Group 10

  • Administrative activities
  • Import/export of documents to and from Pluto
  • Support to EDMS activities and library services –data clean-up, training logs, load of documents, re-indexing, load of articles
  • • Provide review of packaging texts.
  • Contribute to data entry in PLG tools enabling measurements of KPI, metrics for regulatory services supplied by the platform/hub
  • Others
  • Assist in the preparation of Standard Operating Procedures (SOPs) and Working Practice Documents (WPDs).
  • Assist in the management of ProductLife Quality Management System.
  • To participate in training as required for ProductLife staff.
  • Support the Pharmacovigilance group in the production of Regulatory Authority and Ethics Committee documentation.
  • To comply with the company’s policies and procedures to meet statutory, quality and business requirements within the overall strategy and objectives.

Group 12

  • Currently studying for a bachelor or master’s degree related with Library & Information science
  • Is structured and detail-oriented, Excellent organizational and interpersonal skills
  • Used to use and work with IT tools
  • Good understanding of regulatory tracking database software, eDMS, MS Word, MS Excel would be a plus
  • Eager to learn and deliver high quality work
  • Understands and speaks fluent English and Danish for daily contacts
  • Is in the beginning of their studies or has a study period of minimum 2 years left

Student RIMS 626, 627