Manage end-to-end technical changes to production equipment: pump sizing and mechanical design (e.g., pump sizing, piping specifications), planning, coordination of contractors, commissioning and handover to operations in compliance with cGMP and site standards
Act as the engineering point of contact for technical and quality investigations and actively contribute to HSE and continuous improvement initiatives
Lead the design, execution and commissioning of equipment modifications and small installations; coordinate external partners and ensure a smooth handover to operations
Structure and manage work packages, milestones and interfaces with production and maintenance
Provide engineering expertise during investigations (deviations, root cause analyses) and contribute to corrective/preventive action plans
Collaborate cross-functionally (production specialists, maintenance, project managers) to optimize manufacturability and reliability
Promote HSE best practices and continuous improvement on the shop floor and within projects
Requirements
Master’s degree in mechanical engineering or equivalent technical qualification
Strong knowledge of biotech/pharmaceutical production equipment and skids; expertise in mechanical design (e.g., pump sizing, piping specifications)
5+ years of on-site experience in pharmaceutical manufacturing, with proven success in project execution, contractor/work management and commissioning
Strong knowledge of cGMP and regulations applicable to pharmaceutical production
Demonstrated leadership, rapid situational analysis and the ability to manage multiple activities simultaneously (from field work to stakeholder coordination)
Excellent communication skills with internal and external partners; fluent French and a good level of English (spoken and written)
Benefits
Technical and personal support for each project and active career development follow-up
Access to training to develop your professional skills