Top Quality Manager Jobs

Manages quality assurance operations, quality management systems, regulatory compliance, audits, risk assessments, investigations, validation, and continuous improvement for tissue, biologic, and medical device products. Leads QA teams, supports GMP processing and distribution operations, oversees cleanroom and facility quality activities, develops quality metrics, and serves as a regulatory and quality systems subject matter expert.

Leads quality systems staff and manages Management Review, Quality Planning, CAPA, and nonconformance processes. Serves as a subject matter expert for QMR and FSR governance, reviews quality documentation, drives continuous improvement and quality strategies, supports audits and inspections, and partners with cross-functional, site, regional, and global stakeholders to improve compliance and standardization.

Lead Finalis’s quality assurance and risk oversight function within Regulatory Enablement. Responsibilities include supervising audits and continuous monitoring, supporting FINRA Rule 3120 reviews, managing issue escalation and remediation, representing the function on the Risk Committee, overseeing vendor, technology, and cyber-risk testing, and building and managing the Quality & Risk team.

Leads GCP quality assurance activities across clinical development programs, including comprehensive quality strategies, risk and issue management, audit programs, inspection readiness, regulatory interpretation, and clinical quality risk mitigation. Serves as the primary quality liaison across R&D functions and during health authority inspections, influencing cross-functional teams and ensuring compliant, submission-ready clinical data.

Lead the end-to-end quality strategy for distributed call center operations. Own quality assurance frameworks, reporting, dashboards, calibration, CSAT, mystery shopping, data analysis, and continuous improvement. Partner with learning teams, BPO providers, vendors, and senior leaders to improve customer outcomes, operational performance, compliance, and accountability across multiple sites.

Lead quality activities for an aerospace development program from prototype to production readiness. Build and mentor a quality team, establish quality systems and metrics, manage design/configuration control, FRACAS, root cause/corrective actions, verification/validation oversight, production readiness, and compliance with AS9100 and customer requirements to support reliability and mission success.

Supervise transit drivers on the road, evaluate safety and service performance, provide coaching and training, manage post-accident and incident protocols, and serve as the Designated Employer Representative for DOT compliance. Address urgent operational issues, review complaints and documentation, assess training needs, and implement service improvements. The role is primarily field-based, with 85% on-road supervision and 15% training and administrative work.

Lead and support Quality Systems and Compliance activities for clinical development programs. Responsibilities include implementing and improving the QMS, managing deviations, CAPA, change controls, risk assessments, audits, and inspection readiness. The role develops controlled documents and scalable governance frameworks, monitors compliance risks, supports drug production compliance, and coordinates cross-functional quality initiatives with Regulatory, Clinical, R&D, Technology, and external partners.

Lead and sustain site quality systems (ISO/QMS), laboratory operations, customer quality interface, and continuous improvement. Drive SPC usage, KPI monitoring, audits, corrective actions, root-cause analysis, and cross-functional quality improvements while managing quality staff and representing the site in corporate quality forums.

Oversee monitoring quality across multiple oncology clinical trials, including CRO monitoring activities, oversight plans, monitoring reports, risk assessments, corrective actions, SOPs, audits, and inspections. Partner with clinical operations teams and CROs to ensure GCP, regulatory, protocol, and data-quality compliance. Lead training, metrics tracking, process improvements, and senior-management reporting. The role is onsite four days per week in South San Francisco or San Diego and requires up to 80% travel.

Leads the global quality program for Airbnb’s Safety, Premium Support, and CS Labs functions. Owns quality strategy, governance, calibration, QA execution, root-cause analysis, coaching effectiveness, KPI reporting, and partner scorecards. Drives AutoQA and responsible AI quality frameworks, translates insights into product and policy improvements, and presents risks to executives. Manages globally distributed quality leaders and analysts while overseeing vendor governance, performance improvement, and cross-functional alignment across complex, sensitive support environments.

Leads aerospace and spacecraft manufacturing quality control operations, including quality-system development, inspections, testing, audits, documentation, regulatory compliance, and corrective actions. Supervises inspectors, technicians, and auditors; assigns work, coaches staff, and evaluates performance. Partners with engineering, production, and supply chain teams to resolve nonconformances and drive Lean and Six Sigma continuous improvement. Requires expertise in AS9100, aerospace materials, inspection methods, blueprint reading, GD&T, measurement tools, and manufacturing standards.

Leads the standalone quality function for a manufacturing location, owning quality strategy, metrics, audits, supplier corrective actions, root-cause investigations, and continuous improvement. The role uses Lean Six Sigma and statistical analysis to reduce scrap, improve first-pass yield, prevent nonconforming products, maintain calibrated equipment, manage QMS documentation, and coordinate corrective actions across internal teams and suppliers.

The Quality Assurance Manager leads manufacturing quality improvement, QMS compliance, advanced quality planning, corrective and preventive actions, Lean initiatives, audits, and process improvements. The role analyzes quality metrics, manages engineering changes and product introductions, resolves customer and supplier issues, maintains specifications, and trains quality staff. It also supports quality audits and develops plant-wide quality awareness while ensuring production processes meet performance and customer expectations.

Leads Kenco’s corporate quality management system across multiple sites and networks. Establishes quality standards, controls, audits, procedures, training, and continuous-improvement initiatives. Manages corporate and site quality personnel, supports RFPs and IT validations, mentors operating sites, monitors industry standards, and serves as backup quality pillar owner for the Kenco Operating System. Partners with operations, engineering, customers, and corporate departments to resolve quality issues and improve processes.

Manages biological quality control operations across virology, bacteriology, immunology, chemistry, microbiology, environmental monitoring, and animal testing. Ensures vaccine testing, release, documentation, validation, stability programs, and regulatory compliance meet USDA, EU, cGMP, and international requirements. Leads QC departments, training, performance management, audit readiness, inspections, investigations, and regulatory self-inspections while partnering with manufacturing and planning to support timely product release.

Manages site QA oversight of deviations and CAPAs, including triage, investigation review, approvals, training, and process improvement. Leads and develops QA staff, coordinates cross-functional quality systems work, tracks metrics, supports manufacturing and batch release timelines, and manages client communications. Collaborates with global QA, supports audits and regulatory inspections, and ensures compliance with GMP and worldwide biotechnology-product regulations.

Leads hospital quality, governance, and risk functions to support safe patient care and regulatory compliance. Prepares teams for CQC, HIS, and HIW inspections; manages incident and complaint investigations and closure; analyzes clinical governance data; delivers quality and safety training; and coordinates improvement initiatives. The role requires healthcare governance or risk experience, knowledge of national quality standards, root cause analysis expertise, strong communication, project leadership, data analysis, and report-writing skills.

Lead testing and quality processes for IT systems supporting car automation. Develop and execute regression, unit, and integration test plans. Ensure integration requirements, establish and track quality metrics, and coordinate closely between business and IT teams.

Assist in managing the Quality department and oversee quality programs, plant-floor inspection, and SPC. Develop and implement corrective actions and improvement plans, recommend and provide training, maintain TS database as TS QMR, develop policies and procedures, plan resources and control QA budget, and prepare quality reports.

Oversee project-specific quality management for transit and infrastructure projects. Develop and implement Quality Management Plans, inspection and test plans, document control, NCR and corrective actions, audits, material traceability, and training. Coordinate QA/QC staff and third-party labs, support final acceptance and turnover, and ensure compliance with NYCT, MTA, ISO 9001, and contract requirements.

The Quality Manager will enhance the quality management system for IVD products, conduct audits, manage documentation, and ensure compliance with regulations.

The Quality Manager ensures product compliance with legal standards, oversees quality control processes, and manages the quality management system for IVD products.

Lead facility-wide quality assurance transformation, set and maintain quality standards, own plant quality outcomes, drive continuous improvement, coordinate cross-functional teams, and report performance to leadership.

Facility-based quality manager owning execution of Quality Plans and ITPs across design, procurement, fabrication, assembly, testing, and delivery. Approve quality documentation, lead audits/FATs, enforce hold/witness points, manage NCR/CAPA and supplier quality, maintain traceability, drive root cause analysis and continuous improvement, collaborate with engineering/production, train staff, and lead lean initiatives to ensure compliant, on-time shipments.