Head of Quality Control (Relocation Package Available)

Ohio | Commercial Biologics | Head of Quality ControlGlobal Life Science Hub is partnered with a commercial-stage biologics CDMO, a serious force in advanced therapy manufacturing with the resources and reach of a global heavyweight behind it, as it strengthens its quality organization in Ohio. As the site pushes deeper into commercial manufacturing across advanced biologics and cell & gene therapies, we're searching for a Head of Quality Control to take full ownership of the QC function and build it into a best-in-class operation.This is a rare opportunity to step into a pivotal leadership role at a site where quality sits right at the center of the growth story. You'll lead the analytical and microbiology QC organization, partner closely with senior technical and regulatory leadership as the wider quality function continues to evolve, and set the standard for how commercial release is delivered, faster, right-first-time, and inspection-ready.The mandate is clear: bring experienced, commercial-grade quality leadership to a function that underpins every batch that leaves the building.Key ResponsibilitiesLead the QC organization across analytical and microbiology, supporting raw materials, in-process, release, and stability testing for commercial biologics.Drive down cycle times across batch release, investigation closure, and method turnaround, while raising right-first-time performance.Own QC's contribution to investigations, OOS, deviations, and CAPA, with a focus on robust root cause analysis and timely closure.Partner with Analytical Development, MSAT, Manufacturing, and QA to support tech transfer, scale-up, and commercial readiness.Build, mentor, and develop a high-performing QC team, instilling a culture of ownership and transparency.Represent QC in client-facing forums and regulatory inspections, and act as a credible quality voice with senior client counterparts.What We're Looking ForSignificant QC leadership experience in a commercial GMP biologics environment. This is a non-negotiable.A track record of improving quality performance and turnaround times in a commercial manufacturing or CDMO setting.Strong grounding in analytical and microbiological methods for biologics (HPLC, CE, ELISA, cell-based assays, compendial methods).Experience partnering with technical and regulatory leadership, and standing up or restructuring QC functions.Large-molecule biologics background essential; cell & gene therapy exposure a strong plus.Please Note: These are full-time, on-site roles based in Ohio.Relocation assistance is available, and we welcome applications from experienced QC leaders across the U.S. who are open to relocating.