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Quality Systems Manager Jobs in Raleigh, NC (NOW HIRING)

Fujifilm

Manager, All QC

Holly Springs, NC · On-site

... in quality systems and continuous process improvement. * Establishes clear requirements ... Manages complex problem solving, providing mitigation/outcome to management/team. Decisions at this ...

Fujifilm

Manager, All QC

Holly Springs, NC

... in quality systems and continuous process improvement. * Establishes clear requirements ... Manages complex problem solving, providing mitigation/outcome to management/team. Decisions at this ...

Symbiotic Services

Quality Tecnician

Raleigh, NC · On-site

$17.50 - $23.50/hr

Key Responsibilities Maintain calibration systems and measurement accuracy Support CNC operations with quality evaluations and troubleshooting Manage nonconforming materials and MRB processes Assist ...

Siemens

PMO Manager - AIS Systems

Raleigh, NC · On-site

PMO Manager - AIS Systems Here at Siemens, we take pride in enabling sustainable progress through ... Ensure adherence to quality standards for Project Management processes, promoting excellence in ...

MSD

Director, External Quality - Remote

Durham, NC · Hybrid

In this role you will be subject matter expert in EQA and manufacturing quality systems, technology platforms, regulatory expectations, and external manufacturing management, with the opportunity to ...

DSA Doors

Quality Lead - Manufacturing

Raleigh, NC

Own and maintain the company's Quality Management System (QMS) * Lead preparation and execution of internal and external audits * Manage non-conformance (NCR) and corrective action processes end-to ...

DSA Doors

Quality Lead - Manufacturing

Raleigh, NC · On-site

Own and maintain the company's Quality Management System (QMS) * Lead preparation and execution of internal and external audits * Manage non-conformance (NCR) and corrective action processes end-to ...

Mastech Digital

Be Seen First

QC Analyst / Laboratory Technician

Durham, NC · On-site

$24/hr

Job Title: QC Analyst / Laboratory Technician Location: Durham, NC (100% Onsite) Duration: 12 ... Maintain laboratory records and enter data into laboratory systems. * Manage laboratory samples and ...

Endo International

Sr Ops Quality Eng

Raleigh, NC

$86K - $116K/yr

Manages the site Internal Audit program. * Provides guidance and training to Quality Department personnel in all applicable Quality Systems. * Leads compliance efforts for the site. * Responds to ...

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All JobsQuality Systems Manager JobsQuality Systems Manager Jobs in Raleigh, NC

Quality Systems Manager information

See Raleigh, NC salary details

$52.5K

$95.9K

$149.7K

How much do quality systems manager jobs pay per year?

As of Jun 12, 2026, the average yearly pay for quality systems manager in Raleigh, NC is $95,855.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,400.00 and $119,100.00 per year, depending on experience, location, and employer.

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

To thrive as a Quality Systems Manager, you need strong expertise in quality management principles, regulatory compliance, and process improvement, typically supported by a degree in engineering or a related field. Familiarity with ISO standards (like ISO 9001), quality management software, and certifications such as Six Sigma or ASQ Certified Manager of Quality/Organizational Excellence are commonly required. Leadership, analytical thinking, and effective communication are crucial soft skills for coordinating teams and driving continuous improvement. These skills and qualifications are essential to ensure consistent product quality, regulatory adherence, and overall organizational efficiency.

What does a Quality Systems Manager do?

A Quality Systems Manager is responsible for developing, implementing, and maintaining a company's quality management systems to ensure compliance with industry standards and regulations. They oversee quality assurance processes, conduct audits, and work with different departments to improve procedures and product quality. Quality Systems Managers also manage documentation, train staff on quality standards, and analyze data to identify areas for continuous improvement. Their goal is to ensure that products and services consistently meet customer and regulatory requirements.

What is the role of a quality systems manager?

A quality systems manager oversees the development, implementation, and maintenance of quality management systems to ensure products and processes meet industry standards and regulations. They analyze data, conduct audits, and collaborate with teams to improve quality and compliance, often using tools like ISO standards and quality management software. Strong leadership, attention to detail, and knowledge of regulatory requirements are essential for this role.

What is the difference between Quality Systems Manager vs Quality Assurance Manager?

AspectQuality Systems ManagerQuality Assurance Manager
Primary FocusDeveloping and maintaining quality management systems and processesOverseeing product testing and ensuring quality standards are met during production
CertificationsISO 9001 Lead Auditor, CQEASQ certifications, QA certifications
Work EnvironmentQuality management departments, compliance teamsProduction lines, testing labs
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

While both roles focus on quality, the Quality Systems Manager primarily manages the overall quality management system and compliance, whereas the Quality Assurance Manager concentrates on product testing and ensuring quality during production. Understanding these differences helps in selecting the right career path or hiring the appropriate professional.

What is the salary for a quality manager?

The salary for a Quality Systems Manager typically ranges from $70,000 to $120,000 annually, depending on experience, industry, and location. Certifications such as CQE or ISO auditor training can influence earning potential, and managerial roles often include additional benefits and bonuses.

What Does a Quality Systems Manager Do?

As a quality systems manager, your primary responsibilities are monitoring the production processes and ensuring factory machinery/goods are within company and industry requirements. Your duties include weighing, sampling, or testing products for quality and functionality. You may also report the results of quality control tests. You monitor the equipment and people involved, and help with the development and implementation of improved management systems. You are also in charge of creating a standard operating procedure for the specific plant where you work. You check that everything is running at full efficiency and the quality of merchandise is standardized.

What is the average salary of a QA manager in the US?

The average salary of a Quality Systems Manager in the US typically ranges from $80,000 to $130,000 annually, depending on experience, industry, and location. Many QA managers also receive benefits such as bonuses and professional development opportunities, and certifications like ASQ CQE can enhance earning potential.

How does a Quality Systems Manager typically collaborate with cross-functional teams to drive continuous improvement?

A Quality Systems Manager works closely with departments such as manufacturing, engineering, regulatory, and supply chain to ensure that quality standards are consistently met and improved. They often lead or participate in cross-functional meetings to identify process gaps, analyze data, and develop corrective and preventive action plans. Effective communication and project management skills are essential, as the role involves aligning diverse teams toward common quality objectives and facilitating training or audits to support compliance and improvement initiatives.

What jobs pay $500,000 a year in the US?

In the US, high-paying roles such as senior executives, specialized surgeons, and certain investment bankers can earn $500,000 or more annually. For a Quality Systems Manager, reaching this level typically requires extensive experience, advanced certifications, and leadership responsibilities, often supplemented by bonuses or profit-sharing in large organizations.
More about Quality Systems Manager jobs
What are the most commonly searched types of Quality Systems jobs in Raleigh, NC? The most popular types of Quality Systems jobs in Raleigh, NC are:
What are popular job titles related to Quality Systems Manager jobs in Raleigh, NC? For Quality Systems Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Quality Systems Manager jobs in Raleigh, NC look for? The top searched job categories for Quality Systems Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Quality Systems Manager jobs? Cities near Raleigh, NC with the most Quality Systems Manager job openings:
Quality Systems Manager jobs near you
Infographic showing various Quality Systems Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 2% As Needed, 75% Full Time, 21% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $95,855 per year, or $46.1 per hour.
Manager, All QC

Manager, All QC

Fujifilm

Holly Springs, NC • On-site

Other

Posted yesterday

Fujifilm rating

8.3

Company rating: 8.3 out of 10

Based on 66 frontline employees who took The Breakroom Quiz

46th of 518 rated manufacturers

Job description

Position Overview
The Manager, All-QC team is responsible for contributing to key functional, tactical, and operational aspects of the QC group and will lead the 223-shift teams that are responsible for performing routine testing required for Urgent/STAT testing of manufacturing batch samples, clean utility, environmental monitoring. This role is part of a 24x7 team that supports testing/sampling across all the QC laboratories required for urgent testing/Manufacturing support. This role will direct the scheduling across all shifts, initiation of process improvements, serve as a liaison across all QC teams, modeling the leadership competencies, aiding in the development of peers and performing QC approvals, as required.
Company Overview
FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we'll open North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.
We're looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we're proud to cultivate a culture that will fuel your purpose, energy, and drive-what we call Genki. Ready to shape the future of medicine? Let's transform healthcare together!
Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh's thriving tech scene, making it the perfect blend of community and opportunity.
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
Job Description
What You'll Do
  • Ensures and owns GMP-compliant laboratory operations in alignment with EU GMP, 21 CFR Parts 210, 211, 820, 11, and other applicable GMP guidelines.
  • Provides cross-functional leadership and mentorship as the QC laboratory representative.
  • Directs four shift supervisors to ensure 24/7 QC team coverage.
  • Oversees supervision and scheduling across 223 shifts for the All-QC laboratory team.
  • Applies expertise in laboratory methodology and compendial requirements for QC testing that span all the QC labs (e.g., Bioburden, Endotoxin, HPLC, UV280, TOC, etc.) per department Standard Operating Procedures (SOPs) and test methods for samples associated manufactured batches.
  • Acts as primary point of contact for their team and first line escalation point in areas of their responsibility.
  • Coordinates the review of analytical data to support test validation, qualification and certification activities. Performs investigations, manages complex issues, barriers and problems to support team success. Approve data reports within the team and area of discipline/focus, including approval of results
  • Authors protocols, change control requests, and Quality Technical Reports for ensuring successful execution of, qualification, analytical improvement projects, in collaboration with cross-functional teams, as appropriate
  • Provides technical leadership through effective project management, status tracking, presentations, and communication
  • Proactively identifies technical gaps and areas for improvement related to quality. Process and lead internal and external audits proficiently, including commitments on follow up within team & site management, serves as External Leadership cross-functionally.
  • Represents QC interdepartmentally on QC projects with limited support for efficient and collaborative interaction with internal and external stakeholders
  • Provides regular guidance to direct reports; fosters a positive, collaborative work environment that prioritizes team success; mentors junior staff in quality systems and continuous process improvement.
  • Establishes clear requirements, deliverables, measurable goals and targets, and mitigation plans aligned with quality directives, regulatory guidance, and business priorities.
  • Ensures timely and appropriate mitigation of issues and deviations.
  • Manages complex problem solving, providing mitigation/outcome to management/team. Decisions at this level include those that have potential compliance impact to methods, results, product, and/or Quality systems, decisions with impact to customers, or pertaining to personnel issues that must be handled with consultation and recommendations to management. Supports key business strategies
  • Conducts approval of complex reports, data of others; Leads complex problem solving through facilitation/escalation. Conducts impact assessment related to compliance (e.g., global directives, audit finding/readiness, deviations).
  • Provides technical support during audits/inspections
  • Ensures adherence to all regulatory licenses and regulations, serving as a subject matter expert in multiple disciplines, interfacing with key customers
  • Completes required administrative tasks (e.g., timecard approvals, time off approvals, expense reports etc.)
  • Participates in the recruitment process and retention strategies to attract and retain talent, as needed
  • Addresses performance gaps, employee questions and concerns, and partners with HR as needed for resolution
  • Performs other duties, as assigned

Minimum Requirements:
  • Bachelor's degree in chemistry, Microbiology, Biological Sciences, Engineering or related science with 4+ years of related experience OR
  • Master's degree in chemistry, Microbiology, Biological Sciences, Engineering or related science with 2+ years of related experience
    • Degree with emphasis in life science or engineering preferred
    • 4+ years' experience managing people
    • Experience working in a changing, project driven organization
    • Previous experience directly supporting function
    • Experience with regulatory inspections, investigations and change management preferred
    • Experience in pharmaceutical / biological manufacturing operations preferred
    • Experience leading others in a pharmaceutical/biological manufacturing facility preferred

Preferred Requirements:
  • 5+ years of experience in a GMP environment

Physical and Work Environment Requirements:
  • Ability to discern audible cues
  • Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color.
  • Ability to stand for prolonged periods of time (up to 240 minutes)
  • Ability to sit for prolonged periods of time (up to 240 minutes)
  • Ability to conduct activities using repetitive motions that include writs, hands and/or fingers.
  • Ability to conduct work that includes moving objects up to 33 pounds.
  • Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions.

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.
EEO Information
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.
ADA Information
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 (FDBN_PNC@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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