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Quality Control Manager Jobs in Boca Raton, FL (NOW HIRING)

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 ...

The position is responsible for assisting the Quality Control Manager in ensuring consistent, quality concrete within the region. Oversees regional concrete lab(s) and field technicians.

The position is responsible for assisting the Quality Control Manager in ensuring consistent, quality concrete within the region. Oversees regional concrete lab(s) and field technicians.

The position is responsible for assisting the Quality Control Manager in ensuring consistent, quality concrete within the region. Oversees regional concrete lab(s) and field technicians.

The position is responsible for assisting the Quality Control Manager in ensuring consistent, quality concrete within the region. Oversees regional concrete lab(s) and field technicians.

The position is responsible for assisting the Quality Control Manager in ensuring consistent, quality concrete within the region. Oversees regional concrete lab(s) and field technicians.

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Quality Control Manager information

See Boca Raton, FL salary details

$28.9K

$77.2K

$122.9K

How much do quality control manager jobs pay per year?

As of Aug 7, 2026, the average yearly pay for quality control manager in Boca Raton, FL is $77,173.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,400.00 and $94,900.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

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

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

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

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.
What are the most commonly searched types of Quality Control jobs in Boca Raton, FL? The most popular types of Quality Control jobs in Boca Raton, FL are:
What job categories do people searching Quality Control Manager jobs in Boca Raton, FL look for? The top searched job categories for Quality Control Manager jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Quality Control Manager jobs? Cities near Boca Raton, FL with the most Quality Control Manager job openings:
Infographic showing various Quality Control Manager job openings in Boca Raton, FL 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, with an average salary of $77,173 per year, or $37.1 per hour.

Manager, Quality Control (TAS)

Quality

Sunrise, FL

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 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.