Top Quality Manager Jobs

Lead production quality for the TBM Final Assembly Line ensuring compliance with EASA PART‑21G, QMS, and approved design data. Oversee inspections, non‑conformance management, audits, corrective actions, continuous improvement (Six Sigma/Lean), and staff training. Interface with regulators and support aircraft release, delivery, and initial airworthiness.

Lead implementation and continuous improvement of project quality management systems. Coach project staff, conduct audits, manage inspections/testing, track KPIs and QIRs, coordinate with stakeholders, control material/testing quality, and help mitigate risk to improve project efficiency and profitability.

Oversee quality control workflows and systems in manufacturing. Lead a team of 50+ QC technicians, drive continuous improvement, and ensure products meet high standards.

Lead and maintain quality systems and inspections; ensure ISO9001/ISO13485 and regulatory compliance; manage audits, customer quality, supplier monitoring, CAPA, SPC/Minitab, IQ/OQ/PQ, and continuous improvement; recruit and develop staff; implement metrics, budgeting, safety, and documentation to achieve customer acceptance and on-time delivery.

Lead and maintain the Quality Management System, oversee inspections, testing, audits, CAPA, APQP, and continuous improvement. Serve as customer and supplier quality liaison, lead quality projects, mentor a quality team, and apply Lean/Six Sigma methods to drive process improvements and compliance with industry standards.

Oversee all quality aspects of the MFLC contract: collect and report data, ensure QA/QC programs meet contract standards, maintain credentialing and training compliance, facilitate communication between contractor, counselors, and government stakeholders, and implement process improvements to enhance counselor operations.

Lead plant quality function to improve PPM, first pass yield and supplier performance. Manage quality staff, maintain IATF 16949/ISO 9001, run audits, corrective actions, PPAP, PFMEA, control plans, calibration, incoming inspection and continuous improvement activities.

Owns batch-impacting deviation management in Veeva QMS from initiation through closure. Drives cross-functional investigations, reviews technical and compliance quality, supports batch disposition, manages CAPAs and related quality records, tracks KPIs, presents performance data, coaches investigation owners, and improves deviation workflows and procedures in a cGMP biopharmaceutical manufacturing environment.

Manage customer quality for advanced DRAM products supporting Tier 1 customers. Coordinate failure analysis, 8D responses, change notifications, performance reporting, issue tracking, and technical communications across customers and global engineering teams. Align quality requirements, manage response expectations, escalate issues, and drive sustainable solutions. The role requires semiconductor memory expertise, strong technical communication, customer-facing experience, and daily onsite work in San Jose with 20–30% travel.

Lead GCP quality activities for clinical programs, design and execute fit-for-purpose audit programs, drive inspection readiness, manage risk and issues, advise cross-functional teams, present integrated quality strategies, and serve as primary quality liaison during health authority inspections to ensure compliant, submission-ready clinical data.

Responsible for leading Clinical Quality Assurance activities, conducting GCP audits, developing quality systems, and ensuring compliance across clinical research projects.

Lead the QMS and quality team to ensure products meet military, ISO, and customer requirements. Oversee metrology, CMM programming, inspection, calibration (ISO 17025), SPC and capability studies, audits, FAI/PPAP, root cause analysis, corrective actions, supplier quality, and continuous improvement. Train staff and collaborate with engineering and manufacturing to improve manufacturability and measurement strategies.

The Quality Manager oversees the Quality Management System, ensuring compliance with industry standards, supporting continuous improvement, and managing regulatory requirements while engaging with operations and customers.

Lead a team of quality technicians and own quality performance for a stainless-steel manufacturing value stream. Drive root-cause investigations, CAPA, ISO 9001 compliance, APQP activities (PFMEA, control plans, GR&R, FAI), continuous improvement, supplier/customer quality, and cross-functional collaboration to ensure product and process reliability.

The Quality Assurance Manager manages and improves the medical device quality system under FDA, ISO 13485, MDSAP, and ISO 14971 requirements. Responsibilities include internal, supplier, and third-party audits; CAPA and nonconformance investigations; root cause and risk analysis; quality metrics; document and change control; supplier quality agreements; and validation support. The manager leads direct reports, supports regulatory inspections, ensures record accuracy, develops employees, and provides cross-functional quality support.

Evaluates ABA treatment quality and client progress through observations, data review, staff consultation, and caregiver communication. Provides clinical supervision, advanced case consultation, treatment plan modifications, parent training, and IEP participation. Collaborates with clinical directors, program managers, payors, and treatment teams while monitoring outcome trends and maintaining a small to moderate caseload.

Manage and implement the project Quality Control program: coordinate and document inspections and testing, deliver QC reports, run weekly QC meetings, track deficiencies and corrective actions, verify materials and subcontractor compliance, support commissioning and agency inspections, and collaborate with project teams to ensure delivery of high-quality construction outcomes.

Manage and execute the construction Quality Control program: plan and document inspections, run QC meetings, track deficiencies and corrective actions, verify materials and commissioning, ensure subcontractor compliance, and provide reports and recommendations to management.

Leads plant-level quality operations for battery manufacturing, including production support, inspections, containment, nonconforming material disposition, corrective actions, audits, customer and supplier issue resolution, and quality team development. Drives APQP, PPAP, PFMEA, Control Plans, SPC, MSA, process capability, launch readiness, compliance with ISO 9001 and IATF 16949, defect reduction, and continuous improvement.

Support development and implementation of quality management systems for construction projects. Conduct inspections, audits, and compliance checks; manage quality issues, prepare reports, coordinate closeout and commissioning, train staff, and liaise with clients, contractors, and regulators to ensure project standards and safety requirements are met.

Lead the strategy, execution, oversight, and continuous improvement of Heartflow’s global Quality Management System. Manage CAPA, document control, training, audits, management reviews, tool validation, and supplier management. Serve as the QMS subject matter expert during FDA, Notified Body, and other regulatory audits. Lead and develop a quality team, promote a quality-first culture, drive KPI-based decisions, and collaborate with R&D, Production, Regulatory, Clinical, and Product Management teams to support compliant global expansion.

Manages QA/QC for construction projects by developing quality plans and inspection procedures, conducting site inspections, coordinating testing and approvals, reviewing technical documents, resolving non-conformances, maintaining quality records, supporting audits, and promoting quality awareness. The role oversees compliance across civil, structural, architectural, and MEP work while coordinating with clients, consultants, inspectors, subcontractors, and construction teams.

Leads quality control for electrical construction projects, overseeing inspections, testing, documentation, NCR resolution, commissioning readiness, and turnover compliance. Reviews drawings and specifications, implements quality systems and inspection plans, verifies electrical installations and testing, tracks quality metrics, and coordinates with project, field, commissioning, general contractor, owner, and client teams.

Leads project-specific QA/QC planning and execution for mission-critical construction projects. Oversees inspection and testing plans for civil, structural, architectural, and MEP work; coordinates quality teams and trade partners; reviews submittals; conducts inspections, walkthroughs, and quality meetings; tracks deficiencies and corrective actions; supports commissioning, punch lists, turnover, and client communication.

Lead site quality function for aerospace/defense programs: own QMS (AS9100/ISO9001), audits, supplier quality, corrective actions, root cause analysis, SPC, MRB, and continuous improvement.