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

Manager, Quality Systems

Cambridge, MA · On-site

$135 - $150/hr

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

Overall management of quality control activities; oversee the development and implementation of robust systems and procedures to ensure evaluation, measurement and improvement of processes. * Manage ...

Overall management of quality control activities; oversee the development and implementation of robust systems and procedures to ensure evaluation, measurement and improvement of processes. * Manage ...

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 ...

You will establish the quality management system, build the team, and create the standards and systems that ensure our advanced hardware products meet the highest quality bar. This is a high ...

You will establish the quality management system, build the team, and create the standards and systems that ensure our advanced hardware products meet the highest quality bar. This is a high ...

Eaton is a global leader in intelligent power management, serving customers in more than 160 ... We are seeking an experienced Quality Manager to lead quality assurance and compliance efforts ...

Eaton is a global leader in intelligent power management, serving customers in more than 160 ... We are seeking an experienced Quality Manager to lead quality assurance and compliance efforts ...

Quality Manager

Woburn, MA · On-site

$150K/yr

Eaton is a global leader in intelligent power management, serving customers in more than 160 ... We are seeking an experienced Quality Manager to lead quality assurance and compliance efforts ...

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Showing results 1-20

Manager Quality Management information

See Boston, MA salary details

$26.1K

$93.6K

$171.7K

How much do manager quality management jobs pay per year?

As of Sep 3, 2026, the average yearly pay for manager quality management in Boston, MA is $93,604.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,800.00 and $147,800.00 per year, depending on experience, location, and employer.

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

AspectManager Quality ManagementQuality Assurance Supervisor
Primary FocusOversees overall quality management systems and strategic initiativesSupervises daily quality assurance activities and team performance
CertificationsISO 9001 Lead Auditor, Six Sigma Green/Black BeltISO 9001 Internal Auditor, Six Sigma Green Belt
Work EnvironmentManagement level, strategic planning, cross-departmental coordinationOperational, team supervision, hands-on quality checks
Industry UsageCommon in manufacturing, healthcare, and tech industriesPrevalent in manufacturing, pharmaceuticals, and production sectors

The Manager Quality Management typically handles strategic quality initiatives and system oversight, while the Quality Assurance Supervisor focuses on supervising daily QA activities and team management. Both roles require similar certifications and are integral to maintaining quality standards within organizations, but they differ mainly in scope and level of responsibility.

What does a manager quality management do?

A manager of quality management oversees the development and implementation of quality standards and processes within an organization. They analyze data, conduct audits, and lead continuous improvement initiatives to ensure products or services meet customer and regulatory requirements. Strong leadership, analytical skills, and knowledge of quality tools like Six Sigma or ISO standards are essential for this role.

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

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

Infographic showing various Manager Quality Management job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $93,604 per year, or $45 per hour.

Manager, Quality Management Systems & Validations

Ocular Therapeutix

Bedford, MA • On-site

Full-time

Re-posted 4 days ago


Job description

Position Summary:

The Manager, Quality Management Systems & Validations is responsible for overseeing and managing Ocular's QMS and Quality Assurance Validations activities to ensure compliance with regulatory requirements and Ocular standards. Key QMS responsibilities include overseeing the management of Quality Events processes (Deviations, Corrective/Preventive Actions (CAPAs), and Change Controls) as well as the continuous improvement of Ocular's QMS.

Key QA Validations responsibilities include leading and overseeing the validation of GxP systems and processes, managing review and approval of validation activities, ensuring the validated status of the systems, cross-functional collaboration on projects risk assessments and deviations, and continuously improving the QA Validation Program.

This is a critical position within the Quality organization and onsite presence is essential due to the level of cross-functional collaboration that it involves. This position is reporting to the Senior Director, Quality Assurance.

Principal Duties and Responsibilities:

Validations:

  • Maintaining the validated state of all GxP systems to ensure they operate in a state of compliance with internal procedures, regulatory requirements, and industry best practices.
  • Leading, directing, and advising on validation activities, which include the review and approval of validation protocols and documentation.
  • Working cross-functionally with other departments on a variety of projects, including risk assessments, and Quality Events associated with validations.
  • Leading continuous improvement initiatives for the Validation Program to enhance effectiveness and efficiency.
  • Ensuring the integrity of data generated by GxP systems.
  • Maintaining Ocular's QA Validation Program in a state of compliance and inspection readiness.
  • Participating as the SME during regulatory/internal inspections for QA Validations topics.

QMS:

  • Leading, planning, and managing Ocular's QMS, acting as the technical expert of Quality Events topics.
  • Leading/overseeing routine QA activities associated with the lifecycle of the Quality Events, including initiation, investigation, and closure.
  • Developing and implementing policies, schedules, and guidelines for the appropriate management of Ocular's QMS.
  • Leading the Change Control Review Board forum and providing guidance to the owners and collaborators of Change Control records.
  • Supporting the transformation of Ocular's QMS aimed to optimize the systems and add efficiency to the processes.
  • Establishing communication forums to disseminate information on QMS policies and other topics to all Ocular staff.
  • Participating in cross-functional teams to resolve Quality Events potentially impacting Ocular's operations.
  • Developing, trending, and reporting relevant Quality Metrics associated with the Deviations, CAPAs, and Change Controls.
  • Directing and advising on Facility related work orders
  • Maintaining Ocular's QMS in a state of compliance and inspection readiness.
  • Participating as the SME during regulatory/internal inspections for Quality Events topics.
Requirements:
  • Bachelor's Degree in Life Sciences or related field.
  • 10+ years of experience in the pharmaceutical industry with cross-functional experience.
  • Experience leading and working in a GxP setting (commercial and/or clinical).
  • Experience in e-QMS and compliance.
  • Experience supporting the management of Quality Events and validation activities.
  • Knowledge of domestic and international regulatory guidelines such as, CFR 210, 211, USP, FDA, ICH, MHRA, EMA, and others, associated with QMS and validations.
  • Experience with external regulatory inspections (e.g., FDA).
  • Excellent organizational skills and attention to
  • Strong interpersonal, verbal, and written communication
  • Computer literacy, proficiency in MS Word, Excel, PowerPoint,

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