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Quality Associate Jobs in Chester, NY (NOW HIRING)

Hawkins Inc.

Quality Associate

Florida, NY

$23/hr

Learn more about us at ABOUT THE JOB The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe ...

Hawkins

Quality Associate

Florida, NY · On-site

$23/hr

Learn more about us at ABOUT THE JOB The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe ...

Stauber

Quality Associate

Florida, NY · On-site

$23/hr

Learn more about us at ABOUT THE JOB The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe ...

Stauber

Quality Associate

Florida, NY

$23/hr

Learn more about us at ABOUT THE JOB The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe ...

Strides Pharma Inc

QA Associate I

Spring Valley, NY · On-site

$22 - $26/hr

POSITION SUMMARY The Quality Associate I, Operations is responsible for actively participating in "on the floor" Quality activities during product manufacturing and/or packaging. Quality activities ...

Careers at RK Pharma Inc.

QA Associate

Pearl River, NY · On-site

$55K - $95K/yr

About the Role The QA Associate supports production-related quality activities to ensure processes, data, and documentation meet GMP and regulatory expectations. This role works closely with ...

Sysco

Quality Assurance Associate

Florida, NY

Communicate quality issues to buyers, management, and associates. Report all lost product or transfers. * Assure that all inventory is properly blocked and labeled. * Inspects product on production ...

Strides Pharma Inc

QA Associate (QMS)

Spring Valley, NY · On-site

$58K - $65K/yr

Position Summary The QA Associate supports the site's Quality Management System by managing product complaints, adverse events, and investigation activities. This role contributes to deviation and ...

Synerfac Technical Staffing

Quality inspector

Mahwah, NJ · On-site

$24 - $27/hr

Associates degree or higher or equivalent experience * Knowledge of electronics manufacturing * Previous experience as a quality inspector, preferably in a manufacturing environment * IPC620 / J-STD ...

Synerfac Technical Staffing

Quality inspector

Mahwah, NJ

$24 - $27/hr

Associates degree or higher or equivalent experience * Knowledge of electronics manufacturing * Previous experience as a quality inspector, preferably in a manufacturing environment * IPC620 / J-STD ...

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Quality Associate information

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How much do quality associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality associate in Chester, NY is $27.46, according to ZipRecruiter salary data. Most workers in this role earn between $18.61 and $32.12 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 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 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 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.

More about Quality Associate jobs

What job categories do people searching Quality Associate jobs in Chester, NY look for?

The top searched job categories for Quality Associate jobs in Chester, NY are:

What cities near Chester, NY are hiring for Quality Associate jobs?

Cities near Chester, NY with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Chester, NY as of August 2026, with employment types broken down into 43% Full Time, 44% Part Time, and 13% Temporary. Highlights an 100% In-person job distribution, with an average salary of $57,117 per year, or $27.5 per hour.

Quality Associate

Hawkins Inc.

Florida, NY

$23/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago

Job description

About Hawkins

Hawkins, Inc. is a formulator, manufacturer, blender, distributer, and sales agent for thousands of industrial chemicals and reagent grade laboratory chemicals sold to municipalities and businesses throughout the Central United States. Thousands across a variety of industries have depended on Hawkins for the chemical products they need since 1938.

Learn more about us at https://www.hawkinsinc.com/careers/

ABOUT THE JOB

The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe work practices through all stages of manufacturing, packaging, labeling and storage. Completes specific quality-related duties associated with batch manufacturing processes including inspection, monitoring, verification, recordkeeping, and approval. Works with personnel from other departments as needed to identify and resolve quality or production issues. Monitors operations and personnel for compliance with company policy and procedure, GMP, safety and other requirements.  

DUTIES AND RESPONSIBILITIES:

  • Recommend, review, approve, conduct, and/or complete documentation for key activities in support of batch manufacturing and to assure compliance with company policy and cGMP including: line clearances; checking-in jobs (verifying material identify/quantity); required approvals and releases; batch record review including master, in-process and completed batch records; process deviations; product rework plans; other assignments as needed. 
  • Inspect and monitor the batch manufacturing process and personnel work practices for compliance with cGMP and company policy. 
  • Assist with development of programs and writing standard operating procedures, work instructions and other procedural documents. 
  • Complete special request documentation including customer questionnaires. 
  • Handle key activities in conjunction with, and as a back-up to, quality specialist including technical documents, sampling/inspecting/testing materials and products, and maintaining database information. 
  • Alert production and quality managers immediately of problems impacting production.

                        ABOUT YOU:

                        • BS/BA in a Science background preferred but not required; or related experience and/or training; or equivalent combination of education and experience.  
                        • 2+ years’ experience in manufacturing, QC lab, or other environment related to food, dietary ingredient, dietary supplement, or pharmaceutical manufacturing. 
                          Able to multi-task in detail-driven environment. 
                        • Knowledge of relevant SOP's, cGMP, OSHA, FDA, and related requirements preferred. 
                        • Detail oriented. Ability to work independently and change focus to meet changing demands. Able to use independent judgment within company guidelines. 
                        • Bilingual Spanish a plus 
                        • Effective writing and verbal communication skills 
                        • Knowledge of MS Office Systems preferred.  
                        • Excellent analytical and problem-solving skills required. 
                        • Knowledge of CRM and ERP Systems such as JDE preferred 
                        • The person in this position needs to occasionally move about inside the office or production facility. 
                        • Must meet SQF requirements by following all applicable standards and reporting any food safety problems to Lead Process Technician, Plant Manager, or Quality Supervisor/Manager 

                                            TRAVEL

                                            Not required

                                            Expected Compensation: $23.00/hr. + 5% bonus eligibility  

                                            Hawkins offers eligible employees and their dependents comprehensive benefits, which includes medical, dental, vision, life insurance, LTD/STD and more.Other benefits for eligible employees include 401(k) match, Employee Stock Purchase program (ESPP), paid time off, and paid holidays.

                                            For more information on Hawkins benefits, visit:   https://www.hawkinsinc.com/careers/benefits/

                                            Ref. 2027-111

                                            All applications must be received online.  All 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 characteristics protected by law.  Hawkins is a Drug Free workplace.

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