management System, ISO 14971:2019 Risk Management, Directive (ED)93/42/EEC (MDD) European Union Medical Device Directive...
requirements (GMP, ISO, MDD) & JJMT policy & procedure requirements. Excellent ability to convey complex technical information...
, MDD 93/42/EEC and FDA QSR. Duties and Responsibilities: Review and develop process instructions for our products... operations in accordance with ISO 13485, MDD 93/42/EEC and FDA QSR. Duties and Responsibilities: Review and develop process...
investigation compliance with the Food and Drug Administration (FDA), European Union Medical Device Directive (MDD), European Union...
that are compliant and conform to 21 CFR 820, MDD/MDR, and ISO 13485:2016. Responsibilities Under direction, Engineering Interns...
. This involves assuring quality standards (FDA, ISO, CMDCAS, MDD, MDR, MDSAP and Canadian Medical Device requirements... Other duties may be assigned, in addition to those identified below Ensures FDA QSR (GMP), FDA OTC, ISO 13485, MDD, CMDCAS, MDR...
psychology and emerging medications to treat disorders such as MDD, GAD and PTSD empathetic and approachable...
requirements (FDA, ISO-13485, MDD 93/42/EEC, Health Canada regulations, etc.) preferred. Why Apply to Drive DeVilbiss...
processes. Prepare plans and documentation required to participate in the Material Development Decision (MDD), the pre-/post...
communicate this information to stakeholders. EU regulations including, but not limited to, MDD 93/42/EEC and IVDMDD 98/79/EC...