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Quality Associate Jobs in Boston, MA (NOW HIRING)

The Quality Assurance Specialist will work directly with validation project coordinators, technical area representatives and laboratory management Primary responsibilities are reviewing laboratory ...

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

Associate Director, GMP Quality

Boston, MA · On-site

$160K - $180K/yr

About the Role >>> Associate Director GMP Quality As the Associate Director, GMP Quality, reporting to the Head of GMP Quality, you will be responsible for oversight of GMP activities pertaining to ...

Act as a liaison between functions within the organization. * Assist current inspectors and quality engineers with tasks to improve the flow of material. * Assist in tasks to support day to day ...

Showing results 41-60

Quality Associate information

See Boston, MA salary details

$12

$29

$55

How much do quality associate jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for quality associate in Boston, MA is $29.26, according to ZipRecruiter salary data. Most workers in this role earn between $19.86 and $34.23 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 Boston, MA?

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

What are popular job titles related to Quality Associate jobs in Boston, MA?

For Quality Associate jobs in Boston, MA, the most frequently searched job titles are:

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

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

Infographic showing various Quality Associate job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, 5% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $60,858 per year, or $29.3 per hour.
Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees

Full-time

Re-posted 6 days ago


Job description

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.


We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.


Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success.

Job Description

The Quality Assurance Specialist will work directly with validation project coordinators, technical area representatives and laboratory management

Primary responsibilities are reviewing laboratory test protocols and reports, coordinating SOP document revisions, entering electronic training records, maintaining tracking spreadsheets and filing paper copies of laboratory records

Reviewing laboratory testing protocols

Verify that customer information from a questionnaire has been accurately and completely transcribed into a document template

Reviewing lab testing reports. Verify that lab testing data based on the protocol guidance has been accurately captured in the report template

Reviewing data tables and laboratory records

Perform all function of a document controller and training administrator including, but not limited to, processing requests for new documents, revising existing documents, coordinating document validity reviews, entering information into the document and training databases and maintaining associated electronic and hard copy records

Issue controlled documentation for laboratory test data packages

Provide support as needed to administrative staff and validation project coordinators including scanning and filing documents, revising/editing documents, making photocopies and preparing customer mailings. 

Qualifications

Proficient with Microsoft Word and Excel

Attention to detail

Document Proof Reading

Excellent written and verbal communication skills

Documentation preparation and review

Worked in a laboratory

Working knowledge of laboratory information databases

Responsible for document control responsibilities

Responsible for training record maintenance

Experience handling corrective and preventive actions (i.e. CAPA)

Experience with audits

Equipment validation and calibration

Lean and Six Sigma certification

CQA, CQE or CBA 

College education

Additional Information

Kind Regards

Ricky


Integrated Resources logo

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