ZipRecruiter

Log In

2

Part Time Microfluidics Jobs (NOW HIRING)

People also search for

All JobsPart Time Microfluidics Jobs

Part Time Microfluidics information

What are the typical responsibilities and collaborative aspects of a part-time microfluidics position?

In a part-time microfluidics role, you can expect to assist with the design, fabrication, and testing of microfluidic devices, often supporting ongoing research projects or product development. You’ll frequently collaborate with interdisciplinary teams, including biologists, chemists, and engineers, to troubleshoot experiments and analyze data. Communication is key, as you may attend team meetings and contribute to lab documentation. The part-time structure allows for flexibility, but time management is important to balance project milestones and deadlines.

What are the key skills and qualifications needed to thrive as a Part-Time Microfluidics Specialist, and why are they important?

To thrive in a part-time microfluidics role, you typically need a background in engineering, physics, or biology, with hands-on experience in microfluidic device design and analysis. Familiarity with CAD software, microfabrication tools, and laboratory instrumentation such as flow controllers and microscopes is essential. Strong problem-solving skills, attention to detail, and effective communication are important soft skills for collaborating on interdisciplinary projects. These competencies enable accurate experimentation, innovation, and efficient teamwork in fast-evolving research and development environments.

What is the difference between Part Time Microfluidics vs Part Time Microfabrication Technician?

AspectPart Time MicrofluidicsPart Time Microfabrication Technician
Required CredentialsRelevant degrees in biomedical, chemical, or mechanical engineering; certifications in lab techniquesDegrees in materials science, engineering, or physics; certifications in cleanroom procedures
Work EnvironmentLaboratories focused on fluid dynamics, biomedical devices, or lab-on-a-chip systemsCleanroom facilities, microfabrication labs, semiconductor manufacturing environments
Industry UsageBiotech, healthcare, research institutionsSemiconductor, electronics, MEMS device manufacturing

Part Time Microfluidics involves designing and testing micro-scale fluid systems, often in biotech or research settings. In contrast, Part Time Microfabrication Technicians focus on fabricating micro-scale devices in cleanroom environments. While both roles require technical skills and lab experience, they serve different industries and have distinct daily tasks.

What are part time microfluidics jobs?

Part time microfluidics jobs involve working on the design, fabrication, or analysis of devices and systems that manipulate fluids at a very small scale, typically using channels measured in micrometers. These roles may include research assistance, device prototyping, laboratory work, or data analysis related to microfluidic technology, but with a flexible or reduced-hour schedule. Part time positions are common in academic labs, biotech companies, or research institutions, and can be ideal for students, professionals seeking flexible work, or those looking to gain experience in the field. Responsibilities may vary depending on the employer but usually require a background in engineering, chemistry, biology, or related disciplines. These jobs contribute to advancements in areas like medical diagnostics, drug development, and environmental monitoring.
More about Part Time Microfluidics jobs
What are the most commonly searched types of Microfluidics jobs? The most popular types of Microfluidics jobs are:
What job categories do people searching Part Time Microfluidics jobs look for? The top searched job categories for Part Time Microfluidics jobs are:
Part Time Microfluidics jobs near you
Infographic showing various Part Time Microfluidics job openings in the United States as of May 2026, with employment types broken down into 72% Full Time, 25% Part Time, and 3% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution.
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 3 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.