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Manager Of Quality Control Jobs in Boca Raton, FL

The Quality Control Manager is responsible for all of these functions of the QC department, as well as full management of the QC Technicians, staff training and development, and ensuring that the ...

This role is responsible for auditing the quality of work on the production floor, verifying ... The Quality Control Manager serves as a key liaison between Quality Assurance, Safety, Engineering ...

This role is responsible for auditing the quality of work on the production floor, verifying ... The Quality Control Manager serves as a key liaison between Quality Assurance, Safety, Engineering ...

Head Of Quality The Head of Quality leads and oversees all quality functions across the ... Control, Microbiology, Validation, Compliance, and the Quality Management System (QMS). This ...

Supervises inspectors in Quality Control Operations Areas to ensure continuous workflow and ... Familiarity with management of non-conforming product. * Familiarity with sampling plans, and ...

QC Technician

Margate, FL · On-site

$17 - $21.75/hr

This includes supporting the implementation of QA/QC policies, conducting inspections, and ... assisting in vendor evaluations. This job profile is intended for support staff that follows ...

QC Technician

Margate, FL

$17 - $21.75/hr

This includes supporting the implementation of QA/QC policies, conducting inspections, and ... assisting in vendor evaluations. This job profile is intended for support staff that follows ...

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Manager Of Quality Control information

See Boca Raton, FL salary details

$28.9K

$77.2K

$122.9K

How much do manager of quality control jobs pay per year?

As of Aug 12, 2026, the average yearly pay for manager of quality control 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 are common challenges faced by a manager of quality control, and how can they be addressed?

A Manager of Quality Control often encounters challenges such as maintaining consistent quality standards across multiple shifts or teams, managing tight production deadlines while upholding compliance, and implementing new quality protocols. Addressing these challenges requires strong communication skills, effective training programs, and a proactive approach to problem-solving. Collaborating closely with production, engineering, and regulatory teams helps ensure that quality objectives are aligned with business goals, and regular audits or process reviews can help identify and resolve issues early.

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

AspectManager Of Quality ControlQuality Control Supervisor
CertificationsISO 9001, Six Sigma, Quality Management certificationsISO 9001, Six Sigma (preferred but not always required)
Work EnvironmentOversees multiple teams, strategic planning, higher-level managementSupervises daily quality control activities, team management
Industry UsageUsed across manufacturing, pharmaceuticals, food productionCommon in manufacturing, production facilities

The Manager Of Quality Control typically holds a higher strategic role, overseeing quality assurance processes and managing teams, while the Quality Control Supervisor focuses on daily operations and team supervision. Both roles require similar certifications and are integral in maintaining product standards within the same industries.

What skills and qualifications are needed to thrive as a manager of quality control?

To thrive as a Manager of Quality Control, you need expertise in quality assurance processes, statistical analysis, and regulatory compliance, typically supported by a relevant degree and experience in quality management. Familiarity with quality management systems (such as ISO 9001), Six Sigma or Lean certifications, and proficiency with data analysis tools are commonly required. Strong leadership, problem-solving abilities, and effective communication are vital soft skills in this role. These skills ensure consistent product quality, regulatory adherence, and efficient team performance, which are critical for organizational success.

What does a manager of quality control do?

A Manager of Quality Control oversees the quality assurance processes within an organization to ensure that products or services meet established standards. They develop and implement quality control procedures, lead a team of quality inspectors, and work closely with production and engineering teams to resolve quality issues. Additionally, they analyze data, conduct audits, and recommend improvements to enhance product reliability and customer satisfaction.
What are popular job titles related to Manager Of Quality Control jobs in Boca Raton, FL? For Manager Of Quality Control jobs in Boca Raton, FL, the most frequently searched job titles are:
What job categories do people searching Manager Of Quality Control jobs in Boca Raton, FL look for? The top searched job categories for Manager Of Quality Control jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Manager Of Quality Control jobs? Cities near Boca Raton, FL with the most Manager Of Quality Control job openings:

Manager, Quality Control (TAS)

Quality

Sunrise, FL

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 29 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.