- Abbott (St. Paul, MN)
- …improve processes,componentsand products. + Work with cross-functional teams including R&D, Quality , Operations, and Regulatory teams. Collaborate with R&D to ... customers, and vendors. + Comply withU.S. Food and Drug Administration ( FDA ) regulatory requirements, Company policies, operating procedures, processes, and… more
- Fujifilm (St. Paul, MN)
- …others. + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with our MI Marketing Operations team, product owners, sales leadership, finance, quality assurance, legal and order management. The CPQ Product Marketing Manager… more
- Abbott (St. Paul, MN)
- … requirements. + Complies with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, Company policies, operating procedures, ... Our business purpose is to restore health and improve quality of life through the design and provision of...initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and… more
- ManpowerGroup (Fridley, MN)
- …and regulatory requirements. + Drive cross-functional collaboration with R&D, Quality , Regulatory , and Operations teams to ensure program success. + ... medical devices from concept through commercialization. + Deep understanding of FDA , ISO 13485, and design control requirements. + Exceptional communication,… more
- LCI-Lawinger Consulting (Brooklyn Park, MN)
- …Excellent communication, documentation, and leadership skills. Preferred: + Experience working under ISO 13485 and FDA regulatory environments. Powered by JazzHR ... through production. + Develop and optimize molding parameters to ensure part quality , consistency, and efficiency. + Collaborate closely with tool design, quality… more
- Fujifilm (St. Paul, MN)
- …consistently high level of customer satisfaction. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that ... with MI Project Management (PM) team to deliver high quality Synapse product solutions. + Act as primary technical...with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO… more
- Abbott (Minnetonka, MN)
- …processes, components and products. + Work with cross-functional teams including R&D, Quality , Operations, and Regulatory teams. Collaborate with R&D to ensure ... customers, and vendors. + Comply with US Food and Drug Administration ( FDA ) regulatory requirements, Company policies, operating procedures, processes, and task… more
- Teleflex (Minneapolis, MN)
- …by facility requirements. * Responsible for performing all duties in compliance with FDA 's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device ... medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in… more
- Abbott (St. Paul, MN)
- …work environment. + Comply with US Food and Drug Administration ( FDA ) regulations, other regulatory requirements, company policies, operating procedures, ... division. Our mission is to restore health and improve quality of life by designing and providing device and...and attainment goals. + Manage engineers to achieve targeted quality , yield, and continuous improvement (CIP) goals. + Meet… more
- Abbott (Plymouth, MN)
- …new products perform their intended functions safely and comply with our quality system. This role collaborates with clinical, design engineering, regulatory , ... management planning + Assist in requirements development to ensure quality and linkage to the risk management file +...cross-division or enterprise-wide business model + Working knowledge of FDA , GMP, and ISO 13485 + Familiarity with standards… more