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Part Time Automation Testing Jobs in New York (NOW HIRING)

Eulerity

Product Marketing Intern

New York, NY · On-site

$18 - $20/hr

Position Overview At Eulerity, we are building the future of AI-driven marketing automation. To ... testing solutions, and optimizing the "user" (candidate) experience. You will work closely with ...

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Osmo

Contract Sensory Panelist (Fragrance)

Elizabeth, NJ · On-site

$30/hr

We believe in the power of automation and thoughtfully applied AI/ML to solve problems beyond the ... This is a specialized, part-time contract role dedicated exclusively to generating high-quality ...

MTA Headquarters

Manager - Financial Systems

New York, NY · Hybrid

$102K - $113K/yr

Systems Management and Reporting WORK LOCATION: 420 Lexington Avenue FULL/PART-TIME FULL SALARY ... It will also be responsible for the ongoing integration and automation of data exchanges between ...

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How much do part time automation testing jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for part time automation testing in New York is $56.10, according to ZipRecruiter salary data. Most workers in this role earn between $48.41 and $63.89 per hour, depending on experience, location, and employer.

Is automation testing still in demand?

Automation testing remains in high demand as companies seek to improve software quality and accelerate release cycles. Skills in tools like Selenium, TestComplete, and programming languages such as Java or Python are valuable for automation testers in various industries.

What are the typical responsibilities and daily tasks of a Part Time Automation Testing professional?

As a Part Time Automation Testing professional, you will typically write, update, and execute automated test scripts, analyze test results, and report defects to the development team. Your daily work may include collaborating with developers and manual testers to plan and implement testing strategies, maintaining or enhancing automation frameworks, and participating in meetings to discuss project progress. You may also be responsible for troubleshooting test failures and documenting test procedures. Due to the part-time nature, strong time management skills are essential to ensure thorough coverage of assigned tasks and effective communication with the team. This role is valuable for those seeking a balance between hands-on technical work and flexible scheduling.

What are the key skills and qualifications needed to thrive in the Part Time Automation Testing position, and why are they important?

To thrive as a Part Time Automation Testing professional, you need a solid understanding of software testing principles, programming or scripting languages (such as Python, Java, or JavaScript), and experience with automated testing frameworks. Familiarity with tools like Selenium, JUnit, TestNG, or similar, and certifications in software testing or quality assurance are highly valued. Attention to detail, problem-solving abilities, and strong communication skills help you work efficiently and collaborate within a team environment. These skills are crucial for ensuring software quality, integrating seamlessly with development teams, and maximizing productivity in a flexible, part-time setting.

Are QA testers in demand in 2026?

QA testers, including those specializing in automation testing, are expected to remain in demand through 2026 due to ongoing software development and the need for quality assurance. Skills in automation tools like Selenium, programming languages, and continuous integration are valuable for staying competitive in the field.

How much do automation testers get paid?

Automation testers typically earn between $50,000 and $100,000 annually, depending on experience, location, and industry. Entry-level positions may start around $50,000, while experienced professionals with skills in tools like Selenium or Appium can earn higher salaries, especially in tech hubs.

Is QA replaced by AI?

QA roles, including automation testing, are evolving with AI tools that assist in test case generation, bug detection, and data analysis. However, human oversight remains essential for designing tests, interpreting results, and ensuring quality, so QA positions are unlikely to be fully replaced by AI in the near future.

What is a Part Time Automation Testing job?

A Part-Time Automation Testing job involves testing software applications using automated tools and scripts on a flexible or reduced-hour schedule. Professionals in this role design, execute, and maintain automated test scripts to improve software quality while working fewer hours than a full-time equivalent. It's ideal for those looking for work-life balance, freelancing opportunities, or gaining test automation experience while studying or working another job.

What are the most commonly searched types of Automation Testing jobs in New York? The most popular types of Automation Testing jobs in New York are:
What job categories do people searching Part Time Automation Testing jobs in New York look for? The top searched job categories for Part Time Automation Testing jobs in New York are:
What cities in New York are hiring for Part Time Automation Testing jobs? Cities in New York with the most Part Time Automation Testing job openings:
Part Time Automation Testing jobs near you
Infographic showing various Part Time Automation Testing job openings in New York as of June 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $116,685 per year, or $56.1 per hour.
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 12 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.