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Quality Associate Jobs in Worcester, MA (NOW HIRING)

Adecco

Quality Inspector

Devens, MA · On-site

$20/hr

While working as a Quality Inspector for Adecco at our local Customer, you will earn $20.00/hour ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

Quality Inspector

Fitchburg, MA

$18 - $27/hr

Quality Inspector II Location: Fitchburg, MA Pay Range: $18.00 - $27 per hour Schedule: Monday ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

Quality Inspector

Fitchburg, MA

$18 - $27/hr

Quality Inspector II Location: Fitchburg, MA Pay Range: $18.00 - $27 per hour Schedule: Monday ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Lancesoft INC

Quality Technician

Acton, MA · On-site

$30 - $32/hr

Associates Degree in an engineering, or scientific discipline. Preferred Skills and Competencies ... Preferred 2 years in a Quality related function, working with QSR and/or ISO 13485. * Computer ...

New

Replimune

Senior Associate, Quality Systems

Framingham, MA · On-site

$101K - $131K/yr

This position will participate in the improvement of Quality Systems to ensure quality and adherence with current Good Manufacturing Practice (cGMP) and inspection readiness. * This position is based ...

Veranova L P

Senior QA Associate

Devens, MA · On-site

$90K - $105K/yr

Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals ...

medplast

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of ...

medplast

Quality Engineer

Brimfield, MA

$70K - $95K/yr

Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of ...

Viant

Quality Engineer

Brimfield, MA · On-site

$70K - $95K/yr

Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of ...

medplast

Quality Engineer

Brimfield, MA

$70K - $95K/yr

Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, leads each of these groups with capability studies and the application of ...

New England Keyboard Inc

Quality Manager

Fitchburg, MA · On-site

Associate or bachelor's degree in engineering or a related technical field. Experience: Minimum of three to five years of progressive quality experience , with demonstrated leadership experience.

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Quality Associate information

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How much do quality associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for quality associate in Worcester, MA is $26.87, according to ZipRecruiter salary data. Most workers in this role earn between $18.22 and $31.44 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

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

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

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

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

Quality Associate jobs near you
Infographic showing various Quality Associate job openings in Worcester, MA 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 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $55,896 per year, or $26.9 per hour.

Senior Associate, Plant Quality Assurance

Replimune

Framingham, MA • On-site

$99K - $128K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 2 days ago

Job description

Overview
Replimune's mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full-body anti-tumor response, boldly transforming cancer care because patient's lives depend on it.
At Replimune, we live by our values:
United: We Collaborate for a Common Goal.
Audacious: We Are Bold.
Dedicated: We Give Our Full Commitment.
Candid: We Are Honest With Each Other.
People are at the center of everything we do, and when it comes to our employees, we make it personal. With a deep sense of purpose, a strong and evolving culture, a competitive and forward-looking total rewards program, everyone at Replimune has a unique opportunity to impact on the lives of patients, caregivers and themselves.
Join us, as we reshape the future.
Summary of job description:
The Senior Associate, Plant Quality Assurance (PQA) reports to the Manager, Plant Quality Assurance and is responsible for providing day-to-day Quality oversight to support Drug Substance, Drug Product, and Quality Control operations in accordance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and other applicable regulatory requirements.
This position works closely with Manufacturing, Quality Control, and other cross-functional teams to support compliance initiatives, batch record review, quality record review, and maintenance of a quality-focused culture. The Senior Associate serves as a key quality partner on the manufacturing floor and provides guidance to ensure activities are performed in compliance with established procedures and regulatory expectations.
  • This position is based in our Framingham location and typically has a 5-day on-site expectation.

Key responsibilities:
  • Provide on-floor Quality Assurance support during second shift operations to help ensure manufacturing and testing activities are performed in compliance with cGMP requirements and approved procedures.
  • Perform quality walkthroughs and inspections to promote an inspection-ready environment and identify potential compliance concerns.
  • Support the review and timely closure of quality records, including deviations, CAPAs, and change controls.
  • Review production batch records, logbooks, and laboratory documentation for accuracy, completeness, and compliance with established procedures.
  • Assist in authoring, revising, and reviewing quality system documents, including standard operating procedures, training materials, risk assessments, and validation related documentation.
  • Provide guidance and support to manufacturing and support personnel regarding cGMP, GDP, and quality system requirements.
  • Participate in root cause investigations and support development and implementation of corrective and preventative actions.
  • Escalate quality issues and compliance risks to management as appropriate.
  • Support training activities related to procedures, cGMP requirements, and quality systems.
  • Identify, own, and execute continuous improvement initiatives, incorporating cross-functional input and driving projects to timely completion.

Other responsibilities:
  • Support internal and external audits and regulatory inspections as required.
  • Contribute to continuous improvement initiatives within the Quality Management System.
  • Collaborate effectively with cross-functional teams to promote quality and compliance objectives.
  • Perform other duties as assigned.

Educational requirements:
  • BA or BS degree in a scientific discipline or related field, or equivalent combination of education and relevant experience.

Experience and skill requirement:
  • 3-5+ years of experience in the pharmaceutical, biotechnology, or related regulated industry.
  • Minimum of 3 years of experience in Quality Assurance, Quality Control, Manufacturing, or a related GMP-regulated function.
  • Working knowledge of cGMP regulations, GDP requirements, and quality systems.
  • Ability to manage multiple priorities in a fast-paced manufacturing environment.
  • Strong written and verbal communication skills.
  • Experience reviewing GMP documentation and quality records.
  • Demonstrated ability to work collaboratively across multiple departments.
  • Experience providing quality support within a GMP manufacturing environment preferred.

Replimune is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. For this role, the anticipated base pay range is $99,500 -$128,500. The exact base pay offered for this role will depend on various factors, including but not limited to the selected candidate's unique set of qualifications, skills, and experience. Our current organizational needs also play a part in determining your final offer.
At Replimune, base pay is only one part of your total compensation package. The selected candidate will be eligible for an annual performance incentive bonus, new hire equity, and ongoing performance-based equity. Replimune also offers various benefits offerings, including, but not limited to, medical, dental, and vision insurance, 401k match, flexible time off, and a number of paid holidays including year-end shutdown.
About Replimune
Replimune Group, Inc., headquartered in Woburn, MA, was founded in 2015 with the mission to transform cancer treatment by pioneering the development of a novel portfolio of oncolytic immunotherapies. Replimune's proprietary RPx platform is based on a potent HSV-1 backbone intended to maximize immunogenic cell death and the induction of a systemic anti-tumor immune response. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. The RPx product candidates are expected to be synergistic with most established and experimental cancer treatment modalities, leading to the versatility to be developed alone or combined with a variety of other treatment options. For more information, please visit www.replimune.com.
We are an Equal Opportunity Employer.

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