Top Quality Manager Jobs

Lead regional compliance and quality programs across GEODIS sites. Conduct and support regulatory and customer audits, investigate incidents, mentor quality staff, develop quality metrics, and ensure ISO/FDA quality system adherence.

Manage and mature the Quality Management System for a clinical-stage cell therapy company. Own change control, complaints, deviations, CAPA, vendor notifications, and quality reviews while ensuring FDA, EU GMP, ICH, and GxP compliance. Lead eQMS selection, implementation, validation, deployment, governance, and optimization. Support audits and inspections, develop quality metrics, maintain documentation, coach investigation owners, and drive cross-functional process improvements.

Leads the facility’s quality management system, ensuring AS9100 and ISO 9001 compliance. Supervises the quality team, manages internal and external audits, oversees root-cause analysis, develops procedures and continuous-improvement initiatives, and maintains supplier and customer quality relationships. The role also manages IPC training programs, inspections, quality metrics, regulatory compliance, supplier development, and source and first article inspections.

Oversee all quality aspects of the MFLC contract: collect and report data, ensure QA/QC programs meet contract standards, maintain credentialing and training compliance, facilitate communication between contractor, counselors, and government stakeholders, and implement process improvements to enhance counselor operations.

Support Quality Manager implementing and maintaining the project QMS: document and track tests, inspections, submittals, create inspection/test plans, manage material compliance, produce reports, resolve quality issues, and coordinate inspections with stakeholders.

Leads the Companion Diagnostics design quality function and team, overseeing design controls, risk management, verification and validation, clinical performance evaluation, QMS processes, audits, regulatory compliance, investigations, and quality initiatives. Coordinates cross-functional development programs, partner collaborations, resources, budgets, and milestones while ensuring IVD and medical device products meet global regulatory and business requirements. Provides coaching, training, regulatory expertise, and people leadership across CDx development activities.

Oversee project-wide QA/QC for a major semiconductor fabrication facility construction project. Develop quality plans, inspection and testing protocols, documentation systems, and contractor quality requirements. Lead inspectors and quality meetings, manage NCRs, audits, special inspection agencies, commissioning coordination, turnover, warranties, and equipment maintenance. Ensure compliance with semiconductor standards, owner specifications, applicable construction codes, and safety requirements while supporting issue resolution and project closeout.

Lead comprehensive plant quality programs including pre-delivery and finished vehicle inspections, supplier quality assurance, QOS deployment, new model launch quality, audits, corrective actions, and development of quality personnel and communication processes to prevent campaigns and ensure compliance.

Lead creation, integration, and oversight of Quality Management Systems (QMS) for Mentor and client facilities. Manage root cause investigations, inspections, training, vendor management, SLAs, CAPAs, audits, SOPs, and continuous improvement across multiple sites. Provide documentation review/approval, data analysis, and mentorship to ensure regulatory compliance (GMP, GDP, ISO). Travel to support client operations as required.

Leads software engineering teams building scalable communications, notification, telephony, customer engagement, conversational AI, and quality platforms. Establishes technical vision, architecture, engineering standards, automated testing, performance practices, security, reliability, and operational readiness. Partners with product, security, architecture, and business leaders; manages third-party integrations; mentors technical talent; supports hiring and organizational planning; and guides 24x7 enterprise systems handling student and institutional data.

Lead creation, integration, and enforcement of QMS for Mentor and client sites; manage audits, CAPAs, root cause investigations, training, inspection readiness, vendor management, SLAs, SOPs, and continuous improvement across multiple sites while mentoring staff and supporting client operations.

Lead development, implementation and oversight of client Quality Management Systems for FDA-regulated facilities. Manage audits, CAPA, root-cause investigations, inspection readiness, training, vendor management, SLAs, and continuous improvement across multiple sites while mentoring staff and ensuring regulatory compliance (GMP/GDP/ISO).

Lead plant quality function to improve PPM, first pass yield and supplier performance. Manage quality staff, maintain IATF 16949/ISO 9001, run audits, corrective actions, PPAP, PFMEA, control plans, calibration, incoming inspection and continuous improvement activities.

Leads enterprise Quality Engineering and RPA capabilities for a technology organization. Defines testing, automation, governance, CI/CD quality, and intelligent automation strategies; oversees distributed teams, delivery, budgets, vendors, workforce planning, and stakeholder relationships. Establishes RPA Center of Excellence standards, drives AI-enabled automation, manages quality and business value KPIs, and partners with global Engineering, Product, Applications, Infrastructure, and Business leaders.

Lead and scale the clinical Quality Management System (QMS) and QA team, ensuring GCP/ICH and global regulatory compliance across sponsored trials and CRO services. Oversee audits (internal, vendor, investigator site, TMF), vendor qualification, CAPA/non-conformance, document control, inspection support, metrics reporting, and cross-functional QA consultation while driving continuous improvement and QA organizational design.

Own the end-to-end quality and release strategy for Raya’s iOS app. Lead automated and manual testing, regression coverage, release calendars, quality scorecards, readiness criteria, go/no-go decisions, App Store submissions, phased rollouts, and rollback processes. Manage release retrospectives, incident-driven improvements, third-party QA vendors, and cross-functional communication with engineering, product, and leadership.

Owns batch-impacting deviation management in Veeva QMS from initiation through closure. Drives cross-functional investigations, reviews technical and compliance quality, supports batch disposition, manages CAPAs and related quality records, tracks KPIs, presents performance data, coaches investigation owners, and improves deviation workflows and procedures in a cGMP biopharmaceutical manufacturing environment.

Manage customer quality for advanced DRAM products supporting Tier 1 customers. Coordinate failure analysis, 8D responses, change notifications, performance reporting, issue tracking, and technical communications across customers and global engineering teams. Align quality requirements, manage response expectations, escalate issues, and drive sustainable solutions. The role requires semiconductor memory expertise, strong technical communication, customer-facing experience, and daily onsite work in San Jose with 20–30% travel.

Leads mortgage servicing compliance testing and quality assurance programs, managing a team conducting data-driven tests and loan-level reviews. Oversees testing methodologies, findings, reporting, issue remediation, and control effectiveness assessments. Presents trends and risks to leadership, monitors regulatory changes, and collaborates with Compliance, Operations, Legal, Risk Management, and business partners. Responsible for team planning, coaching, performance management, and continuous improvement.

Lead GCP quality activities for clinical programs, design and execute fit-for-purpose audit programs, drive inspection readiness, manage risk and issues, advise cross-functional teams, present integrated quality strategies, and serve as primary quality liaison during health authority inspections to ensure compliant, submission-ready clinical data.

Manages quality assurance programs at an aerospace manufacturing facility. Responsibilities include improving quality metrics, leading continuous improvement and root-cause initiatives, overseeing customer and regulatory audits, managing supplier qualifications, coordinating quality-system reviews, reporting KPIs, and developing quality staff. The role requires aerospace manufacturing quality experience, knowledge of AS9100 and other quality systems, engineering drawings and GD&T, lean manufacturing, and strong leadership skills.

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.