The EDQM knowledge base is accesible free of charge. Details for the glycine monograph can be seen here:
https://extranet.edqm.eu/4DLink1/4DCGI/ ... w/mono/614
There is also a chromatogram (just click on the "availabe" next to "chromatogram").
The first thing that hits the eye is that in your chromatograms the peaks are too early! The first peak elutes at ~2.5 minutes, which corresponds roughly to the dead time of the method (for a 250x4.6mm column at 1mL/min). This means you don't have enough retention. In the exemplary chromatogram, the first peak is at ~4 minutes (which still means very low retention with k~0.6, but at least there is some retention).
Furthermore your peaks don't look very nice concerning asymmetry and width, but the lacking retention is the first thing to care about. Check and double-check that the mobile phase has been prepared correctly, than prepare a new batch of mobile phase and try again. The method uses an ion-pairing reagent, so the column needs some time to get fully equillibrated - to be sure, you may equillibrate the column overnight at a low flow rate.
If this doesn't help to get retention, get hold of a Purospher Star and try that column.