
MEP Engineer
4 days ago
As MEP Engineer, you will be responsible for the design, coordination, installation, testing, commissioning, and maintenance of Mechanical, Electrical, and Plumbing systems in compliance with pharmaceutical GMP standards. You will play a key role in supporting new project setups, cleanroom environments, facility upgrades, and ongoing maintenance in a highly regulated biopharmaceutical manufacturing setting.
Responsibilities:
Design & Coordination
Oversee the design, review, and coordination of MEP systems (HVAC, electrical distribution, fire protection, plumbing, BMS) to meet pharmaceutical regulatory standards.
- Collaborate with process, civil, and instrumentation teams to ensure integrated facility design.
Project Management
Manage MEP components of facility expansion or upgrade projects from concept to completion.
- Supervise contractors, review method statements, and ensure safe execution at site.
- Track project progress, cost control, and ensure adherence to timelines.
Commissioning & Qualification
Participate in FAT/SAT, commissioning, and qualification (IQ/OQ) of MEP systems.
- Work closely with validation, QA, and EHS teams to meet compliance requirements.
Maintenance & Troubleshooting
Oversee preventive and corrective maintenance for all MEP systems, including HVAC, chillers, UPS, electrical panels, and water supply.
- Troubleshoot and resolve system issues in a timely and GMP-compliant manner.
Documentation & Compliance
Prepare and maintain as-built drawings, O&M manuals, risk assessments, and MEP system SOPs.
- Ensure full compliance with local regulations and international GMP requirements.
Requirements:
- Degree or Diploma in Mechanical, Electrical, or Building Services Engineering.
- Minimum 3–5 years of relevant experience, preferably in a pharmaceutical, biotech, or cleanroom manufacturing environment.
- Good knowledge of HVAC systems, cleanroom classification, and regulatory standards.
- Familiarity with AutoCAD/BIM, electrical load calculations, and HVAC balancing tools.
- Experience with regulatory audits (e.g. GMP, EHS) is desirable.
- Good communication, team coordination, and problem-solving skills.
Yvonne Ong EA License No.: 02C3423 Personnel Registration No.: R1549551
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