Quality Systems Specialist: Document Control & eQMS
DEKA Research and Development
DEKA Research and Development, on behalf of Millyard Advanced Medical Products, is seeking a Quality Systems Specialist to join a dynamic Medical Device R&D environment. The position reports to the Director of Quality, with high visibility and direct impact on the QMS. Located in Manchester, NH, the role focuses on documents, records, DCN, training, and change control. You will lead document management, support audits, and promote QMS awareness across DEKA teams. #J-18808-Ljbffr DEKA Research and Development
- ...Research & Development in Manchester, NH, seeks a Quality Systems Specialist to maintain and improve the quality... ...quality records and training. You will manage documents, DCNs, SOPs, and change control, implement an eQMS system, and ensure accuracy and traceability...Suggested
- ...Products, is looking for a Quality Systems Specialis t to work in a dynamic... ...impact: Responsible for documents, records, DCN, and Training... ...Manager to implement an eQMS system Create, implement,... ...numbering, record retention, change control and document distribution...SuggestedContract workWork at office
- ...PCI.Position Title: QA Specialist II - Document ControlLocation:... ...HampshireDepartment: Quality Assurance, Document ControlReporting... ...to ensure only controlled copies are reviewed,... ...Quality Management System tools and supports... ...Document Control and/or eQMS configuration and...SuggestedFull time
- ...Impact That You Will Make Quality Assurance Specialists/Senior Specialists are... ...you will support quality system initiatives, ensuring compliance... ...assessments, and change controls) Participate in root cause... ...processes Own the document control and issuance processes...SuggestedWork experience placement
- ...PCI Pharma Services seeks a QA Specialist II for Document Control in Bedford, New Hampshire to manage... ...document workflows, maintaining quality management systems, and leading continuous improvement... ...Document control and eQMS configuration and system management...Suggested
- SemiGen is seeking a Document Control Administrator to support the Quality Management System, configuration management, and document control across facilities. You will ensure controlled documents are current, approved, and accessible for production and inspections. Responsibilities...
- SemiGen is seeking a Document Control Administrator to join our high-performing team. This role provides administrative support for the Quality Management System, configuration management, quality assurance, engineering, and manufacturing. Ensuring controlled information...
$27.31 - $51.35 per hour
...manufacture and service of aircraft engines and auxiliary power systems and has been revolutionizing modern flight for over 100 years. Join us and help shape the future of aerospace and defense. Quality Management System Auditor Role Overview: Pratt & Whitney, a division...Contract workTemporary workWork experience placementWork at officeRemote workMonday to FridayFlexible hoursShift workDay shift- ...Objective:This position is part of PCI’s Quality Compliance team responsible for the... ...Product Quality Review’s.Support Quality System Events impacting the Supplier Quality program... ..., and file Supplier Qualification documentation from vendors.Track and maintain KPI metrics...Full timeContract work
- ...pioneer and shape the future of PCI.JOB DESCRIPTION:Position Title: Sr. QA Specialist - Supplier QualityLocation: Bedford, New HampshireDepartment: Quality AssuranceReporting To: QA Dir, Quality Systems & ComplianceResponsible For (Staff): NoThis position is part of PCI’s...Full timeContract work
- ...DESCRIPTION:Position Title: QA Specialist ILocation: Bedford,... ...HampshireDepartment: Quality AssuranceReporting To:... ..., and Quality System review. This position... ...Perform review of batch documentation for release of internal... ...Manufacturing, Quality Control, and other investigations...Full time
- ...future of PCI.This position is part of PCI’s Quality Compliance team responsible for the... ...Product Quality Review’s.Support Quality System events impacting the Supplier Quality... ...reconcile, and file Supplier Qualification documentation.Provide support for Quality Council...Full timeContract work
$159.43k
...implement, and maintain the project-specific Quality Assurance Surveillance Plan (QASP) in... ...• Perform daily quality inspections and document work progress to ensure materials,... ...Oversee construction contractor’s Quality Control meetings (Preparatory, Initial, and Follow...Contract workFor contractorsWork experience placementFor subcontractorH1bImmediate startFlexible hours- ...Chief Quality Officer (CQO) About the Company Highly technically advanced hospital network in New England Industry Hospital... ...the quality infrastructure with the clinical services operating system and identifying opportunities to expand and optimize its impact...
- ...Pharma Services seeks a QA Specialist II to oversee supplier qualification... ...compliance with SOPs, quality and regulatory standards... ...maintain supplier qualification documentation and KPI metrics... ...medical device GMP quality systems Exceptional organizational...
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Department: 107100 Quality Location: San Diego, USA- Remote Be a part of a global team... ...device manufacturers. Plan, execute, and document on-site, remote, and hybrid interna/... ...compliance risks as appropriate. Quality Systems & Compliance Support GxP inspection readiness...Contract workTemporary workRemote work- ...products compliant and customers confident. As a Quality Visual Inspector, you’ll move between... ...visual inspections on components and assemblies, document results, and complete FAIs with accuracy and clarity.Strengthen the system: Support and maintain our AS9100 Quality...
- ...Title: QA Operations Specialist I - Floor SupportLocation... ...HampshireDepartment: Quality Assurance,Reporting To... ...product vials, GMP documentation and Batch Record review... ...manufacturing related systems and processes to ensure... ...investigations.Review of Quality Control environmental and...Full timeImmediate startFlexible hoursShift work
$62.7k
...process improvements related to the potential of quality medical care and service to members and to improve documentation of these services for appropriate ICD 10-CM... ...computer literacy and knowledge of information systems and comparative data bases. Working knowledge of...For contractorsWork at officeLocal areaRemote work$20 - $22 per hour
...distribution company in Londonderry, NH to hire Quality Control Associates. This position plays a... ..., and warehouse processes Identify, document, and report quality concerns or... ...issues Utilize warehouse management systems to track inventory and quality information...Hourly payTemporary workLocal areaMonday to FridayShift work$21.1 - $44.99 per hour
...accountable and prioritize safety and quality in everything we do. Join us and be part... ...appropriate, accurate, and supported by clinical documentation in accordance with all state and... ...Coder) or CCS-P (Certified Coding Specialist-Physician) certification required. Minimum...Hourly payFull timeTemporary workWork at officeLocal area- ...QA Specialist I will oversee batch record reviews, lot disposition, and quality system administration for clinical and commercial pharmaceutical... ...Review and approve batch documentation for clinical and commercial... ..., test methods, and change control documentation Lead...
- ...Quality Assurance Specialist supporting clinical and commercial pharmaceutical manufacturing... ...Review and approve batch documentation for clinical and... ...develop, and approve quality system procedures, specifications... ...test methods, and change control documentation Lead...Contract work
- ...Senior QA Operations Specialist responsible for overseeing visual inspection activities, product... ...with cross-functional teams on quality assurance and continuous improvement initiatives... ...Initiate and manage quality systems including deviations, events, and corrective...Work at office
- ...QA Operations Specialist I supports visual inspection and final product sampling, packaging... ...and vial labels Initiate and manage quality systems including deviations, events, and CAPAs... ..., quality assurance, or quality control in pharmaceutical manufacturing (2 years...
- ...PCI Pharma Services seeks a QA Operations Specialist I to support visual inspection and final... ..., and driving continuous improvement in quality assurance processes. Responsibilities... ...vial labels Initiate and own quality system activities including events, deviations,...
- ...Quality Assurance Associate Are you meticulous, technically-minded, and committed to high standards? Become a quality assurance associate... ...life. Your responsibilities: ~ Perform routine quality control (qc) inspections on components, sub-assemblies, or finished...Temporary workImmediate startFlexible hours
- ...Services seeks a QA Operations Specialist II to oversee visual... ...final product sampling, and quality compliance at its Bedford, New... ...Initiate and manage quality systems including deviations, events,... ...Quality Assurance, or Quality Control in pharmaceutical manufacturing...Work at office
- Lactalis USA in Londonderry, NH is seeking an FSQ Customer Support Analyst to ensure product quality and food safety compliance, manage documentation, and support export/import needs. You will work with plant quality, corporate quality, R&D, sales, and external partners...
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