Commissioning Engineer

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