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Associate Quality Manager Jobs in Massachusetts (NOW HIRING)

Globus Medical

Associate Quality Engineer

Methuen, MA · On-site

The Associate Quality Engineer will be responsible for achieving the highest quality level of ... This person will play an integral role in maintaining and improving the quality management system ...

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 ... Knowledge of ISO 9001 or AS9100 quality management systems. * Experience with FMEA, Six Sigma, and ...

Nelson Miller Group

Quality Manager

Fitchburg, MA · On-site

Associate or bachelor's degree in engineering or a related technical field. Experience: Minimum of ... Knowledge of ISO 9001 or AS9100 quality management systems. * Experience with FMEA, Six Sigma, and ...

Nelson Miller Group

Quality Manager

Fitchburg, MA · On-site

Associate or bachelor's degree in engineering or a related technical field. Experience: Minimum of ... Knowledge of ISO 9001 or AS9100 quality management systems. * Experience with FMEA, Six Sigma, and ...

Safariland

Production QA - Quality Manager

Dalton, MA · On-site

The Quality Manager will lead the Quality Management System (QMS), manage internal and external ... want associates to be involved in their work and communities so they can achieve their highest ...

Safariland

Production QA - Quality Manager

Dalton, MA · On-site

The Quality Manager will lead the Quality Management System (QMS), manage internal and external ... want associates to be involved in their work and communities so they can achieve their highest ...

Safariland

Production QA - Quality Manager

Dalton, MA · On-site

The Quality Manager will lead the Quality Management System (QMS), manage internal and external ... want associates to be involved in their work and communities so they can achieve their highest ...

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 ...

Podimetrics

Quality Associate

Somerville, MA · On-site

Podimetrics has since evolved to become a rapidly growing virtual care management company with ... The Quality Associate will work closely with Regulatory Affairs, Quality Engineering, Device ...

Podimetrics

Quality Associate

Somerville, MA

Podimetrics has since evolved to become a rapidly growing virtual care management company with ... The Quality Associate will work closely with Regulatory Affairs, Quality Engineering, Device ...

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All JobsAssociate Quality JobsAssociate Quality Manager JobsAssociate Quality Manager Jobs in Massachusetts

Associate Quality Manager information

See Massachusetts salary details

$13

$27

$55

How much do associate quality manager jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for associate quality manager in Massachusetts is $27.76, according to ZipRecruiter salary data. Most workers in this role earn between $18.89 and $32.55 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 Massachusetts?

The most popular types of Quality Manager jobs in Massachusetts are:

What cities in Massachusetts are hiring for Associate Quality Manager jobs?

Cities in Massachusetts with the most Associate Quality Manager job openings:

Associate Quality Manager jobs near you

Associate Quality Engineer

Methuen, MA • On-site

Globus Medical
Medical Equipment and Supplies Manufacturing • 501 - 1,000 employees

6.7

Company rating: 6.7 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

441st of 544 rated manufacturers

Learn more about Globus Medicalexternal

Full-time

Re-posted 9 days ago

Job description

At Globus Medical, we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and outcomes of surgery so patients can resume their lives as quickly as possible.
Position Summary:
The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be a self-motivated and characterized as an excellent problem solver. This person will play an integral role in maintaining and improving the quality management system, product quality, and manufacturing process quality.
Essential Functions:
  • Provide real-time quality support to manufacturing operations. Assist in identifying defects, performing root-cause analysis, and implementing corrections/corrective actions. Support defect reduction initiatives and process capability improvements.
  • Lead the containment, risk-based evaluation, disposition, and closure of Nonconforming Material records to prevent production delays and ensure consistent product quality
  • Facilitate MRB (Material Review Board) activities by preparing data, coordinating cross-functional input, and ensuring timely documentation
  • Drive continuous improvement in nonconforming material workflows, cycle time, and data accuracy
  • Support timely execution of CAPAs, ensuring proper documentation, risk assessment, and effectiveness verification. Collaborate with cross-functional teams to maintain CAPA compliance and prevent recurrence of issues.
  • Supports the development, implementation, and improvement of production monitoring methods and systems for product inspection and testing
  • Performs measurement systems analysis
  • Conduct thorough review of documentation, including but not limited to Document Change Orders (DCOs), engineering drawings, specifications, risk management files, and Verification & Validation (V&V) protocols and reports. Ensure documents meet regulatory, procedural, and quality system requirements and reflect appropriate risk controls and traceability.
  • Supports the validation of manufacturing processes, including activities associated with equipment installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ)
  • Assess Supplier documentation, including Certificates of Conformance, First Article Inspections, supplier process validations, quality agreements, and supplier responses to SCARs. Ensure suppliers provide adequate objective evidence and that documentation aligns with material, component, and product requirements.
  • Verify that all documentation changes are properly justified, risk-assessed, and approved through the appropriate change control process
  • Collaborate with cross-functional partners-Product Development, Operations, Supply Chain, Regulatory and Field Service-to clarify requirements, close gaps, and drive timely approval of documentation packages
  • Assist in preparation for external and internal audits by organizing documentation, gathering objective evidence, and responding to auditor requests. Support timely closure of audit observations.
  • Utilizes concepts of probability and statistical quality control to guide decisions
  • Establishes, follows, and improves company procedures
  • Provides written and oral reports to supervisor or other management personnel to keep them informed of activities and results. Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies. Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role
  • Represents the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties

Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions.
Qualifications:
  • Bachelor's Degree required (science or engineering preferred)
  • 0-2 years' experience in quality assurance; experience in the medical device industry preferred
  • GMP and ISO experience
  • Strong proficiency in MS Office with knowledge of statistical analysis tools
  • Knowledge of Lean Manufacturing, Six Sigma, and reliability engineering is a plus
  • Must be a team player capable of working in a deadline dictated environment
  • Excellent verbal and written communication skills
  • Self-starter
  • Advanced critical thinking and problems-solving skills

Physical Demands:
The physical demands listed here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
  • Required to sit; climb or balance; and stoop, kneel, crouch or crawl
  • Required to regularly lift and/or move up to 10 pounds, and occasionally lift and/or move up to 25 pounds
  • Required to possess specific visons abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus

Our Values:
Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven.
  • Passionate about Innovation: Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate in our role in improving the lives of patients by continuously developing better solutions.
  • Customer Focused: We listen to our customers' needs and respond with a sense of urgency.
  • Teamwork: Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger.
  • Driven: We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients.

Equal Employment Opportunity:
Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees' talents and support an environment that is inclusive and respectful.
Other Duties:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

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