CQV Engineer

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

CQV Engineer | Pharmaceutical & Biopharmaceutical Projects | Singapore

Looking for your next CQV opportunity?

We’re looking to connect with CQV Engineers in Singapore who are open to exploring opportunities within the Life Sciences industry.

What you’ll be doing

• Supporting Commissioning, Qualification & Validation activities for pharmaceutical/biopharmaceutical facilities, equipment and systems
• Preparing and executing URS, FAT, SAT, DQ, IQ, OQ and PQ documentation
• Supporting equipment start-up, commissioning and qualification activities
• Working closely with Engineering, QA, Automation and Project teams
• Reviewing technical documentation, drawings and vendor documentation
• Supporting deviations, change controls and other CQV-related activities
• Ensuring activities are carried out in line with GMP and project requirements

What we’re looking for

• Degree/Diploma in Engineering, Life Sciences, Biotechnology, Chemistry or a related discipline
• Experience in CQV / C&Q / Commissioning / Qualification / Validation
• Experience within pharmaceutical, biopharmaceutical or other GMP environments
• Familiarity with IQ/OQ/PQ, FAT/SAT, URS and validation documentation
• Good communication and documentation skills

Fresh graduates with relevant internship/project experience may also be considered for junior opportunities.