Quality Assurance Analyst Jobs in Massachusetts
Quality Assurance Analyst jobs in Massachusetts are in steady demand, with openings concentrated in life sciences, medical devices, defense technology, and enterprise software across seniority levels from entry-level associate to senior QA engineer. The heaviest hiring activity is in Greater Boston, Cambridge, and Waltham, where companies like Thermo Fisher Scientific, Raytheon Technologies, and Biogen maintain large operations and ongoing QA needs. The most sought-after specializations in the Massachusetts market are software test automation, regulated-industry quality systems, and medical device compliance. Find a role that fits below and apply directly.
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Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa’s lead investigational candidate – cleminorexton (formerly ORX750) – is being developed for narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions.
Headquartered in Boston, Massachusetts, Centessa was recognized as a Great Place to Work® in 2026.
Description of Role
The Associate Director, Clinical Quality Assurance (CQA) will oversee GCP-focused quality assurance for Centessa-sponsored clinical trials (Early to Late Phase), ensuring compliance with global regulations, ICH guidelines, Centessa SOPs, and industry standards. This role leads daily clinical quality operations, maintains effective quality programs and documentation, and ensures GCP compliance and inspection readiness across all regulatory requirements.
Key Responsibilities
- Lead and maintain GCP QA programs, policies, and procedures.
- Serve as primary GCP QA expert and point of contact.
- Ensure clinical programs comply with global health authority regulations and ICH guidelines.
- Provide QA oversight for protocols, ICFs, CSRs, and other trial documents.
- Monitor evolving GCP regulations and communicate impact to stakeholders.
- Develop and execute global GCP audit strategies and annual plans.
- Conduct and manage audits of investigator sites, CROs, suppliers, systems, and documents.
- Prepare audit reports, evaluate CAPAs, and ensure effective follow-up.
- Lead inspection readiness activities and support regulatory inspections (e.g., FDA, EMA, MHRA).
- Partner with cross-functional teams to ensure compliance.
- Represent CQA on study teams and contribute to protocol design and risk management.
- Collaborate on procedures, forms, and templates related to clinical quality.
- Identify compliance risks and implement mitigation strategies.
- Investigate quality issues, perform root cause analyses, and drive CAPA resolution.
- Prepare and present KPIs, metrics, and audit status updates to leadership.
- Develop and maintain GCP-related SOPs, training materials, and quality metrics.
- Lead process improvement initiatives across QA and broader organization.
- Provide mentorship and leadership to QA staff; may include direct management
Qualifications
- BS or higher in Life Sciences, Chemistry, Pharmacy, or related field.
- 8–10 years of experience in pharmaceutical quality roles.
- Experience with document control software (e.g., ZenQMS, Veeva Vault, MasterControl) required.
Compensation
The annual base salary range for this position is $140,000.00 to $180,000.00. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, job knowledge and location.
In addition to base pay, this role is eligible for a discretionary annual bonus. The Company also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.
Work Location
The Associate Director, Clinical Quality Assurance role is based in the US, with occasional travel.
POSITION: Full-Time, Exempt
EEOC Statement: Centessa Pharmaceuticals, a wholly owned subdisary of Eli Lilly and Company believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. We will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies.
Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders. Centessa’s lead investigational candidate – cleminorexton (formerly ORX750) – is being developed for narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia. Centessa's OX2R agonist portfolio includes additional clinical and preclinical-stage assets with potential utility across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions.
Headquartered in Boston, Massachusetts, Centessa was recognized as a Great Place to Work® in 2026.
Description of Role
The Associate Director, Clinical Quality Assurance (CQA) will oversee GCP-focused quality assurance for Centessa-sponsored clinical trials (Early to Late Phase), ensuring compliance with global regulations, ICH guidelines, Centessa SOPs, and industry standards. This role leads daily clinical quality operations, maintains effective quality programs and documentation, and ensures GCP compliance and inspection readiness across all regulatory requirements.
Key Responsibilities
- Lead and maintain GCP QA programs, policies, and procedures.
- Serve as primary GCP QA expert and point of contact.
- Ensure clinical programs comply with global health authority regulations and ICH guidelines.
- Provide QA oversight for protocols, ICFs, CSRs, and other trial documents.
- Monitor evolving GCP regulations and communicate impact to stakeholders.
- Develop and execute global GCP audit strategies and annual plans.
- Conduct and manage audits of investigator sites, CROs, suppliers, systems, and documents.
- Prepare audit reports, evaluate CAPAs, and ensure effective follow-up.
- Lead inspection readiness activities and support regulatory inspections (e.g., FDA, EMA, MHRA).
- Partner with cross-functional teams to ensure compliance.
- Represent CQA on study teams and contribute to protocol design and risk management.
- Collaborate on procedures, forms, and templates related to clinical quality.
- Identify compliance risks and implement mitigation strategies.
- Investigate quality issues, perform root cause analyses, and drive CAPA resolution.
- Prepare and present KPIs, metrics, and audit status updates to leadership.
- Develop and maintain GCP-related SOPs, training materials, and quality metrics.
- Lead process improvement initiatives across QA and broader organization.
- Provide mentorship and leadership to QA staff; may include direct management
Qualifications
- BS or higher in Life Sciences, Chemistry, Pharmacy, or related field.
- 8–10 years of experience in pharmaceutical quality roles.
- Experience with document control software (e.g., ZenQMS, Veeva Vault, MasterControl) required.
Compensation
The annual base salary range for this position is $140,000.00 to $180,000.00. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, job knowledge and location.
In addition to base pay, this role is eligible for a discretionary annual bonus. The Company also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.
Work Location
The Associate Director, Clinical Quality Assurance role is based in the US, with occasional travel.
POSITION: Full-Time, Exempt
EEOC Statement: Centessa Pharmaceuticals, a wholly owned subdisary of Eli Lilly and Company believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. We will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies.
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Find JobsQuality Assurance Analyst Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
Quality Assurance 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
- Medical Devices
- Distribution & Wholesale
What Massachusetts Employers Look For
The qualifications that appear most often in quality assurance analyst jobs across Massachusetts.
- Bachelor's degree in computer science, engineering, life sciences, or a related field
- Experience with test automation frameworks such as Selenium, Cypress, or equivalent tools
- Familiarity with quality management systems and regulated-industry standards like ISO 13485 or 21 CFR Part 820
- Proficiency in writing and executing test plans, test cases, and defect reports
- Knowledge of Agile or Scrum methodologies and experience working within cross-functional development teams
- Strong written and verbal communication skills for documenting findings and collaborating with engineering stakeholders
Quality Assurance Analyst Jobs in Massachusetts: Frequently Asked Questions
How do you become a quality assurance analyst in Massachusetts?
Most quality assurance analyst roles in Massachusetts require a bachelor's degree in computer science, engineering, information systems, or a life sciences field. There is no state-issued QA analyst license in Massachusetts, but candidates targeting regulated industries such as medical devices or pharmaceuticals benefit from familiarity with FDA quality system regulations and ISO standards. Certifications like the ISTQB Certified Tester or ASQ Certified Quality Auditor strengthen applications considerably across the Massachusetts market.
How much do quality assurance analysts make in Massachusetts?
Quality assurance 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 quality assurance analysts in Massachusetts?
Employers hiring quality assurance analysts in Massachusetts right now include Teleflex, Integrated Pharmacy Solutions, and Replimune, based on current listings on Migrate Mate as of September 2026. Massachusetts's concentration of life sciences, defense, and enterprise software companies means QA roles here frequently require familiarity with regulated-industry quality frameworks alongside traditional software testing skills.
Which Massachusetts cities have the most quality assurance analyst jobs?
Boston, Massachusetts, and Acton account for the largest share of quality assurance analyst openings in Massachusetts. Greater Boston dominates because of the dense cluster of biotech, medical device, and software firms headquartered or with major offices there, while Waltham and Cambridge draw additional volume from life sciences campuses and technology companies that anchor those suburban corridors.
Are there remote quality assurance analyst jobs in Massachusetts?
Yes, and more than most fields, since quality assurance analyst work is largely desk-based and well-suited to remote environments. About 53% of quality assurance analyst openings tied to Massachusetts are remote or hybrid as of September 2026, reflecting broad employer acceptance of distributed QA teams. Software testing and test automation roles tend to be the most remote-friendly, while positions requiring hands-on device inspection or lab-based validation are typically on-site.
How can I get hired as a quality assurance analyst in Massachusetts with little or no experience?
The most realistic entry path is an associate QA or junior test analyst role at a mid-size Massachusetts software or life sciences company, where structured onboarding and mentorship are common. Candidates from adjacent roles like technical support, data entry, or business analysis regularly make the transition. Building a portfolio of documented test plans and defect logs from personal or open-source projects strengthens applications, and earning the ISTQB Foundation Level certification signals readiness to employers who are otherwise hesitant about candidates without direct QA experience.
Where can I find and apply to quality assurance analyst jobs in Massachusetts?
You can find and apply to quality assurance analyst jobs in Massachusetts on Migrate Mate, which lists current openings from employers across the state. Find roles that fit your experience and specialization and apply directly to the ones that match.
See All 104+ Quality Assurance Analyst Jobs in Massachusetts
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