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Computer System Validation Remote Jobs in Hayward, CA

Tempus

Senior Quality Engineer

Redwood City, CA · On-site +1

Lead computer system validation (CSV) activities of Tempus AI applications, software tools, and ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

Vaxcyte

Manager, IT Quality & Compliance

San Carlos, CA · On-site +1

Execute Computer Software Assurance (CSA) and Computer System Validation (CSV) activities for GxP ... Open to Remote; San Carlos, CA Compensation: The compensation package will be competitive and ...

Finance Solutions LLC

Sr. Revenue Accountant

San Francisco, CA · On-site +1

$93K - $122K/yr

Support successful implementation/optimization of revenue systems Additional Notes * Encouraged use of AI tools for contract analysis, documentation, and data validation * Remote/hybrid flexibility

General Motors

Senior ML Validation Engineer

Sunnyvale, CA · On-site +1

$144K - $261K/yr

Collaborate with Simulation, Safety, Systems Engineering, and cross-functional partners. * Author ... MS + 5 years, or PhD + 3 years in ML, Robotics, Computer Science, or work related experience

General Motors

Senior ML Validation Engineer

Sunnyvale, CA · On-site +1

$144K - $261K/yr

Collaborate with Simulation, Safety, Systems Engineering, and cross-functional partners. * Author ... MS + 5 years, or PhD + 3 years in ML, Robotics, Computer Science, or work related experience

Ankura

Model Validation Director

San Francisco, CA · On-site +1

Ideally this role will be hybrid based out of one of our locations; however, remote locations will ... Computer Science, Management Information Systems, or Statistics/Mathematics. * Experience with data ...

Valspec

QA Consultant

San Francisco, CA · Remote

Valspec--a global provider of system validation and lifecycle services--provides commissioning and ... Remote Employment Type: Contract / Consulting (6-12+ months) Start Date: ASAP About the Role: We ...

Oklo

Human Factors Engineer

Santa Clara, CA · On-site +1

... computer-based or paper-based procedure systems. * Plan and execute HFE verification and validation ... Oklo requires remote employees to travel to headquarters (Santa Clara, CA) twice a quarter annually ...

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Computer System Validation Remote information

See Hayward, CA salary details

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

As of Jun 8, 2026, the average hourly pay for computer system validation remote in Hayward, CA is $62.28, according to ZipRecruiter salary data. Most workers in this role earn between $47.93 and $73.85 per hour, depending on experience, location, and employer.

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 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 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 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 are popular job titles related to Computer System Validation Remote jobs in Hayward, CA? For Computer System Validation Remote jobs in Hayward, CA, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Remote jobs in Hayward, CA look for? The top searched job categories for Computer System Validation Remote jobs in Hayward, CA are:
What cities near Hayward, CA are hiring for Computer System Validation Remote jobs? Cities near Hayward, CA with the most Computer System Validation Remote job openings:
Computer System Validation Remote jobs near you

Validation Engineer 1 as 100% Remote

Amicis Global

Sunnyvale, CA • Remote

$74/hr

Contractor

Posted 25 days ago

Job description

Title: Validation Engineer 1
Location: 100% Remote
Duration: 03 Months
Pay Rate: $60.00 - $74.00/- on W2
 
Job Description:
Summary:
This position's primary role is to work closely with the internal IT teams and cross functional departments (Business & PQ-CSV) to support computer system validation activities related to projects and change requests.
 
Roles and Responsibilities:

Top Skills:
Good understanding of CSV, CSA, FDA regulations (21 CFR Part 11 & 820), GAMP5 & GxP regulations.
Essential Job Duties (Specific responsibilities and tasks an individual would be expected to perform in the role. Additional job duties may be determined by functional people manager)
• Responsible for oversight of all GxP-regulated computerized systems at all applicable points of the computerized system lifecycle, ensuring compliance with regulatory requirements, Computer Systems Validation (CSV), and Lifecycle procedures with Data Integrity requirements.
• Provide oversight of validation activities, lead the development and approval of validation documentation and risk assessments, work with project teams to determine which elements should be validated, and conduct impact assessment of proposed changes to computerized systems.
• Perform and/or direct GxP computerized system validation projects in compliance with 21 CFR 820, 21 CFR Part 11, Annex 11, and Data Integrity.
• Ensure that GxP systems meet intended uses and comply with applicable regulations, current industry practices, and *** policies and procedures.
• Development and approval of Validation Plans, IQ, OQ Protocols, Trace Matrices, Risk Assessments and Validation Summary Reports.
• Establish validation standards, develop testing protocols, document test results and maintain records for later analysis.
• Documentation and remediation of deviations resulting from validations/qualifications.
• Provide assistance and guidance in training co-workers on validation protocols and operating procedures.
• Author/Update assigned Operating Procedures (SOPs & DOPs), Policies, validation templates to ensure compliance with Company policies and federal regulations.
• Support regulatory agency inspections/audits, as required.
• Must be familiar with cGMPs and current industry guidelines.
• Interfaces between various internal and external functional areas to assure successful integration and completion of validation activities in overall project schedules.
• Maintains awareness of regulatory requirements.
• Understanding of FDA's new guidance of CSA risk based approach validation
Required Skills and Experience (Specific skills, knowledge, and experience that an individual must possess in order to successfully perform in job)
• Knowledge of fundamental cGMP concepts and FDA/EMA regulations, QSR, 21 CFR Part 820, 21 CFR Part 11, and ISO 9001 Standards.
• Strong knowledge of FDA Regulated manufacturing processes, process validation, computer and equipment validation, and GMPs.
• Hands-on experience in EDMS (Electronic Document Management system) & Test Management tools.
• Understanding of FDA's recent guidance on transition of CSV to CSA.
• Ability to develop clear, concise, and timely oral and written reports. Excellent written and oral communication skills.
• Ability to work on complex projects with general direction and minimal guidance.
• Ability to handle multiple projects and meet deadlines.
• Ability to manage priorities and workflow. Versatility, flexibility, and a willingness to work within constantly changing priorities with enthusiasm.
Required Education and Training (As applicable - Specific education and training that an individual must possess in order to successfully perform in job)
• Bachelor's degree (B.S.) in a related field or equivalent.
• 8 years hands-on experience in Computer System Validation/Quality Compliance in a FDA Regulated industry (Medical Device/Pharma/Life Sciences) with a focus on GxP systems.
Preferred Skills and Experience (As applicable - Specific skills, knowledge, and experience that are not required to perform the job, but are desirable to have)
Hands-on experience with Microsoft Word, Excel, PowerPoint & Visio.
Hands-on experience with EDMS (Electronic Document Management system) & Test Management tools.

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