Contract, initially 4 months (chance of extension)
Project Overview
The role supports a major site expansion project, including a QC lab extension, clean/industrial utilities building, and effluent neutralization plant.
Main Responsibilities
Lead and coordinate technical teams (HVAC, utilities, process, electrical).
Review and validate technical studies and specifications.
Draft and manage contracts with suppliers and subcontractors.
Track project progress, budget, risks, and report regularly.
Identify and resolve technical and organizational issues.
Ensure compliance with GMP and pharmaceutical standards.
Act as a link between engineering firms, developer, and internal teams.
Deliverables
Project plan, specifications, contracts
Meeting minutes, progress reports, KPIs
Planning, budget, cash flow, risk and change documents
Roles and responsibilities matrix
Requirements
15+ years of experience in large pharmaceutical engineeringprojects (>€100M)
Expertise in aseptic processing, clean utilities, GMP batch interface
Strong coordination and stakeholder management skills
Fluent in English
Valid GMP training certificate required before mission starts
