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

Aequor Inc

Validation Engineer

Davie, FL · On-site

Validation Engineer 1 Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to ...

atrion

Quality Engineer

Davie, FL · On-site

$66K - $85.20K/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 ...

TAS Sustaining Engineering

Sustaining Engineer I

Sunrise, FL

$87.30K - $107.30K/yr

Lead TMVs and software validation as necessary * Monitor and improve the efficiency, output, and ... Knowledge of engineering statistics * Technical writing skills for manufacturing instructions, test ...

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How much do validation engineer jobs pay per hour?

As of Jun 4, 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 are Validation Engineers?

Validation Engineers are professionals responsible for ensuring that systems, processes, or equipment meet regulatory standards and function as intended. They typically work in industries such as pharmaceuticals, biotechnology, manufacturing, and medical devices. Their duties involve creating validation protocols, conducting tests, analyzing data, and documenting results to ensure compliance with industry regulations and quality standards. Validation Engineers play a critical role in maintaining product safety and efficacy, as well as helping companies pass audits and inspections.

What jobs make $3,000 a month without a degree?

Validation engineers typically require a degree, but similar roles in fields like sales, customer service, or skilled trades can pay around $3,000 monthly without a degree. Jobs such as commercial drivers, certain technical support roles, or entry-level trades may also meet this income level with relevant experience or certifications. Success in these roles often depends on skills, certifications, and experience rather than formal education.

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.

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 May 2026, with employment types broken down into 90% Full Time, 3% Part Time, and 7% 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 Engineer

Validation Engineer

Aequor Inc

Davie, FL • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Validation Engineer 1

Under general supervision, reviews specifications and determines the critical aspects of facilities, utilities, computer systems and manufacturing equipment with regard to product and process quality, writes qualification protocols for operating systems and records related test results; prepares final reports that identify the results of protocol testing and the conditions of release.

This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks.

  • Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws.
  • Reviews electrical, mechanical, and software/computer specifications in manufacturer and blue print form, and identifies critical parameters.
  • Writes protocols that challenge the critical parameters related to installation, operation, and performance of the related facility, utilities, computer systems, or equipment.
  • Assures that protocols are approved through proper channels; writes and revises validation protocols.
  • Executes validation and qualification protocols per related SOPs and assures that acceptance criterion related to validation and qualification protocols are met.
  • Assures that all test data is gathered and recorded in accordance with cGMP requirements.
  • Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria.
  • Writes final reports and assures that they are approved through proper channels.
  • Develops and communicates project timelines and status.
  • Complies with all GMP and safety requirements, SOP's and Company policies and procedures. Performs equipment and system qualification periodic reviews.
  • Performs related duties as assigned.

Knowledge of:

  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
  • Pharmaceutical principles, practices and applications.
  • English usage, spelling, grammar and punctuation.
  • Principles of mathematical and statistical computations.
  • Personal computer operations and Microsoft applications (Word, Access, and Excel).

Skill in:

  • Interpreting software and ladder logic diagrams and flowcharts.
  • Interpreting electrical, and mechanical blue prints and specifications including HVAC systems and. construction plans.
  • Solving practical problems and considering a variety of concrete variables in situations where only limited standardization exists.
  • Communicating clearly and concisely, both orally and in writing.
  • Establishing and maintaining good relationships with those encountered in the course of work.
  • Operating a personal computer.

Physical Requirements and Working Conditions

Incumbents in this class are subject to extended periods of sitting, standing, walking, pushing and pulling, stooping and crouching climbing and walking, vision to monitor, occasional lifting of equipment or materials weighing up to 25 pounds. Incumbents may be exposed to toxic materials, toxic gases, electrical hazards, and dangerous tools and equipment. Work is performed in a manufacturing environment.

Minimum Qualifications:

Bachelor's degree in Engineering or a related field from an accredited college or university and zero (0) to one (1) year of engineering validation experience, preferably in a pharmaceutical environment, or an equivalent combination of training and experience.

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