QA Jobs in Cambridge, MA

Provides GCP quality oversight for clinical trials, leads audits of sites, CROs, vendors, TMFs, and internal processes, and oversees quality events, investigations, CAPAs, and remediation. Supports clinical QMS development, inspection readiness, regulatory inspections, risk-based document reviews, training, and quality metrics. Requires strong knowledge of global clinical research regulations and willingness to travel domestically and internationally for audits.

The Senior QA Software Engineer ensures software quality through automated and manual testing, focusing on automation frameworks establishment and enhancing software quality standards.

Lead QA for a remote auction marketplace: design and run manual and automated tests for REST APIs and React UIs, build and maintain automation frameworks and test environments, integrate testing into CI/CD, triage defects with engineering, and adopt AI-assisted testing workflows.

Manage QA processes and production support for Harvard Dataverse and related products: design and run functional and performance tests, deploy releases, maintain test infrastructure, troubleshoot production issues, advise support staff, and document QA policies and procedures.

Provide strategic leadership and operational oversight of GCP Quality Assurance for clinical programs. Own GCP quality systems, CRO/vendor oversight, audit strategy, inspection readiness, risk-based QA, quality metrics, SOPs, CAPA, and build/mentor QA capability while partnering cross-functionally to ensure compliance and inspection readiness.

Lead QA activities for CMC supporting clinical GMP manufacturing and CMOs, including document and batch record review, deviations/investigations oversight, product release coordination, GMP metrics, and support for CMC regulatory submissions. Ensures compliance and timely clinical supply release while fostering continuous improvement.

The Executive Director leads Moderna's Quality Assurance strategy in R&D, ensuring compliance across GCP, GLP, GCLP, and GVP. Responsibilities include governance, building a QA team, and overseeing regulatory inspections.

Lead GCP/GLP/GVP quality oversight for clinical studies, manage QMS and vendor audit programs, develop SOPs and training, support regulatory inspections, review clinical and safety documents, identify and mitigate compliance risks, and partner cross-functionally to ensure GCP compliance and quality across programs.

The VP of Quality oversees strategic and operational Quality functions across drug development, ensuring compliance and managing quality systems, audits, and inspections. They lead cross-functional collaborations and maintain quality standards throughout manufacturing and clinical operations.

The role involves defining quality standards, integrating testing with development processes, and implementing AI tools for automation in QA. It requires collaboration with engineering teams and maintaining quality assurance practices aligned with security standards.

Perform independent quality audits of assembled surgical instrument trays: verify contents against count sheets, inspect cleanliness and functionality, document discrepancies, track trends, report findings to leadership, support corrective actions and staff education, and re-audit to confirm improvements.

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.

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.

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.

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.

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.

Audit and validate data labeling outputs, provide structured feedback and hands-on training to annotators, monitor workflows and escalate issues, help apply and improve guidelines, and identify patterns in human and model outputs to maintain high-quality AI training data.