Quality Management Salary at Navien Inc BETA

Thank you for your interest in working for our Company. Recruiting the right talent is crucial to our goals. On April 1, 2024, 3M Healthcare underwent a corporate spin-off leading to the creation of a new company named Solventum. We are still in the process of updating our Careers Page and applicant documents, which currently have 3M branding. Please bear with us. In the interim, our Privacy Policy here: https://www.solventum.com/en-us/home/legal/website-privacy-statement/applicant-privacy/ continues to apply to any personal information you submit, and the 3M-branded positions listed on our Careers Page are for Solventum positions. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Job Description: Site Quality Leader (Solventum) The Impact You’ll Make in this Role As the Site Quality Lead

Manufacturing Quality Manager Arktura is an industry-leading manufacturer of cutting-edge architectural systems and innovative custom solutions, driven by state-of-the-art design & manufacturing technology. We are currently seeking a highly organized, proactive and energetic Quality Manager to join our team of architects, designers, engineers, machinists and software developers at our headquarters in Los Angeles. Responsible for day-to-day tactical leadership of the Quality department to execute the defined Strategic Quality Plan in conjunction with Quality functional leadership. Provides quality assurance support to customers, suppliers, partners and internal manufacturing departments. Leads continuous improvement activities in targeted areas. Ensures compliance to quality standards as it relates to the inspection environment. Oversees the inspection of incoming and assembled parts as well as the day-to-day supervision of employees within QC. Acts as primary contact point for departme

Job Description Job Description Position Overview: American Dawn, Inc., a leading importer and distributor of textile products across diverse industries (food & beverage, health care, and hospitality), is seeking a Quality Manager to join our team. This newly created role, reporting directly to the VP of Supply Chain, will lead product quality and regulatory compliance efforts across our global consumer goods operations. The Quality Manager will be responsible for ensuring product quality, managing compliance with regulations, and overseeing a team of two direct reports. You will collaborate with cross-functional teams such as sourcing, purchasing, product development, and operations. Key Responsibilities: Quality Assurance: Develop and implement quality assurance programs and procedures. Oversee quality control processes, including inspections, testing, and analysis. Monitor product performance and identify opportunities for improvement. Ensure products meet defined quality standards

We Are: Accentures SAP practice, and we bring the New to life using design thinking, agile development methodologies, and the latest smart tech like IoT, automation, and AI. Additionally, as a part of Accenture's Chemicals Practice, you will help power growth and innovation at speed and scale for our clients while being good stewards of our resources. From analytics to sustainability to customer experience, we help Chemical companies transform. SAP technologies power these organizations with modern cloud-based and AI-enabled solutions, and Accenture is the undisputed market leader in this industry. We are continuously expanding our SAP team with advisory skills to continue to drive transformation at scale for our clients. You are: A transformation ace with the skills to help clients meet the challenges of digitization. Your superpower? Using your know-how, creativity and analytical powers to solve clients most complex business problems to help their companies do more. Youre as comforta

Quality Manager Company Profile: Precision Castparts Corp. (PCC) is a leading worldwide, diversified manufacturer of complex metal components and products. It serves the aerospace, power, and general industrial markets. PCC is the market leader in manufacturing large, complex structural investment castings, airfoil castings, and forged components used in jet aircraft engines and industrial gas turbines. The Company is also a leading producer of highly engineered, critical fasteners for aerospace and other general industrial markets, manufactures extruded seamless pipe, fittings, forgings, and clad products for power generation and oil & gas applications, and supplies metal alloys and other materials to the casting and forging industries. PCC is a high-quality business with dominant positions in most segments of the markets in which it serves. Headquartered in Portland, Oregon, this over 10-billion-dollar company employs more than 29,500 people worldwide. PCC has over 160 plants and has

Overview: Monterey Park Hospital, located in the San Gabriel Valley of Los Angeles, is a 101 bed acute care community hospital providing our community with advanced medical and culturally sensitive healthcare services for over 50 years. Monterey Park Hospital is recruiting for a Quality Coordinator (non-clinical) in our Quality Assurance Department. This position reports to the Director of Quality/Risk Management. Responsibilities: The Quality Coordinator (non-clinical) assists the Director of Quality/Risk Management by supporting performance improvement (PI) and Risk Management activities by ensuring PI and Patient Safety Plans are updated annually, reviews policy and procedures, provides education to staff through hospital orientation, skills events, department staff meetings and annual reorientation, reviews occurrence reports timely, processes and documents accurately, abstracts quality data for OPPE evaluations, core measures, falls, risk events and clinical quality indicators for

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