Top Quality Manager Jobs

Coordinate and support quality, validation, and IT security control activities across projects to ensure GxP/CSV/GAMP compliance, maintain audit readiness, execute risk-based reviews, prepare validation documentation, guide teams on validation practices, and drive continuous improvement under defined governance.

Leads quality assurance activities for a medical device manufacturing portfolio, managing quality systems, audits, investigations, CAPA, change management, validation, metrics, training, supplier quality, and continuous improvement. Develops a quality team and partners with Operations, Regulatory Affairs, Global Quality, and suppliers to maintain compliance, audit readiness, product quality, and process performance.

Leads a quality assurance team supporting product quality, process performance, audit readiness, regulatory compliance, and continuous improvement in a regulated medical device manufacturing environment. Oversees quality systems, CAPA, change management, validation, investigations, audits, quality metrics, training, supplier quality, and field-action communications. Partners with manufacturing, regulatory, global quality, and suppliers while supporting strategic planning, acquisitions, and budgeting.

Manage electrical construction quality control and commissioning activities. Coordinate testing, inspections, documentation, QC plans, formal notifications, third-party testing firms, site walks, and deficiency correction. Ensure compliance with testing standards, safety procedures, NFPA requirements, and project specifications. Collaborate with project managers, engineers, superintendents, field personnel, commissioning teams, and clients while maintaining accurate QC reports, logs, test data, and daily documentation.

Leads industrial engineering, quality, Lean, and continuous improvement initiatives in a high-volume warehouse environment. Analyzes workflows, labor utilization, material flow, layouts, capacity, productivity, and operational bottlenecks. Develops labor standards, KPIs, SOPs, dashboards, corrective action plans, and executive reports. Partners with leadership on customer launches, cost reduction, waste elimination, and service improvements while training teams and maintaining safety and quality compliance.

Manage and enforce end-to-end systems and processes to meet internal, external, and legal requirements. Serve as escalation point for LSP super users to global owners, run annual audit programs, collect and drive resolution of issues via training or system/process changes, identify competence gaps and training needs, and lead local implementations of new functionalities and processes.

Leads quality management for Naturium products, including supplier qualification, quality standards, CAPA, product quality incidents, incoming inspections, GMP compliance, and quality activities during new product development. Partners with global quality, sales, marketing, distributors, contract manufacturers, and suppliers to resolve issues and strengthen the supplier quality management system. Travel is required as needed.

Manage and improve the Quality Management System for a precision CNC machining operation supporting aerospace customers. Lead audits, resolve nonconformances, oversee QMS documentation and training, run root-cause and continuous improvement projects, perform hands-on inspections (CMM, micrometers), interface with key clients for FAIs and quality reviews, and supervise a small quality team to ensure compliance with aerospace standards.

Lead quality team and programs to reduce defects, manage warranty and supplier issues, perform audits, ensure compliance with ISO/IATF and automotive standards, drive corrective actions, and use data-driven methods (MSA, SPC, FMEA) to improve product and process quality across operations.

Lead Halo Industries’ production quality roadmap and customer quality strategy for semiconductor wafering operations. Manage customer audits, compliance, certificates of analysis, product change approvals, RMAs, root-cause investigations, and failure analysis. Scale Arena QMS and PLM systems to support IATF 16949, PPAP, and multi-market requirements. Drive quality control, AIAG Core Tools, corrective actions, Kaizen, DMAIC, and process capability improvements while recruiting and developing a quality engineering team.

The Quality & Turnover Project Manager ensures compliance with quality standards in capital projects by developing QA plans, conducting audits, and managing contractors, while facilitating stakeholder communication and continuous improvement.

Lead and maintain the plant Quality Management System (AS9100/ISO9001/NADCAP), oversee audits, supplier quality, corrective actions, non-conforming material disposition, quality planning, continuous improvement, and manage the site quality team to ensure compliance and customer satisfaction.

Supports global Safety, Regulatory Affairs, and Medical Affairs quality assurance activities across AbbVie’s drug, device, and cosmetic portfolio. Responsibilities include GxP compliance, risk assessment, CAPA consultation, audit and inspection readiness, vendor oversight, quality metrics, process improvement, and collaboration with R&D and business partners. The role contributes to regulatory inspections and implementation of global quality strategies.

Build and lead Aether’s quality control system for commercial polymeric manufacturing. Responsibilities include establishing document control, supplier qualification, traceability, inspection and sampling plans, nonconformance and corrective-action processes, lot release, and electronic QMS capabilities. The role provides hands-on oversight at contract manufacturers, investigates failures, qualifies suppliers and manufacturing partners, defines critical-to-quality attributes, trains stakeholders, and supports scalable production quality systems.

Provides GCP and GLP quality assurance support for early-stage clinical programs, including quality planning, risk assessments, audits, inspection readiness, compliance consultation, training, CAPA evaluation, root cause analysis, and regulatory inspection support. Collaborates with cross-functional stakeholders to identify and escalate quality issues, maintain data integrity, and advance GLP/GCP quality strategies across pharmaceutical R&D programs.

Manages a quality engineering team supporting ammunition programs, ensuring contract compliance, QMS adherence, lifecycle quality, regulatory compliance, corrective actions, process improvement, risk mitigation, and quality metrics. Leads technical reviews, approves quality engineering estimates and plans, presents quality data to leadership, and coordinates with supplier quality and mission assurance teams. Supervises 8–10 employees and supports continuous improvement across a highly regulated defense manufacturing environment.

Lead and manage construction quality control to ensure compliance with contract specs and building codes; coordinate inspections, testing, submittals, deficiency logs, punch lists, closeout deliverables, and stakeholder communication while building and training a QC team.

Manage construction quality control to ensure projects comply with contract specifications, owner requirements, and building codes. Lead the Three Phases of Control, submittal reviews, inspections, testing, quality meetings, deficiency tracking, punch lists, and closeout deliverables. Coordinate owners, designers, contractors, inspectors, and testing agencies while developing staff and quality control teams. The role also supports recruiting, business development, stakeholder communication, and executive reporting.

Lead the Quality Management Systems function and team, ensuring compliance with ISO 9001, AS9100, customer, and regulatory requirements. Manage audits, document control, management reviews, CAPA, risk assessments, quality metrics, and continuous improvement. Partner cross-functionally with operations, engineering, supply chain, customer quality, and regulatory teams. Develop employees, support DLA certification, and drive digital transformation and automation of QMS processes.

Leads the Compliance Engineering organization and owns the manufacturing site’s QMS. Ensures AS9100D, ISO 9001, customer, regulatory, and government compliance; directs audits, corrective actions, CAPA, root-cause investigations, management reviews, and quality KPIs. Develops quality engineering talent, partners cross-functionally to resolve manufacturing challenges, and drives Lean, digital, automation, and AI-enabled improvements across multiple sites. Travel up to 25% is required.

Leads the local quality strategy and Quality Management System for a manufacturing organization. Responsibilities include maintaining ISO compliance, managing audits, driving corrective and preventive actions, conducting root cause analysis, applying lean methodologies, analyzing quality trends, reducing scrap and rework, improving processes, and fostering a customer-focused quality culture across cross-functional teams.

Evaluates client treatment progress through in-person observations, data review, and staff and caregiver communication. Provides clinical consultation, supervision, parent training, and treatment-plan modifications for cases not progressing as expected. Collaborates with clinical directors, program managers, treatment teams, and payors, attends IEP meetings, and monitors outcome trends. Maintains a small to moderate caseload while supporting staff development and quality clinical outcomes for clients with autism and special needs.

Leads Document Control and Quality Systems to ensure cGMP, quality, and regulatory compliance in pharmaceutical manufacturing. Oversees controlled document lifecycles, NCRs, CAPAs, and Change Management. Provides quality systems expertise, drives continuous improvement using Lean and Six Sigma, and leads cross-functional compliance initiatives. Manages and develops teams while partnering across the organization to improve manufacturing and quality outcomes.

The Quality Control Manager leads quality management for federal construction projects, administering Contractor Quality Control programs under USACE and NAVFAC requirements. Responsibilities include developing quality plans, managing preparatory, initial, and follow-up control phases, conducting inspections, coordinating testing, reviewing submittals, tracking deficiencies and corrective actions, maintaining project records, and supporting closeout. The role interfaces with government representatives, project teams, trade partners, and safety personnel while ensuring compliance with contract documents, federal standards, specifications, and applicable codes.

Manages quality assurance operations, quality management systems, regulatory compliance, audits, risk assessments, investigations, validation, and continuous improvement for tissue, biologic, and medical device products. Leads QA teams, supports GMP processing and distribution operations, oversees cleanroom and facility quality activities, develops quality metrics, and serves as a regulatory and quality systems subject matter expert.