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Verification And Validation Engineer Jobs in Florida

AMERICAN SYSTEMS

Systems Engineer, Lead

Orlando, FL · Hybrid

$150K - $180K/yr

Guide verification and validation planning and ensure requirements are testable and traceable ... Mentor systems engineers and promote disciplined engineering methods, model quality, and technical ...

AMERICAN SYSTEMS

Systems Engineer, Lead

Orlando, FL · On-site

$96.80 - $161.50/hr

Guide verification and validation planning and ensure requirements are testable and traceable ... Mentor systems engineers and promote disciplined engineering methods, model quality, and technical ...

AMERICAN SYSTEMS

Systems Engineer, Lead

Orlando, FL · On-site +1

$150K - $180K/yr

Guide verification and validation planning and ensure requirements are testable and traceable ... Mentor systems engineers and promote disciplined engineering methods, model quality, and technical ...

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All JobsVerification And Validation Engineer JobsVerification And Validation Engineer Jobs in Florida

Verification And Validation Engineer information

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$38

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How much do verification and validation engineer jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for verification and validation engineer in Florida is $38.86, according to ZipRecruiter salary data. Most workers in this role earn between $29.47 and $47.26 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to thrive as a verification and validation engineer?

To thrive as a Verification and Validation Engineer, you need a solid background in engineering principles, software or hardware testing methodologies, and a relevant degree such as in electrical, computer, or systems engineering. Familiarity with test automation tools (e.g., Selenium, Jenkins), scripting languages, and standards like ISO or IEEE V&V processes is commonly required, along with certifications such as ISTQB. Attention to detail, analytical thinking, and strong communication skills set top performers apart by enabling thorough test coverage and clear reporting. These skills are essential to ensure products meet quality standards, regulatory requirements, and customer expectations before release.

What is the difference between Verification And Validation Engineer vs Quality Assurance Engineer?

AspectVerification And Validation EngineerQuality Assurance Engineer
CredentialsTypically requires engineering degrees, certifications like ISTQB or ASQ CQEOften holds degrees in engineering, quality management, or related fields; certifications like Six Sigma or ISTQB
Work EnvironmentWorks in product development, testing labs, and manufacturing settingsWorks across development, production, and process improvement environments
Industry UsageCommon in electronics, aerospace, automotive, and medical device industriesWidely used in manufacturing, software, and service industries
FocusEnsures products meet specifications through testing and validationEnsures quality processes are followed to prevent defects

While both roles aim to ensure product quality, Verification And Validation Engineers focus on testing and confirming that products meet specifications, whereas Quality Assurance Engineers develop and maintain quality systems and processes to prevent defects. Both roles often collaborate but serve different stages of the product lifecycle.

How does a verification and validation engineer typically interact with development and QA teams during a project?

A Verification and Validation Engineer works closely with both development and QA teams to ensure that products meet specified requirements and function as intended. They often review design documents, develop test plans, and execute test cases in collaboration with developers, providing feedback on potential issues early in the process. Regular communication and coordination with QA are essential to ensure comprehensive test coverage and resolve defects efficiently. This collaborative approach helps maintain product quality and supports a smooth development lifecycle.

What is a verification and validation engineer?

Verification and Validation Engineers are professionals responsible for ensuring that products, systems, or software meet specified requirements and function as intended. They design and execute tests, review documentation, and analyze results to confirm that deliverables are both built correctly (verification) and serve their intended purpose (validation). Their work is crucial in highly regulated industries like aerospace, automotive, and healthcare, where safety and compliance are critical. These engineers collaborate with development teams to identify defects early and help ensure that projects meet quality standards before release.
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Verification And Validation Engineer jobs near you
Infographic showing various Verification And Validation Engineer job openings in Florida as of July 2026, with employment types broken down into 1% As Needed, 72% Full Time, 21% Part Time, 2% Temporary, and 4% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $80,821 per year, or $38.9 per hour.

Senior Quality Engineer, Validation

Exactech

Gainesville, FL

$80K - $108K/yr

Full-time

Posted yesterday

New

Exactech rating

8.0

Company rating: 8.0 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description


This position offers flexibility to align with the candidate's experience level and can be structure as a Senior Validation Engineer role for those with advanced expertise.  

The Validation Engineer provides cross-functional support in V&V development, planning and execution while maintaining corporate engineering and quality systems best practices, policies and procedures. The Validation Engineer is results oriented and has the knowledge and confidence in the areas of Quality Assurance and validation/verification (V&V). 
  • Provide focused, technical, hands-on engineering assistance regarding V&V requirements of medical device processes, materials, equipment and methods including project management, process design, document generation (IQ, OQ, PQ, SOPs, WIs and ETSs), critical process parameter development, protocol execution and summary reports. 
  • Participates in the development and execution of robust inspection and test methods for V&V feasibility and qualification projects and stand alone studies. 
  • Leads or participates in the validation of corporate software packages ensuring adherence to industry requirements. 
  • Use statistical techniques, as necessary, to properly design and execute V&V activities. 
  • Prepare documentation and execute V&V activities utilizing a risk based approach (pFMEA, FMEA, etc.) and Good Engineering Practices (GEPs) ensuring compliance to medical device industry regulations. 
  • Coordinate personnel training, protocol and process documentation/record retrieval, as necessary, supporting timely execution and closure of all corporate V&V activities.  
  • Maintain corporate validation process auditing program ensuring timely completion of auditing activities. 
  • Maintain V&V planning (Validation Project Dashboard) documenting progress towards completion of corporate V&V initiatives in preparation for monthly update meetings. 
  • Lead the identification, maintenance, development and enhancement of corporate systems, processes and standards. 
  • Identify, analyze and correct internal and external manufacturing deviations and/or anomalies related to V&V activities ensuring optimization of production processes. 
  • Successfully contribute to cross-functional project teams in all areas of device cleanliness and manufacturing V&V work such as material testing, specification development, process capability studies, research, and investigation and process/test documentation. 
  • Identify and communicate significant quality and compliance concerns to the Mgr. Validations, QA and associated project team leaders early in the V&V development phase. 
  • Informs Regulatory Affairs of validation projects that may require further reporting/scrutiny (e.g. PMA devices). 
  • Participate in the review and qualification of external supply chain V&V activities. 
  • Take primary responsibility for company-wide validation related Corrective and Preventive Actions that may result from internal/external non-conformances, recalls and/or field actions. 
  • Define and lead third party, customer and regulatory audits as they pertain to validations. 
Education:
  • Bachelor's Degree from an accredited institution required; Master's Degree preferred  
 Experience:
  • Advanced level of technical software proficiency 
  • Excellent Quality System knowledge required 
  • Strong time management and project management skills are necessary. 
  • Experience writing IQ/OQ/PQ V&V protocols. 
  • Working knowledge of principles, concepts and practices of process V&V activities, Risk Management, FDA and ISO Regulations.  
  • General understanding of sterilization and related analytical testing is a plus. 
    Must be able to work independently and in a team environment.  
Functional/Technical Knowledge, Skills and Abilities Required:
  • Statistical expertise in areas such as process capability, process assurance and sampling 
  • Expertise in Microsoft Office products 
  • Ability to work effectively in a team environment 
  • ASQ Certifications preferred 
  • Advanced level of technical software proficiency 
  • Working knowledge of statistical analysis and sampling plans. 
  • Excellent communication (written and verbal) skills. 
  • Excellent organization skills. 

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