Responsibilities:

• Design, configure, and commission automation systems including DCS (e.g., DeltaV), PLC, SCADA, and data historians (e.g., OSI PI).

• Draft, execute, and review commissioning and qualification documentation such as FAT, UAT, IQ, and OQ for automated systems.

• Support system architecture design, control strategies, and library development for manufacturing automation systems.

• Collaborate with manufacturing, QA, and IT teams on system integration, change management, and deviation/non-conformance documentation.

• Perform Computer System Validation (CSV) activities for automated manufacturing equipment and software in compliance with GMP, 21 CFR Part 11, Annex 11, and GAMP5.

• Troubleshoot and resolve automation system issues, ensuring uptime and regulatory compliance.

• Contribute to continuous improvement initiatives for manufacturing automation systems and related processes.

Requirements:

• Bachelor’s degree in Life Sciences, Engineering, Automation, or related field.

• Minimum 4 years of experience in pharmaceutical, medical device, or related manufacturing environments.

• Hands-on experience in automation system commissioning (DCS/PLC/SCADA) and/or data historian systems (OSI PI, DeltaV).

• Strong understanding of manufacturing operations, process control, and automation hardware.

• Knowledge of computerized system requirements in pharma: 21 CFR Part 11, Annex 11, and industry best practices (GAMP5, ISA-88, ISA-95).

• Experience with FAT, IQ, OQ and supporting CSV documentation for automated manufacturing systems.

• Strong problem-solving, cross-functional collaboration, and documentation skills.

• Relevant certifications in automation, CSV, or process systems is a plus.

Interested candidates please apply online or send your latest CV to [email protected]

AlwaysHired Pte Ltd

Reg No: R1549345

EA: 24C2293

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