Top Quality Manager Jobs

Lead the Quality Engineering and Inspection team, manage the ISO-certified quality system, maintain policies and procedures, monitor supplier quality, support proposals and cross-functional product development, and ensure compliance with ISO, aerospace, customer, and government requirements. The role requires extensive durable-goods manufacturing experience, familiarity with RF electronics and navigation systems, limited worldwide travel, and successful completion of a U.S. government background investigation.

Lead and maintain the Quality Management System for VBAT production, ensuring AS9100 compliance, manufacturing quality, inspections, MRB/CAPA management, and mentoring quality staff while partnering with production, supply chain, and engineering to improve processes and product conformity.

Oversee project-wide quality assurance governance for complex engineering, procurement, and construction projects. Develop and maintain quality plans, manage audits, nonconformances, corrective actions, vendor quality, documentation, KPIs, and compliance. Coordinate with engineering, construction, supply chain, HSE, project management, suppliers, and clients. Promote quality culture, root-cause analysis, continual improvement, training, and customer satisfaction while ensuring compliance with applicable codes, standards, contracts, and ISO 9001 principles.

Leads a Failure Analysis team and laboratory, establishing testing standards, investigation workflows, documentation requirements, and performance metrics. Oversees complex failure investigations, root-cause analysis, technical reporting, resource allocation, and cross-functional risk mitigation. Manages hiring, coaching, performance development, succession planning, and team capability building. Drives continuous improvement, ensures safety and quality-system compliance, and communicates findings and recommendations to Engineering, Operations, Procurement, Quality, and executive stakeholders.

Leads the plant quality strategy and Quality Management System, ensuring customer satisfaction, product compliance, and manufacturing excellence. Manages the quality team, customer and supplier relationships, audits, problem-solving, process capability, SPC, continuous improvement, warranty reduction, and quality budgets. Partners with Production and Engineering to reduce defects, scrap, rework, supplier nonconformances, and cost of poor quality while maintaining safe work practices.

Manages a multi-shift Quality Assurance department in a food manufacturing environment. Oversees food safety and quality systems, audits, corrective actions, environmental monitoring, testing, nonconformance investigations, customer complaints, documentation, regulatory compliance, and certification requirements. Provides staff training, coordinates cross-functional continuous improvement, supports external audits, and serves as backup for recall and food defense coordination.

Leads quality control activities for civil construction projects, including inspections, material testing, sample collection, equipment calibration, audits, corrective actions, documentation, and project submittals. Manages quality personnel, interprets plans and specifications, records and analyzes test results, maintains document-control databases, coordinates with government agencies, and supports project schedules, budgets, safety, and regulatory compliance.

Lead Huckleberry’s globally distributed QA organization of 12 engineers across manual and automated testing. Own QA strategy, staffing, standards, quality KPIs, process improvement, and release-readiness decisions. Partner with engineering and product leadership to identify risks, negotiate release trade-offs, reduce post-release defects, and implement shift-left and AI-enabled QA practices. Mentor team members, manage performance, and collaborate with outsourcing partners to scale quality capacity.

Leads CMC Quality Control oversight for gene therapy programs, including external laboratory management, analytical method lifecycle activities, stability and release testing, investigations, specifications, reference standards, comparability, and regulatory submissions. Partners with Analytical Development, Technical Operations, Regulatory Affairs, Quality Assurance, and external vendors to support clinical development, process validation, and commercial readiness. Coordinates sample submissions, shipments, and testing activities while ensuring cGMP and global regulatory compliance.

Leads a team of sustaining design quality engineers supporting medical device products throughout their lifecycle. Oversees design controls, Design History File integrity, verification and validation, risk management, CAPAs, design changes, regulatory submissions, audits, and compliance improvements. Partners cross-functionally to address technical and quality challenges, allocates resources, and mentors engineering talent while ensuring product safety, performance, and regulatory compliance.

Leads the Sealants Quality Laboratory, managing daily testing, product release, staffing, training, resources, audits, and compliance with customer, AS9100, and Nadcap requirements. Oversees investigations, root-cause analysis, corrective actions, laboratory performance, and continuous improvement. Partners with Manufacturing, Quality, Science and Technology, and other functions to resolve product and process issues while ensuring safe, accurate, and timely laboratory operations.

Manage and continuously improve an environmental laboratory’s quality management system. Oversee regulatory compliance, internal and external audits, accreditation, document control, proficiency testing, nonconformances, corrective actions, client complaints, vendor approvals, and quality personnel. Maintain accurate training and audit records while ensuring adherence to safety and organizational standards.

Leads the Document Control team within QA Operations, overseeing controlled document issuance, revision workflows, records management, eQMS administration, change controls, metrics, and inspection readiness. Manages team performance, training, and development while partnering with manufacturing, quality, laboratory, and cross-functional stakeholders. Drives documentation process improvements, supports system validation and upgrades, and ensures compliance with GMP requirements and regulatory expectations.

Serves as the primary quality contact for customers and commercial teams, investigating product issues, conducting root cause analysis, implementing containment and corrective actions, and coordinating rework or recalls. Supports supplier quality, incoming inspection, new product introductions, FMEA, continuous improvement, and KPI reporting. Maintains quality documentation, communicates findings to customers and management, supports manufacturing processes, and leads cross-functional quality initiatives.

Oversee quality assurance and control for translation and interpretation service contracts. Responsibilities include maintaining the QMS and Quality Management Plan, monitoring performance metrics, conducting audits and inspections, managing corrective actions, investigating nonconformances, supporting customer assessments, overseeing subcontractor quality, preparing reports, and driving continuous improvement.

Leads regional Quality and Operations teams, ensuring electronic and semiconductor components meet customer requirements. Oversees inspection accuracy, product acceptability, failure analysis, corrective actions, quality training, and compliance with quality standards. Coordinates with customers, Purchasing, Sales, and service providers to resolve quality concerns and improve operational effectiveness. This is an onsite leadership role in Austin, Texas.

Manages construction quality control programs for federal projects, including QC plans, three-phase quality control, inspections, testing, submittals, RFIs, deficiency resolution, and documentation. Coordinates with superintendents, safety professionals, and subcontractors while maintaining quality records and ensuring compliance with contract, USACE, NAVFAC, and federal construction requirements.

Manages regulatory affairs and quality assurance project execution across pharmaceutical development programs, from clinical development and NDA submissions through health authority review, approval, launch readiness, and post-approval activities. Coordinates cross-functional teams, submission plans, regulatory interactions, inspection readiness, CAPA, quality systems, risks, commitments, vendors, budgets, dashboards, and executive reporting.

Manages construction quality assurance and quality control programs across projects, ensuring compliance with plans, specifications, codes, regulations, and quality management standards. Develops quality plans, procedures, metrics, training, and reporting processes; conducts site evaluations; manages quality personnel; addresses deficiencies; and coordinates with field teams, subcontractors, clients, architects, consultants, vendors, and authorities.

Leads a quality engineering team while remaining hands-on with AI-powered test automation across API, UI, integration, and end-to-end workflows. Evaluates AI tools, improves test frameworks and regression efficiency, supports release readiness, analyzes defects, tracks quality metrics, and partners with Engineering, Product, DevOps, and Release teams. Coaches employees on AI-native quality practices, prompt engineering, responsible AI use, and evaluating AI-generated tests.

Manages aircraft maintenance quality control operations, inspectors, compliance surveillance, documentation, training, budgets, and regulatory adherence. Ensures maintenance work follows company policies, Federal Aviation Regulations, manufacturer-approved data, and safety requirements. Oversees inspections including Required Inspection Items, nondestructive testing, borescope work, and receiving acceptance. Prepares management reports, supports personnel actions, and maintains facility and technical-data compliance.

Leads global quality assurance, audit, supplier quality, inspection readiness, and compliance programs for biologics manufacturing and outsourced GxP operations. Oversees audits, supplier qualification, quality agreements, risk management, corrective actions, regulatory inspections, SOPs, and approved supplier list maintenance. Manages and develops audit and supplier quality teams while driving cross-functional improvement initiatives and supporting regulatory submissions.

The Quality Manager will lead a team to ensure quality standards in manufacturing water filtration equipment, manage reports and processes, and achieve ISO 9001 certification.

Lead and maintain the plant Quality Management System, drive continuous improvement and COPQ reduction, manage supplier and manufacturing quality, lead audits and RCCAs, and develop a quality team to support production and customer requirements.

Lead a 4-5 person engineering team to build clinician-facing quality platform: define technical/product direction, ship AI-assisted workflows from transcripts to chart notes, partner with clinical/product/design/data, hire and develop engineers, ensure reliability, observability, privacy, and measure care quality and outcomes.