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New Generation Wellness

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Quality Assurance Supervisor

Colorado Springs, CO · On-site

$60K - $80K/yr (+ commission)

Support root-cause analysis and track CAPA effectiveness * Manage change-control documentation to ... Coordinate QA-related training programs in collaboration with HR and department leaders * Ensure ...

Celularity

Lead, Quality Assurance

Florham Park, NJ · On-site

$90K - $115K/yr

... CAPA activities, audits, regulatory interactions and cross-functional QA guidance to maintain ... compliance with cGMP, GTP, applicable health authority regulations, and Celularity quality ...

CELULARITY LLC

Lead, Quality Assurance

Florham Park, NJ · On-site

$90K - $115K/yr

... CAPA activities, audits, regulatory interactions and cross-functional QA guidance to maintain ... compliance with cGMP, GTP, applicable health authority regulations, and Celularity quality ...

Celularity Inc.

Lead, Quality Assurance

Florham Park, NJ · On-site

$90K - $115K/yr

... CAPA activities, audits, regulatory interactions and cross-functional QA guidance to maintain ... compliance with cGMP, GTP, applicable health authority regulations, and Celularity quality ...

Globalchannelmanagement

QA Engineer

Fort Worth, TX

$59K - $60K/hr

... CAPA, Root Cause Analysis, 8D, Fishbone Analysis, 5 Why, PFMEA, DFMEA, Statistical Process Control (SPC), Lean Manufacturing, Six Sigma, Minitab, ERP Systems, Microsoft Office, Quality Metrics, FPY ...

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Capa Quality Assurance information

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How much do capa quality assurance jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for capa quality assurance in the United States is $23.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $24.28 per hour, depending on experience, location, and employer.

What is CAPA Quality Assurance?

Capa Quality Assurance refers to the processes and practices used to ensure that products and services meet regulatory and organizational quality standards, particularly through the Corrective and Preventive Action (CAPA) system. CAPA is a critical component in industries like pharmaceuticals, medical devices, and manufacturing, where it helps identify, investigate, and resolve quality issues to prevent their recurrence. Quality Assurance professionals in CAPA are responsible for monitoring compliance, analyzing root causes of problems, and implementing solutions to improve overall product quality and safety.

How does a CAPA Quality Assurance professional collaborate with other departments to address quality issues?

As a CAPA Quality Assurance professional, you will regularly work with cross-functional teams such as manufacturing, engineering, and regulatory affairs to investigate, document, and resolve quality issues. Collaboration often involves facilitating root cause analysis meetings, reviewing corrective and preventive action plans, and ensuring timely implementation of solutions. Effective communication and project management skills are essential, as you must coordinate with various stakeholders to monitor progress and verify that actions have successfully mitigated the identified risks.

What are the key skills and qualifications needed to thrive as a CAPA Quality Assurance professional?

To thrive as a CAPA Quality Assurance professional, you need a solid understanding of quality management systems, regulatory compliance, root cause analysis, and typically a degree in a scientific or engineering field. Familiarity with CAPA management software, ISO standards (such as ISO 13485 or ISO 9001), and documentation tools is often required. Strong attention to detail, analytical thinking, and effective communication are crucial soft skills for investigating issues and implementing solutions. These competencies ensure that process failures are thoroughly addressed and prevented, maintaining product quality and regulatory compliance.

What is the difference between Capa Quality Assurance vs Quality Control Inspector?

AspectCapa Quality AssuranceQuality Control Inspector
Primary FocusPreventive measures, process improvement, ensuring compliance with CAPA proceduresDetecting defects, inspecting products, verifying quality at various stages
CredentialsISO certifications, quality assurance training, knowledge of CAPA processesQuality inspection certifications, technical skills in product testing
Work EnvironmentDocumentation review, process audits, collaboration with production teamsOn-site inspections, sampling, testing products or components
Industry UsageManufacturing, pharmaceuticals, medical devices

While Capa Quality Assurance focuses on preventing issues through process improvements and CAPA procedures, Quality Control Inspectors primarily identify defects through product inspections. Both roles are essential for maintaining quality but differ in their approach and scope within the quality management system.

What are popular job titles related to Capa Quality Assurance jobs?

For Capa Quality Assurance jobs, the most frequently searched job titles are:

Infographic showing various Capa Quality Assurance job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $48,237 per year, or $23.2 per hour.

Quality Assurance Manager

Cincinnati, OH • On-site

Kutol-Product
See more jobs at Kutol-Productexternal

Other

Medical, Dental, Vision, PTO

Posted 25 days ago

Key responsibilities

  • Lead QA activities for OTC drug and cosmetic manufacturing operations to ensure compliance with regulatory standards.

  • Manage and develop the Quality Management System, including deviations, CAPA, change control, and audit management.

  • Oversee investigations, root cause analysis, and CAPA effectiveness related to deviations, nonconformances, and customer complaints.

Job description

Lead Quality - Drive Compliance - Shape the Future

Kutol Products Company, a recognized leader in hand hygiene and skin care solutions, is seeking an experienced Quality Assurance Manager to lead our QA operations and play a critical role in advancing our quality culture. This is an exciting opportunity for a quality professional who is passionate about regulatory compliance, continuous improvement, and building strong quality systems that support operational excellence.

As the Quality Assurance Manager, you will lead QA activities for our OTC drug and cosmetic manufacturing operations, ensuring compliance with current Good Manufacturing Practices (cGMP), FDA regulations, Health Canada requirements, and internal quality standards. You will serve as a key leader in strengthening our Quality Management System (QMS), driving investigation and CAPA effectiveness, supporting audit readiness, and partnering cross-functionally to ensure product quality and regulatory compliance.

If you thrive in a fast-paced manufacturing environment and enjoy leading teams, solving complex quality challenges, and driving continuous improvement initiatives, we'd love to hear from you.

Key Areas of Responsibility Include:
  • Lead and develop the QA Team including QA Technicians, Specialists and Incoming Inspection
  • Lead the Quality Management System with regard to deviations, CAPA's, change and document control, and audit management
  • Ensure regulatory compliance and inspection readiness for FDA, Health Canada, customer, supplier and internal audits
  • Lead complex investigations, root cause analysis and CAPA effectiveness involving deviations, nonconformances, OOS/OOT results and customer complaints
  • Provide product quality and documentation oversight including SOP's, specs, master mfg records, validation protocols, etc.
  • Support Microbiological risk management providing oversight for environment monitoring programs, water systems, preservation strategies, and micro risk assessments
  • Manage supplier quality and quality risk by supporting supplier qualification and ongoing performance management, supplier audits and quality agreements
  • Support validation and change management providing quality oversight for equipment, process, cleaning and method validations
  • Monitor and report out metrics, analyze trends and identify/lead initiatives for systemic improvement
  • Bachelor's degree in Chemistry, Microbiology, Biology, Pharmaceutical Sciences, Engineering, or a related scientific field.
  • 5+ years of Quality Assurance experience in a regulated manufacturing environment.
  • 3+ years of leadership or supervisory experience.
  • Strong working knowledge of:
    • cGMP regulations
    • FDA requirements
    • OTC drug manufacturing
    • Quality Management Systems
    • Investigations and CAPA processes
  • Experience leading audits, inspections, and regulatory interactions.
  • Excellent problem-solving, communication, and leadership skills.

Competitive salary range with a comprehensive benefit package including medical, dental, vision, paid time off and more. Our shared fate culture has resulted in a strong track record of company-wide profit sharing, a goal that every Teammate works to achieve annually.

More about us:

Kutol manufactures hand soaps, sanitizers, and other skin care products in our LEED Silver Certified, FDA-registered facility. Our company boasts a rich 100+ year history while being uniquely positioned for significant growth. As a $60M company, Kutol hand care products and dispensers can be found across the US and Canada in schools, restaurants, offices, medical buildings, and industrial/manufacturing facilities.

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