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

Actalent

Validation Specialist

Boca Raton, FL · On-site

$36.06 - $45.67/hr

Collaborate closely with Engineering, Production, Quality Control, Microbiology, and Quality Assurance teams to plan and execute validation activities. * Support commissioning activities for new or ...

atrion

Quality Engineer

Davie, FL · On-site

$66K - $85K/yr

Manages engineering projects. Supports the internal and external audit program. Uses statistical ... Generate, review and approve ECOs and Validation Reports. * Provide oversight to the Supplier ...

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How much do validation engineer jobs pay per hour?

As of Aug 12, 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.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often working in industries like pharmaceuticals, biotech, or manufacturing. The role typically requires knowledge of regulatory requirements, validation protocols, and tools like GxP or SOPs, and can offer stable employment with opportunities for advancement. Job satisfaction depends on individual interests in quality assurance, technical skills, and industry stability.

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 regulatory standards and experience with validation tools are also important.

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 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.

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.
More about Validation Engineer jobs
What job categories do people searching Validation Engineer jobs in Boca Raton, FL look for? The top searched job categories for Validation Engineer jobs in Boca Raton, FL are:
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 87% Full Time, 8% Part Time, and 5% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $102,633 per year, or $49.3 per hour.

Validation Specialist

GL Staffing Services, Inc.

Boca Raton, FL • On-site

Full-time

Posted 4 days ago

Job description

We are seeking an experienced Validation Specialist / Validation Engineer to support qualification and validation activities within an FDA-regulated sterile injectable pharmaceutical manufacturing environment. This role is responsible for planning, executing, documenting, and maintaining validation activities to ensure facilities, equipment, utilities, processes, and computerized systems comply with FDA and cGMP requirements.

Responsibilities
  • Prepare, execute, review, and maintain validation documentation, including:
  • Validation Master Plans (VMP)
  • User Requirement Specifications (URS)
  • Design Qualification (DQ)
  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Requalification protocols
  • Perform equipment qualification for sterile injectable manufacturing equipment, including compounding vessels, filling machines, isolators/RABS, vial washers, depyrogenation tunnels, lyophilizers, autoclaves, visual inspection equipment, and packaging systems.
  • Support qualification of critical utilities, including HVAC, Purified Water (PW), Water for Injection (WFI), Clean Steam, Compressed Air, Nitrogen, and Environmental Monitoring systems.
  • Execute process validation, media fill studies, and cleaning validation activities.
  • Review validation data, investigate deviations, and prepare validation summary reports.
  • Participate in change control assessments and determine validation impact.
  • Support equipment commissioning, validation scheduling, and periodic requalification activities.
  • Collaborate with Engineering, Manufacturing, Quality Assurance, Quality Control, and Microbiology teams.
  • Support internal audits, customer audits, and regulatory inspections.
  • Ensure compliance with FDA regulations, cGMP, 21 CFR Parts 210 & 211, Annex 1, Data Integrity (ALCOA+), and company procedures.
  • Participate in continuous improvement initiatives to enhance validation and compliance programs.
Qualifications
  • Bachelor's degree in Engineering, Chemistry, Pharmacy, Biotechnology, Microbiology, or a related scientific discipline.
  • 5–10 years of validation experience in pharmaceutical manufacturing.
  • Sterile injectable manufacturing experience is required.
  • Strong experience with equipment qualification, utility qualification, process validation, and cleaning validation.
  • Computer System Validation (CSV) experience is a plus.
  • Knowledge of FDA cGMP regulations, 21 CFR Parts 210 & 211, Annex 1, change control, deviation investigations, risk assessments, and data integrity principles.
  • Excellent technical writing, documentation, analytical, and problem-solving skills.

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