- Aerotek (Shakopee, MN)
- …+ Uphold Good Manufacturing Practices (GMP) with a strong commitment to quality and safety. + Work independently and prioritize assignments effectively. + Contribute ... years of relevant experience in a regulated industry (eg, FDA , ISO). + Proficiency with Microsoft applications. + Ability...960 regular hours worked. Benefit from having an on-premise manager for instant communication and enjoy the perk of… more
- Medtronic (Fridley, MN)
- …and technical debt. + Translate business and user needs into high- quality engineering and product requirements within technical, schedule, and cost constraints. ... compliance, including IEC 60601, IEC 62304, ISO 14971, and FDA 21 CFR 820.30 for Class I-III devices. +...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Fujifilm (St. Paul, MN)
- …engineers. + Maintains a high level of success with yearly goals provided by your manager and metrics defined on a team level. + Working outside of normal business ... the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job… more
- Medtronic (Minneapolis, MN)
- …understanding of designs, documentation of compliance to requirements and timely, high- quality product launches that satisfy patient needs and reduce customer ... Medical Device Industry experience. + Familiarity with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Medtronic (Plymouth, MN)
- …or similar + Working understanding of medical device regulation including ISO-13485, US FDA CFR Part 820 + Knowledge of Good Manufacturing Practices (GMP) and ... applicable Quality System and Regulatory Requirements **Physical Job Requirements** The...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Medtronic (Fridley, MN)
- …such as pressure gauges and tension meters. + May monitor and verify quality in accordance with statistical process or other control procedures. + Perform ... intervals, and out-of-tolerance reporting. + Familiar with these regulations: FDA 21 CFR Part 820 cGMP, ISO 13485, ISO...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Medtronic (Minneapolis, MN)
- …and other legal and compliance professionals, as needed, to deliver the highest quality practical and strategic advice to sales, finance, and other stakeholders to ... HIPAA, state data privacy and security laws, software licensing, FDA law, IP and other legal risk areas governing...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Medtronic (Brooklyn Center, MN)
- …Manufacturing, you will have responsibility for supporting manufacturing of high- quality components used in implantable medical devices. The Brooklyn Center ... Good Manufacturing Practices (GMP). + Experience working in regulated environments ( FDA , ISO). + Previous Medical Manufacturing experience. + Strong problem-solving… more
- Fujifilm (St. Paul, MN)
- …opinion leaders in the Endoscopy space. The role of the Business Development Manager is to understand and define our internal and external endoscopic customers' ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
- Fujifilm (St. Paul, MN)
- …engineers. + Maintains a high level of success with yearly goals provided by your manager and metrics defined on a team level. + Working outside of normal business ... the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job… more