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Quality Assurance Systems Jobs (NOW HIRING)

The Role The QA Systems Manager is responsible for technical and documentation aspects of our ISO 9001 based Quality Management System, which includes the Integrated Management System Manual, work ...

The Role The QA Systems Manager is responsible for technical and documentation aspects of our ISO 9001 based Quality Management System, which includes the Integrated Management System Manual, work ...

QA Systems Manager At Guerbet, we build lasting relationships so that to enable people to live better . This is Our Purpose. We are a global leader in medical imaging, offering an extensive portfolio ...

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The Food Safety & Quality (FSQ) Systems Lead assists FSQ Management in the maintenance and improvement of overall product quality and safety programs, procedures, and policies. This position will be ...

At Samuel Packaging Systems Group, we are committed to providing our customers with innovative, high quality, cost-effective packaging systems, supplies and solutions. Our technical expertise takes ...

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Quality Assurance Systems information

What are some common challenges faced by professionals in Quality Assurance Systems and how can they be addressed?

Professionals in Quality Assurance Systems often encounter challenges such as keeping up with evolving industry standards, ensuring cross-departmental compliance, and managing documentation for audits. These challenges can be effectively addressed by fostering strong communication with other teams, regularly participating in training to stay current with regulations, and implementing robust document management systems. Proactively engaging in continuous improvement initiatives also helps QA teams adapt to changes and maintain high standards consistently.

What are Quality Assurance Systems?

Quality Assurance Systems are structured processes and procedures used by organizations to ensure that their products or services meet specific quality standards and regulatory requirements. These systems involve creating guidelines, conducting audits, monitoring performance, and continuous improvement to prevent defects and maintain consistency. By implementing Quality Assurance Systems, companies can increase customer satisfaction, reduce errors, and comply with industry regulations. They are commonly used in industries such as manufacturing, healthcare, and software development.

What is the difference between Quality Assurance Systems vs Quality Control Inspectors?

AspectQuality Assurance SystemsQuality Control Inspectors
Primary FocusDeveloping and maintaining quality processes and systemsInspecting products to identify defects
CredentialsCertifications like ASQ CQE, ISO auditor trainingTraining in inspection techniques, sometimes certifications like Certified Quality Inspector
Work EnvironmentDesigning procedures, audits, process improvementsConducting physical or visual product inspections
Industry UsageUsed across manufacturing, software, healthcare for system developmentCommonly found in manufacturing, production lines, warehousing

While Quality Assurance Systems focus on creating and improving quality processes, Quality Control Inspectors are responsible for checking products for defects. Both roles are essential in ensuring product quality but differ in their approach and responsibilities.

What are the key skills and qualifications needed to thrive as a Quality Assurance Systems professional, and why are they important?

To thrive as a Quality Assurance Systems professional, you need a strong understanding of quality management principles, process improvement methodologies, and industry regulations, often supported by a degree in engineering or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and audit software is typically required, and certifications like Six Sigma or ASQ are highly valued. Attention to detail, problem-solving abilities, and strong communication skills help professionals excel when identifying issues and collaborating across departments. These skills are crucial for maintaining high product standards, ensuring compliance, and driving continuous improvement within an organization.
More about Quality Assurance Systems jobs
Infographic showing various Quality Assurance Systems job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 89% Full Time, 7% Part Time, and 3% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.
Quality Assurance Systems Manager

Quality Assurance Systems Manager

Fujifilm

Pueblo, CO • On-site

Full-time

Posted 19 days ago


Fujifilm rating

8.3

Company rating: 8.3 out of 10

Based on 66 frontline employees who took The Breakroom Quiz

47th of 516 rated manufacturers


Job description

FUJIFILM Electronic Materials, U.S.A., Inc., is a global leader in chemical solutions which enable the semiconductor industry and the digital universe. We have an exciting opportunity at our Pueblo, CO facility for a Quality Assurance Systems Manager!

With state-of-the-art manufacturing facilities in the U.S., Europe, Taiwan, China, Korea and Japan, local sales offices throughout the world and on-site applications support, FUJIFILM Electronic Materials supplies the world's top tier semiconductor manufacturers with a broad array of products and services used throughout the semiconductor manufacturing process.

The Role

The QA Systems Manager is responsible for technical and documentation aspects of our ISO 9001 based Quality Management System, which includes the Integrated Management System Manual, work procedures and instructions, related employee training, document control, internal audits, and continuous improvement.

This individual will ensure the IMS system is effective, efficient, and intuitive, and all processes within it continually evolve to meet the ongoing needs of the company, customers, and employees.

The dimensions of the job include interacting with all members of the Site Manager’s staff, and all members of Quality Departments. Interface with all the key Business unit leaders.


FUJIFILM Electronic Materials, U.S.A. fuels innovation in the semiconductor industry—where chemistry meets technology. Our advanced materials and formulations enable manufacturers to build the microchips that power Artificial Intelligence, computers, electric vehicles, smartphones, and more.


We’re a global business-to-business supplier of chemical formulations and advanced materials used for manufacturing and packaging semiconductors. Our chemical formulations allow top manufacturers to produce microchips that both power and connect our digital world. Think you’ve got what it takes to build a more connected world? Then connect with us today and challenge the boundaries of what’s possible—for the world and your future.


We have six U.S. manufacturing and Research & Development facilities, located in: Mesa, Arizona; Castroville, California; Hollister, California; Carrollton, Texas; and North Kingstown, Rhode Island—each offering unique local experiences, from vibrant cultural scenes to historic charm.


Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers


Key responsibilities for this role include:

  • Support the Pueblo site with ISO 9001, 14001 and 45001 certification maintenance.
  • Coordinate the preparation for external certifications.
  • Lead and maintain IMS related system permissions.
  • Lead regulatory audits for the 3 ISOs (9001/14001/45001) in coordination with EHS and other departments, as required.
  • Actively lead and participate in internal and external customer quality audits.
  • Coordinate and lead the response to customer quality surveys.
  • Support the administration of ETQ Software. Partner with the Document Control and Training Administrator to resolve issues and identify areas where functionality and utility can be improved.
  • Support the implementation and maintenance of IMS tools to achieve desired results.
  • Coordinate annual Integrated Management Review with upper management and all stakeholders.
  • Define internal audit schedule to cover all areas required to be audited by IMS.
  • Coordinate the internal audit process. Manage progress against and closure of any resulting CARs.
  • Maintain and certify internal auditors to support audit schedule.
  • Manage the Management of Change (MOC) meetings and repository for MOC history.
  • Support consistent metrics (process capability, control charts, measurement quality) for monitoring systems effectiveness.
  • Continually monitor all existing IMS processes and identify opportunities to streamline processes and/or better align processes to the needs of the business.
  • Implement and maintain appropriate IMS tools to achieve desired results.
  • Support regional alignment of IMS tools
  • Lead the site record retention program, including maintenance and 3rd party service management.
  • Serve as a quality assurance resource for data analysis, problem identification, resolution, and continuous improvement.
  • Support root-cause analysis and other problem-solving activities to identify effective corrective actions and process improvements
  • Support Quality Assurance introduction training day for new hires in coordination with HR & EH&S.
  • Provide supervision, guidance, and coaching to the Document Control and Training Administrator. Define objectives for annual performance reviews, timecard checks, and training for the Administrator.
  • Partner with the Document Control and Training Administrator to ensure facility documentation control and training requirements are in compliance per ISO (9001/14001/45001) and regulatory standards.
  • Interact with customers to identify opportunities to improve quality and establish feedback with manufacturing and development personnel.
  • Perform other duties, as required.

REQUIREMENTS

  • Minimum of a Bachelor’s degree in Chemical Engineering, Chemistry, Industrial Engineering, or Quality Engineering or other technical discipline.
  • 5+ years of experience in Quality Assurance systems, semiconductor industry preferred.
  • Prior supervisory experience is preferred.
  • Direct experience utilizing, implementing, and managing ISO 9001 or equivalent Quality Management Systems and associated QMS.
  • Experience utilizing, implementing, and managing ISO.
  • Prior experience working with semiconductor manufacturers or within the semiconductor industry supplier base is strongly preferred.
  • Strong knowledge and experience for problem solving techniques preferred, such as 5 Why’s, Fishbone, Process Mapping, etc., to identify root cause and define CAPA.
  • Broad knowledge of theory and principles of statistics and statistical process control, helpful.
  • Strong organizational skills, good attention to detail, and the ability to lead and/or function effectively as part of a cross-functional team.
  • Must have the ability to communicate professionally and effectively at all levels (verbal/written/presentations).
  • Must have experience as a quality assurance resource for data analysis, problem identification, resolution, and continuous improvement.
  • Must have excellent computer skills (PowerPoint, Excel, and statistical software tools).
  • Ability to travel up to 20% domestically
  • This is a safety-sensitive position that requires candidates to successfully pass a post-offer drug screening prior to employment. One of the essential job functions is the ability to work in a constant state of alertness and in a safe manner.

ADDITIONAL REQUIREMENTS

We value a professional, adaptable, and collaborative work environment. The following competencies are essential for success in any role and reflect our commitment to effective teamwork, problem solving, and workplace communication. 

  • Resilience -Ability to adapt to workplace challenges, maintain professionalism, and manage responsibilities effectively.
  • Communication -Capacity to clearly and professionally exchange ideas, interact respectfully with colleagues and customers, and foster positive workplace relationships. 
  • Reasoning & Decision Making -Ability to analyze information, follow verbal and written instructions, and make logical, sound decisions.
  • Comprehension -Capability to understand and complete tasks as assigned and solve problems effectively.
  • Organizational Skills -Competence in managing multiple priorities, maintaining accuracy, and staying focused despite potential workplace distractions. 

PAY RANGE: The pay range for this role is estimated $110,000/yr. - $120/000/yr. with actual wage based on candidate’s qualifications and experience.

To all agencies: Please, no phone calls or emails to any employee of Fujifilm about this requisition. All resumes submitted by search firms/employment agencies to any employee at Fujifilm via-email, the internet or in any form and/or method will be deemed the sole property of Fujifilm, unless such search firms/employment agencies were engaged by Fujifilm for this requisition and a valid agreement with Fujifilm is in place. In the event a candidate who was submitted outside of the Fujifilm agency engagement process is hired, no fee or payment of any kind will be paid.


Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.


If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (feus.humanresources@fujifilm.com).


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About Fujifilm

Sourced by ZipRecruiter

With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.

Industry

Chemical manufacturing

Company size

10,000+ Employees

Headquarters location

Minato-ku, Tokyo, JP

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