Pharmaceutical CQV Engineer Contract Lead

RMA Projects; Singapore; On-site; SGD 70,000 - 100,000; Full time

Job summary

RMA Projects is seeking a Pharmaceutical Engineer - CQV (Contract) for an on-site role in Tuas/Singapore region. The candidate will lead commissioning, qualification and validation activities, develop CQV strategies, and coordinate with EPCM teams and vendors to ensure timely, safe delivery.

The role emphasizes experience in CQV execution, risk-based validation methodologies, and drug linker knowledge, including ATEX and pharmaceutical engineering standards.

Qualifications

• Bachelor degree in Engineering; familiar with Risk Based Validation.
• Extensive experience in areas/systems under future responsibility.
• Minimum of 5 years field CQV execution experience.
• For Drug Linker: knowledge of ATEX, process safety, and pharmaceutical engineering standards.

Responsibilities

• Lead CQV strategy development and execution.
• Plan and execute commissioning activities for allocated areas.
• Coordinate with EPCM/vendors and stakeholders.
• Review CQV test scripts and manage discrepancies and deviations.
• Ensure CQV activities meet site EHS standards and regulatory expectations.

Skills

CQV execution

Risk Based Validation

Field CQV experience

Education

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

Job description

RMA Projects is seeking a Pharmaceutical Engineer - CQV (Contract) for an on-site role in Tuas/Singapore region. The candidate will lead commissioning, qualification and validation activities, develop CQV strategies, and coordinate with EPCM teams and vendors to ensure timely, safe delivery.

The role emphasizes experience in CQV execution, risk-based validation methodologies, and drug linker knowledge, including ATEX and pharmaceutical engineering standards.