Commissioning Support Engineer Back to jobs **Commissioning Support Engineer** **Job details** Posted 22 October 2026 Salary USD Negotiable Start date 02 November 2026 LocationPerth Job type Contract Discipline Pharmaceutical Reference170691 Job Function Commissioning Engineer , Support Engineer **Job description** **Regional C&Q; Support Engineer** **Location:** Singapore (Extensive Regional & International Travel Required) **Contract Position** **About our client** Our client is proud to design and build projects and careers. We are committed to fostering a welcoming and cooperative work environment that encourages big-picture thinking, brings out the best in our personnel, and helps us develop innovative solutions that contribute to building a better world together. If this sounds like a culture you would like to work in, you are invited to apply for this role We are seeking an experienced **Regional C&Q; Support Engineer** to join a major pharmaceutical manufacturing project. This role will play a critical part in supporting Commissioning & Qualification (C&Q;) activities across a network of equipment suppliers, ensuring packaged systems are designed, tested, documented, and delivered in accordance with GMP and project requirements. The successful candidate will act as the key liaison between equipment vendors and the project team, driving C&Q; readiness from design through Factory Acceptance Testing (FAT) and handover to site execution teams. **Key Responsibilities** **Vendor & Supplier Management** + Act as the primary regional point of contact between equipment suppliers and project stakeholders. + Support and coordinate supplier activities throughout the C&Q; lifecycle. + Manage vendor deliverables including Vendor Turnover Packages (VTOPs), FAT protocols, SAT protocols, Inspection Test Plans (ITPs), and associated documentation.



+ Ensure supplier documentation is complete, accurate, and suitable for transition into site qualification activities. **Commissioning & Qualification Support** + Facilitate delivery of key C&Q; documentation including: + User Requirement Specifications (URS) + Requirements Traceability Matrix (RTM) + Design Qualification (DQ) + Receipt Verification (RV) + Factory Acceptance Testing (FAT) + Stage Gate Reviews + Vendor Turnover Packages (VTOP) + Support alignment of supplier testing strategies with Validation Master Plans and C&Q; Execution Plans. + Drive readiness for Design Reviews, Pre-FAT and FAT activities. + Monitor fabrication, testing and documentation progress to ensure systems are delivered ready for qualification. **Quality & Compliance** + Ensure all supplier activities comply with GMP, quality, regulatory and SHE requirements. + Review technical documentation including P&IDs;, specifications and control strategies against project requirements. + Maintain audit-ready documentation and adherence to Good Documentation Practices (GDP). + Identify and escalate quality risks, deviations, design changes and compliance issues. **Project Controls & Reporting** + Track supplier progress, risks, issues and schedule performance. + Provide regular status reporting and recovery planning where required. + Support risk management and change control processes throughout the project lifecycle. + Identify constraints that may impact project delivery and implement mitigation strategies.



**About You** **To be successful in this role, you will ideally have:** + Degree qualification in Engineering or a related technical discipline. + Demonstrated experience in Commissioning, Qualification and Validation (CQV) within pharmaceutical, biotechnology, life sciences, or highly regulated manufacturing environments. + Experience managing vendor-packaged equipment and supplier interfaces. + Strong understanding of GMP requirements and validation methodologies. + Hands-on experience supporting FAT, SAT, Design Qualification (DQ), URS development and Requirements Traceability Matrix (RTM) management. + Ability to review technical documentation, engineering drawings and control system documentation. + Excellent stakeholder management and communication skills. + Strong organisational skills with the ability to manage multiple suppliers and deliverables simultaneously. + Willingness to undertake regional and international travel to supplier facilities as required. **What's on Offer?** + Opportunity to contribute to a major pharmaceutical manufacturing project. + Exposure to global suppliers and advanced manufacturing technologies. + Collaborative project environment with international stakeholders. + Long-term contract opportunity with significant project visibility. If you have a strong background in pharmaceutical CQV and enjoy working at the interface between engineering, suppliers, and quality teams, we'd love to hear from you. We are an equal opportunity employer. All qualified individuals will receive consideration for employment without regard to race; color; age; sex; sexual orientation; gender identity; religion; national origin; disability; veteran status; genetic information; or any other criteria protected by governing law.

📌 Commissioning Support Engineer (Perth)
🏢 Fluor
📍 Perth