Science,Science|Quality Assurance Scientist,Science|Quality Control Scientist Jobs

Job Description:

Core Focus: Lead End-to-End (E2E) testing and subject matter expertise for Vanguard workplace systems, focusing on retirement plan contributions, payroll rules, and proprietary Vanguard platform infrastructure.

Key Workstreams:

• Execute E2E 403(b)/402 contribution monitoring, including eligibility determination, transaction processing, limit monitoring, and exception handling.
• Test and validate proprietary Vanguard applications such as client, PE Web, My Plan Manager, eSetup, Infocap, PRS, VISTA, and VISION, alongside PRDS payroll deduction rules.
• Perform functional, regression, integration, and system testing, backed by deep data integrity testing and custom DB2 query analysis.
• Technical & Testing Scope: Validate complex workflows, track defects in Jira, execute test automation (TestComplete, Spring Boot, Core Java), and ensure multi-device/OS mobile compatibility.
• Requirements: Mandatory background in Vanguard workplace experience, deep domain knowledge of retirement plan recordkeeping/payroll rules, and strong technical testing competencies (Mainframe, DB2, Java-based automation).

And Here is the JD for QA lead:

We are looking for a Global QA Lead who is self-motivated, creative, and proactive to work successfully in a fast-paced environment, including multiple platforms and architectures, diverse technologies, and Cloud environments. The individual will work closely with various stakeholders throughout the SDLC, executing automated test iterations, tracking & reporting test results, troubleshooting, and coordinating bug fixes. The individual should have a strong understanding of agile processes and the related Quality lifecycle and automation methodology.

Responsibilities:

• Advance product quality via testing innovations and process improvement.

• Collaborate with Client, Architects & Developers in designing testable applications.

• Technical roadmaps & plans for implementing enterprise/program test strategies.

• Design & manage technical proof-of-concept and feasibility studies.

• Resolve technical issues,

Required Skills:

• Expert in writing automated scripts using scripting languages like SQL, Java, Python, and JavaScript.

• Expert in designing and building automated testing frameworks using Behavior Driven Development and Test Driven development tools like Cucumber, JBehave, Jasmine, and Selenium.

• Expert in building and implementing CI/CD automation strategies for testing using tools like Jenkins, Bamboo, and Azure DevOps.

• Expert in designing automated test scripts for testing Operational/Relational/OLAP databases and data warehouses.

• Expert in designing automated test scripts and validations for ETL/ELT solutions for multiple parallel processing pipelines.

• Expert in testing APIs and microservices for both the UI layer and the data layer for data extraction, preparation, and consumption modules.

• Good Understanding and familiarity with SQL databases (Azure SQL DB, Azure DW), ETL tools like Talend, Azure Data Factory, and Cloud Storage tools.

SHIFT - FRI, SAT, SUN 6PM - 6AM + 1 DAY EVERY OTHER WEEK + MANDATORY OVERTIME

General Information:

• Recommend SOP and batch record changes as needed
• Review proposed SOP revisions and provide feedback to management
• Real-time audit of batch records in the production suites for completeness, documentation, calculation errors and conformance to critical process parameters
• Perform room and equipment clearances per procedure following cleaning conducted by production.
• Perform microbial swabbing of equipment and room surfaces for environmental monitoring.
• Maintain a full understanding of all client s SOPs and policies along with all cGMP and CFR guidance that are applicable to the manufacturing of solid oral dosage pharmaceutical products.
• Perform routine testing of in-process and finished product samples including particle size, bulk density, moisture analysis, appearance, and AQL testing real-time.
• Monitor production manufacturing areas for compliance to SOP/cGMP/batch record and safety requirements in order to identify and resolve routine errors and prevent possible deviations that affect production real-time.
• Works cross functionally to assess impact for potential deviations and assist in identifying if an investigation is required.
• Initiate deviation problem reports in Trackwise for issues discovered by QA, providing sufficient detail of the incident so that a full investigation by the responsible department can be conducted.
• Manage quality status of WIP and finished good materials on physical inventory and in inventory system (JD Edwards)
• Other assignments as needed within the scope of QA Associate training curriculum.
• Assist in investigations for deviations by supporting data gathering and root cause analysis
• Enforcement of GMP Compliance.
• Promotes teamwork and good communication.
• Provide training and coaching to manufacturing staff as needed
• Support site process improvements (training, efficiency projects, implementation of CAPAs)
• Completes investigations of customer complaints

Education or Equivalent Requirements:

Minimum education and experience required to perform the job:

Quality Assurance Associate

• Bachelors degree; OR
• Associates with 1 year of related work experience; OR
• High School Diploma/GED with 2 years of related work experience

SHIFT - FRI, SAT, SUN 6PM - 6AM + 1 DAY EVERY OTHER WEEK + MANDATORY OVERTIME

General Information:

• Recommend SOP and batch record changes as needed
• Review proposed SOP revisions and provide feedback to management
• Real-time audit of batch records in the production suites for completeness, documentation, calculation errors and conformance to critical process parameters
• Perform room and equipment clearances per procedure following cleaning conducted by production.
• Perform microbial swabbing of equipment and room surfaces for environmental monitoring.
• Maintain a full understanding of all client s SOPs and policies along with all cGMP and CFR guidance that are applicable to the manufacturing of solid oral dosage pharmaceutical products.
• Perform routine testing of in-process and finished product samples including particle size, bulk density, moisture analysis, appearance, and AQL testing real-time.
• Monitor production manufacturing areas for compliance to SOP/cGMP/batch record and safety requirements in order to identify and resolve routine errors and prevent possible deviations that affect production real-time.
• Works cross functionally to assess impact for potential deviations and assist in identifying if an investigation is required.
• Initiate deviation problem reports in Trackwise for issues discovered by QA, providing sufficient detail of the incident so that a full investigation by the responsible department can be conducted.
• Manage quality status of WIP and finished good materials on physical inventory and in inventory system (JD Edwards)
• Other assignments as needed within the scope of QA Associate training curriculum.
• Assist in investigations for deviations by supporting data gathering and root cause analysis
• Enforcement of GMP Compliance.
• Promotes teamwork and good communication.
• Provide training and coaching to manufacturing staff as needed
• Support site process improvements (training, efficiency projects, implementation of CAPAs)
• Completes investigations of customer complaints

Education or Equivalent Requirements:

Minimum education and experience required to perform the job:

Quality Assurance Associate

• Bachelors degree; OR
• Associates with 1 year of related work experience; OR
• High School Diploma/GED with 2 years of related work experience

• 10+ years of experience in Software Quality Assurance.
• 5+ years of Test Automation experience.
• 3+ years of experience testing AI/ML or Generative AI solutions.
• Experience leading QA teams and enterprise testing programs.

AI Quality Engineering Leadership

• Define and implement enterprise-wide AI testing and quality assurance strategies.
• Establish testing standards, governance, and best practices for AI/ML and Generative AI applications.
• Lead QA activities across AI product lifecycle from development through production deployment.
• Drive AI-powered quality engineering transformation initiatives.

AI & Generative AI Testing

• Validate LLMs, Chatbots, Copilots, and GenAI applications.
• Develop test scenarios for:

1. Prompt validation
2. Hallucination detection
3. Bias and fairness testing
4. Security and privacy testing
5. Performance and scalability testing
6. Explainability validation

• Define AI model quality metrics and monitoring standards.
• Automation & Quality Engineering
• Design and implement automated testing frameworks.
• Integrate automated testing into CI/CD pipelines.
• Establish AI-assisted test generation and test optimization strategies.
• Drive shift-left and continuous testing practices.

Summary:

• Location: East Hanover, NJ
• Duration: 12 Months

Responsibilities:

• Conduct chemical and physical laboratory tests on solid materials, liquids, and gases.
• Analyze test data.
• Operate performance testing equipment and analytical instrumentation.
• Ensure proper maintenance, calibration, and repairs of equipment.
• Perform detailed ASTM, SAE, and FTM testing of raw materials, intermediates, production batches, and R&D/Technical Service samples.
• Conduct aviation-specific performance testing, viscometric testing, tribology testing, foam/emulsion testing, and grease testing.
• Characterize ultra-clean requirements using spectroscopic light scattering particle counters.
• Perform quantitative gravimetric Millipore filtration analysis.
• Utilize wet chemical titration methods including Karl Fisher, total acid/base number.
• Determine specific gravity, pour/flash/fire point, and electrical properties.
• Conduct analytical analysis using ICP, HPLC, GC, and FTIR.
• Perform routine control charting on critical tests and troubleshoot/communicate deviations or trends.
• Operate production laboratory to test inline packaged material and authorize line approvals for packaging manufactured products.
• Provide support to production for maintaining product quality and integrity.
• Maintain accurate, well-organized, and defensible documentation of all results using software such as SAP.
• Participate in both internal quality audits and external customer audits of laboratory performance.
• Perform PTHAs, JSAs, and support plant/department safety and 5S initiatives.

Requirements:

• BS in Sciences or AS with lab experience preferred.
• First shift: 8:00 am to 4:30 pm
• Second shift: 3:00 pm to 11:30 pm

Preferred Skills:

• Replacement Position

At Thorlabs, we design and manufacture components, instruments, and systems that transform the world by identifying, enabling, and accelerating key photonics (i.e., light-based) technologies. Backed by a dedicated workforce of more than 3,000 employees worldwide, Thorlabs contributes to cutting-edge research and real-world innovation.

Whether you're early in your career or bringing years of experience, you’ll find opportunities to grow, take ownership, and make meaningful contributions from day one. We know every employee brings unique talents and perspectives that fuel our success, and we seek driven individuals who are excited to make an impact in a fun, fast-moving culture.

 

This position effectively assures vendor & manufacturing compliance to Thorlabs ISO9001 quality standards protecting customers. Inspectors perform visual and dimensional inspection of precision parts and make quick, accurate pass/fail decisions on many types of optics including filters, mirrors, crystals, prisms, and lenses as well as mechanical components used in conjunction with optical components. Visual surface quality inspections are often performed under 100 watt bulb in low lit room. Although the location of the position is in Newton, NJ, from time to time it may be required to undertake duties at other Thorlabs locations.

Essential Job Functions include the following, but are not limited to:

• Introduction to visual and mechanical measurement of parts using metrology devices such as eye loupes, microscopes, calipers, micrometers, and indicators.

• Identify non-conformances through specified inspection methods.

• Ability to perform extremely detailed visual inspections on intricate and delicate parts occasionally performed under microscopes.

• Inspections are performed efficiently, with attention to detail.

• Low friction interface to peers/vendors/others in interaction with regards to inspection.

• Inspection of products against manufacturing prints.

• Handle and Clean Specialty Fiber Optics, Precision Optics, and mechanical components.

• Maintain proper records in our Manufacturing Database.

• Ask questions when instructions are not understood or clear.

• Comply with the company safety program and maintain a clean and organized work area.

In addition to the essential functions and duties listed above, all positions are also responsible for:

• Meeting company standards pertaining to quantity and quality of work performed on an ongoing basis, performing all work-related tasks in a manner that is in compliance with all Company policies and procedures.

• Adhering to Company policies, procedures, and directives regarding standards of workplace behavior in completing job duties and assignments.

The Company retains the right to change or assign other duties to this position.

Requirements

Physical Activities: Work may be active, could stand or sit for long durations and/or perform repetitious work at times. The employee may lift or move objects up to 20 pounds. Employees must grasp, manipulate, or assemble parts and components that are often very small. The noise level in the work environment is usually moderate, however, may be noisy at times. Must be able to wear appropriate clothing and personal protective equipment such as but not limited to masks, glasses, gloves, and specialty garments. The required PPE and training allow for the safe handling and processing of chemicals like adhesives, lubricants and solvents, and safe operation of job-related equipment and tools.

Qualifications

Experience:

• 1 year experience in a similar position preferred.

Education:

• High School Diploma or equivalent work experience.

Specialized Knowledge and Skills:

• Ability to learn, understand, and effectively apply sampling plans.

• Good verbal and written communication skills to operate in both individual and team environments.

• Capable of reading mechanical drawings and interpret dimensional tolerances.

• Adaptable to process and procedure changes.

• Ability to meet department standards for productivity and quality.

• Computer literacy using Microsoft product suite is desired.

• Must have the ability to cross train in all areas of the department, including but not limited to visual and dimensional inspection, data entry.

• High attention to detail.

The hourly rate for this position is $18.00 - $20.00 D.O.E.

Thorlabs values its diverse environment and is proud to be an Equal Employment Opportunity/Affirmative Action Employer. All qualified individuals will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age or veteran status. Job descriptions are not intended as and do not create employment contracts. The organization maintains its status as an at-will employer. Employees can be terminated for any reason not prohibited by law.

Benefits

Thorlabs offers a complete benefits package that includes medical, dental and vision insurance, company paid life insurance, a generous PTO package, a 401(k) plan, and tuition reimbursement just to name a few.

 

 

Must be available for 1st shift - 6:30am - 3pm plus overtime.

• Inspecting automotive parts to make sure they meet customer and company specifications.
• Performing initial, in-process, and final inspections of parts.
• Using measuring and inspection equipment to verify dimensions and quality.
• Identifying defective or nonconforming parts and determining whether they can be accepted or need correction.
• Performing audits of production processes and finished products.
• Checking incoming materials/parts before they enter production.
• Recording inspection results and maintaining quality documentation.
• Working with production employees and supervisors to correct quality problems.
• Following work instructions, company quality procedures, and automotive quality-system requirements.
• Helping identify the cause of defects and prevent them from recurring.
• Maintaining a strong focus on safety, accuracy, and customer requirements.

COM015

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Checking Quality of Parts Building 2 3rd shift

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.