Life Sciences Project Manager Automation Engineer – Brussels/Wallonia

About Capgemini

Capgemini is a global leader in partnering with companies to transform and manage their business by harnessing the power of technology. The Group is guided everyday by its purpose of unleashing human energy through technology for an inclusive and sustainable future. It is a responsible and diverse organization of 270,000 team members in nearly 50 countries. With its strong 50 year heritage and deep industry expertise, Capgemini is trusted by its clients to address the entire breadth of their business needs, from strategy and design to operations, fueled by the fast evolving and innovative world of cloud, data, AI, connectivity, software, digital engineering and platforms. The Group reported in 2020 global revenues of €16 billion.
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Your role

  • Lead the automation design end to end with engineering office / contractors
  • Responsible for the approval for the conceptual & basic of design + design specification documents
  • Ensure smooth communication & follow-up along with automation experts, stakeholders & engineering offices
  • Ensure the compliance with GMP, Eudralex, FDA & EHS requirements
  • Responsible of finding the best solutions for technical problems / issues and their implementation according to GMP quality requirements
  • Automation contractor follow-up & management (set-up & challenge of the offers, capacity management (CAPA Plan), progress & invoicing follow-up; quality delivery tracking (KPIs), governance management, …)
  • Cross-planning integration along with the mechanical validation according to overall CAPEX project’s milestones in place
  • Day to day coordination:
    • Tier meeting (check-in / check-out (if needed))
    • Project stakeholders/SMEs/Client/… overall coordination and alignment
    • Dashboard follow-up and communication (planning, KPIs, CAPA plan, actions plans, issues log,
    • EHS requirements monitoring
    • Site compliance tracking (training matrix, access, multi-zone/site/MPU control)
    • Quality spot-check of ongoing deliverables done by both the internal & external CSV/autom validation team (RFT)
    • Technical support (if needed)
  • Work in full collaboration along with the Start-up Service contract SPOC
  • Use existing templates & Wow of Stratup Service contract (PFU project follow-up template, planning, governance & reporting, KPIs, …)
  • Standardize automation approach & delivery across CAPEX project at GSK
  • Gain efficiency on overall validation with a firm alignment along with the mechanical one
  • Priority & emergency management
  • Coordinate & develop a multi-skills competency center to offer best automation solution for each project (multi supplier diversification + internal support hub development.

Your profile

  • A Master in Engineering with at least 5 to 10 years of experience
  • An automation know-how: Archestra, Wonderware, DCS, Osi-PI, Siemens …
  • A validation know-how: CSV, V-Cycle, ASTM2500 (as a plus), GAMP 5
  • A “change management” approach
  • A GMP background / pharmaceutical industry
  • A 5 years (min) as automation engineer (other industries other than the pharmaceutical is relevant)
  • A good communicator & team player
  • An autonomous, rigorous & proactive drive
  • The capacity to adapt quickly in complex environment
  • A project management expertise (certification is a plus)
  • A planning & cost capabilities with proven experience on this role
  • A native ( or very fluent) French speaker & fluent in English



Posted on:

June 2, 2021

Experience level:


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