Validation Engineer
Palm Coast, FL · On-site
Develop, review, and approve validation master plans, protocols, reports, and supporting documentation. * Partner with Manufacturing, Engineering, Quality, Regulatory, and Supply Chain to support new ...
Validation Engineer
Palm Coast, FL · On-site
Develop, review, and approve validation master plans, protocols, reports, and supporting documentation. * Partner with Manufacturing, Engineering, Quality, Regulatory, and Supply Chain to support new ...
Validation Engineer
Palm Coast, FL · On-site
Develop, review, and approve validation master plans, protocols, reports, and supporting documentation. * Partner with Manufacturing, Engineering, Quality, Regulatory, and Supply Chain to support new ...
Validation Engineer
Palm Coast, FL · On-site
Develop, review, and approve validation master plans, protocols, reports, and supporting documentation. * Partner with Manufacturing, Engineering, Quality, Regulatory, and Supply Chain to support new ...
The Process Validation Engineer will work closely with the existing Cleaning Validation and Commissioning & Qualification teams while owning the process validation program. This role reports directly ...
The Process Validation Engineer will work closely with the existing Cleaning Validation and Commissioning & Qualification teams while owning the process validation program. This role reports directly ...
The company is primarily focused on information technology, engineering, healthcare, financial ... Design, write and execute test plans to validate VoIP application functionality. Own and maintain ...
The company is primarily focused on information technology, engineering, healthcare, financial ... Design, write and execute test plans to validate VoIP application functionality. Own and maintain ...
You in this Role The Test & Validation Engineer defines and executes structured test programs for motor systems, covering dynamometer characterization, endurance testing, environmental exposure, and ...
You in this Role The Test & Validation Engineer defines and executes structured test programs for motor systems, covering dynamometer characterization, endurance testing, environmental exposure, and ...
You in this Role The Test & Validation Engineer defines and executes structured test programs for motor systems, covering dynamometer characterization, endurance testing, environmental exposure, and ...
You in this Role The Test & Validation Engineer defines and executes structured test programs for motor systems, covering dynamometer characterization, endurance testing, environmental exposure, and ...
You in this Role The Test & Validation Engineer defines and executes structured test programs for motor systems, covering dynamometer characterization, endurance testing, environmental exposure, and ...
Quick apply
You in this Role The Test & Validation Engineer defines and executes structured test programs for motor systems, covering dynamometer characterization, endurance testing, environmental exposure, and ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Senior Validation Engineer Responsibilities: This role leads the process of Clean Room qualification and the associated validation of related equipment such as incubators, cryo freezers, and HVAV.
Senior Validation Engineer Responsibilities: This role leads the process of Clean Room qualification and the associated validation of related equipment such as incubators, cryo freezers, and HVAV.
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation activities include testing in both vehicle environments and Hardware-in-the-Loop (HIL) simulation systems. The engineer will execute DVP&R test procedures, perform initial root-cause ...
Validation Engineer information
See Florida salary details
$16.89 - $20.66
2% of jobs
$20.66 - $24.43
6% of jobs
$24.43 - $28.20
13% of jobs
$29.38 is the 25th percentile. Wages below this are outliers.
$28.20 - $31.98
13% of jobs
$31.98 - $35.75
11% of jobs
The median wage is $37.63 / hr.
$35.75 - $39.52
12% of jobs
$39.52 - $43.29
9% of jobs
$46.20 is the 75th percentile. Wages above this are outliers.
$43.29 - $47.07
13% of jobs
$47.07 - $50.84
13% of jobs
$50.84 - $54.61
6% of jobs
$54.61 - $58.38
3% of jobs
$16
$38
$58
How much do validation engineer jobs pay per hour?
As of Jul 2, 2026, the average hourly pay for 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 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?
| Aspect | Validation Engineer | Quality Assurance Engineer |
|---|---|---|
| Certifications | GMP, ISO, Six Sigma | ISO, Six Sigma, CQA |
| Work Environment | Regulated industries like pharma, biotech, medical devices | Manufacturing, software, and product development |
| Primary Focus | Ensuring products meet specifications through validation processes | Preventing defects through process and system improvements |
| Common Usage | Regulatory compliance, validation protocols | Process 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.
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.
More about Validation Engineer jobs
What are the most commonly searched types of Validation Engineer jobs in Florida? The most popular types of Validation Engineer jobs in Florida are:
What are popular job titles related to Validation Engineer jobs in Florida? For Validation Engineer jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Validation Engineer jobs in Florida look for? The top searched job categories for Validation Engineer jobs in Florida are:
- Director Computer System Validation Csv
- Weekend Labware Lims Developer
- Summer 21 Cfr Part 11 Validation
- Medical Device Validation Engineer
- Computer System Validation Csv Remote
- Validation Manager
- Validation Engineer Biomedical
- Vehicle Validation Engineer
- Verification And Validation
- Embedded System Validation Engineer
What cities in Florida are hiring for Validation Engineer jobs? Cities in Florida with the most Validation Engineer job openings:
What are popular job titles related to Validation Engineer jobs in FL? For Validation Engineer jobs in FL, the most frequently searched job titles are:
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 13 days ago
Job description
Location
Palm Coast, United States of America
About the role
In this mid-level role, you will plan, execute, and document validation activities that support compliant operations across the product and process lifecycle while partnering with cross-functional teams throughout BU Medical.
About you
You bring 3-7 years of experience in equipment, process, or system validation within a regulated manufacturing environment such as medical device, pharmaceutical, biotechnology, or a comparable industry. You have demonstrated experience creating and executing VMP, IQ, OQ, and PQ activities, and you hold a bachelor's degree in Engineering, Life Sciences, or a related technical discipline such as Mechanical, Chemical, Biomedical, or Industrial Engineering. To succeed in this role, you need strong technical judgment, attention to detail, and the ability to work effectively across Quality, Engineering, Manufacturing, and other cross-functional teams. You are comfortable working in a structured, regulated environment and can balance compliance, quality, and business needs while supporting consistent validation practices across sites. Just as importantly, you value collaboration and understand that every role matters in building reliable processes that support better healthcare.
What you can expect from us
Why Alleima, BU Medical?
We don't just make components; we enable breakthroughs. Whether it's helping someone with diabetes live more freely or supporting the next generation of neurostimulation devices, our work is purpose-driven and technically sophisticated. Are you ready to take on this challenge together with us? Join us on our journey! www.alleima.com
Palm Coast, United States of America
About the role
In this mid-level role, you will plan, execute, and document validation activities that support compliant operations across the product and process lifecycle while partnering with cross-functional teams throughout BU Medical.
- Lead and execute equipment, process, and system qualification and validation activities, including VMP, IQ, OQ, and PQ, in line with internal procedures and applicable regulatory requirements.
- Develop, review, and approve validation master plans, protocols, reports, and supporting documentation.
- Partner with Manufacturing, Engineering, Quality, Regulatory, and Supply Chain to support new product introductions, capacity expansions, equipment transfers, and site expansion activities.
- Ensure validation practices meet customer requirements, internal standards, and regulatory expectations, including FDA and ISO requirements.
- Maintain validation lifecycle compliance through change control, revalidation, periodic review, and support for deviations, CAPAs, and nonconformances.
- Participate in internal audits, customer audits, and regulatory inspections, including preparation of validation evidence and responses.
- Provide technical guidance to site teams and contribute to continuous improvement through standardization, templates, best practices, and risk mitigation.
- Ability and willingness to travel internationally up to 50% of the time as required by business needs.
About you
You bring 3-7 years of experience in equipment, process, or system validation within a regulated manufacturing environment such as medical device, pharmaceutical, biotechnology, or a comparable industry. You have demonstrated experience creating and executing VMP, IQ, OQ, and PQ activities, and you hold a bachelor's degree in Engineering, Life Sciences, or a related technical discipline such as Mechanical, Chemical, Biomedical, or Industrial Engineering. To succeed in this role, you need strong technical judgment, attention to detail, and the ability to work effectively across Quality, Engineering, Manufacturing, and other cross-functional teams. You are comfortable working in a structured, regulated environment and can balance compliance, quality, and business needs while supporting consistent validation practices across sites. Just as importantly, you value collaboration and understand that every role matters in building reliable processes that support better healthcare.
What you can expect from us
- A workplace built on care, for better healthcare, for our customers, and for each other.
- A culture that values unique, novel solutions and high-quality standards.
- Opportunities to contribute to medical innovations that make a real difference.
- A collaborative, decentralized environment where your voice matters.
- Competitive compensation, benefits, and global career development.
- Heath, Dental, and Vision coverage after 30 days
- 401K with company contribution of 5% plus matching after 30 days
- 88 paid holiday hours per year
- Paid time off (up to 120 hours paid time off after one year)
Why Alleima, BU Medical?
We don't just make components; we enable breakthroughs. Whether it's helping someone with diabetes live more freely or supporting the next generation of neurostimulation devices, our work is purpose-driven and technically sophisticated. Are you ready to take on this challenge together with us? Join us on our journey! www.alleima.com