Quality Manager Iovino EnterprisesQuality ManagerBrooklyn, New YorkFinal compensation will be based on a combination of: · Relevant work experience · Education · Project size · Project location · Required working hours · Candidate subject matter expertise and/or specialty · Ability to be approved by agencies/owners as required · *Final salary determination is negotiable* Join our “ track” record of success, we are looking to grow our most valuable asset … our employees! Certified Quality Engineer (CQE) as recognized by the American Society for Quality (ASQ) or a certified ISO-9000 Lead Auditor as recognized by the Registrar Accreditation Board (RAB) preferred.
Safety/Quality Coordinator Metals USASafety/Quality CoordinatorFairless Hills, PA$28–$32 / hourStand, walk, sit, hearing, talking, use of hands and fingers, hand-eye coordination, reach outward, reach above shoulder, climb, squat or kneel or bend . Monitors working conditions across the entire facility--including warehouse, office areas, external property, and parking lots--to ensure compliance with local, state, and federal safety regulations.
Assistant Vice President - Planning & Quality Metropolitan Transportation AuthorityAssistant Vice President - Planning & QualityNew York, NY$177,069–$210,268.25 / yearLead the development of long-range, strategic plans for maintenance and upgrades of the rolling stock fleet and facilities aligned to service needs, including but not limited to fleet maintenance, fleet composition, yard and maintenance facility requirements. Provide key input from long-range planning and forecasting in the development of the annual budget submission and ensure that the MofE department operates within the established budget by designing and instituting the necessary internal processes, protocols and controls.
Quality Specialist AB CorporateQuality SpecialistSouth Plainfield, New JerseyWork with customers for confirming information related to new items and attend new start-ups to ensure all requirements are met. Confers with manufacturing/sales/management about quality assurance of new products designed and manufactured products on market to rectify problems.
QA Specialist - 1 year contract Novartis AGQA Specialist - 1 year contractEast Hanover, NJEnsure reporting and follow up of all spontaneous adverse events (AE) and technical complaints for all Novartis Corporate products according to respective SOP.Essential RequirementDegree in Life Sciences or related fieldsLicensed Pharmacist, eligible to be registered as an Import Manager for the purpose of batch release approval activities. Ensure the quality of the finished products that are imported and distributed by Country Organization is complied with both a) Korea Pharmaceutical Law and the related regulation and b) Novartis Corporate Quality Manual and Policies (Quality manual and the relevant SOP) including cGxP requirements.
Lead (Quality) Benjamin Moore & CoLead (Quality)Newark, NJ$31–$41 / hourIn this position, the Plant Quality Lead performs quality related testing of all production batches, conducts batch related quality activities including pre- and post-manufacturing review of production orders, advises on batch adjustments, and manages quality records and retains. Laboratory Skills: Capable of using laboratory equipment including weighing balances, viscometers, pH meters, gloss/sheen meters and spectrophotometers.
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.
QA Manager Operations Novartis AGQA Manager OperationsEast Hanover, NJCollaboration in GxP audits/inspectionsOversight of Quality OperationsMaster Batch Record review and approvalAs site QP or delegation to release productQA for Quality Control & AS&TQA Operational ExcellenceWork Experience:Good Manufacturing Practices (cGMP)Audit & Inspection ManagementRelease ManagementQuality AssuranceQuality ComplianceQuality Management SystemsTechnological ExpertiseSkills:CollaborationContinuous Improvement mindsetDealing With AmbiguityRegulatory requirements knowledgeProblem Solving SkillsLeadershipCommunication skillsData IntegrityDigital savvinessLanguages:English. Successfully Support continuous improvement ProjectsExecutes batch release in compliance with registrationAs per local regulatory requirement and global guidance/SOP to set up local documentation hierarchyQuality system management (e.g., Change Control, Deviation, Audit &Inspection, CAPA, QE, CONDO, etc.)Validation Batch Record review; Validation protocols review; Deviation management; On site Quality monitoringSupport and oversight validation activitiesAudit and Inspection preparation and readinessFunction representative to be involved in global and/or local project if any.
NewSenior Quality Technician Synerfac Technical StaffingSenior Quality TechnicianRiverdale, NJMastery of both digital and non-digital shop measuring tools, including micrometers with vernier scales and calipers, complemented by strong Excel skills for data analysis. This senior role demands expertise in mechanical inspection, CMM programming, and AS9100D compliance, with a focus on tight tolerances down to ±0.0003.
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.
Quality Testing Technician I-MPA Americhem IncQuality Testing Technician I-MPAPAChanges machine settings throughout the process, with the guidance of the team leader, by adjusting functional parts of devices and control instruments using various types of settings and tools to assure product quality; recording changes on the FFC sheet. Runs a sample mold by combining the resin and compound in a plastic bag, loading a saved slot on the injection mold machine, and dropping the concentrate/resin mixture into the machine hopper to create a sample plaque.
Quality Assurance Coordinator (Home Care Agency-Brooklyn) YELM US Associates, LLCQuality Assurance Coordinator (Home Care Agency-Brooklyn)Brooklyn, NYOur mission is to provide and restore client dignity and independence in their homes through individualized care plans that reduce caregiver role strain and stress on family members while helping clients avoid nursing homes and assisted living facilities. Our office team works behind the scenes to ensure patients receive exceptional care — giving families true peace of mind — while also providing the coordination, resources, and support our field staff need to succeed.
QA Specialist I WuXi Biologics Cayman IncQA Specialist ICranbury, NJ$72,800–$116,500 / yearResponsibilities: Perform On-The-Floor QA activities pertaining to Drug Substance Manufacturing Operations, including QA observation of Upstream (USP) and Downstream (DSP) processing, real time executed batch record review, corrections, logbook review, room clearance/changeover, and data integrity checks of electronic systems. WuXi Biologics is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop, and manufacture biologics from concept to commercial manufacturing.
Staff Quality Engineer, Design & Reliability Assurance Integra LifeSciences Holdings CorpStaff Quality Engineer, Design & Reliability AssurancePlainsboro, 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.
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.
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.
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.
Unarmed Security Officer for Corporate Location Doyle Security Services, Inc.Unarmed Security Officer for Corporate LocationWARREN, New JerseyPart timeAbout Doyle Security Services: Doyle Security Services (DSS) is a leading provider of customized security solutions and investigative services. Securing premises and personnel by patrolling property; monitoring surveillance equipment; inspecting buildings, equipment, and access points; permitting entry.
NewUnarmed Security Officer for Warehouse Doyle Security Services, Inc.Unarmed Security Officer for WarehouseELIZABETH, New JerseyPart timeAbout Doyle Security Services: Doyle Security Services (DSS) is a leading provider of customized security solutions and investigative services. Securing premises and personnel by patrolling property; monitoring surveillance equipment; inspecting buildings, equipment, and access points; permitting entry.