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Csv Manager Jobs in Florida (NOW HIRING)

Lonza

ERP Head (SAP)

Tampa, FL · On-site

$210 - $320/hr

GxP Compliance & Computer Systems Validation (CSV) GxP Compliance & Computer Systems Validation (CSV): Manage the ERP environment in strict compliance with life science quality regulations; ensure ...

Lonza

ERP Head (SAP)

Tampa, FL · On-site

GxP Compliance & Computer Systems Validation (CSV): Manage the ERP environment in strict compliance with life science quality regulations; ensure all system lifecycle phases, data migrations, and ...

Lonza

ERP Head (SAP)

Tampa, FL · On-site

GxP Compliance & Computer Systems Validation (CSV): Manage the ERP environment in strict compliance with life science quality regulations; ensure all system lifecycle phases, data migrations, and ...

Strive Pharmacy

GMP Systems Administrator

Alachua, FL · On-site +1

Support the CSV lifecycle: author or review URS, FDS and Configuration Specifications and execute IQ/OQ protocols for new systems, upgrades and patches. * Manage the periodic review program for all ...

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

TekWissen group is a workforce management provider throughout the USA and many other countries in ... Exposure to computerized system validation (CSV). * Experience in biologics, pharmaceutical, or ...

Noblesoft Technologies

GxP Test Lead

Boca Raton, FL · On-site

$45 - $61.50/hr

... CSV , and FDA 21 CFR Part 11 standards. * Strong leadership, test planning, estimation, and cross-functional communication skills. * Experience in testing SAAS/COTS/Bespoke , CRM , Life sciences ...

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Csv Manager information

See Florida salary details

$21.7K

$78.1K

$88.2K

How much do csv manager jobs pay per year?

As of Aug 13, 2026, the average yearly pay for csv manager in Florida is $78,148.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,200.00 and $87,100.00 per year, depending on experience, location, and employer.

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 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 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 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 popular job titles related to Csv Manager jobs in Florida?

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

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

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

What cities in Florida are hiring for Csv Manager jobs?

Cities in Florida with the most Csv Manager job openings:

Csv Manager jobs near you
Infographic showing various Csv Manager job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 13% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $78,148 per year, or $37.6 per hour.

Sr. Software Quality Engineer (Computer Software Validation-CSV)

MDAEdge

Jacksonville, FL • On-site

Full-time

Re-posted 19 days ago

Job description

Job Summary:
MDAEdge is a company focused on software quality in the medical device sector, and they are seeking a Senior Software Quality Engineer to lead Computer Software Validation (CSV) projects. The role involves managing software validation documentation, supporting compliance efforts, and promoting cross-functional collaboration within the organization.
Responsibilities:
• Lead Computer Software Validation (CSV) project planning activities, including the creation and updates of User Requirements Specifications (URS), Software Design Specifications (SDS), and Requirements Traceability Matrices (RTM).
• Develop, review, and approve software validation documentation.
• Create and execute qualification protocols, document reports, and review and approve software test scripts and code reviews.
• Evaluate and approve internal and vendor software packages and test documentation.
• Prioritize and manage all assigned projects within the software validation department.
• Implement and support policies, procedures, and processes related to CSV, Software Development Life Cycle (SDLC), and software validation for computerized systems.
• Serve as the Software Quality Engineering (SQE) representative in the Change Control Board (CCB) to facilitate change validation.
• Lead Installation Qualification (IQ) activities for manufacturing lines.
• Drive CSV improvement initiatives within the manufacturing environment.
• Promote cross-functional collaboration across different teams, sites, and operating companies in the area of CSV.
• Identify and resolve obstacles that impact business needs.
• Work closely with Franchise Quality to implement and sustain Quality System initiatives at the site level.
• Support compliance efforts by ensuring audit readiness and participating in internal and external audits related to CSV.
• Act as the Subject Matter Expert (SME) for CSV, leading investigations, responses, and remediation of site-specific CSV audit findings.
Qualifications:
Required:
• Strong working knowledge of FDA and European medical device regulations (QSR and ISO).
• Expertise in software validation requirements for both medical device production and Quality System software.
• Proficiency in GAMP5 and SDLC methodologies.
• In-depth understanding of regulations for electronic records, electronic signatures, and data integrity.
• Experience in change management with strong technical writing skills.
• Hands-on experience with SCADA and/or Manufacturing Execution Systems (MES), with a background in manufacturing/operations.
• Minimum of 4 years of experience in a regulated environment.
• 2-4 years of experience in medical device regulations.
• Strong knowledge of FDA and European medical device regulations (QSR and ISO).
• Expertise in software validation for medical device production and Quality System applications.
• Working knowledge of GAMP5 and SDLC.
• Understanding of electronic records, electronic signatures, and data integrity regulations.
• Experience with change management and technical writing.
• Hands-on experience with SCADA and/or MES in a manufacturing/operations setting.
Preferred:
• Medical device process validation experience.
• Experience in Quality Auditing and notified body inspections.
• Background in Quality Systems process development, support, integration, or enhancement.
• Experience in training or coaching others.
• Certification as a Software Quality Engineer (CSQE) or Quality Engineer (CQE).
Company:
The world doesn't have a talent shortage. It has a talent alignment problem. MDA Edge exists to fix that. Founded in , the company is headquartered in Sheridan, WY, US, , with a team of 51-200 employees. The company is currently Growth Stage.

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