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Responsibilities:
Experience in pharmaceutical cGxP setting with the ability to generate CSV deliverables
Experience in GMP regulated environment.
Proven attention to detail and organization in project work
Capable of working on assigned tasks without mentorship.
General understanding of capital equipment implementation and process knowledge
Verifying system drawings including ability to review and as built P&IDs (piping and instrumentation drawings) and I&C (instrumentation and controls) drawings as well as verifying electrical schematics with support of an electrical engineer
Date Posted: 20 May 2024
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