QA Analyst Jobs in Massachusetts
QA Analyst jobs in Massachusetts are in strong demand, concentrated in life sciences, medtech, financial services, and enterprise software, with openings at every level from entry-level tester through senior QA engineer. Boston, Cambridge, and Worcester anchor most of the hiring, with established employers like Thermo Fisher Scientific, Liberty Mutual, and MathWorks maintaining consistent QA teams across the state. The most sought-after specialties in Massachusetts listings include automation testing, regulatory compliance QA for FDA-regulated products, and performance testing for financial platforms. Find a role that fits below and apply directly.
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The RQA Senior Director is a strategic leadership role responsible for management of day-to-day GCP/GLP/GVP Quality Operations including, goal setting, budgeting, hiring, team development, strategic execution and oversight of the Akebia RQA operational strategy. This position will be a member of the Quality Leadership Team and will report to the Vice President (VP)/Sr. Vice President (SVP) of Quality.
This individual will oversee, assess, and directly work to continuously improve Research and Development Quality processes at Akebia. This is an opportunity to continue the development of the GCP/GLP/GVP QA function and ensure high quality execution of non-clinical and clinical trials from first in human through commercial marketing authorization.
This position will also be responsible for interactions with regulatory agencies in regard to GCP, GVP and GLP matters.
Essential Functions and Duties
- Drive achievement of strategic Quality objectives through leadership & coaching of direct reports and cross-functional influence at the senior level
- Develop strong relationships, collaborate, and interact with various departments (i.e., Clinical Development, Clinical Operations, Statistics & Data Management, Drug Safety and Pharmacovigilance, Non-clinical) and levels of management at Akebia to accomplish company objectives.
- Develop strong relationships and partner with external collaborators to ensure the appropriate processes, systems, and activities are in place to protect the rights, safety, and welfare of study subjects.
- Ensure GCP/GLP/GVP projects and programs are conducted in accordance with current GCP/GLP/GVP regulations and ICH guidelines.
- Provide consultation on, and interpretation of, regulations, guidance documents and industry standards.
- Communicate and escalate critical risks to Senior Leadership: requires diplomatic and objective representation of the issue(s), robust root cause analysis and effective CAPA implementation for nonconformances.
- Ensure Quality Agreements are established, as necessary, with Akebia's key GCP/GLP/GVP vendors.
- Lead inspection readiness preparations (internal and external) including hosting and interacting with regulatory agencies during inspections on GCP/GLP/GVP related matters.
- Assist in the development and management of the annual budget for Quality Assurance Basic Qualifications
Basic Qualifications
- Bachelor's degree in a scientific discipline is required.
- Minimum of 10 years of progressive responsibility in pharmaceutical/biotech GCP, GVP and GLP-related Quality environments.
- 8+ years direct and indirect management level experience required.
Preferred Qualifications
- An advanced degree in a scientific discipline is strongly preferred.
- In-depth working knowledge of the applicable GCP/GLP/GVP regulations and guidelines.
- In-depth working knowledge of the non-clinical and clinical research process.
- Must be able to efficiently utilize the computer hardware and software programs provided to plan, manage, conduct and track deliverables and to communicate with internal and external team members.
- Ability to travel approximately 25% to various meetings including overnight trips. Some international travel may be required.
The RQA Senior Director is a strategic leadership role responsible for management of day-to-day GCP/GLP/GVP Quality Operations including, goal setting, budgeting, hiring, team development, strategic execution and oversight of the Akebia RQA operational strategy. This position will be a member of the Quality Leadership Team and will report to the Vice President (VP)/Sr. Vice President (SVP) of Quality.
This individual will oversee, assess, and directly work to continuously improve Research and Development Quality processes at Akebia. This is an opportunity to continue the development of the GCP/GLP/GVP QA function and ensure high quality execution of non-clinical and clinical trials from first in human through commercial marketing authorization.
This position will also be responsible for interactions with regulatory agencies in regard to GCP, GVP and GLP matters.
Essential Functions and Duties
- Drive achievement of strategic Quality objectives through leadership & coaching of direct reports and cross-functional influence at the senior level
- Develop strong relationships, collaborate, and interact with various departments (i.e., Clinical Development, Clinical Operations, Statistics & Data Management, Drug Safety and Pharmacovigilance, Non-clinical) and levels of management at Akebia to accomplish company objectives.
- Develop strong relationships and partner with external collaborators to ensure the appropriate processes, systems, and activities are in place to protect the rights, safety, and welfare of study subjects.
- Ensure GCP/GLP/GVP projects and programs are conducted in accordance with current GCP/GLP/GVP regulations and ICH guidelines.
- Provide consultation on, and interpretation of, regulations, guidance documents and industry standards.
- Communicate and escalate critical risks to Senior Leadership: requires diplomatic and objective representation of the issue(s), robust root cause analysis and effective CAPA implementation for nonconformances.
- Ensure Quality Agreements are established, as necessary, with Akebia's key GCP/GLP/GVP vendors.
- Lead inspection readiness preparations (internal and external) including hosting and interacting with regulatory agencies during inspections on GCP/GLP/GVP related matters.
- Assist in the development and management of the annual budget for Quality Assurance Basic Qualifications
Basic Qualifications
- Bachelor's degree in a scientific discipline is required.
- Minimum of 10 years of progressive responsibility in pharmaceutical/biotech GCP, GVP and GLP-related Quality environments.
- 8+ years direct and indirect management level experience required.
Preferred Qualifications
- An advanced degree in a scientific discipline is strongly preferred.
- In-depth working knowledge of the applicable GCP/GLP/GVP regulations and guidelines.
- In-depth working knowledge of the non-clinical and clinical research process.
- Must be able to efficiently utilize the computer hardware and software programs provided to plan, manage, conduct and track deliverables and to communicate with internal and external team members.
- Ability to travel approximately 25% to various meetings including overnight trips. Some international travel may be required.
See All 105+ QA Analyst Jobs in Massachusetts
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Find QA Analyst JobsQA Analyst Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
QA Analyst Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Technology & Software
- Electronics & Hardware
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
- Food & Beverage
What Massachusetts Employers Look For
The qualifications that appear most often in QA analyst jobs across Massachusetts.
- Bachelor's degree in computer science, engineering, information systems, or a related field
- Hands-on experience with test automation frameworks such as Selenium, Cypress, or TestNG
- Proficiency writing and executing manual and automated test cases across web and mobile applications
- Familiarity with Agile and Scrum methodologies and tools such as Jira or Azure DevOps
- Experience with FDA 21 CFR Part 11 or GxP validation requirements for life sciences or medtech environments
- Strong written communication skills for producing test plans, defect reports, and traceability documentation
QA Analyst Jobs in Massachusetts: Frequently Asked Questions
How do you become a qa analyst in Massachusetts?
Most qa analyst roles in Massachusetts require at minimum a bachelor's degree in computer science, information technology, engineering, or a related discipline. There is no state-issued license for qa analysts in Massachusetts, so hiring decisions turn on demonstrated testing skills and relevant certifications. Industry credentials such as ISTQB Foundation or Certified Software Tester are recognized by Massachusetts employers, particularly in life sciences and financial services, and a portfolio of automation work or hands-on testing projects strengthens any application significantly.
How much do QA analysts make in Massachusetts?
QA analysts in Massachusetts earn a median of about $122,210 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $68,050 for the lowest 10% to over $168,000 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire qa analysts in Massachusetts?
Employers hiring qa analysts in Massachusetts right now include Insulet Corporation, Teleflex, and Maverick Tech, based on current listings on Migrate Mate as of October 2026. Massachusetts's concentration of biotech, medtech, and fintech firms means many of these openings require specific domain knowledge such as FDA validation or financial systems testing alongside core QA skills.
Which Massachusetts cities have the most qa analyst jobs?
Boston, Acton, and Cambridge account for the largest share of qa analyst openings in Massachusetts. Boston and Cambridge drive volume through the region's dense cluster of biotech companies, financial institutions, and enterprise software firms, while Worcester's growing healthcare and manufacturing base generates consistent demand for QA professionals with validation and compliance experience.
Are there remote qa analyst jobs in Massachusetts?
Yes, and more than most fields. About 57% of qa analyst openings tied to Massachusetts are remote or hybrid as of October 2026, reflecting how naturally the analytical and documentation-heavy parts of QA work translate to distributed teams. Roles focused on manual test execution for physical devices or regulated lab environments are more likely to require on-site presence, while automation engineering and test strategy positions are the most consistently remote-eligible.
How can I get hired as a qa analyst in Massachusetts with little or no experience?
The most realistic entry path is applying for associate or junior QA roles at Massachusetts's large life sciences and software employers, where structured onboarding programs often bring in candidates who demonstrate testing fundamentals even without years of experience. Companies such as Thermo Fisher Scientific and mid-size Cambridge biotech firms regularly post entry-level quality associate and validation analyst positions that are accessible to new graduates. Earning an ISTQB Foundation certification and building a small automation portfolio using open-source tools are the credentials that move entry-level Massachusetts applicants to the top of candidate pools.
Where can I find and apply to qa analyst jobs in Massachusetts?
You can find and apply to qa analyst jobs in Massachusetts on Migrate Mate, which lists current Massachusetts openings updated in real time. Search the listings for the city, seniority level, or specialty that fits your background, then apply directly to the roles that match.
See All 105+ QA Analyst Jobs in Massachusetts
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