Pharmaceutical Engineer - CQV (Contract - Tuas)

Scope ofWork • 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, proces ssafety, 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 be contacted. By sending us your personal data, you are deemed to consent to RMA Consultants PteLtd and its affiliates collecting, using and disclosing your personal data for the purposes set out in our Data Protection Policy at http://rmabpo.com/policy This is in partnership with the Employment and Employability Institute Pte Ltd (“e2i”). e2i is the empowering network for workers and employers seeking employment and employability solutions. e2i serves as a bridge between workers and employers, connecting with workers to offer job security through job-matching, career guidance and skills upgrading services,and partnering employers to address their manpower needs through recruitment,training, and job redesign solutions. e2i is a tripartite initiative of the National Trades Union Congress set up to support nation-wide manpower and skills upgrading initiatives. By applying for this role, you consent to RMA Group’s PDPA and e2i’s PDPA. EA Licence No: 93C4403 EA Regn No: R1326974