QA Lead Jobs in Massachusetts
QA Lead jobs in Massachusetts are in strong demand, with consistent openings concentrated in life sciences and biotech, financial technology, enterprise software, and defense systems across a range of levels from associate QA lead through senior and principal. The largest hiring centers are Boston and Cambridge, with significant activity in Worcester and the Route 128 technology corridor, where employers like Biogen, MathWorks, and Raytheon Technologies maintain substantial QA and quality engineering teams. Automated testing, regulatory compliance quality assurance in FDA-regulated environments, and Agile-based QA leadership are the most sought-after specialties in the Massachusetts market. Find a role that fits below and apply directly.
Find QA Lead JobsOverview
Showing 5 of 65+ QA Lead 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 65 QA Lead Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
Find QA Lead JobsQA Lead Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
QA Lead Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
- Technology & Software
- Food & Beverage
What Massachusetts Employers Look For
The qualifications that appear most often in QA lead jobs across Massachusetts.
- Bachelor's degree in computer science, engineering, or a related technical field required
- Proven experience leading QA teams and defining test strategy for complex software products
- Hands-on proficiency with automated testing frameworks such as Selenium, Cypress, or Playwright
- Experience with Agile and Scrum methodologies in a cross-functional product development environment
- Strong knowledge of CI/CD pipelines and integrating automated tests into DevOps workflows
- Familiarity with FDA or regulated industry quality standards preferred for life sciences roles
QA Lead Jobs in Massachusetts: Frequently Asked Questions
How do you become a qa lead in Massachusetts?
Most qa leads in Massachusetts reach the role by combining a technical degree in computer science, software engineering, or a related field with several years of hands-on QA experience before stepping into a leadership position. No state-issued license is required, but certifications like ISTQB Advanced Level Test Manager carry real weight with Massachusetts employers, particularly in the life sciences and fintech sectors. Building experience with automated testing tools and Agile delivery methods accelerates the path considerably.
Which companies hire qa leads in Massachusetts?
Employers hiring qa leads in Massachusetts right now include Replimune, Redwire Space, and Boston Scientific, based on current listings on Migrate Mate as of August 2026. Massachusetts's concentration of biotech, defense, and enterprise software companies means qa lead openings here often require domain-specific quality experience alongside core testing leadership skills.
Which Massachusetts cities have the most qa lead jobs?
The cities with the most qa lead openings in Massachusetts are Boston, Marlborough, and Waltham. Boston and Cambridge dominate because of the region's dense cluster of biotech, fintech, and enterprise technology employers, while Worcester and the Route 128 corridor draw significant hiring from defense contractors and established software firms with long-standing Massachusetts operations.
Are there remote qa lead jobs in Massachusetts?
Yes, and more than most fields. About 53% of qa lead openings tied to Massachusetts are remote or hybrid as of August 2026, reflecting the desk-based and digital nature of most QA lead work. The parts of the role most commonly done remotely include test planning, code review, and team coordination, while on-site presence is more often expected in regulated industries like medical devices or defense.
How can I get hired as a qa lead in Massachusetts with little or no experience?
The most realistic entry path is moving into a junior QA engineer or QA analyst role first, then building toward leadership. Large Massachusetts employers in life sciences and enterprise software, including companies along the Route 128 corridor, regularly hire for associate QA positions that develop into lead roles over time. Earning an ISTQB Foundation certificate and building a portfolio of automated test scripts using open-source tools gives candidates a clear edge when competing for these entry points.
Where can I find and apply to qa lead jobs in Massachusetts?
You can find and apply to qa lead jobs in Massachusetts on Migrate Mate, which lists current Massachusetts openings. Find the roles that fit your experience and apply directly to each one.
See All 65 QA Lead Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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