Top Quality Manager Jobs

Lead product development of an AI-ready data quality platform on Databricks, embedding schema enforcement, data contracts, observability, anomaly detection, CI/CD validation, and driving data product ownership, governance, and reproducibility for ML workloads.

Responsible for developing, implementing, and maintaining a Quality Management System across Architectural Metals sites to ensure compliance and drive continuous improvement.

Manage and oversee quality control operations, lead and develop a QC team, implement procedures, ensure regulatory compliance, investigate and resolve quality issues, track metrics, and drive continuous improvement.

Lead and optimize escalation and field action processes and systems to ensure compliance with global regulations and J&J policies. Manage QRB/RMB activities, support field corrective actions, prepare regulatory reporting and recall documentation, monitor QMS performance, drive process improvements, and provide SME leadership and training across cross-functional teams.

Lead quality oversight for clinical studies by ensuring GCP compliance, managing risk assessments, investigations, CAPAs, and inspection readiness. Partner with internal and external stakeholders, support audit planning, approve controlled documents, and drive process improvements across RD&M.

Inspect and evaluate new home construction to ensure compliance with plans, specifications, and local codes. Document defects, complete scheduled QA acceptance, maintain inspection records with photos/reports, communicate findings to contractors and customers, conduct new home orientations, and recommend training to improve quality standards.

Lead the Manufacturing Quality organization, ensuring compliance with quality standards, managing a team, and driving continuous improvement in processes.

Manage QA processes and production support for Harvard Dataverse and related products: design and run functional and performance tests, deploy releases, maintain test infrastructure, troubleshoot production issues, advise support staff, and document QA policies and procedures.

Serve as the single quality contact for CMOs, ensuring GMP/GDP compliance, managing QTAs, audits, CAPA/deviations, change control, product release support, risk assessments, KPIs, regulatory inspection readiness, and cross-functional coordination for external manufacturing.

Manage and drive performance improvement for Medicaid managed care quality metrics (NCQA HEDIS, CMS Core). Develop and implement system-wide improvement projects and corrective action plans, analyze and report data, supervise improvement staff, collaborate across internal teams and external stakeholders (AHCCCS, providers), monitor provider performance, and ensure contractual compliance. Hybrid role requiring Arizona residency and full-time availability.

Lead author for Module 3 CTD sections supporting biologics regulatory submissions. Provide analytical CMC subject-matter expertise in methods, validation, reference standards, and stability. Collaborate cross-functionally to ensure compliant, accurate submission documents, resolve technical issues, identify risks, and drive timelines for regulatory approvals.

Manage a 20–25 person clinical quality team to ensure clinical accuracy, regulatory compliance (FDA), and high-volume service delivery. Oversee performance metrics, coaching, escalation/recovery, training, budget/headcount, and continuous improvement initiatives. Collaborate cross-functionally on quality programs, policies, and operational efficiencies while using workflow automation and dashboards to drive outcomes.

Lead and oversee analytical QC testing for clinical and commercial drug substance and drug product in a GMP and select-agent regulated lab. Manage laboratory capacity, method lifecycle (validation/transfer), stability and release testing, regulatory inspection readiness, biosafety/biosecurity, investigations (OOS/OOT/CAPA), and develop QC staff to ensure compliant, timely product release and continual process improvement.

Lead and govern the OTC quality program to ensure FDA and Health Canada compliance across development, manufacturing, testing, release, and post-market. Oversee QMS integration, audits/inspections, stability testing, supplier and third-party oversight, investigations/CAPAs, and validation. Manage and mentor a team, drive risk-based decisions, and implement continuous improvements to maintain inspection readiness.

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.

Lead QA for retail technology products, driving testing strategy, automation adoption, CI/CD integration, people leadership, cross-functional collaboration, and QA process governance to ensure release quality and stability.

Lead and manage a global GCP audit program: hire and develop staff, plan and conduct internal and external GxP/GCP audits, provide compliance input cross-functionally, drive process improvements, support regulatory inspections, and deliver training to Global Development QA and partner teams.

Lead and support system-level clinical engineering regulatory and quality operations, develop standards and processes, ensure compliance with healthcare regulations (TJC, DNV, NFPA, CAP, AAMI, CISA), manage vendor/contract labor strategy, track KPIs, and support transitions, continuous improvement, and cross-functional alignment.

Lead and manage site quality assurance activities for pharmaceutical, biologic, device, and combination product manufacturing. Oversee QA policies, regulatory compliance (FDA/EMA/ICH), inspections, deviations/CAPA, quality metrics, training, and cross‑functional projects to ensure product and process compliance from raw materials through final shipment.

Lead and grow quality engineering through automation, CI/CD integration, and shift-left practices. Design and scale test frameworks for web, API (REST/GraphQL), integrations, and mobile web; mentor QA teams; partner with Engineering, DevOps, and Product; drive AI-assisted testing, test reliability, observability, and release confidence across the platform.

Lead development and execution of internal communications strategy for the Quality department. Manage communications specialists, create targeted messaging and multi-channel content, oversee templates and centralized sites, support change management, and partner with leaders to drive employee engagement and consistent communications.

Oversees clinical quality for assigned caseloads by observing client programs, reviewing outcome data, providing supervision and feedback to staff, consulting on non-progressing cases, training parents, attending IEPs as needed, and collaborating with clinical leadership and payors to improve treatment outcomes.

Develop, implement, and continuously improve GxP training and personnel qualification programs. Manage LMS/eQMS training systems, ensure inspection readiness, create role-based curricula and competency frameworks, link training to quality systems (deviations, CAPA, change control), and drive cross-functional compliance and training effectiveness.

Lead and manage Operations QA at RayzeBio Indianapolis, overseeing GMP/GDP compliance across CDMOs and site operations. Supervise up to eight direct reports, provide on-floor QA oversight, review batch records, drive deviation/CAPA investigations, author SOPs, develop KPIs, and build a strong quality culture in a radiopharmaceutical manufacturing cleanroom environment.

Lead and develop Quality Engineering teams supporting design transfer, risk management, statistical analysis, deviations, change control, supplier nonconformance, and product launches. Serve as SME for design control, risk management (ISO 14971), and quality systems (ISO 13485, FDA 21 CFR 820). Oversee investigations, validation strategies, MSA/GR&R, test method transfer, resource planning, metrics, audits, and regulatory inspections.