QA Manager Jobs in Massachusetts
QA Manager jobs in Massachusetts are in strong demand, concentrated in the state's robust life sciences, medtech, and defense sectors, with openings at every level from quality assurance coordinator up through senior QA director. Boston, Cambridge, and Worcester anchor most of the hiring activity, with established employers like Thermo Fisher Scientific, Raytheon Technologies, and Boston Scientific maintaining consistent QA manager needs across manufacturing, regulatory compliance, and software quality functions. Professionals with experience in FDA-regulated environments or AS9100 aerospace standards are especially sought after in the Massachusetts market. Find a role that fits below and apply directly.
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Showing 5 of 70+ QA 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 70 QA Manager Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
Find QA Manager JobsQA Manager Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
QA Manager Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals
- Healthcare & Medical Services
- Consulting & Professional Services
- Technology & Software
- Food & Beverage
What Massachusetts Employers Look For
The qualifications that appear most often in QA manager jobs across Massachusetts.
- Bachelor's degree in engineering, life sciences, or a related technical field
- Five or more years of quality assurance experience in a regulated Massachusetts industry
- Demonstrated knowledge of FDA regulations, GMP, or ISO 13485 standards
- Proficiency with quality management systems such as MasterControl or Veeva Vault
- Experience leading root cause analysis, CAPA processes, and internal audits
- Certified Quality Manager or Six Sigma Black Belt credential preferred
QA Manager Jobs in Massachusetts: Frequently Asked Questions
How do you become a qa manager in Massachusetts?
Most qa managers in Massachusetts enter the field through a bachelor's degree in engineering, biology, chemistry, or a related discipline, then build experience in quality assurance roles within FDA-regulated industries like pharmaceuticals, medtech, or aerospace. Massachusetts does not require a state-issued license for qa managers, but employers strongly favor credentials such as the ASQ Certified Quality Manager or a Six Sigma Black Belt. Advancing to a management role typically requires several years in quality technician, specialist, or engineer positions at Massachusetts-based manufacturers or biotech firms.
Which companies hire qa managers in Massachusetts?
Employers hiring qa managers in Massachusetts right now include Replimune, Redwire Space, and Boston Scientific, based on current listings on Migrate Mate as of August 2026. Massachusetts's dense concentration of life sciences companies, defense contractors, and medtech manufacturers means qa manager hiring stays active year-round across the greater Boston corridor and I-495 technology belt.
Which Massachusetts cities have the most qa manager jobs?
The Massachusetts cities with the most qa manager openings are Boston, Waltham, and Marlborough. Boston and Cambridge drive much of the demand through their concentration of biotech, pharmaceutical, and academic medical institutions, while Worcester and the I-495 corridor attract strong hiring from medical device manufacturers and defense contractors that have long maintained operations in central and metrowest Massachusetts.
Are there remote qa manager jobs in Massachusetts?
Yes, but they are less common than in purely desk-based fields. About 53% of qa manager openings tied to Massachusetts are remote or hybrid as of August 2026, reflecting that many QA functions require on-site presence for facility audits, production floor oversight, and hands-on equipment validation. The portions of the role most compatible with remote work include documentation review, supplier audits conducted by video, and quality system analysis.
How can I get hired as a qa manager in Massachusetts with little or no experience?
The most realistic entry path is landing a quality technician, quality control inspector, or manufacturing associate role at a Massachusetts life sciences or defense manufacturer, then building toward management over time. Large employers such as Thermo Fisher Scientific and Boston Scientific hire quality associates and rotational program participants directly out of college. Earning an ASQ Certified Quality Improvement Associate credential before applying gives candidates a concrete edge, and internships through UMass or Northeastern's cooperative education programs frequently convert to full-time quality roles.
Where can I find and apply to qa manager jobs in Massachusetts?
You can find and apply to qa manager jobs in Massachusetts on Migrate Mate, which lists current openings from Massachusetts employers across the life sciences, defense, medtech, and technology sectors. Find roles that fit your experience and apply directly to the employers posting them.
See All 70 QA Manager Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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