Support the management of project documentation, from initiation to handover, meeting all milestones within the project program to ensure timely project progression.
Current Good Manufacturing Practices (cGMP) in biopharmaceutical manufacturing environment
General understanding on biopharmaceutical manufacturing processes
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Possesses a working knowledge of chemical reaction mechanisms and is proficient in chemical synthesis unit operations. Capable of independently, safely, and accurately executing key steps in the laboratory for various chemical reactions, including charging, in-process control (IPC), quenching, work-up, and crystallization.
Perform preliminary analysis of spectra such as NMR, HPLC, and LCMS with minimal supervision.
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Coordinate and support planned maintenance activities so work is executed safely, to schedule, and to the right standard.
Apply reliability methods to reduce repeat failures using data, structured problem solving, and condition-based insights (e.g., vibration/alignment/oil analysis/ultrasonic checks where relevant).
Support reliability strategy activities such as asset criticality, functional analysis, FMEA, and risk-based maintenance planning, helping ensure the right work at the right time.
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Coordinate and support planned maintenance activities so work is executed safely, to schedule, and to the right standard.
Apply reliability methods to reduce repeat failures using data, structured problem solving, and condition-based insights (e.g., vibration/alignment/oil analysis/ultrasonic checks where relevant).
Support reliability strategy activities such as asset criticality, functional analysis, FMEA, and risk-based maintenance planning, helping ensure the right work at the right time.
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