, 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...
that are compliant and conform to 21 CFR 820, MDD/MDR, and ISO 13485:2016. Responsibilities Under direction, Engineering Interns...
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...
. Prepare plans and documentation required to participate in the Material Development Decision (MDD), the pre-/post-Acquisition...
), Multi-Department Direction’s (MDD), and Department Instructions (DI’s). Qualifications: Education/Experience: High...
devices (e.g., ISO, MDD/MDR) High level of competency in Windows environment and with Microsoft Office Tools (Word, Excel...
of relevant Domestic and International Regulations and Industry Standards (e.g. ISO, QSR, UL, MDD, TGA etc.) Proficient in...
, FDA, MDD and regulations applicable to the design and development of medical device/science/technology. Encounters...
, validation, and manufacturing. Exceptional verbal and written communication skills. Familiarity with ISO 13485, MDD, and FDA...