- Agiliti Health (Logan Township, NJ)
- …equipment inspection, maintenance, calibration, and repair service on a variety of medical devices including medical beds, infusion pumps, patient ... power to change a life. We are a nationwide company of passionate medical equipment management experts who proudly serve hospitals and healthcare facilities to… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …field required; _Master's degree preferred_ + Expert-level proficiency in ISO 13485, Medical Device Regulation (MDR), and FDA requirements with demonstrated ... ISO frameworks, GMP/GDP protocols, and USP-EP guidelines as they apply to medical device environments + Demonstrated capability to align technical decisions… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. * QA experience in the medical device… more
- Integra LifeSciences (Plainsboro, NJ)
- …a quantitative standpoint. The candidate must be familiar with process flow of a medical device organization, including the regulatory impact of change and ... in a Validation or Quality Assurance role for a medical device or pharmaceutical environment. + Demonstrates excellent organizational and communication… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device… more
- Fresenius Medical Center (East Brunswick, NJ)
- …success. + Directs data entry related activities such as patient admission, regulatory reporting, billing, physician orders, lab results, vital signs, patient status ... any other treatment related data into systems. + Ensures regulatory , compliance, and audit activities are accomplished on time....There is a two-person assist program and "material assist" devices for the heavier items. + This position requires… more
- System One (Mahwah, NJ)
- …Engineer Location: Mahwah, NJ Compensation: $53.00- $70.00 Type: Contract Overview Global Medical Device company looking for experienced Engineer to join their ... up to and including that necessary to support a regulatory submission. Requirements + A minimum of BS degree...analysis and familiarity with Minitab and/or MS Excel. + Medical device or similar regulated industry experience… more
- Integra LifeSciences (Plainsboro, NJ)
- …Manufacturing Center) to ensure the safety, efficacy, and quality of our medical devices . This includes assigning and monitoring weekend (Friday through ... all established costs, quality, and delivery commitments are met, working within FDA medical device regulations, and applicable ISO standards. + Responsible for… more