required documentation within designated timelines. Work with internal databases to record and document accurate
Supervisor.
repairs to Supervisor. Compiling and filing of documentations related to product inspection and test results Compiling and storing of final product COC/COA documents. Conduct weekly and/or monthly verification of
innovation.
Qualifications:
reviewing QMS documentation in relation to activities – provide input where documentation can be improved
Albert Heijn Capturing of compliance related documents and procedures, as well as generating reports and Safety). Capturing of compliance related documents and procedures, as well as generating reports
activities Review and ensure essential regulatory documentation available and up to date across all studies Operating Procedures (SOPs), and Regulatory Essential Documents per sponsor requirements Coordinate staff training studies and SOPs, knowledge of clinical research documentation Computer literate with the ability to create
activities Review and ensure essential regulatory documentation available and up to date across all studies Operating Procedures (SOPs), and Regulatory Essential Documents per sponsor requirements Coordinate staff training studies and SOPs, knowledge of clinical research documentation Computer literate with the ability to create
activities
ASSURANCE