Lead Scheduler – CQV / Pharma

Pennsylvania

Perm or Contract

My client, a leading built environment construction consultant, are seeking an experienced Lead Scheduler to be site based with their Client in Pennsylvania, USA, to support a major capital investment programme at a manufacturing and R&D campus.

You will own and maintain the Integrated Master Schedule (IMS) across all project phases including design, procurement, construction, CQV, and handover.

The back end focus is key and you will take ownership of the CQV schedule as a standalone workstream, integrating it fully within the IMS.

You will have a minimum 10 years of project scheduling experience on capital projects, with demonstrable pharma or biotech sector experience and extensive hands-on CQV scheduling experience — must be able to demonstrate ownership of IQ/OQ/PQ scheduling at system level.

email stephen@ruetwo.com