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Quality Control Associate Jobs in Wilton, CT (NOW HIRING)

Title: QC Chemist Job Type: Full-time | On-site Company Summary: Radienz Living is a leading North ... Associate or Bachelor's degree in chemistry or related science preferred. High school diploma with ...

QC Chemist

Commack, NY · On-site

$22 - $27/hr

Title: QC Chemist Job Type: Full-time | On-site Company Summary: Radienz Living is a leading North ... Associate or Bachelor's degree in chemistry or related science preferred. High school diploma with ...

Associate's or Bachelor's degree in Chemistry, Materials Science, or related field preferred * Relevant laboratory experience may be considered in lieu of degree * 1-3 years of laboratory or QC ...

Associate's or Bachelor's degree in Chemistry, Materials Science, or related field preferred * Relevant laboratory experience may be considered in lieu of degree * 1-3 years of laboratory or QC ...

Associate's or Bachelor's degree in Chemistry, Materials Science, or related field preferred * Relevant laboratory experience may be considered in lieu of degree * 1-3 years of laboratory or QC ...

Associate's or Bachelor's degree in Chemistry, Materials Science, or related field preferred * Relevant laboratory experience may be considered in lieu of degree * 1-3 years of laboratory or QC ...

Associate's or Bachelor's degree in Chemistry, Materials Science, or related field preferred * Relevant laboratory experience may be considered in lieu of degree * 1-3 years of laboratory or QC ...

What We're Looking For: • High school diploma or equivalent; associate degree or certification in quality control, engineering, or a related field is preferred. • Proven experience as a quality ...

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How much do quality control associate jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for quality control associate in Wilton, CT is $26.37, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $32.12 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 cities near Wilton, CT are hiring for Quality Control Associate jobs? Cities near Wilton, CT with the most Quality Control Associate job openings:
Quality Control Chemist

$22/hr

Other

Posted 4 days ago


Job description

Title: QC Chemist

Job Type: Full-time | On-site

Company Summary:

Radienz Living is a leading North American manufacturer of home and personal care products, such as unit dose laundry and dish products, facial wipes, and baby wipes. With manufacturing plants and warehouses in Chicago and Long Island, NY, the company provides customers with private-label solutions and contract manufacturing services for products found in retail and institutional markets. Through its commitment to agility, innovation, trust and reliability, and sustainable creation, Radienz Living is passionate about providing its customers with products that support a cleaner way of living and a more radiant world.


The company has undergone a remarkable transformation over the years, focusing on two product lines: Unit Dose products, where it is the undisputed leader in Private Label and Contract Manufacturing, and Personal Care Wipes, where it manufactures the wipes for the country's #1 beauty care brand.


Our commitment to operational excellence is supported by robust quality systems, multiple GMP certifications, and a comprehensive suite of in-house labs—including FDA/EPA-certified microbiology, quality control, chemistry, and R&D facilities. This infrastructure enables us to deliver innovation, safety, and performance at every stage of the product lifecycle.


Background:

The Chemist applies knowledge and skills to perform diverse and complex laboratory procedures

and /or specialized technical, administrative services requiring application of equivalent technical knowledge in a quality control laboratory.


Responsibilities:

  • Perform organoleptic evaluation, pH analysis, titrations and routine analytical testing of raw materials, in-process samples and finished goods
  • Maintain GLP lab records and issue test reports.
  • Experience with HPLC and FTIR in manufacturing setting a plus
  • Calibrate and maintain lab instruments, ensuring a clean and organized workspace.
  • Adhere to safety protocols, GMP (Good Manufacturing Practices), and Standard Operating Procedures (SOPs) that are in effect assuring the quality and quantity of product produced.
  • Openness to learn new instruments methods and positions. Experience with HPLC and FTIR in manufacturing setting a plus


Qualifications:

  • 1-3 years analytical laboratory experience preferred
  • Openness to learn new instruments methods and positions.
  • Associate or Bachelor's degree in chemistry or related science preferred. High school diploma with relevant laboratory experience would be accepted.
  • Previous experience in production, manufacturing, or chemical industries (food or pharma preferred). Strong attention to detail, proficiency in basic lab equipment (e.g., pH meters, viscometers), and good
  • documentation practices.


Work Environment:


  • Work is performed primarily in a laboratory and manufacturing environment where exposure to biological agents, chemicals, and disinfectants may occur.
  • The role requires adherence to all safety procedures, including the use of PPE and compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • The noise level in the work environment is generally moderate but may vary depending on production activity.
  • The laboratory environment is temperature-controlled, but occasional work in production or warehouse areas may be required.
  • The employee must maintain a clean, organized, and safe workspace in accordance with company and regulatory standards.


Why Join Us?


At Radienz Living, we take pride in making high-quality personal care and household products that people trust every day. As part of our team, you’ll join a company that values safety, teamwork, and continuous improvement. We believe in investing in our people — providing hands-on experience, training, and opportunities to grow your career in manufacturing, quality, and operations.


You’ll work in a clean, professional, and collaborative environment where your contributions make a direct impact on the products we deliver to leading brands and consumers. At Radienz Living, we’re more than a manufacturing company — we’re a community built on respect, reliability, and shared success.


The approximate hourly pay for this position is $22-00-$27.00*. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to knowledge, skills and abilities as well as geographic location.


Radienz Living is an equal employment opportunity employer. All applicants will receive

consideration for employment without regard to race, color, religion, sex, sexual orientation,

gender identity, national origin, disability, or veteran status or any other characteristic

protected by applicable law. Prior to the next step in the recruiting process, we welcome you to

inform us confidentially if you may require any special accommodation to participate fully in

our recruitment experience. Contact us at hrny@radienzliving.com.


The company participates in the E-Verify program to confirm the employment eligibility of all new hires. This position is not eligible for Visa Sponsorship.