Quality Technician Bio-TechneQuality TechnicianDevens, Massachusetts$23.20–$31.90 / hourBy joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Performs facility monitoring tasks including: o Daily monitoring of temperature-controlled areas using calibrated devices.
CT - 5237 Quality Engineer I All Coghlin CompaniesCT - 5237 Quality Engineer IWestborough, Massachusetts$70,000–$85,000 / yearCollaborate with Project Managers (PM’s) to analyze customer ECN’s and ensure effective implementation to the production floor through proper use of the Engineering Change Order (ECO) process, including reviewing and communicating impacts of any changes (e.g., financial, inventory, WIP, open supplier orders, etc.) as it pertains to Quality. Collaborate with all internal groups and customers to help determine root cause of customer issues, Complaints, and CAPAs using various techniques including but not limited to Reenactment, PFMEA, Control Plans, Five Whys, Ishikawa (fishbone) Diagrams, Pareto Analysis, etc.
Quality Engineer I Coghlin CompaniesQuality Engineer IWestborough, MAFull timeCollaborate with Project Managers (PM’s) to analyze customer ECN’s and ensure effective implementation to the production floor through proper use of the Engineering Change Order (ECO) process, including reviewing and communicating impacts of any changes (e.g., financial, inventory, WIP, open supplier orders, etc.). Collaborate with all internal groups and customers to help determine root cause of customer issues, Complaints, and CAPAs using various techniques including but not limited to Reenactment, PFMEA, Control Plans, Five Whys, Ishikawa (fishbone) Diagrams, Pareto Analysis, etc.
NewQuality Assurance Representative Canadian Nuclear Laboratories LtdQuality Assurance RepresentativeBurlington, MARemoteFrom building the next generation of clean nuclear and hydrogen energy technologies, to developing targeted cancer treatments, to continuing our global leadership in environmental remediation-we are driven by impact, innovation, and purpose. At a minimum, a Bachelor''''s (Honours) in Engineering, Chemistry, Physics or equivalent from a university of recognized standing; or membership in an engineering or scientific organization authorized by statute to establish qualification for membership in that organization.
Supplier Quality Engineer Hydration Labs IncSupplier Quality EngineerBoston, MA$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.
QA Tech (Food Production) - Milford, MA Legal Sea FoodsQA Tech (Food Production) - Milford, MAMilford, MAMaintain a clean and sanitary laboratory, including but not limited to keeping benchtops sanitized and free of clutter, washing lab floor and cleaning all glassware/metal instruments used in the testing process. Works closely with the QA Manager in ensuring all specifications are met in conjunction with the departments that impact food quality, including receiving, portioning and sanitation.
Sr Quality Engineer, Design Assurance Integra LifeSciences Holdings Corp.Sr 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.
Lead Auditor, Quality Compliance Integra LifeSciences Holdings Corp.Lead Auditor, Quality ComplianceBraintree, MA$109,250–$149,500 / yearThe Lead Auditor, Quality Compliance will form part of the Corporate Audit team and will lead, coordinate and perform corporate audits of the Quality Management System (QMS) as part of Integra LifeScience's quality internal audit program across more than 15 design, manufacturing, and distribution facilities and a diverse portfolio of leading medical devices. The incumbent will possess extensive GMP audit experience and practical skills including: the ability to write objective technical audit reports, evaluate and make objective judgments on technical issues arising during the audit, utilize multi-cultural sensitivity while driving audits forward consistently and on time, as well as project and time management.
NewTranslation Quality Assurance Specialist (Bilingual Portuguese) Framingham Public SchoolsTranslation Quality Assurance Specialist (Bilingual Portuguese)Framingham, MAThe requirements listed below represent the knowledge, skills, and abilities required: Linguistic & Editing Expertise: High-level proofreading, editing, and machine-translation post-editing skills; exceptional grasp of grammar, syntax, and cultural nuances in English, and Portuguese. This role utilizes district-approved AI-powered translation software to initiate translations and performs meticulous proofreading, editing, and post-editing to guarantee absolute accuracy, cultural consistency, and regulatory compliance.
Project Controls - Senior Director - Project Farma PerkinElmer US LLCProject Controls - Senior Director - Project FarmaBoston, MAAt more senior levels, this role is accountable for shaping strategy, leading leaders, and driving sustained business impact across a significant area of the organization, while influencing enterprise-level decisions, ensuring operational excellence, and developing leadership talent to balance short-term execution with long-term growth objectives. Project Farma (PF) team members collaborate with cross-functional teams to build trusted client relationships, deliver an exceptional customer experience, and contribute to business growth by identifying opportunities and applying data-driven insights to support project planning, cost, schedule, and performance management.
QA Manager (Manager, Quality Assurance) Redwire SpaceQA Manager (Manager, Quality Assurance)Marlborough, Massachusetts$126,000–$165,000 / yearTo 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.
QA Manager/Hardware Manufacturing (Manager, Quality Assurance) Redwire SpaceQA Manager/Hardware Manufacturing (Manager, Quality Assurance)Marlborough, Massachusetts$126,000–$165,000 / yearTo 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.
Quality Change Control, Project Manager (Contract) 665 Vertex PharmaceuticalsQuality Change Control, Project Manager (Contract) 665Boston, Massachusetts$58–$65 / hourFull timeAgreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners. Excellent oral and written communication skills, including presentation and facilitation skills, to effectively inform key updates & issues across all levels of the organization.
Quality Operations Program Manager - Document Control Veeva Systems IncQuality Operations Program Manager - Document ControlBoston, MARemote$100,000–$150,000 / yearServe as System Administrator of Veeva's internal electronic Document Management System (eDMS), responsible for system configuration, user administration, lifecycle management, and continuous improvement of the system and its governed processes. We're not just any public company - we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
QA officer (Controls Testing) Syntricate Technologies IncQA officer (Controls Testing)Nashua, FLAppropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Banking, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behaviour, conduct and business practices, and escalating, managing and reporting control issues with transparency. Help contribute to the Lessons Learned Policy, including monitoring of control breaches and dissemination and learnings across other business units for process improvement to limit the occurrence of similar future events and where similar risk exposure might exist.
Quality Engineer Merrimack ManufacturingQuality EngineerManchester, NHDevelop and approve technical documents to plan work, such as Master Validation Plans, Quality Plans, and Qualification Protocols; support execution of work product. Lead investigations resulting in root cause and corrective actions through use of data analysis, inductive and deductive reasoning, and problem solving skills.
Principal Associate I, Plant Quality Assurance - 2ND SHIFT ReplimunePrincipal Associate I, Plant Quality Assurance - 2ND SHIFTFramingham, MassachusettsThe Principal Associate I/II, Plant Quality Assurance (PQA) reports to the Associate Director, Quality Assurance and is responsible for on-going Quality oversight to ensure real time quality oversight for Drug Substance, Drug Product, and all other production and QC testing activities according to current good manufacturing practices (cGMP), good documentation practices (GDP) and other applicable regulations. 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.
Associate Quality Engineer Globus Medical Inc.Associate Quality EngineerMethuen, MAPosition Summary: The Associate Quality Engineer will be responsible for achieving the highest quality level of manufacturing quality and quality system performance while ensuring compliance with all company policies and procedures and maintaining compliance with US FDA and international medical device regulations and ISO 13485 quality system requirements. Conduct thorough review of documentation, including but not limited to Document Change Orders (DCOs), engineering drawings, specifications, risk management files, and Verification & Validation (V&V) protocols and reports.
NewQuality Engineer III Mercury Systems IncQuality Engineer IIIHudson, NHExperience with systems such as Product Lifecycle Management software (Agile or similar), ERP system (Oracle or similar), Manufacturing Execution System (Factory Logix or similar), and issue and project tracking software (Jira, Confluence, or similar). This position will focus on delivering quality product that meets customer requirements, identifying opportunities for yield improvement, process improvement, and product cost-reduction methods.
Quality Systems Specialist I Cirtec Medical CorpQuality Systems Specialist ILowell, MA$70,000–$80,000 / yearOur expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems. Must Have: Associates of Science Degree in Manufacturing, Engineering, or Technical Field, or equivalent of directly transferrable industry work experience (Engineering or Quality discipline preferred).