CQV Engineer — GMP Pharma & Biopharma Validation

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

Job summary

EFOR in Singapore is seeking a CQV Engineer to support commissioning, qualification and validation activities for pharmaceutical facilities and systems. The role involves preparing URS, FAT, SAT, IQ/OQ/PQ documentation and collaborating with QA, Engineering and Project teams.

Ideal candidates have a degree/diploma in engineering or life sciences and experience in GMP environments. Fresh graduates may be considered for junior opportunities.

Qualifications

• CQV/ C&Q, commissioning, qualification and validation
• Experience in GMP environments
• Familiarity with IQ/OQ/PQ, FAT/SAT and validation docs
• Strong written and verbal communication skills

Responsibilities

• Support commissioning, qualification and validation activities for pharma facilities, equipment and systems
• Prepare and execute URS, FAT, SAT, DQ, IQ, OQ and PQ documentation
• Assist with equipment start-up, commissioning and qualification tasks
• Collaborate with Engineering, QA, Automation and Project teams
• Review technical documents, drawings and vendor docs
• Support deviations, change controls and CQV-related activities
• Ensure all CQV activities align with GMP standards and project requirements

Skills

CQV / C&Q / Commissioning / Validation

GMP experience

IQ/OQ/PQ / FAT/SAT

Documentation skills

Communication skills

Education

Degree/Diploma in Engineering or Life Sciences

Job description

EFOR in Singapore is seeking a CQV Engineer to support commissioning, qualification and validation activities for pharmaceutical facilities and systems. The role involves preparing URS, FAT, SAT, IQ/OQ/PQ documentation and collaborating with QA, Engineering and Project teams.

Ideal candidates have a degree/diploma in engineering or life sciences and experience in GMP environments. Fresh graduates may be considered for junior opportunities.