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.
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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 104+ QA Lead Jobs in Massachusetts
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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
- Electronics & Hardware
- Biotechnology & Pharmaceuticals
- Consulting & Professional Services
- Food & Beverage
- Medical Devices
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 Insulet Corporation, Teleflex, and Maverick Tech, based on current listings on Migrate Mate as of October 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, Acton, and Cambridge. 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 59% of qa lead openings tied to Massachusetts are remote or hybrid as of October 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 104+ QA Lead Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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