Lead Product Quality Engineer, Aerospace & Defense VulcanFormsLead Product Quality Engineer, Aerospace & DefenseDevensThis role goes beyond individual task execution to shape how quality is built into the program from the outset, mentor and develop other quality engineers supporting the program, and represent quality engineering in cross-functional product development & ongoing production initiatives. Independently investigate complex product non-conformances (NCRs), lead material review boards (MRBs), and drive the execution of Corrective and Preventive Actions (CAPAs) to eliminate systemic failure modes.
Clinical Laboratory Quality Coordinator - Onsite LabCorpClinical Laboratory Quality Coordinator - OnsiteWestborough, MA$26–$30 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Senior Product Quality Engineer, Consumer Technology VulcanFormsSenior Product Quality Engineer, Consumer TechnologyDevensThe Senior Product Quality Engineer, Consumer Technology manages quality systems, implements robust process controls, and drives continuous improvement across advanced manufacturing programs within our consumer technology business unit. Root Cause & CAPA: Independently investigate complex product non-conformances (NCRs), lead material review boards (MRBs), and drive the execution of Corrective and Preventive Actions (CAPAs) to eliminate systemic failure modes.
Senior Product Quality Engineer, Aerospace & Defense VulcanFormsSenior Product Quality Engineer, Aerospace & DefenseDevensVulcanForms is seeking a Senior Product Quality Engineer, Aerospace & Defense to manage quality systems, implement robust process controls, and drive continuous improvement across advanced manufacturing programs within our aerospace & defense business unit. Serve as a core member of our quality engineering team, supporting designated product lines and managing product lifecycle quality from initial validation through steady-state production.
Validation Quality Technician LancesoftValidation Quality TechnicianActon, MA$28The Quality Technician collaborates with Quality Engineering to ensure new and existing products conform to the *** Quality System, Quality System Regulation, ISO 13485 and ISO14971 throughout the design transfer to manufacturing process as well as product lifecycle. The Quality Technician is responsible for executing Test Method Validations, Process Validations, and other engineering studies in accordance with written protocols and procedures to maintain the validated state of ***’s product manufacturing and quality processes.
Senior Director, Quality Repligen CorporationSenior Director, QualityWaltham, Massachusetts$191,250–$260,000 / yearAs a member of the Global Quality Leadership Team, reporting directly to the VP Global Quality, you will partner closely with Operations, Commercial, Product Management, Supply Chain, Regulatory Affairs, and senior business leaders to establish a culture of quality excellence, operational performance, and continuous improvement throughout the network. Lead and execute the quality strategy across Repligen’s Filtration & System networks, with accountability for Quality Assurance, Quality Systems, Quality Compliance, Validation, Quality Control, Supplier Quality partnership, and Customer Quality activities.
Director Of Quality Catalent Pharma Solutions, Inc.Director Of QualityChelsea, MA$168,750–$257,800 / yearDemonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience; The anticipated salary range for this position in Massachusetts is $168,750-$257,800. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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.
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.
NewValidation Contractor, Quality Assurance BelcanValidation Contractor, Quality AssuranceWestborough, MACollaborates with cross-functional stakeholders regarding quality events (e.g., deviations, Corrective / Preventative Actions (CAPAs), etc.), assisting in investigations and ensuring quality records are clearly written, technically sound, and provide thorough root cause analysis and risk assessment. * Authors technical documents such as User Requirement Specifications (URS), Regulatory Assessment and System Categorization (RASC), Functional Specification (FS), Configuration Specification (CS), Traceability Matrix (TM), deviations, and risk assessments.
Enterprise Data Quality Leader, Vice President State StreetEnterprise Data Quality Leader, Vice PresidentBoston, MassachusettsThe successful candidate will play a key role in strengthening enterprise capabilities for data quality management, controls, measurement and reporting, exception and issue management, and BCBS 239-aligned risk data aggregation and reporting outcomes using the Collibra Platform and related technologies. Define strategy to governance structure to drive continuous improvement of enterprise Data Quality Error Management and Data Quality Issue Management processes, including effective escalation paths, and senior management engagement as needed.
NewManager, Quality Engineering ImprivataManager, Quality EngineeringWaltham, MA$177,000–$180,000 / year40% telecommuting permitted in U.S. Requires up to 10% travel throughout the U.S. Minimum Qualifications : Must have a Bachelor’s degree in Engineering, Computer Science, or closely related field and 3 years of experience in Quality Control Engineering / Quality Assurance, or a substantially similar position, including the mobile applications for iOS and Android, white box and black box testing, testing applications on Windows, MacOS, iOS, Android and Linux, working in Agile environment, and testing in and managing virtual environments including VMware and Citrix. Position Duties : Manage a team of Quality Engineers primarily tasked with verifying the quality of new feature development, maintenance, and integration with existing platforms through manual and automated testing.
Quality Manager What we do- AspenQuality ManagerEast Providence, Rhode IslandThe ideal candidate must be able to lead through ambiguity, stabilize quality performance during supplier/process changes, support customer escalations, and develop a high-performing Quality Engineering team capable of sustaining IATF 16949 expectations, automotive core tools, product validation, traceability, and continuous improvement. The Quality Manager will ensure that quality processes are not only documented but effectively implemented on the manufacturing floor including control plans, quality gates, incoming inspection, process controls, layered audits, nonconformance management, APQP, PPAP, supplier qualification, and customer-specific requirements.
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.
Raw Material Quality and Supplier Management Engineer DuPont Electronic Materials InternationalRaw Material Quality and Supplier Management EngineerMarlborough, MassachusettsAt Qnity , we’re more than a global leader in materials and solutions for advanced electronics and high-tech industries – we’re a tight-knit team that is motivated by new possibilities, and always up for a challenge. Interact closely with vendors to ensure clear communication of DuPont’s expectations, including regular audits, technical meetings, and on-site visits.
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 ComplianceMansfield, 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.
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.
Product Quality Technician Shyft6Product Quality TechnicianFall River, MassachusettsConduct quality audits and influence the proper execution of culinary and cook methods so that product will meet desired quality levels. Aids and Supports facility teams on investigating, analyzing, containing, and correcting quality issues related to customer complaints.
Senior Associate, Plant Quality Assurance ReplimuneSenior Associate, Plant Quality AssuranceFramingham, Massachusetts$99,500–$128,500 / yearThe 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.