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Associate Quality Manager Jobs in Boston, MA (NOW HIRING)

Replimune

Senior Associate, Quality Systems

Framingham, MA · On-site

$101K - $131K/yr

Manage and prioritize document-related requests through the Jira ticketing system, ensuring timely ... Support Quality Records, VEEVA system. Create reports, dashboards, ability to pull metrics and ...

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All JobsAssociate Quality JobsAssociate Quality Manager JobsAssociate Quality Manager Jobs in Boston, MA

Associate Quality Manager information

See Boston, MA salary details

$13

$27

$54

How much do associate quality manager jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for associate quality manager in Boston, MA is $27.61, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $32.40 per hour, depending on experience, location, and employer.

What does an associate quality manager do?

An Associate Quality Manager assists in overseeing quality assurance processes within an organization to ensure products or services meet established standards. They help develop and implement quality control procedures, monitor compliance, and collaborate with various departments to address quality issues. Additionally, they may analyze data, support audits, and provide training to staff on quality best practices. Their work helps maintain customer satisfaction and regulatory compliance.

What are some common challenges faced by an associate quality manager, and how can they be effectively addressed?

Associate Quality Managers often encounter challenges such as ensuring consistent compliance with evolving quality standards, managing cross-departmental communication, and balancing multiple projects with tight deadlines. To address these, it's important to stay up-to-date with industry regulations, foster open communication channels with production and engineering teams, and utilize project management tools to track progress. Proactive problem-solving and continuous process improvement are also key strategies to overcome these challenges and drive quality initiatives forward.

What are the key skills and qualifications needed to thrive as an associate quality manager, and why are they important?

To thrive as an Associate Quality Manager, you need a solid understanding of quality assurance processes, problem-solving abilities, and a relevant degree in engineering, science, or a related field. Familiarity with quality management systems such as ISO 9001, statistical analysis tools, and process improvement methodologies like Six Sigma is typically required, and certifications such as CQE or Lean Six Sigma are highly valued. Strong attention to detail, effective communication, and leadership skills help you drive quality initiatives and collaborate across teams. These competencies are crucial for ensuring product compliance, minimizing defects, and supporting continuous improvement within an organization.

What is the difference between Associate Quality Manager vs Quality Control Specialist?

AspectAssociate Quality ManagerQuality Control Specialist
CertificationsISO 9001, Six Sigma, ASQ certificationsISO 9001, Six Sigma, ASQ certifications
Work EnvironmentManufacturing, healthcare, or tech industries overseeing quality processesManufacturing, production lines, labs focusing on product inspection
Employer & Industry UsageUsed in companies with quality management systems, often in managerial support rolesUsed in production and manufacturing settings for product inspection and testing

The Associate Quality Manager and Quality Control Specialist roles share similar certifications and work environments but differ in scope. The Associate Quality Manager typically oversees broader quality processes and supports quality management systems, while the Quality Control Specialist focuses on inspecting and testing products to ensure quality standards are met.

What are the most commonly searched types of Quality Manager jobs in Boston, MA?

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

Associate Quality Manager jobs near you

QA Associate, Quality Operations

Integrated Resources, Inc

Norton, MA

$40 - $46/hr

Full-time

Posted 8 days ago

Job description

Title: QA Associate, Quality Operations
Location: Norton, MA
Duration: 6months+
Pay: $40-46/hr. on w2
About the Role:
The QA Associate will help ensure that life-changing biopharmaceutical products are manufactured to the highest standards. The QA Associate will provide day-to-day QA support across manufacturing, validation, materials, QC, engineering and facility operations at our Norton site, partnering with cross-functional teams to maintain GMP compliance and inspection readiness.
Key Responsibilities:
  • Provide raw material support, including review/approval of incoming material documentation and release for GMP use.
  • Deliver on-the-floor QA support to manufacturing, including area clearance and changeover operations, ensuring readiness for production activities.
  • Review and approve SOPs, master batch records (MBRs), specifications, risk assessments, and quality documents.
  • Generate and maintain Quality-related SOPs and controlled forms.
  • Review and approve validation documents and protocol executions to confirm compliance with approved procedures and regulatory requirements.
  • Review and approve QC laboratory qualification documents, including equipment qualification.
  • Perform executed batch record review and approval to ensure accuracy and compliance.
  • Review and approve deviations, CAPAs, Change Controls and related investigations in the quality management system.
  • Support partner audits and regulatory inspections, including document retrieval and subject matter input.
  • Approve work orders in the maintenance system to verify equipment maintenance and calibration compliance.
  • Collaborate with internal cross-functional teams at the Norton facility to drive continuous improvement and quality excellence.
Qualification/Skills:
  • Bachelor’s degree in a scientific or engineering discipline (Biology, Chemistry, Biotechnology, etc.) or equivalent experience.
  • 2–4 years of GMP experience in Quality, Manufacturing, or QC.
  • Knowledge of cGMP regulations (21 CFR Parts 210/211/11, ICH Q7/Q10) and Good Documentation Practices.
  • Strong attention to detail, organizational skills, and the ability to communicate effectively across teams.
  • Experience with quality systems (e.g., Veeva, SAP) is a plus.
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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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