Top Quality Manager Jobs

Manage Quality Management System processes including document control, complaint management, post-market activities, CAPA, training, audits, risk management, and compliance. Lead investigations, root-cause analysis, process improvements, and cross-functional quality decisions. Ensure adherence to FDA 21 CFR 820, ISO 13485, MDSAP, EU regulations, and company procedures while supporting audit readiness and patient safety. The role also requires team leadership, stakeholder collaboration, and maintaining current regulatory and industry knowledge.

Manage the Quality Management System and lead Quality Engineers/Supervisors to drive root-cause analysis, warranty reduction, PCP and APQP/PPAP activities, customer and supplier quality interactions, corrective/preventive actions, and continuous improvement (Lean) across production.

Responsible for leading Clinical Quality Assurance activities, conducting GCP audits, developing quality systems, and ensuring compliance across clinical research projects.

Oversee construction quality to ensure compliance with contract documents, codes, and owner requirements. Manage QC plans, inspections, submittals, testing coordination, deficiency logs, punch lists, closeout deliverables, and lead a quality control team while collaborating with owners, design teams, contractors, and executive management.

The Quality Manager will lead Quality Assurance, ensure ISO 9001 compliance, manage quality systems, and develop strategies while supervising personnel.

Lead the QMS and quality team to ensure products meet military, ISO, and customer requirements. Oversee metrology, CMM programming, inspection, calibration (ISO 17025), SPC and capability studies, audits, FAI/PPAP, root cause analysis, corrective actions, supplier quality, and continuous improvement. Train staff and collaborate with engineering and manufacturing to improve manufacturability and measurement strategies.

Oversee technical quality across North American laboratories to ensure ISO/IEC 17025 conformance. Lead method validation, verification, transfers, technical audits, QC and PT/RR performance monitoring, statistical evaluation, LIMS review, corrective actions, training, and client complaint assessments. Coordinate with operations, chief chemists, and quality teams and may perform site audits and backup duties for the Quality Systems Manager.

Manage the DRC Quality Assurance program compliant with ISO 9001, oversee quality personnel, address customer needs, and drive continuous improvement initiatives.

The Quality Manager leads quality functions in a manufacturing environment, ensuring compliance, driving continuous improvement, and mentoring quality personnel.

The Quality Manager oversees the Quality Management System, ensuring compliance with industry standards, supporting continuous improvement, and managing regulatory requirements while engaging with operations and customers.

Lead a team of quality technicians and own quality performance for a stainless-steel manufacturing value stream. Drive root-cause investigations, CAPA, ISO 9001 compliance, APQP activities (PFMEA, control plans, GR&R, FAI), continuous improvement, supplier/customer quality, and cross-functional collaboration to ensure product and process reliability.

Leads the creation and implementation of an enterprise Quality Management System for title insurance operations. Responsibilities include developing quality metrics and composite scores, quantifying poor-quality costs, driving process improvements, establishing governance and executive reporting, building a maturity roadmap, automating data collection with technology teams, and securing cross-functional leadership alignment.

Evaluates client treatment progression through observation, data review, and staff and caregiver communication. Provides clinical consultation, supervision, parent training, intervention support, and treatment-plan modifications for autism services. Collaborates with clinical directors, program managers, and outcome teams to monitor case quality and trends. Maintains a small to moderate caseload, participates in IEP meetings, and supports staff development across home, school, community, clinic, telehealth, and military-base settings.

Manages Quality Control and Data Entry workflows for clinical studies, including staff supervision, workload planning, regulatory compliance, sponsor and auditor communication, SOP development, metrics tracking, data review, and process improvement. Ensures accurate, timely, and compliant clinical data processing while leading problem solving, inspections, audits, and employee development.

Manages pharmaceutical QA compliance programs involving supplier qualification, vendor audits, internal audits, quality agreements, risk assessments, CAPA reviews, regulatory inspection support, and compliance databases. Coordinates cross-functional and supplier activities, prepares reports and management reviews, maintains approved vendor and audit records, supports process improvements, and serves as backup to the Senior Manager. Requires strong knowledge of GMP and quality systems, leadership, negotiation, communication, and problem-solving skills.

The Quality Assurance Manager manages and improves the medical device quality system under FDA, ISO 13485, MDSAP, and ISO 14971 requirements. Responsibilities include internal, supplier, and third-party audits; CAPA and nonconformance investigations; root cause and risk analysis; quality metrics; document and change control; supplier quality agreements; and validation support. The manager leads direct reports, supports regulatory inspections, ensures record accuracy, develops employees, and provides cross-functional quality support.

The job description provides no substantive responsibilities or duties beyond the title Senior Manager of Innovation and Quality.

Oversee quality assurance for government construction projects across design, modernization, renovation, and construction phases. Inspect contractor workmanship, materials, equipment, testing, documentation, and compliance with contract requirements. Manage deficiency correction, RFIs, submittals, punch lists, final inspections, site meetings, daily reports, project schedule reviews, and closeout activities. Report critical issues, verify corrective actions and test results, and support zero-defect walkthroughs.

Manages pharmaceutical QA compliance programs covering supplier qualification, internal audits, quality agreements, regulatory inspections, CAPA closure, and management reporting. Coordinates supplier risk assessments, audit activities, approved vendor lists, quality agreement reviews, and tracking databases. Supports process improvements, annual supplier evaluations, product APQR data, and implementation assessments. Serves as backup to the Senior Manager and requires strong knowledge of GMP and regulated quality systems.

Leads enterprise software testing and quality engineering across the application lifecycle. Develops QA standards, governance, test strategies, and automation programs; oversees functional, integration, regression, performance, API, and user acceptance testing. Manages defects, release readiness, quality metrics, vendors, and distributed QA resources. Partners with business, product, development, and operations teams to embed quality into Agile and DevOps practices while mentoring testing professionals and driving continuous improvement.

Lead and maintain the local quality management system, prevent and investigate nonconformities, manage customer quality claims and audits, drive continuous improvement, and develop the local quality team to meet automotive standards.

Lead and implement project quality management systems, inspections, testing, and documentation. Coach project teams, manage KPIs and QIRs, perform audits, coordinate testing and materials, and drive risk mitigation to improve project quality, safety, and profitability.

Manage and implement the project Quality Control program through inspections, documentation, and corrective actions. Coordinate QC meetings and reports, verify materials and subcontractor work, support testing and commissioning, ensure regulatory inspections for TCO/CO, and collaborate with project teams to drive site-specific quality, safety compliance, and resolution of deficiencies.

Lead KPI validation, monitoring, and reporting for cargo operations to ensure real-time visibility and drive continuous improvement. Produce actionable daily/weekly/monthly reports, analyze operational trends and delay causes, validate scan compliance, track ramp and departure performance, and serve as a backup for data/reporting leadership while collaborating with stakeholders to improve processes and mitigate operational risk.

Develops and manages QA/QC systems, quality plans, procedures, and audits for commercial construction projects. Identifies corrective actions, addresses constructability concerns, trains project teams, and ensures compliance with client, design, contract, and regulatory requirements. The role supports multiple mission-critical, healthcare, and tenant-improvement projects, assists with emergent problem-solving, represents the company in project and business-development activities, and supervises the QA/QC team.