Job Summary:
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 an added advantage.
- Good communication, team coordination, and problem-solving skills.
