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Quality Associate Jobs in Mansfield, MA (NOW HIRING)

NYGCI

Quality Assurance Associate II

Framingham, MA · On-site

We provide IT Professional Services to local, regional and global customers and reduce their IT risk and maximize their IT performance. The QA Product Release Associate is responsible for ensuring ...

NYGCI

Quality Assurance Associate II

Framingham, MA

We provide IT Professional Services to local, regional and global customers and reduce their IT risk and maximize their IT performance. The QA Product Release Associate is responsible for ensuring ...

CEDENT

Quality Assurance Associate I

Cumberland, RI · On-site

The QA Associate II/III independently conducts quality assurance audits of production records (manufacturing, analytical and quality control records) and facility records assuring company standards ...

Randstad

Quality Control Associate I

Norwood, MA

$35 - $38/hr

Quality Control Associate I * Location: Norwood, MA (100% On-Site) * Job Type: 6-Month Contract * Pay Rate: Up to $38.00 / hour (commensurate with experience) * Target Start Date: September 7, 2026

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Quality Associate information

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How much do quality associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for quality associate in Mansfield, MA is $28.51, according to ZipRecruiter salary data. Most workers in this role earn between $19.33 and $33.32 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 Mansfield, MA?

The most popular types of Quality jobs in Mansfield, MA are:

What job categories do people searching Quality Associate jobs in Mansfield, MA look for?

The top searched job categories for Quality Associate jobs in Mansfield, MA are:

What cities near Mansfield, MA are hiring for Quality Associate jobs?

Cities near Mansfield, MA with the most Quality Associate job openings:

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Mansfield, MA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 3% Contract, and 2% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $59,301 per year, or $28.5 per hour.

QA Documentation Associate

Integrated Resources INC

Cambridge, MA

Contractor

Re-posted 12 days ago

Job description

Company Description

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Job Description: 

The Quality Assurance Associate I is responsible for contributing to the oversight of key functional, tactical, and operational aspects within Quality Assurance at the Company CAM facility. 

The Quality Documentation Associate I responsibilities include, but are not limited to: 

1. An Associate I is responsible for supporting key functional, tactical, and operational aspects of the Quality Assurance department. 

2. An Associate I should possess a fundamental understanding of the Company Quality Systems and apply it in their daily support functions. 

3. Additional responsibilities include ensuring adherence to all regulatory licenses and regulations, review/approval of GMP procedures, protocols and reports, support the development and performance of GxP Quality systems-related training, participate in internal/external compliance audits. 

4. Interfacing with key Quality, manufacturing, and PO&T customers. 

5. The Associate I will also support the Quality Management for activities related to archiving, imaging, and maintaining archived documents. 

6. The Associate I should have a working knowledge of Library Sciences and be able to work computerized data management systems. 


Job Responsibilities 

Utilizing Library Sciences maintain QA archive room, to include routine scanning, cataloging and filing of Quality Controlled data and documents. 

Coordinate shipping of records to and from offsite storage facilities. 

Work within an electronic document management system to review and provide final Quality approval of Standard Operating Procedures, Master Production Records, Solution Lot Records and other related GMP records. Perform the issuance and printing of quality controlled documents effectively and efficiently ensuring customer needs and schedules are maintained. 

Provide Quality Assurance representation and guidance at Technical Transfer meetings for manufacturing campaigns. Provide technical assistance to manufacturing operations as related to compliance requirements. 

Support the inspection documentation room activities during regulatory agency inspections; to include assembling, printing, tracking and refiling/archiving of all documentation requests. 

Supports and/or assists in GxP quality systems-related training. 

Responsible for scanning, archiving and shipping of GxP documentation and data. 

Responsible for providing final review of GxP documents in support of the Pharmaceutical Operation and Technology business unit. 



Qualifications

Required Experience: 

Incumbent should have a Bachelor of Science Degree or Bachelors in Library Science or 3 years related industry experience. 

Prior experience in pharmaceutical, biotech manufacturing or library science environment is preferred. 

Additionally, prior experience with regulatory audits is also preferred. 



Additional Information

Warm Regards,


Amanpreet Kaur

Clinical Recruiter

Integrated Resources Inc.

IT LIFE SCIENCES ALLIED HEALTHCARE CRO 

Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012, 2013 & 2014 (8th Year)

Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70

(W) 732-429-1913| (F) 732-549-5549





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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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