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Yesterday
N

Nvidia Senior Test Methodology Engineer United States, California

Limitless High-tech career opportunities - Expoint
Define, develop, implement, and support ATE test program solutions for the next generation of GPUs and AI server products. ATE test method code development and debugging. Scripting and automation tools...
Description:
US, CA, Santa Clara
time type
Full time
posted on
Posted Yesterday
job requisition id

We need a creative individual who will help transfer GPU gaming and compute products from design engineering to mass production. You will be exposed to various aspects of building and testing NVIDIA products, from GPUs to assembled boards. In addition, your responsibilities will include working with overseas manufacturing teams to increase yields, test coverage and capacity, and reduce production costs. If you are passionate about building the highest quality server products that will change the world, then we really want to hear from you.

What you'll be doing:

  • Define, develop, implement, and support ATE test program solutions for the next generation of GPUs and AI server products.

  • ATE test method code development and debugging

  • Scripting and automation tools development and debugging

  • Actively participate in cross function team including Product Development Engineering, DFT, and IC design to efficiently debug any product failures and implement optimal solutions

What we need to see:

  • Completion of bachelor's degree or higher in Electrical Engineering/Computer Engineering (or equivalent experience).

  • 5+ years of relevant work experiencein the semiconductor industry.

  • Knowledge of silicon verification, testing and manufacturing

  • Have knowledge in Advantest 93K ATE platform is essential

  • Experienced with Linux, and programming languages such as C/C++/Java and/or Perl/Python

  • Good communication skills and works well in a group environment and with cross functional teams that spans across continents

  • Experience with SRAM testing and familiarity with 2.5D or MCM assembly

  • Understanding of DFT insertion techniques including SCAN, ATPG, MBIST and IOBIST

  • Knowledge of system level testing/validation is a plus

  • Utilizing the AI in ATE testing is a plus and make you standout.

You will also be eligible for equity and .

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Yesterday
3M

3M Lead Design Operations Project Manager United States, Minnesota

Limitless High-tech career opportunities - Expoint
Focus on leading a diverse array of projects from simple to highly complex global packaging artwork through production art, approvals and through printing. Ability to lead creative / design and...
Description:

The Impact You’ll Make in this Role

As a
Lead Design Operations Project Manager , you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by:

  • Focus on leading a diverse array of projects from simple to highly complex global packaging artwork through production art, approvals and through printing.
  • Ability to lead creative / design and adaptation projects if needed.
  • Drive global artwork consistency and design content accuracy within brand guidelines, while effectively managing details and proof-reading artwork.
  • Understand packaging artwork requirements, including working with die lines, net contents, regulatory and warning texts, color and printing methods.
  • Collaborate across many functions/disciplines within 3M (marketing, manufacturing, packaging engineering, regulatory, etc.) and with external agencies and printing companies.
  • Strong problem solving and collaboration skills, keeping projects on brand, budget and on time.
  • Manage project estimates, budget and timelines with internal and external partners.
  • Strong knowledge of consumer brand design methodologies, including managing large global packaging redesigns from concept through production art to print.
  • Adapt and work well with defined approaches, systems, best practices and processes.
  • Ability to learn and adapt to new systems and processes as needed.
  • Build and maintain relationships with key internal and external agency partners.

Your Skills and Expertise

To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:

  • High school diploma/ GED equivalent (completed and verified prior to start)
  • Ten (10) years combined working experience in project management for packaging on production art within corporate, creative, agency and /or printing industry in a private, public, government or military environment
  • Ten (10) years of experience in consumer packaging industry.
  • Ten (10) years of experience in packaging artwork production with strong graphic design acumen.


Additional qualifications that could help you succeed even further in this role include:

  • In-depth packaging design knowledge and experience with print production.
  • Knowledge of packaging regulation and uniform packaging laws is important.
  • Knowledge of consumer goods packaging industry.
  • Experience in consumer healthcare industry.
  • Understanding of current print and pre-press industry processes (offset, flexo, digital,
    gravure, etc.).
  • Working knowledge of review tools, project management software, and Power BI applications.
  • Ability to manage high volumes, shifting priorities, and tight timelines.
  • Strong skills in communication, collaboration, time management and attention to detail, combined with a strategic approach.

Work location:

  • This role follows an on-site working model, requiring the employee to work at least four days a week at the 3M Center in Maplewood, MN.

Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.

Please access the linked document by clicking select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.

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23.11.2025
WP

West Pharma QA Measurement Tech United States, Pennsylvania, Williamsport

Limitless High-tech career opportunities - Expoint
Prioritizing assigned workload, works independently to identify quality problems and recommend action to be taken (i.e., continuing production) based on specifications, procedures and GMP. Determining product acceptability by performing various...
Description:
Essential Duties and Responsibilities
  • Prioritizing assigned workload, works independently to identify quality problems and recommend action to be taken (i.e., continuing production) based on specifications, procedures and GMP.
  • Determining product acceptability by performing various visual, functional and dimensional evaluations using various types of measurement devices such as micrometers, calipers, digital or dial indicators, comparators, force testers, and torque testers to determine product acceptability.
  • Providing assistance in the development of sampling plans, as required.
  • Basic understanding of Statistical terminology is required to evaluate data and make a determination as to process capability; providing written summarization of study data to engineering or other groups as requested.
  • Using Minitab software to create summarized data and graphs in support of engineering activities.
  • Assisting in the training of manufacturing and support personnel in quality assurance related subjects, including certification to the QA equipment.
  • Performing internal quality audits as part of the internal audit team.
  • Support new product development working with Engineering to perform dimensional and functional testing.
  • Obtaining 6S Green Belt Certification.
  • Evaluating current processes for improvement opportunities.
  • Performing in-process inspections in support of the manufacturing group.
  • Ability to evaluate dimensional and functional test results to determine compliance to specifications.
  • Performing calibration tasks for equipment and gauges in support of the Calibration Program.
  • Performing raw material inspection and testing, as back –up to the Quality Assurance Inspector.
  • Verify effectiveness of operator’s inspection process by performing selective product sampling audits.
  • Work with Quality Assurance Engineer to design/develop fixtures for existing and new product types.
Education
  • A High School Diploma or GED is required.
  • A 2-year certification in Quality Assurance or commensurate training is preferred.
Work Experience
  • 1+ year of manufacturing experience is required.
Preferred Knowledge, Skills and Abilities
  • Demonstrate proficiency through literacy testing.
  • Must be familiar with computers and various software programs such as Microsoft Word and Microsoft Excel.
    • Master Control and Mattec experience is a plus.
  • Understanding of Statistical Process Control, blueprint reading, and use of measuring/testing equipment.
  • Must have excellent interpersonal & problem-solving skills & be able to interface with employees in all levels of the organization; must possess good organization, time-management, negotiating & conflict resolution skills; excellent computer skills (including MS Office experience using Word & Excel) required.
  • Ability to understand an interpret dimensional drawings.
  • Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description.
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target.
  • Able to comply with the company’s safety policy at all times.
  • Able to comply with the company’s quality policy at all times.
Travel Requirements
None: No travel required
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
What We Offer

3rd Shift: Sunday-Thursday from 11:30PM - 8AM.

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23.11.2025
JE

Johnson Electric Lead Process Engineer United States, Illinois

Limitless High-tech career opportunities - Expoint
Innovative Environment : Work on cutting-edge technologies and innovative projects that push the boundaries of what’s possible. Professional Growth : Opportunities for continuous learning and professional development through training programs...
Description:

As our next, you’ll play a key role in introducing new products to the production line efficiently and effectively. Your expertise will ensure smooth transitions from prototype to full-scale production while maintaining quality and reducing waste.


Why You’ll Love Working Here:

  • Innovative Environment : Work on cutting-edge technologies and innovative projects that push the boundaries of what’s possible.

  • Professional Growth : Opportunities for continuous learning and professional development through training programs and workshops.

  • Collaborative Culture : A supportive and collaborative work environment where teamwork and knowledge sharing are encouraged.

  • Competitive Compensation : Attractive salary packages and comprehensive benefits that reward your hard work and dedication.

  • Global Presence : Be part of a global company with diverse teams and the opportunity to work on international projects.

What You’ll Be Doing:

  • Running IQ (Installation Qualifications), OQ (Operational Qualifications), and PQ (Performance Qualifications), FQ (Fixture Qualifications) protocols to qualify products.

  • Conduct test method validations to ensure new testers meet their requirements.

  • Facilitate prototype runs, documenting issues in planned production methods.

  • Run and document Pilot builds to determine product readiness for production.

  • Help create work instructions to allow smooth transitions to production.

  • Help confirm cycle times to ensure engineering estimates are accurate.

  • Train operators in the start of production on the new processes.

  • Collaborate with other functional areas to resolve problems and develop improved manufacturing processes.

  • Make efforts to reduce manufacturing waste and process complexity.

  • Travel required 5-10% internationally and/or domestically

What We’re Looking For:

  • Minimum of 5 years’ experience manufacturing environments.

  • Able to use the required measurement equipment for taking measurements during qualification runs.

  • Keen eye for detail in ensuring new processes are developed appropriately.

  • Willingness to highlight issues which will cause waste or potential quality issues in the future.

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23.11.2025
BS

Boston Scientific Sr Software Test Engineer United States, Massachusetts, Waltham

Limitless High-tech career opportunities - Expoint
Design, develop and execute test cases to ensure the quality of the product by proving system functionality, verify business and user requirements are met in Electrophysiology domain area. Manual execution...
Description:

The OPAL Mapping System is a 3D mapping and navigation system and is an effective diagnostic tool for cardiac electrophysiology (EP) procedures. It provides real-time visualization of intracardiac catheters and a display of 3D cardiac maps in selected formats in minimally invasive procedures to assist the physician in identifying the origin of the arrhythmia within the heart chamber. As a physician probes the heart with a catheter, the system generates an accurate anatomical model of the chamber. High-performance rendering and algorithmic techniques are vital to creating a stunning view and providing the physician with instant feedback.

Your responsibilities will include:

  • Design, develop and execute test cases to ensure the quality of the product by proving system functionality, verify business and user requirements are met in Electrophysiology domain area.
  • Manual execution of tests or execute automated test scripts.
  • Create, execute automated test scripts.
  • Debug and fix issues on the automated test scripts within its verification points
  • Debug and fix issues that may be related to the automation framework.
  • Execute automation runs to test JIRA items and coordinate with multiple scrum teams
  • Ensure that tests have been conducted in accordance with written procedures.
  • Document test results and write test reports.
  • Diagnose problems and report bugs and enhancements in a bug tracking system.
  • Share knowledge and demonstrate product areas to other team members on ad hoc basis.
  • Assist in determining test methodology, test strategy and test data setup.
  • Participate in daily scrum meetings, product review meetings, bug triage meetings etc.
  • Work closely with software development team, hardware engineering team, field support team, and other cross-functional teams.

Required qualifications:

  • Bachelor’s degree along with 5+ years of software test engineer or related experience or 3+ years with a master’s degree or advanced degree, preferably BS/MS in Computer Science, Biomedical Engineering, or equivalent.
  • Minimum of 3 years of Python programming experience is required
  • Prior experience with source code management tool such as Git and BitBucket.
  • Working experience of databases.
  • Strong written and verbal communication skills
  • Strong analytical and problem-solving skills

Preferred qualifications:

  • Programming experience such as HTML, CSS, JavaScript, C or C++.
  • A strong product quality and testing experience preferably in medical device domain
  • Experience with ultrasound medical devices
  • Working knowledge of test automation under Linux/Unix environment
  • A natural attention to detail and a penchant for organizing and documenting.
  • A good learner who can master complex software and quickly adapt to new tools and technologies.
  • Experience working in Agile Scrum development environment.
  • Ability to think logically and analytically in a problem-solving environment.
  • Ability to work independently as well as work collaboratively as part of a team.
  • Follow company policy regarding ISO and FDA documentation and compliance for medical device.

Maximum Salary: $ 164500

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).


For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

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23.11.2025
BS

Boston Scientific Team Lead Production Supervisor - Weekend Shift United States, Minnesota

Limitless High-tech career opportunities - Expoint
Produce high quality products, safely, on time for the customer at the lowest cost. Facilitate and partner with a cross functional production team of production, quality and manufacturing engineering team...
Description:

:

Your Responsibilities will Include:

  • Produce high quality products, safely, on time for the customer at the lowest cost
  • Facilitate and partner with a cross functional production team of production, quality and manufacturing engineering team members to achieve annual safety, quality, service and cost goals while maintaining a high engagement & high-performance culture
  • Identify customer requirements to deliver the right products at the right time
  • Be responsive & flexible to customer demands
  • Achieve & exceed product cost goals
  • Support new product development readiness activities for the line team
  • Manufacture products to the highest quality standards and ensure compliance to all Boston Scientific policies and regulations
  • Promote safety, quality & compliance among the team while maintaining Good Manufacturing Practices
  • Foster teamwork and enable a culture of Operational Excellence throughout the entire cross-functional team
  • Ensure effective two-way communication between the production line team and cross-functional support teams
  • Manage, motivate, develop, and involve product builders through coaching and performance management
  • Embed the company values through demonstration & recognition of individual & team behaviors
  • Utilize production area planning tools to ensure all resources are in place to achieve team commitments such as Direct Labor Staffing, Equipment Capacity, Support Team, and Space
  • Ensure product builder training is effective & efficient and maintain training versatility across entire team
  • Utilize leader standard work to ensure lines are meeting standards and escalate appropriately
  • Lead & create team engagement around continuous improvement goals for safety, quality, service, cost and space through the utilization of lean and operational excellence tools and best practices
  • Benchmark and share best practices
  • Partner with materials management team for build planning and material delivery systems and tools
  • Analyze build plan requirements and provide forward looking monthly production commitments
  • Anticipate requirements and position resources to meet & exceed the customer needs
  • Provide appropriate input into the long-term planning of the production area


Required Qualifications:

  • Bachelor’s Degree or equivalent combination of education and experience will be considered in lieu of degree
  • 4 years’ minimum of manufacturing and/or engineering experience
  • 4 years’ minimum of supervisor/management experience
  • Solid computer skills required including Microsoft Excel, Word, and PowerPoint
  • Demonstrated Lean tools/systems experience

Preferred Qualifications:

  • Experience in a regulated environment
  • Medical device industry experience
  • Strong written and verbal communication skills with the ability to communicate at all levels of the organization
  • Ability to be flexible and agile
  • Ability to be a self-starter

Maximum Salary: $ 156900

Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).


For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.

Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.

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23.11.2025
I

Incyte Associate Director Senior PMO Capacity Management Lead United States, Delaware, Wilmington

Limitless High-tech career opportunities - Expoint
Clinical Cost Modeling: Lead the creation of robust cost models for clinical trials, factoring in variables such as patient recruitment, site management, drug supply, and regulatory requirements. Refine cost models...
Description:

Director, PMO (Project Management Office) Capacity Management Leadoperations, financial processes, and resource management concepts.This role will provide support and guidance to key R&D partners on capacity management systems, tools, data, and processes. You will lead the design, and support the development and delivery, of various activity-based models within our Planisware system.

Key Responsibilities

  • Clinical Cost Modeling: Lead the creation of robust cost models for clinical trials, factoring in variables such as patient recruitment, site management, drug supply, and regulatory requirements. Refine cost models for clinical trials, incorporating financial assumptions and benchmarks.
  • Activity-Based Forecasting: Oversee the development of forecasts for clinical trial activities, incorporating timelines, resource demands, and project milestones to guide R&D planning. Direct the calculation of estimate to complete (ETC) while leveraging remaining timeline assumptions to ensure accurate projections and forecasts.
  • Planisware Algorithm Oversight: Manage and validate Planisware algorithm models for financial forecasting, ensuring transparency in inputs (e.g., cost drivers, trial milestones), calculations (e.g., cost allocation formulas), and assumptions. Maintain clear documentation and reporting of Planisware algorithm inputs, calculations, and assumptions to support auditability and stakeholder confidence.
  • Strat Plan, Budget, and Forecasts: Support annual budgeting and forecasting processes with workforce related financial insights. Support the alignment of financial and resource data with project and study assumptions for the annual Strategic Planning and Budget Processes. Provide information necessary to support quarterly Forecast and Monthly Planning and Control Processes.
  • Orphan Drug Credits: Oversee the tracking and optimization of tax credits and incentives for orphan drug development, maximizing financial benefits
  • Business Analysis and Reporting: Prepare and deliver recurring and ad-hoc financial reports to finance leadership and business partners. Provide actionable financial insights through variance analysis, cost-benefit analysis, scenario planning, and other reporting solutions. Translate complex financial/resource management data into clear, actionable insights for both finance and non-finance audiences. Analyze headcount, labor cost, and utilization data to support resource planning
  • Cross-Functional Collaboration: Partner with Finance (FPA), clinical operations, regulatory, and development project management teams to ensure forecasting aligns with trial milestones and operational needs. Collaborate with the Business Intelligence Resources within the PMO Team to deliver requirements and develop dashboards to manage resource spending and capacity planning.
  • Process Improvement and Oversight: Oversee the design, implementation, and standardization of forecasting and budgeting processes, ensuring consistency, efficiency, and compliance with industry best practices. Lead initiatives to identify inefficiencies, streamline workflows, and implement process enhancements to improve forecasting accuracy and budgeting effectiveness.

Additional Responsibilities

  • Advanced Analytics and Forecasting Innovation

Investigate alternative design approaches for forecasting and capacity management, ensuring scalability, flexibility, and alignment with organizational goals. Lead discussions on system transitions, model redesigns, and the incorporation of advanced analytics to support long-term strategic objectives.

Qualifications

Bachelor’s degree in Finance, Accounting, Business Administration, Life Sciences, or a related field (MBA, CPA, or advanced degree preferred)

10+ years of experience in financial planning, forecasting, or budgeting within pharmaceutical R&D or a related industry.

Proven expertise in clinical cost modeling, activity-based forecasting, portfolio management, and process improvement.

Experience with Planisware or similar systems for resource and financial management.

Skills and Competencies:

  • Deep understanding of pharmaceutical R&D processes, including clinical trial phases and clinical trial budgeting models.
  • Strong analytical and financial modeling skills, with proficiency in advanced analytics and forecasting algorithms.
  • Experience working with AI-based models for forecasting, including knowledge of machine learning frameworks and data science principles.
  • Ability to ensure transparency through documentation of forecasting models, including inputs, calculations, and assumptions.
  • Ability to partner with technical and operational teams to drive financial insight while managing multiple priorities
  • Strong business acumen with the ability to work independently and manage multiple priorities.
  • Understanding of project-based accounting or resource planning principles.
  • Excellent leadership, communication, and stakeholder management skills.

Technical Proficiencies:

  • Advanced proficiency in Planisware, ERP systems, and financial reporting tools; Proficient in Excel and financial reporting tools; experience with SQL, Power BI, Tableau, or similar platforms preferred.
  • Familiarity with financial systems (e.g., Oracle, SAP, Adaptive Insights, Hyperion) and project costing concepts.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Learn more at:

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process .

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Limitless High-tech career opportunities - Expoint
Define, develop, implement, and support ATE test program solutions for the next generation of GPUs and AI server products. ATE test method code development and debugging. Scripting and automation tools...
Description:
US, CA, Santa Clara
time type
Full time
posted on
Posted Yesterday
job requisition id

We need a creative individual who will help transfer GPU gaming and compute products from design engineering to mass production. You will be exposed to various aspects of building and testing NVIDIA products, from GPUs to assembled boards. In addition, your responsibilities will include working with overseas manufacturing teams to increase yields, test coverage and capacity, and reduce production costs. If you are passionate about building the highest quality server products that will change the world, then we really want to hear from you.

What you'll be doing:

  • Define, develop, implement, and support ATE test program solutions for the next generation of GPUs and AI server products.

  • ATE test method code development and debugging

  • Scripting and automation tools development and debugging

  • Actively participate in cross function team including Product Development Engineering, DFT, and IC design to efficiently debug any product failures and implement optimal solutions

What we need to see:

  • Completion of bachelor's degree or higher in Electrical Engineering/Computer Engineering (or equivalent experience).

  • 5+ years of relevant work experiencein the semiconductor industry.

  • Knowledge of silicon verification, testing and manufacturing

  • Have knowledge in Advantest 93K ATE platform is essential

  • Experienced with Linux, and programming languages such as C/C++/Java and/or Perl/Python

  • Good communication skills and works well in a group environment and with cross functional teams that spans across continents

  • Experience with SRAM testing and familiarity with 2.5D or MCM assembly

  • Understanding of DFT insertion techniques including SCAN, ATPG, MBIST and IOBIST

  • Knowledge of system level testing/validation is a plus

  • Utilizing the AI in ATE testing is a plus and make you standout.

You will also be eligible for equity and .

Show more
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