Editorial summary

The company is seeking a Pharmaceutical Engineer specialized in Commissioning, Qualification, and Validation (CQV) for a contract position in Tuas, with a salary of SGD 20,000. The role involves developing strategies and procedures, planning and executing commissioning activities, and leading C&Q efforts in collaboration with EPC teams, engineering, operations, and external vendors. Candidates should have experience in CQV activities within pharmaceutical or related industries. The position offers an opportunity to contribute to critical validation projects within a dynamic environment.

This summary is AI-generated and may contain inaccuracies. Please refer to the full job description below.

Job description

[This job https://singapore.job-q.com/jobs/detail/pharmaceutical-engineer-cqv-contract-tuas-34888 first appeared in Job-Q.com on 28 Sep 2026]

Scope of Work

• Ensure that Commissioning, Qualification, and Validation (CQV) activities are executed in accordance with the Commissioning and Qualification (C&Q) Execution Plan and supporting Plans.
• Development of strategies and procedures that support their execution scope.
• Overall planning and execution of the commissioning activities related to allocated areas or systems.
• Leading and coordinating the C&Q execution effort supported by C&Q EPC teams,Engineering, Operations, and external vendors and contractors
• Support development of C&Q schedule for associated scope.
• Coordinating the planning and scheduling of activities with supporting disciplines (HSE,Automation, Electrical, Instrumentation, Operation and Engineering, etc.
• Guiding C&Q documentation preparation effort to ensure correctness, completeness and alignment across different areas/systems.
• Lead preparation activities (e.g. start-up, procurement, vendors selection, etc)
• Coordination and interfacing with vendors for C&Q execution related activities.
• Lead coordination meetings to fine-tune the commissioning preparation and execution with all involved parties
• Reporting of C&Q status, progress and issues during project stakeholders meetings (e.g.Tier 2 meetings, Wall meetings).
• Review and approve CQV test scripts
• Ensure discrepancies encountered are adequately reviewed and approved in accordance with CQEP. Tracking of these deficiencies, including planning and executing there mediation actions
• Support the control of changes, ensuring cost, schedule and compliance are correctly assessed.
• C&Q execution milestones are completed as per baseline schedule
• Ensures C&Q field execution is completed in a safely manner and following Site EHS standards. 
• Liaising with EPCM/Vendors on design and construction issues.
• Participate in construction walk-downs and snag list of these systems for Mechanical Completion.
• Ensure that quality standards are followed during C&Q execution. No significant observations in external regulatory inspections for allocated process area.
• This role reports to the C&Q Manager
• This role is outsourced to our Client.

Requirements

• Bachelor's degree in Engineering (Chemical, Mechanical, Process, or related discipline)
• Familiar with methodologies related Risk Based Validation
• Extensive experience in areas/systems under future responsibility. Minimum of 5 years is preferable
• Field CQV execution experience. 
• For Drug Linker: Knowledge of ATEX, processsafety, and pharmaceutical engineering standards

If you are keen to know more about this role, please email Mary at and send your resume in MS Word format. Note that only shortlisted candidates will becontacted.

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