Top Quality Manager Jobs

The Quality Risk Manager ensures compliance with quality systems, manages site risk registers, coordinates risk assessments, and provides guidance on risk mitigation strategies.

As the Manager of QA Operations, you will oversee the quality assurance department, ensuring compliance with ISO standards, managing audits, and improving quality processes.

The Quality Control Manager leads facility quality control activities, supervises personnel, ensures compliance with quality management standards, and fosters continuous improvement.

The Manager, QA Operations leads the Quality Assurance department, ensuring compliance with production quality standards and overseeing the Quality Management System, including implementing policies and training for performance management.

The Quality Manager oversees product disposition for Finished Goods, ensuring compliance with regulations, managing projects, and collaborating with stakeholders to maintain product quality.

Lead a team of Quality Engineers to ensure manufacturing quality and process control for medical devices, employing Lean and Six Sigma methodologies for improvements.

The Quality and Compliance Manager will oversee complaint management processes, audit compliance, and improve operational efficiencies in the lending service environment.

The HR Manager serves as a strategic partner to business leaders, focusing on talent management, organizational effectiveness, and HR program delivery to meet business needs.

Lead the development and strategy for Moloco Ads in areas like supply exchange integrations and invalid traffic mitigation, overseeing a large engineering team.

The Quality Assurance Manager will lead the development of a QMS for regulatory compliance, oversee product quality assurance, and drive continuous improvement initiatives.

Lead design, implementation, and continual improvement of a pharmaceutical quality assurance function and quality management system. Oversee SOPs, document control, batch record review, deviations, change control, CAPA, internal and vendor audits, regulatory submission support, and quality IT (e.g., Veeva). Manage quality training, vendor programs, inspections, and quality metrics to ensure regulatory compliance and product development readiness.

Lead design, implementation, and continuous improvement of a Quality Management System supporting clinical development and regulatory approval. Oversee SOPs, document control, batch record review, deviation/change control, CAPA, audits, vendor management, regulatory submission support, and inspection readiness while managing a quality team and cross-functional quality activities.

Lead and manage cGMP quality systems for the QC laboratory, including SOP creation, CAPA/change control review, audits (internal and 3rd party), vendor/CDMO oversight, analytical method review, batch record review, HA inspection hosting, and QA team supervision. Support regulatory responses and manage day-to-day QA operations.

Lead and manage the Quality Assurance function, enforce quality systems and procedures, oversee audits and corrective actions, drive continuous improvement, and ensure product/process compliance with standards and customer requirements.

Lead operational execution of testing, inspection, and product release for technology hardware. Manage QC team, develop SOPs, analyze defects, oversee kitting and BOM verification, and drive process improvements to ensure products meet quality standards before shipment.

The Quality Assurance Manager ensures compliance with quality systems based on ISO/IEC 17025 and 21 CFR standards, oversees audits, leads quality initiatives, manages documentation, and interacts with clients and regulatory bodies.

Manage and improve the design and development program within regulatory compliance. Oversee quality engineering team, set goals, and drive product development initiatives.

The Quality Assurance Manager oversees complex projects, manages process improvements, leads cross-functional teams, coordinates with stakeholders, and supervises staff to ensure quality standards are met.

The Quality Conformance Manager ensures product quality meets regulatory requirements, conducts non-conformity analyses, manages quality improvement projects, and collaborates with multi-functional teams.

Lead QA/QC programs and a team of inspectors to ensure welding and construction work meets industry codes and company standards. Conduct audits, review documentation, provide training, and collaborate with project teams to resolve quality issues while maintaining organized quality records.

Lead transition from paper-based processes to a compliant electronic Quality Management System (eQMS). Manage quality systems (document control, training, deviations, CAPA, change control, audits), ensure GxP and regulatory compliance (GLP/GCP/GMP, FDA/EMA), support inspection readiness and regulatory submissions, validate computerized systems, oversee vendor oversight, and provide cross-functional quality leadership and training across drug development lifecycle.

Provide QA oversight for GCP/GCLP/GPP activities across clinical studies, manage end-to-end GCP audit program, assess deviations and CAPAs, support inspection readiness, qualify GCP service providers, author and review QA processes, produce audit and quality metrics, and act as QA representative during inspections and cross-functional initiatives.

Lead GCP/GCLP quality oversight for clinical studies: manage audits, assess deviations and CAPAs, support inspection readiness, qualify GCP service providers, author QA processes, and report audit/CAPA metrics across the organization.

Lead external quality oversight for contract manufacturing organizations (CMOs), ensuring GMP/GDP compliance, managing QTAs, product release, audits, deviations/CAPA, change control, KPIs, risk assessments, inspection readiness, and cross-functional quality activities to support reliable product supply.

Lead and continuously improve product assurance and quality systems for power distribution products. Align quality programs with business goals, manage audits and regulatory compliance, resolve supplier and technical quality issues, and drive cross‑functional quality initiatives across engineering, production, and vendors.