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Quality Associate Jobs in Newtown, CT (NOW HIRING)

BIOWAVE CORPORATION

Quality Systems Associate

Westport, CT · On-site

$50K - $60K/yr

Quality Systems Associate Quality Department Reports to Sr. Manager Quality Systems 19 Newtown Turnpike, Westport, CT 06880 Full-time on-site position ​ About BioWave BioWave is a Medtech company ...

The Rizzo Companies

QA/QC Associate

Danbury, CT

Quality Assurance/Quality Control Associate Position Summary Rizzo Corporation is seeking a full-time Quality Assurance/Quality Control (QA/QC) Associate. This individual is responsible for ...

The Rizzo Companies

QA/QC Associate

Danbury, CT · On-site

Quality Assurance/Quality Control Associate Position Summary Rizzo Corporation is seeking a full-time Quality Assurance/Quality Control (QA/QC) Associate. This individual is responsible for ...

Total Mortgage

Quality Control Associate

Milford, CT · On-site

$65 - $90/hr

Purpose and Scope This position works with the Quality Control Manager for pre- and post-closing quality control, investor post purchase requests, mortgage insurance company and investor audit ...

Posted today

Adecco

Quality Inspector

Milford, CT

$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 ...

Adecco

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 ...

Cadence Inc

Quality Inspector

Watertown, CT · On-site

High school diploma or equivalent; associate degree in a related field preferred. * 1-2 years of inspection experience in a manufacturing environment. * Proven experience in quality control or ...

Ametek

Quality Inspector

Bridgeport, CT

As the Quality Inspector you will perform dimensional and functional inspection of in process ... other associates in procedures and use of equipment. * Maintain work area in a clean and safe ...

LanceSoft Inc

Senior Quality Engineer

North Haven, CT

$88K - $119K/yr

Oversee and provide leadership for Quality Engineers, Associate Quality Engineers and other personnel as necessary. Tracking timelines and facilitating the required Quality Engineering Tools.

Hamilton by Gunnebo

Quality Specialist

Milford, CT · On-site

$65 - $80/hr

The Quality Specialist focuses on writing work instructions and is detail‑oriented, analytical ... Associates Degree in Engineering, Operational Management, or other related field * Experience with ...

LanceSoft Inc

Quality Engineer III

North Haven, CT · On-site

$71K - $92K/yr

Oversee and provide leadership for Quality Engineers, Associate Quality Engineers and other personnel as necessary. Tracking timelines and facilitating the required Quality Engineering Tools.

Ametek

Quality Inspector

Bridgeport, CT · On-site

$35K/yr

As the Quality Inspector you will perform dimensional and functional inspection of in process ... other associates in procedures and use of equipment. * Maintain work area in a clean and safe ...

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All JobsQuality Associate JobsQuality Associate Jobs in Newtown, CT

Quality Associate information

See Newtown, CT salary details

$11

$27

$52

How much do quality associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for quality associate in Newtown, CT is $27.74, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $32.45 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.

More about Quality Associate jobs

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

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

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

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

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Newtown, CT as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 17% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $57,704 per year, or $27.7 per hour.

Quality Systems Associate

BIOWAVE CORPORATION

Westport, CT • On-site

$50K - $60K/yr

Full-time

Posted 4 days ago

Job description


Quality Systems Associate

Quality Department

Reports to Sr. Manager Quality Systems

19 Newtown Turnpike, Westport, CT 06880

Full-time on-site position

​

About BioWave

BioWave is a Medtech company redefining pain management through our innovative, non-invasive technology that delivers powerful relief without drugs or surgery. We offer a range of products designed to meet the unique needs of different markets, delivering effective, customized pain relief solutions where they’re needed most. Our technology is backed by clinical evidence and real-world results, helping patients reduce pain, restore function, and reclaim their lives. Trusted by healthcare professionals, athletes, veterans, and individuals alike, BioWave targets pain at its source to provide long-lasting results.

Vision & Mission

Our Vision is to transform pain management by solving complex pain conditions with innovative, patented, drug-free technology and patient-first, collaborative support - empowering clinicians to deliver better outcomes and enabling people to reclaim their lives with less pain and more possibility. 

Our Mission is to help people win their battle with severe pain.

Job Description

Support the maintenance and day-to-day administration of BioWave’s Quality System. This entry-level role assists with document control, training records, change management, nonconformances, CAPA, complaints, and risk management activities, while helping the organization maintain compliance and quality objectives for BioWave.

Duties and Responsibilities

To perform this job successfully, an individual must be able to perform the following satisfactorily (other duties may be assigned). Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Assist with maintaining quality system records and reports, including CAPA, nonconformance, document control, training, and audit tracking logs.
  • Support CAPA and nonconformance processes by following up on due dates, collecting documentation, and helping ensure records are complete and current.
  • Assist with document control activities, including formatting, routing, issuance, revision updates, and archival of quality system documents.
  • Help support internal and external audit readiness by organizing records, preparing documentation, and assisting with follow-up actions.
  • Maintain training records and help ensure employees are assigned and complete required quality system training.
  • Provide administrative and coordination support for quality system improvements and electronic QMS activities, as assigned.
  • Additional responsibilities as required by management. 

Required Experience/Skills

Competencies: To perform the job successfully, an individual should demonstrate the following competencies.

  • Achievement focus – demonstrates persistence and overcomes obstacles. Measures self against standard of excellence. Recognizes and acts on opportunities.  Sets and achieves challenging goals.  Takes calculated risks to accomplish goals.
  • Business Ethics – Inspires the trust of others. Keeps commitments. Treats people with respect. Upholds organizational values. Works with integrity and ethically.
  • Communications – exhibits good listing and comprehension. Expresses ideas and thoughts in written form. Expresses ideas and thoughts verbally. Keeps others adequately informed. Selects and uses appropriate communication methods.
  • Quality Management – Foster’s quality focus in others. Improves processes, products and services. Measures key outcomes. Sets clear quality requirements. Solicits and applies customer feedback.
  • Teamwork – balances team and individual responsibilities. Contributes to building a positive team spirit. Exhibits objectivity and openness to other views Gives and welcomes feedback. Puts success of team above own interests.

Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education/Experience:

Bachelor's degree from a four-year college or university, or equivalent combination of education and experience, with approximately two years of related quality systems, quality assurance, or regulated industry experience.

Experience in a medical device company or other ISO 9001/13485-regulated environment is preferred.

Language Ability:

Read, analyze and interpret scientific and technical journals, financial reports and legal documents. Respond to inquiries or complaints from customers, agencies or members of the business community. Write speeches and articles for publication. Working knowledge of/Fluency in the English language (spoken and written).

Mathematical Ability:

Apply advanced concepts such as exponents, logarithms, quadratic equations and permutations. Apply operations to such tasks as frequency distribution, test reliability/validity, variance analysis, correlation technique, sampling theory and factor analysis.

Reasoning Ability:

Define problems, collect data, establish facts and draw valid conclusions. Interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

Computer Skills:

To perform this job successfully, an individual should have knowledge of 

  • Working to intermediate knowledge of Microsoft Office applications (e.g., Word, Excel, PowerPoint, Outlook)
  • Exposure to electronic Quality Management Systems is preferred

Certificates and Licenses:

  • None required.
  • Certified auditor or other Quality Certification is a bonus

Supervisory Responsibilities: N/A

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

No hazardous or significantly unpleasant conditions.  Standard office environment and/or remote work.