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Senior Quality Systems Engineer Jobs in Florida (NOW HIRING)

CIRCOR International, Inc.

Senior Quality Engineer

Tampa, FL · On-site

$83K - $113K/yr

Sr Quality Engineer ORGANIZATIONAL STRUCTURE BUSINESS: Leslie Controls, Inc LOCATION: Tampa, FL ... Conduct and participate in quality system, process, and product audits * Provide technical ...

Danaher

Senior Quality Engineer

Pensacola, FL · On-site

$83K - $113K/yr

And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact ... The Senior Quality Engineer is responsible for ensuring the quality of membrane products and ...

Danaher

Senior Quality Engineer

Pensacola, FL

$83K - $113K/yr

And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact ... The Senior Quality Engineer is responsible for ensuring the quality of membrane products and ...

ECS

Senior Systems Engineer

Orlando, FL · On-site

$120K - $130K/yr

Review test plans, procedures, and results to ensure quality outcomes Senior Systems Engineer will bring strong systems engineering fundamentals, experience with virtual training technologies, and ...

Vhr_unither

Senior Quality Engineer

Jacksonville, FL · On-site

$82K - $111K/yr

Who You Are The Senior Quality Control Engineer performs activities supporting the full equipment ... Troubleshoot and resolve equipment, system, and process issues using established procedures and ...

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All JobsQuality Systems Engineer JobsSenior Quality Systems Engineer JobsSenior Quality Systems Engineer Jobs in Florida

Senior Quality Systems Engineer information

See Florida salary details

$45.2K

$78.7K

$109.5K

How much do senior quality systems engineer jobs pay per year?

As of Aug 10, 2026, the average yearly pay for senior quality systems engineer in Florida is $78,684.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,100.00 and $89,700.00 per year, depending on experience, location, and employer.

What are some typical challenges senior quality systems engineers face when implementing new quality management processes?

Senior Quality Systems Engineers often encounter challenges such as aligning new quality processes with existing company workflows, ensuring cross-departmental buy-in, and managing documentation compliance with industry standards like ISO 9001 or FDA regulations. Balancing the need for thorough process controls while maintaining operational efficiency can also be demanding. Success in this role often depends on strong communication and project management skills to lead teams through change and continuous improvement initiatives.

What is the difference between Senior Quality Systems Engineer vs Quality Engineer?

AspectSenior Quality Systems EngineerQuality Engineer
CertificationsISO 9001, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentManufacturing, aerospace, medical devices, regulated industriesManufacturing, electronics, consumer products
ResponsibilitiesDeveloping quality systems, ensuring compliance, process improvementProduct testing, inspection, process monitoring

The Senior Quality Systems Engineer typically focuses on developing and maintaining quality management systems, ensuring compliance with industry standards, and leading process improvements. Quality Engineers often concentrate on product testing, inspection, and day-to-day quality assurance tasks. Both roles require similar certifications and work in related industries, but the senior role involves more strategic oversight and system-level responsibilities.

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

To thrive as a Senior Quality Systems Engineer, you need a deep understanding of quality management principles, regulatory standards (such as ISO 9001 or FDA QSR), and a degree in engineering or a related field. Familiarity with tools like CAPA systems, audit management software, and certifications such as Six Sigma or ASQ Certified Quality Engineer are typically required. Strong analytical skills, attention to detail, and the ability to communicate effectively across teams are crucial soft skills. These competencies ensure robust quality systems, regulatory compliance, and continuous improvement in product and process quality.

What does a senior quality systems engineer do?

A Senior Quality Systems Engineer is responsible for developing, implementing, and maintaining quality management systems within an organization. They ensure that processes comply with industry standards and regulatory requirements, often leading audits, analyzing data, and driving continuous improvement initiatives. These professionals collaborate with cross-functional teams to resolve quality issues, develop documentation, and provide training on quality best practices. Their work helps ensure products and services consistently meet customer and regulatory expectations.
What are popular job titles related to Senior Quality Systems Engineer jobs in Florida? For Senior Quality Systems Engineer jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Senior Quality Systems Engineer jobs in Florida look for? The top searched job categories for Senior Quality Systems Engineer jobs in Florida are:
What cities in Florida are hiring for Senior Quality Systems Engineer jobs? Cities in Florida with the most Senior Quality Systems Engineer job openings:
Senior Quality Systems Engineer jobs near you
Infographic showing various Senior Quality Systems Engineer job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $78,684 per year, or $37.8 per hour.

Sr. Quality Systems Engineer (TAS)

Terumo Corporation

Sunrise, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

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

Job description

At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to find the right fit for each patient anatomy.
The company has over 1,250 associates around the world with manufacturing facilities in Glasgow, Scotland and Sunrise, Florida.
Terumo Aortic is focused on the continuing development of new and innovative products driving the growth of the business globally. Associates are part of a stimulating and exciting environment in which they can develop their skills and achieve career goals. Working for the company, each associate's role contributes greatly to helping to save or improve the lives of patients in over 100 countries worldwide.
At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients.
Join us and help shape wherever we go next!
Advancing healthcare with heart
www.terumoaortic.com
Job Summary
Provides technical support to the maintenance and improvement of the quality systems. Develops quality standards and controls. Develops, process and systems qualification protocols for new systems and existing manufacturing production lines. Advises company management on quality assurance requirements. Review non-conformance reports along with product risk assessment and performs root cause investigations.
Job Details/Responsibilities
Quality engineering, system and process validation, project team leadership and participation, document generation and control, data analysis, corrective and preventive action.
  • Prepares and implements quality standards, operating procedures and reporting systems.
  • Conducts training to end-users of Quality Management Systems, specifically the CAPA process.
  • Supports CAPA and auditing programs and performs assigned actions to address quality issues.
  • Interacts with cross-functional teams to obtain system requirements and feedback to implement preventive and/or corrective actions.
  • Manages and provides status of assigned projects to the management team. Identifies areas of risk and recommends mitigation actions.
  • Prepares and implements proposals of improvement to the quality management system. Provides follow-up actions as necessary.
  • Develops quality plans, validation plans, risk assessments and other validation related deliverables for the implementation of the CAPA Process.
  • Ensures quality system compliance for areas of responsibility.
  • Reviews, approves changes under the change management system, as required.
  • Initiate investigations and product performance risk analysis for issues related to the quality management system.
  • Leads CAPA Review Board meetings

Job Responsibilities (continued)
Working Conditions/Physical Requirements
QUALITY REQUIREMENTS
  • Maintain awareness of the relevance and importance of activities performed and how they contribute to the achievement of quality objectives
  • Work within the QMS at all times, ensure accurate completion of records and highlight issues to immediate supervisor any issues affecting quality
  • Responsible to ensure facility, processes and documentation remain in a state of audit readiness at all times

EH&S REQUIREMENTS
  • Take care of your own health and safety and that of others who maybe affected by your actions
  • Work co-operatively to highlight issues affecting Environmental Health and Safety

Knowledge, Skills and Abilities (KSA)
  • Excellent Written and Verbal Communication
  • Understanding of quality system regulations (ISO13485, 21CFR820)
  • Working knowledge of Computerized System Validation requirements for Medical Devices (21CFR Part 11).
  • Ability to interact with all levels within organization
  • Analytical skills for compiling and analyzing data
  • Systems and customer service oriented.
  • Knowledge of DOE, SPC, Gage R&R, and sampling plans
  • Computer and software skills
  • Ability to motivate others and work independently

Qualifications/ Background Experiences
  • Bachelor's degree in a technical discipline, or equivalent, with a minimum of five years of experience in medical device quality assurance.
  • Experience with class III cardiovascular medical devices
  • Thorough understanding of quality system regulations (e.g. 21CFR820, ISO 13485)

It is Terumo's policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.
Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program.

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