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Quality Associate Jobs in Meriden, CT (NOW HIRING)

Quality Clinical Associate

Branford, CT · On-site

$20 - $27.50/hr

Assists Manager and others in the Quality Department in recognizing unmet needs within the organization and assists in planning and development of corrective actions * Works closely with the ...

Associate Quality Engineer

Torrington, CT · On-site

$82K - $95K/yr

The Associate Quality Engineer is responsible for ensuring the quality output of internal manufacturing processes and the quality levels for incoming purchased materials used in the manufacturing ...

Quality Starts With You What You'll Earn & Enjoy: * Comprehensive healthcare * Paid holidays & vacation * Retirement savings benefits * Employee discount program * Discounted Sysco stock (SYY) JOB ...

Quality Specialist We are looking for a Quality Specialist (Technician) to join our New Britain, CT team! Our Quality Technician is responsible for ensuring that products, materials, and processes ...

Quality Specialist We are looking for a Quality Specialist (Technician) to join our New Britain, CT team! Our Quality Technician is responsible for ensuring that products, materials, and processes ...

Quality Specialist We are looking for a Quality Specialist (Technician) to join our New Britain, CT team! Our Quality Technician is responsible for ensuring that products, materials, and processes ...

This is a great opportunity to further your existing quality assurance and inspection skills while ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco is hiring a night shift Quality Inspector for a leading personal care products manufacturer ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Quality Inspector

Milford, CT · On-site

$18.50/hr

Adecco is hiring a night shift Quality Inspector for a leading personal care products manufacturer ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Quality Technician

Berlin, CT · On-site

$17.75 - $24/hr

What we are looking for: 3 years + experience in Quality Control performing audit, inspection ... Associates degree in a technical field preferred. * Good mechanical, analytical, mathematical and ...

Quality Technician

Berlin, CT · On-site

$17.75 - $24/hr

What we are looking for: 3 years + experience in Quality Control performing audit, inspection ... Associates degree in a technical field preferred. * Good mechanical, analytical, mathematical and ...

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Quality Associate information

See Meriden, CT salary details

$10

$26

$49

How much do quality associate jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for quality associate in Meriden, CT is $26.40, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $30.87 per hour, depending on experience, location, and employer.

What is a quality associate?

Quality Associates are professionals responsible for ensuring that products or services meet established quality standards before reaching customers. They assist in monitoring production processes, performing inspections, and documenting quality issues or defects. Quality Associates also help implement quality control procedures and work closely with other departments to resolve any quality-related problems. Their role is essential in maintaining compliance with regulatory requirements and ensuring customer satisfaction.

What does a quality associate do?

A quality associate works as part of a team, typically in the manufacturing industry, to inspect and audit a factory to ensure that production follows the necessary protocols and delivers the expected results. In this role, your responsibilities involve all aspects of quality control. You test procedures and make adjustments as required to meet goals and deadlines. As part of your duties, you log your findings and implement a plan for the smooth operation of the line for the long-term. Some people in this career specialize in a particular facet of the manufacturing process.

What are the key skills and qualifications needed to thrive as a quality associate, and why are they important?

To thrive as a Quality Associate, you need attention to detail, knowledge of quality control principles, and often a degree in science, engineering, or a related field. Familiarity with quality management systems (such as ISO 9001), statistical analysis tools, and documentation software is typically required. Strong analytical thinking, communication skills, and problem-solving abilities help you collaborate across teams and address process issues effectively. These skills and qualities ensure that products and processes consistently meet standards, minimizing errors and maintaining compliance.

What are some common challenges quality associates face when working on cross-functional teams?

Quality Associates often collaborate with departments like manufacturing, engineering, and regulatory affairs to ensure product quality standards are met. One common challenge is balancing differing priorities—while production teams may be focused on output and speed, Quality Associates must prioritize compliance and thorough documentation. Navigating these competing interests requires strong communication skills and a proactive approach to problem-solving. Building positive relationships across teams and fostering a culture of quality can help overcome these challenges and ensure successful outcomes.

What is the difference between Quality Associate vs Quality Technician?

AspectQuality AssociateQuality Technician
Required CredentialsHigh school diploma or equivalent; some roles may prefer certifications like ASQ CQPAHigh school diploma; certifications like CQTA are common but not always required
Work EnvironmentOffice settings, manufacturing floors, labsManufacturing plants, labs, production lines
Employer & Industry UsageManufacturing, healthcare, aerospace, automotiveManufacturing, electronics, pharmaceuticals
Common Search & ComparisonOften compared for entry-level quality rolesSimilar roles but more technical focus

While both roles focus on quality assurance, a Quality Associate typically handles documentation, audits, and process improvements, often in office or administrative settings. A Quality Technician usually performs hands-on inspections, testing, and data collection directly on the production floor. Both roles are essential in maintaining product quality but differ in their daily tasks and work environments.

What are the most commonly searched types of Quality jobs in Meriden, CT?

The most popular types of Quality jobs in Meriden, CT are:

What cities near Meriden, CT are hiring for Quality Associate jobs?

Cities near Meriden, CT with the most Quality Associate job openings:

Infographic showing various Quality Associate job openings in Meriden, CT as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 5% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $54,903 per year, or $26.4 per hour.

QUALITY ASSOCIATE -PHARMACEUTICAL MFG.

TOWER LABORATORIES LTD.

Clinton, CT • On-site

Full-time

Medical, Dental, Life, Retirement

Posted 6 days ago


Job description

QA ASSOCIATE


Tower Laboratories is a leading effervescent product manufacturer in the U.S. We develop and manufacture over-the-counter medications, prescription pharmaceuticals, nutritional supplements, soft drink tablets and other consumer products on a contract basis. We are continually expanding our effervescent product base and currently have several new and interesting products in the research and development phase right now. We are a family owned company and have been in business for over 40 years. www.towerlabs.com.
 
POSITION SUMMARY:

This is a 2nd shift, salary exempt position. Minimum hours will be Monday to Friday, 3:50PM to 12:20AM.

Responsible for the enforcement of Tower Laboratories, Ltd. quality system which ensures production of a consistently high quality product. 

Work closely with production staff to ensure that our effervescent tablets and powders are manufactured in accordance with applicable procedures, specifications and in a cGMP (current Good Manufacturing Practices) compliant manner. Partners with manufacturing throughout production life cycle to assure that procedures are followed and activities are appropriately documented.   

ESSENTIAL FUNCTIONS:

  • Perform product manufacturing audits throughout process through observation and by conducting in-process testing to ensure product meets specifications.  
  • Conduct packaging audit ensuring final product meets packaging specifications and is within the allowed accepted quality limits (AQL); inspect all incoming packaging components, ensuring specifications are met by performing appropriate tests following determined component specifications.
  • Conduct investigations as directed and collect information to assess root causes when product or processes are not meeting specifications.
  • Assist in the conduct of internal audits of cGMP to ensure compliance to cGMP and internal procedures and policies.
  • Audit finished/completed batch production documents for procedural or mathematical errors prior to final review and release of product by the QA Manager.
  • Communicate identified manufacturing deficiencies to key personnel (Machine Operator, Quality Supervisor/Manager, Production Manager, etc.).  
  • Verify that all instrumentation used are calibrated and perform equipment calibrations as identified.
  • Work as a team member; be cooperative with all departments and staff to meet company objectives.
  • Perform all work in accordance with established Safety, cGMP and company procedures.
  • Other responsibilities as assigned.

ESSENTIAL SKILLS AND EXPERIENCE:

  • Minimum of 2 years’ experience in either pharmaceutical, food/beverage, nutritional supplement or another highly regulated environment.
  • Demonstrated strong attention to detail.
  • Knowledge of cGMP regulations highly preferred.
  • Working knowledge of MS Word and MS Excel.
  • Must be able to read and follow directions, complete paperwork and communicate effectively in English.
  • Excellent organizational skills.
  • Good interpersonal skills; ability to communicate effectively with all levels of plant personnel.
  • Strong team player, demonstrated team attitude and behaviors.

PHYSICAL DEMANDS:

  • Lift, push, pull up to 25lbs. on occasional basis
  • Climb stairs, walking throughout manufacturing/warehouse areas
  • Must be able to wear safety shoes & safety glasses when in manufacturing/warehouse areas
  • Must be able to wear sanitary attire such as gloves, hairnet, face mask and lab coat.

EDUCATION:  

High school diploma or equivalent; degree desirable.

This medium sized family business is headquartered in the scenic town of Centerbrook in Southeastern Conn., and offers a clean, humidity & temperature controlled, friendly working environment and complete benefit package, including: medical, dental, short term and long term disability, life and AD&D insurances, Flexible Spending Accounts, Health Savings Accounts, 401(k) with company match, tuition assistance, free counseling with EAP, free uniforms, safety shoe and glasses reimbursements. 

Qualified candidates apply today to start the conversation! Tower Labs is a Socially Responsible Employer and a great place to work! 


We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law