Science,Science|Quality Assurance Scientist,Science|Quality Control Scientist,Administration,Administration|Data Entry Jobs

Libra Solutions helps simplify and ease the burden of legal processes for plaintiffs, heirs, and the attorneys and doctors who serve them. By combining financial strength with technology-driven innovation, we simplify difficult legal processes, reduce delays, and help people access both money and the care they need, when they need it most. Our companies are leaders in their industries! MoveDocs streamlines the coordination of medical, financial, and professional services for personal injury cases—improving efficiency for attorneys, care providers, and their clients. Oasis Financial is the largest and most recognized plaintiff funding brand in the nation, having helped 400,000+ plaintiffs access more than $2 billion in funding while their personal injury cases progress. And through Probate Advance, we enable heirs to access their inheritance without waiting through the lengthy probate process.

Together, under the Libra Solutions banner, we support a nationwide network of more than 45,000 attorneys and 10,000 healthcare providers – creating a powerful platform to deliver faster, more seamless outcomes for our customers.

The Quality Control Analyst is responsible for conducting independent quality control reviews of company accounts to evaluate the accuracy, completeness, and adherence of underwriting and operational activities to established policies, procedures, and documentation standards

The Quality Control Analyst performs detailed QC audits, documents findings and exceptions, identifies potential errors or process gaps, and escalates findings requiring additional review to Quality Control management. The role supports the overall effectiveness of the Quality Control program by providing accurate, consistent, and well-documented audit results.

This is an in-person position that can be based out of one of our offices located in Denver, CO, Las Vegas, NV, Rosemont, IL or Charlotte, NC.

Responsibilities:             

• Perform detailed quality control audits of company accounts using established QC procedures, review criteria, and audit tools.
• Review underwriting decisions, due diligence, account documentation, case information, agreements, payment terms, and other relevant account data for accuracy, completeness, and adherence to established requirements.
• Clearly document audit results, findings, exceptions, and supporting information in designated QC tools and records.
• Apply QC standards consistently and exercise sound judgment when evaluating potential errors, discrepancies, or exceptions.
• Escalate significant, unusual, or unclear findings to QC management for review and determination.
• Support the identification of recurring errors, trends, process gaps, and potential areas of risk through observations identified during QC reviews.
• Participate in discussions with QC management and business partners to clarify findings and promote consistent application of policies and procedures.
• Assist with the development and refinement of QC procedures, checklists, audit tools, and reviewer resources.
• Support validation or follow-up reviews when additional review of audit findings is required.
• Maintain organized and accurate QC documentation in accordance with established recordkeeping practices.
• Participate in system, process, or procedural changes by providing feedback from a QC and reviewer perspective.
• Serve as a resource to other QC reviewers and assist with reviewer consistency and knowledge sharing, as needed.
• Complete assigned QC reviews within established timelines while maintaining accuracy and thoroughness.

Requirements

• Bachelor’s degree in Business, Finance, or a related field, or equivalent relevant experience preferred.
• 3+ years of experience in underwriting, quality control, auditing, operations, or a related function within consumer funding, healthcare, legal, insurance, or a similar industry.
• Strong understanding of underwriting, due diligence, documentation, and operational processes.
• Knowledge of applicable privacy, documentation, and compliance requirements.
• Strong attention to detail with the ability to identify discrepancies and evaluate information across multiple documents and systems.
• Strong analytical, critical-thinking, and problem-solving skills.
• Ability to apply established standards consistently while exercising appropriate judgment when unusual circumstances arise.
• Strong organizational and prioritization skills with the ability to manage assigned reviews and meet established deadlines.
• Strong written and verbal communication skills, including the ability to clearly document and explain QC findings.
• Experience working with case management, document management, or similar operational systems.
• Proficiency in Microsoft Excel and other reporting or data-analysis tools.
• Prior experience performing quality control reviews or audits is preferred.

Benefits

We believe taking great care of our customers starts with taking great care of our people. That’s why we offer competitive compensation and a comprehensive benefits package, including a choice of multiple medical plans, dental, vision, and life insurance, a 401(k) with generous company match, flexible spending accounts for medical and dependent expenses, and time off to recharge.

Job Description:
The Quality Control Analyst I is an entry level laboratory role responsible for performing routine testing and sampling to support QC operations. The role focuses on developing foundational technical skills while ensuring all activities comply with cGMPs, SOPs, and data integrity principles.
Responsibilities:
Primary Responsibilities:

• Perform routine testing and sampling (EM, utilities, raw materials, in process, finished goods).
• Document, review, and report data accurately per GDP and ALCOA+.
• Execute assigned testing and support activities within defined timelines.
• Support lab operations: housekeeping, inventory, basic equipment care.
• Identify and escalate deviations, atypical results, or compliance concerns.

Secondary Responsibilities:

• Assist with sample coordination and shipments to external labs.
• Support SOP revisions and documentation updates.
• Participate in training to build proficiency across assays.
• Support validation or innovation projects as assigned.

Lab Time Expectations:

• ~80 90% laboratory-based work.
• Majority of time spent performing routine testing and sampling activities.
• Limited non lab responsibilities (mainly documentation and training).

Key Competencies:

• Foundational laboratory skills and aseptic technique.
• Strong attention to detail and data integrity awareness.
• Basic prioritization and time management (with guidance).
• Clear written and verbal communication.
• Ability to follow procedures and learn new techniques.

Requirements:

• Required: High School Diploma.
• Preferred: Bachelor's Degree in a Scientific Discipline.
• Entry Level 0 to 4 years.
• Laboratory experience and basic cGMP exposure.

Job Description: The QC Environmental Monitoring Analyst supports cleanroom operations by performing routine environmental monitoring, microbiological testing, documentation, and lab maintenance. This role ensures compliance with GMP standards and supports investigations related to environmental excursions.
Roles & Responsibilities:

• Perform environmental monitoring in cleanrooms (At Rest & In Operation).
• Conduct microbiological tests for media, raw materials, and product release.
• Perform microbial isolations and identifications.
• Support environmental investigations and write excursion/deviation reports.
• Maintain lab equipment, supplies, and general lab upkeep.
• Prepare data summaries, trend reports, and documentation.
• Write and revise SOPs and qualification reports.
• Maintain training compliance and assist in training new analysts.

Requirements:

• BS degree preferred (Microbiology, Biology, Biotechnology, or related field).
• Degree not required if candidate has relevant experience.
• 1 3 years' experience in environmental monitoring or microbiology.
• Experience in GMP/cleanroom environments preferred.

Additional Requirements:

• 100% on site role.
• Work hours: 7/8 AM 5 PM (flexibility required).
• Gowning training provided.
• Ability to lift up to 50 lbs.
• Must be comfortable using stairs, ladders, and step stools .

Job Description: The QC Environmental Monitoring Analyst supports cleanroom operations by performing routine environmental monitoring, microbiological testing, documentation, and lab maintenance. This role ensures compliance with GMP standards and supports investigations related to environmental excursions.
Roles & Responsibilities:

• Perform environmental monitoring in cleanrooms (At Rest & In Operation).
• Conduct microbiological tests for media, raw materials, and product release.
• Perform microbial isolations and identifications.
• Support environmental investigations and write excursion/deviation reports.
• Maintain lab equipment, supplies, and general lab upkeep.
• Prepare data summaries, trend reports, and documentation.
• Write and revise SOPs and qualification reports.
• Maintain training compliance and assist in training new analysts.

Requirements:

• BS degree preferred (Microbiology, Biology, Biotechnology, or related field).
• Degree not required if candidate has relevant experience.
• 1 3 years' experience in environmental monitoring or microbiology.
• Experience in GMP/cleanroom environments preferred.

Additional Requirements:

• 100% on site role.
• Work hours: 7/8 AM 5 PM (flexibility required).
• Gowning training provided.
• Ability to lift up to 50 lbs.
• Must be comfortable using stairs, ladders, and step stools .

Provides business and technical expertise to help design and develop analytics processes, tools, dashboards and applications for a business function or business unit. Applies advanced consulting skills and/or extensive technical expertise; full industry knowledge. Develops innovative solutions to complex problems. Works without considerable direction; mentors and may supervise team members

Key Responsibilities

Develop detailed test plans and test scripts for CLM modules, workflows, templates, permissions, and integrations. Execute functional, regression, integration, and user acceptance test scenarios aligned with program milestones. Validate system outputs, including clauses, contract metadata, templates, approval routing, and workflow behavior, against business requirements. Coordinate defect logging, triage, and retesting with functional SMEs, developers, and system integrators. Validate data flowing into and out of CLM, ensuring alignment with mapping rules and upstream or downstream systems. Conduct testing across multiple environments, including SIT, UAT, and Pre Prod, and support readiness for go live cutover. Maintain test evidence, documentation, and audit ready artifacts consistent with Keystone QA and compliance standards.

Due to the nature of work performed within this facility, U.S. citizenship is required.

Qualifications

· 3+ years of experience in QA or testing supporting enterprise SaaS implementations

· 3+ years of experience testing complex COTS products in an enterprise setting

· 3+ years of experience creating clear defect reports and partnering with cross functional teams to drive resolution

· Experience with Jira and Zephyr for test execution and defect tracking

· Experience using tools such as Playwright or Selenium for test automation, including designing or supporting automated regression scripts

· Experience executing SIT and UAT cycles and validating requirements traceability

· Bachelor's degree

Job Title: Quality Control Analyst I
Location: Ridgefield, NJ
Duration: 24 months

Job Description:
How you will make an impact:
The Quality Control Analyst I is responsible to perform environmental monitoring (EM) of aseptic manufacturing operations in Grade A, B, C and D clean room environments and other classified areas as required.

What you will do:
Perform daily Viable and Non-viable EM in production facility.
Assist with manufacturing operations during periods of inactivity as required.
Perform product sampling, EM, or other related activities as directed.
Maintain batch record documentation and logs as required by corporation and regulatory agencies.
Maintain all associated documentation for EM and operations being performed.
Follow ALCOA principals with right first time, legible and contemporaneous entries.
Perform cleaning and sanitizing of EM equipment.
Maintain supply/stock of required materials for EM operations.
Prepare plates daily required for EM operations.
Assist in process and system validation activities as required.
Serve as witness to routine unit operational tasks for batch record signing.
Review and revision of EM standard operating procedures (SOPs) and batch production records (BPRs).
Author and assist with out-of-specification and non-conformance EM investigations.

JOB TITLE: Senior QA Analyst
JOB TYPE: Contract
LOCATION: Norristown, PA (Hybrid, 2 days onsite per week)
START DATE: November/December 2026
SHIFT: Monday–Friday, First Shift
 
We are seeking a Senior QA Analyst to support the quality and reliability of complex software applications. This hands-on role focuses on software testing, database validation, test automation, and data management throughout the development lifecycle. The ideal candidate will bring extensive technical QA experience and work closely with development teams and business stakeholders to deliver high-quality software solutions.

Responsibilities

• Develop and execute testing strategies covering functional, integration, system, regression, acceptance, and non-functional testing.
• Analyze business requirements, application architecture, and data flows to design comprehensive test cases, including boundary conditions and error scenarios.
• Perform manual and automated testing of complex applications, identifying defects and verifying functionality against established requirements.
• Validate Oracle database functionality, including views, stored procedures, functions, and data migration processes, while maintaining consistency across testing environments.
• Develop and manage test data sets, including extracting and modifying production data to support realistic testing scenarios.
• Create and maintain scripts for database setup, test data preparation, file generation, and environment cleanup.
• Write SQL queries and develop methods to compare expected and actual results across databases, application interfaces, and external data sources.
• Monitor testing progress, evaluate completion criteria, adjust testing activities, and provide status updates to project teams and business stakeholders.
• Collaborate with developers, project managers, and business users to support acceptance testing and ensure compliance with established testing standards.

Qualifications

• 7+ years of professional QA or software testing experience, including hands-on testing of complex technical applications.
• Professional experience working with Salesforce.
• Proficiency with Oracle databases and SQL, including database queries, data validation, and testing stored procedures, functions, and views.
• Extensive experience with test planning, test case development, functional testing, integration testing, regression testing, and user acceptance testing.
• Experience using automated testing tools such as SOAPUI, Tricentis Tosca, or scriptless automation platforms.
• Scripting experience and hands-on involvement in test data preparation, management, and database cleanup.
• Experience with Agile Scrum methodologies and test-driven development (TDD) or behavior-driven development (BDD).
• Familiarity with Atlassian tools, including Confluence.
• Experience applying user-centered design principles and conducting usability testing.
• Experience supporting large development teams and projects involving multiple business owners, including communicating testing results to business leadership and stakeholders.

EOE STATEMENT:
We are an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law.

PSR Associates is a consulting and talent solutions firm that connects qualified IT professionals with great opportunities. Whether you're looking for a contract or permanent position, we can help you find the right fit for your skills and experience. We have a team of experienced recruiters who know the IT industry inside and out, and we work with you every step of the way to ensure a smooth and successful transition. PSR Connecting Talent, Crafting Success.

Quality Assurance Analyst Position Description

We are looking for a motivated Quality Assurance Analyst ready to take us to the next level! If you have 5+ years in software quality assurance, 5+ years of creating test cases, test scripts, and acceptance criteria, and are looking for your next career move, apply now.
The selected candidate will work a hybrid schedule consisting of three (3) days each week onsite in Trenton, NJ and two (2) days each week remotely.

Summary:
We are looking for a Quality Assurance Tester to ensure software systems meet functional, non-functional, business, and technical requirements.
What You'll Do:

• Review project requirements, specifications, and business expectations to develop comprehensive testing plans
• Create functional and non-functional test cases, test scripts, and acceptance criteria
• Execute test cases under varying conditions to validate system functionality, performance, and reliability
• Document, evaluate, and communicate testing results to stakeholders
• Detect, log, track, and report software defects and program bugs
• Troubleshoot issues and collaborate with development teams to resolve defects
• Create testing procedures, user guidance, and training materials to support application quality initiatives
• Identify, recommend, and implement appropriate testing methodologies and quality assurance strategies
• Participate in Agile development processes, including sprint planning, reviews, and testing activities
• Collaborate with project team members regarding application development, customer issues, and security requirements
• Support testing efforts for systems containing K-12 education data
• Assist with validation and quality assurance activities involving Snowflake, Salesforce, Tableau, and automated testing solutions when applicable

What You'll Need:
Required:

• Bachelor's degree or higher from an accredited college or university in a related technical field
• 5+ years of experience in software quality assurance and testing
• 5+ years of experience creating test cases, test scripts, and acceptance criteria
• 5+ years of experience executing test cases under varying circumstances
• 5+ years of experience documenting and evaluating test results
• 5+ years of experience detecting, logging, and reporting software defects and program bugs
• 5+ years of experience tracking defects and troubleshooting errors
• 5+ years of experience creating test procedures and training materials
• Experience working in Agile development environments
• Strong analytical, problem-solving, and communication skills
• Experience collaborating with cross-functional project teams

Preferred:

• 3+ years of experience working with K-12 education data
• 3+ years of experience using Snowflake, Salesforce, and Tableau
• 3+ years of experience with automation testing tools and methodologies
• Experience supporting large-scale government or public-sector technology initiatives

Physical Demands:

• Ability to safely and successfully perform the essential job functions consistent with the ADA and other federal, state, and local standards
• Sedentary work that involves sitting or remaining stationary most of the time with occasional need to move around the office to attend meetings and collaborate with team members
• Ability to conduct repetitive tasks on a computer, utilizing a mouse, keyboard, and monitor

*** Please note that any false information on your resume or application could lead to the offer being withdrawn or even termination after hire.***

Title: Quality Assurance Analyst
Location: Trenton, NJ – Hybrid Role (3 days Onsite, 2 days Remote)
Duration: 12 months

Note: Only candidates with work authorization that do not require sponsorship now or in the future will be considered.

Job Summary
5+ years of experience in software quality assurance and testing
5+ years of experience creating test cases, test scripts, and acceptance criteria
5+ years of experience executing test cases under varying circumstances
5+ years of experience documenting and evaluating test results
5+ years of experience detecting, logging, and reporting software defects and program bugs
5+ years of experience tracking defects and troubleshooting errors
5+ years of experience creating test procedures and training materials

Job Description
We are looking for a motivated Quality Assurance Analyst ready to take us to the next level! If you have 5+ years in software quality assurance, 5+ years of creating test cases, test scripts, and acceptance criteria, and are looking for your next career move, apply now. We are looking for a Quality Assurance Tester to ensure software systems meet functional, non-functional, business, and technical requirements.

Job Description
What You'll Do
Review project requirements, specifications, and business expectations to develop comprehensive testing plans
Create functional and non-functional test cases, test scripts, and acceptance criteria
Execute test cases under varying conditions to validate system functionality, performance, and reliability
Document, evaluate, and communicate testing results to stakeholders
Detect, log, track, and report software defects and program bugs
Troubleshoot issues and collaborate with development teams to resolve defects
Create testing procedures, user guidance, and training materials to support application quality initiatives
Identify, recommend, and implement appropriate testing methodologies and quality assurance strategies
Participate in Agile development processes, including sprint planning, reviews, and testing activities
Collaborate with project team members regarding application development, customer issues, and security requirements
Support testing efforts for systems containing K-12 education data
Assist with validation and quality assurance activities involving Snowflake, Salesforce, Tableau, and automated testing solutions when applicable

What You'll Need
Required:
Bachelor's degree or higher from an accredited college or university in a related technical field
5+ years of experience in software quality assurance and testing
5+ years of experience creating test cases, test scripts, and acceptance criteria
5+ years of experience executing test cases under varying circumstances
5+ years of experience documenting and evaluating test results
5+ years of experience detecting, logging, and reporting software defects and program bugs
5+ years of experience tracking defects and troubleshooting errors
5+ years of experience creating test procedures and training materials
Experience working in Agile development environments
Strong analytical, problem-solving, and communication skills
Experience collaborating with cross-functional project teams

Preferred:
3+ years of experience working with K-12 education data
3+ years of experience using Snowflake, Salesforce, and Tableau
3+ years of experience with automation testing tools and methodologies
Experience supporting large-scale government or public-sector technology initiatives

Immediate need for a talented Quality Control Analyst (QC Analyst). This is a 12+ Months Contract opportunity with long-term potential and is located in Fredrick, MD (Hybrid). Please review the job description below and contact me ASAP if you are interested.

Job ID:(phone number removed)

Pay Range: $28 - $30/hour. Traveler benefits as per agency package. (Benefits vary by vendor and assignment.)
 
Key Responsibilities:

• Perform QC analytical testing of raw materials, intermediates, drug substances, and final drug products according to approved analytical methods and SOPs.
• Perform laboratory assays including Flow Cytometry, ELISA, qPCR/PCR, cell-based bioassays, and other applicable biopharmaceutical analytical methods.
• Review and trend laboratory data and complete routine review of test results and supporting documentation.
• Support in-process testing and drug substance/drug product release activities.
• Provide testing information and analytical data to support Certificate of Analysis (CoA) generation.
• Maintain laboratory instruments and equipment, including calibration, routine maintenance, and troubleshooting activities.
• Work with internal and external resources to maintain the laboratory in an optimal, compliant, and inspection-ready condition.
• Author, revise, and maintain SOPs, qualification/validation protocols, reports, and other controlled documents.
• Support laboratory investigations associated with Out-of-Specification (OOS) results.
• Participate in deviation investigations and assist with root-cause analysis related to analytical procedures.
• Ensure accurate and timely documentation of laboratory activities in accordance with GMP and data integrity requirements.
• Monitor applicable GMP quality systems and ensure compliance with established procedures and policies.
• Support review of proposed changes to laboratory systems, procedures, analytical methods, and related regulatory documentation.
• Gather and analyze laboratory metrics to support continuous improvement.
• Communicate testing status, laboratory activities, issues, and priorities during daily and weekly meetings.
• Collaborate effectively with Quality, Manufacturing, Analytical, Scientific, and Technical teams.
• Perform other QC laboratory duties as assigned.

Key Requirements and Technology Experience:

• Bachelor's degree in Biology, Biochemistry, Chemistry, Biotechnology, Microbiology, or a related scientific field; OR
• Associate's degree + 2 years of experience in biotechnology or a related field with Quality Control experience; OR
• High School Diploma/GED + 3 years of experience in biotechnology or a related field with Quality Control experience.
• Experience working in a biotechnology, biopharmaceutical, pharmaceutical, or biologics laboratory.
• Hands-on experience in a GMP Quality Control environment.
• Strong understanding of GMP, SOPs, laboratory quality systems, and QC processes.
• Experience with OOS investigations, deviations, root-cause analysis, and investigation documentation.
• Hands-on experience with one or more of the following:
• Flow Cytometry / FACS
• ELISA
• qPCR / PCR
• Cell-based assays
• Bioassays
• Other analytical methods used for biopharmaceutical testing
• Working knowledge of 21 CFR Part 11, 21 CFR Part 210, and 21 CFR Part 211.
• Experience with laboratory instrument calibration, maintenance, and troubleshooting.
• Experience writing or revising SOPs, protocols, validation/qualification documents, and technical reports.
• Strong understanding of laboratory documentation and data integrity requirements.
• Proficiency with Microsoft Word, Excel, PowerPoint, and other standard laboratory applications.
• Strong written and verbal communication skills.
• Ability to work independently while collaborating effectively with scientific and technical personnel.
• Strong attention to detail and ability to work effectively in a fast-paced, regulated environment.

 
Our client is a leading Pharmaceutical Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
 
Pyramid Consulting, Inc. 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.

By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

#St

Job Description: The QC Environmental Monitoring Analyst supports cleanroom operations by performing routine environmental monitoring, microbiological testing, documentation, and lab maintenance. This role ensures compliance with GMP standards and supports investigations related to environmental excursions.
Roles & Responsibilities:

• Perform environmental monitoring in cleanrooms (At Rest & In Operation).
• Conduct microbiological tests for media, raw materials, and product release.
• Perform microbial isolations and identifications.
• Support environmental investigations and write excursion/deviation reports.
• Maintain lab equipment, supplies, and general lab upkeep.
• Prepare data summaries, trend reports, and documentation.
• Write and revise SOPs and qualification reports.
• Maintain training compliance and assist in training new analysts.

Requirements:

• BS degree preferred (Microbiology, Biology, Biotechnology, or related field).
• Degree not required if candidate has relevant experience.
• 1 3 years' experience in environmental monitoring or microbiology.
• Experience in GMP/cleanroom environments preferred.

Additional Requirements:

• 100% on site role.
• Work hours: 7/8 AM 5 PM (flexibility required).
• Gowning training provided.
• Ability to lift up to 50 lbs.
• Must be comfortable using stairs, ladders, and step stools .