Manufacturing Automation Engineer (CSV, Pharmaceutical)

ALWAYSHIRED PTE. LTD.; Singapore; On-site; SGD 60,000 - 85,000; Full time

Job summary

A Singapore-based automation solutions provider is seeking an experienced Automation Systems Engineer to design, configure, and commission complex automation systems. Candidates should hold a Bachelor's degree in Engineering or related fields, with at least 4 years of experience in the pharmaceutical or medical device industries. Responsibilities include collaborating across teams and ensuring compliance with industry standards. Interested candidates can apply online or send their CV to the provided email.

Qualifications

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

Responsibilities

• Design, configure, and commission automation systems including DCS, PLC, and SCADA.
• Support system architecture design and control strategies.
• Collaborate with teams on system integration and documentation.

Skills

Automation system commissioning

Problem-solving

Cross-functional collaboration

Education

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

Tools

DCS (e.g., DeltaV)

PLC

SCADA

Data historians (e.g., OSI PI)

Job description

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 [e-mail]

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