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Quality Systems Jobs in Massachusetts (NOW HIRING)

VulcanForms

Quality Systems Engineer

Harvard, MA · On-site

$75.41 - $103.69/hr

As a Quality Systems Engineer , you will be responsible for helping to ensure the QMS is established and maintained in accordance with applicable regulatory requirements. A candidate must have ...

CYNET SYSTEMS

Quality Systems Analyst

Boston, MA · On-site

$120 - $125/hr

Strong computer skills - Word, Excel, and other electronic Quality systems. Responsibilities: * Assist in Quality oversight for external GMP production and testing activities for clinical stage ...

VulcanForms

Quality Systems Engineer

Devens, MA · On-site

$75K - $103K/yr

As a Quality Systems Engineer, you will be responsible for helping to ensure the QMS is established and maintained in accordance with applicable regulatory requirements. A candidate must have ...

Editas Medicine

Manager, Quality Systems

Cambridge, MA · On-site

$135K - $150K/yr

Oversee Quality Systems ensuring health, effectiveness, and compliance. * Support the management and administration of the electronic document management system (Veeva QualityDocs), the electronic ...

Editas Medicine

Manager, Quality Systems

Cambridge, MA · On-site

$135 - $150/hr

Oversee Quality Systems ensuring health, effectiveness, and compliance. * Support the management and administration of the electronic document management system (Veeva QualityDocs), the electronic ...

Editas Medicine

Manager, Quality Systems

Cambridge, MA · On-site

$135K - $150K/yr

Oversee Quality Systems ensuring health, effectiveness, and compliance. * Support the management and administration of the electronic document management system (Veeva QualityDocs), the electronic ...

Gentuity

Quality Systems Manager

Sudbury, MA · On-site

ISO 13485 and FDA Quality System Regulation * Strong knowledge of Quality Systems programs including but not limited to Document Control, Record Control, Change Control, Training, and Device Master ...

Gentuity LLC

Quality Systems Manager

Sudbury, MA · On-site

$145K - $165K/yr

... Quality Systems programs including but not limited to Document Control, Record Control, Change Control, Training, and Device Master Record (DMR) • Demonstrated experience in administration of ...

USPRO

Quality Systems Manager

Lanesborough, MA

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

USPRO

Quality Systems Manager

North Adams, MA · On-site

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

USPRO

Quality Systems Manager

Florida, MA

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

Adecco

Quality Systems Engineer

Devens, MA · On-site

$80K - $105K/yr

This is an excellent opportunity for a quality professional with experience in ISO-compliant Quality Management Systems who is looking to join a global organization that offers long-term career ...

USPRO

Quality Systems Manager

Williamstown, MA

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

USPRO

Quality Systems Manager

Lee, MA · On-site

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

Gentuity

Quality Systems Manager

Sudbury, MA · On-site

... Quality System Regulation Strong knowledge of Quality Systems programs including but not limited to Document Control, Record Control, Change Control, Training, and Device Master Record (DMR ...

USPRO

Quality Systems Manager

Stockbridge, MA

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

USPRO

Quality Systems Manager

Hinsdale, MA

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

USPRO

Quality Systems Manager

West Stockbridge, MA · On-site

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

USPRO

Quality Systems Manager

Pittsfield, MA · On-site

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

USPRO

Quality Systems Manager

Washington, MA · On-site

$110K/yr

The Quality Control Manager will provide hands-on leadership across inspection, testing, documentation, quality systems, and continuous improvement activities. Working closely with Production and ...

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All JobsQuality Systems JobsQuality Systems Jobs in Massachusetts

Quality Systems information

See Massachusetts salary details

$59K

$107.7K

$168.2K

How much do quality systems jobs pay per year?

As of Sep 5, 2026, the average yearly pay for quality systems in Massachusetts is $107,698.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,500.00 and $133,800.00 per year, depending on experience, location, and employer.

What is a quality system?

Quality Systems are structured processes and procedures that organizations establish to ensure their products or services consistently meet defined quality standards and regulatory requirements. These systems typically include documentation, training, auditing, corrective actions, and continuous improvement practices. Quality Systems are essential in industries like manufacturing, pharmaceuticals, and healthcare to maintain compliance and customer satisfaction. Implementing a robust Quality System helps organizations minimize errors, improve efficiency, and comply with industry regulations.

How does a quality systems professional typically collaborate with other departments to maintain compliance and improve processes?

Quality Systems professionals work closely with departments like Manufacturing, Regulatory Affairs, and Research & Development to ensure that quality standards and compliance requirements are consistently met. They facilitate communication between teams, conduct audits, and coordinate corrective actions to address any issues. Collaboration often involves leading training sessions, reviewing documentation, and implementing continuous improvement initiatives based on feedback from various stakeholders. This cross-functional teamwork is essential for maintaining certifications and driving process excellence throughout the organization.

What are the key skills and qualifications needed to thrive as a quality systems professional, and why are they important?

To thrive as a Quality Systems professional, a solid understanding of quality management principles, process improvement methodologies, and compliance standards such as ISO 9001 is essential, often supported by a relevant degree or certification. Familiarity with quality management software (QMS), audit tools, and document control systems is typically required. Strong attention to detail, problem-solving abilities, and effective communication are vital soft skills that distinguish top performers in this role. These capabilities are crucial for maintaining regulatory compliance, driving continuous improvement, and ensuring consistent product or service quality.

What is the difference between Quality Systems vs Quality Assurance?

AspectQuality SystemsQuality Assurance
FocusDeveloping, implementing, and maintaining quality management systemsMonitoring and verifying product quality through audits and inspections
CertificationsISO 9001, ISO 13485, QS standardsISO 9001, industry-specific standards
Work EnvironmentQuality departments, compliance teamsProduction lines, inspection units
Employer UsageManufacturers, healthcare, aerospaceManufacturers, service providers

While both roles aim to ensure product quality, Quality Systems focuses on establishing and maintaining the overall quality management framework, whereas Quality Assurance emphasizes verifying and validating that products meet quality standards through testing and inspections.

What does a quality systems specialist do?

A quality systems specialist develops, implements, and maintains quality management systems to ensure products and processes meet industry standards and regulations. They analyze data, conduct audits, and collaborate with teams to improve quality and compliance, often using tools like ISO standards and quality software. Certification in quality management, such as ISO 9001, is common in this role.

What are the most commonly searched types of Quality Systems jobs in Massachusetts?

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

What are popular job titles related to Quality Systems jobs in Massachusetts?

For Quality Systems jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Quality Systems jobs in Massachusetts look for?

The top searched job categories for Quality Systems jobs in Massachusetts are:

Quality Systems jobs near you
Infographic showing various Quality Systems job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 1% Temporary, 4% Contract, and 2% Nights. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $107,698 per year, or $51.8 per hour.

Quality Systems Engineer

VulcanForms

Harvard, MA • On-site

$75.41 - $103.69/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Key responsibilities

  • Ensure that a Quality System is established and maintained in accordance with applicable regulatory requirements

  • Write, review, and approve changes to QMS documentation and support the NCR, CAPA, and internal audit programs

  • Support the tracking, trending, and analysis of quality metrics and KPIs to identify areas for improvement

Job description

Founded in 2015 to develop the world’s first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We build and operate advanced digital infrastructure that enables innovation, accelerates growth, and supports sustainability across aerospace, defense, medical, and other essential industries. Through our vertically integrated capabilities, including scalable additive manufacturing and precision machining, we deliver true end-to-end production at scale by combining cutting-edge technology with a foundation of proven industrial craftsmanship. Our team brings deep expertise in manufacturing, materials science, software, automation, and operations, united by a shared commitment to quality, curiosity, and accountability. We foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because we believe diverse perspectives lead to better outcomes.

Job Purpose
  • As a Quality Systems Engineer, you will be responsible for helping to ensure the QMS is established and maintained in accordance with applicable regulatory requirements. A candidate must have knowledge of quality systems, CAPA, NCR, and document control. This position is responsible for writing and updating QMS procedures and is accountable for ensuring quality processes are executed compliantly. QMS compliance will be met by ensuring that activities previously noted are conducted according to prescribed procedures, policies, and regulations.
Key Responsibilities
  • Ensure that a Quality System is established and maintained to the highest levels of accordance with applicable regulatory requirements
  • Write, review, and approve the release of changes to QMS documentation
  • Support the NCR program
  • Support the internal audit program
  • Support the CAPA program
  • Support the preparation of Management Review
  • Support the QMS training program
  • Work with other functions to ensure accurate, complete, and efficient change processing and document control activities
  • Support the tracking and trending of quality metrics/KPIs (e.g., CAPAs, NCs, SCARs, complaints, deviations, internal audit findings, calibration, etc.
  • Identify areas of improvement through data-driven trending and bring solutions to management
  • Lead/support Quality System projects effectively
  • Develop innovative and practical solutions to complex and unique process problems and systematic improvements through the use of best practices
  • Identify/escalate any compliance issues and their potential impact and provide potential solutions/actions so that they can be effectively resolved
  • Support audits and inspections as needed (e.g., coordinate preparation activities, FR/BR support, track resolution activities
  • Lead or support additional projects as assigned by QS Leadership
Qualifications
  • 3+ years’ experience working in the medical device or aerospace fields with experience in FDA regulatory requirements, ISO 13485, and/or AS9100/ISO9001
  • Experience in writing QMS procedures
  • Experience in NCR and CAPA
  • Excellent communication, interpersonal and leadership skills
  • Experience working with and evaluating Quality metrics and KPIs
Preferred Qualifications
  • Experience with Start-ups
  • Experience in audit support
  • Experience leading and influencing across functional groups and leadership levels

VulcanFormsoffers a competitive salary and equitypackage.Actual compensation is based on factors such as the candidate's skills, qualifications, and experience.In addition,VulcanFormsprovides comprehensive benefits including medical, dental, vision, and life insurance; generous paid time off; and a 401(k) plan with companymatch.

The annual base salary range for this position is $75,413.00 to $103,692.00.

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