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Contract Csv Engineer Jobs (NOW HIRING)

Lonza

Senior Validation Engineer - CSV (OT)

Vacaville, CA · On-site

$93K - $155K/yr

Paid Time Off The Senior Validation Engineer - CSV at Lonza will be responsible for leading and ... Peer review/approve validation protocols, and summary reports generated by junior and contract ...

Intellectt INC

Automation Engineer

New Albany, OH · On-site

My name is Mahalakshmi , and I'm reaching out from Intellectt Inc. regarding an exciting contract ... Collaborate with Packaging, Warehouse, Quality, CSV, IT/OT teams, vendors, and system integrators.

Pinnaql

Validation Engineer

Atlanta, GA

FAT, SAT, CSV, equipment integration, and startup. * Drive process design for new equipment and ... Collaborate with Procurement and Legal on vendor contracts. * Create and maintain engineering ...

Pinnaql

Validation Engineer

Atlanta, GA · On-site

FAT, SAT, CSV, equipment integration, and startup. * Drive process design for new equipment and ... Collaborate with Procurement and Legal on vendor contracts. * Create and maintain engineering ...

AEG

Sr. Solutions Engineer - Mulesoft

Scottsdale, AZ · On-site

$55.50 - $71.75/hr

... XML, CSV, and other payload formats. • Configure and manage API deployments to CloudHub ... API interfaces, contracts, error handling patterns, and reusable assets in alignment with ...

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Contract Csv Engineer information

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$39K

$101.8K

$137.5K

How much do contract csv engineer jobs pay per year?

As of Jun 28, 2026, the average yearly pay for contract csv engineer in the United States is $101,752.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What are some common challenges Contract CSV Engineers face when joining new projects, and how can they adapt quickly?

Contract CSV Engineers often step into projects at various stages, which can pose challenges such as understanding existing validation documentation, aligning with specific company SOPs, and quickly adapting to unique project timelines. To adapt effectively, it's important to proactively communicate with project managers and team members, thoroughly review current validation protocols, and clarify expectations early on. Familiarizing oneself with the company’s preferred validation tools and systems also helps ensure a smoother transition and fosters effective collaboration.

What are the key skills and qualifications needed to thrive as a Contract CSV Engineer, and why are they important?

To thrive as a Contract CSV (Computer System Validation) Engineer, you need a solid background in computer science or engineering, knowledge of regulatory standards (such as FDA 21 CFR Part 11), and experience in validation processes. Familiarity with validation lifecycle documentation, risk management tools, and software like TrackWise or Veeva Vault is typically required. Strong analytical thinking, attention to detail, and effective communication skills help in managing projects and collaborating with cross-functional teams. These competencies ensure compliance, system integrity, and successful project delivery in regulated industries such as pharmaceuticals and biotechnology.

What are Contract CSV Engineers?

Contract CSV Engineers are professionals hired on a contract basis to oversee Computer System Validation (CSV) processes within organizations, particularly in regulated industries like pharmaceuticals and biotechnology. They ensure that computer systems used for processes such as manufacturing, laboratory analysis, and data management comply with regulatory standards (like FDA 21 CFR Part 11). Their responsibilities include developing validation protocols, performing risk assessments, executing testing, and documenting results to ensure data integrity and system reliability. Contract positions allow companies to access specialized expertise for specific projects or during peak workloads without a long-term employment commitment.

What is the difference between Contract Csv Engineer vs Data Analyst?

AspectContract Csv EngineerData Analyst
Required CredentialsTypically requires a degree in computer science, engineering, or related field; proficiency in CSV processing tools and scripting languagesUsually requires a degree in statistics, mathematics, or related field; skills in data visualization and analysis tools
Work EnvironmentOften project-based, working with data pipelines, ETL processes, and database managementPrimarily office-based, analyzing data sets, creating reports, and providing insights
Employer & Industry UsageUsed by tech companies, data firms, and organizations needing data pipeline supportCommon in finance, marketing, healthcare, and consulting industries

The Contract Csv Engineer focuses on building and maintaining CSV data pipelines and tools, often in a technical environment, while the Data Analyst interprets data to generate insights and reports. Both roles require strong data skills but differ in their primary functions and work settings.

More about Contract Csv Engineer jobs
What cities are hiring for Contract Csv Engineer jobs? Cities with the most Contract Csv Engineer job openings:
What are the most commonly searched types of Csv Engineer jobs? The most popular types of Csv Engineer jobs are:
What states have the most Contract Csv Engineer jobs? States with the most job openings for Contract Csv Engineer jobs include:
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Contract Csv Engineer jobs near you
Infographic showing various Contract Csv Engineer job openings in the United States as of June 2026, with employment types broken down into 58% Full Time, 22% Part Time, 1% Temporary, and 19% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $101,752 per year, or $48.9 per hour.

Validation Engineer

Validation & Engineering Group, Inc

Holly Springs, NC

Full-time

Posted 14 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Validation Engineer

Description:

The role demands deep technical expertise across the full validation lifecycle — including URS development, FAT/SAT execution, and Computer System Validation (CSV) — as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.

Key Responsibilities:

  • Develop User Requirement Specifications (URS).
  • Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
  • Drive process design for new equipment and ensure product design requirements are met.
  • Execute commissioning and qualification activities for new and existing equipment.
  • Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
  • Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
  • Collaborate with Procurement and Legal on vendor contracts.
  • Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
  • Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
  • Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
  • Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
  • Apply statistical analysis and SPC systems to support data-driven decision-making.
  • Manage multiple priorities and maintain equipment qualification schedules.

Qualifications:

  • Bachelor's degree in Engineering or Science.
  • Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
  • Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
  • Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
  • Strong experience executing capital projects within GMP-regulated manufacturing environments.
  • Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
  • Ability to work independently and lead solutions under general direction.
  • Strong organization, and communication skills

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.