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Manufacturing Quality Manager Jobs in Spring Hill, FL

Leads the Quality Team in managing and conducting the final quality and safety inspections of all products from each value stream which is manufactured within the operations, ensuring that each ...

Leads the Quality Team in managing and conducting the final quality and safety inspections of all products from each value stream which is manufactured within the operations, ensuring that each ...

In depth knowledge of electronic manufacturing processes including SMT, through-hole technology, assembly and test, and box build assembly * Thorough knowledge of quality management systems and ...

The Site Quality Manager is responsible for providing clear leadership for the development of an ... Six Sigma/Lean Manufacturing experience * Experience dealing with customers and suppliers

The Site Quality Manager is responsible for providing clear leadership for the development of an ... Six Sigma/Lean Manufacturing experience * Experience dealing with customers and suppliers

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The Operations Manager will work closely with Sales, Supply Chain, Quality, Engineering, and senior leadership to align manufacturing capabilities with customer and business requirements. We are ...

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QC Microbiologist I

Tampa, FL · On-site

$24 - $31.75/hr

Partner with manufacturing, quality, and external laboratories to ensure compliance and timely ... Experience using laboratory systems such as LIMS and electronic quality management systems.

Manage the issuance and receipt of gages to and from appropriate departments using Gagetrak ... manufacturing, quality, or related field · Solid knowledge of quality processes and measurement ...

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Manufacturing Quality Manager information

See Spring Hill, FL salary details

$55.1K

$85.4K

$109K

How much do manufacturing quality manager jobs pay per year?

As of Aug 22, 2026, the average yearly pay for manufacturing quality manager in Spring Hill, FL is $85,439.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,400.00 and $97,600.00 per year, depending on experience, location, and employer.

What does a manufacturing quality manager do?

A Manufacturing Quality Manager ensures that products meet quality standards and regulatory requirements in a production environment. They develop and implement quality control processes, conduct audits, and analyze data to identify areas for improvement. They also collaborate with teams to resolve production issues and enhance efficiency while maintaining compliance. Their role is crucial in minimizing defects, improving customer satisfaction, and ensuring operational excellence.

What are the key skills and qualifications needed to thrive as a manufacturing quality manager?

To thrive as a Manufacturing Quality Manager, you need strong knowledge of quality assurance processes, regulatory compliance, and manufacturing operations, usually supported by a bachelor's degree in engineering or a related field. Familiarity with quality management systems (like ISO 9001), statistical process control, Six Sigma methodologies, and relevant certifications such as CQE or Lean are commonly required. Strong leadership, problem-solving skills, and effective communication help you excel in team settings and drive continuous improvement initiatives. These competencies ensure consistent product quality, support regulatory requirements, and foster a culture of excellence on the manufacturing floor.

What are the most common challenges a manufacturing quality manager faces in a typical day?

Manufacturing Quality Managers often navigate challenges such as maintaining consistent product quality during high-volume production, investigating and resolving quality issues quickly, and ensuring compliance with changing industry standards. They regularly collaborate with production, engineering, and supply chain teams to implement process improvements and corrective actions. Balancing quality expectations with tight deadlines and cost pressures can be demanding, but effective managers use data-driven strategies and strong teamwork to achieve results. This role is dynamic and requires adaptability, attention to detail, and a commitment to ongoing process optimization.

What are popular job titles related to Manufacturing Quality Manager jobs in Spring Hill, FL?

For Manufacturing Quality Manager jobs in Spring Hill, FL, the most frequently searched job titles are:

What job categories do people searching Manufacturing Quality Manager jobs in Spring Hill, FL look for?

The top searched job categories for Manufacturing Quality Manager jobs in Spring Hill, FL are:

What cities near Spring Hill, FL are hiring for Manufacturing Quality Manager jobs?

Cities near Spring Hill, FL with the most Manufacturing Quality Manager job openings:

Infographic showing various Manufacturing Quality Manager job openings in Spring Hill, FL as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 19% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $85,439 per year, or $41.1 per hour.

Engineering Quality Manager

Composite Motors, Inc.

Brooksville, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago


Job description

ENGINEERING QUALITY MANAGER
Full-Time Monday-Friday
Benefits: Medical (UHC), Dental, Vision, Critical Illness, Short Term Disability, Life Insurance, 401k w/company match, paid holidays and PTO.
Position Overview:
The Engineering Quality Manager collaborates with the engineering team, supporting both New Product Development and ongoing manufacturing activities for medical devices. This professional collaborates closely with Engineering, Production and Operations to ensure that all products and processes meet applicable ISO 13485, ISO 9001, and 21 CFR 820 quality and regulatory requirements.
This role combines hands-on process verification and SPC activities with strategic improvement initiatives – ensuring design-transfer integrity, robust process capability, and sustainable quality controls. The position requires a self-motivated individual who can work independently while effectively partnering across departments. It is expected that this role will evolve into a broader Quality Management position, providing leadership continuity as the current Quality Manager advances within the organization.
Essential Job Functions:
  • Partner with Engineering on New Product Development projects to ensure quality is embedded throughout the design and development lifecycle.
  • Develop and maintain NPI quality documentation, including Process Flow Diagrams, PFMEAs, Control Plans, and Validation Protocols (IQ/OQ/PQ).
  • Perform and document process verifications, first article inspections, and SPC studies to establish baseline process capability and identify improvement opportunities.
  • Participate in design transfer and process validation activities to confirm that production processes consistently meet product requirements.
  • Analyze quality data, process trends, and CPK results to support data-driven decisions and corrective/preventive actions (CAPA).
  • Lead or support root cause analyses, nonconformance investigations, and risk management updates.
  • Update and maintain Methods of Manufacture (MOMs), tool and equipment documentation, and change notices as part of the document-control process.
  • Drive the creation and revision of SOPs, work instructions, and control procedures aligned with current best practices and regulatory expectations.
  • Train and mentor employees in quality control principles, process capability, and regulatory compliance to strengthen organizational quality culture.
  • Work independently to identify improvement opportunities, propose and implement corrective actions, and introduce new or refined controls that enhance product and process quality.
  • Support internal and external audits, supplier evaluations, and management reviews as required.
Required Qualifications:
  • Experience in Quality Engineering, Quality Assurance, or Manufacturing Quality within the medical-device or regulated manufacturing industry.
  • Strong working knowledge of ISO 13485, 21 CFR 820, and ISO 9001 Quality Management Systems.
  • Hands-on experience with Statistical Process Control, process verification/validation, root cause analysis, and CAPA systems.
  • Proficiency in developing and maintaining PFMEA, Control Plans, and validation protocols.
  • Demonstrated ability to lead cross-functional teams, communicate effectively, work independently, and drive sustainable improvements.
  • Exceptional attention to detail and organizational discipline in managing documentation and data.