MES Automation Engineer (Pharmaceutical) - Choa Chu Kang

Responsibilities:

• Lead the automation engineering team in performing project activities such as Batch Design, implementation, and testing.
• Collaborate with engineers, designers, partners, and clients to deliver advanced control systems that enhance process efficiency, product quality, and profitability.
• Design and implement Distributed Control Systems (DCS) aligned with S88 standards for manufacturing plants.
• Contribute to system architecture, design specifications, control strategies, and library development.
• Support testing, on-site commissioning, and qualification of control systems.
• Prepare lifecycle documents, electrical panel designs, control architectures, and wiring drawings in accordance with GMP standards.
• Provide day-to-day support for automation systems in manufacturing operations.
• Develop engineering standards to improve project execution efficiency and accuracy.
• Participate in the design and implementation of MES systems and electronic Batch Records (eBR) for pharmaceutical manufacturing processes.

Requirements:

• Bachelor’s degree in Engineering or a related field.
• Minimum 3 years of relevant experience, preferably within the pharmaceutical industry in projects or operations.
• Hands-on experience with Emerson DeltaV DCS is a strong plus.
• Good understanding of Batch S88 standards (Control Modules, Equipment Modules, Phases, Recipes, Units, etc.).
• Experience with MES platforms and eBR systems is highly desirable.
• Preferably with hands-on exposure to eBR systems beyond user-level (e.g., configuration, design, troubleshooting).
• Knowledge of automation hardware and industrial networking technologies.
• Interest or experience in pharmaceutical and biologics GMP processes, including computer systems validation.
• Familiarity with the Validation Lifecycle (URS, FAT/SAT, Commissioning, IQ/OQ/PQ protocols), international regulations, and industry best practices.
• Experience interacting with or preparing documentation for management and regulatory agencies is an advantage.
• Background in handling manufacturing deviations, determining product impact, root cause analysis, and implementing corrective/preventive actions (CAPA).

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

AlwaysHired Pte Ltd

EA: 24C2293

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