The spinel group is a growing family of materials with general formulation AB₂X₄ (the X anion typically being a chalcogen like O and S) with many advanced applications for energy. At the time being, the spinel zinc gallate (ZnGa₂O₄) arguably is the ternary ultra-wide bandgap bipolar oxide semiconductor with the largest bandgap (~5eV), making this material very promising for implementations in deep UV optoelectronics and ultra-high power electronics. In this work, we further demonstrate that, exploiting the rich cation coordination possibilities of the spinel chemistry, the ZnGa₂O₄ intrinsic conductivity (and its polarity) can be controlled well over 10 orders of magnitude. p-type and n-type ZnGa₂O₄ epilayers can be grown by tuning the pressure, oxygen flow and cation precursors ratio during metal-organic chemical vapor deposition. A relatively deep acceptor level can be achieved by promoting antisites (Zn_Ga) defects, while up to a (n > 10¹⁹ cm^-3) donor concentration is obtained due to the hybridization of the Zn-O orbitals in the samples grown in Zn-rich conditions. Electrical transport, atomic and optical spectroscopy reveal a free hole valence band conduction (at high temperature) for p-ZnGa₂O₄ while for n-ZnGa₂O₄ a (Mott) variable range hopping (VRH) and negative magnetoresistance phenomena take place, originated from “self-impurity” band located at Ev+ ~3.4 eV. Among arising ultra-wide bandgap semiconductors, spinel ZnGa₂O₄ exhibit unique self-doping capability thus extending its application at the very frontier of current energy optoelectronics.