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Medical Device Commercialization Consultant Jobs

Cordis

QC Technician - Medical Device

Irvine, CA · On-site

$20.63 - $25.65/hr

... commercialization of advanced drug device combination products for the treatment of coronary and ... High School diploma or equivalent education required * 1 year of experience in a medical device or ...

Cordis

QC Technician - Medical Device

Irvine, CA · On-site

$20.63 - $25.65/hr

... commercialization of advanced drug device combination products for the treatment of coronary and ... High School diploma or equivalent education required * 1 year of experience in a medical device or ...

LexisNexis

Sr. Account Executive - Medical Device

Do you have a background in consultative sales specializing in PIM/ UDI/ GDSN compliance and ... Senior Account Executive - Medical Device (New Business) About our Team LexisNexis Reed Tech brings ...

RELX

Sr. Account Executive - Medical Device

Do you have a background in consultative sales specializing in PIM/ UDI/ GDSN compliance and ... Senior Account Executive - Medical Device (New Business) About our Team LexisNexis Reed Tech brings ...

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Medical Device Commercialization Consultant information

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$31K

$148.2K

$399K

How much do medical device commercialization consultant jobs pay per year?

As of Sep 12, 2026, the average yearly pay for medical device commercialization consultant in the United States is $148,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $181,500.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Commercialization Consultant vs Regulatory Affairs Specialist?

AspectMedical Device Commercialization ConsultantRegulatory Affairs Specialist
CredentialsIndustry experience, certifications like RAC or ISO 13485Regulatory certifications, such as RAC or RAPS membership
Work EnvironmentConsulting firms, client sites, project-basedMedical device companies, regulatory departments
Industry UsageAdvises on market entry, product launch, and commercialization strategiesEnsures compliance with regulations, prepares submissions

The main difference is that Medical Device Commercialization Consultants focus on bringing devices to market through strategic planning and project management, while Regulatory Affairs Specialists concentrate on ensuring regulatory compliance and managing submissions. Both roles require industry knowledge and certifications but serve different stages of the product lifecycle.

What cities are hiring for Medical Device Commercialization Consultant jobs?

Cities with the most Medical Device Commercialization Consultant job openings:

What states have the most Medical Device Commercialization Consultant jobs?

States with the most job openings for Medical Device Commercialization Consultant jobs include:

What are popular job titles related to Medical Device Commercialization Consultant jobs?

For Medical Device Commercialization Consultant jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Commercialization Consultant job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $148,159 per year, or $71.2 per hour.

Senior Device Engineer

San Diego, CA • On-site

Ventura Solutions LLC
Medical Equipment and Supplies Manufacturing • 11 - 50 employees
Learn more about Ventura Solutions LLCexternal

$70 - $90/hr

Full-time

Medical, Dental, Retirement, PTO

Re-posted 20 days ago

Job description

We are seeking an experienced Senior Device Engineer to support client device development programs focused on autoinjector and combination products. The successful candidate will serve as an extension of the client team, leading day-to-day development activities, managing design control deliverables, coordinating external partners, and ensuring program objectives are achieved.

The ideal candidate brings deep hands-on experience in medical device and combination product development, with the ability to independently manage design control activities, risk management deliverables, technical documentation, and cross-functional project execution while contributing to overall program strategy.

Responsibilities

  • Support autoinjector and combination product development activities across multiple programs.
  • Develop and maintain integrated project schedules and Gantt charts.
  • Coordinate activities across device vendors, fill-finish partners, assembly sites, and other suppliers.
  • Prepare and manage design control and risk management deliverables.
  • Draft development plans, verification plans, and supporting technical documentation.
  • Manage day-to-day execution of assigned programs while receiving strategic direction from client leadership.
  • Work independently on design control processes and deliverables.
  • Communicate effectively across technical and cross-functional teams.

Qualifications

  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related discipline.
  • Approximately 5–10 years of relevant experience in device or combination product development (preferred).
  • Direct, hands-on autoinjector development and commercialization experience (preferred).
  • Experience with controls and risk management.
  • Willingness and ability to perform detailed, hands-on execution work in addition to any strategic input.
  • Strong project management skills, including schedule development and cross-functional coordination.
  • Strong written and verbal communication skills.

Location

  • On-site in San Diego, CA

Employment Type

  • W2 Contract

Compensation & Benefits

  • Hourly range: $70-$90 depending on experience
  • Medical and dental insurance
  • Paid vacation time
  • 401(k) after 90 days

About Ventura Solutions

Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.


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