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Freelance Medical Device Consulting Jobs (NOW HIRING)

Building Block Co

FL · On-site

Foot and Ankle Medical Device Sales Representative Position Overview: Are you thrilled by the ... trusted consultant to our clients, while driving revenue growth to new heights. Join our team ...

HealthTrust

AVP Strategic Sourcing

Lebanon, TN · On-site

The goals of SurgIntel analytics, medical device consulting, and physician engagement are to illustrate implant utilization, supply cost variation, deep clinical categorization, and price ...

HealthTrust

AVP Strategic Sourcing

Murfreesboro, TN · On-site

The goals of SurgIntel analytics, medical device consulting, and physician engagement are to illustrate implant utilization, supply cost variation, deep clinical categorization, and price ...

HealthTrust

AVP Strategic Sourcing

Franklin, TN · On-site

The goals of SurgIntel analytics, medical device consulting, and physician engagement are to illustrate implant utilization, supply cost variation, deep clinical categorization, and price ...

HealthTrust

AVP Strategic Sourcing

Nashville, TN · On-site

The goals of SurgIntel analytics, medical device consulting, and physician engagement are to illustrate implant utilization, supply cost variation, deep clinical categorization, and price ...

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 ...

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Freelance Medical Device Consulting information

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How much do freelance medical device consulting jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for freelance medical device consulting in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

What is freelance medical device consulting?

Freelance medical device consulting involves providing expert advice and support to medical device companies or startups on a contract or project basis. Consultants may assist with regulatory compliance, product development, quality assurance, clinical trial design, and market entry strategies. Unlike full-time employees, freelance consultants work independently and typically serve multiple clients, offering flexible and specialized expertise tailored to each project's needs. This role requires in-depth knowledge of medical device regulations, industry standards, and often a background in engineering, science, or regulatory affairs.

What are the key skills and qualifications needed to thrive as a freelance medical device consultant?

To thrive as a Freelance Medical Device Consultant, you need a solid background in biomedical engineering, regulatory affairs, and industry standards, often backed by relevant degrees and experience in medical device development. Familiarity with FDA and EU MDR regulations, quality management systems (like ISO 13485), and project management tools is essential. Strong communication, problem-solving, and client management skills set top consultants apart. These competencies ensure successful navigation of complex compliance landscapes and effective delivery of solutions to clients.

What are some common challenges faced by freelance medical device consultants, and how can they be addressed?

Freelance medical device consultants often encounter challenges such as keeping up-to-date with rapidly changing regulatory requirements and building a steady client base. Staying current with evolving FDA or EU MDR regulations is essential, so regular professional development and networking are crucial. Additionally, freelancers must proactively market their services and establish clear communication with clients to ensure project expectations are met. Being adaptable and organized helps consultants successfully manage multiple projects and deadlines.

What is the difference between Freelance Medical Device Consulting vs Medical Device Regulatory Affairs Specialist?

AspectFreelance Medical Device ConsultingMedical Device Regulatory Affairs Specialist
CredentialsVaries; often requires industry experience, certifications like RAC beneficialTypically requires a degree in life sciences or engineering, plus regulatory certifications
Work EnvironmentIndependent, project-based, remote or on-siteEmployed by companies or consultancies, office or lab settings
Employer & Industry UsageSelf-employed, serving multiple clients in medical device industryFull-time employee or contractor within medical device companies or regulatory firms

Freelance Medical Device Consulting involves independent project work advising clients on product development, compliance, and market entry. In contrast, a Medical Device Regulatory Affairs Specialist is typically employed full-time within a company, focusing on regulatory submissions and compliance. Both roles require industry knowledge, but freelancing offers flexibility and diverse projects, while specialists provide ongoing regulatory expertise within organizations.

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What are the most commonly searched types of Medical Device Consulting jobs?

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Freelance Medical Device Consulting jobs near you
Infographic showing various Freelance Medical Device Consulting job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Medical Device/Combination Product Engineer

Ventura Solutions LLC

Vernon Hills, IL • On-site

$60K - $75K/yr

Full-time

Medical, Dental, Vision, PTO

Re-posted 21 days ago

Job description

We are seeking passionate and driven Medical Device/Combination Product Engineers to join our medical device consulting team. This is an ideal opportunity for recent graduates or those with limited experience who are excited to apply their academic knowledge in real-world product development.
If you have a strong interest in medical devices, pharmaceuticals, and combination products, and are eager to gain hands-on experience in product development, design controls, and risk management, we want to meet you!
As a Medical Device/Combination Product Engineer, you will support the development and maintenance of medical devices and combination products by assisting with technical documentation, testing, and cross-functional collaboration. You'll contribute to the creation of Design History Files (DHF), risk management files, and other engineering documentation in accordance with industry regulations and standards such as FDA 21 CFR 820 and ISO 14971.
Responsibilities
  • Assist in developing and maintaining Design History Files (DHF) and Risk Management Files for medical devices and combination products
  • Support product development activities, including gathering user needs, design inputs, and testing requirements
  • Participate in risk assessment activities, such as creating or supporting FMEAs
  • Help prepare and review technical documentation for design verification and validation
  • Research applicable regulations, standards, and guidance documents to support compliance efforts
  • Work closely with cross-functional teams, including Quality, Regulatory, Manufacturing, Human Factors, and Clinical
  • Contribute to design control activities and help ensure traceability from requirements through testing
  • Support documentation for inspections and regulatory submissions

Qualifications
  • Bachelor's degree in Biomedical Engineering or related engineering discipline (e.g., Mechanical, Chemical, Electrical)
  • Strong academic foundation in engineering principles and a desire to apply them in a regulated industry
  • Understanding of or exposure to design control, risk management, and product development lifecycle through coursework, internships, or academic projects
  • Strong written and verbal communication skills
  • Detail-oriented with good documentation and organizational skills
  • Team-oriented with a willingness to learn and grow in a fast-paced environment

Preferred (Not Required) Experience
  • Internship, co-op, or project work related to medical devices, drug delivery, or combination products
  • Familiarity with standards like ISO 13485, ISO 14971, or FDA design control regulations
  • Exposure to tools such as FMEA, DHF documentation, or verification test planning
  • Experience with engineering software (CAD, Minitab, MATLAB, etc.)

Location
  • Northwest Chicago Suburbs or remote for the right candidate

Employee Type
  • W2 Employee

Compensation and Benefits
  • Salary: $60,000 - $75,000 annually, depending on experience
  • Choice of medical, dental, and vision plans
  • Paid Vacation Time
  • Competitive base salary

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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