Process/CQ Engineers
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 protocols
• Reviews and approves Basis of Design (BOD) and detail design of assigned systems i.e. PFDs, P&IDs etc.
• Tracks HAZOP action items
• Attends 30%, 60% and 90% model reviews
• Supervises and executes Site Acceptance Testing (SAT) and commissioning activities
• Ensures Vendor Document Requirements (VDR) meet requirements

EDUCATION AND EXPERIENCE:

• Bachelor degree in relevant field
• Experience in pharmaceutical industry
• Experience with manufacturing process equipment such as Bioreactors, HTST, Viral Filtration, Formulation/filling
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