1,006 Results for

Quality Assurance Lead Jobs in Boston, MA

Jobs

Quality Assurance Lead Virtusa Corp

US-MN-Minneapolis'',''US-MN-Minneapolis'',''US-IN-Indianapolis'',''US-IN-Indianapolis'','''','''','''','''','''','''',''Full-time'',''Full Time'',''Full Time'',''Individual Contributor'',''Experienced'',''Experienced'',''No'',''No'',''05/05/2026, 5:09:29 PM'',''05/05/2026, 5:09:29 PM'',''100000'',''100000'',''120000'',''120000'',''false'',''923802'',''923802'',''true'',''923802'',''false'',''Submission for the position: Quality Assurance Lead - (Job Number: CREQ254972)'',''false'',''923802'',''false'',''true''. ''923802'',''true'',''923802'',''false'',''Submission for the position: Quality Assurance Lead - (Job Number: CREQ254972)'',''false'',''923802'',''false'',''true'',''Quality Assurance Lead'',''CREQ254972'',''!*!

30+ days ago

Director / Senior Director, GCP Quality Assurance Lead (US/IL/EU) Prilenia

Europe, Massachusetts

Remote

About Prilenia Prilenia Therapeutics, a clinical-stage biotechnology company focused on the urgent mission of developing novel therapeutics to slow the progression of neurodegenerative diseases and neurodevelopmental disorders, is looking for a Director/Senior Director, GCP Quality Assurance Lead, to support programs in both Huntington’s Disease and ALS. The ideal candidate is both a hands-on quality practitioner and a strategic partner to Clinical Development, Regulatory Affairs, Drug Safety, and Biostatistics, combining deep GCP/GvP/GLP expertise with the executive presence to influence cross-functional teams and senior leadership.

30+ days ago

Training and Quality Assurance Lead Old Colony Elder Services

Brockton, MA

Full time

Our mission: Through the talents of an experienced and diverse workforce, OCES supports the independence and dignity of older adults and individuals with disabilities by providing essential information and services that promote healthy, safe living which positively impacts our community. They will work with agency leadership to provide industry intelligence and actionable solutions to programmatic staff resulting in improvement in OCES' clinical, designation and strategic goals.

30+ days ago

Product Quality Lead (APQR & QA CMC Support) Genetix Biotherapeutics

Somerville, Massachusetts

The Product Quality Lead (APQR & QA CMC Support) is a key member of the QA Compliance organization, responsible for ensuring quality oversight of regulatory submissions and lifecycle management for Genetix Biotherapeutics (GTX) products. Additionally, the Associate Director partners cross-functionally and with external vendors to support health authority inspection readiness activities, mock inspections and internal audits.

28 days ago

Director, U.S. Commercial QA Lead (GMP) Pharvaris NV

Boston, MA

$195,000–$225,000 / year

Strategic thinking, business acumen, analytical mindset with strong attention to details, with proven ability to motivate, influence, negotiate, and collaborate with internal and external stakeholders through efficient management of relationship within a cross-functional matrix. We aim at bringing new, more convenient options to bradykinin-mediated angioedema patients who suffer sudden and prolonged attacks of swelling in multiple areas of the body including the airway, which can be life-threatening.

30+ days ago

Lead SDET Quality Assurance Engineer oneZero Financial Systems LLC

Somerville, MA

$115,000–$145,000 / year

Promotes automation first approach to test plans that incorporate both positive and negative scenarios Identifies functional interdependencies between squads that optimizes testing of related/dependent features that are cross-squad and cross-team Participates and leads in postmortem activities to better understand and automate escapes and implement process improvements Understands each tier of the testing pyramid and the how to use the different automation solutions for them Helps ensure both stories and epics meet both Definition of Ready (DoR) and Definition of Done (DoD) Applies test-first BDD and TDD best practices. EXPERIENCE/EDUCATIONAL REQUIREMENTS: Bachelor's/Master's degree in the Hard Sciences (Computer Science, Math, Engineering preferred) 10+ years of software development or automation development or technical team leadership experience Demonstrable experience with some of CI/CD, BDD/TDD, C#, Relational Databases and Python/JavaScript Experience with performance tools like Neoload/JMeter/Etc Familiarity with Playwright Experience managing technical automation QA teams in an agile and CI/CD environment Finance industry experience Experience using generative AI within a development environment.

30 days ago

QA Test Lead Capital Markets Artech LLC

North Quincy, MA

$38–$44 / hour

Desirable Skills: Keyword: Skills: Manual Testing Processes and Management~Capital Markets and Financial Services. Should have experience in functional| regression| performance testing Should have experience in offshore co-ordination Should have experience in stakeholer management at onsiteNice to have.

14 days ago

Quality Assurance Team Lead ZOLL Medical

Chelmsford, Massachusetts

Remote

The Acute Care Technology division of ZOLL Medical Corporation develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. The Quality Assurance Team Leader supervises a small team of Quality Assurance Technicians and is responsible for monitoring and ensuring products are safe and meet customer expectations.

3 days ago

Quality Assurance Automation Lead Faro Health Inc

We are a hybrid workplace where San Diego employees work from their homes as well as in our stunning main headquarters enjoying a gym with classes and (early next year) spa services, outdoor lawn work area, and steeply discounted food hall. Faro is a mission driven company seeking world class people who share our passion for improving drug availability and patient outcomes through better clinical trial design.

30+ days ago

QA Manager/Hardware Manufacturing (Manager, Quality Assurance) Redwire Space

Marlborough, Massachusetts

$126,000–$165,000 / year

To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. These cutting-edge capabilities address cost and performance limitations that are helping to revolutionize spaceflight and are currently being utilized on missions with NASA, the Department of Defense, and several commercial space companies.

23 days ago

Senior Quality Assurance Engineer (OT / Security Platforms) Industrial Defender, Inc. (Inactive)

Boston, MA

$115,000–$140,000 / year

We are looking for a Senior Quality Assurance Engineer to join our experienced QA team working on a multi-tier security platform for industrial and operational environments. This role is intended for an experienced QA engineer who can independently execute complex testing contribute to quality discussions and raise issues early.

30+ days ago

Director, Clinical Quality Assurance Seaport Therapeutics

Boston, Massachusetts

$198,000–$225,000 / year

The ideal candidate will embrace a collaborative, innovative culture that embodies our values of service to patients impacted by mental health conditions, with a “we own it” mentality, demonstrating entrepreneurial spirit and technical excellence while fostering teamwork and continuous improvement. Seaport Therapeutics is seeking an experienced Director, Clinical Quality Assurance to manage clinical quality activities supporting clinical development programs, ensuring compliance with regulatory requirements and company policies.

30+ days ago

Quality Associate, QA Operations Obsidian Therapeutics Inc

Bedford, MA

$95,500–$117,000 / year

Provide timely QA support for change controls, GMP investigations, associated CAPAs, and effectiveness checks by reviewing records, supporting impact assessments, tracking action items, and helping ensure quality system activities are completed accurately and within required timelines. Serve as a point of coordination for QA support across manufacturing operations by partnering with CMC, QA Operations, and Supply Chain/materials management teams to review documentation, resolve quality-related questions, and support timely execution of GMP activities.

2 days ago

Senior Specialist, Field Quality QA Operations Bristol-Myers Squibb Co

$89,530–$108,490 / year

The Senior Field QA Specialist is responsible for reviewing Manufacturing Batch Records (MBRs), performing real time on-the-floor exceptions reviews and logbooks, conducting GMP area walkthroughs, and supporting timely return-to-service (RTS) walkthroughs to confirm that manufacturing areas and equipment are properly cleaned, calibrated, and ready for production use. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.

30+ days ago

Aerospace QA Engineer (Quality Engineer) Redwire Space

Marlborough, Massachusetts

$85,000–$110,000 / year

3 days ago

Manager, CDx Quality Assurance Foundation Medicine Inc

Boston, MA

$123,600–$154,500 / year

Partnering closely with Regulatory Affairs, Quality Systems, Complaints, Risk Management, Diagnostic Development and Validation, Clinical Operations, R&D, and Global Lab Operations, this role provides leadership, governance, and operational oversight to ensure CDx programs are executed with patients and users at the forefront, safety, and high quality as the north star. Partner with cross functional stakeholders (Quality, Regulatory Affairs, Diagnostic Development and Validation, Clinical Operations Product, Research and Development, Operations, Laboratory, IT, and Clinical/Lab interfaces) to ensure Medical Device Products and IVD are developed with patient safety first and right the first time mentality.

30+ days ago

Director, Clinical Quality Assurance Oruka Therapeutics

Waltham, Massachusetts

Remote

This role will establish, improve, and lead phase-appropriate clinical quality processes, ensure robust oversight of clinical trial execution and vendor performance, and drive inspection readiness for global health authority inspections, including FDA Bioresearch Monitoring (BIMO) inspections. The Director, Clinical Quality Assurance is responsible for providing strategic quality leadership, support, and oversight for Oruka’s clinical development activities, with primary focus on Good Clinical Practice (GCP) and related quality systems supporting clinical trials.

30+ days ago

Associate Director / Director, Clinical Quality Assurance Beam Therapeutics

Cambridge, MA

$185,000–$260,000 / year

Reporting to the Senior Director, Clinical Quality Assurance, this role will provide strategic and operational leadership for inspection readiness, program quality oversight, and vendor oversight as Beam advances toward its first regulatory submission and potential associated inspections. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA.

30+ days ago

Associate Director / Director, Clinical Quality Assurance Beam Therapeutics Inc

Cambridge, MA

$185,000–$260,000 / year

30+ days ago

Director, Clinical Quality Assurance Oruka Therapeutics Inc

Waltham, MA

Remote

$213,000–$240,000 / year

Role Overview: The Director, Clinical Quality Assurance is responsible for providing strategic quality leadership, support, and oversight for Oruka's clinical development activities, with primary focus on Good Clinical Practice (GCP) and related quality systems supporting clinical trials. This role will establish, improve, and lead phase-appropriate clinical quality processes, ensure robust oversight of clinical trial execution and vendor performance, and drive inspection readiness for global health authority inspections, including FDA Bioresearch Monitoring (BIMO) inspections.

30+ days ago

Associate Director, GMP QA Operations Dyne Therapeutics Inc

Waltham, MA

$160,000–$195,000 / year

Role Summary: The Associate Director, QA Operations serves as the QA technical lead for external manufacturing and testing project teams, ensuring the effective development, implementation, and continuous improvement of Quality Systems, procedures, policies, and metrics supporting GMP activities. 5+ years of related work experience in Quality Assurance or closely related role within Medical Device, Diagnostic, Pharmaceutical, or other similar regulated industry, preferably with experience overseeing CMO/CDMO organizations.

17 days ago

Quality Assurance Specialist III Raw Material/Batch Record Review Nitto Denko Avecia Inc

Milford, MA

$73,700–$89,177 / year

Perform QA-related entries and reviews in inventory management systems (e.g., SAP or LIMS) related to raw material status changes (quarantine/release/reject). Attend or lead all raw material meetings including interaction with other departments such as QC, Milford Supply Chain, Cincinnati Supply Chain, etc.

20 days ago

Aerospace QA Engineer (Quality Engineer) Redwire Corp

Marlborough, MA

$85,000–$110,000 / year

These cutting-edge capabilities address cost and performance limitations that are helping to revolutionize spaceflight and are currently being utilized on missions with NASA, the Department of Defense, and several commercial space companies. To conform to U.S. Government space technology export regulations, including the International Traffic in Arms Regulations (ITAR) you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State.

3 days ago

Associate Director, GMP Quality Assurance Operations Kiniksa Pharmaceuticals International Plc

Lexington, MA

Kiniksa is seeking an experienced Associate Director, GMP Quality Assurance Operations to be a key leader within the Quality organization, responsible for providing hands-on-Quality Operations oversight for GMP manufacturing activities supporting clinical programs. Responsibilities (including, but not limited to): Lead and execute GMP QA activities for development programs, including manufacture of master cell bank, working cell bank, drug substance and drug product/finished goods, in alignment with Kinika's Quality System.

30+ days ago

Sr. Manager, Design Quality Assurance Foundation Medicine Inc

Boston, MA

$153,200–$191,500 / year

Partnering closely with Product Development, Regulatory Affairs, Quality Systems, Complaints, Risk Management, R&D, and Global Lab Operations, this role provides strategic leadership, governance, and operational oversight to ensure products are designed and developed with patients and users at the center, safe, high quality, and inspection ready. Partner with senior Quality leadership to align Medical Device and IVD Product Development governance with broader FMI organization responsible for Product Development, including but not limited to Regulatory Affairs, Clinical Operations, Product, Research and Development, Operations.

30+ days ago

Manager/Sr. Manager QA Supply Chain Oruka Therapeutics

Waltham, Massachusetts

The Manager / Senior Manager, QA Supply Chain is responsible for providing quality oversight of clinical supply chain activities supporting Phase 2 and Phase 3 programs, including packaging, labeling, distribution, and cold chain management. This role ensures that all supply chain operations are conducted in compliance with cGMP, GCP, and GDP requirements, with a focus on IRT-driven clinical supply management, temperature control, and investigational product traceability.

30+ days ago

Senior Software Quality Assurance Engineer Karwell Technologies

Andover, MA

Job Description: As a Senior Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end to end design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. Working directly with cross-functional teams, you will drive adherence to design controls, risk management, and SDLC best practices from concept through commercialization and post market activities.

30+ days ago

Senior Software Quality Assurance Engineer Katalyst Healthcares & Life Sciences

Andover, MA

Job Description As a Senior Design Quality Engineer (DQE) for our medical device manufacturer client in the Greater Boston region, you will be responsible for ensuring end to end design quality and compliance across the product development lifecycle for Class II/III medical devices, including software-driven and active implantable products. In this role you will play a key role in: Serving as the quality lead on product development teams, ensuring compliance with design controls across all lifecycle phases (planning, inputs/outputs, verification, validation, transfer, and change management).

30+ days ago

Senior Quality Assurance Software Engineer Cooley LLP

Boston, MA

$103,000–$150,000 / year

We offer a full range of elective benefits including medical, health savings account (with applicable medical plan), dental, vision, health and/or dependent care flexible spending accounts, pre-tax commuter benefits, life insurance, AD&D, long-term care coverage, backup care for children and/or adults and other parental support benefits. In addition to elective benefit options, benefited employees receive firm-paid life insurance, AD&D, LTD, short term medical benefits as well as 21 days of Paid Time Off ("PTO") and 10 paid holidays each year.

30+ days ago

Quality Assurance Tech I :26-01079 Akraya Inc.

North Reading, MA

$36–$41 / hour

Most recently, we were recognized Stevie Employer of the Year 2025, SIA Best Staffing Firm to work for 2025, Inc 5000 Best Workspaces in US (2025 & 2024) and Glassdoor's Best Places to Work (2023 & 2022)! Primary Skills: Electromechanical Assembly (Proficient), Schematic Interpretation (Expert), Electrical Troubleshooting (Expert), Test Execution (Proficient), Linux Usage (Intermediate), Contract Type: W2 Only.

30+ days ago

Quality Assurance Tech III: 26-02115 Akraya Inc.

Wilmington, MA

$35–$41 / hour

Most recently, we were recognized Stevie Employer of the Year 2025, SIA Best Staffing Firm to work for 2025, Inc 5000 Best Workspaces in US (2025 & 2024) and Glassdoor's Best Places to Work (2023 & 2022)! Primary Skills: Mechanical inspection (Proficient), MRB Process Management (Advanced), Calibration system administration (Expert), Root cause analysis (Advanced), Reading technical drawings (Proficient).

1 day ago

Group Risk Specialist - Quality Assurance The Toronto-Dominion Bank

Boston, MA

$91,000–$145,600 / year

Additional Responsibilities: The Group Risk Manager is an enterprise role which works with various stakeholders across Risk Management and Technology, including but not limited to, Non-Financial Risk Management, Compliance, Financial Crimes, Audit, Enterprise Protect, and Platforms and Technology teams that support Risk. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition.

2 days ago

Senior Data Quality Assurance Analyst TalentBurst, Inc.

Quincy, MA

$64–$67 / hour

This includes creating a consolidated Enterprise Data Platform on modern cloud tools (including AWS & Snowflake,) and re-platforming existing business data applications from solutions such as SAS and legacy databases to the new platform. This position works collaboratively with epidemiologists, program staff, analytics teams, developers, and external partners to maintain data integrity across state public health information systems and reporting processes.

23 days ago

Senior Manager, Clinical Quality Assurance Kura Oncology Inc

Boston, MA

$160,000–$187,000 / year

ESSENTIAL JOB FUNCTIONS: Reporting to the Executive Director of Quality Assurance, the Senior Manager, Clinical Quality Assurance (CQA) is responsible for supporting the development and implementation of processes and programs that provide quality and compliance oversight utilizing proactive end to end strategies for all clinical development programs. Kura developed and is commercializing KOMZIFTI (ziftomenib), the FDA-approved once-daily, oral menin inhibitor for the treatment of adults with relapsed or refractory NPM1-mutated acute myeloid leukemia, and continues to pioneer advancements in menin inhibition and farnesyl transferase inhibition.

30+ days ago

Manager/Sr. Manager QA Supply Chain Oruka Therapeutics Inc

Waltham, MA

$146,000–$161,000 / year

Role Overview: The Manager / Senior Manager, QA Supply Chain is responsible for providing quality oversight of clinical supply chain activities supporting Phase 2 and Phase 3 programs, including packaging, labeling, distribution, and cold chain management. This role ensures that all supply chain operations are conducted in compliance with cGMP, GCP, and GDP requirements, with a focus on IRT-driven clinical supply management, temperature control, and investigational product traceability.

30+ days ago

Director, Quality Assurance (Operations) Zevra Therapeutics Inc

Boston, MA

10+ years of progressive experience in pharmaceutical/biotech industry with expertise in establishing effective and efficient systems and processes supporting pre-clinical, clinical and commercial programs, 7+ years of Quality leadership experience with a successful track record in vendor oversight and managing relationship with external stakeholders as well as internal QA systems in a virtual environment, 7+ years' experience in the establishing and administering of GCP-, GLP- and GDP compliant systems, Bachelors or Advanced degree in a scientific or related discipline, Understanding of worldwide requirements of GxP compliance and quality systems for clinical and commercial products, Leadership role in the management of regulatory/health authorities inspections, Experience with new product launch and implementation of serialization systems and commercial product complaint processes is a plus, Strong team player that has a customer service approach and is solution oriented, Ability to travel both domestically and internationally as needed, likely to be ~10 15%, The candidate will need to embrace Zevra's mission and core values, Ability to effectively communicate with inspiration, lead and influence individuals from multiple functional departments at all levels of the organization, Strong organizational and time management skills to balance working on multiple projects and initiatives in parallel, A proven self-starter capable of high performance with limited direction and oversight, Excellent people leader with strong mentorship skills. This includes, but is not limited to, audit planning and execution, reporting and coordination with external contractors, Supports periodic GxP training and ensure that training requirements are consistently met, as required, In collaboration with Head of Quality and other department heads, prepare, review, approve, and implement SOPs as required, Responsible for Quality Review Boards, providing technical expertise for product quality decisions, Responsible for manufacturing investigations, in collaboration with the Manufacturing Team, ensuring appropriate corrective and preventive actions are taken as required, Support continuous improvement initiatives to optimize Zevra's quality and compliance position, Cross-train and serve as back-up for Quality Systems, as assigned.

14 days ago

Senior Quality Assurance Director Compass Group

Boston, Massachusetts

$125,000–$130,000

This role oversees brand wide food safety programs, supplier controls, operational audits, crisis management, and regulatory compliance across all jurisdictions. The director partners closely with Operations, Supply Chain, Training, and Culinary to ensure safe execution of menu items and consistent guest experience.

7 days ago

Director of Software Quality Assurance PreVeil

Boston, Massachusetts

You will set testing strategy, mentor and grow the QA team, and work closely with Engineering, Security, and Compliance so that every release — especially file sync, sharing, and storage functionality — holds up under real-world usage and regulatory scrutiny alike. Reporting to the VP of Engineering, you will take ownership of a QA function that today is largely manual and hands-on — deeply skilled at finding real-world, at-scale issues in our web, Windows, and macOS applications — and grow it into a more mature, automation-forward organization without losing that rigor.

4 days ago

Senior QA Auditor - 60% - 80% Healx Ltd

Cambridge, MA

Maintain and improve Healx's Quality Management System (QMS), including delivery of training and tracking of training across company, change control (including regulatory impact assessment in coordination with Regulatory Affairs), deviations, CAPAs, and risk assessments, in cooperation with the management team (MT), department directors and with support from the Clinical Team. Healx is looking for a part-time (60% - 80%) experienced Senior QA Auditor to join the team to lead strong analytical, problem-solving activities that ensure all clinical research (GCP) and manufacturing (GMP) related activities performed by Healx personnel and vendors are carried out in accordance with industry expectations, SOPs, and international regulations.

30+ days ago

Business Systems Analyst / QA (Data & Automation) Manulife

Boston, Massachusetts

Manulife offers eligible employees a wide array of customizable benefits, including health, dental, mental health, vision, short- and long-term disability, life and AD&D insurance coverage, adoption/surrogacy and wellness benefits, and employee/family assistance plans. As part of the US Retirement Technology team, you will partner with Business Operations, Data Engineering, and QA teams to deliver transformation initiatives and improve system efficiency, data quality, and automation maturity.

22 days ago

Senior Group Risk Analyst - Quality Assurance The Toronto-Dominion Bank

Boston, MA

$72,280–$117,520 / year

Additional Role Responsibilities: The Group Risk Specialist is an enterprise role which works with various stakeholders across Risk Management and Technology, including but not limited to, Non-Financial Risk Management, Compliance, Financial Crimes, Audit, Enterprise Protect, and Platforms and Technology teams that support Risk. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition.

2 days ago

QA Automation Engineer Creatio EMEA LTD

Boston, MA

Team composition: 3 Developers, 1 QA, 1 Technical Lead, 1 Agile Coach, 1 Product OwnerResponsibilities:Create and maintain E2E automated tests with Playwright (in TypeScript)Perform exploratory and manual testing for new features and complex workflowsCover UI/API/business logic scenariosWork closely with developers and analysts to identify edge cases and improve test coverageContribute to improving our QA processes, tools, and reportingRequirements:Knowing testing techniques and applying them. Will be a plus: Experience conducting load testing of web applications; Experience with Continuous Integration tools: TeamCity, Jenkins; Test automation experience: Selenium WebDriver, Cucumber, Chai, Mocha, Selenoid/Selenium Grid; Understanding the principles of OOP.What you should expect from us:Growth & Development: Clear career paths, mentorship opportunities, and access to continuous learning to help you reach your full potential.

30+ days ago

International Quality Assurance Manager AngioDynamics Inc

Marlborough, MA

AngioDynamics is dedicated to improving patient outcomes by focusing on the development of disruptive and differentiated technologies that address unmet patient needs and supporting professional healthcare providers around the world in the delivery of high-quality patient care. Operate with a hands-on management approach, actively engaging in key quality activities as needed to support the team, resolve issues, and ensure timely execution in a dynamic, fast-paced environment.

30+ days ago

Manufacturing Quality Assurance Engineer Emerson Electric Co

Mansfield, MA

$80,000–$110,000 / year

Through our deep domain expertise and legacy of flawless execution, Emerson helps customers in critical industries like life sciences, energy, power and renewables, chemical and advanced factory automation operate more sustainably while improving productivity, energy security and reliability. We have built an engaged community of inquisitive, dedicated people who thrive knowing they are welcomed, trusted, celebrated, and empowered to solve the world's most complex problems - for our customers, our communities, and the planet.

9 days ago

Data Warehouse QA Tester Lancesoft

Quincy, MA

Must have Tools: Selenium, Client Load Runner, TOAD for Oracle 12.6, Python, Oracle SQL Developer 18.2, PL/SQL, UNIX, AWS, FileZilla, Microsoft Visio, WinSCP, Java, MS Office, Atlassian JIRA, Putty, COGNOS. Responsible for System testing of Ad-Hoc Query Packages in Cognos which involves execution of Ad-hoc reports and corresponding test SQLs based on various join conditions and filters and calculations.

30+ days ago

Director Of Quality Assurance - CMO/ CDMO RPM ReSearch

Waltham, Massachusetts

Has knowledge and skills across a range of Quality practices, procedures, and principles, with an astute ability to easily rank priorities based on importance and feel comfortable making decisions on quality issues. Demonstrate knowledge of and instruct department procedures and company policies, pay attention to detail in all areas, and ensure all the paperwork is completed completely, neatly, and fully.

23 days ago

Sr Quality Assurance Documentation Specialist Candel Therapeutics Inc

Needham, MA

$88,000–$100,000 / year

Essential Areas of Responsibility: Administers Document Management Program and provides support to end users for the creation, revision, and retirement of documents including: Reviews GxP documents and records for completeness and compliance with internal procedures and applicable regulations and ensures ALCOA++ principles are followed to ensure data robustness. Administers the Training Management Program and provides support to end users for the maintenance of training activities including: Maintains user roles, training curricula, and training assignments.

2 days ago

Senior QA Specialist I Pfizer

Massachusetts

Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Applicant must have a bachelor's degree with at least 4 years of experience; OR a master's degree with at least 2 years of experience; OR a PhD with 0+ years of experience; OR as associate's degree with 8 years of experience; OR a high school diploma (or equivalent) and 10 years of relevant experience.

4 days ago

Associate Director, Clinical Quality Assurance Kailera Therapeutics

Waltham, Massachusetts

Plan, coordinate, review and approve internal, external, and clinical site audits using risk-informed strategy to ensure GCP/GVP compliance in clinical studies and pharmacovigilance operations. through helping to facilitate the identification of critical data and critical data processes, and risks associated with them, establishing, monitoring and reporting out on Quality Tolerance Limits (QTLS)).

30+ days ago

Sr Director, QA- GxP Systems Candel Therapeutics Inc

Needham, MA

$258,333–$280,000 / year

System Validation & Governance: Own all CSV (computer system validation) activities, including SOP development, vendor questionnaires, test scripts, reports, periodic reviews, and revalidations. serve as a strategic partner across departments, while independently owning vendor oversight, computer system validation, and overall GxP system effectiveness.

10 days ago

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Quality Assurance Lead Jobs in Boston, MA

Quality Assurance Lead Virtusa Corp

Director / Senior Director, GCP Quality Assurance Lead (US/IL/EU) Prilenia

Training and Quality Assurance Lead Old Colony Elder Services

Product Quality Lead (APQR & QA CMC Support) Genetix Biotherapeutics

Director, U.S. Commercial QA Lead (GMP) Pharvaris NV

Lead SDET Quality Assurance Engineer oneZero Financial Systems LLC

QA Test Lead Capital Markets Artech LLC

Quality Assurance Team Lead ZOLL Medical

Quality Assurance Automation Lead Faro Health Inc

QA Manager/Hardware Manufacturing (Manager, Quality Assurance) Redwire Space

Senior Quality Assurance Engineer (OT / Security Platforms) Industrial Defender, Inc. (Inactive)

Director, Clinical Quality Assurance Seaport Therapeutics

Quality Associate, QA Operations Obsidian Therapeutics Inc

Senior Specialist, Field Quality QA Operations Bristol-Myers Squibb Co

Aerospace QA Engineer (Quality Engineer) Redwire Space

Manager, CDx Quality Assurance Foundation Medicine Inc

Director, Clinical Quality Assurance Oruka Therapeutics

Associate Director / Director, Clinical Quality Assurance Beam Therapeutics

Associate Director / Director, Clinical Quality Assurance Beam Therapeutics Inc

Director, Clinical Quality Assurance Oruka Therapeutics Inc

Associate Director, GMP QA Operations Dyne Therapeutics Inc

Quality Assurance Specialist III Raw Material/Batch Record Review Nitto Denko Avecia Inc

Aerospace QA Engineer (Quality Engineer) Redwire Corp

Associate Director, GMP Quality Assurance Operations Kiniksa Pharmaceuticals International Plc

Sr. Manager, Design Quality Assurance Foundation Medicine Inc

Manager/Sr. Manager QA Supply Chain Oruka Therapeutics

Senior Software Quality Assurance Engineer Karwell Technologies

Senior Software Quality Assurance Engineer Katalyst Healthcares & Life Sciences

Senior Quality Assurance Software Engineer Cooley LLP

Quality Assurance Tech I :26-01079 Akraya Inc.

Quality Assurance Tech III: 26-02115 Akraya Inc.

Group Risk Specialist - Quality Assurance The Toronto-Dominion Bank

Senior Data Quality Assurance Analyst TalentBurst, Inc.

Senior Manager, Clinical Quality Assurance Kura Oncology Inc

Manager/Sr. Manager QA Supply Chain Oruka Therapeutics Inc

Director, Quality Assurance (Operations) Zevra Therapeutics Inc

Senior Quality Assurance Director Compass Group

Director of Software Quality Assurance PreVeil

Senior QA Auditor - 60% - 80% Healx Ltd

Business Systems Analyst / QA (Data & Automation) Manulife

Senior Group Risk Analyst - Quality Assurance The Toronto-Dominion Bank

QA Automation Engineer Creatio EMEA LTD

International Quality Assurance Manager AngioDynamics Inc

Manufacturing Quality Assurance Engineer Emerson Electric Co

Data Warehouse QA Tester Lancesoft

Director Of Quality Assurance - CMO/ CDMO RPM ReSearch

Sr Quality Assurance Documentation Specialist Candel Therapeutics Inc

Senior QA Specialist I Pfizer

Associate Director, Clinical Quality Assurance Kailera Therapeutics

Sr Director, QA- GxP Systems Candel Therapeutics Inc

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