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Quality Control Manager Jobs in Garner, NC (NOW HIRING)

Fujifilm

QC LIMS Developer

Durham, NC · On-site

Position Overview The QC LIMS Developer designs, configures, validates, and supports Laboratory Information Management System (LIMS) capabilities for Quality Control laboratories. This role builds ...

Fujifilm

QC LIMS Developer

Research Triangle Park, NC · On-site

The QC LIMS Developer designs, configures, validates, and supports Laboratory Information Management System (LIMS) capabilities for Quality Control laboratories. This role builds compliant digital ...

CMC Hotels

Quality Control Inspector

Raleigh, NC · On-site

Quality Control Inspector - Housekeeping Westin Raleigh Durham Airport Are you looking for a ... Communicate effectively with the Executive Housekeeper, management team, Front Desk, Maintenance ...

Acrotech Biopharma inc.

QC INVESTIGATOR

Durham, NC · On-site

$75 - $90/hr

The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality control and regulatory affairs. In addition to several formulations ...

Scorpion Therapeutics

QC Microbiologist

Chapel Hill, NC · On-site

$60 - $85/hr

Who You Are The QC Microbiologist I ensures contamination control of manufacturing facilities by ... Troubleshoot instruments; coordinate with lab manager/equipment technical services; perform ...

Guerbet

QC Analyst

Raleigh, NC · On-site

$60 - $80/hr

The QC Analyst is responsible for evaluating material and product quality by performing various ... Notify management of unsafe conditions or practices, unlawful activities and activities which ...

Fujifilm

Analyst 1, QC Compendial Testing

Holly Springs, NC · On-site

$20.75 - $28/hr

Assists the QC Manager in the implementation of new technologies. * Authors and reviews procedures, protocols, reports and specifications related to compendial testing of materials under supervision ...

LeadStack Inc.

QC Laboratory Analyst

Durham, NC · On-site

$21.75 - $29.25/hr

The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. Job ...

LeadStack Inc.

QC Laboratory Analyst

Durham, NC · On-site

$21.75 - $29.25/hr

The QC Analyst I, reporting to the Manager of Quality Control, will be responsible for serving as a performing routine GMP testing on analytical methods in the Quality Control laboratories. Job ...

Guerbet

QC Chemistry Lead

Raleigh, NC · On-site

$80 - $100/hr

The QC Chemistry Lead is responsible for overseeing analytical testing and quality assurance ... Perform other duties as assigned by management. Qualifications * Education: Bachelor's or Master ...

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All JobsQuality Control JobsQuality Control Manager JobsQuality Control Manager Jobs in Garner, NC

Quality Control Manager information

See Garner, NC salary details

$27.2K

$72.5K

$115.4K

How much do quality control manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for quality control manager in Garner, NC is $72,490.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,900.00 and $89,100.00 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 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 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 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 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.

Is a Quality Control Manager a high paying job?

A Quality Control Manager typically earns a salary above the national average for managerial roles, with pay varying based on industry, experience, and location. They often require skills in inspection, testing, and quality assurance, and may hold certifications such as Six Sigma or ISO auditor training. Overall, it is considered a well-compensated position within manufacturing, production, and related sectors.

What is the work of a quality control manager?

A quality control manager oversees the inspection and testing of products or services to ensure they meet quality standards and specifications. They develop quality control procedures, analyze data, and coordinate with production teams to address issues, often using tools like inspection equipment and quality management systems. The role requires attention to detail, problem-solving skills, and knowledge of industry regulations.
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Quality Control Manager jobs near you
Infographic showing various Quality Control Manager job openings in Garner, NC as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 18% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $72,490 per year, or $34.9 per hour.

QC LIMS Developer

Fujifilm

Durham, NC • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Fujifilm rating

8.5

Company rating: 8.5 out of 10

Based on 70 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Position Overview
The QC LIMS Developer designs, configures, validates, and supports Laboratory Information Management System (LIMS) capabilities for Quality Control laboratories. This role builds compliant digital workflows for sample lifecycle, stability, specifications, CoAs, instrument/data integrations, and reporting, ensuring data integrity, GMP compliance, and on-time product/material release.
Company Overview
At FUJIFILM Biotechnologies, we're leading the charge in advancing tomorrow's medicines. If you want to be a part of life-impacting projects alongside today's most innovative biopharmaceutical companies, FUJIFILM Biotechnologies could be the right place for you.
From our Bioprocess Innovation Center to our cGMP-compliant manufacturing site, we thrive on collaboration, creativity, and purpose. Whether your expertise lies in research, manufacturing, or production, you'll find a home here where your efforts directly improve patients' lives. Together, let's shape the future of healthcare.
Situated at the cross-section of Morrisville and Research Triangle Park (RTP), North Carolina, our site is at the heart of a booming biotech hub surrounded by top universities, vibrant communities, and various outdoor opportunities.
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:
  • Solution design and configuration
    • Translate QC business requirements into LIMS workflows (sample login, testing, results entry/review/approval, CoA generation, stability, EM, utilities, raw materials, in-process/finished product).
    • Configure master data: tests, methods, specifications, limits, calculations, units, instruments, users/roles, security, audit trails, electronic signatures.
    • Build dashboards, queries, and reports (KPIs, turnaround time, RFT metrics, EM trending, stability pulls) using native LIMS tools and reporting platforms.
  • Integrations and automation
    • Integrate instruments and systems (CDS such as Empower; ELN; ERP like SAP/Oracle)
    • Implement results parsing and automated calculations; manage instrument metadata and result mapping.
  • Compliance and validation (GxP)
    • Author and execute CSV deliverables: URS, FRS, HDS, configuration specs, risk assessments, test scripts (IQ/OQ/PQ), validation summary reports.
    • Ensure 21 CFR Part 11 / EU Annex 11 adherence, ALCOA+ data integrity, and Good Documentation Practices; maintain change control and periodic review.
    • Support audits/inspections; maintain audit-readiness for LIMS and connected systems.
  • Operations and support
    • Provide application support, incident/problem management, and root-cause analysis; monitor job/integration health and performance.
    • Manage environments and releases (dev/test/qual/prod), versioning, and migrations; follow SDLC and Agile/Scrum practices.
    • Lead data migration/cleanup projects; build scripts for bulk loads and master data maintenance.
    • Create user guides/SOPs/WIs; train end users (multiple departments).
  • Continuous improvement
    • Identify digital opportunities to reduce cycle time and errors; implement templates, macros, and standardized builds across sites/products.
    • Partner with QC, QA, Validation/CSV, IT Security, and Manufacturing to align solutions with contamination control strategy and right-first-time goals.
Qualifications
  • Bachelor's in Computer Science/Information Systems, Chemistry, Biochemistry, or related field; Master's a plus.
  • 3-7 years configuring and supporting LIMS in GMP environments (pharma/biotech/med device).
    • Hands-on with one or more platforms (e.g., LabWare, LabVantage, SampleManager, Nautilus, STARLIMS).
    • Proven CSV experience and familiarity with FDA 21 CFR 210/211/11, EU Annex 11, GAMP 5, ICH Q9/Q10.
    • Understanding of QC lab processes (raw materials, compendial testing, stability, EM/utilities, microbiology, chromatography workflows).

Knowledge & Capabilities:
  • Scripting/config: SQL; LabWare LIMS Basic or LabVantage Java/Groovy; .NET/Java/Python for integrations; XML/JSON.
  • Databases: Oracle and/or SQL Server
  • Interfaces: file-based integrations; experience with CDS (Empower/Chromeleon), ELN/LES, and label systems.
  • Reporting: Crystal Reports, Jasper, Power BI/Tableau; LIMS native query/report tools.
  • Strong requirements gathering, documentation, and communication.
  • Analytical problem solving; ability to translate lab needs into scalable, compliant solutions.
  • Stakeholder management and training aptitude; comfortable in fast-paced, regulated settings.
  • Strong analytical and problem-solving skills.
Preferred Qualifications
  • Knowledge of LabWare LIMS version 8 table relationships.
  • Experience with Crystal reports.
  • Excellent verbal and written communication skills.

Physical Requirements:
  • Will work in environment which may necessitate respiratory protection
  • Ability to discern audible cues
  • Ability to inspect or perform a task with 20/20 corrected vision, visual acuity, including distinguishing color
  • Ability to ascend or descend ladders, scaffolding, ramps, etc.
  • Ability to stand for prolonged periods of time (240 minutes)
  • Ability to sit for prolonged periods of time (240 minutes)
  • Ability to conduct activities using repetitive motions that include wrists, hands, and/or fingers
  • Ability to conduct work that includes moving objects up to 33lbs
  • Ability to bend, push or pull, reach to retrieve materials from 18" to 60" in height, and use twisting motions.
  • Will work in warm/cold environments (0-100F range)

Benefits
Our programs are designed to focus on maintaining and enhancing all pillars of health with a robust benefits package including medical, dental, vision and prescription drug coverage with the option of a Health Savings Account with company contributions. In addition, we offer an industry leading 401(k) savings plan, insurance coverage, employee assistance programs and various wellness incentives. We support life-work balance with paid vacation time, sick time, and company holidays. Explore a supportive environment that enriches both your personal and professional growth!
*#LI-onsite
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 (HR_FDBU@fujifilm.com).

What Fujifilm employees say

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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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