Senior Quality Manager Jobs in Massachusetts
Senior Quality Manager jobs in Massachusetts are in strong demand, with the highest concentration in medical devices, biopharmaceuticals, defense systems, and advanced manufacturing. Boston, Lowell, and Worcester anchor most of the hiring, and established employers like Raytheon Technologies, Boston Scientific, and Thermo Fisher Scientific maintain deep quality leadership teams across the state. The most sought-after specialties include regulatory quality systems, supplier quality assurance, and FDA-regulated manufacturing compliance. Find a role that fits below and apply directly.
Find Senior Quality Manager JobsOverview
Showing 5 of 102+ Senior Quality Manager jobs
- Provide expertise in Risk Management, Design Verification and Validation, Process Validation, Statistical Methods and Design Controls.
- Drive Design Assurance activities throughout Product Life Cycle management.
- Drive quality system execution to U.S. regulations (21 CFR 820), International regulations and standards( IVDR and ISO 13485)
- Assist in maintaining and improving the quality management system documentation and processes to meet or exceed all applicable requirements
- Develop and validate test methods and inspection procedures and implement process control systems to support the development, qualification, and on-going manufacturing of products.
- Drive continuous improvement and CAPA projects, and proactively identify and implement best-in-class quality engineering practices.
- Support supplier quality management, including maintaining the Approved Supplier List, performing audits of sub-contractors and material / component suppliers.
- Apply systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues.
- Execute and review engineering change orders and document change requests
- Facilitate product risk management activities (e.g., Risk Management Plans, Risk Management Reports, Risk Management Files, Hazard Analyses, FMEAs)
- Identify, prioritize, communicate and resolve quality issues given dynamic business needs
- Identify and implement effective process controls to support the development, qualification, and manufacturing of products.
- Generate quality metrics, perform trend analyses, and identify preventive / corrective actions to drive product quality and process improvements through the CAPA process or other methods.
- Participate in developing inspection requirements for procured and manufactured products.
- Lead MRB and Nonconformance activities
- Participate in internal and external audits and other quality system maintenance/improvement activities to be compliant with various regulatory standards and regulations, such as Management Review
- Provide support to the complaint handling function as required
- Provide support in design control activities as required.
- Perform other duties as assigned
- Bachelor of Science Degree in Engineering or Science
- At least 4 years’ experience in OEM medical device manufacturing of FDA approved or 510k cleared product
- Able to use Microsoft Office (Microsoft Word, Excel, PowerPoint)
- Extensive working knowledge of GMP, FDA regulations (21 CFR Part 820), ISO 13485
- Ability to write, review, and execute deviations, nonconformance reports, CAPAs, and complaints.
- Previous experience with electronic document management systems preferred
- Ability to read, understand and follow all company SOPs and guidelines.
- Utilize critical thinking skills to problem solve and troubleshoot.
- Ability to communicate (written and verbal) and interact effectively with all levels of the organization.
- Good organizational skills and strong attention to detail.
- Must be able to perform job requirements independently with minimal supervision.
- Adjusts easily and readily to a fast-paced work environment with changing priorities
- Travel up to 5%
- Compensation: $120k to $140k with a 7% target bonus.
- Provide expertise in Risk Management, Design Verification and Validation, Process Validation, Statistical Methods and Design Controls.
- Drive Design Assurance activities throughout Product Life Cycle management.
- Drive quality system execution to U.S. regulations (21 CFR 820), International regulations and standards( IVDR and ISO 13485)
- Assist in maintaining and improving the quality management system documentation and processes to meet or exceed all applicable requirements
- Develop and validate test methods and inspection procedures and implement process control systems to support the development, qualification, and on-going manufacturing of products.
- Drive continuous improvement and CAPA projects, and proactively identify and implement best-in-class quality engineering practices.
- Support supplier quality management, including maintaining the Approved Supplier List, performing audits of sub-contractors and material / component suppliers.
- Apply systematic problem-solving methodologies to identify, prioritize, communicate, and resolve quality issues.
- Execute and review engineering change orders and document change requests
- Facilitate product risk management activities (e.g., Risk Management Plans, Risk Management Reports, Risk Management Files, Hazard Analyses, FMEAs)
- Identify, prioritize, communicate and resolve quality issues given dynamic business needs
- Identify and implement effective process controls to support the development, qualification, and manufacturing of products.
- Generate quality metrics, perform trend analyses, and identify preventive / corrective actions to drive product quality and process improvements through the CAPA process or other methods.
- Participate in developing inspection requirements for procured and manufactured products.
- Lead MRB and Nonconformance activities
- Participate in internal and external audits and other quality system maintenance/improvement activities to be compliant with various regulatory standards and regulations, such as Management Review
- Provide support to the complaint handling function as required
- Provide support in design control activities as required.
- Perform other duties as assigned
- Bachelor of Science Degree in Engineering or Science
- At least 4 years’ experience in OEM medical device manufacturing of FDA approved or 510k cleared product
- Able to use Microsoft Office (Microsoft Word, Excel, PowerPoint)
- Extensive working knowledge of GMP, FDA regulations (21 CFR Part 820), ISO 13485
- Ability to write, review, and execute deviations, nonconformance reports, CAPAs, and complaints.
- Previous experience with electronic document management systems preferred
- Ability to read, understand and follow all company SOPs and guidelines.
- Utilize critical thinking skills to problem solve and troubleshoot.
- Ability to communicate (written and verbal) and interact effectively with all levels of the organization.
- Good organizational skills and strong attention to detail.
- Must be able to perform job requirements independently with minimal supervision.
- Adjusts easily and readily to a fast-paced work environment with changing priorities
- Travel up to 5%
- Compensation: $120k to $140k with a 7% target bonus.
See All 102+ Senior Quality Manager Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
Find Senior Quality Manager JobsSenior Quality Manager Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
Senior Quality Manager Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
- Vertex Pharmaceuticals10
- Raytheon5
- Katalyst Healthcares & Life Sciences4
- Boston Scientific3
- Hologic2
Top Industries Hiring
- Medical Devices
- Consulting & Professional Services
- Biotechnology & Pharmaceuticals
- Manufacturing
- Healthcare & Medical Services
What Massachusetts Employers Look For
The qualifications that appear most often in senior quality manager jobs across Massachusetts.
- Bachelor's degree in engineering, life sciences, or a related technical discipline required
- Minimum seven years of quality management experience in regulated manufacturing environments
- Demonstrated experience with FDA 21 CFR Part 820 or ISO 13485 quality system standards
- Proven ability to lead corrective and preventive action programs across cross-functional teams
- ASQ Certified Quality Manager or Certified Quality Engineer credential strongly preferred
- Proficiency with quality management software such as Veeva Vault, MasterControl, or TrackWise
Senior Quality Manager Jobs in Massachusetts: Frequently Asked Questions
How do you become a senior quality manager in Massachusetts?
Most senior quality managers in Massachusetts follow a path that begins with a technical or scientific bachelor's degree, followed by progressive quality roles in a regulated industry such as medical devices, biotech, or defense. There is no state-issued license for this role, but employers in Massachusetts consistently require credentials such as the ASQ Certified Quality Manager or Certified Quality Engineer. Building deep experience with FDA regulations or ISO standards is the clearest way to reach a senior level.
How much do senior quality managers make in Massachusetts?
Senior quality managers in Massachusetts earn a median of about $148,050 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $99,920 for the lowest 10% to over $227,080 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire senior quality managers in Massachusetts?
Employers hiring senior quality managers in Massachusetts right now include Vertex Pharmaceuticals, Raytheon, and Katalyst Healthcares & Life Sciences, based on current listings on Migrate Mate as of August 2026. Massachusetts's dense concentration of medical device, biopharmaceutical, and aerospace firms means demand for senior quality leadership is consistent throughout the year.
Which Massachusetts cities have the most senior quality manager jobs?
Boston, Andover, and Waltham have the most senior quality manager openings in Massachusetts. Greater Boston drives the largest share of demand because of its cluster of biotech and medical device headquarters along Route 128, while Lowell and Worcester draw openings from established defense contractors and precision manufacturing companies with long-standing operations in those areas.
Are there remote senior quality manager jobs in Massachusetts?
Yes, but they are rare. Senior quality manager work is heavily tied to physical production lines, regulated manufacturing floors, and in-person audits, which limits full remote opportunities. About 54% of senior quality manager openings tied to Massachusetts are remote or hybrid as of August 2026, and those arrangements tend to apply to quality systems, documentation, or supplier oversight functions rather than direct manufacturing oversight.
How can I get hired as a senior quality manager in Massachusetts with little or no experience?
The most realistic entry path is a quality engineer or quality specialist role at a Massachusetts medical device or biotech company, where structured rotational or associate programs at employers like Boston Scientific or Thermo Fisher Scientific give candidates hands-on exposure to regulated quality systems. Pursuing an ASQ Certified Quality Auditor credential early and targeting internal promotions within a single quality organization is how most professionals in the state build toward a senior title without starting at that level.
Where can I find and apply to senior quality manager jobs in Massachusetts?
You can find and apply to senior quality manager jobs in Massachusetts on Migrate Mate, which lists current Massachusetts openings. Find roles that fit your background and apply directly to the ones that match.
See All 102+ Senior Quality Manager Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
Find Senior Quality Manager Jobs