ZipRecruiter

Log In

1

Validation Engineer Biomedical Jobs in Florida (NOW HIRING)

Alleima

Validation Engineer

Palm Coast, FL

... Biomedical, or Industrial Engineering. To succeed in this role, you need strong technical judgment ... supporting consistent validation practices across sites. Just as importantly, you value ...

Alleima

Validation Engineer

Palm Coast, FL · On-site

... Biomedical, or Industrial Engineering. To succeed in this role, you need strong technical judgment ... supporting consistent validation practices across sites. Just as importantly, you value ...

Baptist Health Care

Biomedical Technician II

Pensacola, FL · On-site

$22.25 - $29.50/hr

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

GE HealthCare

$21.75 - $28.75/hr

Associate's or Bachelor's degree in Electrical Engineering, Biomedical Engineering, Mechanical ... Must have valid driver's license and ability to maintain license. * The successful applicant must ...

next page

Showing results 1-20

All JobsValidation Engineer Biomedical JobsValidation Engineer Biomedical Jobs in Florida

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, and why are they important?

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 the biomedical field?

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 are popular job titles related to Validation Engineer Biomedical jobs in Florida? For Validation Engineer Biomedical jobs in Florida, the most frequently searched job titles are:
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:
Validation Engineer Biomedical jobs near you
Infographic showing various Validation Engineer Biomedical job openings in Florida as of July 2026, with employment types broken down into 2% Internship, 1% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, and 1% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution.

Validation Engineer

Alleima

Palm Coast, FL

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 25 days ago

Job description

LocationPalm Coast, United States of AmericaAbout 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 after30 days

  • 88 paid holiday hours per year

  • Paid time off (up to120 hourspaid 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

Apply