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Director Medical Device Jobs (NOW HIRING)

Kellton Tech

Medical Device Assembler

Madison, WI · On-site

$23 - $24/hr

Medical device, pharmaceutical industry Competencies: Self-directed Teamwork Good communication skills Proficient with computer systems Critical thinking Decision making Quality focused ...

SmartTalent

Medical Device Assembler

Redmond, WA · On-site

$23 - $26/hr

Paid Weekly, Direct Deposit, Affordable Health Care, Full-Time, Career Advancement Opportunities ... Medical device experience is a plus. Apply today and one of our recruiters will help you get ...

SlingShot Connections

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Medical Device Assembler

San Clemente, CA · On-site

$20.25 - $22.27/hr

Work under direction from management or engineering staff with direct oversight * Other duties as ... Comfortable working in a regulated environment (medical device experience is a plus) * Ability to ...

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Kelly Services

Medical Device Assembler

Maple Plain, MN

$20 - $24/hr

Join our team as a Medical Device Assembler! If you enjoy working with precision, take pride in ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

Kelly Services

Medical Device Assembler

Maple Plain, MN

$20 - $24/hr

Join our team as a Medical Device Assembler! If you enjoy working with precision, take pride in ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

Kelly Services

Medical Device Assembler

Lake Zurich, IL · On-site

$19.50 - $23.50/hr

... medical device preferred) * Strong attention to detail and manual dexterity * Ability to use hand ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

Kelly Services

Medical Device Assembler

Lake Zurich, IL · On-site

$19.50 - $23.50/hr

... medical device preferred) * Strong attention to detail and manual dexterity * Ability to use hand ... Requests for accommodation related to our application process can be directed to the Kelly Human ...

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How much do director medical device jobs pay per year?

As of May 31, 2026, the average yearly pay for director medical device in the United States is $177,191.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,000.00 and $203,500.00 per year, depending on experience, location, and employer.

What is a Director Medical Device job?

A Director of Medical Devices is a senior leadership role responsible for overseeing the development, regulatory compliance, and commercialization of medical devices. They manage cross-functional teams, ensuring products meet industry standards and regulatory requirements. This role often involves strategic planning, budget management, and collaboration with R&D, quality assurance, and marketing teams. Directors also play a key role in ensuring patient safety and product effectiveness while driving business growth.

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

To thrive as a Director Medical Device, you need deep knowledge of medical device regulations, product development, and leadership, often supported by a degree in engineering, life sciences, or a related field. Familiarity with tools like quality management systems (QMS), regulatory submission platforms, and certifications such as PMP or Six Sigma are highly valuable. Strategic thinking, cross-functional communication, and change management are vital soft skills that help drive innovation and lead diverse teams. These competencies are essential to ensure product quality, regulatory compliance, and successful market delivery in a complex and rapidly evolving industry.

What are some of the main challenges Directors of Medical Device face in leading product development teams?

Directors of Medical Device often encounter challenges such as managing regulatory compliance across multiple markets, ensuring seamless collaboration between cross-functional teams, and keeping projects on track amid evolving industry standards. They must also balance innovation with risk mitigation to bring new products to market safely and efficiently. Navigating these demands requires strong leadership and a deep understanding of both engineering and regulatory requirements, as well as the ability to adapt to new technologies. Overcoming these challenges is key to driving organizational success and maintaining a competitive edge within the medical device sector.
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What cities are hiring for Director Medical Device jobs? Cities with the most Director Medical Device job openings:
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Director Medical Device jobs near you
Infographic showing various Director Medical Device job openings in the United States as of May 2026, with employment types broken down into 30% Full Time, 10% Part Time, and 60% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $177,191 per year, or $85.2 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 26 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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