Manager, Site Quality Salary at Ventra Inc BETA

Quality Manager – Aerospace Contract Manufacturing Location: Burbank, Ca Reports To: Director of Quality About the Role: We are seeking a Quality Manager to lead quality assurance, compliance, and continuous improvement in our aerospace manufacturing operations. This role is critical in ensuring our products meet AS9100, ISO 9001, FAA regulations, and customer expectations. The ideal candidate has a strong background in electrical components, quality systems, root cause analysis, supplier quality, and continuous improvement methodologies. They must be a hands-on leader who fosters a culture of quality, accountability, and operational excellence. Key Responsibilities: Quality Assurance & Compliance; Continuous Improvement & Problem-Solving; Supplier & Customer Quality Management; Leadership & Team Development Maintain and oversee the Quality Management System (QMS) in compliance with AS9100, ISO 9001, and FAA regulations. Lead internal and external audits, ensuring adherence to aerospac

Project Details 6-Month contract. (Extension/Conversion likely). On-site, 5 days per week. (40 hours). Key Responsibilities: Oversee core quality functions: CAPA, change control, audits, training, and complaints. Manage and develop quality team members. Act as the Quality Management Representative, reporting on QMS performance and promoting regulatory awareness. Ensure audit readiness and lead interactions with regulatory bodies. Maintain and improve quality procedures and documentation. Qualifications: 5+ years of quality experience in medical devices. Strong understanding of ISO 13485, 21 CFR Part 820, ISO 14971; MDSAP and MDR knowledge a plus. Experienced in eQMS tools and audit processes. ISO 13485 Lead Auditor certification required; ASQ certifications preferred.

Founded in 1984, Best Formulations LLC, a diversified nutraceutical and personal care company headquartered in City of Industry, California, is a contract manufacturer of thousands of branded SKUs, including high quality nutritional supplements. At the core of our ethos is a dedication to personal care, where every product is crafted with meticulous attention to detail and the highest standards of quality. Our longstanding expertise in contract manufacturing of dietary supplements has uniquely positioned us as leaders in research, regulatory compliance, and quality assurance. About the role: Best Formulations Personal Care continues the legacy of excellence established by Best Formulations, drawing on over 30 years of success in the dietary supplement industry. Our commitment to quality, innovation, and customer satisfaction remains unwavering as we venture into the realm of Personal Care. As Manager of Quality, they lead our Analytical & Microbiology Laboratories. This role ensures co

POSITION SUMMARY: The Quality Manager at Irvine, will work to apply knowledge in the implementation of an integrated Quality Management System (QMS) to ensure full compliance and a continual product, process, and supplier improvement culture. This individual will work closely with all cross-functional teams to create quality strategies that support customer needs and overall business objectives. Work on and provide solutions to a wide range of difficult problems relating to the quality aspects of design, validation, and manufacture of medical devices. The Quality Manager serves as owner and administrator of several aspects of the quality system, including but not limited to supplier management, customer feedback, process control, internal audits, change management, and design control. This quality and compliance professional will be responsible for assuring conformance to product serve as the sites lead ISO Representative. ESSENTIAL JOB FUNCTIONS: Plans, implements, and directs quality

SUMMARY: Primarily responsible for maintaining, measuring, and evaluating the effectiveness of the quality management system to assure products and services meet or exceed VSE Aviation quality standards, customer requirements, and applicable legal or regulatory requirements. DUTIES & RESPONSIBILITIES: Responsibilities include, but are not limited to: Accountable for leading annual internal and 3rd party audits. Ensures QMS processes are established, implemented, and properly maintained, including the oversight and control of all documents and data related to the requirements of the QMS system. Manages quality metrics, trends and activities to improve cost, quality, and customer satisfaction. Develops written quality plans by conducting analyses, identifying critical control points, and implementing preventive measures and verification procedures. Accountable for assessing Customer Satisfaction by conducting an annual customer satisfaction survey and overseeing customer complaints and p

Central Transport LLC is one of the nation’s most reliable and technologically advanced LTL (Less-than-Truckload) carriers to date. We are privately owned and have been servicing manufacturing & retail companies of all sizes for over 90 years. With over 200 locations around the country, we pride ourselves on the continuous expansions that we have made and are still making strides to improve our operation systems to better service our wide network of clientele. For example, we have recently implemented 25 next-day hubs in our network to provide immediate, essential services for our customers overnight. We also hold the industry’s most modern fleet with our tractors & trailers having an average age of 2.5 years old. Earlier this year, our business levels have reached the highest they’ve ever been; breaking our personal record that had been set the previous year. We like to credit our growing success with our ability to develop and provide opportunity for our team of employees so they can

Description Title: Site Quality Manager Department: Business Planning & Operations Location: Project-Based Rotation Supervisor: Associate Director of Quality FLSA Status: Exempt Position Status: Permanent, Full-time Work Status: Hybrid SITE QUALITY MANAGER Hanwha Qcells USA Corp (Qcells USA), headquartered in Irvine, CA, specializes in providing utility-scale modules, solar photovoltaic (PV), and battery energy storage systems (BESS) project development, along with Engineering, Procurement, and Construction (EPC) services for solar and BESS projects nationwide. Qcells USA delivers comprehensive turnkey solutions encompassing the entire utility-scale project lifecycle. By choosing Qcells USA for turnkey solutions, customers can reduce uncertainty and risk, leading to enhanced investment returns and contributing to a more sustainable future. Qcells USA's complete turnkey solutions seamlessly integrate the expertise of our Development, Module, and EPC teams, while ensuring close coordinat

Job Description Job Description SUMMARY: Manages the development and implementation of the Quality Engineering function to ensure that VACCO Space Products and Services meet specifications and contractual agreements. ESSENTIAL DUTIES AND RESPONSIBILITIES: Maintain a high level of communication and credibility with DCMA, Customer Representatives, Regulatory Agencies and other external quality personnel. Recommend Quality Management System changes to the Director of Quality or his designee when changes are required by industry, contract requirements or audit findings. Support audits by Space customers, government, and regulatory agencies and reports the results to the Director of Quality or his designee for necessary action. Submit information to the Director of Quality or his designee in order to update action items to conform to the results of internal and customer audits. Implement all necessary corrective actions requirements by results of Internal or customer audits. Implement requi