CQV Engineer

No deviation; Singapore; On-site; SGD 90,000 - 150,000; Full time

Job summary

[Unknown Company] CQV Engineer role in Singapore focuses on commissioning, qualification, validation and lifecycle management of GMP equipment, utilities and controlled temperature storage systems.

The position requires planning temperature mapping studies, developing URS, generating protocols/reports, and periodic reviews to maintain GMP/regulatory compliance throughout the equipment lifecycle.

Qualifications

• Fair knowledge and experience of the practical and theoretical requirement of validation program in a GMP facility.
• Experience in validation of facility, equipment, utility, lab equipment and/or sterilization.
• Familiarity with Regulatory requirements and Standards (e.g., FDA, EMEA, GAMP and ICHQ7)
• Ability to read and interpret technical documentation, system specifications, and validation protocols.
• Strong analytical, problem-solving, and organizational skills.
• Excellent communication skills and ability to work in a team-oriented environment.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
• Willingness to learn and adapt in a fast-paced, regulated industry.

Responsibilities

• Develop, execute, and document IQ, OQ, PQ protocols and reports for new qualification.
• Investigate and resolve discrepancies/incidents arising from qualification activities.
• Perform Periodic review Site Validation Maintenance Program, ensuring systems remain in a validated state throughout their lifecycle.
• Support other day-to-day validation activities, ensuring adherence to approved Validation SOPs, Plans, and Policies.
• Work closely with End-Users, Quality, and Engineering functions to ensure validation activities are completed as planned.

Skills

Validation knowledge

Analytical skills

Communication skills

Kneat

Trackwise

Tools

Kneat

Trackwise

Job description

Position Overview

The CQV Engineer is responsible for the commissioning, qualification, validation, and lifecycle management of GMP equipment, utilities, and controlled temperature storage systems. The role involves planning and executing temperature mapping studies, developing User Requirement Specifications (URS), generating qualification protocols and reports, and performing periodic reviews to ensure continued compliance with GMP and regulatory requirements.

Position Overview

The CQV Engineer is responsible for the commissioning, qualification, validation, and lifecycle management of GMP equipment, utilities, and controlled temperature storage systems. The role involves planning and executing temperature mapping studies, developing User Requirement Specifications (URS), generating qualification protocols and reports, and performing periodic reviews to ensure continued compliance with GMP and regulatory requirements.

Key Responsibilities

• Develop, execute, and document protocols (IQ, OQ, PQ) and reports for new qualification.
• Investigate and resolve discrepancies/incidents arising from qualification activities.
• Perform Periodic review Site Validation Maintenance Program, ensuring systems remain in a validated state throughout their lifecycle.
• Support other day-to-day validation activities, ensuring adherence to approved Validation SOPs, Plans, and Policies.
• Work closely with End-Users, Quality, and Engineering functions to ensure validation activities are completed as planned.,

Required Qualifications

• Fair knowledge and experience of the practical and theoretical requirement of validation program in a GMP facility
• Relevant experience in validation of facility, equipment, utility, lab equipment and/or sterilization
• Familiarity with Regulatory requirements and Standards (e.g., FDA, EMEA, GAMP and ICHQ7)
• Ability to read and interpret technical documentation, system specifications, and validation protocols.
• Strong analytical, problem-solving, and organizational skills.
• Excellent communication skills and ability to work in a team-oriented environment.
• Proficiency in electronic systems such as Kneat and Trackwise will be a plus.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook).
• Willingness to learn and adapt in a fast-paced, regulated industry.