Lead CQV for Packaging & Warehouse Systems (Pharma)

RMA CONSULTANTS PTE LTD; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

RMA Consultants Pte Ltd is seeking an experienced CQV professional to lead commissioning and qualification activities for a major pharmaceutical facility in Singapore. The role focuses on packaging lines, storage, and serialization systems, with responsibilities spanning strategy development, scheduling, and vendor coordination.

The incumbent will oversee CQV execution with cross-functional teams, ensure adherence to cGMP, and drive documentation quality and regulatory readiness throughout the

Qualifications

• Field CQV execution experience.
• Extensive familiarity with cGMP.
• Knowledge of ATEX, process safety and pharmaceutical engineering standards.

Responsibilities

• Execute and lead CQV activities in accordance with CQV plans and supporting plans.
• Develop strategies and procedures to support execution scope.
• Plan and manage commissioning activities for allocated areas or systems.
• Lead CQV execution with EPCM teams, Engineering, Operations and external vendors.
• Support the development of CQV schedules for the scope.
• Coordinate planning with HSE, Automation, Electrical, Instrumentation and Operations.
• Guide CQV documentation to ensure correctness and alignment across areas/systems.
• Lead start-up, procurement and vendor selection activities.
• Coordinate and interface with vendors for CQV execution.
• Lead meetings to align commissioning preparation and execution.
• Report CQV status and progress at stakeholder meetings.
• Review and approve CQV test scripts.
• Track and remediate discrepancies per CQEP and plan remediation actions.
• Support changes ensuring cost, schedule and compliance.

Skills

CQV execution

cGMP experience

ATEX knowledge

Process safety

Education

Bachelor's degree in Engineering (Chemical, Mechanical, Process, or related)

Third Level or Professional Qualification

Job description

RMA Consultants Pte Ltd is seeking an experienced CQV professional to lead commissioning and qualification activities for a major pharmaceutical facility in Singapore. The role focuses on packaging lines, storage, and serialization systems, with responsibilities spanning strategy development, scheduling, and vendor coordination.

The incumbent will oversee CQV execution with cross-functional teams, ensure adherence to cGMP, and drive documentation quality and regulatory readiness throughout the