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Senior Csv Engineer Jobs in Florida (NOW HIRING)

Bond-Pro Inc

Senior Software Engineer

Tampa, FL · On-site +1

$115K - $152K/yr

SENIOR SOFTWARE ENGINEER Overview We're looking for a Senior Software Engineer who can operate ... Design and implement systems that handle structured (CSV, relational), semi-structured (JSON ...

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

... CSV). * Create, review, and approve SOPs, Change Controls, CAPAs, deviations, forms, reports, and ... Perform additional duties as assigned by the Senior Manager of QA Operations. Required ...

Adasoft

Senior Automation Engineer

Plantation, FL · On-site

$103K - $135K/yr

We are looking for an Industrial Automation Engineer to join our team and participate in industrial ... Knowledge of GxP, GMP or CSV environments. * Experience with industrial communication protocols ...

GL Staffing Services, Inc.

Validation

Boca Raton, FL · On-site

$75K - $95K/yr

The Validation Specialist / Validation Engineer is responsible for planning, executing, documenting ... Senior Manager, Quality Assurance Employment Type: Full-Time Salary Range: $75,000-$95,000, based ...

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Senior Csv Engineer information

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.

What are the most commonly searched types of Csv Engineer jobs in Florida?

The most popular types of Csv Engineer jobs in Florida are:

What are popular job titles related to Senior Csv Engineer jobs in Florida?

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

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

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

What cities in Florida are hiring for Senior Csv Engineer jobs?

Cities in Florida with the most Senior Csv Engineer job openings:

Senior Csv Engineer jobs near you
Infographic showing various Senior Csv Engineer job openings in Florida as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution.

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

MDAEdge

Jacksonville, FL • On-site

Full-time

Re-posted 8 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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