Project Engineer (Pharma) (SG)
Job Description We’re looking for a Project Engineer to drive on-site project implementation and contribute directly to our business growth. This role is crucial for managing the entire lifecycle of engineering projects at GMP facility. Key Responsibilities Manage medium sized capital engineer projects, from feasibility studies through commissioning and handover. Collaborate cross-functionally with stakeholders to […]
Mechanical Engineer – HVAC & Cleanroom (Pharma) (SG)
Job Description We’re looking for an experienced Mechanical Engineer specializing in HVAC and Cleanroom systems to join our team in Singapore. This role focuses on project execution in regulated manufacturing environments. Key Responsibilities Manage HVAC and cleanroom project phases, primarily focusing on construction, testing, and commissioning. Coordinate stakeholders including clients, contractors, and consultants. Review project documentation like shop drawings and as-builts. Perform cleanroom […]
Mechanical Technician (Pharma) (SG)
Job Description We’re hiring a dedicated Mechanical Technician to ensure the operational excellence of GMP manufacturing production and facility equipment in Tuas, Singapore.This is an 8-hour shift-based role, with shifts from 7:30 AM to 4:00 PM and 3:30 PM to 12:00 AM. Key Responsibilities Troubleshoot & Repair: Perform repairs on production, packaging, and critical utility systems (e.g., compressed air, steam, refrigeration, […]
Utilities Engineer (Pharma) (SG)
Job Description We are seeking a highly skilled Utilities Engineer to join our pharmaceutical project team in Singapore. In this role, you will be responsible for the design, commissioning, qualification, and validation (CQV) of utility systems, ensuring that all processes meet stringent regulatory and quality standards. Your expertise will be essential in the successful delivery […]
CSV Engineer (Pharma) (SG)
Job Description We are urgently seeking a highly experienced CSV Engineer to join our pharmaceutical team in Singapore. The ideal candidate will have a minimum of 5-7 years’ experience in the pharmaceutical manufacturing environment, with a strong proficiency in computer system validation (CSV) protocols and reports execution and review Key Responsibilities Prepare, execute, and review […]