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This communication presents a comprehensive investigation into the impact of mixing on the synthesis of water-in-water Pickering emulsions. The approach employs commercial-grade oppositely charged nanoparticles within two distinct fluid phases, facilitating self-assembly and the formation of aggregates with variable sizes and compositions. Enhanced interfacial area, achieved through aggregate adsorption at the interface, elevates the Gibbs detachment energy of particles between the two aqueous phases, leading to stable emulsion formation. We further explore the effect of various mixing devices, including high-pressure and sonic wave mixing. Our findings reveal that mixing within the aqueous phase critically influences emulsion size, with sonicator-assisted mixing producing smaller droplets than homogenizer mixing. Both devices yield poly-dispersed droplet size distributions. Interestingly, the droplet size correlates well with the Hinze scale (hd), and the Kolmogorov length scale (ld) exhibits good correspondence within a specific operating range. The proposed method introduces a streamlined, one-step synthesis process for easy preparation, demonstrating excellent stability for a minimum of 30 days. This study pioneers the investigation of mixing effects within an aqueous two-phase system utilizing a Pickering emulsion template.