Polymer chains undergoing adsorption are expected to show universal critical behavior which may be investigated using partition function zeros. The focus of this work is the adsorption transition for a continuum chain, allowing for investigation of a continuous range of the attractive interaction and comparison with recent high-precision lattice model studies. The partition function (Fisher) zeros for a tangent-hard-sphere N-mer chain (monomer diameter σ) tethered to a flat wall with an attractive square-well potential (range λσ, depth ε) have been computed for chains up to N=1280 with 0.01≤λ≤2.0. In the complex-Boltzmann-factor plane these zeros are concentrated in an annular region, centered on the origin and open about the real axis. With increasing N, the leading zeros, w_{1}(N), approach the positive real axis as described by the asymptotic scaling law w_{1}(N)-y_{c}∼N^{-ϕ}, where y_{c}=e^{ε/k_{B}T_{c}} is the critical point and T_{c} is the critical temperature. In this work, we study the polymer adsorption transition by analyzing the trajectory of the leading zeros as they approach y_{c} in the complex plane. We use finite-size scaling (including corrections to scaling) to determine the critical point and the scaling exponent ϕ as well as the approach angle θ_{c}, between the real axis and the leading-zero trajectory. Variation of the interaction range λ moves the critical point, such that T_{c} decreases with λ, while the results for ϕ and θ_{c} are approximately independent of λ. Our values of ϕ=0.479(9) and θ_{c}=56.8(1.4)^{∘} are in agreement with the best lattice model results for polymer adsorption, further demonstrating the universality of these constants across both lattice and continuum models.