Job Description:
The project scope involves the full lifecycle from detail design phase all the way through to the commissioning and qualification of the new plant.
Generation User Requirement Specification (URS), reviews and approves system lifecycle documentation, generates FAT, SAT and commissioning protocolsReviews and approves Basis of Design (BOD) and detail design of assigned systems i.e. PFDs, P&IDs etc.Tracks HAZOP action itemsAttends 30%, 60% and 90% model reviewsSupervises and executes Site Acceptance Testing (SAT) and commissioning activitiesEnsures Vendor Document Requirements (VDR) meet requirements
Education and experience:
Bachelor degree in relevant fieldExperience in pharmaceutical industryExperience with manufacturing process equipment such as Bioreactors, HTST, Viral Filtration, Formulation/filling