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Computer System Validation Csv Jobs in Florida (NOW HIRING)

TekWissen LLC

Quality Assurance Engineer

Tampa, FL · On-site

$25 - $35/hr

... computer systems, validation, and laboratory instruments. * Contribute to continuous improvement ... Exposure to computerized system validation (CSV). * Experience in biologics, pharmaceutical, or ...

Compunnel

CSV Technical Specialist

Coral Springs, FL · On-site

$106K/yr

... validated state of systems by implementing and documenting controlled technical changes in ... Required Qualifications • Bachelor's degree in Information Technology, Computer Science ...

Jj

Senior Software Quality Engineer

Jacksonville, FL · On-site

Support Computer Software Validation (CSV) project planning activities including the creation or ... Support CSV programs / policies / procedures and improvement initiatives for computerized systems.

Unicon Pharma Inc.

CQV Lead

Davie, FL · On-site

$45 - $50/hr

... System Validation (CSV), data integrity, and 21 CFR Part 11 compliance. 5. Strong understanding of OSD unit operations and equipment (e.g., blending, granulation, compression, coating, encapsulation ...

Cordis

MES Engineer I (Onsite)

Miami Lakes, FL · On-site

Support computerized system validation (CSV) activities, including IQ/OQ/PQ protocols, under supervision. * Assist in the creation and maintenance of technical documentation, work instructions, and ...

IT EXCEL LLC

Qa Analyst

Orlando, FL

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. WE ARE LOOKING FOR FRESH GRADUATES FOR QA and Validation POSITIONS. Qualifications ...

IT EXCEL LLC

Qa Analyst

Orlando, FL · On-site

We specialize in the following technologies- QA/Software Testing, Business Analysis and Computer System Validation. WE ARE LOOKING FOR FRESH GRADUATES FOR QA and Validation POSITIONS. Qualifications ...

Leidos

Computer Systems Engineer

Saint Petersburg, FL

$131K - $237K/yr

Guide electromagnetic modeling, array simulation, beamforming architecture development, and performance validation activities. * Develop and review technical documentation including system ...

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Computer System Validation Csv information

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How much do computer system validation csv jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for computer system validation csv in Florida is $38.71, according to ZipRecruiter salary data. Most workers in this role earn between $29.09 and $48.12 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Computer System Validation Csv position, and why are they important?

To thrive as a Computer System Validation (CSV) professional, you need a solid understanding of computer science, regulatory compliance (such as FDA 21 CFR Part 11), and validation methodology, often supported by a degree in a scientific or technical field. Familiarity with documentation tools, validation protocols, and quality management systems, as well as certifications like PMP or Six Sigma, is highly beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills enable effective cross-functional collaboration. Mastering these skills ensures accurate validation processes, regulatory compliance, and smooth project execution in highly regulated environments.

What is a Computer System Validation (CSV) job?

A Computer System Validation (CSV) job involves ensuring that computerized systems used in regulated industries, such as pharmaceuticals and medical devices, comply with industry standards and regulatory requirements (e.g., FDA 21 CFR Part 11, GxP). CSV professionals develop validation protocols, conduct testing, and document system performance to ensure data integrity, reliability, and compliance. Their role is critical in maintaining system quality and avoiding regulatory risks.

What are some typical challenges faced by Computer System Validation professionals and how are they addressed?

Computer System Validation (CSV) professionals often encounter challenges such as keeping up with evolving regulations, managing complex documentation requirements, and ensuring robust communication between IT, quality assurance, and business teams. Navigating system upgrades while maintaining compliance with strict regulatory standards requires careful planning and thorough risk assessment. Successful candidates address these challenges by staying current with industry guidance, utilizing validation templates and checklists, and fostering strong teamwork across various departments. Building collaborative relationships and maintaining meticulous records help ensure both audit readiness and smooth project completion.

What are the most commonly searched types of Computer System Validation Csv jobs in Florida? The most popular types of Computer System Validation Csv jobs in Florida are:
What are popular job titles related to Computer System Validation Csv jobs in Florida? For Computer System Validation Csv jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Computer System Validation Csv jobs in Florida look for? The top searched job categories for Computer System Validation Csv jobs in Florida are:
Computer System Validation Csv jobs near you
Infographic showing various Computer System Validation Csv job openings in Florida as of June 2026, with employment types broken down into 1% Locum Tenens, 37% Full Time, 59% Part Time, 2% Temporary, and 1% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $80,519 per year, or $38.7 per hour.
Quality Engineer CSV & Digital Systems

Quality Engineer CSV & Digital Systems

Unicon Pharma Inc.

Davie, FL • On-site

$35 - $36/hr

Contractor

Posted 7 hours ago

Job description

Description:

Title: Quality Engineer – CSV & Digital Systems
Shift Details: Monday to Friday 8am – 5 pm (40 hours per week)
Assignment Duration: 6 months with possible extension
Location: Davie, FL

Convert to Perm: Depending on opens and performance

Core Essential skill sets (must have):

  • Recent Master’s graduate Master's degree in Engineering, Computer Science, Life Sciences, or related field.
  • Min 3 years experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization
  • Min 3 years hands-on CSV experience reviewing and approving validation documentation.
  • Direct experience supporting manufacturing or utilities systems (not just lab systems).
  • Medical screening requirements:

Key Responsibilities:

Computer System Validation (CSV)

  • Review and approve CSV lifecycle documents (VMP, URS, FRS, HDS, Risk Assessments, IQ/OQ/PQ, RTM, Summary Reports).
  • Ensure risk-based validation approaches aligned with GAMP 5, 21 CFR Part 11, and Data Integrity (ALCOA+) principles.
  • Evaluate system changes through change control, assessing GxP impact and validation requirements.
  • Support periodic reviews and re-validation activities for existing systems.
  • Digital Systems & Platforms
  • Act as Quality reviewer/approver for systems including:
  • MES / EBR platforms (e.g., Werum PAS-X or similar)
  • Historians (OSIsoft PI or equivalent)
  • Advanced analytics tools (Seeq, used for GxP trending)
  • Empower and other lab systems
  • Review configurations related to data acquisition, time stamping, audit trails, access control, and electronic records/signatures.
  • Ensure proper segregation between GxP vs non-GxP analytics use cases.

Data Integrity & Compliance:

  • Assess and approve data flows, interfaces, and integrations between systems.
  • Support regulatory inspections (FDA, EMA) and internal audits related to computerized systems.
  • Cross-Functional Collaboration
  • Partner with Engineering, Automation, MS&T, IT, and Operations to:
  • Enable faster project execution with compliant validation strategies
  • Avoid over-validation while maintaining inspection readiness
  • Provide Quality input during project design, FAT/SAT, and commissioning phases.

Required Qualifications:

Education:

  • Master's degree in Engineering, Computer Science, Life Sciences, or related field.

Experience:

  • 3-5 years experience in pharmaceutical or regulated manufacturing; out of which 2 years in quality organization
  • 3+ years hands-on CSV experience reviewing and approving validation documentation.
  • Direct experience supporting manufacturing or utilities systems (not just lab systems).

Required Technical Skills

  • Strong working knowledge of:
  • CSV lifecycle & GAMP 5
  • 21 CFR Part 11 / Annex 11
  • Data Integrity (ALCOA+)
  • Practical experience with:
  • MES / EBR systems
  • Process Historians (PI, etc.)
  • Advanced analytics platforms (Seeq) in a GxP context
  • Ability to evaluate risk-based validation for dashboards, reports, and models.
  • Familiarity with change control, deviations, and CAPA systems.

Preferred / Nice-to-Have

  • Experience with:
  • Werum PAS-X, Seeq, PI Vision, Power BI (for regulated trending)
  • Agile or lean validation approaches
  • Commissioning & Qualification (C&Q) integration with CSV
  • Prior involvement in:
  • FDA inspections related to computerized systems
  • Site digitalization or Industry 4.0 initiatives

Key Competencies

  • Risk-based decision making with quality and compliance focus
  • Strong documentation review and technical writing skills
  • Ability to challenge constructively while remaining solution-oriented
  • Comfortable working at the intersection of Quality, Engineering, and IT
  • Pragmatic mindset: compliant and business-enabling