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Medical Device Development Jobs (NOW HIRING)

Aerotek

Medical Device Assembler

Dallas, TX

$21 - $22/hr

... development. Work Environment This role is based in a medical device warehouse and production ... environment, working closely with a team of approximately 5-10 people. Standard hours are first ...

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$53.4K

$81K

How much do medical device development jobs pay per year?

As of Jun 10, 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 June 2026, with employment types broken down into 2% As Needed, 75% Full Time, 13% Part Time, and 10% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $53,418 per year, or $25.7 per hour.
Director/Sr. Director, Medical Device Development

Director/Sr. Director, Medical Device Development

Liquidia Corporation

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 6 days ago

Job description

Job Description
Liquidia is deeply passionate and committed to the discovery, engineering, and development required to bring novel therapies to patients who need them most, and to the healthcare providers who care for them. Our current drive is toward improving the treatment of pulmonary hypertension (PH). We will continue to combine our proprietary, innovative PRINT® Technology with new and established medications, offering the potential for both better precision and improved clinical outcomes. Our team members include some of the industry's top scientists, clinicians, business strategists, engineers, and pharmaceutical executives. We work together to help people lead longer, healthier, and happier lives.
Job Summary
The Senior Director or Director of Medical Device Development will lead the development and lifecycle management of inhalation drug delivery systems, with a strong focus on inhalation technologies and drug-device combination products.
This role is responsible for driving robust inhalation device development and innovation, and ensuring compliance with the latest regulations for the successful combination use of device and drug across all development stages, from early feasibility. The role also requires deep technical expertise in nebulizers, DPIs and SMIs, aerosol science, device engineering, statistics and combination product development.
Job Requirements
Education and Experience
  • PhD, MS, or equivalent degree in Industrial Design, Mechanical Engineering, Electrical Engineering, Human Factors Engineering, Aerosol Science, Pharmaceutical Sciences, Statistics, or another relevant field.
  • Proven track record (15+ years) in development of medical devices, including mesh nebulizers, SMIs, and drug-device combination products.
  • Experience supporting regulatory submissions and responding to deficiencies related to inhalation devices and inhaled drug-device combination products.
  • Proven ability to lead cross-functional development programs and provide support for commercial launches.
Knowledge, Skills, and Abilities
  • Mesh nebulizer technology (including mechanical, electrical, and software engineering)
  • SMI engineering
  • Human factors engineering
  • Design controls, risk management and preparation of DHF authoring
  • Design verification and validation
  • Statistics for samples size calculations and SPEC settings as applied to the development of medical devices and combination products
  • CFR 820. Part 4 / ISO 13485, medical devices quality framework and in-depth knowledge of GMP, GXP, FDA and EU regulatory requirements for medical devices
  • Strong program leadership and decisive decision-making
  • Management of external device partners
  • Excellent communication and stakeholder management

Job Responsibilities
  • Collaborates in developing device development strategies that support and align with pipeline needs.
  • Acts as the technical lead for nebulizers, SMIs, other inhalation delivery technologies, and oversees mechanical, electrical, software, human factors engineering, as well as statistical analysis of sample sizes for design verification.
  • Oversees device design, prototyping, verification, validation, and transfer processes.
  • Ensures development of drug-device combination products follow design control and risk management requirements in accordance with FDA and international regulations.
  • Leads preparation of Design History File (DHF).
  • Identifies issues and proposes mitigating plans to facilitate decision-making
  • Works collaboratively with contract development and manufacturing organizations (CDMOs) and device vendors.
  • Drives cross-functional alignment among R&D, Clinical, Quality, Regulatory, and Manufacturing teams.
  • Supports preparation of device sections for regulatory filings and responses to deficiencies.

Job Benefits
Liquidia offers a competitive compensation package (base salary and commission) as well as a comprehensive benefits package that includes Medical, Dental, Vision, STD, LTD, 401(k) Savings Retirement Plan, ESPP, Unlimited Paid Time Off and more!
Liquidia is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Reasonable accommodation may be made to enable qualified individuals with disabilities to perform the essential functions of this position.
Recruiting Agencies, Please Note :
Liquidia will not accept unsolicited assistance from recruiting/search agencies for this employment opportunity. Please, no phone calls or emails. All resumes submitted by recruiting or search agencies to any employee at Liquidia via email, the Internet or in any form and/or method without a valid written search/recruitment agreement in place for this position will be deemed the sole property of Liquidia. No fee will be paid in the event the candidate is hired by Liquidia as a result of the referral or through other means.

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