Pharmaceutical Engineer - CQV (Contract - Tuas)
at RMA Projects in Geylang, S00, SG. This Full time on site position offers great opportunities for career growth.
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‑down(s) 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.
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, process safety, and pharmaceutical engineering standards.
This role reports to the C\&Q Manager. This role is outsourced to our Client.