Quality Manager (Manufacturing) Coyote Technical & Executive SourcingQuality Manager (Manufacturing)Hopkinton, MADirector of SourcingQuality Manager– Webster, MA#CNC#QualityManager#QualityControl#QualityAssurance#CMMProgrammer#PCDMIS#Calypso#Massachusetts#Manufacturing#Jobs Manage CSM Quality Team: delegate daily inspections and shipments, approve work schedules/vacations, execute yearly appraisals, and provide training.
Supplier Quality Engineer BeviSupplier Quality EngineerBoston, Massachusetts$94,690–$116,970 / yearApply an Advanced Product Quality Planning (APQP) framework to drive defect prevention at the supplier, owning the PPAP submission and approval process (PFMEA, control plan, process flow, MSA, dimensional/capability studies) for assigned parts. Serve as the lead supplier quality interface triaging field issues to root cause at the suppliers driving 8D corrective action, and verifying fixes hold against top-level quality metrics.
Post Closing/HMDA Quality Assurance Specialist Dean Co-operative BankPost Closing/HMDA Quality Assurance SpecialistFranklin, MAWorking in conjunction with the VP Loan Servicing Operations Officer in developing an internal quality assurance auditing program and after identifying areas of concern, the Post Closing/HMDA Quality Assurance Specialist will assist in creating a subsequent training program to enhance post-closing and create efficiencies in loan audits, loan funding, post-closing and servicing. Post-Closing: Assist the VP Loan Servicing Operations Officer in developing an internal pre-funding and post-closing Quality Assurance review process identifying adherence to department procedures, bank policies, regulatory compliance and investor guidelines.
QA Automation Engineer Creatio EMEA LTDQA Automation EngineerBoston, MATeam 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.
Sr. Aerospace Quality Engineer Analog DevicesSr. Aerospace Quality EngineerUs, MassachusettsADI combines analog, digital, AI, and software technologies into solutions that combat climate change, reliably connect humans and the world, and help drive advancements in automation and robotics, mobility, healthcare, energy and data centers. For positions requiring access to technical data, Analog Devices, Inc. may have to obtain export licensing approval from the U.S. Department of Commerce - Bureau of Industry and Security and/or the U.S. Department of State - Directorate of Defense Trade Controls.
Senior Data Quality Analyst IQVIA Holdings IncSenior Data Quality AnalystBurlington, MA$56,100–$140,300 / yearIn this highly visible role, you will partner with Engineering, Product, Data Operations, Client Support, and offshore teams to validate data, investigate and resolve quality issues, strengthen governance practices, and drive continuous improvement across the data lifecycle. As a Senior Data Quality Analyst at Cedar Gate Technologies, an IQVIA business, you will play a critical role in ensuring the accuracy, integrity, and reliability of healthcare data that powers our industry-leading analytics platform.
Product Quality Technician Straumann Holding AGProduct Quality TechnicianMA$26.61–$32.52 / hourWe develop, manufacture, and supply dental implants, clear aligners, instruments, CADCAM prosthetics and biomaterials for use in esthetic dentistry, tooth replacement and restoration solutions or to prevent tooth loss. We empower our employees to perform and make an impact, to question the status quo, to drive change, to stay ahead of the competition.
Quality Technician Johnson Controls International PlcQuality TechnicianBurlington, MA$42,600–$63,800 / yearJohnson Controls, a global leader in thermal management, mission-critical building systems, energy efficiency, and decarbonization, helps customers use energy more productively, reduce carbon emissions, and operate with the precision and resilience required in rapidly expanding industries such as data centers, healthcare, pharmaceuticals, advanced manufacturing, and higher education. Enabled by the Stack Forging process, JCI produces high-performance thermal components and cooling loop solutions - purpose-built for direct integration into AI, HPC, and mission-critical systems.
NewDirector, QA for QC Intellia Therapeutics IncDirector, QA for QCCambridge, MA$213,063–$260,411 / yearThis role partners closely with Analytical Development to ensure effective method design, lifecycle transfer, performance characterization, and alignment of analytical control strategies from early development through commercialization, and partners with QA GMP Operations, Global Technical Operations, Process Development, Regulatory Affairs, and external testing laboratories/CMOs. Provide Quality and technical oversight of analytical method validation, verification, lifecycle management, and method transfers in close collaboration with Analytical Development, including review of validation design, acceptance criteria, and method performance trends across novel and platform-specific assays.
NewAir Quality Compliance Manager Pinellas CountyAir Quality Compliance ManagerBoston, MAIf you are passionate about protecting air resources, enjoy a variety of work projects, and bring expertise in air quality compliance, enforcement and data management, this may be the perfect opportunity for you to join a stellar group of Environmental Professionals as an Environmental Program Manager 1 with Pinellas County's Division of Environmental Management (DEM). Bachelor's degree with major course work in physical, natural or biological science, environmental engineering, or related field, and five (5) years of progressively more responsible professional level experience that includes supervision or supervisor training; or an equivalent combination of education, training and/or experience.
Quality Engineer III Mercury Systems IncQuality Engineer IIINHThis role will participate and/or lead failure analysis in manufacturing and for field failures, develop troubleshooting & repair schemes, develop manufacturing process controls and documentation, interface with manufacturing and quality personnel to train and transfer processes & knowledge for successful volume production launches, and engage with suppliers as needed to drive improvement and implement process controls. Experience with systems such as Product Lifecycle Management software, Agile, or similar ERP system (Oracle, similar), Manufacturing Execution System (Factory Logix, similar), and issue and project tracking software (Jira, Confluence, similar).
Quality Manager (Heavy Civil Construction) Skanska ABQuality Manager (Heavy Civil Construction)Boston, MAHeshe develops plans directs and supervises project quality control functions and activities in conformance with the Company or project required Quality Program. The Quality Manager assists and supports Project Engineer Project Manager and Superintendent on assigned projects.
Lead Auditor, Quality Compliance Integra LifeSciences Holdings CorpLead Auditor, Quality ComplianceMansfield, MA$109,250–$149,500 / yearExperience with Corporate, divisional, site, supplier GMP, GDP, GLP or GCP (as applicable) audits as a Lead Auditor for multi-national manufacturing companies in the medical devices or pharmaceutical sector.\n \n\n Related quality/operations GMP work experience in a medical device or pharmaceutical manufacturing site or an equivalent combination of education and work experience in QS/QA/QC/OPS or a technical management and supervisory function.\n \n\n Experience auditing technical files for conformance with EU regulations for CE-marked medical devices.\n Master's degree preferred.\n \n\n Formal Auditor certification by a recognized body (e.g., IRCA, ASQ CQA, BSI, Exemplar Global).\n \n\n Minimum 15 years of experience in auditing in quality, manufacturing, or engineering, or equivalent education and years of experience.\n \n\n Experience in FDA controlled environment.\n \n\n* Strong collaboration skills and experience working in a matrix environment.\n \n\n \nSalary Pay Range:\n \n$109,250.00 - $149,500.00 USD Salary\n \nOur salary ranges are determined by role, level, and location.
Sr Quality Engineer, Design Assurance Integra LifeSciences Holdings CorpSr Quality Engineer, Design AssuranceBraintree, MA$81,650–$112,700 / yearThe Design Quality Assurance Engineer (DQA) is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, as well as risk management work for new and existing products. Writing & coordinating efforts for the development and implementation of new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development documentation, SOPs to support development and sustaining/remediation projects.
Quality Engineer II - Design & Reliability Assurance Integra LifeSciences Holdings CorpQuality Engineer II - Design & Reliability AssuranceBraintree, MA$71,300–$97,750 / yearThe Design Quality Assurance Engineer (DQA) is responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, as well as risk management work for new and existing products. Writing & coordinating efforts for the development and implementation of new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development documentation, SOPs to support development and sustaining/remediation projects.
Staff Quality Engineer, Design & Reliability Assurance Integra LifeSciences Holdings CorpStaff Quality Engineer, Design & Reliability AssuranceBraintree, MA$109,250–$149,500 / yearThe Staff Design Quality Assurance Engineer (DQA) is a subject matter expert responsible for the efficient and compliant support of New Product Development (NPD) and Sustaining/Remediation project(s) of varying scope and complexity in the Tissue Technology (TT) division, as well as risk management work for new and existing products. Writing & coordinating efforts for the development and implementation of new and updated Quality System procedures for ISO/QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development documentation, SOPs to support development and sustaining/remediation projects.
Specialist, Quality Assurance Moderna IncSpecialist, Quality AssuranceNorwood, MA$89,900–$143,800 / yearHere's What You'll Bring to the Table: Minimum requirements: Requires a Master's degree, or foreign equivalent, in Engineering Management, Engineering (any), Biology, Chemistry, or related field and 3 years of experience as a Quality Assurance Associate, QA Testing Engineer, Supervising Engineer, Graduate Apprentice, or related position. Must have 3 years of experience with the following: Writing and ensuring compliance to SOPs; Documenting processes, deviations, and corrective actions to maintain quality records; Root Cause Analysis; Technical writing; and.
Senior Associate, Plant Quality Assurance ReplimuneSenior Associate, Plant Quality AssuranceFramingham, MassachusettsThe Senior Associate, Plant Quality Assurance (PQA) reports to the Manager, Plant Quality Assurance and is responsible for providing day-to-day Quality oversight to support Drug Substance, Drug Product, and Quality Control operations in accordance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and other applicable regulatory requirements. The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response.
Senior QA Specialist Editas Medicine, Inc.Senior QA SpecialistCambridge, MA$110,000–$120,000 / yearDecoding The Role: The primary focus of this role in the next 12 months is to advance our lead in vivo development candidate, EDIT-401, into the clinic to establish human proof of concept by ensuring compliance with FDA, cGMP, and international regulatory requirements across manufacturing, testing, product disposition, and quality event management. Author, review, and approve GMP documentation (SOPs, batch records, protocols, technical reports, test methods, specifications, and summary reports) supporting GMP manufacturing.
Product Quality Engineer VulcanForms IncProduct Quality EngineerMA$75,000–$94,000 / yearFounded in 2015 to develop the world's first industrially scalable laser metal additive manufacturing solution, VulcanForms is reshaping how the world manufactures critical products. We foster an inclusive culture where people take ownership, solve meaningful problems, and continuously learn, because we believe diverse perspectives lead to better outcomes.