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Principal Quality Engineer Jobs in Florida (NOW HIRING)

Quality Engineer

Crestview, FL · On-site

$61K - $78K/yr

Perform other duties as assigned Principal Responsibilities and Accountabilities: * Excellent ... ASQ Quality Engineering Certification with 5-7 years of quality and/or engineering related ...

New

Quality Engineer

Crestview, FL · On-site

$61K - $78K/yr

Perform other duties as assigned Principal Responsibilities and Accountabilities: * Excellent ... ASQ Quality Engineering Certification with 5-7 years of quality and/or engineering related ...

New

Quality Sr Engineer I

Jacksonville, FL · On-site

$82K - $111K/yr

How You'll Create Impact Principal Duties and Responsibilities: Formulates procedures, specifications, and standards for Zimmer products and processes. Provides leadership for quality engineering ...

Principal Engineer - Land Development and Water Resources About KEITH: We are a multidisciplined ... Provide high-level design expertise, review, and technical oversight to ensure quality, efficiency ...

Principal Engineer - Land Development and Water Resources About KEITH: We are a multidisciplined ... Provide high-level design expertise, review, and technical oversight to ensure quality, efficiency ...

Principal Engineer - Land Development and Water Resources About KEITH: We are a multidisciplined ... Provide high-level design expertise, review, and technical oversight to ensure quality, efficiency ...

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Showing results 1-20

Principal Quality Engineer information

See Florida salary details

$48.2K

$93.8K

$127.8K

How much do principal quality engineer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for principal quality engineer in Florida is $93,769.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,600.00 and $112,100.00 per year, depending on experience, location, and employer.

What is a principal quality engineer?

A Principal Quality Engineer is a senior-level professional responsible for overseeing quality assurance and quality control processes within an organization. They develop and implement quality standards, conduct audits, and collaborate with cross-functional teams to ensure product and process compliance. Their role often includes mentoring junior engineers, driving continuous improvement initiatives, and ensuring products meet regulatory and customer requirements.

What are the day-to-day responsibilities of a principal quality engineer?

As a Principal Quality Engineer, your daily responsibilities often include leading quality improvement initiatives, analyzing production or service processes, and conducting root cause investigations to address quality issues. You’ll collaborate closely with engineering, manufacturing, and operations teams to develop and implement quality standards, review product designs, and ensure compliance with industry regulations. The role may also involve mentoring junior quality engineers, facilitating audits, and compiling reports for senior management. This dynamic position requires a balance of hands-on problem-solving and strategic oversight to drive excellence throughout the organization.

What are the key skills and qualifications needed to thrive as a principal quality engineer?

To thrive as a Principal Quality Engineer, you need deep expertise in quality assurance, process improvement, and engineering principles, usually backed by a relevant bachelor’s or master’s degree and extensive industry experience. Familiarity with quality management systems such as ISO 9001, Six Sigma, root cause analysis tools, and proficiency in statistical analysis software are typically required, along with certifications like ASQ CQE or Lean Six Sigma. Strong leadership, problem-solving abilities, and clear communication skills set outstanding candidates apart in this role. These competencies are crucial for driving continuous improvement, ensuring product reliability, and leading cross-functional teams towards quality objectives.

Are principal quality engineers paid well?

Principal quality engineers typically earn high salaries due to their advanced expertise, leadership responsibilities, and experience in quality assurance and process improvement. Compensation varies by industry and location but generally includes competitive base pay, bonuses, and benefits reflecting their senior role.

What does a principal quality engineer do?

A principal quality engineer leads quality assurance efforts within an organization, developing and implementing testing strategies, ensuring product compliance with standards, and mentoring QA teams. They often utilize tools like test automation software and require strong analytical, communication, and leadership skills to improve product quality and process efficiency.

What are popular job titles related to Principal Quality Engineer jobs in Florida?

For Principal Quality Engineer jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Principal Quality Engineer jobs?

Cities in Florida with the most Principal Quality Engineer job openings:

What are popular job titles related to Principal Quality Engineer jobs in FL?

For Principal Quality Engineer jobs in FL, the most frequently searched job titles are:

Infographic showing various Principal Quality Engineer job openings in Florida as of August 2026, with employment types broken down into 95% Full Time, and 5% Nights. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $93,769 per year, or $45.1 per hour.

Principal Quality Engineer- Georgia

FloodGate Medical

Tampa, FL • On-site

Full-time

Medical, Life, Retirement, PTO

Posted 2 days ago

New


Job description

About Zywie
Founded in 2014, Zywie is a founder-led, privately held remote cardiac monitoring company on a mission to transform cardiovascular care. Our flagship product, the ZywieNano™ MCT Patch - the smallest cardiac monitoring patch on the market - delivers up to 30 days of continuous ECG monitoring paired with ZywieAI™, our proprietary AI-driven arrhythmia detection platform.
We have monitored over 500,000 patients, analyzed more than 1 trillion heartbeats, and generated 4.5 million unique clinical notifications. We are profitable, self-funded, and scaling fast - growing our commercial team from 3 to nearly 25 reps in five years. We are now entering the most exciting chapter of our growth: developing and bringing our own proprietary hardware to market. That's where you come in.
The Opportunity
As we transition from a software and services company to a full medical device manufacturer, we're building our Quality organization from the ground up - and we need a Principal Quality Engineer to lead that build. Our first proprietary hardware device is already in active FDA 510(k) submission, with three more devices behind it in our R&D pipeline. This is a foundational, highly visible role: you'll design, implement, and scale our Quality Management System while directly supporting the development and commercialization of our hardware portfolio, reporting to our Sr. Director, Quality & Regulatory Affairs.
What You'll Do
  • Design, implement, and maintain an ISO 13485 and FDA 21 CFR Part 820/QMSR compliant Quality Management System
  • Lead Design Control activities across the product lifecycle, including Design Inputs, Outputs, Verification, Validation, and Design Reviews
  • Lead ISO 14971 Risk Management processes - hazard analysis, FMEA, benefit-risk analysis, and risk management reporting
  • Support software development teams to ensure compliance with IEC 62304, and review software lifecycle and verification documentation
  • Build and manage our supplier quality program, including audits and qualification for our contract manufacturer
  • Lead CAPA, nonconformance, change control, and complaint handling processes
  • Support process validation, manufacturing readiness, and Design Transfer activities
  • Lead implementation and validation of our electronic Quality Management System (eQMS)
  • Prepare the organization for FDA inspections and ISO 13485 certification, including all supporting documentation
  • Partner cross-functionally with Engineering, Clinical, Operations, Regulatory Affairs, and Manufacturing
  • Mentor future Quality Engineers as our organization grows

What You'll Bring
  • Bachelor's degree in Engineering or a related technical discipline; Master's preferred
  • 5+ years of Quality Engineering experience in the medical device industry
  • Demonstrated experience building or significantly enhancing a Quality Management System - not just operating within one
  • Deep knowledge of FDA 21 CFR Part 820/QMSR, ISO 13485, ISO 14971, and IEC 62304
  • Experience supporting Class II and/or Class III medical devices
  • Experience supporting FDA inspections and ISO certification audits
  • Strong Design Controls and Risk Management expertise
  • Experience implementing electronic Quality Management Systems
  • Excellent communication and leadership skills
  • Preferred: experience in startup or high-growth medical device companies, and experience supporting software-enabled devices (SaMD/SiMD), including AI/ML-enabled devices
  • Preferred: ASQ Certified Quality Engineer (CQE), CQA, or equivalent certification

Compensation & Benefits
  • Competitive base salary plus performance bonus, commensurate with experience
  • Full travel reimbursement - flight, hotel, transportation, and daily meal stipend for Atlanta office visits
  • Health Insurance
  • PTO and Holidays
  • 401(k) with company match
  • Life Insurance & AD&D Insurance
  • Direct access to senior leadership and the opportunity to build something that matters
  • A lean, entrepreneurial culture that rewards results and moves fast when the right person is identified

Zywie is an Equal Opportunity Employer. Zywie does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.