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Remote Director Medical Device Jobs (NOW HIRING)

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Director, Business Development - Medical Device

OR · Remote

$153K - $210K/yr

... medical device sector to join our dynamic and empowered Business Development team as Director ... This remote role is primarily based on the East Coast of the United States, with consideration for ...

Danaher

Sales Representative Medical Device

Wilmington, DE · On-site +1

$90K - $100K/yr

... directed by annual performance objectives and quota. This position reports to the Regional Sales ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Sales Representative Medical Device

Richmond, VA · On-site +1

$90K - $100K/yr

... directed by annual performance objectives and quota. This position reports to the Regional Sales ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Sales Representative Medical Device

Baltimore, MD · On-site +1

$90K - $100K/yr

... directed by annual performance objectives and quota. This position reports to the Regional Sales ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Sales Representative Medical Device

Philadelphia, PA · On-site +1

$90K - $100K/yr

... directed by annual performance objectives and quota. This position reports to the Regional Sales ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Sales Representative Medical Device

Raleigh, NC · On-site +1

$90K - $100K/yr

... directed by annual performance objectives and quota. This position reports to the Regional Sales ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Airspace

Enterprise Account Manager (Medical Device)

OR · Remote

$100K - $120K/yr

They report to the Director, Enterprise Sales and Account Management. This role serves as the ... Comfortable working with high accountability at a distributed, highly remote company with remote ...

Bausch + Lomb

Research Fellow, Medical Device Toxicologist

OR · On-site +1

$150K - $200K/yr

The Research Fellow - Medical Device Toxicologist will provide cross functional Preclinical medical ... Remote All qualified applicants will receive consideration for employment without regard to race ...

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Remote Director Medical Device information

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$76.5K

$177.2K

$304.5K

How much do remote director medical device jobs pay per year?

As of Jun 7, 2026, the average yearly pay for remote 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 the difference between Remote Director Medical Device vs Remote Regulatory Affairs Director?

AspectRemote Director Medical DeviceRemote Regulatory Affairs Director
Required CredentialsMedical device industry certifications, engineering or clinical backgroundRegulatory affairs certifications (e.g., RAC), science or law background
Work EnvironmentMedical device companies, manufacturing, R&D teamsRegulatory agencies, medical device firms, compliance departments
Employer & Industry UsageMedical device manufacturers, biotech firmsPharmaceutical and medical device companies, regulatory agencies
Common Search & ComparisonYesYes

The Remote Director Medical Device focuses on overseeing product development, quality, and compliance within medical device companies, often requiring engineering or clinical expertise. In contrast, the Remote Regulatory Affairs Director specializes in navigating regulatory requirements, submissions, and compliance with agencies like the FDA. Both roles require regulatory knowledge but differ in their core focus areas and industry applications.

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What cities are hiring for Remote Director Medical Device jobs? Cities with the most Remote Director Medical Device job openings:
What are the most commonly searched types of Remote Medical Device jobs? The most popular types of Remote Medical Device jobs are:
What states have the most Remote Director Medical Device jobs? States with the most job openings for Remote Director Medical Device jobs include:
What job categories do people searching Remote Director Medical Device jobs look for? The top searched job categories for Remote Director Medical Device jobs are:
Remote Director Medical Device jobs near you
Infographic showing various Remote Director Medical Device job openings in the United States as of May 2026, with employment types broken down into 78% Full Time, 11% Part Time, and 11% Contract. Highlights an 100% 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 3 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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