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Director Quality Systems Jobs in Florida (NOW HIRING)

Boeing

Experienced Quality Systems Specialist

Hialeah, FL · On-site

$79K - $112K/yr

Experienced Quality Systems Specialist Company: Boeing Distribution, Inc. Boeing Global Services ... Ability to influence without direct authority Conflict of Interest: * Successful candidates for ...

Boeing

Experienced Quality Systems Specialist

Hialeah, FL · On-site

$79K - $112K/yr

Experienced Quality Systems Specialist Company: Boeing Distribution, Inc. Boeing Global Services ... Ability to influence without direct authority Conflict of Interest: * Successful candidates for ...

Malibu Boats Inc.

Quality Director

Fort Pierce, FL · On-site

Lead all aspects of the Quality Management System (QMS). * Establish quality goals, KPIs, and ... director level. * Experience in marine, automotive, recreational vehicle, aerospace, heavy ...

Advita Ortho

Manager, Quality Engineering

Gainesville, FL · On-site

$90 - $120/hr

Director, Quality Management Systems Description Provide quality engineering leadership by inspiring individuals and teams while creating an environment of organizational excellence to deliver ...

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Director Quality Systems information

See Florida salary details

$23.2K

$93.9K

$159.5K

How much do director quality systems jobs pay per year?

As of Sep 4, 2026, the average yearly pay for director quality systems in Florida is $93,860.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,000.00 and $112,800.00 per year, depending on experience, location, and employer.

What is a director quality systems?

A Director of Quality Systems is a senior management professional responsible for overseeing the development, implementation, and maintenance of an organization's quality management systems. They ensure that products and processes comply with industry standards, regulatory requirements, and company policies. This role often involves leading teams, developing quality strategies, conducting audits, and driving continuous improvement initiatives across the organization. Directors of Quality Systems play a critical part in safeguarding product quality, customer satisfaction, and regulatory compliance.

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

To thrive as a Director of Quality Systems, you need deep expertise in quality management principles, regulatory compliance, process improvement, and typically a relevant degree such as in engineering or life sciences. Familiarity with quality management systems (QMS) like ISO 9001, FDA regulations, and proficiency with tools such as CAPA, risk management software, and internal audit systems is essential. Strong leadership, strategic thinking, and effective communication distinguish top performers in this role. These skills ensure the organization maintains high quality standards, meets regulatory requirements, and drives continuous improvement across all operations.

What are some common challenges faced by a director quality systems when implementing new compliance standards across an organization?

A Director of Quality Systems often encounters challenges such as resistance to change from staff, alignment of existing processes with new regulatory requirements, and ensuring consistent training across departments. Effective communication and cross-functional collaboration are key to overcoming these hurdles. The role typically involves working closely with leadership, operations, and regulatory teams to ensure that new standards are understood and integrated smoothly, minimizing disruptions while maintaining compliance.

What is the difference between Director Quality Systems vs Quality Manager?

AspectDirector Quality SystemsQuality Manager
ResponsibilitiesOversees quality systems, compliance, and strategic quality initiatives across departmentsManages daily quality operations, audits, and team supervision
CertificationsISO 9001 Lead Auditor, CQE, Six SigmaISO 9001 Lead Auditor, CQE, Six Sigma
Work EnvironmentStrategic planning, cross-departmental collaborationOperational focus, team management
Industry UsageCommon in regulated industries like pharmaceuticals, medical devicesWidely used in manufacturing, production facilities

The main difference between a Director Quality Systems and a Quality Manager lies in scope and strategic focus. The Director typically oversees the entire quality system, ensuring compliance and strategic alignment, while the Quality Manager handles daily quality operations and team supervision. Both roles often require similar certifications and work in regulated industries, but the Director's role is more strategic and cross-departmental.

What are the most commonly searched types of Quality Systems jobs in Florida?

The most popular types of Quality Systems jobs in Florida are:

What are popular job titles related to Director Quality Systems jobs in Florida?

For Director Quality Systems jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Director Quality Systems jobs in Florida look for?

The top searched job categories for Director Quality Systems jobs in Florida are:

What cities in Florida are hiring for Director Quality Systems jobs?

Cities in Florida with the most Director Quality Systems job openings:

Director Quality Systems jobs near you
Infographic showing various Director Quality Systems 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 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $93,860 per year, or $45.1 per hour.

Director, Quality and Compliance

Gift of Life Marrow Registry Inc

Boca Raton, FL • On-site

Full-time

Posted yesterday

New

Job description

Education

Bachelor’s degree in biology, biochemistry or related scientific field required

Summary Statement

The Director of Quality and Compliance reports to the Chief Quality and Compliance Officer and provides onsite support to the quality and compliance strategies of the organization. The position strives to ensure that the product or service the organization provides is fit for its purpose and meets customer expectations and regulatory standards and compliance.

Responsibilities: 

  • Oversee quality system requirements to ensure the organization complies with federal (i.e. FDA) and state (i.e. Department of Health) regulatory requirements and standards promulgated by relevant accrediting bodies (i.e. WMDA, FACT, NMDP, AABB)
  • Keeps abreast of laws and regulations that may affect the organization’s policies, on an ongoing basis through industry bulletins, journals, meetings and seminars 
  • Works with Associate Director, Quality and Compliance to ensure smooth daily operations within the QA department.
  • Works with departmental directors to apply for relevant accreditations in the industry
  • Maintains organization’s existing and future accreditations and certifications
  • Provides training across the organization regarding applicable quality and regulatory issues
  • Promotes quality achievement and performance improvement throughout the organization
  • Enforces QA compliance objectives and ensures that targets are achieved
  • Other duties as assigned

Knowledge, Skills and Experience:

  • Certified Quality Auditor or other quality certification required
  • Minimum of 10 years’ experience in Biopharmaceutical quality assurance with practical knowledge in quality systems, FDA, cGMPs, cGTPs, cGLPs and ATMP regulations
  • At least 5 years’ direct QA experience in cell and gene therapy or biologics manufacturing.
  • Prior experience with obtaining and maintaining FACT accreditation required
  • Strong leadership ability, mentoring skills, and demonstrated ability to guide, train and provide constructive feedback to staff
  • Strong commitment to quality practices
  • Prior experience hosting regulatory inspections and providing oversite for cleanroom environments
  • Strong background in aseptic processing and environmental monitoring data analysis
  • Experience with autologous and allogeneic donor workflows
  • Excellent organizational skills, attention to detail, ability to multi-task effectively and customer service skills 
  • Effective, clear and concise oral and written English communication abilities
  • Knowledge of business principles relating to goal attainment 
  • Knowledge of measurement / benchmarking techniques for continuous process improvement

Physical Demands

This position is basically sedentary with some walking, standing, stooping and lifting required.  Occasional lifting of objects weighing in excess of 20 pounds.  Travel may also be required.


This job description is not intended to be all inclusive.  Duties and/or responsibilities may be added or deleted as management requires to meet the ongoing needs of the organization.