Top Quality Manager Jobs

Manage and maintain the Quality Management System for ISO 13485 and medical device regulatory compliance. Oversee QA/QC activities, CAPA, complaints, internal audits, receiving inspection, and QC lab operations. Lead and coach direct and indirect reports, support eQMS use, perform quality data and trend analysis, drive corrective actions, support validation and audit readiness, and partner cross-functionally to resolve quality issues and support continuous improvement.

Manage and implement the Quality Control and site-specific Safety Plans for range and airfield grounds maintenance. Conduct inspections, hazard assessments, incident reporting, enforce OSHA and AR 385-10 compliance, coordinate emergency responses, maintain safety and environmental records, and ensure personnel certifications and airfield operational safety requirements are met.

Manage and implement the Quality Control Program: develop QC plans, perform inspections and surveillance, track deficiencies and corrective actions, conduct root cause analysis and trend reporting, coordinate audits and validate compliance with PWS requirements.

Lead and develop the quality team and oversee quality processes from incoming materials to final product release. Establish standards, inspections, KPIs, and dashboards; investigate issues, lead root-cause analysis and CAPA; audit processes; train staff; partner with Production, Engineering, Purchasing, and Operations; troubleshoot on the production floor and drive continuous improvement to reduce rework and improve first-pass quality.

Lead plant quality and safety programs, direct the QMS, drive continuous improvement, manage production scheduling, conduct safety training and inspections, perform root cause analysis for customer complaints, maintain incident/workers' compensation records, and ensure GMP/SOP compliance.

Lead and scale a QA automation team for store technology systems. Define and implement test automation strategies and frameworks, oversee UI/API/performance testing, integrate automation into CI/CD, maintain QA lab, drive TDD/BDD adoption, coordinate end-to-end testing across teams, mentor engineers, and continuously improve QA processes.

Build and lead Helion's quality function for fusion hardware: design quality systems, hire and mentor teams, own supplier and inspection strategies, manage nonconformance/MRB/CAPA, and drive root-cause analysis and continuous improvement across manufacturing and testing.

Lead and manage metrology and software teams for a calibration laboratory. Oversee software quality, inspections, V&V, process improvement, CMMI implementation, metrics, root-cause analysis, and stakeholder coordination to ensure compliant, reliable calibration software and equipment tracking systems.

Build and lead a QA automation function: define strategy, select tooling, integrate tests into CI/CD, write automated tests and framework components, hire and coach automation engineers, drive risk-based testing and quality gates, and evaluate/adopt AI-assisted testing while maintaining human review and trusted quality metrics.

Manage site Quality Operations including change control, CAPA, complaints, data integrity, and quality metrics. Lead review boards, Quality Council, investigations, and inspection readiness. Collaborate cross-functionally, drive corrective actions, and apply AI to improve team execution.

Lead system and clinical quality improvement using clinical data to standardize care, reduce variation, improve outcomes, support QAPI and regulatory reporting, present analyses, perform chart reviews, and educate clinicians and leaders.

Lead and develop a QA Operations team to ensure compliant GMP execution across manufacturing, manage batch record review, change control, CAPAs, audit readiness and client quality interactions, support technology transfers, drive continuous improvement, and maintain quality metrics and training.

The Senior Manager, Robotics Quality Assurance will lead test engineering strategy, automation development, and validate models for robotics products, ensuring quality across hardware and software.

The Quality Control and Contracts Manager ensures compliance with quality standards across projects, manages contracts, and oversees quality control programs while mentoring teams and maintaining project documentation.

The Quality Control Manager develops quality control programs, oversees project quality assurance, manages contracts, and ensures compliance with regulations.

Provide QA leadership and oversight for Manufacturing and QC at the Foster City biologics site. Ensure GMP/GLP compliance during design, startup, and operation of a single-use drug substance facility and QC lab. Oversee batch record review and product release, external lab oversight, method lifecycle, investigations (OOS/OOT), CAPA, change control, audits, risk assessments, and continuous improvement.

Lead and manage QA automation projects, define test automation strategy, coordinate cross-functional teams, track delivery, timelines, risks, and stakeholder communications to ensure high-quality software releases.

The ATS Quality Division Manager leads the quality assurance efforts at ATS, ensuring compliance with standards and promoting a culture of quality across the organization and its suppliers. Responsibilities include setting quality targets, managing corrective actions, developing employees, and collaborating with various teams to deliver defect-free products. This role requires strategic vision, strong leadership, and extensive experience in quality management.

The Quality Systems Manager oversees the Quality Management System, ensuring compliance and managing quality initiatives across Nextern US sites.

Lead Computer System Validation and Computer Software Assurance for GxP computerized systems across Information Sciences. Provide technical guidance on FDA 21 CFR Part 11, EU Annex 11, GAMP5 and data integrity, develop validation strategies and deliverables, mentor teams, manage deviations/CAPAs/change controls, support inspections, and drive continuous improvement of risk-based validation and CSA practices.

Lead and manage QA for assigned PET radiopharmaceutical manufacturing sites, overseeing batch record review, product disposition, investigations, validation, change control, training, regulatory interactions, and quality metrics to ensure cGMP and FDA compliance. Supervise QA staff, drive corrective actions, and provide regional quality coverage across multiple sites with significant travel.

The Quality Assurance and Documentation Manager leads quality management activities, oversees contractual documentation, and ensures compliance in a large automated photo enforcement program. Responsibilities include maintaining requirements traceability, conducting audits, and managing SharePoint documentation for contractual deliverables, ensuring audit readiness and quality standards are met.

Lead Accreditation and Quality operations for FEP, set strategy for QCR measures, ensure compliance with HEDIS/NCQA/URAC, manage cross-functional accreditation projects, develop programs to improve member care, oversee budgets, and lead a department to meet Plan and accreditor requirements.

Manage and coordinate the hospital's Quality/Performance Improvement program under DCQI direction. Track and analyze quality and infection prevention data, lead improvement initiatives, ensure regulatory compliance (Joint Commission, state), collaborate with department leaders, and prepare reports. Support meetings, corrective action plans, and hospital-wide performance improvement activities.

Lead and facilitate hospital quality improvement, patient safety, and regulatory readiness efforts. Monitor quality metrics, run root-cause analyses, develop corrective action plans, support QAPI, prepare for surveys, maintain dashboards, present outcomes to leadership, and collaborate with clinical and operational teams to improve outcomes and compliance.