Top Quality Manager Jobs

Lead QA and compliance for hardware and software products: manage audits and certifications (UL/CE), monitor regulations, investigate fielded product issues, develop test suites and training, collaborate cross-functionally, and drive continuous improvement to ensure regulatory and quality standards are met.

Manage and apply software quality practices to identify defects, plan quality-control resources, monitor performance across lifecycle, support metrics reporting, and maintain system quality and efficiency.

Manage and implement quality program for data center construction projects. Lead daily QC activities, inspections, documentation, submittal reviews, testing tracking, root cause analysis, corrective actions, and weekly QC meetings with stakeholders. Train and oversee project teams to ensure work conforms to contract documents and project quality standards; support turnover, punch lists, and client walkthroughs.

Lead Quality Control for clinical and commercial drug substance and product programs, managing analytical testing, release and stability programs, reference standards, specifications, OOS/OOT investigations, vendor/CMO oversight, regulatory CMC QC content, audits, and cross-functional collaboration to ensure cGMP and ICH compliance.

Manage and maintain QC systems to ensure compliance with regulations and BRC standards. Supervise lab supervisors and technicians, support manufacturing and sales on quality issues, provide technical product support, and assist product/process development projects.

Lead establishment and maintenance of Product and Client Quality Assurance programs, drive continuous improvement and global harmonization, own quality metrics and data analysis, manage CAPA/change control/design quality, implement QRM and supplier assessment, collaborate on regulatory compliance, and provide cross-functional leadership to align QA/QC resources with corporate and supply chain objectives.

Lead quality oversight of global supply chain activities for clinical programs, ensuring GMP/GDP compliance across suppliers, CMOs, warehouses, and logistics. Manage supplier qualification, audits, deviation/CAPA investigations, shipping validations, and quality agreements while partnering with cross-functional teams to maintain timely, compliant supply of clinical materials.

Lead and improve the Quality Management System for a regulated medical device manufacturer. Oversee audits, CAPA/NCR/complaints, supplier quality, DHR and documentation control, risk-based decision-making, quality metrics, and training. Partner with Operations and Engineering to ensure compliant manufacturing and drive continuous improvement and regulatory readiness.

Manage quality of the driver fleet and independent contractors for final-mile deliveries: perform site visits for claims and meet trucks, negotiate settlements, organize repairs, train and onboard contractors, conduct ride-alongs and performance surveys, coordinate routes and service orders, assist with large installs, and resolve escalated issues while liaising with sales and customers.

Lead and grow a team of quality engineers in an Agile environment to embed quality into AspenTech's Performance Engineering Suite. Drive adoption of testing technologies and best practices, create and execute behavior tests using Gherkin, collaborate with product owners and technical leads on testable features, and improve quality metrics and KPIs for software delivered to customers.

The Quality Control Manager oversees compliance with sanitation and quality standards in dietary services, producing reports and conducting inspections.

Manage Wallingford site Quality Management System activities including document control, training, validations, CAPA, NCMRs, deviations, process improvements, and validation approvals. Lead and develop quality personnel, collaborate on new product/process design, support software validation, and ensure compliance with safety and quality procedures.

As a QA Manager, you will develop and maintain quality assurance processes, collaborate with cross-functional teams, conduct inspections and audits, and drive continuous improvement initiatives.

The QA Manager ensures A-dec's Quality Management System meets regulatory standards, leads QA teams, drives quality initiatives, and improves quality processes.

The US Regional Quality Systems Manager will lead the development and sustainability of Quality Management Systems for Large Form Factor sites ensuring compliance with ISO standards and driving continuous improvement.

The role involves leading the integration and sustainability of Quality Management Systems for new US manufacturing sites, ensuring ISO 9001 certification readiness and promoting a culture of quality and continuous improvement across operations.

The QCM/SSHO will manage the Quality Management System, ensure compliance with safety standards, conduct audits, and lead safety protocols on healthcare and military construction projects.

The Quality Control Manager leads inspection and compliance activities in manufacturing, ensuring product quality and regulatory adherence. They oversee QC teams, drive continuous improvement initiatives, and manage nonconformance processes to enhance operational efficiency.

Manage and execute software QA strategy across web, mobile, API, mainframe and databases. Lead hands-on testing and automation, define QA KPIs, plan test activities, supervise SQA engineers, drive process improvements, and support modernization and compliance-focused test cycles.

Manage plant Quality Assurance Labs, coordinate product releases and specifications compliance, oversee laboratory data and noncompliance resolutions, and support supplier quality monitoring programs.

The Staff Product Manager will drive pricing strategies and build tools for pricing performance, collaborating with teams to support brand success and growth.

Lead and develop site Quality Engineering, QC, and Inspection teams; maintain and improve the QMS and certifications; manage customer failure analysis, MRB, CAPA, supplier quality, NPI quality activities, audits, and DLA interactions to ensure product and process compliance and continuous improvement.

Lead CMC Quality Assurance strategy for radiopharmaceutical drug candidates at the Indianapolis site. Provide QA input across development through lifecycle, manage change control, oversee deviations/investigations/CAPAs, review and approve analytical and stability documentation, perform risk assessments, support regulatory filings (IND/BLA/NDA), and act as QA approver for GMP documentation and investigations. Collaborate with cross-functional CMC and Regulatory teams; may support multiple sites and CMOs.

The Manager for Supplier Quality ensures compliance with cGMPs, oversees vendor qualification, manages material lifecycle, and leads quality improvement initiatives.

The Services Engagement Manager ensures successful implementations for Quality Cloud customers, oversees project charters, and contributes to sales efforts while leveraging industry knowledge.