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Timestamp
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1792475906
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Fetch Consultant ID
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51
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Unique ID
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1f0a5
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Running No
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10179
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Method
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Solo
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Edit
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No
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Frontend
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True
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Role
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Consultant
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Requestor View
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No
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Status
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Accepted
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| Who's Hiring? |
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Consultant In Charge
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Kimberly Wong
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Company Profile
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Astrazeneca Singapore Pte Ltd
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UEN
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199002462M
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Client Manager
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Mohamed Osman – C – Valid
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Designation
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Global CAPEX Procurement
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Type of Placement
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Contract (KF)
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Urgency
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Normal
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Mode of Communication
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Email
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Visibility
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Publish
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Job Posting Date
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20/10/2026
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Posting Validity (Days)
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30
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| Job Posting Details |
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Enable AI
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No
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| Basic Details |
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Job Title
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Regional C&Q Support
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Job Type
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Contract
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SSOC
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Manufacturing engineer
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Number of Headcount Required
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1
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Expected Date to Join
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01/12/2026
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Work Hours Per Week
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40
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No.
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6
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Period
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Months
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Salary Type
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Range
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Hide Salary
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No
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Negotiable
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Yes
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Currency
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SGD
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Min
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7,000
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Max
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9,000
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Period
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Monthly
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Add Allowance
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No
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| Entitlements |
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Work from home
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No
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Primary Work Location
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Singapore, Singapore
Singapore
Map It
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Nearest MRT station(s)
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Country
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Afghanistan
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| Job-Specific Details |
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Level of Competency
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Senior Position
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Years of Relevant Experience
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5
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Classification
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Technical
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Sector
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Manufacturing
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Project Experience
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- Pharmaceutical Manufacturing
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Specialization
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- Commissioning & Qualification (C&Q)
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Professional Characteristics
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- Pharmaceutical Manufacturing Equipment
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Primary Responsibilities
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- Supplier Coordination and On-site Support: Work primarily at the main supplier’s factory during design, fabrication, Factory Acceptance Testing (FAT), and pre-shipment phases. Travel to and work alongside other vendors or suppliers during critical project execution and preparation, as required.
- C&Q Lifecycle Coordination: Liaise closely with packaged equipment and system suppliers to align on Commissioning and Qualification (C&Q) test approaches and deliverables in accordance with the Validation Master Plan (VMP) and C&Q Execution Plan (CQEP), ensuring adherence to agreed scope, schedule, quality, and safety requirements.
- Stakeholder and Interface Management: Act as the regional focal point between suppliers and internal stakeholders, including the C&Q Program Manager, C&Q Lead, Quality Lead, Subject Matter Experts (SMEs), and System Owners, to align on C&Q requirements and deliverables.
- Supplier Deliverables Management: Manage supplier documentation and deliverables, including Vendor Turnover Packages (VTOPs), Construction Turnover Packages (CTOPs), Inspection Test Plans (ITPs), FAT protocols, and Site Acceptance Testing (SAT) protocols, where applicable.
- Documentation and Readiness Management: Ensure VTOPs are complete and meet quality requirements to facilitate the transition to site C&Q activities, including CTOP, SAT, Installation Qualification (IQ), and Operational Qualification (OQ). Drive supplier readiness for Design Qualification (DQ), pre-FAT, and FAT by ensuring that documentation, test protocols, and systems are aligned and approved before execution.
- Quality and Regulatory Compliance: Ensure all project deliverables comply with applicable regulatory, quality, safety, health and environmental (SHE) standards. Implement global standards and procedures, maintain audit-ready documentation, and ensure adherence to Good Documentation Practices (GDP).
- Technical Design Review: Review supplier design documentation, including P&IDs, specifications, and control strategies, to verify compliance with User Requirement Specifications (URS) and Good Manufacturing Practice (GMP) requirements, where applicable. Identify and escalate construction changes that deviate from approved designs without the required client approval or notification.
- Quality and Performance Monitoring: Establish performance metrics and take corrective action when necessary, particularly in cases involving non-compliance, quality risks, or deviations from approved requirements.
- Project Controls and Reporting: Establish and maintain controls for project risks, changes, issues, and progress. Monitor fabrication, documentation, and construction testing activities, report progress against established baselines and the master plan, and escalate issues while driving recovery actions where required.
- Risk and Constraint Management: Identify and communicate risks and constraints, including fabrication limitations, local practices, and workshop constraints, that may affect project delivery.
- Schedule Management: Own and manage scope schedules, track commitments, forecasts, and variances, and ensure schedule performance remains within approved project parameters.
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| Competencies |
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Minimum Qualifications
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Bachelor's Degree or equivalent
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Specify the Field of Study
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Yes
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Field of Study
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Language Spoken
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Language Written
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Key Skills
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Are the Key Skills selections good enough?
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Yes
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Key Skills
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- C&Q Coordination
- Supplier Management
- FAT/SAT
- GMP Compliance
- Technical Documentation
- Project Scheduling
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| Summary of Key Requirements |
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Must-Have Requirements and Preferences
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- Relevant qualifications or experience in engineering, commissioning and qualification (C&Q), quality assurance, or a related technical discipline.
- Experience coordinating packaged equipment or system suppliers in a manufacturing, engineering, pharmaceutical, or regulated industry environment.
- Familiarity with C&Q lifecycle deliverables, including URS, Requirements Traceability Matrix (RTM), Receipt Verification (RV), ITP, Design Review (DR), Design Qualification (DQ), pre-FAT, FAT, SAT, and vendor turnover documentation.
- Knowledge of Good Manufacturing Practice (GMP), Good Documentation Practices (GDP), quality standards, and applicable regulatory and SHE requirements.
- Ability to review technical design documentation, such as P&IDs, equipment specifications, and control strategies, against approved user requirements.
- Experience in supplier management, documentation review, testing readiness, and project schedule coordination.
- Strong stakeholder management and communication skills, with the ability to coordinate effectively with suppliers, project teams, quality teams, and technical stakeholders.
- Good understanding of project controls, risk management, change management, issue resolution, and progress reporting.
- Willingness to travel and work on-site at supplier facilities, including during design, fabrication, testing, and pre-shipment phases.
- Strong organisational skills and attention to detail, with the ability to manage multiple deliverables and maintain audit-ready documentation.
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Featured
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No
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On Hold
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No
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