Being client representative for all Process-related activities and installations
Supporting the E.O in getting the necessary information at the battery limits of the package
Ensuring alignment between equipment suppliers and client Specification and Guidance
Reviewing design and technical documentation
Following-up construction & all testing activities falling under the package' scope
Ensure systems start-up and punch list solving
Provide projects support in terms of technical expertise, contractors' management and troubleshooting capabilities.
Facilitating handover process towards the end user
Review documents for ITT process & contractors' selection
Detailed design studies review with contractors, including follow up of yellow reviews, functional specifications, piping and vessel design, 3D-model
Works supervision, Walkdowns performed, FAT, SAT, IQ, OQ + punch list follow-up
Provisional and final acceptances
Final handover for process packages and systems.
Experience in the Bio-Pharmaceutical industry
Perform his/her work in an EHS and cGMP high-demanding environment.
Chemical or Process engineering degree is required.
10 years of experience in the field of Bio or Vaccine Process engineering is required, ranging from early design to facility start-up.
Deep knowledge of commissioning and qualification of similar production trains is a must.
Experience with Centrifugation and Ultrafiltration systems is a must.