a) Write, review and update plans, protocols and reports, including DA/DV, DA/DV Shelf Life, DV Transportation, Engineering Reports and Summary reports.
b) Prepare Pre-Requisites to Execute and Component Information Matrix before DV activities start. Double check and confirm the components’ revisions, batch numbers, component approval references are correct.
c) Check Test Instructions’ revisions are applicable for DV activities and confirm engineers’ training record are complied with the TIs.
d) Use MiniTab for different statistical methods for data analyses.
e) Deviation Tracking Sharepoint application and maintenance.
f) Syringe application and disposal for all projects.
g) Join regular weekly meeting with Sweden Office and customer (Pfizer) to discuss project progress.