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Validation Engineer Jobs in Boca Raton, FL (NOW HIRING)

DSN-IT

QA Engineer

Boca Raton, FL · On-site

$90 - $130/hr

Senior QA Automation Engineer (TypeScript) Location: Boca Raton, FL - Onsite (W2) About the Role We ... Test across platforms - validate application behavior across iOS, Android, Windows, and macOS ...

DSN

QA Engineer

Boca Raton, FL · On-site

Senior QA Automation Engineer (TypeScript) Location: Boca Raton, FL - Onsite (W2) About the Role We ... Test across platforms - validate application behavior across iOS, Android, Windows, and macOS ...

DSN

QA Engineer

Boca Raton, FL

Senior QA Automation Engineer (TypeScript) Location: Boca Raton, FL -- Onsite (W2) About the Role ... Test across platforms -- validate application behavior across iOS, Android, Windows, and macOS ...

Inficare Technologies

QA Engineer

Sunrise, FL · On-site

... validate: • Completeness and edge cases • Performance and reliability • Scalability and ... DevOps, etc.). • Experience with defect tracking and source control tools (e.g., Jira, Git). • ...

Globaltech, Inc.

Project Engineer (E1)

Boca Raton, FL · On-site

Globaltech, Inc. is a design-build company of engineers and contractors that serves primarily ... Possess a valid Florida Driver License and able to pass a motor vehicle record search * Able to ...

Assa Abloy

Field Support Engineer

Fort Lauderdale, FL · On-site

Configuring, integrating, and validating physical access control system environments for testing ... Coordinating with product engineering for two-way feedback (requesting assistance when needed and ...

ASSA ABLOY

Field Support Engineer

Fort Lauderdale, FL · On-site

Configuring, integrating, and validating physical access control system environments for testing ... Coordinating with product engineering for two-way feedback (requesting assistance when needed and ...

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Validation Engineer information

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$21

$49

$74

How much do validation engineer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for validation engineer in Boca Raton, FL is $49.34, according to ZipRecruiter salary data. Most workers in this role earn between $37.40 and $60.00 per hour, depending on experience, location, and employer.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

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

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often in regulated industries like pharmaceuticals or manufacturing. The role typically requires attention to detail, knowledge of validation protocols, and familiarity with tools like GxP or FDA regulations. It can offer stable employment and opportunities for specialization and advancement.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of industry standards and experience with validation tools are also important.
More about Validation Engineer jobs

What job categories do people searching Validation Engineer jobs in Boca Raton, FL look for?

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What cities near Boca Raton, FL are hiring for Validation Engineer jobs?

Cities near Boca Raton, FL with the most Validation Engineer job openings:

Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Boca Raton, FL as of August 2026, with employment types broken down into 89% Full Time, 8% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $102,633 per year, or $49.3 per hour.

Quality Engineer, CSV & Digital Systems

Unicon Pharma Inc.

Davie, FL • On-site

$35 - $36/hr

Contractor

Re-posted 24 days ago

Job description

Details
Description:   Title: Quality Engineer – CSV & Digital Systems
Assignment Duration: 6 months with possible extension
Davie, FL
Shift Details: Monday to Friday 8am – 5 pm (40 hours per week)
 
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:
o       MES / EBR platforms (e.g., Werum PAS-X or similar)
o       Historians (OSIsoft PI or equivalent)
o       Advanced analytics tools (Seeq, used for GxP trending)
o       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:
o       Enable faster project execution with compliant validation strategies
o       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:
o       CSV lifecycle & GAMP 5
o       21 CFR Part 11 / Annex 11
o       Data Integrity (ALCOA+)
•       Practical experience with:
o       MES / EBR systems
o       Process Historians (PI, etc.)
o       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:
o       Werum PAS-X, Seeq, PI Vision, Power BI (for regulated trending)
o       Agile or lean validation approaches
o       Commissioning & Qualification (C&Q) integration with CSV
•       Prior involvement in:
o       FDA inspections related to computerized systems
o       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