PMO Doc Control Lead

PMO Doc Control Lead – US, Ohio – Initial 12-Month Contract – Life Sciences

Be part of a next-generation pharmaceutical project that’s transforming how medicines are made. We’re supporting a major new-build facility in Ohio, a multi‑billion‑dollar investment designed to push the boundaries of science and engineering. We’re looking for a PMO Doc Control Lead to support this project and help deliver this world‑class program.

• Define, document and govern the end-to-end flow of design documents, CTOPs, VTOPs, addenda and MC/TCCC approvals from EPCM delivery through PM, CQ/TMP and Operations handover.
• Identify the approved repository for each document set and ensure the TMP integrates and uses EIDA, Kneat, MCPlus, EPIC, Aconex, Procore and Unifier in line with the agreed architecture.
• Ensure EPIC remains the master repository for construction turnover documentation and Aconex controls correspondence, transmittals and formal document workflows.
• Own the document requirements and deliverable obligations embedded in Client contracts; translate them into clear expectations for PMs, EPCMs, CMs, vendors, CQ firms and the TMP.

• Bachelor's degree in Engineering, Science, Information Management or a related discipline. Equivalent senior-level experience may be considered only if accepted by the hiring manager.
• Extensive document control / information management on large capital programs.
• GMP pharmaceutical or biotechnology manufacturing capital-project experience.
• Technical ownership of contractor deliverable registers, transmittals, review