CQV Project Lead - Biopharma & GxP

Esco Aster Pte. Ltd.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

Esco Aster Pte Ltd, part of Esco Lifesciences Group in Singapore, invites a proactive Project Coordinator to join our CQV-focused team. You will plan, coordinate and monitor validation activities across CQV lifecycle in a fast-paced regulated environment.

You will partner with Engineering, Facilities, Manufacturing and Quality to ensure on-time delivery, compliant documentation and risk-managed progress, while developing cross-functional expertise.

Qualifications

• Diploma or Bachelor's in Engineering, Life Sciences or related field; Bachelor's preferred.
• At least 1 year in project coordination/ management in regulated environment.
• Familiar with GxP, GDP, and CQV lifecycle basics.
• Strong organisational and time-management skills; able to work under pressure.

Responsibilities

• Coordinate project plans, schedules, milestones and deliverables.
• Liaise with management and vendors to align requirements and scope.
• Serve as main coordinator between teams and external stakeholders.
• Monitor resources and adjust plans to meet timelines and budgets.
• Support CQV activities including URS, DQ, FAT/SAT, IOQ and PQ.
• Maintain risk tracking, reports and project documentation.

Skills

Project coordination

Project management

GxP familiarity

Documentation practices

CQV lifecycle understanding

Education

Diploma in Engineering or Life Sciences

Bachelor’s degree

Job description

Esco Aster Pte Ltd, part of Esco Lifesciences Group in Singapore, invites a proactive Project Coordinator to join our CQV-focused team. You will plan, coordinate and monitor validation activities across CQV lifecycle in a fast-paced regulated environment.

You will partner with Engineering, Facilities, Manufacturing and Quality to ensure on-time delivery, compliant documentation and risk-managed progress, while developing cross-functional expertise.