- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... policies, and procedures. + Effective communication within FUJIFILM IVD organization of sales, quality and compliance issues. + Utilization of the IVD reporting… more
- Jabil (Maple Grove, MN)
- …electrical systems. + HVAC experience preferred. + Experience in a regulated or medical device manufacturing environment is a plus. Knowledge, Skills, Abilities: ... its surrounding premises. You will oversee preventive maintenance, environmental compliance , vendor management, and emergency response while driving continuous… more
- Abbott (St. Paul, MN)
- …of FDA, IEC 60601, GMP, ISO 13485, and ISO 14971 + Prior medical device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more about our ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Philips (Plymouth, MN)
- …experience in strategic account management or corporate sales leadership within the medical device or healthcare industry. + Strong understanding of imaging ... + Ensures compliance performance within the designated market, addresses compliance issues, and collaborates with legal, quality , and regulatory functions… more
- Actalent (Minneapolis, MN)
- …ISO Quality Management Systems. + Experience with ANSI/AAMI/ISO standards for medical device risk management. + High aptitude for learning and innovation. ... devices. This role focuses on advancing the development of innovative medical products, ensuring compliance with industry standards and regulatory requirements.… more
- WSP USA (Minneapolis, MN)
- …grounding touch and step potentials, short circuit study, protective device coordination, one-line diagram development, protective relaying, and substation ... and ensuring project work conforms with specifications, permit applications, compliance documentation, and regulatory and technical analysis memos. + Prepare… more
- Medtronic (Mounds View, MN)
- …documentation skills for recording test results and preparing reports. + Experience in medical device or other highly regulated industries. + Familiarity with ... tools (eg, Excel, Minitab) for test result interpretation. + Understanding of quality systems and regulatory compliance requirements. + Strong verbal and… more
- Actalent (Minneapolis, MN)
- …+ Knowledge of RTOS and real-time environments. + 2+ years of experience in medical device or safety-critical software development. + 2+ years of experience in ... II to design and develop software applications that support a range of medical devices used in various environments, including labs, hospitals, and remote settings.… more
- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... consistently high level of customer satisfaction. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that… more
- Edwards Lifesciences (Minneapolis, MN)
- …assigned studies + Contributing to additional initiatives that shape the future of medical device development **What you'll need (Required):** + Ph.D. or ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more