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Csv Manager Jobs in Delaware (NOW HIRING)

Prophecy Technologies

R&D CSV Engineer

Wilmington, DE · On-site

Manage deviations and Corrective and Preventive Actions (CAPA), ensuring full compliance with ... Core expertise in Computer System Validation (CSV). * In-depth knowledge of regulatory frameworks ...

MDAEdge

LabWare LIMS-LES Developer

Port Penn, DE · On-site

... Management System (LIMS) and Lab Execution System (LES). The role involves configuring, customizing ... CSV), change control, and regulatory requirements (FDA 21 CFR Part 11, GxP). • Good analytical ...

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Csv Manager information

See Delaware salary details

$29K

$104.7K

$118.1K

How much do csv manager jobs pay per year?

As of Aug 25, 2026, the average yearly pay for csv manager in Delaware is $104,665.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,100.00 and $116,600.00 per year, depending on experience, location, and employer.

What is a CSV manager?

A CSV Manager is a software tool or professional responsible for handling, organizing, and processing CSV (Comma-Separated Values) files. These files are commonly used for storing and exchanging data in a simple text format, making them popular for data imports and exports in various applications. A CSV Manager ensures that the data within these files is correctly formatted, validated, and sometimes transformed for compatibility with databases or other systems. They may also automate workflows involving large amounts of CSV data to improve efficiency and accuracy.

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

To thrive as a CSV (Computer System Validation) Manager, you need a strong background in GxP regulations, validation methodologies, and a degree in life sciences, engineering, or a related field. Familiarity with validation lifecycle documentation, risk assessment tools, and regulatory standards like FDA 21 CFR Part 11 is typically required. Outstanding project management, attention to detail, and strong communication skills make a CSV Manager stand out in ensuring compliance and leading cross-functional teams. These competencies are crucial for ensuring validated systems meet regulatory requirements and support business operations in highly regulated industries.

What are some common challenges faced by a CSV manager in maintaining regulatory compliance across multiple projects?

A CSV (Computer System Validation) Manager often manages several projects simultaneously, each with unique regulatory requirements. One major challenge is ensuring that all validation documentation remains current and audit-ready, despite frequent software updates or process changes. Additionally, coordinating with cross-functional teams such as IT, Quality Assurance, and Operations can be demanding, as priorities and timelines may differ. Staying updated with evolving industry regulations and effectively training team members are also essential to maintaining consistent compliance.

What is the difference between Csv Manager vs Data Analyst?

AspectCsv ManagerData Analyst
Required CredentialsExperience with CSV data management, basic database skillsDegree in statistics, data science, or related field; proficiency in data analysis tools
Work EnvironmentData management teams, IT departmentsBusiness analysis teams, research departments
Employer & Industry UsageUsed in industries handling large CSV datasets, such as logistics and financeUsed across industries for interpreting data, reporting, and decision-making

The Csv Manager primarily focuses on managing and organizing CSV data files, ensuring data integrity and accessibility. In contrast, a Data Analyst interprets data, creates reports, and provides insights. While both roles work with data, Csv Managers specialize in data handling, whereas Data Analysts focus on analysis and interpretation.

What are popular job titles related to Csv Manager jobs in Delaware?

For Csv Manager jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Csv Manager jobs in Delaware look for?

The top searched job categories for Csv Manager jobs in Delaware are:

Csv Manager jobs near you
Infographic showing various Csv Manager job openings in Delaware as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $104,665 per year, or $50.3 per hour.

R&D CSV Engineer

Prophecy Technologies

Wilmington, DE • On-site

Full-time

Posted 12 days ago

Job description

Role Overview:
This role is for a Computer System Validation (CSV) Engineer with strong R&D domain knowledge, focusing on ensuring GxP compliance for various systems. The engineer will be responsible for applying core CSV principles and regulatory expertise within a pharmaceutical or life sciences R&D environment.
Key Responsibilities:
  • Ensure strict adherence to regulatory standards including 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, and ITIL.
  • Author critical validation documentation such as User Requirement Specifications (URS), Functional Specifications (FS), protocols, final reports, and comprehensive validation plans/reports.
  • Conduct activities related to audit/inspection readiness, periodic reviews, access roster management, and audit trail reviews.
  • Manage deviations and Corrective and Preventive Actions (CAPA), ensuring full compliance with Standard Operating Procedures (SOPs) and company policies.
  • Implement risk-based testing methodologies in alignment with Computer Software Assurance (CSA) fundamentals.

Required Skills:
  • Core expertise in Computer System Validation (CSV).
  • In-depth knowledge of regulatory frameworks including 21 CFR Part 11/820, GxP, GAMP 5, SOX, EU Annex 11/22, ISO 9001, and ITIL.
  • Experience in authoring URS/FS, protocols, final reports, and validation plans/reports.
  • High-level understanding of Veeva Vault suites.
  • Proficiency in risk-based testing aligned to CSA fundamentals.
  • Experience with audit/inspection readiness, periodic reviews, access roster, and audit trail reviews.
  • Competence in Deviation/CAPA management and SOP/policy compliance processes.
  • High-level understanding of R&D domains such as Biostatistics, Clinical, Discovery, Medical Affairs, Pharmacovigilance, Regulatory Affairs, RPA GxP BOTs, and R&D AI GxP.

Qualifications:
  • Bachelor of Science OR Bachelor of Technology OR Bachelor's in Pharmacy.
  • Over 8+ years of overall experience.
  • At least 5 years of experience specifically in Computer System Validation for GxP systems.

Preferred Skills:

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