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Remote Qa Validation Jobs (NOW HIRING)

SmartIPlace

100% REMOTE QA Requirement

Irving, TX · Remote

$45 - $50/hr

... Validate data and reports using SQL and other tools (where needed) • Report QA metrics and testing status • Identify, document, and track issues found during testing • Coordinate with ...

Actifio

Senior QA Enginerer

Waltham, MA · Remote

You will also work with cross-functional teams work with developers, Product Managers and Remote QA teams to develop software tests which verify and exercise product requirements. The candidate must ...

Xometry

Quality Assurance Engineer

Gaithersburg, MD · Remote

$84K - $109K/yr

This person will work closely with Case Management, Partner Support, and remote Quality Engineering ... Strong Quality Assurance / Supplier Development experience * Effective communicator with data at ...

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Remote Qa Validation information

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How much do remote qa validation jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for remote qa validation in the United States is $56.31, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $70.43 per hour, depending on experience, location, and employer.

What is the difference between Remote Qa Validation vs Remote Software Tester?

AspectRemote Qa ValidationRemote Software Tester
Required CredentialsQA certifications, testing methodologiesTesting certifications, programming knowledge
Work EnvironmentCollaborative teams, testing labs, remoteDevelopment teams, remote or onsite
Industry UsageQuality assurance, software developmentSoftware development, quality assurance
Common Search IntentQA validation roles, remote QA jobsSoftware testing roles, remote testing jobs

Remote Qa Validation focuses on verifying that software meets quality standards through validation processes, often requiring specific QA certifications. Remote Software Testers primarily execute testing scripts and identify bugs, sometimes with programming skills. Both roles are integral to software quality but differ in scope and skill requirements.

What are the key skills and qualifications needed to thrive as a Remote QA Validation specialist, and why are they important?

To thrive as a Remote QA Validation specialist, you need a solid background in software testing principles, validation methodologies, and often a degree in computer science or a related field. Familiarity with test management tools like Jira, automation frameworks such as Selenium, and relevant certifications like ISTQB are typically required. Attention to detail, strong problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies ensure accurate validation of software products, efficient defect resolution, and clear collaboration across distributed teams.

What are Remote QA Validation jobs?

Remote QA Validation jobs involve testing and verifying the quality and functionality of software products or systems from a remote location. Professionals in these roles design and execute test cases, identify bugs or issues, and ensure that the software meets specified requirements and standards. Remote QA Validation specialists often use various tools to track defects, report results, and collaborate with development teams online. The goal is to maintain high-quality software releases while working independently or with distributed teams.

What are some common challenges faced by Remote QA Validation professionals, and how can they be overcome?

Remote QA Validation professionals often encounter challenges such as coordinating effectively with distributed teams, maintaining clear communication, and ensuring that all validation protocols are strictly followed without in-person oversight. To overcome these hurdles, it is important to utilize collaborative tools for documentation and communication, establish regular check-ins with team members, and leverage test management platforms to track progress. Clear documentation and proactive communication are key to ensuring validation processes run smoothly and compliance standards are met.
More about Remote Qa Validation jobs
What cities are hiring for Remote Qa Validation jobs? Cities with the most Remote Qa Validation job openings:
What are the most commonly searched types of Qa Validation jobs? The most popular types of Qa Validation jobs are:
What states have the most Remote Qa Validation jobs? States with the most job openings for Remote Qa Validation jobs include:
What job categories do people searching Remote Qa Validation jobs look for? The top searched job categories for Remote Qa Validation jobs are:
Remote Qa Validation jobs near you
Infographic showing various Remote Qa Validation job openings in the United States as of June 2026, with employment types broken down into 98% Full Time, 1% Part Time, and 1% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $117,123 per year, or $56.3 per hour.
Quality Assurance Validation Manager

Quality Assurance Validation Manager

Thermo Fisher Scientific

Teterboro, NJ • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 401 frontline employees who took The Breakroom Quiz

187th of 519 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Location: Ridgefield, New Jersey - Sterile Fill-Finish & Packaging Site
Our state-of-the-art sterile fill-finish and packaging facility in Ridgefield, NJ, is dedicated to meeting the growing needs of biotech and pharmaceutical drug developers. With expanded capabilities in pre-filled syringe and liquid vial manufacturing, the site increases U.S. capacity to manufacture the medicines patients rely on every day.
As part of Thermo Fisher Scientific's global network, Ridgefield complements our world-class contract development and manufacturing services and strengthens our sterile fill-finish footprint-now spanning seven sites worldwide, including three in the U.S. (Greenville, NC; Plainville, MA; and Ridgefield, NJ). Strategically located along the East Coast to streamline logistics and attract top talent, the 360,000 sq. ft. Ridgefield site plays a vital role in the global pharmaceutical supply chain, with products distributed to more than 67 countries across all continents.
Join Thermo Fisher Scientific and play a critical role in supporting the delivery of life-changing therapies and products to patients worldwide. As a Quality Assurance Validation Manager, you will lead validation activities that ensure product quality, operational excellence, and compliance with global regulatory requirements. Working in a highly collaborative environment, you will partner with Quality Assurance, Manufacturing, Engineering, Regulatory Affairs, and other cross-functional teams to maintain the validated state of systems and processes that support the manufacture of therapeutics and other critical products.
You'll have the opportunity to influence validation strategy, lead complex projects, and develop a high-performing team while contributing to a culture of quality, continuous improvement, and innovation.
Discover Impactful Work:
As a Quality Assurance Validation Manager, you will provide leadership and oversight for validation programs across equipment, utilities, facilities, computer systems, cleaning processes, analytical instruments, and manufacturing operations. You will ensure validation activities are executed in accordance with cGMP requirements, quality standards, and industry best practices while supporting business objectives, new product introductions, and technology transfer initiatives. In partnership with Quality Assurance and cross-functional teams, you will help maintain compliance and the validated state of critical systems and processes that support the manufacture of therapeutics and other life-changing products.
A Day in the Life:
  • Lead and manage validation activities across manufacturing, laboratory, utility, facility, computerized systems, and analytical instruments
  • Develop and maintain validation strategies, validation master plans, and project timelines
  • Oversee the planning, coordination, execution, review, and approval of validation protocols and reports
  • Partner with project managers and cross-functional stakeholders to establish priorities, monitor progress, and communicate project status
  • Ensure validation activities comply with FDA, EU, and applicable global regulatory requirements and Quality Assurance standards
  • Support equipment qualification, process validation, cleaning validation, utility qualification, computer system validation, and analytical instrument qualification programs
  • Apply risk assessment methodologies and statistical tools to support validation decisions
  • Drive continuous improvement initiatives to enhance validation processes and operational efficiency
  • Manage change control activities and assess validation impacts associated with process or system changes
  • Ensure adherence to data integrity requirements and governance standards across validation activities
  • Support regulatory inspections, customer audits, and quality assessments
  • Mentor, develop, and lead validation professionals while fostering a culture of accountability and excellence

Keys to Success:
Education
  • Advanced Degree with 8+ years of validation experience, or
  • Bachelor's Degree with 10+ years of validation experience
  • Preferred fields of study include Engineering, Chemistry, Biology, Life Sciences, or related technical disciplines

Experience
  • Significant experience in validation within pharmaceutical, biotechnology, medical device, or other regulated manufacturing environments
  • Experience coordinating, planning, executing, and approving validation activities across multiple disciplines
  • Demonstrated success managing complex validation projects, programs, and teams
  • Experience partnering with project managers to establish priorities and drive project execution
  • Experience participating in regulatory inspections and customer audits
  • Experience with validation master planning, change control systems, and quality management systems
  • Expertise in process validation and analytical instrument qualification
  • Proficiency in data integrity compliance, governance, and regulatory expectations related to data lifecycle management

Knowledge, Skills, Abilities
  • Strong knowledge of cGMP regulations, including FDA, EU, and global regulatory requirements
  • Expertise in equipment qualification, process validation, cleaning validation, computer system validation, utility qualification, and analytical instrument qualification
  • Strong understanding of ALCOA+ principles, data integrity requirements, and data governance practices
  • Proficiency in risk assessment methodologies and statistical analysis
  • Strong technical writing, documentation, and report review capabilities
  • Excellent leadership, communication, and interpersonal skills
  • Ability to influence stakeholders and collaborate effectively across functions and organizational levels
  • Knowledge of Lean Manufacturing and continuous improvement methodologies
  • Proficiency with Microsoft Office and standard business software applications
  • Strong organizational and problem-solving skills with the ability to manage multiple priorities

Relocation assistance is not provided
Must be legally authorized to work in the United States now or in the future without sponsorship
Must be able to pass a comprehensive background check, which includes a drug screening
Compensation and Benefits
The salary range estimated for this position based in New Jersey is $112,500.00-$168,750.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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