CQV Engineer

EFOR; Singapore; On-site; SGD 60,000 - 100,000; Full time

Job summary

EFOR in Singapore is seeking Commissioning, Qualification and Validation (CQV) Engineers to support pharmaceutical and life sciences projects.

You will prepare, execute and review CQV documentation and collaborate with engineering, quality and vendor teams to ensure GMP compliance and audit-ready records.

All experience levels are welcome to apply.

Qualifications

• Experience in CQV within a GMP-regulated environment.
• Knowledge of GMP and validation practices.
• Good documentation and communication skills.
• Eligibility to work in Singapore.

Responsibilities

• Prepare, execute and review CQV documentation.
• Support commissioning and qualification activities for equipment, utilities and facilities.
• Ensure work meets GMP and regulatory requirements.
• Work closely with engineering, quality and vendor teams.
• Maintain audit-ready records.

Skills

CQV experience

GMP knowledge

Documentation skills

Communication skills

Eligibility to work in Singapore

Job description

We are looking for Commissioning, Qualification and Validation (CQV) Engineers to join our pharmaceutical and life sciences clients in Singapore.

Key Responsibilities

• Prepare, execute and review CQV documentation
• Support commissioning and qualification activities for equipment, utilities and facilities
• Ensure work meets GMP and regulatory requirements
• Work closely with engineering, quality and vendor teams
• Maintain accurate, audit-ready records

Requirements

• Experience in CQV within a GMP-regulated environment
• Knowledge of GMP and validation practices
• Good documentation and communication skills
• Eligibility to work in Singapore

All experience levels are welcome to apply.