Pharmaceutical Engineer - CQV (Contract - Tuas) at RMA Projects

RMA Projects

Singapore

On-site

SGD 70,000 - 100,000

Full time

9 days ago
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Job summary

RMA Projects is seeking a Pharmaceutical Engineer - CQV (Contract) for an on-site role in Tuas/Singapore region. The candidate will lead commissioning, qualification and validation activities, develop CQV strategies, and coordinate with EPCM teams and vendors to ensure timely, safe delivery.

The role emphasizes experience in CQV execution, risk-based validation methodologies, and drug linker knowledge, including ATEX and pharmaceutical engineering standards.

Qualifications

  • Bachelor degree in Engineering; familiar with Risk Based Validation.
  • Extensive experience in areas/systems under future responsibility.
  • Minimum of 5 years field CQV execution experience.
  • For Drug Linker: knowledge of ATEX, process safety, and pharmaceutical engineering standards.

Responsibilities

  • Lead CQV strategy development and execution.
  • Plan and execute commissioning activities for allocated areas.
  • Coordinate with EPCM/vendors and stakeholders.
  • Review CQV test scripts and manage discrepancies and deviations.
  • Ensure CQV activities meet site EHS standards and regulatory expectations.

Skills

CQV execution
Risk Based Validation
Field CQV experience

Education

Bachelor's degree in Engineering (Chemical, Mechanical, Process, or related discipline)

Job description

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.

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