The person will be responsible for performing source data verification (SDV) and technical (Novstyle) quality control (QC) of NIBR submission documents (simple to medium complexity) to ensure both content and format fulfil requirements, collaborate with globally located NIBR scientific personnel to ensure finalization of the documents, according to timelines and quality requirements. The person will compile, integrate and publish applicable documents with state-of-the-art word pro-cessing, electronic publishing and document management systems in collaboration with the responsible author(s).You will resolve technical document or workflow issues as applicable on the documents being processed.
Document Quality Specialist
Unser Kunde ist im Medien Bereich tätig.
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
As per Industry
3-5 years of relevant work experience with electronic document management systems and document review is required with basic understanding of clinical and nonclinical information contained in a submission dossier.
Deutsch: Of value
Englisch: Very good
If you are interested then kindly send your resume to firstname.lastname@example.org