- Philips (Plymouth, MN)
- ** Labeling Designer (Plymouth, MN)** You are part of the Labeling group that reports up through the R&D department of the Image Guided Therapy Devices BU. ... The labeling group is dedicated to ensuring the accuracy and...Instruction For Use (IFUs) documents, including product illustrations, layout design , and illustrative material and copy. + Utilize existing… more
- Medtronic (Fridley, MN)
- …+ Coordinate with Product Release and Quality Systems to prepare and route product design documentation. + Perform audits of labeling and packaging components. + ... prepare, process, and implement quality systems, configuration assurance, and product design documentation deliverables to support Neuromodulation and Pelvic Health … more
- Medtronic (Fridley, MN)
- …risks for products in the field. This includes trends in complaint data, labeling , software, and hardware related issues. You will also provide risk and reliability ... engineering support for released product design and process changes. **Careers That Change Lives** A...Plans, directs and implements all aspects of the company's design and development of new medical device products or… more
- Medtronic (Fridley, MN)
- …risks for products in the field. This includes trends in complaint data, labeling , software, and hardware related issues. You will also provide risk and reliability ... engineering support for released product design and process changes. The Reliability Engineer II ensures...of software anomalies. + Evaluate reliability impact of proposed design and manufacturing changes on existing market released product.… more
- Medtronic (Minneapolis, MN)
- …specialist also assists with the license maintenance including renewals, design /manufacturing change notification, QMS audit, and Manufacturing site registrations. ... support for currently marketed products as necessary. This includes reviewing labeling and changes to existing devices and documentation. Prepare submissions and… more
- Abbott (Plymouth, MN)
- …new or modified, are distributed to appropriate personnel. + Reviews device labeling for compliance with FDA submissions and applicable regulations. + Supports the ... medical device regulations and submissions. + Experience with risk management, design verification, or process validation work. + Proficient with MS Office… more
- AECOM (Minneapolis, MN)
- …site descriptions and contributions to reports. + Processing artifacts (washing, labeling , and cataloging) and performing basic analysis of artifacts. **About ... professional services throughout the project lifecycle - from advisory, planning, design and engineering to program and construction management. On projects spanning… more