Commissioning Support Engineer

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 collaborative 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.

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 Valuable Documentation Practices (GDP).





- Identify and elevate 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 pharmaceutic

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