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Quality Associate Jobs in Worcester, MA (NOW HIRING)

Adecco

Quality Inspector

Devens, MA

$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 ...

Central Wire

Quality Supervisor

Pomfret Center, CT · On-site

Associate's or Bachelor's degree in Engineering, Quality, Manufacturing, or a related field. * Experience in an ISO 13485 regulated manufacturing environment. * AS9100 Internal Auditor or Lead ...

Posted today

Alkermes

Associate Director, Clinical QA

Waltham, MA

$166K - $181K/yr

This position is an integral part of the CQA team and provides oversight for and participates in, auditing services in support of Alkermes Clinical Programs by conducting clinical site, vendor ...

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 ...

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 ...

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 ...

AIS

Quality Technician

Leominster, MA

$16.50 - $23/hr

Associate's or Bachelor's in a Technical field required * 3+ years of experience in a quality role within a manufacturing sector. * Familiarity with Lean, Quality Tools, Six Sigma, Audits, or ...

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All JobsQuality Associate JobsQuality Associate Jobs in Worcester, MA

Quality Associate information

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How much do quality associate jobs pay per hour?

As of Jul 31, 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 are Quality Associates?

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 are the most commonly searched types of Quality jobs in Worcester, MA? The most popular types of Quality jobs in Worcester, MA are:
What are popular job titles related to Quality Associate jobs in Worcester, MA? For Quality Associate jobs in Worcester, MA, the most frequently searched job titles are:
What job categories do people searching Quality Associate jobs in Worcester, MA look for? The top searched job categories for Quality Associate jobs in Worcester, MA are:
What cities near Worcester, MA are hiring for Quality Associate jobs? 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 July 2026, with employment types broken down into 1% As Needed, 66% Full Time, 30% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $55,896 per year, or $26.9 per hour.

Associate Director, Clinical Quality Assurance

Kailera Therapeutics, Inc.

Waltham, MA

Other

Re-posted 12 days ago

Job description

Responsibilities:

  • Oversee and ensure compliance with GCP/GVP regulations, guidelines, and internal policies throughout clinical trial and pharmacovigilance activities
  • Develop and implement quality assurance plans and strategies for clinical studies and related activities
  • In collaboration with internal stakeholders, ensure risk-based quality management is applied as appropriate to specific studies (e.g. through helping to facilitate the identification of critical data and critical data processes, and risks associated with them, establishing, monitoring and reporting out on Quality Tolerance Limits (QTLS))
  • Monitor and track quality metrics to identify trends and areas of improvement
  • Ensure the timely completion of quality assurance activities, including audits, investigations, and inspection readiness
  • Facilitate review of potential Serious Breach and Urgent Safety Measure assessments arising from clinical program
  • Plan, coordinate, review and approve internal, external, and clinical site audits using risk-informed strategy to ensure GCP/GVP compliance in clinical studies and pharmacovigilance operations
  • Assess audit findings and develop corrective and preventative actions (CAPA)
  • Lead investigations into quality issues and deviations, identifying root causes and implementing appropriate CAPA
  • Ensure that investigations are conducted in a timely and thorough manner, following established procedures
  • Develop and implement inspection readiness plans and procedures, ensuring that clinical studies and related activities are ready for Health Authority inspections
  • Provide guidance and support to cross-functional teams during Health Authority inspections
  • Collaborate with cross-functional teams to support data integrity during audits, inspections and clinical trial activities by adhering to GxPs standards and applicable regulations governing clinical data
  • Provide training and guidance to cross-functional teams on GCP/GVP regulations, Quality Assurance procedures, and audit protocols
  • Serve as a subject matter expert on GCP/GVP quality assurance matters
  • Participate in the selection and evaluation of Vendors, ensuring that they meet quality standards and regulatory requirements
  • Review and approve GCP/GVP-related documentation, including study protocols, study reports, and other relevant documents
  • Ensure that documentation is accurate, complete, and compliant with regulations
  • Facilitate/participate in Quality Oversight Committee meetings with Vendors and develop and maintain quality agreements with Vendors

Qualifications:

  • Minimum of 10 or more years of experience in FDA regulated industry
  • Previous hands-on experience with Veeva Quality Docs, Veeva Training, and Veeva QMS required
  • A strong customer focus and ability to prioritize and adapt to business needs are required
  • Strong business partner with a focus on collaborating and delivering results
  • Self-motivated, detail oriented, well organized, and able to demonstrate success with managing multiple projects simultaneously and other priorities
  • Understanding and knowledge of applicable industry regulations
  • Ability to interact constructively and efficiently within and across functional areas and management
  • Ability to resolve day-to-day issues efficiently while maintaining compliance
  • Clear, concise writing skills and good verbal communication and presentation skills
  • Proficiency in Microsoft Word, Power Point, Excel, Adobe, and SharePoint
  • Comply with Company quality standards/SOPs and implementation of new quality systems
  • Provide imaginative, thorough, and practical solutions to problems
  • Solve conflict and address workplace issues in a professional and collaborative manner

Education:

  • Bachelor's degree required

Apply