Top Quality Manager Jobs

Leads risk-based quality management across global clinical trials, including quality risk assessments, control tracking, issue management, CAPA, trend analysis, inspection readiness, and audit responses. Partners with clinical study teams, monitoring groups, CROs, and quality leadership to manage site risks and escalate significant events. Oversees staff onboarding, coaching, performance discussions, training, process improvement, and team administration.

Own and deploy supplier quality engineering processes including supplier appraisal, APQP, supplier assessments, non-conformance management, PPAP/FAI oversight, audits, metrics, and continuous improvement to ensure product and regulatory quality in the production supply chain.

Provide program leadership and direction for Community Integration Services for adults with I/DD and complex behavioral health needs. Oversee day habilitation program operations, supervise staff, coordinate with clinical teams, ensure safe person-centered, community-integrated services, and maintain documentation and compliance.

Lead and optimize the quality management system, manage the Quality and Inspection team, oversee inspections, PPAP, PFMEA and calibration programs, handle corrective actions and failure analysis, ensure ISO9001/AS9100 compliance, drive continuous improvement using Six Sigma and Lean, and manage engineering project scheduling to meet customer and regulatory requirements.

Lead the site Quality Management System for circular manufacturing products, ensuring specification compliance and alignment with ISO, automotive, and environmental standards. Oversee sampling, testing, laboratory operations, quality KPIs, SPC, root-cause analysis, CAPA, supplier quality, management of change, customer complaints, audits, and product qualifications. Partner with Operations, Maintenance, Engineering, and Commercial teams to improve process reliability, customer satisfaction, traceability, and ESG compliance.

Manages facility quality assurance, inventory control, audits, inspections, recalls, non-conformities, and warehouse quality processes. Oversees value-added services, receiving, picking, shipping, inventory accuracy, and customer service requirements. Leads quality improvements, researches discrepancies, coordinates audits and cycle counts, supports operational efficiency, and trains warehouse personnel on equipment and procedures.

The Quality Manager leads quality initiatives, develops quality plans, ensures product quality compliance, manages a quality team, and drives continuous improvement efforts, focusing on customer satisfaction and operational excellence.

Manages medical-device quality control activities, inspectors, and inspection processes. Develops and improves quality systems, oversees nonconformance investigations, supports manufacturing and new product development, and ensures compliance with FDA QSR, ISO 13485, MDSAP, and MDR requirements. Leads audits, continuous improvement initiatives, staff training, performance management, and complaint investigations while maintaining product quality and regulatory compliance.

Manage and implement the internal quality program across facility operations, serving as central point of contact for quality matters. Oversee progress control, quality data analysis, and statistical sampling to ensure maintenance, repair, and operations meet contractual and safety requirements in support of Defense and Intelligence facilities.

Manages national healthcare quality performance initiatives, including quality data collection, analytics, reporting, data validation, regulatory audit readiness, and care-gap improvement. Coordinates projects, stakeholders, vendors, documentation, and delivery timelines across a matrixed organization. Analyzes HEDIS, CAHPS, health equity, SDOH, provider performance, EHR, and HIE data to identify improvement opportunities and communicate risks and progress.

Leads quality engineering teams and programs supporting complaint handling, post-market surveillance, regulatory compliance, audits, and continuous improvement for medical devices. Oversees talent strategy, KPIs, quality investigations, customer-facing discussions, quality system processes, budgets, and warranty costs. Partners cross-functionally to identify product quality trends, mitigate risks, and improve operational performance in a regulated environment.

Leads quality assurance for mission-critical products in a manufacturing and technical environment. Develops quality plans and process improvements, oversees audits and corrective actions, validates documentation and metrics, partners with engineering and operations, manages quality personnel, analyzes quality trends, and supports safety, regulatory, import/export, and customer compliance requirements.

Leads quality engineering teams and programs supporting medical device complaint handling, post-market surveillance, regulatory compliance, audits, quality system processes, and continuous improvement. Analyzes complaint and product quality data, manages KPIs, budgets, and warranty costs, investigates customer-impacting issues, and partners cross-functionally with sales and field teams. Oversees talent strategy, team development, and operational performance in a regulated environment.

Manages medical device quality systems and regulatory compliance for a production unit. Leads CAPA, complaint investigations, internal and external audits, change control, document control, inspection readiness, and corrective improvements. Develops compliance strategy, reports quality-system health to management, represents the organization during FDA and regulatory inspections, and drives cross-functional QMS initiatives. Provides leadership, coaching, escalation, and communication across local, global, and divisional quality teams.

Lead the Test, Manufacturability, Reliability & Quality organization for GPU, SoC, and CPU programs. Ensure technical execution, resolve multi-functional failures, and develop a high-performing engineering team.

Manages hospital and professional coding quality and education programs. Oversees coding audits, monitors accuracy and documentation compliance, communicates regulatory and guideline changes, develops training for coding staff and physicians, identifies documentation trends, reports findings to leadership, and supports process improvement across Revenue Integrity, Clinical Documentation Integrity, and related departments.

Lead quality assurance and quality control across multiple manufacturing facilities. Maintain the ISO 9001:2015 quality management system, develop quality strategy and KPIs, reduce quality costs, oversee inspections and audits, manage nonconformances and corrective actions, and drive continuous improvement. The role also involves leading quality teams, partnering cross-functionally, supporting customer and supplier quality activities, and serving as a key quality advisor to business leadership.

Leads a QA team responsible for testing quality across software products and initiatives. Oversees manual, automated, exploratory, regression, and risk-based testing; drives quality throughout the SDLC; expands automation and CI/CD testing; and champions responsible AI use in QA workflows. Manages delivery, metrics, risks, team development, and cross-functional collaboration with Engineering and Product to improve release confidence, efficiency, and software quality.

Manages clinical quality assurance and quality oversight for GCP/GCLP activities, including audit management, deviations, CAPAs, risk assessments, inspections, and clinical study support. Provides quality guidance, prepares audit and quality metrics, qualifies GCP service providers, reviews contracts and quality agreements, supports inspection readiness, and authors or reviews global QA processes. The role collaborates cross-functionally across Sobi and requires strong knowledge of ICH GCP, FDA, EMA, and related regulatory requirements.

Owns supplier quality strategy and execution across U.S. pharmaceutical manufacturing sites. Leads regulatory inspection readiness, supplier audits, risk reporting, deviation response, CAPAs, vendor remediation, performance improvement, and quality-system deployments. Manages global supplier relationships and serves as the U.S. account lead for Integrated Facility Management partners. Drives cross-functional supply chain quality projects, supplier compliance, risk mitigation, and uninterrupted delivery of safe, compliant materials.

Manages owner quality assurance and commissioning activities for data center construction projects. Oversees CxA and GC quality teams, ensures stage-gate and milestone compliance, tracks testing, checklists, issues, NCRs, warranties, and escalations, and provides project and program-level readiness reporting. Serves as the site-level quality and commissioning point of contact while coordinating suppliers, project managers, and facilities stakeholders.

Lead and advance quality management across manufacturing: develop and maintain QMS, drive continuous improvement, lead investigations and corrective actions, manage audits and compliance, collaborate cross-functionally, monitor KPIs, and hire/train quality staff to improve product quality and operational performance.

Lead global design assurance for medical devices and IVD product development, providing strategic governance, inspection readiness, risk management, KPI oversight, and people leadership to ensure safe, compliant, and scalable product development across functions and sites.

Lead and manage site quality operations ensuring regulatory compliance and patient safety. Develop and implement quality systems, oversee audits and responses, train and manage quality staff, conduct Site Quality Management Reviews, report KPI metrics, identify trends, and make product release decisions.

Oversee clinical quality for assigned ABA cases through observations, data review, staff consultation and parent communication. Provide supervision, advanced clinical consultation, parent training, IEP participation, and outcome monitoring to ensure treatment aligns with plans.