Manager of Quality Improvement for School Age Programs RFCUNY Research Foundation of the City University of New YorkManager of Quality Improvement for School Age ProgramsNew York, New York$80,000–$85,000 / yearUnder the direct supervision of the Senior Director of QUALITYstarsNY, the Manager of School-Age Programs will work closely with leaders of the QSNY team and external partners to define, plan, build, and launch the rollout of our quality rating and improvement model with programs serving school-aged children. While the Manager of School Age Programs is modeled after other positions on QSNY's early childhood quality improvement team, it is a new position within the team and requires a leader who can take the reins and chart a clear path for success for SACC programs across the state that apply and are selected to participate.
NewQuality Manager Synerfac Technical StaffingQuality ManagerRidgefield, NJYou will coach and develop a high-performing quality organization, ensure appropriate resourcing, represent site quality leadership in executive meetings, contribute to alignment with corporate quality strategy, and participate in strategic planning and facility expansion discussions. The role requires expert-level proficiency in cGMPs, 21 CFR Parts 210/211, ICH, and USP requirements, as well as demonstrated success leading FDA and customer audits, maintaining inspection readiness, and developing and verifying effective remediation plans.
NewQA / UAT Lead FuntonetworkQA / UAT LeadLong Island City, New YorkAt FuntoNetwork, we connect experienced consultants with Upcoming project opportunities through a mobile-first platform built for discovery, review, application submission, payment tracking, and consultant support. Once you complete AI vetting and are approved, you will log in to the FuntoNetwork mobile app to track relevant opportunities, application status, contracts, earnings, payments, withdrawals, and related records.
Quality Engineer III Volt Information Sciences IncQuality Engineer IIIClifton, NJDay to Day Responsibilities• Establishes robust quality evaluation and control systems for assembly integration and test of complex electronic & mechanical assemblies• Leads support activities across programs ranging from hardware inspections evaluation of incoming material electrical test and inspection of build of assemblies• Expert with FRBMRB activities overseeing issue closure and strategic cross-company implementation of systemic preventive corrective actions• Expert RCCA practitioner of problem-solving methodologies• Strong performance history with generating professional presentations technical reports and in-depth case studies• Uses metrics to identify signals and initiate tactical course corrections and manages key performance areas KPIs to meet established goals• Responsible for providing guidance coaching and training to other employees related to all quality processes• Initiates complex projects and leads continuous improvement activities including driving ZDP execution in accordance with business strategy• Communicates within and outside of own function or business area and has responsibility for communicating with parties external to the organization e.g. At Volt our greatest strength is our peopleVolt is immediately hiring for a Quality Engineer in Clifton NJJob descriptionAs a Quality Engineer your responsibilities will include Delivers mission success and excellence throughout the integrated product lifecycle resulting in defect-free work products and delighted customers.
Document Control Analyst Exp Global IncDocument Control AnalystNew York, NY$50,000–$80,000 / yearHere, you join a team that leverages differences, harnesses their entrepreneurial spirit in an employee-owned company, that believes diversity is what gives us strength, seeks sustainable results and shares ambitions for each other, our clients and the communities we are part of and serve. We are an entrepreneurial, multidisciplinary firm of approximately 5,000 professionals across North America with a history of successfully delivering some of the most complex infrastructure projects across North America.
Staff Quality Engineer, Design & Reliability Assurance Integra LifeSciences Holdings CorpStaff Quality Engineer, Design & Reliability AssurancePrinceton, NJ$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.
Sr Quality Engineer, Design Assurance Integra LifeSciences Holdings CorpSr Quality Engineer, Design AssurancePrinceton, NJ$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 AssurancePrinceton, NJ$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.
Principal Auditor (Experienced Senior Auditor) Audit Practices - Quality Assurance (Hybrid) Capital One Financial CorpPrincipal Auditor (Experienced Senior Auditor) Audit Practices - Quality Assurance (Hybrid)New York, NY$109,900–$125,400 / yearThe uality Assurance and Improvement Program executes quality assurance and quality control reviews to maintain high audit quality and inform department-wide methodology, and training needs. Candidates hired to work in other locations will be subject to the pay range associated with that location, and the actual annualized salary amount offered to any candidate at the time of hire will be reflected solely in the candidate's offer letter.
Lead Auditor, Quality Compliance Integra LifeSciences Holdings CorpLead Auditor, Quality CompliancePlainsboro, NJ$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.
NewSupplier Quality Coordinator TW O'Neal Industries, Inc.Supplier Quality Coordinator TWMonroe, NJPosition Summary: The Supplier Quality Coordinator assists the Quality team by promptly resolving supplier issues and serves as a key point of communication between suppliers and internal quality functions. Responsibilities include maintaining supplier records, certifications, and various databases such as supplier contacts, specification libraries, and material qualification software.
Test Engineer - Equipment & Cloud QA (Chinese-Speaking) myHR PartnerTest Engineer - Equipment & Cloud QA (Chinese-Speaking)Langhorne, PA$70,000–$90,000 / yearAs their Test Engineer for Equipment & Cloud QA located in Langhorne, PA, you will own quality control and validation testing across the full product lineup, from physical hardware (batteries, inverters, gateways, and firmware) to the Fortress cloud platform, portal, and mobile/web applications. Direct experience with battery energy storage systems (BESS), inverters, or power electronics, including bench testing with lab instrumentation (e.g., multimeter, oscilloscope, power analyzer, programmable loads/sources).
Quality Assurance Technician, 2nd Shift Bruker CorpQuality Assurance Technician, 2nd ShiftCarteret, NJ$20–$23 / hourThe base salary for the role will depend on several job-related factors, including, but not limited to, education, training, experience, the geographic location of the successful candidate, skills, competencies, job-related knowledge, and travel requirements for this position. Our customers include government agencies with primary applications in fusion energy, wind turbine technology, and high energy physics, as well as private industries around the world for medical, pharmaceutical, and industrial applications.
Corporate Vice President - Delivery Lead, Quality Engineering & Automation New York Life Insurance CoCorporate Vice President - Delivery Lead, Quality Engineering & AutomationNew York, NY$119,000–$170,000 / yearThis leader will oversee a team of quality engineers and automation experts, providing both strategic and technical direction while partnering across delivery, engineering, and platform teams to embed quality throughout the software lifecycle. The ideal candidate will bring strong hands-on SDET (Software Development Engineer in Test) experience, combined with proven leadership in scaling modern QE practices, test data management, cloud platforms, and AI-driven validation.
Managing Director - Assurance Professional Practice Group - Quality Management Baker Tilly Advisory Group, LPManaging Director - Assurance Professional Practice Group - Quality ManagementIselin, New JerseyBaker Tilly Advisory Group, LP and Baker Tilly US, LLP, trading as Baker Tilly, are independent members of Baker Tilly International, a worldwide network of independent accounting and business advisory firms in 141 territories, with 43,000 professionals and a combined worldwide revenue of $5.2 billion. Baker Tilly is a leading advisory, tax and assurance firm, providing clients with a genuine coast-to-coast and global advantage in major regions of the U.S. and in many of the world's leading financial centers - New York, London, San Francisco, Los Angeles, Chicago and Boston.
Quality Engineer Whippany Actuation Systems, LLCQuality EngineerWhippany, NJ$82,000–$105,000 / yearThe Quality Engineer develops and implements systems to ensure products or services are designed and produced to meet or exceed customer requirements and expectations and establishes the principles of product and service quality evaluation and control for the quality management system. This role participates in the change management process to assure the products or services continue to meet customer requirements and provides independent oversight and review of the project deliverables throughout the lifecycle.
Cybersecurity Control Testing Lead, VP Mitsubishi UFJ Financial GroupCybersecurity Control Testing Lead, VPJersey City, New JerseyThis position will serve as a team leader within a broader Cybersecurity GRC control assurance operating model, accountable for directing testing activities, developing team capability, influencing control quality, and providing insight to engineering, security architecture, application, infrastructure, audit, risk, and compliance stakeholders. Demonstrated experience testing technical controls, including access management, privileged access, change management, vulnerability management, logging and monitoring, encryption, backup and recovery, incident response, configuration management, and network security.
Quality Coordinator (Hybrid position) Concordance Health Solutions LLCQuality Coordinator (Hybrid position)Edison, NJThe role will work in collaboration with the Emergency Preparedness and Response Manager, Operations Manager, Program Manager, and Compliance Manager to maintain and enhance the quality management system (MasterControl) and ensure consistent quality practices across all distribution operations. Concordance Healthcare Solutions, LLC is committed to being the most respected, innovative, national, multi-market healthcare solutions company earning the highest level of trust by operating with integrity, unwavering commitment and exceptional service through our culture of excellence.
Quality Coordinator (Hybrid position) Concordance Healthcare Solutions CareersQuality Coordinator (Hybrid position)Edison, New JerseyThe role will work in collaboration with the Emergency Preparedness and Response Manager, Operations Manager, Program Manager, and Compliance Manager to maintain and enhance the quality management system (MasterControl) and ensure consistent quality practices across all distribution operations. Support external audits with customers, regulatory bodies, and third-party auditors and track audit findings with assisting in timely implementation and verification of corrective actions.
Senior Specialist, Quality Assurance Validation Bristol-Myers Squibb CoSenior Specialist, Quality Assurance ValidationNew Brunswick, NJ$78,980–$95,708 / yearBased 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. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.