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Capa Jobs in Ohio (NOW HIRING)

Track observations, grade findings, and drive CAPA effectiveness through to verified closure. * Trend audit data, prepare dashboards/metrics, and present results in quality reviews and readiness ...

Manages closure of multiple quality records simultaneously and in a timely matter (Deviations, Change Controls, ENs, SICARs, CAPA, CAPA-EV). * Collaborate closely with External Supply Quality, ES SRE ...

You'll oversee HACCP, SQF, FSMA, GMPs, SSOPs, sanitation, allergen controls, traceability, labeling, CAPA, recalls, and regulatory compliance while serving as a key point of contact for USDA/FSIS ...

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Capa information

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$13

$38

$64

How much do capa jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for capa in Ohio is $38.55, according to ZipRecruiter salary data. Most workers in this role earn between $29.23 and $44.83 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a CAPA specialist?

A CAPA specialist is responsible for investigating quality issues, identifying root causes, and implementing corrective and preventive actions to ensure ongoing compliance and product integrity. Their typical day involves reviewing nonconformance reports, collaborating with cross-functional teams, documenting findings, and tracking the progress of CAPA initiatives using specialized software. CAPA specialists also prepare reports for audits and may facilitate meetings to drive continuous improvement activities. This role often requires balancing multiple projects and deadlines in a regulated environment, making organizational and communication skills crucial for success.

What are the key skills and qualifications needed to thrive in the CAPA position, and why are they important?

To thrive as a CAPA (Corrective and Preventive Action) specialist, you need expertise in quality management systems, root cause analysis, and compliance with industry standards, typically backed by a degree in engineering, life sciences, or a related field. Familiarity with CAPA software, regulatory frameworks (such as ISO 13485 or FDA 21 CFR Part 820), and document control systems is essential. Strong analytical thinking, attention to detail, and effective communication skills are vital soft skills for this role. These skills ensure effective problem-solving and sustained compliance, which are essential for maintaining product quality and meeting regulatory requirements.

What is a CAPA?

A CAPA (Corrective and Preventive Action) job involves identifying, investigating, and resolving quality issues in industries like manufacturing, healthcare, and pharmaceuticals. CAPA professionals analyze root causes of defects or process failures and implement corrective actions to prevent recurrence. They ensure compliance with regulatory standards, document findings, and improve overall quality management systems. Their role is critical in maintaining product safety, efficiency, and regulatory adherence.

What are the most commonly searched types of Capa jobs in Ohio?

The most popular types of Capa jobs in Ohio are:

What are popular job titles related to Capa jobs in Ohio?

For Capa jobs in Ohio, the most frequently searched job titles are:

What cities in Ohio are hiring for Capa jobs?

Cities in Ohio with the most Capa job openings:

Infographic showing various Capa job openings in Ohio as of August 2026, with employment types broken down into 81% Full Time, 11% Part Time, 1% Temporary, 6% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $80,178 per year, or $38.5 per hour.

Quality Assurance Manager

Kutol Products Company

Cincinnati, OH • On-site

Full-time

Medical, Dental, Vision, PTO

Re-posted 8 days ago


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

Requirements
  • 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.

Benefits
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.