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Part Time Biomedical Engineering Consultant Jobs

Rutgers University

Coadjutant Non-Teaching

Piscataway, NJ · On-site

$14.25 - $18/hr

... Biomedical Engineering Salary Details 5400 Offer Information The final salary offer may be ... Position Status Part Time Posting Number 26FA0538 Posting Open Date Posting Close Date ...

Advocate Aurora Health

Endoscopy Technician

Elgin, IL · On-site

Endoscopy Technician * Part time - 20 Hours a Week * First week: Two 8-hour shifts. Second week ... and Biomedical Engineering immediately. 5)Performs chemical and biological monitoring per ...

Advocate Aurora Health

Endoscopy Technician * Part time - 20 Hours a Week * First week: Two 8-hour shifts. Second week ... and Biomedical Engineering immediately. 5)Performs chemical and biological monitoring per ...

Grant Engine

This position is a part-time opportunity. Deliverables: · Review grants from various agencies and ... Required Qualifications: · PhD in biological sciences, biomedical engineering, or other life ...

North Memorial Health

Biomedical Technician

Robbinsdale, MN · On-site

$32.94 - $43.95/hr

Most part-time and all full-time positions are eligible for benefits. * Health & Welfare Benefit ... Local 70 Engineers/BioMed Hours per two week pay period: 80 Shift: Days 8 hours Weekend Requirement:

St. Joseph's Health

Equipment Technician

Wayne, NJ

... Biomedical Engineering, Maintenance, etc.) to effectively and efficiently meet the needs of OR as ... Benefits Eligibility : (Full-time and Part-time Employees-over 20 hours a week) * Competitive ...

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Part Time Biomedical Engineering Consultant information

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$41K

$94.8K

$140K

How much do part time biomedical engineering consultant jobs pay per year?

As of Jun 29, 2026, the average yearly pay for part time biomedical engineering consultant in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What does a biomedical engineer consultant do?

A biomedical engineer consultant provides expert advice on the design, development, and evaluation of medical devices and healthcare systems. They analyze technical problems, ensure compliance with industry standards, and often collaborate with healthcare professionals and regulatory agencies to improve medical technologies.

How does a part-time biomedical engineering consultant typically balance multiple projects or clients, and what support can they expect from employers or clients?

As a part-time biomedical engineering consultant, you may juggle several projects or clients simultaneously, often requiring strong organizational and communication skills. Most employers and clients provide clear project scopes, deliverables, and timelines, but time management remains largely your responsibility. You can expect to collaborate remotely or onsite with cross-functional teams, such as clinicians, regulatory specialists, or product designers, depending on the project's needs. Many consultants find that proactive communication and regular check-ins with stakeholders help manage expectations and ensure project success.

Can a biomedical engineer work part-time?

Yes, biomedical engineers can work part-time, especially in consulting roles where flexible schedules are common. Part-time positions may involve project-based work, contract consulting, or supporting specific tasks such as equipment evaluation or regulatory compliance, often requiring relevant certifications and technical skills.

What is a part-time biomedical engineering consultant?

A part-time biomedical engineering consultant is a professional who provides expert advice and services in biomedical engineering on a flexible, as-needed basis rather than as a full-time employee. These consultants may help healthcare organizations, medical device companies, or research institutions with tasks such as product development, regulatory compliance, troubleshooting, and technology assessment. Working part-time allows them to take on multiple clients or projects, offering specialized expertise without long-term commitment. Their role often involves problem-solving, strategic planning, and ensuring that biomedical devices and systems meet industry standards.

What are the key skills and qualifications needed to thrive as a Part Time Biomedical Engineering Consultant, and why are they important?

To thrive as a Part Time Biomedical Engineering Consultant, you need a solid background in biomedical engineering, problem-solving skills, and typically a relevant degree or certification. Familiarity with medical device regulations, CAD software, and laboratory testing equipment is often required. Excellent communication, project management, and adaptability help consultants effectively collaborate with clients and navigate diverse project needs. These skills and qualities are crucial for delivering expert guidance, ensuring regulatory compliance, and maximizing client satisfaction in a dynamic field.

What engineering jobs pay $500,000?

Senior biomedical engineering consultants or specialized roles in medical device development can reach annual salaries of $500,000 or more, especially with extensive experience, advanced certifications, and leadership responsibilities. High-paying engineering positions often require advanced degrees, strong technical skills, and a track record of successful project management or innovation.

What is the difference between Part Time Biomedical Engineering Consultant vs Biomedical Equipment Technician?

AspectPart Time Biomedical Engineering ConsultantBiomedical Equipment Technician
CredentialsTypically requires a bachelor's degree in biomedical engineering or related field; certifications like CBET are commonRequires an associate degree or certification in biomedical equipment technology; often certified as CBET
Work EnvironmentConsults with healthcare facilities, designs solutions, and provides technical advice; often project-based and flexible hoursPerforms maintenance, repairs, and calibration of medical equipment on-site in hospitals or clinics
Employer & Industry UsageEmployed by consulting firms, hospitals, or as independent contractors in healthcare and medical device industriesEmployed directly by healthcare facilities or service companies, focusing on equipment upkeep and troubleshooting

In summary, a Part Time Biomedical Engineering Consultant primarily offers expert advice, design, and project-based services, often with flexible hours, while a Biomedical Equipment Technician focuses on hands-on maintenance and repair of medical devices on-site. Both roles require relevant technical credentials but differ in scope and work environment.

Can biomedical engineers make 200k?

Biomedical engineers typically earn less than $200,000 annually in most roles, especially at entry and mid-career levels. Achieving a $200,000 salary often requires senior positions, extensive experience, advanced certifications, or working in specialized areas such as research, management, or consulting. Part-time biomedical engineering consultants may have variable earnings depending on their client base and hours worked, but reaching that salary level part-time is uncommon.
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Part Time Biomedical Engineering Consultant jobs near you
Senior Assay Development Consultant / Contractor POC IVD Clinical Chemistry

Senior Assay Development Consultant / Contractor POC IVD Clinical Chemistry

Essenlix

Monmouth Junction, NJ • On-site

$93K - $127K/yr

Part-time

Posted 27 days ago

Job description

Job Title:
Senior Assay Development Consultant / Contractor POC IVD Clinical Chemistry | Lab-on-Spin-Disk | Lyophilized
Reagent Beads
Location:
Monmouth Junction, New Jersey 08852
On-site preferred; part-time / project-based consulting arrangement
Employment Type:
Consultant / Contractor / Part-Time / Hybrid
About Essenlix Corporation:
 Essenlix Corporation is a fast-growing medical device company focused on developing innovative point-of-care diagnostic platforms for decentralized clinical testing. Our technologies integrate microfluidics, precision instrumentation, imaging, automation, and scalable manufacturing to enable accessible, high-quality diagnostics worldwide.
Our overseas manufacturing facility is ISO 13485 certified. We are expanding our U.S.-based assay development and product development capabilities while advancing next-generation POC diagnostic platforms from feasibility through commercialization. 
Position Summary:
We are seeking an experienced POC IVD Assay Development Consultant / Contractor to support and accelerate the development of clinical chemistry assays for a Lab-on-Spin-Disk / centrifugal microfluidic diagnostic platform. 
This role is intended for a consultant with strong hands-on experience developing biochemical or clinical chemistry assays that can be translated into manufacturable IVD products, especially assays using dry reagent formats, lyophilized reagent beads, or stabilized reagent systems.
The consultant will help design, optimize, troubleshoot, and productize assays for analyzer-based POC diagnostic systems. Prior experience with Lab-on-Disk, Lab-on-Spin-Disk, cartridge-based clinical chemistry platforms, or similar POC IVD systems is highly preferred. 
Target assay areas may include, but are not limited to: 
glucose, albumin, creatinine, lipid panel, triglycerides, cholesterol, metabolic panel, electrolyte panel, and liver function markers such as AST and ALT. 

 Key Responsibilities:
  • Develop, optimize, and troubleshoot biochemical and clinical chemistry assays for POC IVD platforms. 
  • Support assay development on Lab-on-Spin-Disk, Lab-on-Disk, centrifugal microfluidic, or equivalent cartridge/analyzer-based systems. 
  • Design and optimize reagent formulations, including enzyme systems, buffers, calibrators, stabilizers, surfactants, preservatives, and dry reagent formats.
  • Develop or improve lyophilized reagent bead formulations suitable for product integration and manufacturing transfer.
  • Evaluate assay performance, including precision, accuracy, linearity, sensitivity, specificity, reportable range, interference, and matrix effects.
  • Conduct method comparison studies against reference analyzers or established clinical chemistry systems.
  • Support real-time and accelerated stability studies for liquid, dried, and lyophilized reagent formats.
  • Troubleshoot assay performance issues related to reagent chemistry, sample matrix, disk/cartridge design, fluidics, optical detection, and instrument interaction.
  • Work closely with engineering, instrumentation, software, manufacturing, QA/QC, and regulatory teams to ensure assay-platform compatibility.
  • Provide technical guidance to accelerate assay development from feasibility to productready design.
  • Support transfer of assays from R&D to manufacturing and quality control. 

Required Qualifications:
  •  PhD in Biochemistry, Analytical Chemistry, Clinical Chemistry, Chemistry, Biomedical Engineering, or a related field;     or MS/BS with significant relevant industry experience.
  •  5+ years of hands-on IVD assay development experience, preferably in POC diagnostics, clinical chemistry, or     analyzer-based system. 
  • Strong experience developing assays for automated analyzers, cartridge-based systems, Lab-on-Disk platforms, or    similar diagnostic platforms.
  • Solid understanding of enzymatic assays, colorimetric/spectrophotometric assays, clinical chemistry principles, and reagent formulation.
  • Experience translating assays from feasibility into robust product development.
  • Experience with assay verification, validation, performance characterization, and troubleshooting.
  • Proven ability to identify root causes of assay failure and improve assay robustness.
  • Ability to work independently as a senior technical consultant while collaborating with cross-functional teams.

Preferred Qualifications:
• Direct experience with Lab-on-Spin-Disk, Lab-on-Disk, centrifugal microfluidics, or  similar POC diagnostic platforms. • Experience developing multi-analyte clinical chemistry panels.
• Experience with dry chemistry, lyophilized reagent beads, reagent stabilization, or dry reagent manufacturing for IVD
   applications.
• Experience with clinical chemistry panels such as glucose, albumin, creatinine, lipid panel, metabolic panel, electrolyte
   panel, liver panel, AST, ALT, and related assays.
• Experience with product commercialization, design transfer, or regulatory submissions for IVD products.
• Familiarity with statistical tools for assay evaluation, including regression analysis, correlation studies, Bland–Altman
  analysis, precision studies, and method comparison.
• Prior experience at diagnostics companies such as Abaxis, Abbott, Roche Diagnostics, Siemens Healthineers,
  Beckman Coulter, Ortho Clinical Diagnostics, or similar companies.
Ideal Candidate Profile:
The ideal candidate is not only a strong assay scientist, but someone who has previously helped bring clinical chemistry assays into real diagnostic products. We are especially interested in candidates who understand the practical challenges of converting liquid reagent chemistry into stable dry or lyophilized formats for POC platforms.
The candidate should be able to provide senior-level technical direction, quickly diagnose assay development bottlenecks, and help the internal team accelerate development toward a manufacturable and commercially viable product.
Soft Skills:
• Strong hands-on problem-solving ability in assay development.
• Practical understanding of product development, not only academic assay design.
• Strong experimental rigor and attention to detail.
• Ability to communicate technical findings clearly to scientific, engineering, and business teams.
• Comfortable working in a fast-paced startup/product development environment.
• Able to work independently with limited supervision.
• Collaborative mindset across assay, engineering, manufacturing, QA/QC, and regulatory functions.
What We Offer:
• Flexible consulting / contractor arrangement.
• Competitive hourly or project-based compensation.
• Opportunity to contribute directly to commercial POC IVD product development.
• Hands-on involvement in next-generation Lab-on-Spin-Disk diagnostic platform development.
• Collaborative cross-functional R&D environment.
• Opportunity for technical leadership and potential longer-term collaboration.
How to Apply:
Please submit your resume and a brief summary of your relevant experience in POC IVD assay development, clinical chemistry assay development, Lab-on-Disk/Lab-on-Spin-Disk systems, or lyophilized reagent bead development.