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Computer System Validation Remote Jobs in Columbus, OH

Supports computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc), ERP ...

Supports computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc), ERP ...

Supports computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information management), analytical lab instruments (e.g., HPLC, UHPLC, PCR instruments, plate readers etc), ERP ...

They provide support to resolve system issues within Service Level Agreements. Duties ... Remote roles will also have the opportunity to come together in our offices for moments that matter.

They provide support to resolve system issues within Service Level Agreements. Duties ... Remote roles will also have the opportunity to come together in our offices for moments that matter.

They provide support to resolve system issues within Service Level Agreements. Duties ... Remote roles will also have the opportunity to come together in our offices for moments that matter.

They provide support to resolve system issues within Service Level Agreements. Duties ... Remote roles will also have the opportunity to come together in our offices for moments that matter.

This position is remote and requires an active Secret clearance or higher. Maximus TCS (Technology ... and system validation - Develop test documentation and procedures supporting verification ...

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Computer System Validation Remote information

See Columbus, OH salary details

$10

$52

$83

How much do computer system validation remote jobs pay per hour?

As of May 29, 2026, the average hourly pay for computer system validation remote in Columbus, OH is $52.47, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $62.21 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Computer System Validation (CSV) professional working remotely, and why are they important?

To excel as a Computer System Validation Remote professional, you need a solid understanding of regulatory compliance (such as FDA 21 CFR Part 11), risk management, and validation lifecycle processes, often supported by a degree in computer science, engineering, or a related field. Familiarity with validation software, quality management systems (QMS), and documentation tools is typically required, along with certifications like GAMP or Six Sigma being advantageous. Strong attention to detail, analytical thinking, and effective remote communication are crucial soft skills for this role. These competencies ensure validated systems meet compliance standards, minimize risks, and support seamless collaboration in a regulated, distributed environment.

What are some common challenges faced by Computer System Validation professionals working remotely, and how can they be addressed?

Remote Computer System Validation (CSV) professionals often encounter challenges such as coordinating validation activities across distributed teams and ensuring secure access to sensitive documentation. Effective communication and use of collaborative tools are crucial for managing documentation reviews, test execution, and issue resolution. Establishing clear validation protocols and regular virtual check-ins with cross-functional teams can help maintain compliance and project momentum. Additionally, leveraging secure cloud-based validation platforms can streamline approvals and maintain data integrity while working remotely.

What is computer system validation (CSV) in a remote job context?

Computer system validation (CSV) is a process used to ensure that IT systems and software used in regulated industries (such as pharmaceuticals or healthcare) work as intended and comply with relevant regulations. In a remote job context, CSV professionals perform validation tasks, documentation, and system testing from an offsite location, often collaborating with teams via digital tools. This remote work typically involves reviewing validation protocols, writing reports, and ensuring compliance with standards like FDA 21 CFR Part 11, all while leveraging secure online platforms to communicate and manage documentation.

What is the difference between Computer System Validation Remote vs Computer System Validation on-site?

AspectComputer System Validation RemoteComputer System Validation on-site
Work EnvironmentPerforms validation tasks remotely, often from home or a different location from the client site.Works directly at the client or company site, conducting validation activities in person.
Required CredentialsTypically requires certifications like GxP, 21 CFR Part 11, and validation experience, applicable in both settings.Same certifications as remote roles, with additional familiarity with on-site equipment and facilities.
Industry UsageCommon in industries like pharmaceuticals and biotech where remote oversight is feasible.Traditional in regulated industries requiring on-site validation activities.

Both roles require similar certifications and industry knowledge, but the main difference lies in the work environment—remote versus on-site. Remote validation offers flexibility, while on-site validation involves direct interaction at the facility.

What are popular job titles related to Computer System Validation Remote jobs in Columbus, OH? For Computer System Validation Remote jobs in Columbus, OH, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Remote jobs in Columbus, OH look for? The top searched job categories for Computer System Validation Remote jobs in Columbus, OH are:
What cities near Columbus, OH are hiring for Computer System Validation Remote jobs? Cities near Columbus, OH with the most Computer System Validation Remote job openings:
Validation Engineer, CSV Biopharma (JP12934-R)

Validation Engineer, CSV Biopharma (JP12934-R)

3 Key Consulting

New Albany, OH

$35 - $40/hr

Other

Posted 16 days ago


Job description

Job Title:Validation Engineer, CSV Biopharma (JP12934-R)
Location: New Albany, OH. 43054
Business Unit: Ops Digital Technology Innovation
Employment Type: Contract
Duration: 6+ months with likely extension
Rate: $35-40/Hr with benefits
Posting Date:3/18/2025
Notes: Onsite New Albany, OH - must be local. Standard hours.
3 Key Consulting is hiring! We are recruiting a Validation Engineer for a consulting engagement with our direct client, a leading global biotechnology company.
Job Description:
Primarily responsible for ensuring adherence to computer validation standards and procedures for computer related systems. Responsibilities include participation in system design, preparation of test protocols, analysis of test results and preparation of summaries. Provides guidance and sets standards in producing quality documentation, serves as the liaison between the IS and Quality functions, provides testing and IT compliance guidance, and provides timely and effective response and follow-through in the resolution of IT Quality/Project compliance issues.
This role is for a strong background in IT Business systems validation, IT Automation systems validation, ensuring that our Information technology systems and processes meet regulatory requirements and industry standards, particularly within the framework of GxP (Good manufacturing Practice) in projects. Integrates a variety of systems technologies to provide systems related solutions to meet business needs. Supports the creation and maintenance of client's Ohio computer systems validation.
Top Must Have Skill Sets:
  • Experience with testing tools (ALM, or Kneat or ValGenesis).
  • Experience with ServiceNow (Change Module), Track wise (CAPA, Deviations, Change), Veeva document management, CAPA, Deviations, Change Management.
  • Knowledge of cGMP regulations and guidelines including but not limited to U.S. code of Federal Regulations 21 CFR Part 11 and Part 211.
  • Understanding of industry standards and best practices for computer system validation such as GAMP 5.
  • Must have experience with deviations
  • IT infrastructure tools is highly preferred but not required (example: backup and restore, disaster recovery)

Day to Day Responsibilities:
  • Perform Deviations, CAPA, Change records for DTI computer systems (E.g: MES, SCADA, ASRS, ServiceNow, QBAS, SAP/ERP, Serialization, etc).
  • Provide support to system owners on completing Design Spec, URS, Traceability, IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification) draft copies.
  • Provide support on completion of validation deliverables as required per the project.
  • Develop and execute test scripts in ALM, Kneat test tools to support system owners/IT Application Owners.
  • Ensure and track computer systems periodic reviews and periodic access reviews are completed as per schedule to maintain system maintenance phase.
  • Ensures that systems are maintained in a compliant manner according to the DTI quality systems standards.
  • Support regulatory inspections and internal audits as required.

Basic Qualifications:
  • Master degree OR Bachelor degree in Engineering and 2 years of experience OR Associate degree and 6 years of experience OR High school diploma / GED and 8 years of experience
  • 2. 5+ years relevant experience in computer system validation (E.g: MES, SCADA, Building Management system (BMS, QBAS), Serialization, QC systems).
  • Experience with ALM or Kneat testing tool is plus.
  • 2. Experience with ServiceNow, Track wise (CAPA, Deviations), Veeva document management, CAPA, Deviations, Change Management.
  • 3. Knowledge of cGMP regulations and guidelines including but not limited to U.S. code of Federal Regulations 21 CFR Part 11 and Part 211.
  • 4. Understanding of industry standards and best practices for computer system validation such as GAMP 5.

Why is the Position Open?
Supplement additional workload on team.
Red Flags:
  • cannot support onsite operations
  • Overly long or irrelevant resume
  • Exaggerated or vague job titles and responsibilities
  • Lack of achievements or quantifiable results

Interview Process:
WebEx or onsite.
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.