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Manager Qc Jobs in Florida (NOW HIRING)

Quality

Manager, Quality Control (TAS)

Sunrise, FL

Management of QA/QC staff, GMP and ISO compliance. Job Details/Responsibilities * Manages Production Quality staff overseeing Receiving Inspection, Cleanroom, and Final Release areas, including all ...

CACI International, Inc.

Quality Control Manager

Tampa, FL · On-site

$65K - $136K/yr

Quality Control Manager Job Category: Project and Program Management Time Type: Full time Minimum Clearance Required to Start: TS/SCI Employee Type: Regular Percentage of Travel Required: Up to 10% ...

Cape Fox Corporation

Site Quality Control (QC) Manager

FL · On-site

$95K - $125K/yr

Job Title Site Quality Control (QC) Manager This position is contingent upon award. Cape Fox, subsidiary Mountain Point is seeking a qualified Site Quality Control (QC) Manager. This candidate will ...

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Manager Qc information

See Florida salary details

$17.9K

$64.4K

$118.1K

How much do manager qc jobs pay per year?

As of Jul 27, 2026, the average yearly pay for manager qc in Florida is $64,386.00, according to ZipRecruiter salary data. Most workers in this role earn between $32,900.00 and $101,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Manager QC, and why are they important?

To thrive as a Manager QC (Quality Control), you need a solid background in quality assurance processes, analytical testing, and industry regulations, typically supported by a degree in science or engineering. Familiarity with quality management systems (like ISO standards), statistical analysis software, and certification such as Six Sigma or ASQ is often required. Strong leadership, problem-solving, and communication skills help drive team performance and handle complex quality issues. These skills are essential for maintaining product standards, ensuring regulatory compliance, and supporting continuous improvement within the organization.

What are Manager QC responsibilities?

A Manager QC (Quality Control Manager) is responsible for overseeing the quality assurance processes within a company to ensure that products meet required standards and specifications. They develop and implement quality control procedures, supervise QC staff, conduct audits, and analyze quality data to identify areas for improvement. Additionally, they collaborate with other departments to resolve quality issues and ensure compliance with industry regulations. Their ultimate goal is to maintain consistent product quality and customer satisfaction.

What is the difference between Manager Qc vs Quality Assurance Supervisor?

AspectManager QcQuality Assurance Supervisor
ResponsibilitiesOversees quality control processes, manages teams, implements quality policiesSupervises QA team, conducts inspections, ensures compliance with standards
CredentialsBachelor's degree in related field, experience in quality management, certifications like CQEBachelor's degree, experience in quality assurance, certifications like CQE or ASQ certifications
Work EnvironmentManagement level, strategic planning, cross-department collaborationOperational level, hands-on inspections, team supervision
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, electronics, consumer goods

The main difference between a Manager Qc and a Quality Assurance Supervisor lies in scope and level of responsibility. The Manager Qc typically handles strategic oversight and manages multiple teams, while the QA Supervisor focuses on daily supervision and operational tasks. Both roles require similar credentials and are vital in quality management across industries.

What are some common challenges a Manager QC faces when balancing regulatory compliance with production timelines?

A Manager QC (Quality Control) often faces the challenge of ensuring that all products meet strict regulatory standards while also supporting the company's production goals. This balancing act requires effective communication with production and regulatory teams, as well as proactive planning to anticipate potential bottlenecks. Managers must remain vigilant about documentation and testing, and be prepared to address unforeseen quality issues without causing significant delays. Success hinges on strong leadership, a detail-oriented mindset, and the ability to adapt quickly to changing priorities.
What are the most commonly searched types of Qc jobs in Florida? The most popular types of Qc jobs in Florida are:
What cities in Florida are hiring for Manager Qc jobs? Cities in Florida with the most Manager Qc job openings:
Manager Qc jobs near you
Infographic showing various Manager Qc job openings in Florida as of July 2026, with employment types broken down into 84% Full Time, 14% Part Time, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $64,386 per year, or $31 per hour.
Manager, Quality Control (TAS)

Manager, Quality Control (TAS)

Quality

Sunrise, FL

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago

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

Responsible for supporting the quality control staff in the receiving inspection, in-process and finished product and maintaining processes and methods in accordance with the company standards. Reporting on the performance of the assigned quality areas. Management of QA/QC staff, GMP and ISO compliance.

Job Details/Responsibilities
  • Manages Production Quality staff overseeing Receiving Inspection, Cleanroom, and Final Release areas, including all inspectors, analysts, and technicians that report into the supervisors of those areas.
  • Identifies, Reports and Monitors Nonconforming events for the Receiving, Cleanroom, Final Packaging and Release areas.
  • Performs product failure investigations and implements corrective and preventive actions to prevent reoccurrence.
  • Interacts with cross-functional teams to resolve quality issues. 
  • Quality Control, product release authorizations, and quarantine of all suspect or discrepant product.
    Develops Quality Instructions and Quality Standards.
    Support in the development, validation, and implementation of Test Methods.
  • Reviews and approves engineering changes to support product life cycle.
  • Provides adequate QA support to the assigned areas and responds to Internal Audits, and takes actions as appropriate based on CAPAs, Complaints investigations, Nonconforming events, etc.
  • Supports the Corrective and Preventive Action (CAPA) System.
  • Identifies and evaluates fundamental compliance issues for major functional areas through assessment of quality system compliance.
  • Establishes Quality Assurance objectives and assignments, and delegates assignments to subordinates.
  • Involved in executing company policies.  
  • Recommends decisions on administrative or operational matters and ensures Quality Assurance(s) effective achievement of objectives.
  • Ensure compliance with all quality systems regulatory requirements such as, but not limited to, ISO 13485, 21 CFR Part 820, MDSAP, MDD (93/42/EEC) and MDR (EU 2017/745)
  • Responsible for addressing issues within the QMS without undue delay as evidenced by on time completion of actions on the Single Action Tracker (SAT)
Job Responsibilities (continued)
Working Conditions/Physical Requirements
Knowledge, Skills and Abilities (KSA)
  • Works with all levels within the company.
  • Strong communication skills (written and oral)
  • Ability to organize and conduct multiple, parallel tasks.
  • Ability to seek and utilize varied resources.
  • Ability to influence others.
  • Understanding of medical device design and process controls per FDA Quality System Requirements (QSRs) and ISO 13485.
  • Understanding of required standards / regulations impacting Medical Devices.
  • Leadership ability and organizational skills.
  • Strong team-oriented professional with good interpersonal skills who is hands-on with a high energy approach to work.
Qualifications/ Background Experiences
  • A bachelor’s degree or equivalent experience in Engineering, Quality Engineering or Sciences.
  • 8+ years of related experience in a regulated environment in Quality Assurance and or Manufacturing/ Engineering environment.
  • Must have experience handling nonconforming events.
  • Packaging/Labelling process experience is a plus.
  • SAP knowledge is a plus.

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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