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Risk Management Quality Engineer Jobs in Florida

atrion

Quality Engineering Manager

Davie, FL · On-site

Apply basic risk management principles to all aspects of the quality system. Qualifications : Required * Technical Engineering or Science degree at the Bachelor level or above. * 8+ years of quality ...

Mainstream Engineering

Quality Engineer

Rockledge, FL · On-site

$63K - $82K/yr

... risk management process * Maintaining quality records that document the quality status of incoming ... AS or BS in Engineering, Quality Assurance, Manufacturing, or applicable technical field and/or a ...

Mainstream Engineering

Quality Engineer

Rockledge, FL · On-site

$63K - $82K/yr

... risk management process * Maintaining quality records that document the quality status of incoming ... AS or BS in Engineering, Quality Assurance, Manufacturing, or applicable technical field and/or a ...

Comrise

Quality Engineer

Miami, FL · On-site

$90/hr

Track and manage quality non-conformances identified through production audits and vehicle release ... Risk Mitigation (PFMEA & Control Plans): Support the development, review, and optimization of ...

Mainstream Engineering

Quality Engineer

Rockledge, FL · On-site

$63K - $82K/yr

Position SummaryThe Quality Engineer for Mainstream is responsible for developing and leading all ... risk management processMaintaining quality records that document the quality status of incoming ...

Denken Solutions, Inc.

Quality Engineer

Miami, FL · On-site

$91.50/hr

Manage quality issue tracking to implement Containment, drive Root Cause Analysis and Corrective ... Support develop and review of PFMEA and Control Plans to ensure compliance and robust risk ...

atrion

Quality Engineer

Davie, FL · On-site

$66K - $85K/yr

Manages engineering projects. Supports the internal and external audit program. Uses statistical ... Develop and maintain risk management files and quality control plans for components, devices and ...

VIVEX BIOLOGICS INC

Manager, Quality Engineer

Miami, FL · On-site

$68K - $88K/yr

Job purpose The Quality Engineer Manager will be responsible for developing, revising, and ... Responsible for initiating and leading technical investigations, risk assessments (including FMEA ...

Socket.dev

Manager, Quality Engineer

Miami, FL · On-site

$120 - $180/hr

Job purpose The Quality Engineer Manager will be responsible for developing, revising, and ... Responsible for initiating and leading technical investigations, risk assessments (including FMEA ...

VIVEX Biologics, Inc.

Manager, Quality Engineer

Miami, FL · On-site

$68K - $88K/yr

Job purpose The Quality Engineer Manager will be responsible for developing, revising, and ... Responsible for initiating and leading technical investigations, risk assessments (including FMEA ...

Honeywell

Sr Supplier Quality Engineer

Palmetto, FL · On-site

As a Sr Quality Engineer here at Honeywell, you will play a pivotal role in ensuring the quality ... Maintain Supply Chain Risk Management Plans and develop and maintain Supplier Management (Quality ...

Danaher

Senior Quality Engineer

Pensacola, FL · On-site

$83K - $113K/yr

The Senior Quality Engineer is responsible for ensuring the quality of membrane products and ... Lead root cause analysis and implement CAPA for nonconformities using the risk management processes.

CACI

Program Quality Engineer

Melbourne, FL · On-site

$66K - $86K/yr

Engineering and Technical Support Time Type: Full time Minimum Clearance Required to Start: None ... risk management, and compliance. Provide end-to-end quality oversight across planning, design ...

Treace

Quality Engineer

Ponte Vedra, FL · On-site

$65K - $84K/yr

Responsible for creating and maintaining process risk management files to meet FDA and ISO ... Quality Engineering) within an FDA compliant Title 21 section 820 environment Additional ...

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All JobsRisk Management Quality Engineer JobsRisk Management Quality Engineer Jobs in Florida

Risk Management Quality Engineer information

What is the difference between Risk Management Quality Engineer vs Quality Engineer?

AspectRisk Management Quality EngineerQuality Engineer
CertificationsISO 9001, Six Sigma, Risk Management certificationsISO 9001, Six Sigma, Quality Management certifications
Work EnvironmentManufacturing, aerospace, automotive, industries with risk assessment focusManufacturing, software, healthcare, quality assurance roles
Primary FocusIdentifying and mitigating risks to ensure product safety and complianceEnsuring product quality, process improvements, defect reduction

The Risk Management Quality Engineer focuses on identifying and mitigating risks to ensure safety and compliance, often working in industries like aerospace and automotive. In contrast, a Quality Engineer concentrates on improving product quality and reducing defects across various sectors. While both roles require similar certifications and work environments, their core responsibilities differ in scope and focus.

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

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Risk Management Quality Engineer jobs near you
Infographic showing various Risk Management Quality Engineer job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution.

Quality Engineering Manager

atrion

Davie, FL • On-site

Full-time

Re-posted 10 days ago

Job description

JD534-016: 

Position:

Manager, Quality Engineering

Department:

Reports To:

Vice President, Quality Assurance & Regulatory Affairs

FLSA Status:

JD Number:

JD534-016

Revision:

A

Summary:

Manages the Quality Engineering team to support new product development, process quality, CAPA, post-market compliance, supplier management, project management, internal & external auditing, and risk management activities with respect to global regulatory requirements and MDSAP (FDA, ISO, EU MDR, ANVISA, MHLW, and TGA). 

 

 

General Duties and Responsibilities:

 

  • Ensure the ongoing integrity, adequacy, and appropriateness of the Quality Management System and associated processes.  
  • Provide technical support, leadership and quality guidance to multi-functional teams, including Quality, Regulatory, R&D, Operations, Engineering, and Marketing.
  • Select, develop, and evaluate Quality Engineering staff to support all aspects of design and manufacturing quality.
  • Act as assistant to the Management Representative during regulatory and customer audits.
  • Develop and implement and improve efficient quality systems processes. 
  • Utilize project management strategy at a department level to successfully execute multiple projects with competing resources and prioritization. 
  • Establish and maintain quality metrics and utilizes KPIs to drive improvements.
  • Manage the CAPA program (to include Complaints, SCARs, NCMRs, Audit Non-Conformances and Corrective & Preventive Action projects).  Ensure thorough investigations and implement effective corrective actions to prevent recurring issues.
  • Utilize root cause analysis and statistical techniques for complex problem solving of technical product and manufacturing issues.  
  • Ensure a high level of supplier quality through effective supplier evaluation, approval, and monitoring processes.  Collaborate with internal supply chain and external suppliers to drive continual improvement of supplier quality. 
  • Develop and maintain FMEAs, Controls Plans, and SOPs to identify and mitigate risks. 
  • Support the development and validation of new products and production lines.  
  • Write, review, and approve documents (SOPs, Protocols, Reports, and ECOs) pertaining to key quality system elements affecting product quality.
  • Apply basic risk management principles to all aspects of the quality system.

 

Qualifications:

Required

  • Technical Engineering or Science degree at the Bachelor level or above.
  • 8+ years of quality engineering experience in a highly regulated industry.
  • 3+ years managing team members with varied backgrounds, experience, and technical capabilities.
  • Excellent working knowledge of medical device regulations and industry standards pertaining to manufacturing (FDA 21 CFR Part 820, ISO 13485, EU MDR (2017/745), the Medical Device Single Audit Program (MDSAP), and ISO 14971), IEC 60601.. 
  • Demonstrated project management skills, including the ability to prioritize and manage multiple project workloads in a highly dynamic production environment.
  • Solid working background utilizing quality management methods and tools (CAPA, Root Cause Analysis, FMEA, Control Plans, Statistical Techniques, MSA, etc.)
  • Demonstrated experience using trending and analysis reporting to drive organizational improvements.
  • Ability to develop and deliver clear communications (written and verbal), ensuring timely and relevant communication.
  • Some travel, domestic or international, may be required (up to 25%).

 

Preferred

  • ASQ Certified Quality Manager or Certified Quality Engineer
  • ISO 13485 Lead Auditor
  • Lean Six Sigma Green Belt or Black Belt
  • Working knowledge of IEC 60601 and IEC 62366
  • Experience with sterile product assembly and packaging
  • Experience with electronics assembly

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