[Hiring] Technical Project Manager @GMP Pros, Inc.

Role Description

The TPM owns the delivery. This is not a coordination or reporting role — the TPM is responsible for:

• Detailed MS Project schedule
• Critical path
• Risk identification and escalation
• Cross-workstream dependency management
• Full accountability for GMP Pros' performance under the Oxford subcontract

The TPM also owns the validation documentation layer, which includes:

• Protocol planning
• Kneat incident coordination
• Veeva VQD documentation oversight across both workstreams

This person must be comfortable operating in a three-party governance structure (GMP Pros / Oxford / GSK) with competing priorities and significant schedule pressure.

Qualifications

• 5+ years of project management experience in FDA-regulated pharmaceutical or biopharmaceutical manufacturing environments
• Direct experience managing MES or eBR implementation projects (Siemens OpCenter, Rockwell PharmaSuite, Emerson DeltaV Batch, or equivalent) from design through PPQ
• Proficiency with MS Project for schedule development, critical path definition, and baseline management — not just Gantt creation, but active schedule management under pressure
• Working knowledge of 21 CFR Part 11, EU Annex 11, and the CSV/CQV lifecycle: IQ/OQ/PQ structure, validation protocol authorship, and documentation requirements in regulated systems
• Experience with Kneat or an equivalent electronic validation management system for protocol authorship and incident management
• Experience with Veeva Vault QualityDocs (VQD) or an equivalent QMS/DMS for managing validation lifecycle documentation
• Demonstrated ability to manage risk registries, escalate proactively, and protect schedule without creating noise — GSK will be watching this closely
• Prior experience in a prime/subcontract delivery model or multi-vendor program environment preferred

Requirements

• PMP certification or equivalent project management credential preferred
• Direct experience with Siemens OpCenter Execution Pharma (formerly SIMATIC IT)
• Experience supporting PPQ execution and post-go-live hypercare activities
• Familiarity with GSK, Pfizer, Merck, Lilly, or other large pharma MES environments
• Familiarity with SAP-MES and OSI-PI integrations in a pharma manufacturing context

Key Tools & Platforms

• MS Project (required)
• Kneat (preferred)
• Veeva VQD (preferred)
• Siemens OpCenter (familiarity required)
• SAP
• OSI-PI / PI System
• Microsoft Teams / SharePoint