- Integra LifeSciences (Plainsboro, NJ)
- …to advance patient outcomes and set new standards of care. SUMMARY DESCRIPTION The ** Quality Inspector II** will be responsible for performing quality ... on purchased components, manufactured sub-assemblies and final product. The Quality Inspector will perform all duties in...corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable… more
- Integra LifeSciences (Plainsboro, NJ)
- …treatment pathways to advance patient outcomes and set new standards of care. The **Lead Quality Inspector ** serves as a Lead Associate, Quality Inspector ... quality inspectors and provide guidance to current quality inspectors. Lead Associate, Quality Inspector...corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable… more
- Fujifilm (Wayne, NJ)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... or degree preferred, but will consider applicants with repair experience in electronics, medical device , mechanical, or a similar field. + Soldering experience… more