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Timestamp
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1781663955
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Fetch Consultant ID
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51
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Unique ID
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b6f62
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Running No
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10100
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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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High
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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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17/06/2026
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Posting Validity (Days)
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90
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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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Equipment Package Lead
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Job Type
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Contract
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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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13/07/2026
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Work Hours Per Week
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40
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Period
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Months
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No.
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1
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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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9,000
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Max
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12,000
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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 339510
Singapore
Map It
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Classifications of Location
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Tuas
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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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- Pharmaceutical Engineering / Biopharmaceutical Manufacturing
- Process Equipment Engineering (GMP-regulated environments)
- Chemical / Mechanical / Process Engineering
- Equipment Package Management (procurement to commissioning)
- High-containment / hazardous chemical handling systems
- Thermal Oxidizer / Scrubber / Solvent systems
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Professional Characteristics
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- Strong ownership mindset for end-to-end equipment delivery
- Hands-on technical problem solver with attention to detail
- Able to manage multiple vendors and stakeholders confidently
- Comfortable working in fast-paced project environments
- Strong coordination and communication across engineering
- QA
- EHS
- and CQV teams
- Proactive
- structured
- quality-driven approach
- Willing to travel for vendor FAT and project support
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Primary Responsibilities
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- The Equipment Package Lead will be responsible for end-to-end technical ownership of assigned process equipment packages for a pharmaceutical manufacturing facility. This includes leading technical procurement, vendor management, design coordination, and execution through installation, commissioning, and qualification phases.
- Lead technical development of equipment packages, including User Requirement Specifications (URS), P&IDs, functional specifications, and RFP documentation. Ensure alignment with GMP, safety (OEB/OEL), containment, CIP/WIP, and ATEX requirements.
- Coordinate cross-functional inputs from engineering, CQV, EHS, QA, and process teams to ensure complete and compliant technical specifications.
- Manage end-to-end vendor selection process, including RFQ issuance, technical/commercial bid evaluations, vendor clarifications, and recommendation reports.
- Serve as primary technical owner for assigned equipment packages (e.g., thermal oxidizers, scrubber systems, solvent storage and transfer systems, and associated utilities).
- Oversee vendor design execution, fabrication progress, and interface coordination with site construction teams.
- Develop and execute Factory Acceptance Testing (FAT) protocols and manage vendor FAT activities.
- Ensure readiness for installation, commissioning, and qualification, including Pre-Startup Safety Review (PSSR), Mechanical Completion, and turnover documentation.
- Support CQV activities, including IQ/OQ execution, validation planning, and risk-based commissioning strategies (ASTM E2500 aligned).
- Enforce construction quality standards through inspection and test plans (ITPs), punch list management, and as-built documentation control.
- Maintain project schedules, risk registers, and provide regular progress updates to the Technical Project Manager.
- Participate in cross-functional project meetings to ensure alignment across engineering, procurement, CQV, operations, EHS, and QA teams.
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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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- Chemical Engineering
- Chemical Process Technology
- Engineering
- Mechanical Engineering
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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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| Summary of Key Requirements |
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Summary of Key Requirements
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- Bachelor’s degree in Chemical, Mechanical, Process, or related engineering discipline.
- Minimum 5 years of experience in pharmaceutical or GMP-regulated manufacturing projects with direct equipment package ownership.
- Strong experience in equipment lifecycle management including design, procurement, FAT/SAT, installation, commissioning, and qualification.
- Technical knowledge of process equipment such as thermal oxidizers, scrubbers, solvent storage and transfer systems, and related utility systems.
- Experience working in GMP environments with knowledge of FDA, EMA, or PIC/S regulatory requirements.
- Familiarity with high-containment or potent compound manufacturing environments is highly preferred.
- Understanding of ATEX, process safety, hazardous chemical handling, and pharmaceutical engineering standards.
- Proven ability to manage vendors, review technical documentation, and resolve engineering issues during execution phases.
- Strong communication and stakeholder management skills across engineering, CQV, EHS, QA, and operations teams.
- Willingness to travel internationally to vendor sites (e.g., China, Europe).
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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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