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Quality Control Associate Jobs in Ohio (NOW HIRING)

Vantage Specialty Chemicals

QC Chemist

Englewood, OH · On-site

The Role QC Chemist POSITION SCOPE The creating of methods as needed and verification and ... A minimum of an associate's degree in physical science and a minimum of 3 years of laboratory ...

Core and Main LP

Quality Control Engineer

Boardman, OH · On-site

Core & Main's 5,700 associates are committed to helping their communities thrive with safe and reliable infrastructure. Visit coreandmain.com to learn more. Job Summary The Quality Control Engineer ...

Tjx

Accuracy Control Associate

Ashville, OH

$20 - $22/hr

Ensure quality and accuracy of items being distributed to stores and customers * Conduct research ... to Associate errors * Communicate with Merchandise Control team on errors that may be impacting ...

Adecco

Quality Control Technician

Bedford, OH · On-site

$20 - $21/hr

Quality Control Technician (Night Shift) Location: Walton Hills, OH Pay: $20-$21/hour + $0.75 shift ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

TJX Companies

Accuracy Control Associate

Ashville, OH · On-site

$20 - $22/hr

Ensure quality and accuracy of items being distributed to stores and customers * Conduct research ... to Associate errors * Communicate with Merchandise Control team on errors that may be impacting ...

Adecco

Quality Control Technician

Bedford, OH

$20 - $21/hr

Quality Control Technician (Night Shift) Location: Walton Hills, OH Pay: $20-$21/hour + $0.75 shift ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

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All JobsQuality Control Associate JobsQuality Control Associate Jobs in Ohio

Quality Control Associate information

See Ohio salary details

$10

$24

$36

How much do quality control associate jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for quality control associate in Ohio is $24.21, according to ZipRecruiter salary data. Most workers in this role earn between $17.60 and $29.47 per hour, depending on experience, location, and employer.

What does a Quality Control Associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

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

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges Quality Control Associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

Is a degree needed to be a QC?

A degree is not always required to become a Quality Control Associate, but many employers prefer candidates with a high school diploma or equivalent, along with relevant skills such as attention to detail and knowledge of quality standards. Some positions may require or prefer post-secondary education or certifications in quality management or related fields. Practical experience and familiarity with testing tools can also be valuable for this role.

Which is higher position, QA or QC?

In the context of a Quality Control Associate role, Quality Assurance (QA) is generally considered a higher-level function that focuses on preventing defects through process improvements, while Quality Control (QC) involves inspecting products to identify defects. QA roles often involve more strategic responsibilities and may require broader skills or certifications, whereas QC roles are more focused on testing and inspection tasks.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

Is QC a hard job?

Quality Control Associate roles can be challenging due to the need for attention to detail, adherence to strict standards, and sometimes repetitive tasks. The job often requires good observation skills, knowledge of quality procedures, and sometimes certifications, but the difficulty varies depending on the industry and specific responsibilities.

What does a QC associate do?

A Quality Control (QC) Associate inspects and tests products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to address issues, often using tools like inspection equipment and quality management systems. Attention to detail and knowledge of industry standards are essential for this role.
What are the most commonly searched types of Quality Control jobs in Ohio? The most popular types of Quality Control jobs in Ohio are:
What are popular job titles related to Quality Control Associate jobs in Ohio? For Quality Control Associate jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Quality Control Associate jobs in Ohio look for? The top searched job categories for Quality Control Associate jobs in Ohio are:
What cities in Ohio are hiring for Quality Control Associate jobs? Cities in Ohio with the most Quality Control Associate job openings:
What are popular job titles related to Quality Control Associate jobs in OH? For Quality Control Associate jobs in OH, the most frequently searched job titles are:
Quality Control Associate jobs near you
Infographic showing various Quality Control Associate job openings in Ohio as of June 2026, with employment types broken down into 2% As Needed, 76% Full Time, and 22% Part Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $50,351 per year, or $24.2 per hour.
QC Chemist

QC Chemist

Vantage Specialty Chemicals

Englewood, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Job description

The Role
QC Chemist
POSITION SCOPE
The creating of methods as needed and verification and validation of pre-existing methods to establish as a Standard Operating Procedure for the testing of raw materials and finished good products.
Maintain equipment and laboratory compliance for all equipment used. Ensure solutions and standards are made and available, and up to date. Ensure laboratory is clean and safe for the handling of chemicals.
Carry out QC lab analysis of raw materials, in process samples and final products so that results are accurately determined, carried out in a timely way, properly communicated to customers, and carried out within the framework of the Quality System ISO 9000 and FSSC 22000/22002 with cGMP applying. This ensures that the manufacturing operation is well supported, and outside customers promptly served with the correct product, quality and information.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Key responsibilities include, but are not limited to the following:
  • Carry out QC analytical work and the requirements exactly to the required written methods and using the correct equipment, so that information to internal and external customers is accurate, timely and properly reported and in compliance as applicable per product type. (food, drug)
  • Carry out all work to the appropriate Quality Standards - ISO 9000 as well as FSSC 22000/22002 also applying cGMP food safety/ drug safety related to designated area. Knowledge and access to USP monograph for drug testing.
  • Immediately report any accidents or hazardous incidents including any issues with food/drug safety, food/drug raw materials, finished goods or any concerns whatsoever regarding food and drug products as required by the FDA and GFSI standards to management immediately.
  • Comply, maintain, train, and enforce contractors to ensure all third parties have been qualified to meet all cGMP, GFSI, ISO, food safety requirements as applicable for the overall site.
  • Communicate fully with internal and external customers so that their requirements and results are fully understood and any interpretation of the information is properly supplied.
  • Work independently, as well as in a team, so that work is smoothly and efficiently handled, shift hand-over is completed with a full understanding of ongoing issues, production operators are supported in their in-process testing and the lab manager/supervisor is kept appraised of issues and how they are being handled.
  • Spot and troubleshoot questionable results and equipment problems so that resolution of the matter is obtained in a timely manner, and the proper people kept informed or asked for guidance.
  • Calibrate all lab equipment and keep records to the appropriate Quality Standards so that the equipment is always ready for use.
  • Suggest and run small projects, within the general scope of work done in the QC Lab, so that the lab improvements can be made.
  • Follow all Company policies, procedures, and instructions using cGMP so that work is properly and safely done, the quality system maintained, and good housekeeping is carried out.
  • Internal audit certification is required to audit to ISO 9001:2015 and FSSC 22000:2018, GMP ICHQ7 Standards.
  • The ability to conduct investigations on out of specification results, customer complaints and assist the QC team with investigation, root cause analysis and Corrective and Preventive Actions.
  • The ability to review documentation to ensure there are no unapproved deviations, and for accuracy using Good Documentation Practices.
  • Physically inspecting equipment, conducting swabs for approval to use in clean room environments.

Note: The duties listed above are not all inclusive and may be subject to periodic updating or revision.
The Ideal Candidate
Desired Background
  • A minimum of an associate's degree in physical science and a minimum of 3 years of laboratory experience.
  • Must be able to apply good safety practice, good laboratory practice (GLP) - cGMP, and operate to the quality regime, i.e. ISO 9000 as well as FSSC 22000/22002 and have a basic understanding of cGMP requirements, CFR requirements for the sampling and testing of USP pharmaceutical products.
  • Must be fully conversant with all the instrumental analysis and wet chemistry in the QC Lab and in particular the following techniques: HPLC, automated titrations, physical property testing, color measurement, and spectroscopic techniques; as well as be able to teach the techniques, demonstrate good lab practice, do basic troubleshooting, and maintain good records including lab books. A good sense of smell is required for organoleptic testing.

Knowledge, Skills & Talents
More specifically, we would seek the following attributes and competencies for the position:
  • Computer skills are required as the chemists must be able to use databases, spreadsheets, word processing software, LIMS and computer controlled instruments.
  • Must have good written and verbal communication skills. Good organizational skills, decision-making and record keeping skills are also required. The ability to work in a team environment as well as independently with minimal supervision is necessary.
  • Flexibility to work any other shifts and be able to work overtime as required.

Pay
The estimated base pay range for this position is $26.00/hr - $30.00/hr. Actual pay will be determined based on education, certifications, experience, qualifications, skills and geographic location. This position is eligible to participate in a short-term incentive program.
Benefits
Vantage offers a comprehensive benefits package to eligible employees, including:
  • Medical, HSA, dental, vision
  • FSA (limited purpose, dependent care, and commuter/parking)
  • Life and AD&D insurance
  • Accident, hospital indemnity and critical illness insurance
  • Short- and long-term disability
  • EAP, identity theft protection
  • Paid time off, Parental Leave
  • 401(k) with company match

Equal Employment Opportunity
Vantage is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status or any other protected category.
About Vantage
Vantage provides natural solutions to our customers' technical performance and marketing needs through a unique combination of chemistry, application expertise and service. Underpinned by our broad portfolio of formulations, ingredients and actives that are built on a backbone of sustainable oils, fats and their derivatives, Vantage targets selected markets and applications including personal care, food, surface treatment, agriculture, pharma, and consumer and industrial performance. Vantage is headquartered in Deerfield, IL., operates in 11 countries worldwide and employs more than 1,000 talented professionals focused on delivering exceptional customer experiences with every interaction.
We are a dynamic people-centered organization where you'll be part of a collaborative global team. Embracing our cultural diversity, we learn from each other to constantly improve, adapt and iterate. We value the voices and talents of our colleagues, empowering them to drive their unique ideas to completion. We're convinced that exceptionally motivated employees produce outstanding results, and we celebrate them by fostering a culture of recognition, development, learning, excellence and shared achievement. Most importantly, we know you're going to like it here. For more information visit: vantagegrp.com or LinkedIn/vantage.

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