Document Control Specialist

Náplň práce, pravomoci a zodpovědnosti

Ref. č.: 16-14-262314. The Document Control Specialist will compile and maintain control records, quality documents and files related to the release of medical device software, drawings, components and documents for a cross functional set of groups including engineering, manufacturing, quality and purchasing. The Document Control Specialist is responsible for the creation and release of Engineering Change Orders (ECO’s), Deviations and maintenance of the training process.ESSENTIAL FUNCTIONS:Work with ECO originators to complete ECO packages and Deviations in Arena PLMFollow NDS documented standard operating proceduresManage and monitor training quality system elements as neededMaintain effective change and version control of all documents, components and device itemsWrite and update documentation and processes as needed

Osobnostní předpoklady a dovednosti
Minimum 1 year Document Control Specialist experience (Arena PLM highly desired/Agile PLM acceptable)Direct experience in Medical Device Quality Systems preferredExperience with a variety of software programs (particularly MS Excel, MS Word and Adobe Acrobat)Ability to analyze complex information and summarize into a concise, easy to read text for reviewersExcellent interpersonal skills, communication and organizational skills particularly across multiple levels of managementAbility to speak and write English fluentlyExcellent typing skills (>50 words per minute)Strong customer service skills and time managementDetail oriented and accurate

Práce v oboru: Školství, vzdělávání, věda, výzkum

Lokality: Brno-město, Brno-venkov