Mechanical Design MEP Engineer (Pharmaceutical facilities/ Greenfield projects)

Manpower Staffing Services; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A staffing agency in Singapore is seeking an experienced individual to manage Mechanical, Electrical, and Plumbing (MEP) systems for pharmaceutical facilities. The role involves design coordination, project management, and ensuring compliance with quality standards. Candidates should have a strong background in engineering and project execution within the pharmaceutical sector.

Responsibilities

• Design, review, and coordinate MEP systems for pharmaceutical facilities.
• Manage MEP aspects of new projects from concept to completion.
• Ensure designs comply with local codes and safety regulations.

Job description

Responsible for designing, coordinating, and overseeing Mechanical, Electrical, and Plumbing (MEP) systems for pharmaceutical facilities to ensure compliance with GMP standards. Key duties include developing design drawings and specifications, collaborating with cross-functional teams, managing project execution, conducting site inspections, performing commissioning and qualification (IQ, OQ, PQ) activities, and ensuring all work adheres to safety and regulatory requirements.

Design and coordination

• Design, review, and coordinate MEP systems like HVAC, electrical distribution, fire protection, and plumbing to meet pharmaceutical GMP standards.
• Develop detailed design drawings, specifications, bills of materials, and technical reports.
• Collaborate with architects, civil engineers, and other teams to ensure integrated facility design.

Project management and execution

• Manage MEP aspects of new projects, expansions, or upgrades from concept to completion.
• Supervise contractors and ensure safe execution of work on-site.
• Conduct site visits and inspections to monitor progress and ensure design compliance.
• Assist with project budgeting, scheduling, and cost control.

Compliance and qualification

• Ensure designs comply with local codes, safety regulations, and pharmaceutical industry standards.
• Participate in and oversee testing, commissioning, and qualification (IQ, OQ, PQ) activities.
• Collaborate with Quality Assurance (QA) and Validation teams to meet compliance requirements.

Technical support and maintenance

• Provide technical support during project execution, troubleshooting, and commissioning phases.
• Participate in equipment improvement efforts and contribute to operational excellence initiatives.