Quality Engineer – Singapore – Beverage Plant Expansion (Contract Engagement)

The Project: Capex Value - $35m SGD Brownfield Project (Plant Expansion)

The Location: Singapore

Duration & Working Week: 12 Month Contract – Possible extension

40 – 45 hours per week minimum

The Company

Working on behalf of a multidisciplinary project management and design consultancy. This is an international company with a large footprint across the South East Asia, New Zealand and Australian markets.

The Role

• Lead the engineering and execution Quality lifecycle
• Maintain Site Quality Master plan. Responsibilities include oversight for the development, completion, logging and archiving of documentation on protocols, Quality Master Plans, and quality Summary Packages
• Generates the quality schedule, drives execution of workload and monitors performance to plan and tracks status of quality activities and documentation
• Approves quality protocols prior to execution of work, ensuring content is accurate and in a timely manner to meet schedule requirements
• Oversee the development and lead the closure of key validation packages / stages. (DQ, IQ, OQ, PQ)
• Ensure validation packages are following Quality plan and PGCS standards
• Establish and maintain system lifecycle documentation (e.g. Validation Plans/URS/FRS/IQ/OQ/PQ/FAT/SAT/TM) and associated final reports
• Evaluates data from executed validation protocols and ensures summary reports are generated and approved, Ensuring quality, accuracy, and completeness of commissioning, qualification, and validation documentation and deliverables
• Establish quality compliance checklists, FAT checklists and others as required.
• Develop and present project status updates to relevant stakeholders
• Support development and tracking of project related training requirements
• Support HAZOP’s, documentation squad checks, risk assessments, design reviews, workshops and other project related activities.
• Updating relevant PGCS standards as required
• Manage closeout of corrective actions associated with validation activities
• Generates or approves Quality Risk Assessment documents in relation to executed quality activities
• Ensure that the Change Control Procedure is implemented and maintained throughout the project lifecycle

Education / Experience

• Bachelor’s degree in science or engineering and a minimum of 5 years' validation experience in the F&B or pharmaceutical industry
• Hands on quality experience with manufacturing equipment including tanks, Homogenizers, Pumps, sterilizers, parts washer, HVAC, controlled environmental chambers and utilities
• Demonstrated proficiency and knowledge of CGMPs, industry validation practices, and change control practices
• Demonstrated ability to effectively write technical documents, including test plans, protocols, and reports
• Excellent people management skills including collaboration and influencing with key stakeholders

Strong change management skills, experience of driving initiative