ZipRecruiter

Log In

1

Contract Csv Engineer Jobs (NOW HIRING)

AMRI

CSV Systems Engineer II/III

Albany, NY

$90K - $112K/yr

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ... CSV Systems Engineer II: $73,000-$112,000 per year. CSV Systems Engineer III: $90,000 - $112,000 ...

Curia, Inc.

CSV Systems Engineer II/III

Albany, NY · On-site

$90K - $112K/yr

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of ... CSV Systems Engineer II: $73,000-$112,000 per year. CSV Systems Engineer III: $90,000 - $112,000 ...

next page

Showing results 1-20

People also search for

All JobsContract Csv Engineer Jobs

Contract Csv Engineer information

See salary details

$39K

$101.8K

$137.5K

How much do contract csv engineer jobs pay per year?

As of May 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 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 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 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:
What job categories do people searching Contract Csv Engineer jobs look for? The top searched job categories for Contract Csv Engineer jobs are:
Contract Csv Engineer jobs near you
Infographic showing various Contract Csv Engineer job openings in the United States as of May 2026, with employment types broken down into 50% Full Time, 17% Temporary, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $101,752 per year, or $48.9 per hour.
Validation Engineer/CSV Engineer

Validation Engineer/CSV Engineer

Katalyst Healthcares & Life Sciences

Walnut Creek, CA

Contractor

Posted 6 days ago

Job description

Company Description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.
Job Description

Job Description:

  • Develop, implement, and maintain software quality assurance processes for non-product software used in medical device development.
  • Ensure adherence to regulatory standards (FDA, ISO 13485, IEC 62304) and industry best practices for non-product software.
  • Support audits and inspections by regulatory bodies, ensuring that non-product software systems comply with quality and documentation standards.
  • Ensure computerized systems are appropriately validated Assessment of applicability & criticality of GxP and 21 CFR Part 11.
  • Creation and review of validation deliverables including but not limited to.

Responsibilities:

  • Requirement Specifications (User, Functional).
  • Plan.
  • Qualification Protocol (Installation, Operational, Performance) Reports (Summary, Exception) of protocol execution.
  • Traceability Matrix.
  • Periodic Reviews.
  • System Retirement/Decommissioning.
  • Execution of Dry/Test protocol run.
  • Conduct Periodic Reviews to determine if system is in a validated state and take appropriate actions.
  • Perform System Retirement/Decommissioning of systems not in business .
  • Work closely with software development and IT teams to establish best practices for quality and compliance.
  • Provide expertise and guidance on quality assurance processes for non-product software to ensure robust software management.
  • Drive continuous improvement initiatives in software development processes, ensuring alignment with the company's quality management system.

Requirements:

  • A Minimum bachelor's degree in engineering, Science or related technical field.
  • Minimum of 4-5 years of experience in software quality assurance or software validation, preferably within the medical device industry.
  • Strong understanding of quality standards and regulatory requirements (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 62304).
  • Experience with non-product software validation, including tools for development, testing, and maintenance.
  • Good knowledge and experience of CSV activities but not limited to.
  • GxP and 21 CFR Part 11 applicability/criticality assessment.
  • Identification, Preparation and Review of validation deliverables such as Requirements, Plan, Protocols, Test specifications, Reports, Traceability Matrix etc.
  • Execution of Dry/Test protocols.
  • Conduct Periodic Reviews of systems.
  • Perform System Retirement of systems that are not in business.
  • Understanding of Medical Device Quality and Compliance.
  • Good knowledge of GxP, GAMP and 21CFR Part 11 guidelines.
  • Working experience in Product Lifecycle Management (PLM) too.
  • sound knowledge of computer system development lifecycles.
  • Knowledge of JIRA, JAMA software and test automation is a plus. "
  • Computer System Validation, 21 CFR Part 11, GxP, FDA, 21 CFR Part 11, ISO 13485, IEC 62304.
Additional Information

All your information will be kept confidential according to EEO guidelines.

Katalyst Healthcares & Life Sciences logo

About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

Social media

FacebookTwitter

View All Katalyst Healthcares & Life Sciences Jobs

Apply