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Senior Csv Engineer Jobs (NOW HIRING)

Senior CSV Engineer

Indianapolis, IN ยท On-site

$110 - $160/hr

About the Job Performance Validation is seeking a Senior CSV Engineer to join our Indianapolis team. To be clear about scope up front: this is OT-side validation - process automation, control systems ...

$120 - $170/hr

The Opportunity Adryan is looking for an experienced Senior Computer System Validation (CSV) Engineer / MES Validation Lead to support a pharmaceutical manufacturing site in Oregon. The successful ...

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CSV Engineer I

Indianapolis, IN ยท On-site

$68K - $88K/yr

The CSV Engineer will work under the guidance of senior CSV team members to execute and document validation activities, support deviation resolution, verify system functionality against approved ...

CSV Engineer I

Indianapolis, IN ยท On-site

$68K - $88K/yr

The CSV Engineer will work under the guidance of senior CSV team members to execute and document validation activities, support deviation resolution, verify system functionality against approved ...

CSV Engineer III

Indianapolis, IN ยท On-site

$68K - $88K/yr

This is a senior-level Computer System Validation (CSV) role for an experienced validation ... The CSV Engineer III will support validation activities for systems used in quality control ...

CSV Engineer III

Indianapolis, IN ยท On-site

$68K - $88K/yr

This is a senior-level Computer System Validation (CSV) role for an experienced validation ... The CSV Engineer III will support validation activities for systems used in quality control ...

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to ... Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark ...

IT CSV Engineer

Redmond, WA ยท On-site

$115K - $135K/yr

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to ... Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark ...

IT CSV Engineer

Redmond, WA ยท On-site

$115K - $135K/yr

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to ... Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark ...

Senior Validation Engineer

Portsmouth, NH ยท On-site

$35 - $45/hr

Senior Validation Engineer Location: Portsmouth, NH - 03801 Duration: 7 Months Job Type: Temporary ... Hybrid Summary The CSV Engineer will act as an individual contributor responsible for ensuring ...

IT CSV Engineer Location: Seattle, WA OR Redmond, WA Reports to ... Senior Manager/Group Leader, CSV About Us: At Just-Evotec, we believe that curiosity is the spark ...

The Senior Computer System Validation (CSV) Engineer is responsible for leading the validation of complex computerized systems, custom-developed applications, enterprise databases, data platforms ...

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Senior Csv Engineer information

See salary details

$59.5K

$126.6K

$183.5K

How much do senior csv engineer jobs pay per year?

As of Aug 24, 2026, the average yearly pay for senior csv engineer in the United States is $126,557.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,500.00 and $143,500.00 per year, depending on experience, location, and employer.

What is a senior CSV engineer?

Senior CSV Engineers are experienced professionals who specialize in Computer System Validation (CSV) within regulated industries such as pharmaceuticals, biotechnology, and medical devices. Their main responsibility is to ensure that computer systems used in these industries comply with regulatory standards and function as intended. They lead validation projects, develop validation protocols, conduct risk assessments, and work closely with IT and quality assurance teams. Senior CSV Engineers also provide guidance on regulatory requirements, troubleshoot validation issues, and help maintain audit-ready documentation.

What are the key skills and qualifications needed to thrive as a senior CSV engineer?

To excel as a Senior CSV (Computer System Validation) Engineer, you need expertise in validation methodologies, regulatory compliance (such as FDA 21 CFR Part 11, GAMP 5), and a relevant engineering or scientific degree. Proficiency with validation lifecycle documentation, risk management tools, and quality management systems is typically required, as are certifications like PMP or Six Sigma. Strong analytical skills, attention to detail, and effective communication are crucial soft skills for coordinating cross-functional teams and ensuring compliance. These skills are essential to maintaining regulatory standards, minimizing risks, and ensuring the integrity and reliability of computerized systems in regulated industries.

What are common challenges faced by senior CSV engineers when ensuring regulatory compliance across multiple projects?

Senior CSV Engineers often encounter the challenge of managing varying compliance standards and documentation requirements across multiple projects, especially when working with global teams. Keeping up-to-date with evolving regulations (such as FDA 21 CFR Part 11 or EU Annex 11) and ensuring that validation activities are harmonized across different systems can be demanding. Strong project management skills, proactive communication with cross-functional stakeholders, and meticulous attention to detail are essential for overcoming these challenges and maintaining audit-ready documentation.

What is the difference between Senior Csv Engineer vs Data Engineer?

AspectSenior Csv EngineerData Engineer
Required CredentialsBachelor's in Computer Science, Data Science, or related field; experience with CSV processingBachelor's or higher in Computer Science, Data Engineering, or related; often includes knowledge of databases and ETL tools
Work EnvironmentData processing teams, analytics departments, data pipelines involving CSV filesData infrastructure teams, big data environments, cloud platforms, and data pipelines
Employer & Industry UsageTech companies, finance, healthcare, any industry handling large CSV datasetsTech firms, finance, e-commerce, and industries requiring large-scale data integration

The main difference is that a Senior Csv Engineer specializes in managing and optimizing CSV data workflows, while a Data Engineer has a broader role in designing and maintaining comprehensive data infrastructure, including databases, pipelines, and big data systems. Both roles require similar foundational skills but differ in scope and complexity.

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Infographic showing various Senior Csv Engineer job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $126,557 per year, or $60.8 per hour.

Senior CSV Engineer

Performance Validation, Inc

Indianapolis, IN โ€ข On-site

$115K - $135K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago


Job description

About Us
Here at Performance Validation, Inc. (PV) we have been providing Commissioning, Qualification, and Validation services to the life science industries for over 30 years! We are a 100% employee-owned company with teams in Indiana, Michigan, Illinois, Kansas, Washington, Wisconsin, and North Carolina, and we support clients throughout the US and overseas. As an employer, PV is committed to providing growth opportunities to our employees through professional development, implementation of new services, and cultivation of new geographical areas.
About the Job
Performance Validation is seeking a Senior CSV Engineer to join our Indianapolis team. To be clear about scope up front: this is OT-side validation โ€” process automation, control systems, and manufacturing equipment on the plant floor, not enterprise IT systems. If your background is in DCS and PLC platforms rather than ERP and business applications, you are in the right place.
This is a senior technical role for someone who has moved past executing other people's protocols and is ready to define the strategy โ€” deciding how a system should be qualified, not just running the test.
You will serve as our technical leader in automation lifecycle management, computer system validation, commissioning and qualification, data integrity, and regulatory compliance. Our clients bring us their hardest automation problems: greenfield facilities, complex DCS and PLC platforms, data integrity remediation, systems where the right validation approach is not obvious. You will be the person they ask, and you will work directly alongside their quality, engineering, IT, and manufacturing teams to build validation strategies that hold up to regulatory scrutiny and still let the project move.
What You Will Do
Validation Strategy and Execution
  • Develop qualification and testing strategies for process automation systems across the full system lifecycle, applying risk-based principles to determine appropriate qualification scope, testing approach, and lifecycle controls.
  • Lead the planning, development, execution, and review of C amp;Q and CSV documentation โ€” User Requirements, Functional and Design Specifications, Validation Plans, Risk Assessments, Traceability Matrices, IQ/OQ/PQ protocols, Summary Reports, and software lifecycle documentation.
  • Execute validation activities in GMP environments including protocol walkdowns, field testing, discrepancy resolution, commissioning support, and turnover to operations.
  • Perform Data Integrity assessments for computerized systems and support remediation in line with regulatory expectations.
Automation and Technical Depth
  • Perform source code reviews and participate in design reviews to ensure automation solutions meet quality, validation, cybersecurity, and compliance expectations.
  • Contribute to electrical system design, automation software, PLC programming, and debugging as project needs require.
  • Support commissioning and qualification planning for GMP manufacturing facilities and process automation systems.
Leadership and Client Partnership
  • Advise clients on industry best practices, and serve as the subject matter expert for automation validation, Data Integrity, GAMP, and risk-based validation methodologies.
  • Provide technical leadership during audits, inspections, client assessments, and regulatory interactions.
  • Mentor and empower colleagues, and influence both technical and management teams through collaboration and sound engineering judgment.
  • Build standardized validation templates, testing approaches, and reusable documentation that make every subsequent project faster and more consistent.
  • Serve as a key resource in developing new services, technologies, standards, and best practices for the firm.

Requirements You Will Need โ€‹
Education
  • A four-year degree in Electrical Engineering, Computer Engineering, Chemical Engineering, Mechanical Engineering, Computer Science, Life Sciences, or another related technical discipline.

Experience
  • Five or more years supporting pharmaceutical, biotechnology, or other regulated manufacturing environments, including automation engineering, C amp;Q, CSV, process automation.
  • Demonstrated experience executing validation testing in GMP manufacturing environments, including protocol execution, discrepancy management, and final report generation.
  • Experience developing validation strategies and lifecycle documentation for automation and computerized systems.
  • Experience with commissioning and qualification of automation platforms and manufacturing systems.
  • Experience collaborating across Quality, Engineering, Manufacturing, IT, Operations, and external suppliers.

Technical Knowledge
  • Working knowledge of risk-based cGMP principles, FDA regulations, EU Annex 11, Data Integrity guidance, and GAMP 5.
  • Strong understanding of the computerized system validation lifecycle from concept through retirement.
  • Control systems experience โ€” Emerson DeltaV DCS, Rockwell Automation/Allen-Bradley PLCs, Siemens PLCs, FactoryTalk/RSView, or comparable platforms.
  • Ability to perform and facilitate Data Integrity assessments for computerized systems.

How You Work
  • Excellent written and verbal communication, with the ability to translate complex technical concepts for both engineering and business audiences.
  • Self-motivated, professional, and enthusiastic, with proven leadership and mentoring skills.
  • Diplomacy, respect, and a service mindset in every client interaction.

Nice to Have
  • Experience supporting pharmaceutical API, Drug Substance, Drug Product, or biotechnology manufacturing facilities.
  • Experience on large capital expansion projects and greenfield manufacturing facilities.
  • Experience developing enterprise CSV standards, templates, and best practices.
  • Experience with MES, historians, SCADA systems, and enterprise automation architectures.
  • Familiarity with automated warehouses and material handling systems.
  • Multi-level industrial network infrastructure design and cybersecurity considerations.
  • Knowledge of virtualization, high availability, and clustered automation environments.
  • Programming experience in VBA, .NET, SQL, scripting languages, or other automation-related tools.
  • Experience supporting global project teams and multi-site implementations.
  • Advanced degrees or professional certifications. Published research, technical presentations, or recognized industry participation are a plus.

What We Have to Offer
  • Competitive base salary and biannual profit share
  • Employee stock ownership program (ESOP) and 401(k) company match
  • Medical, vision, and dental coverage
  • Disability and life insurance
  • Paid vacation and holidays
  • Internal and external training opportunities
  • Cellphone stipend
  • Company-sponsored team building outings

Additional Information
Position type: Full-time, exempt. This role reports to the Account Director and is assigned to one or more project teams.
Travel: Occasional travel is required in support of project and client needs.
Qualified candidates must be legally authorized to be employed in the United States. Performance Validation, Inc. does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this position.