184 qa manager jobs at 124 companies in Holden, MA
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QA Manager- Finished Goods Commercial
Boston, Massachusetts, United States
$118k-$178k/yrHybridFull Time
Vertex PharmaceuticalsNASDAQ: VRTX: Develops and sells prescription drugs for serious genetic diseases.
4+ YOE4+ years in pharmaceutical manufacturing/QA/finished goods disposition; strong GMP knowledge; data analysis skills; excellent communication and project management.
Zealand PharmaNasdaq Copenhagen: ZEAL: Develops peptide-based medicines for obesity and metabolic health.
Master's degree in life science or pharmacy, life sciences industry experience, complaint processing experience, GMP and quality systems knowledge, eQMS experience, strong communication skills, and willingness to travel.
Dyne TherapeuticsNASDAQ: DYN: Developing therapeutics for genetically driven neuromuscular diseases.
6+ YOEBachelor's in engineering/science (Master's preferred), 6+ years cGMP experience, 4+ years QA experience, knowledge of FDA/EMA regulations, GxP QA systems, CAPA, investigations, and proficiency with MS Office, SmartSheet, and Veeva.
Emergent BioSolutionsNYSE: EBS: Develops and manufactures vaccines and therapeutics for health threats.
8+ YOEBachelor's in scientific discipline, 8+ years GMP quality experience in pharma/biologics, QA operations and people leadership, inspection readiness, deviations/CAPA/change control, validation, risk management, MS Office and eQMS proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, eQMS
PCI Pharma Services: Integrated pharmaceutical development, manufacturing, and global packaging services.
3+ YOE3+ years QA GMP experience preferred; ability to manage supplier qualification, audits, non-conformances, and QA documentation; proficiency in MS Office and strong communication and organizational skills.
Invaluable: Online auction marketplace for fine art and collectibles.
5+ YOE5+ years QA experience; testing REST APIs and modern UIs (React); strong manual and automated testing skills with Selenium/Playwright/Cypress; programming for automation; CI/CD and test environment management; AWS/Docker/Kubernetes preferred.
Trivelta: Builds modular technology for social-first sportsbooks and casinos
Manual QA testing experience, strong attention to detail, bug tracking and test management tool familiarity, clear communication, and passion for sports and games.
Providence or Arizona or Connecticut or Florida or Georgia or Louisiana or Massachusetts or North Carolina or Oklahoma or Rhode Island or South Carolina or Texas or Virginia
$94k-$140k/yrRemoteFull Time
Blue Cross & Blue Shield of Rhode Island: Provides health and dental insurance plans to Rhode Islanders.
5+ YOEBachelor's degree or equivalent experience; 5–7 years of QA or software testing experience, including significant Salesforce enterprise testing, agile QA leadership, integrations, regression, security, and release validation.
Salesforce, Sales Cloud, Service Cloud, Experience Cloud, Financial Services Cloud, Data Cloud, Apex, Lightning Web Components, Flow, APIs, SOQL, Platform Events, AppExchange, CI/CD
Viridian TherapeuticsNASDAQ: VRDN: Developing optimized treatments for rare autoimmune conditions.
5+ YOE5+ years QA experience in biotech/pharma/medical device, Bachelor's in Life Science or Engineering, complaint handling, experience with CDMOs, Veeva eQMS, knowledge of US/global GMP and ICH guidelines.
Veeva Quality Management System, Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook, Microsoft SharePoint
HEICONYSE: HEI: Manufactures specialty electronic components and niche aircraft parts.
Bachelor of Science or equivalent RF/microwave industry experience; knowledge of drawing standards and military specifications; experience with supplier quality, audits, controls, documentation, training, and corrective actions.
Ionis PharmaceuticalsNASDAQ: IONS: Discovers and develops RNA-targeted medicines for serious diseases.
3+ YOEBachelor's degree in a science-related field, 3+ years quality assurance experience in pharmaceutical/biotech, strong knowledge of GxP/GMP and quality systems, familiarity with AI in GxP desirable, strong communication and problem-solving.
GCP & GLP QA Lead (Nonclinical & Clinical Quality Assurance)
Boston, Massachusetts, United States
$171k-$257k/yrHybridFull Time
Tango TherapeuticsNasdaq Capital Market: TNGX: Develops precision cancer medicines using synthetic lethality principles.
8+ YOEBachelor's in life sciences, 8+ years GLP/GCP QA experience, CRO/vendor oversight and inspection experience (FDA BIMO), GCP/GLP auditor certification preferred, knowledge of ICH E6/E8, TMF, data integrity, and audit execution.
QA Validation Engineer for AI Initiatives (Teradyne, North Reading, MA)
North Reading, Massachusetts, United States
$126k-$202k/yrOnsiteFull Time
TeradyneNASDAQ: TER: Designs and manufactures automated test equipment and advanced robotics systems.
7+ YOERequires 7+ years in QA/validation engineering, 2+ years with AI/ML or data-intensive systems, coding experience, database knowledge, and a bachelor's degree; master's preferred.
Python, Java, SQL, test automation frameworks, ML metrics, data profiling tools, Generative AI, API, ETL, ELT
Bowman Consulting GroupNASDAQ: BWMN: Provider of engineering and infrastructure consulting services.
8+ YOEBachelor's degree in civil engineering or related field, 8+ years of professional engineering experience, transportation project leadership, EIT registration, design experience, QA/QC skills, and proficiency with engineering software.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, MicroStation, AutoCAD, AutoTurn, GuideSIGN, Department of Transportation (DOT), QA/QC, Personal Protective Equipment (PPE)
Intellia TherapeuticsNASDAQ: NTLA: Develops curative gene-editing treatments using CRISPR technology.
10+ YOE10+ years industry experience with GMP QC oversight; advanced degree (MS/PhD preferred); experience with stability, reference standards, analytical methods, audits, and regulatory interactions.
EDMS, LIMS, JMP, MINITAB, GraphPad Prism, PLA, HPLC, UPLC, CE
Genezen: Produces viral vectors for cell and gene therapy programs.
6+ YOEBachelor's degree in science or related field; 6–8+ years in pharmaceutical or biologics quality assurance; GMP, investigations, quality systems, cross-functional leadership, and mentoring experience.
Veeva, 21 CFR Part 11, 21 CFR 210, 21 CFR 211, 21 CFR 600, 21 CFR 610, EudraLex Volume 4, ICH Quality Guidelines, EMA, ISO