Top Quality Manager Jobs

Lead harmonization of global quality practices, implement continuous quality improvements, oversee audits, CAPA, deviations, document control, change management, coach quality teams, and drive cultural change across multi‑site pharmaceutical/biotech operations.

Manage and supervise a Clinical Quality team to ensure cGMP-compliant quality activities, training, audits, deviations/CAPAs, calibration, preventive maintenance, qualification/validation, and customer-facing quality metrics. Coordinate with project management, business units, and customers to drive continuous improvement and meet site quality objectives.

Manage and monitor production quality and compliance with codes and company standards. Conduct inspections, review change orders, track service trends, initiate corrective actions, maintain QA documentation and training, ensure testing and reporting (HUD, Energy Star) are completed, and communicate findings to management.

Lead the plant QA team to ensure product quality and food safety. Maintain HACCP and food safety systems, troubleshoot quality issues, deliver KPI reporting, and coach QA staff to meet company standards.

Manage and maintain Kymera's electronic Quality Management System (Veeva Vault) including document control, training program administration, compliance monitoring, metrics reporting, and inspection-ready records. Support SOP lifecycle, vendor qualification, and continuous improvement to sustain QMS operations during late-stage development and commercialization.

Lead and maintain the quality management system, internal audits, supplier quality, CAPA, complaints and field actions. Develop SOPs, monitor program effectiveness, manage staff performance, and support customer and supplier audits to ensure FDA and ISO compliance.

Manage the Bioanalytical Quality Assurance Unit to ensure GLP/GCLP compliance, supervise QAU staff, conduct audits, review CAPAs and deviations, support customer audits/questionnaires, implement continuous improvement, and train/mentor laboratory staff.

Build and scale QA and enablement programs for email, chat, and phone support. Develop scorecards, audits, calibration, coaching, Help Center content, macros, and reporting. Use data and AI to analyze quality trends, reduce contact rates, and partner cross-functionally to improve customer experience and operational KPIs.

Lead and develop the global disposable/single-use quality team; drive quality, compliance, and continuous improvement. Oversee audits, CAPA, change control, vendor qualification, calibration, product and equipment validation. Ensure compliance with SOPs, GDP, cGMP, and quality systems; monitor quality metrics, support customer audits, and partner with cross-functional global stakeholders.

Lead manufacturing and quality engineering for medical device products: manage product development, NPI implementation, continuous improvement, CAPA and QMS activities, statistical process analysis, staff supervision, customer quality issue resolution, and regulatory compliance (ISO 13485, 21 CFR 820).

Build and scale QA and enablement programs for email, chat, and phone support. Create scorecards, audits, calibration, coaching, and reporting. Own Help Center, macros, voice-and-tone standards, training, and AI-driven improvements to reduce contact rate and improve team performance.

Lead and supervise site quality and EHS functions within a NADCAP QMS environment. Manage audits (internal, customer, regulatory), maintain AS9100/NADCAP certifications, develop process and inspection plans, perform root cause analysis and corrective actions, review contractual requirements, maintain training records, and support continuous improvement while managing a small quality team.

Lead product complaint management and CAPA program oversight, including pharmacovigilance vendor oversight, complaint investigations, trend analysis, inspection readiness, audits, and cross-functional coordination to ensure regulatory compliance and continuous improvement of the pharmaceutical quality system.

Lead air permitting strategy and regulatory approvals for a Direct Reduced Iron and integrated steel plant. Manage permit applications (PSD, NSR, Title V), emissions inventories, dispersion modeling, and technical liaison with regulators. Integrate permitting into engineering, construction, commissioning, and operations, monitor schedules, support EIAs, audits, compliance, and maintain permitting documentation.

Lead development and improvement of ISO 9001-compliant quality management systems; oversee QA/QC and lab operations; manage audits, KPIs, RCA, CAPA, and continuous improvement in chemical manufacturing.

Manage quality assurance and risk by identifying, analyzing, and mitigating operational and regulatory risks. Interface with payers and state agencies, aggregate and analyze quality data, lead projects and investigations, perform root cause analyses, support improvement plans and annual QA/Risk plans, ensure compliance, coordinate inspections, and help develop technology to support quality management.

Build, implement, and continuously improve a commercial ISO 9001-based Quality Management System. Lead audits, corrective actions, supplier quality, metrics, training, and cross-functional coordination while interfacing with Nuclear Quality Assurance and supporting assessments.

Manage driver fleet quality and final-mile service: perform site visits for claims and meet trucks, negotiate settlements, organize repairs, train and onboard independent contractors, monitor deliveries and performance, assist with escalations and customer relations.

Develop, implement, and manage quality control processes and systems. Supervise inspection and testing, investigate customer quality issues, analyze data and specifications, document standards and inspection procedures, support continuous improvement, coordinate with engineering and purchasing on vendor quality, and ensure compliance with safety and regulatory standards.

Manage HACCP and food safety programs in a 30,000-sf facility: maintain HACCP/Food Safety records, oversee CCP/SSOP deviations, analyze pathogen testing, train staff on GMPs, coordinate with inspectors and external partners, prepare audits, and support QA team operations.

Oversee quality systems and aseptic manufacturing operations, ensuring compliance with regulations and leading a team to meet quality standards.

Lead and maintain the airline's quality assurance and Continuous Analysis and Surveillance Program (CASP), promote safety and regulatory compliance with 14 CFR, audit vendors, perform safety risk analyses, maintain CASP and safety database records, and manage QA inspections, reporting, and related documentation.

Drive QA and Developer Experience programs at HP IQ, enhancing engineering velocity and ensuring quality across AI product portfolio while collaborating with multiple teams.

Lead ISO 9001 implementation and certification, maintain quality and safety programs, perform audits and inspections, investigate incidents, drive root cause analysis and corrective actions, apply Lean/Six Sigma for continuous improvement, manage and train QA and safety teams, and report KPIs to management in a metal fabrication manufacturing environment.

Manage and implement the Quality and Performance Improvement Program for assigned services, ensuring patient safety, regulatory readiness, and clinical quality. Lead PI projects, perform root cause and statistical analyses, develop dashboards and reports, use Epic chart review for quality assessments, and recommend improvements to departments and committees.