minimum of four years experience in quality systems management.
  • Minimum of four years experience in medical device development, manufacture and/or testing, with demonstrated knowledge of US, Canada and EU medical device regulatory requirements, experience with device submittals and knowledge of risk management principles such as ISO 14971.
  • Passed or ability to pass an accredited 40-hour ISO 9001 or ISO 13485 lead auditor course.
  • Experience in implementation of ISO 13485, MDD and/ or CMDCAS desired.

EEO is the Law
Right to Work Poster (English)
DQS Inc. is an Equal Opportunity Employer. Minorities/Women/Veterans/Disabled
EQUAL EMPLOYMENT OPPORTUNITY (EEO)
Qualified applicants are considered for employment without regard to race, religion, sex, national origin, age, marital status, sexual orientation, veteran status, disability, or other protected characteristic.
The employer is subject to certain governmental recordkeeping and reporting requirements for the administration of civil rights laws and regulations. In order to comply with these laws, the employer invites employees to voluntarily self-identify their race or ethnicity. Submission of this information is voluntary and refusal to provide it will not subject you to any adverse treatment. The information obtained will be kept confidential and may only be used in accordance with the provisions of applicable laws, executive orders, and regulations, including those that require the information to be summarized and reported to the federal government for civil rights enforcement. When reported, data will not identify any specific individual.
Right to Work Poster (English)
EEO is the Law

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