PMO Document Control Lead — Life Sciences (Contract)

QCS Staffing; Kentucky; On-site; USD 90,000 - 130,000; Full time

Job summary

QCS Staffing seeks a PMO Doc Control Lead for a US-based, Ohio project in Life Sciences. The role governs design documents, approvals, and turnover packages across EPCM and operations handover, ensuring master repositories and proper workflow.

You will own document requirements, manage transmittals and reviews, and coordinate with PMs, EPCMs, vendors and the TMP to ensure compliance and timely delivery.

Qualifications

• Bachelor's degree or equivalent senior-level experience considered with approval.
• Extensive document control / information management on large capital programs.
• GMP pharmaceutical or biotechnology capital‑project experience.
• Technical ownership of contractor deliverable registers and transmittals.

Responsibilities

• Define and govern end-to-end flow of design documents and approvals.
• Identify approved repositories and ensure integrations with project tools.
• Ensure master repositories and controls for turnover documentation.
• Translate contract requirements into clear expectations for PMs and vendors.

Skills

Document control

Information management

GMP experience

Capital projects

PM/CM coordination

Contract/workflows

Education

Bachelor's degree in Engineering/Science/IM

Equivalent senior-level experience

Tools

EPIC

Aconex

Procore

Unifier

Kneat

EIDA

MCPlus

Job description

QCS Staffing seeks a PMO Doc Control Lead for a US-based, Ohio project in Life Sciences. The role governs design documents, approvals, and turnover packages across EPCM and operations handover, ensuring master repositories and proper workflow.

You will own document requirements, manage transmittals and reviews, and coordinate with PMs, EPCMs, vendors and the TMP to ensure compliance and timely delivery.