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Quality Management System Manager Jobs in Massachusetts

The Raytheon Quality Management System (QMS) is a collection of business processes focused on consistently meeting customer requirements and enhancing customer satisfaction. We are seeking an ...

The Raytheon Quality Management System (QMS) is a collection of business processes focused on consistently meeting customer requirements and enhancing customer satisfaction. We are seeking an ...

Role Summary The Director, Quality Management Systems is a quality leader responsible for designing ... Leads the evolution of the QMS into a commercial-ready, globally scalable system aligned with ICH ...

Enforce compliance to quality management system, develop and maintain quality processes, and support audits of the quality management system. * Manage compliance of products to regulatory ...

Manager, Quality Systems

Cambridge, MA · On-site

$135K - $150K/yr

Support the management and administration of the electronic document management system (Veeva QualityDocs), the electronic quality management system (Veeva QMS), and the electronic learning ...

Manager, Quality Systems

Cambridge, MA · On-site

$135K - $150K/yr

Support the management and administration of the electronic document management system (Veeva QualityDocs), the electronic quality management system (Veeva QMS), and the electronic learning ...

Quality Manager

Dudley, MA · On-site

$110K - $130K/yr

Essential Duties and Responsibilities Quality Management System & Regulatory Compliance * Maintain and continually improve the HSWoA Quality Management System in compliance with FDA Quality System ...

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Quality Management System Manager information

What is the difference between Quality Management System Manager vs Quality Assurance Manager?

AspectQuality Management System ManagerQuality Assurance Manager
Primary FocusDeveloping, implementing, and maintaining quality management systemsOverseeing quality assurance processes and testing
CertificationsISO 9001 Lead Auditor, CQEASQ CQE, Six Sigma Green/Black Belt
Work EnvironmentQuality departments, compliance teamsProduction, manufacturing, or service delivery areas
Industry UsageManufacturing, healthcare, aerospaceManufacturing, software, healthcare

The Quality Management System Manager focuses on establishing and maintaining comprehensive quality systems, ensuring compliance with standards like ISO 9001. In contrast, the Quality Assurance Manager concentrates on testing, inspections, and ensuring products or services meet quality requirements. Both roles are essential for quality improvement but differ in scope and daily responsibilities.

What does a quality management system manager do?

A quality management system manager oversees the development, implementation, and maintenance of quality management systems to ensure products and services meet company standards and regulatory requirements. They analyze processes, conduct audits, and coordinate continuous improvement initiatives, often using tools like ISO standards and quality metrics. Strong leadership, communication skills, and knowledge of quality tools are essential for this role.

What is the role of a quality management system manager?

A quality management system manager oversees the development, implementation, and maintenance of quality management systems to ensure products and services meet industry standards and customer requirements. They analyze processes, conduct audits, and coordinate with teams to improve quality, often utilizing standards like ISO 9001. Strong organizational, analytical, and communication skills are essential for this role.

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

The most popular types of Quality Management System jobs in Massachusetts are:

Infographic showing various Quality Management System Manager job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 10% Part Time, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Quality Management System Lead

Boston, MA • On-site

Tango Therapeutics
Biotechnology Research and Development • 11 - 50 employees

$151K - $226K/yr

Full-time

Re-posted 4 days ago


Job description

Company Overview
Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.
Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.
This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.
The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts.
Summary
Own and continuously improve the QMS framework to ensure processes, document control, training, and quality records support consistent compliance across functions and regions.
Your Role:
  • Define and maintain QMS structure: policies, SOPs, work instructions, templates, and governance
  • Ensure harmonization across GxP domains (GMP/GLP/GCP) and alignment with applicable regulations/standards
  • Oversee document lifecycle management (authoring standards, review/approval, periodic review, archival)
  • Ensure change control processes exist and are followed (QMS changes and cross-functional change impacts)
  • Oversee GxP training framework (curricula, assignment rules, effectiveness checks, compliance reporting)
  • Partner with functional owners to define role-based training requirements
  • Ensure QMS records are complete, traceable, audit-ready, and meet data integrity principles
  • Establish metrics and trending for QMS health (cycle time, overdue items, training compliance)
  • Lead QMS simplification/optimization, including CAPA prevention initiatives based on trending and learnings
  • Prepare Quality Management Review packages: KPIs, risks, audit outcomes, CAPA effectiveness, and improvement plans

What You Bring:
  • Bachelor's degree in Life Sciences, Quality, or related discipline (required)
  • Quality-related certification preferred (e.g., ASQ, ISO Lead Auditor, Quality Systems)
  • Training in electronic QMS platforms advantageous
  • 8-12 years in Quality Assurance or Compliance
  • Hands-on experience managing QMS in regulated GxP environments
  • Experience supporting QMS-related inspections and audits
  • QMS design, lifecycle management, and governance
  • GxP training systems and compliance tracking
  • Data integrity and document control standards
  • Process-oriented, structured, and detail focused
  • Strong communication and training skills
  • Ability to simplify complex processes and drive alignment

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
Salary range
$151,200-$226,800 USD