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Process Quality Manager Jobs in Florida (NOW HIRING)

atrion

Quality Engineering Manager

Davie, FL · On-site

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 ...

The Walsh Group

Quality Manager

Fort Lauderdale, FL · On-site

Responsible for leading and managing quality processes such as work planning, pre-activity meetings, material management, Quality Incident Reports, Lesson Sharing and follow-up inspections.

Dometic

Quality Manager

Stuart, FL · On-site

Responsible for ensuring that all managers, process owners and supervisors develop and maintain their part of the quality management system. Ensure that customer requirements and expectations have ...

Smurfit-Westrock

Quality Manager

Jacksonville, FL · On-site

As a Quality Manager you will ensure that quality standards are met and maintained by understanding, implementing, and enforcing customer, regulatory, and Smurfit Westrock processes, policies, and ...

Xylem

Quality Manager

Jacksonville, FL · On-site

$90K - $130K/yr

Join our campus in Thomasville, GA. (Onsite) Relocation assistance is available as required Quality Manager - People & Process Leader with 5+ Years of Quality Experience and a BS in Engineering or ...

Australia-Employment

Quality Manager

Sanford, FL · On-site

$110K - $120K/yr

Manage quality control processes across production, including testing, inspection, and documentation. * Investigate non-conformances and implement corrective and preventive actions (CAPA)

New

InSpec Solutions LLC

Be Seen First

Quality Manager

Holly Hill, FL · On-site

$50K - $80K/yr

Design and execute document control processes, including electronic batch records, deviations, CAPAs, and change management. * Oversee product quality systems: incoming inspection, in-process checks ...

iMPact Business Group, Inc.

Quality Manager

Tampa, FL · On-site

Quality Manager Establishes, implements and maintains processes and programs that yield high quality products while creating and maintaining both a quality-centric and quality-focused culture for all ...

Wire Experts Group Inc.

Quality Manager

Naples, FL · On-site

Description : The Quality Manager leads continuous improvement, Lean Six Sigma execution ... Identify and prioritize improvements related to scrap, rework, cable defects, process variation ...

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Process Quality Manager information

What is a process quality manager?

Process Quality Managers are professionals responsible for ensuring that an organization's processes and products meet established quality standards. They design and implement quality control procedures, monitor production processes, and work to identify areas for improvement. These managers also lead audits, analyze data to prevent defects, and collaborate with various departments to uphold compliance with industry regulations. Their goal is to maintain high levels of customer satisfaction by ensuring consistent product or service quality.

What are some common challenges faced by process quality managers, and how can they be addressed?

Process Quality Managers often encounter challenges such as resistance to change from team members, balancing strict quality standards with production efficiency, and managing cross-functional communication. To address these issues, successful managers proactively engage stakeholders, provide clear training on quality processes, and foster a culture of continuous improvement. Collaboration and transparent communication with production, engineering, and leadership teams are key to overcoming obstacles and ensuring that quality initiatives are effectively implemented.

What are the key skills and qualifications needed to thrive as a process quality manager, and why are they important?

To thrive as a Process Quality Manager, you need a strong background in quality management, process improvement methodologies (such as Six Sigma or Lean), and a relevant degree in engineering, manufacturing, or a related field. Familiarity with quality management systems (QMS), statistical process control (SPC) tools, and certifications like Six Sigma Green/Black Belt or ISO 9001 Auditor are typically required. Outstanding analytical thinking, problem-solving abilities, leadership, and effective communication are vital soft skills for this position. These competencies ensure that quality standards are consistently met, processes are optimized, and teams are aligned to achieve organizational goals.

What is the difference between Process Quality Manager vs Quality Assurance Specialist?

AspectProcess Quality ManagerQuality Assurance Specialist
CertificationsSix Sigma, Lean, ISO certificationsISO, Six Sigma, or QA-specific certifications
Work EnvironmentManufacturing, production, or operational settingsProduct development, software, or service industries
ResponsibilitiesOversees process improvements, ensures process compliance, manages quality metricsTests products/services, identifies defects, implements QA procedures

The Process Quality Manager focuses on optimizing and maintaining manufacturing or operational processes, ensuring efficiency and compliance. In contrast, the Quality Assurance Specialist concentrates on testing and verifying products or services to meet quality standards. Both roles require similar certifications and often work within manufacturing or production environments, but their core responsibilities differ in scope and focus.

What cities in Florida are hiring for Process Quality Manager jobs?

Cities in Florida with the most Process Quality Manager job openings:

Process Quality Manager jobs near you
Infographic showing various Process Quality Manager 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.

Quality Engineering Manager

Davie, FL • On-site

atrion
Manufacturing • 501 - 1,000 employees
Learn more about atrionexternal

Full-time

Re-posted 18 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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