Communicate with customers on quality issues and coordinate with regional Quality Teams to resolve concerns.
Review customer quality requirements and integrate them into the Quality Management System.
Support APQP and PPAP activities and ensure manufacturing techniques meet specifications.
MISUMI Americas provides standard, configurable, and custom manufacturing solutions with a digital manufacturing platform. The company serves innovative companies in the Americas with operations in San Francisco Bay Area and Chicago.
Support the development and implementation of quality management systems and continuous improvement initiatives.
Track performance metrics, identify process optimization opportunities, and collaborate with cross-functional teams.
Participate in root cause analysis, quality inspections, and assist in training staff on quality practices.
Hitachi Energy is a global technology company leading the energy transition with innovative solutions and services. The company fosters a diverse and inclusive workplace with a strong focus on quality and continuous improvement.
Design and develop quality screening strategies, business rules, and disposition plans for centralized quality systems.
Analyze large manufacturing datasets to identify abnormal signatures, trends, and emerging quality risks using statistical methodologies.
Collaborate with cross-functional teams to standardize quality practices, support root-cause investigations, and drive continuous improvement initiatives.
This global quality engineering organization is responsible for centralized quality operations across semiconductor manufacturing sites in Asia and the United States. They focus on safeguarding product quality through automated screening, statistical risk assessment, and data-driven operational controls, offering broad exposure to manufacturing and engineering teams.
Own quality oversight and production troubleshooting with CMO partners.
Verify products and run stability testing end to end.
Generate claims evidence and manage US ingredient and regulatory requirements.
We are a DTC Health & Wellness brand that provides conscious, high-quality & innovative supplement products. In just 5 years, we scaled to USD$100M+ in annual sales, serving more than 3,000,000 customers worldwide, and have been ranked among APAC’s top High-Growth Companies.
Own GTI's QA/QC policies, SOPs, and quality management system across a multi-state network, driving consistency and continuous improvement.
Direct company-wide sanitation and QC practices ensuring product purity, consistency, and compliance with regulatory standards.
Manage nonconformance records, CAPA processes, and complaint investigations to drive systemic improvements and regulatory compliance.
Green Thumb Industries is a multi-state cannabis operator involved in cultivation, manufacturing, and production of cannabis products. The company emphasizes a culture of quality, food-safety, and compliance excellence across its network.
Provides quality oversight of QC laboratory activities, ensuring compliance with global GxP regulations across multiple indications.
Manages GMP testing at CMOs and contract testing laboratories, including raw data review and exceptions management.
Collaborates with CMC Manufacturing, Quality Assurance, and Regulatory Affairs to align testing timelines with corporate goals.
Immunovant is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. They are a publicly traded, clinical-stage biopharmaceutical company with a dynamic, fast-paced, entrepreneurial culture.
Lead implementation and improvement of quality management systems, including certifications. - Develop solutions for complex quality challenges and provide training on quality processes. - Conduct audits, manage non-conformance investigations, and drive continuous improvement.
The partner company is a technology-driven organization focused on safety, reliability, and continuous improvement. It operates globally and emphasizes quality management and operational excellence, with a culture of collaboration and innovation.
Monitor technical aspects of SGS Natural Resources, Energy, North American Operations in conjunction with Quality Management System and ISO/IEC 17025 requirements.
Establish and maintain lean and effective method validation, verification, and consistency to align with technical requirements.
Support corrective actions, liaise with site operations and quality managers, and contribute to training technical staff.
SGS is the world's leading testing, inspection and certification company, recognized as the global benchmark for sustainability, quality and integrity. With 99,600 employees operating a network of 2,600 offices and laboratories, they work together to enable a better, safer and more interconnected world.
Implement and maintain best-in-class quality systems in compliance with FDA, ICH, 21 CFR Part 11, and ISO 9001.
Foster a culture of quality excellence and continuous improvement across the organization.
Manage day-to-day activities of a lean, high-performing quality team and optimize workflows.
N-Power Medicine aims to reinvent drug development by transforming clinical trials through better integration with clinical practice. They are building a multi-disciplinary team with diverse expertise in healthcare, engineering, technology, and regulatory, sharing a core value of empowering community through generosity, curiosity, and humility.