The prefrontal cortex (PFC) maintains goal information for action planning, but how recurrent circuits preserve it in an action-usable form over behavioral timescales remains unclear. Here we ask whether short-term synaptic plasticity (STP) can stabilize goal information as action-usable, goal-conditioned dynamics. We incorporated STP into a PFC-inspired reservoir computing model with basal-ganglia-inspired temporal-difference readout learning, and evaluated paired models with and without STP across 100 independently generated networks in a multistep goal-directed action-selection task with delayed execution. Goal identity was highly decodable during the delay even without STP, so STP was not required to form a linearly readable goal representation. Under state noise, however, success without STP fell from 75.8% to 49.5%, whereas the model with STP remained essentially unchanged (91.8% without noise versus 89.2% under noise; paired Cohen's dz=1.31). Time-resolved decoding, state-space separability, and action-value-difference analyses showed that STP preserved goal information as action-relevant goal-conditioned dynamics available at later action opportunities. Gain-matched and STP-state perturbation controls argued against a simple fixed recurrent-scaling explanation and supported online, history-dependent synaptic modulation. Effective-connectivity analyses showed delay-period goal-specific patterning that increased toward the later part of the trial with STP, where it should be read as goal- and task-state-conditioned patterning; effective connectivity without STP was time-invariant. A grid search identified a facilitation-dominant range of STP time constants associated with high success rates. These results suggest that STP supports robust goal-conditioned dynamics through dynamic modulation of goal-dependent effective recurrent connectivity.