QA Specialist Jobs in Massachusetts
QA Specialist jobs in Massachusetts are consistently active, with strong demand concentrated in the state's life sciences, medtech, and enterprise software sectors, and openings at every level from entry-level test associate through senior quality engineer. Boston, Cambridge, and Marlborough anchor most of the hiring, where employers like Thermo Fisher Scientific, Raytheon Technologies, and Boston Scientific maintain large quality teams. The most sought-after specialties in Massachusetts are software QA automation, FDA-regulated medical device quality, and GMP compliance testing. Find a role that fits below and apply directly.
Find QA Specialist JobsOverview
Showing 5 of 77+ QA Specialist 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 77 QA Specialist Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
Find QA Specialist JobsQA Specialist Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
QA Specialist 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 specialist jobs across Massachusetts.
- Bachelor's degree in life sciences, engineering, computer science, or a related field
- Hands-on experience with test planning, test case execution, and defect tracking tools
- Familiarity with FDA 21 CFR, ISO 13485, or GMP quality standards for regulated industries
- Proficiency with automation frameworks such as Selenium, Cypress, or comparable tools
- ASQ Certified Quality Auditor or CSTE certification preferred by Massachusetts employers
- Strong documentation and written communication skills for quality records and reports
QA Specialist Jobs in Massachusetts: Frequently Asked Questions
How do you become a qa specialist in Massachusetts?
Most qa specialist roles in Massachusetts require a bachelor's degree in engineering, life sciences, computer science, or a closely related field. There is no state-issued license for the role, but employers in Massachusetts's regulated industries strongly favor candidates who hold ASQ certifications such as the Certified Quality Engineer or Certified Quality Auditor. Building experience through internships at a medtech or biotech company gives candidates a meaningful edge in this market.
Which companies hire qa specialists in Massachusetts?
Employers hiring qa specialists in Massachusetts right now include Vertex Pharmaceuticals, Genezen, and Replimune, based on current listings on Migrate Mate as of August 2026. Massachusetts's dense concentration of FDA-regulated medtech and pharmaceutical companies means quality roles here are particularly deep in compliance and validation work compared to national averages.
Which Massachusetts cities have the most qa specialist jobs?
Boston, Marlborough, and Waltham have the most qa specialist openings in Massachusetts. Boston and Cambridge drive volume through their concentration of biotech, software, and research institutions, while Marlborough and the Route 495 corridor attract significant medical device and defense manufacturing quality roles anchored by employers like Boston Scientific and Raytheon Technologies.
Are there remote qa specialist jobs in Massachusetts?
Yes, though availability depends heavily on the industry. About 51% of qa specialist openings tied to Massachusetts are remote or hybrid as of August 2026, reflecting a split market. Software QA and test automation roles can run fully remote, while positions in medical device manufacturing, GMP environments, or hardware validation typically require on-site presence at a Massachusetts facility.
How can I get hired as a qa specialist in Massachusetts with little or no experience?
The most realistic entry path is through a QA associate or junior test analyst role at a Massachusetts software company or contract research organization. Large Massachusetts employers like Biogen and MathWorks have historically hired new graduates into quality associate and analyst programs. Completing an ASQ-recognized quality fundamentals course, building a portfolio of test cases from open-source projects, or transitioning from a related role such as technical support analyst or laboratory technician are the moves that get candidates through the door.
Where can I find and apply to qa specialist jobs in Massachusetts?
You can find and apply to qa specialist jobs in Massachusetts on Migrate Mate, which lists current Massachusetts openings across software, medtech, manufacturing, and enterprise sectors. Find the roles that fit your experience and apply directly from the listing.
See All 77 QA Specialist Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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