Pharma Engineering Project Manager (CAPEX)

No-Deviation-Pte.-Ltd; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

No deviation in Singapore is seeking an experienced Project Manager (Engineering) to lead pharmaceutical engineering and CAPEX projects from initiation to handover. You will drive project planning, cost and schedule control, risk management and supplier coordination to ensure safe, compliant delivery within scope and budget.

The role requires strong stakeholder management, experience with multi-phase projects and a focus on HSE, quality and regulatory alignment in a GMP environment.

Qualifications

• Degree in Engineering or related technical discipline.
• Strong experience in engineering project management / CAPEX project delivery within regulated manufacturing.
• Proven ability to manage projects across Concept, Definition Design, Procurement, Construction, Commissioning, Handover.

Responsibilities

• Develop Project Charters, Business Cases, CAPEX requests and initiation docs.
• Define project scope, execution strategy and delivery objectives.
• Develop and maintain: schedules, WBS, CBS, cost estimates and forecasts, execution and controlling plans.
• Conduct risk assessments for safety, quality, technical and execution risks.
• Establish change control, risk management and reporting processes.
• Coordinate sourcing, tendering, vendor selection and contract award.
• Lead engineering consultants, vendors and contractors; oversee safety and quality.

Skills

Engineering project management

CAPEX project delivery

Stakeholder management

Cost forecasting

Education

Engineering degree

Job description

No deviation in Singapore is seeking an experienced Project Manager (Engineering) to lead pharmaceutical engineering and CAPEX projects from initiation to handover. You will drive project planning, cost and schedule control, risk management and supplier coordination to ensure safe, compliant delivery within scope and budget.

The role requires strong stakeholder management, experience with multi-phase projects and a focus on HSE, quality and regulatory alignment in a GMP environment.