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Remote Validation Engineer Jobs in Kansas (NOW HIRING)

Harris

Candidates must hold a current, valid passport and be legally eligible to travel. This includes ... Proven experience as a Software Engineer or similar role. * Proven proficiency in MSSQL and ...

Harris

Candidates must hold a current, valid passport and be legally eligible to travel. This includes ... Proven experience as a Software Engineer or similar role. * Proven proficiency in MSSQL and ...

Harris

This remote role welcomes candidates anywhere in Canada and the US ... Travel is required as needed, approximately 10%. Candidates must hold a current, valid passport and ...

Harris

This remote role welcomes candidates anywhere in Canada and the US ... Travel is required as needed, approximately 10%. Candidates must hold a current, valid passport and ...

NinjaOne

C++ Staff Software Engineer

Kansas, KS · On-site +1

... validate patches across Windows, macOS, and Linux. This means working close to the metal with ... Location - We are flexible on remote working from home, if you are located in the USA and reside in ...

Locatee AG

$125K - $165K/yr

Develop automated workflows to ingest, transform, and validate large volumes of structured and semi ... Flexible Work Environment Whether remote, hybrid, or in-office, we support work arrangements that ...

Locatee Ag

$125K - $165K/yr

Develop automated workflows to ingest, transform, and validate large volumes of structured and semi ... Flexible Work Environment Whether remote, hybrid, or in-office, we support work arrangements that ...

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How much do remote validation engineer jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for remote validation engineer in Kansas is $46.37, according to ZipRecruiter salary data. Most workers in this role earn between $35.14 and $56.39 per hour, depending on experience, location, and employer.

What is a remote validation engineer?

A Remote Validation Engineer is responsible for testing and verifying that products, systems, or software meet required specifications and function correctly. They develop test plans, run simulations, analyze data, and document results—all while working remotely. This role is common in industries like automotive, semiconductor, and software development, ensuring quality and compliance with standards. Strong technical skills, attention to detail, and proficiency with validation tools are essential.

What are the typical day-to-day responsibilities of a remote validation engineer?

Remote Validation Engineers are responsible for developing and executing test plans, analyzing results, and documenting findings to ensure products meet required standards and specifications. They often collaborate virtually with design, development, and quality teams to identify issues and recommend improvements. Daily tasks may include running automated tests, preparing validation reports, participating in team meetings, and troubleshooting system behaviors. Adapting to shifting project requirements and effectively communicating in a remote setting are also integral parts of the role.

What are the key skills and qualifications needed to thrive as a remote validation engineer, and why are they important?

To thrive as a Remote Validation Engineer, you need a strong background in engineering or computer science, expertise in validation protocols, and experience with testing methodologies. Familiarity with validation tools such as simulation software, automated test platforms, and knowledge of industry compliance standards (e.g., ISO, FDA, or automotive standards) is typically required, and certifications like ISTQB can be beneficial. Excellent problem-solving skills, attention to detail, and strong written and verbal communication are important for collaborating across distributed teams. These skills ensure the effectiveness and reliability of complex products or systems while supporting seamless teamwork in a remote work environment.

Are remote validation engineers in demand?

Remote validation engineers are in demand due to the increasing need for quality assurance and compliance in various industries, especially in technology and manufacturing. They often require skills in testing tools, automation, and industry standards, making remote work a viable option for qualified professionals.

Do remote validation engineers make good money?

Remote validation engineers typically earn competitive salaries that vary based on experience, location, and industry. They often require skills in testing, automation tools, and quality assurance, which can influence earning potential. Overall, the role can offer a solid income, especially with specialized skills and certifications.

What are the most commonly searched types of Validation Engineer jobs in Kansas?

The most popular types of Validation Engineer jobs in Kansas are:

What are popular job titles related to Remote Validation Engineer jobs in Kansas?

For Remote Validation Engineer jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Remote Validation Engineer jobs in Kansas look for?

The top searched job categories for Remote Validation Engineer jobs in Kansas are:

What cities in Kansas are hiring for Remote Validation Engineer jobs?

Cities in Kansas with the most Remote Validation Engineer job openings:

Remote Validation Engineer jobs near you
Infographic showing various Remote Validation Engineer job openings in Kansas as of August 2026, with employment types broken down into 6% Internship, 71% Full Time, and 23% Contract. Highlights an 100% Remote job distribution, with an average salary of $96,456 per year, or $46.4 per hour.

6500 - Lead CQV Engineer / Lead Validation Engineer

Verista, Inc.

Wichita, KS • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago

Job description

Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines & Values:
  • We empower and support our colleagues
  • We commit to client success at every turn
  • We have the courage to do the right thing
  • We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
  • We constantly acquire new skills and learn from our experiences to enhance our collective expertise

Senior Validation Engineer Responsibilities:
  • Lead and execute validation and qualification activities for facilities, utilities, manufacturing equipment, laboratory systems, and/or computerized systems within GxP-regulated environments.
  • Author, review, and approve validation deliverables, including URS, validation plans, risk assessments, protocols, test scripts, IQ/OQ/PQ documentation, deviations, traceability matrices, and validation/qualification summary reports.
  • Plan, coordinate, and perform hands-on validation execution, including protocol execution, field verification, system walkdowns, functional testing, punch-list management, and acceptance testing.
  • Serve as the validation technical lead for assigned projects, providing direction on validation strategy, scope, execution approach, documentation, and issue resolution.
  • Coordinate with Engineering, Quality, Operations, Automation, IT, vendors, and other stakeholders to ensure validation activities, project milestones, and deliverables are completed on schedule.
  • Review engineering and vendor documentation, including drawings, specifications, manuals, FAT/SAT documentation, and commissioning records, to establish validation requirements and execution strategies.
  • Lead the identification, investigation, and resolution of deviations, discrepancies, change controls, and validation-related issues.
  • Ensure validation documentation and execution activities comply with cGMP, GAMP 5, ASTM E2500, data integrity principles, Good Documentation Practices, and applicable regulatory requirements.
  • Track validation deliverables, project schedules, risks, action items, and dependencies; proactively communicate status and escalate issues that may impact project timelines or compliance.
  • Provide technical leadership, coaching, and mentoring to validation engineers and less experienced team members.
  • Support development and continuous improvement of validation procedures, templates, standards, and best practices.
  • Maintain strong working relationships with project stakeholders and provide clear communication regarding validation strategy, progress, risks, and execution status.

Job Requirements:
  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
  • 7+ years of validation/CQV experience within the pharmaceutical, biotechnology, medical device, or other regulated life sciences industries.
  • Demonstrated hands-on experience with both authoring and execution of validation and qualification deliverables.
  • Strong experience developing and executing IQ/OQ/PQ protocols, validation test scripts, commissioning documentation, and validation/qualification reports.
  • Experience leading validation activities across one or more of the following: manufacturing equipment, process equipment, facilities, utilities, laboratory systems, automation, or computerized systems.
  • Strong understanding of cGMP requirements, validation lifecycle principles, and risk-based validation approaches.
  • Experience managing deviations, change controls, punch lists, action items, and resolution of validation issues.
  • Demonstrated ability to independently manage multiple validation activities and deliverables while meeting project timelines.
  • Project Lead or Project Management experience, including responsibility for coordinating project teams, schedules, deliverables, resources, risks, and stakeholder communication.
  • Experience serving as a Validation Lead or CQV Lead on pharmaceutical or biotechnology capital projects.
  • Experience managing validation workstreams from planning and requirements development through execution and final closeout.
  • Strong knowledge of GAMP 5, ASTM E2500, risk-based qualification, data integrity/ALCOA+, and applicable FDA/EMA regulatory expectations.
  • Experience coordinating and managing third-party vendors, contractors, and cross-functional project teams.
  • Experience with project scheduling and tracking tools such as Microsoft Project, Smartsheet, Jira, or similar platforms.
  • This role is hybrid - on-site presence between Wichita, KS and Boston, MA may be required.

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
*Verista is an equal opportunity employer.
National (US) Range
$90,937-$136,225 USD
Benefits
Why Choose Verista?
  • High growth potential and fast-paced organization with a people-focused culture
  • Competitive pay plus performance-based incentive programs
  • Company-paid Life, Short-Term, and Long-Term Disability Insurance.
  • Medical, Dental & Vision insurances
  • FSA, DCARE, Commuter Benefits
  • Supplemental Life, Hospital, Critical Illness and Legal Insurance
  • Health Savings Account
  • 401(k) Retirement Plan (Employer Matching benefit)
  • Paid Time Off (Rollover Option) and Holidays
  • As Needed Sick Time
  • Tuition Reimbursement
  • Team Social Activities (We have fun!)
  • Employee Recognition
  • Employee Referral Program
  • Paid Parental Leave and Bereavement

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.
For more information about our company, please visit us at Verista.com

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