QA Jobs in Cambridge, MA

Lead test execution for banking platform transformation projects by designing and implementing test strategies, coordinating test case generation and automation, managing defects, collaborating with cross-functional teams, and coaching team members to ensure quality and timely delivery.

The QA Automation Engineer II will design and enhance automated tests across Enterprise Applications, focusing on Salesforce integrations and ensuring system reliability and quality under various testing methodologies.

Lead QA for an enterprise wealth-management platform: design and execute test plans, write and run API and integration tests, debug multi-layer issues, improve test coverage, mentor engineers, review release notes, and use tools/automation to ensure product quality.

Lead asset-level quality strategy by embedding Quality by Design, mapping risks/opportunities, conducting due diligence for in-licensed assets, driving audit-readiness for acquisition/commercial transitions, and applying global regulatory expectations (FDA/EMA/ICH) in AI-accelerated and digital environments.

Lead QA for AI-enabled software: design and execute test strategies, identify and resolve defects, automate browser and regression tests (Selenium), validate model outputs and data, perform compatibility and post-go-live support, and provide client-facing QA process design and mentoring.

Lead and grow engineering, QA, DevOps, support, and data architecture teams to deliver scalable, secure software. Drive agile delivery, CI/CD, IaC, SRE, test automation, and platform initiatives. Operationalize AI with governance and production patterns, ensure compliance and security, manage budgets and vendors, and align technology strategy with business outcomes.

Design, build, and maintain automated test frameworks and scripts. Lead test strategy, planning, and execution across functional, load, integration, security, server-side, and ETL testing. Create test artifacts, run automated tests, analyze results, report defects, participate in CI/CD, code reviews, and agile ceremonies, and drive issue resolution.

Lead quality management system implementations and regulatory compliance strategies for medical device clients, leveraging AI technology.

The Quality Manager oversees product disposition for Finished Goods, ensuring compliance with regulations, managing projects, and collaborating with stakeholders to maintain product quality.

Senior QA Specialist provides GMP quality oversight for EDIT-401 clinical candidate: batch record review, lot disposition, QA review of assay validation and test methods, CDMO oversight, authoring and approving GMP documentation, maintaining quality systems, vendor management, and supporting quality event management to ensure regulatory compliance for clinical manufacturing.

Support data quality in the Apricot case management database: identify and correct missing data, perform spot checks, generate simple reports, assist documentation clean-up, and help draft/update user tutorials and trainings under the Data & Impact Manager's guidance.

Lead QA oversight for analytical QC and development across cell and gene programs, including method validation/transfer, stability, release testing, investigations (OOS/OOT), CAPA/RCA, vendor/CMO QA oversight, regulatory submission support, audits, and implementation of digital quality systems and analytics to improve quality and compliance.

Perform quality assurance for sonos.com ecommerce experiences: plan and execute tests, audit content, run UAT with stakeholders, troubleshoot code/configuration issues, and QA emails and in-app communications to ensure cross-device and cross-browser accuracy.

Manual QA tester responsible for functional, regression, integration, conversion, reports, and end-to-end testing. Work includes PRPC (Pega) rule verification, performance analysis with PAL, use of PRPC developer tools, test management in HP Quality Center, and collaboration with offshore teams in Agile/Waterfall environments. Biopharma/GxP familiarity is desirable.

Design, implement, and maintain automated test frameworks and test suites for embedded wireless products (headphones, mobile speakers). Develop Python automation, integrate CI/CD, execute automated validation across UI, embedded, and application components, manage test cases and issues, perform troubleshooting and root cause analysis, and support cross-functional teams through all software lifecycle phases.

Lead QA oversight for QC activities supporting development through commercial manufacture of gene editing products. Provide technical authority on analytical control strategies, method validation/transfers, stability programs, reference standards, investigations, trending/predictive quality, and regulatory inspection readiness. Mentor QA/QC staff and partner cross-functionally to mature QC capabilities for commercial supply.

Perform IQC and OQC inspections of incoming materials and finished products, operate measurement equipment, raise and track NCRs, maintain lot traceability and document control, execute internal and supplier audits to ISO 9001, evaluate engineering changes and FMEA impacts, support CAPA and failure analysis, and collaborate with cross-functional teams and external semiconductor partners to ensure product quality and manufacturing readiness.

In-person QA Analyst role requiring minimum 5 years' experience. Responsibilities include integration work using SQL, strong SDLC knowledge, and working with Agile teams. Candidate must be self-motivated, able to work independently, and have excellent communication skills. Face-to-face interview in Massachusetts is mandatory.

As a Senior QA Engineer, you will design and maintain automated testing frameworks, support CI/CD environments, and mentor junior engineers while collaborating across teams to enhance gaming quality solutions.

The Quality Assurance Analyst will define testing objectives, write test plans and scripts, and ensure software integrity through various testing approaches including regression and stress testing.

Seeking a Midlevel/Senior QA professional with expertise in Advent Collateral Management and Dynamic Margin Methodology for Securities Lending. Responsibilities include general QA functions like test planning and defect tracking.

Lead and manage deviation and QMS activities for internal cell & gene manufacturing. Oversee investigations (OOS/OOT), root cause analysis, CAPA, change control, and audit readiness. Provide on‑floor quality support, partner cross-functionally (Manufacturing, QC, MSAT, Supply Chain, Regulatory), drive continuous improvement, track metrics, and ensure regulatory compliance (cGMP, FDA/EMA) from startup through commercialization.

Looking for a Senior Software QA Engineer with 6+ years of QA experience in enterprise software, strong problem-solving skills, and expertise in Linux/Unix configuration and scripting.

Lead RA/QA strategy and business integration, partnering with Product, R&D, and Operations to embed regulatory and quality perspectives across development. Drive governance, process simplification, resource prioritization, external engagement with biopharma and industry forums, and position RA/QA as a strategic enabler of innovation and speed.

Lead global companion diagnostic (CDx) quality for medical devices and IVDs, overseeing end-to-end product development quality, inspection readiness, risk management, CAPA, KPIs, and a team of quality professionals while partnering cross-functionally to ensure patient safety and continuous improvement.