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Medical Device Consulting Jobs (NOW HIRING)

AstrixTechnology LLC

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Medical Device Assembler

Santa Rosa, CA · On-site

$20 - $25/hr

... technology consulting, regulatory advisory services and staffing solutions to the scientific ... Medical device, Petrochemical and Clinical Research.

Medix

Medical Device Specialist

Westminster, CO · On-site

$25 - $35/hr

Job Summary Our client is looking for a dedicated Medical Device Specialist to manage cardiac ... Conduct real-time device interrogation and reprogramming during patient consultations to assist ...

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Medical Device Consulting information

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$49

$96

How much do medical device consulting jobs pay per hour?

As of Jul 3, 2026, the average hourly pay for medical device consulting in the United States is $49.84, according to ZipRecruiter salary data. Most workers in this role earn between $35.10 and $59.62 per hour, depending on experience, location, and employer.

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

To thrive in Medical Device Consulting, you need a strong background in biomedical engineering, regulatory knowledge, and experience with product development or commercialization, often supplemented by a relevant degree and industry certifications. Expertise with FDA regulations, ISO standards, clinical trial management systems, and common project management tools is highly valued. Exceptional problem-solving, client communication, and adaptability are crucial soft skills for success. These competencies are vital to effectively guide clients through compliance, market entry, and product lifecycle challenges in a complex, high-stakes industry.

What does a Medical Device Consultant do?

A Medical Device Consultant provides expertise to companies developing, manufacturing, or marketing medical devices. They help navigate regulatory requirements, ensure compliance with FDA or EU MDR guidelines, conduct quality assessments, and offer strategic advice on product development. Consultants may also assist with clinical trials, risk management, and market entry strategies. Their goal is to help companies bring safe and effective medical devices to market efficiently while meeting industry regulations.

What are some typical daily responsibilities for professionals in Medical Device Consulting?

Day-to-day tasks for Medical Device Consultants often include advising clients on regulatory strategy, preparing submissions for compliance agencies, assessing product safety and efficacy data, and coordinating with cross-functional teams such as R&D, quality assurance, and marketing. You may also conduct audits, lead training sessions, and assist clients in navigating clinical trial requirements or post-market surveillance. Collaboration and regular communication with client stakeholders are essential, as is staying current on evolving industry standards. This dynamic role provides exposure to diverse projects and the opportunity to make a tangible impact on the development and approval of innovative medical technologies.

What are the Big 4 consulting firms in healthcare?

The Big 4 consulting firms in healthcare are Deloitte, PwC (PricewaterhouseCoopers), EY (Ernst & Young), and KPMG. These firms provide strategic, regulatory, and operational consulting services to healthcare organizations, including medical device companies, often requiring strong analytical skills and industry knowledge.

What does a medical device consultant do?

A medical device consultant advises companies on the development, regulatory compliance, and market strategy of medical devices. They often review design, assist with FDA submissions, and ensure products meet safety and quality standards, utilizing industry knowledge and regulatory tools. Their work supports bringing safe, effective devices to market efficiently.

Is 30 too old to get into consulting?

Medical device consulting is a field that values experience and industry knowledge, and individuals often enter at various ages. Being 30 is generally not too old, especially if you have relevant skills, certifications, or prior healthcare or engineering experience. Success in consulting depends more on expertise and network than age alone.

How to get into medical device consulting?

To enter medical device consulting, professionals typically need a background in biomedical engineering, healthcare, or related fields, along with experience in regulatory compliance, quality assurance, or product development. Gaining certifications such as ISO 13485 or regulatory affairs credentials can enhance credibility, and developing strong project management and communication skills is essential for client interactions. Entry often involves networking within the industry and applying for roles at consulting firms or medical device companies seeking external expertise.
More about Medical Device Consulting jobs
What cities are hiring for Medical Device Consulting jobs? Cities with the most Medical Device Consulting job openings:
What are the most commonly searched types of Medical Device Consulting jobs? The most popular types of Medical Device Consulting jobs are:
What states have the most Medical Device Consulting jobs? States with the most job openings for Medical Device Consulting jobs include:
What job categories do people searching Medical Device Consulting jobs look for? The top searched job categories for Medical Device Consulting jobs are:
Medical Device Consulting jobs near you
Infographic showing various Medical Device Consulting job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 89% Full Time, 1% Part Time, and 9% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $103,662 per year, or $49.8 per hour.
Medical Device/Combination Product Engineer

Medical Device/Combination Product Engineer

Ventura Solutions LLC

Vernon Hills, IL • On-site

$60K - $75K/yr

Full-time

Medical, Dental, Vision, PTO

Posted 3 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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