Pharmaceutical Engineer - CQV (Contract - Tuas)

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 marymarquez@rmagroup.com.sg and send your resume in MS Word format. Note that only shortlisted candidates will becontacted.

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