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Validation Engineer Biomedical Jobs in Florida (NOW HIRING)

Familiarity with HIPAA, CLIA, CAP, validation processes, change management, and audit readiness. * Bachelor's degree in Computer Science, Software Engineering, Information Systems, Biomedical ...

Biomedical Technician III

Pensacola, FL · On-site

$23.75 - $31.75/hr

... clinical engineering setting (required) * Strong expertise in complex systems, diagnostics ... Valid driver's license; ability to travel as needed If you're ready to lead from the front and make ...

Maintains a valid driver's license and satisfactory driving record. Qualifications Minimum Education * Associates Degree Electrical Engineering, Mechanical Engineering, Related field, Biomedical ...

Design and execute tests to simulate product use for verifying and validating product performance ... Educational and Experience Requirements * BS in Engineering (Mechanical, Bioengineering, Biomedical ...

Design and execute tests to simulate product use for verifying and validating product performance ... Educational and Experience Requirements * BS in Engineering (Mechanical, Bioengineering, Biomedical ...

Showing results 41-60

Validation Engineer Biomedical information

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

AspectValidation Engineer BiomedicalQuality Assurance Engineer Biomedical
CertificationsGMP, ISO, FDA validation certificationsGMP, ISO, audit and compliance certifications
Work EnvironmentDesign, develop, and execute validation protocols for medical devicesDevelop and maintain quality systems, audits, and process improvements
Industry UsagePrimarily in medical device manufacturing and regulatory validationAcross medical device, pharmaceutical, and biotech industries

Validation Engineer Biomedical focuses on ensuring medical devices meet regulatory validation requirements through testing and protocols. Quality Assurance Engineer Biomedical emphasizes maintaining quality systems, compliance, and process improvements. Both roles are essential in the biomedical industry but serve different functions related to validation versus quality assurance.

What are some typical challenges faced by validation engineers in the biomedical industry and how can they be addressed?

Validation Engineers in the biomedical field often face challenges such as keeping up with evolving regulatory requirements, managing complex documentation, and ensuring equipment or processes meet stringent quality standards. Navigating audits and working cross-functionally with R&D, manufacturing, and quality assurance teams can also be demanding. To address these challenges, staying current with industry regulations, developing strong organizational and communication skills, and maintaining meticulous records are essential for success and career growth in this role.

What are the key skills and qualifications needed to thrive as a validation engineer in biomedical?

To thrive as a Validation Engineer in Biomedical, you need a solid background in engineering or life sciences, knowledge of regulatory standards (such as FDA or ISO 13485), and experience with validation protocols. Familiarity with technical tools like statistical analysis software, calibration equipment, and documentation systems is essential, and certifications such as Six Sigma or CQE can be advantageous. Strong problem-solving, attention to detail, and effective communication skills help you excel in cross-functional teams and ensure compliance. These skills are crucial for maintaining product quality, meeting regulatory requirements, and ensuring patient safety in biomedical environments.

What does a validation engineer do in biomedical?

A Validation Engineer in the biomedical industry ensures that equipment, processes, and systems used in the production of medical devices or pharmaceuticals meet regulatory standards and function as intended. Their work involves planning and executing validation protocols, documenting results, and troubleshooting any deviations. This role is crucial for maintaining product quality, patient safety, and compliance with regulatory agencies such as the FDA. Validation Engineers often collaborate with quality assurance, manufacturing, and research teams to establish and maintain validated systems throughout a product's lifecycle.

What job categories do people searching Validation Engineer Biomedical jobs in Florida look for?

The top searched job categories for Validation Engineer Biomedical jobs in Florida are:

What cities in Florida are hiring for Validation Engineer Biomedical jobs?

Cities in Florida with the most Validation Engineer Biomedical job openings:

Infographic showing various Validation Engineer Biomedical job openings in Florida as of August 2026, with employment types broken down into 78% Full Time, and 22% Contract. Highlights an 80% In-person, and 20% Hybrid job distribution.

On-Site Service Engineer (3rd Shift)

Labcorp

Tampa, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,140 frontline employees who took The Breakroom Quiz

97th of 120 rated laboratories


Job description

Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our global scale and deep expertise, you'll do meaningful work, grow your career and make a real impact. Together, we're improving health and improving lives.


Labcorp is seeking a On-Site Service Engineer (3rd Shift) to join our team in Tampa, FL.

Location: Tampa, FL (On-Site)

Schedule: This is a full time position assigned to a third shift schedule. Standard hours are Monday through Friday, 12:00 a.m. to 8:30 a.m. Business needs may occasionally require weekend, after-hours, or emergency support.

Travel: Approximately 25% domestic travel required

Job Responsibilities

  • Execute Factory Acceptance Testing (FAT) of laboratory automation equipment at Protedyne's manufacturing facility in Windsor, CT.
  • Install laboratory automation instruments at customer locations and perform Site Acceptance Testing (SAT).
  • Perform preventive maintenance on laboratory automation equipment according to established schedules.
  • Conduct equipment qualification and validation testing.
  • Troubleshoot, diagnose, and repair automation instruments and systems.
  • Provide emergency service support and repairs as requested by customers.
  • Maintain assigned inventory and ensure inventory accuracy.
  • Document and communicate customer feedback, service issues, and resolutions to the Customer Care Manager.
  • Deliver customer support in laboratory and production environments.
  • Complete service-related documentation, including time reports, expense reports, inventory reports, equipment checklists, and field service reports.
  • Provide operator training on system operation and maintenance as needed.
  • Support field upgrades, enhancements, and equipment improvements.
  • Perform additional duties as assigned.

Minimum Qualifications

  • High school diploma with 7 or more years of experience supporting automation systems, instrumentation, or field service operations; or Associate degree in Engineering Technology, Electronics, Mechanical Technology, or Biomedical Equipment Technology with 3 or more years of experience supporting automation systems, instrumentation, or field service operations; or Bachelor's degree in Engineering, Engineering Technology, Electronics, Mechanical Engineering, or Biomedical Engineering with 1 or more years of experience supporting automation systems, instrumentation, or field service operations
  • 3 or more years of field service experience supporting complex automation systems.
  • 3 or more years of experience troubleshooting electrical, pneumatic, and mechanical systems.
  • 1 or more years of experience using diagnostic and testing equipment including digital voltmeters (DVMs), oscilloscopes, micrometers, or similar instrumentation.
  • 1 or more years of experience with Microsoft Office applications including Excel, Word, and Outlook.
  • 1 or more years of experience performing equipment installation, repair, preventive maintenance, qualification, or validation activities.
  • Ability to lift and carry 50 pounds or more on a regular basis.

Preferred Qualifications

  • 1 or more years of field service experience supporting medical, laboratory, diagnostic, or healthcare automation systems.
  • 1 or more years of experience performing Factory Acceptance Testing (FAT), Site Acceptance Testing (SAT), equipment qualification, or validation activities.
  • 1 or more years of experience providing customer training on technical equipment or instrumentation.
  • 1 or more years of experience supporting laboratory automation, robotic systems, or automated instrumentation platforms.

Additional Job Standards

Technical Skills

  • Working knowledge of troubleshooting and root-cause analysis methodologies.
  • Ability to diagnose issues remotely based on customer-reported symptoms.
  • Ability to triage service requests and develop solutions that minimize operational downtime.
  • Ability to instruct customers on equipment operation and maintenance procedures.

Customer Service & Communication

  • Strong customer relationship and customer satisfaction skills.
  • Strong interpersonal and communication skills.
  • Ability to communicate technical information effectively to customers and internal stakeholders.

Problem Solving & Decision Making

  • Strong analytical and problem-solving capabilities.
  • Ability to make sound technical decisions in field service environments.
  • Ability to work independently with minimal supervision.

Professionalism

  • Ability to maintain a professional demeanor in demanding customer environments.
  • Commitment to continuous learning and technical skill development.

About the Role

The On-Site Service Engineer is responsible for providing installation, preventive maintenance, troubleshooting, repair, qualification, validation, and customer support services for complex laboratory automation systems. This role serves as a key customer-facing technical resource, ensuring equipment performance, reliability, and operational continuity while supporting customers through service, training, and technical expertise. The position requires independent judgment, strong technical troubleshooting skills, and a commitment to delivering exceptional customer support in a fast-paced environment.

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.Employees who are regularly scheduled toworka 7 on/7 off schedule are eligible to receive all the foregoing benefits except PTO or FTO. For more detailed information, pleaseclick here.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.


We encourage all to apply

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