Commissioning Engineer
Summary
Commissioning Engineer supports start-up and operational readiness for pharma/biotech manufacturing, executing qualification protocols and troubleshooting DeltaV control systems in GMP-compliant environments.
Main Responsibilities:
Support commissioning, qualification, start-up, and operational readiness activities for pharmaceutical/biotechnology manufacturing facilities and process systems.
Execute commissioning and qualification protocols for process equipment, utilities, and automation systems in compliance with GMP requirements.
Monitor and optimize process control systems, including temperature control, pressure control, flow control, and TCU
Support and troubleshoot DeltaV control system operations during commissioning, start-up, and manufacturing campaigns.
Perform system testing, loop checks, functional testing, and operational verification activities.
Support CIP (Clean-in-Place) and SIP (Steam-in-Place) operations, troubleshooting, and performance verification.
Work closely with engineering, automation, validation, operations, and project teams to ensure successful project execution.
Identify, investigate, and resolve commissioning and operational issues to minimize downtime and ensure project milestones are achieved.
About You:
Degree/ Diploma in Chemical Engineering, Biotechnology, Pharmaceutical
Engineering, Mechanical Engineering, Electrical Engineering, or related disciplines.
Experience in pharmaceutical, biotechnology, biologics, or life sciences manufacturing environments.
Must have ex-biotech experience or project engineers with commissioning experience.
Able to work on 12 hours rotating shifts, morning shift/ night shift, 24/7 operations.
Contract Duration: 6 months